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    will contact tutor – 2 years ago **files (1)** – ## W1Assignment.docx **## W1Assignment.docx** 5 **Set The Change for Change** 2 4 ## 1 **Identifying Organizational Change Using Kotter’s 8-Step Process** **Introduction** This means that change is another key factor central for sustaining long-run su…

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    **files (1)**

    – ## W1Assignment.docx

    **## W1Assignment.docx**

    5

    **Set The Change for Change**

    2

    4

    ## 1

    **Identifying Organizational Change Using Kotter’s 8-Step Process**

    **Introduction**

    This means that change is another key factor central for sustaining long-run success, even though it poses significant concerns to organizations as well as individuals. In both personal and business environments, bringing effective change involves planning, teaming, and acting now. This paper is centered on a plan for implementing change in a selected organization and Kotter’s 8-Step Change Model as a theoretical guide (Williams et al., 2023). The proposed institution for this study is a healthcare clinic in which strategic transformations are required to enhance synchronized points concerning those gaps in clinic appointment schedules. The context of the organization in question, the change that is required, and why the change is required are described in this paper – why this situation is perfect for implementing Kotter’s framework.

    **Context of the Organization**

    The organization chosen for this analysis is a mid-sized primary care and chronic disease clinic. This clinic targets diverse people, whereby about 60% of the patients are from disadvantaged background. Even though the clinic is reputed to offer quality services, patient appointment has proved to be a major issue. At the moment, appointments are often blocked by time, often booked by more than one patient, or rescheduled as a result of silent conflict between administration personnel.

    The clinic works with a limited number of employees in the administration while providing scheduling services for more than 20 physicians and NP’s. Scheduling is still cumbersome and mostly paper based or complete reliance on word of mouth. Therefore, patients are able to be envious and have to wait a lot of time, and this gives a poor impression of the care, not to mention lost time to make some important interventions. More so, there is enormous pressure in the number of patients each clinician attends to that leads to compromise of the circulation time through presentation of unscheduled appointments that affect job satisfaction among clinicians.

    **The Change Needed**

    To satisfy these demands, the clinic needs a sufficient modification of the existing system of appointments’ taking. The proposed change is shifting from a manual system of scheduling to an integrated EHR schedule with a scheduling component. It will replace manual appointment bookings because it will help the clinic give the patients real time updates on their appointments and the patients will be able to book their appointments online. Enacting this change will involve a training of staff, modification of operational procedures and cooperation from all employees across all ranks.

    **Why the Change is Needed**

    This has to occur for several reasons. First, the current scheduling system causes tactics that introduce the waste, patient frustrations, and resulting high no-show percentages. The literature review also shows that ineffective and inefficient management of appointments is a major factor in reduced access to quality health care, especially in minority communities (Kim et al., 2022). When used as the clinic has done above, an EHR can help reduce time wastage, eliminate scheduling errors that are always associated with manual systems, and serve the intended clientele within the time that is required.

    Second, on the issue of scheduling, there is sufficient evidence to support that there is a problem that results in cost implications on the clinic. He resigned to the fact that unscheduled appointments and wrong schedules result in reduced revenue and more bills to pay. These problems can be reduced by implementing an integrated scheduling mechanism, which will enhance resources management as well as clinic workflow.

    In addition, this change is also inevitable to boost staff morale and staff retention. While the administrative staff complained of stress brought by manual schedule, the clinicians complained of stress brought by changes in their schedules at the last moment. These challenges lead to burnout which is becoming rampant in healthcare organizations (Dennis et al., 2021). These stressors can be reduced by adopting a less complex system an aspect that helps increase personnel satisfaction and efficiency.

    **Why the Organization is a Good Candidate for the Project**

    The healthcare clinic is the right place for this project as it is already prepared for the change and it will be seen tangible benefits once the scheduling system is improved. The leaders of the organization have verbally conveyed some form of intended adoption of technology in enhancing their operation hence a good sign of embracing change. Moreover, the clinic is rather small to introduce and analyze modifications because it does not have many layers of management compared to the large-scale organizations.

    More importantly, this change has undertaken the clinic’s goal of delivering quality and personalized services. Depending on the organization of the work schedule, the clinic can optimize the accessibility of its services and respond to the background of patients’ inequalities, which, in turn, will contribute to improving the outcomes of patients’ treatment. Looking beyond the specifics of this organization, another benefit of the proper completion of this plan is the fact that it can and should be used by other similar clinics that face comparable difficulties and obstacles to those outlined above.

    **Conclusion**

    Therefore, there is the need to transform the functions of the healthcare clinic and to integrate an EHR-based scheduling system. Using Kotter’s 8-Step Change Model, changes are possible and easy to achieve because the organization is able to handle the change process carefully, engage the stakeholders and get their support. The clinic is prepared for change, and due to possible advantages for patients, employees, and financial results, it is suitable for this project. At the end of this course, the outlined steps of Kotter’s model are going to be used to outline a detailed successful implementation plan.

    **References**

    Kim, H., Park, S., & Lee, J. (2022). Barriers to access and strategies for improvement in healthcare appointment scheduling: A systematic review. Journal of Health Management, 24(2), 145-160.
    [https://doi.org/10.1177/09720634211058034](https://doi.org/10.1177/09720634211058034)

    Dennis, R., Johnson, T., & Nguyen, P. (2021). Addressing staff burnout in healthcare: The role of technology in improving work environments. Journal of Occupational Health Psychology, 26(4), 372-382.
    [https://doi.org/10.1037/ocp0000302](https://doi.org/10.1037/ocp0000302)

    Williams, L., Carter, E., & Davis, M. (2023). Electronic health records as a tool for reducing disparities in healthcare access: Evidence from community clinics. Health Informatics Journal, 29(1), 45-60.
    [https://doi.org/10.1177/14604582221106187](https://doi.org/10.1177/14604582221106187)

    **## W1Assignment.docx**

    5

    **Set The Change for Change**

    2

    4

    ## 1

    **Identifying Organizational Change Using Kotter’s 8-Step Process**

    **Introduction**

    This means that change is another key factor central for sustaining long-run success, even though it poses significant concerns to organizations as well as individuals. In both personal and business environments, bringing effective change involves planning, teaming, and acting now. This paper is centered on a plan for implementing change in a selected organization and Kotter’s 8-Step Change Model as a theoretical guide (Williams et al., 2023). The proposed institution for this study is a healthcare clinic in which strategic transformations are required to enhance synchronized points concerning those gaps in clinic appointment schedules. The context of the organization in question, the change that is required, and why the change is required are described in this paper – why this situation is perfect for implementing Kotter’s framework.

    **Context of the Organization**

    The organization chosen for this analysis is a mid-sized primary care and chronic disease clinic. This clinic targets diverse people, whereby about 60% of the patients are from disadvantaged background. Even though the clinic is reputed to offer quality services, patient appointment has proved to be a major issue. At the moment, appointments are often blocked by time, often booked by more than one patient, or rescheduled as a result of silent conflict between administration personnel.

    The clinic works with a limited number of employees in the administration while providing scheduling services for more than 20 physicians and NP’s. Scheduling is still cumbersome and mostly paper based or complete reliance on word of mouth. Therefore, patients are able to be envious and have to wait a lot of time, and this gives a poor impression of the care, not to mention lost time to make some important interventions. More so, there is enormous pressure in the number of patients each clinician attends to that leads to compromise of the circulation time through presentation of unscheduled appointments that affect job satisfaction among clinicians.

    **The Change Needed**

    To satisfy these demands, the clinic needs a sufficient modification of the existing system of appointments’ taking. The proposed change is shifting from a manual system of scheduling to an integrated EHR schedule with a scheduling component. It will replace manual appointment bookings because it will help the clinic give the patients real time updates on their appointments and the patients will be able to book their appointments online. Enacting this change will involve a training of staff, modification of operational procedures and cooperation from all employees across all ranks.

    **Why the Change is Needed**

    This has to occur for several reasons. First, the current scheduling system causes tactics that introduce the waste, patient frustrations, and resulting high no-show percentages. The literature review also shows that ineffective and inefficient management of appointments is a major factor in reduced access to quality health care, especially in minority communities (Kim et al., 2022). When used as the clinic has done above, an EHR can help reduce time wastage, eliminate scheduling errors that are always associated with manual systems, and serve the intended clientele within the time that is required.

    Second, on the issue of scheduling, there is sufficient evidence to support that there is a problem that results in cost implications on the clinic. He resigned to the fact that unscheduled appointments and wrong schedules result in reduced revenue and more bills to pay. These problems can be reduced by implementing an integrated scheduling mechanism, which will enhance resources management as well as clinic workflow.

    In addition, this change is also inevitable to boost staff morale and staff retention. While the administrative staff complained of stress brought by manual schedule, the clinicians complained of stress brought by changes in their schedules at the last moment. These challenges lead to burnout which is becoming rampant in healthcare organizations (Dennis et al., 2021). These stressors can be reduced by adopting a less complex system an aspect that helps increase personnel satisfaction and efficiency.

    **Why the Organization is a Good Candidate for the Project**

    The healthcare clinic is the right place for this project as it is already prepared for the change and it will be seen tangible benefits once the scheduling system is improved. The leaders of the organization have verbally conveyed some form of intended adoption of technology in enhancing their operation hence a good sign of embracing change. Moreover, the clinic is rather small to introduce and analyze modifications because it does not have many layers of management compared to the large-scale organizations.

    More importantly, this change has undertaken the clinic’s goal of delivering quality and personalized services. Depending on the organization of the work schedule, the clinic can optimize the accessibility of its services and respond to the background of patients’ inequalities, which, in turn, will contribute to improving the outcomes of patients’ treatment. Looking beyond the specifics of this organization, another benefit of the proper completion of this plan is the fact that it can and should be used by other similar clinics that face comparable difficulties and obstacles to those outlined above.

    **Conclusion**

    Therefore, there is the need to transform the functions of the healthcare clinic and to integrate an EHR-based scheduling system. Using Kotter’s 8-Step Change Model, changes are possible and easy to achieve because the organization is able to handle the change process carefully, engage the stakeholders and get their support. The clinic is prepared for change, and due to possible advantages for patients, employees, and financial results, it is suitable for this project. At the end of this course, the outlined steps of Kotter’s model are going to be used to outline a detailed successful implementation plan.

    **References**

    Kim, H., Park, S., & Lee, J. (2022). Barriers to access and strategies for improvement in healthcare appointment scheduling: A systematic review. Journal of Health Management, 24(2), 145-160.
    [https://doi.org/10.1177/09720634211058034](https://doi.org/10.1177/09720634211058034)

    Dennis, R., Johnson, T., & Nguyen, P. (2021). Addressing staff burnout in healthcare: The role of technology in improving work environments. Journal of Occupational Health Psychology, 26(4), 372-382.
    [https://doi.org/10.1037/ocp0000302](https://doi.org/10.1037/ocp0000302)

    Williams, L., Carter, E., & Davis, M. (2023). Electronic health records as a tool for reducing disparities in healthcare access: Evidence from community clinics. Health Informatics Journal, 29(1), 45-60.
    [https://doi.org/10.1177/14604582221106187](https://doi.org/10.1177/14604582221106187)

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    1. Describe causes of Upper respiratory infections and drug therapy 2. Discuss triggers of asthma and treatment options 3. Discuss corticosteroids 4. Describe chronic bronchitis and treatment options **Submission Instructions:** – Your initial post should be at least **500 words**, formatted and cit…

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    1. Describe causes of Upper respiratory infections and drug therapy
    2. Discuss triggers of asthma and treatment options
    3. Discuss corticosteroids
    4. Describe chronic bronchitis and treatment options

    **Submission Instructions:**

    – Your initial post should be at least **500 words**, formatted and cited in the current APA style with support from at least 2 academic sources.

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    1. Describe health and illness practices that may augment problems associated with the treatment of hypertension for Chinese-American clients. 2. Describe the locus-of-control variable that some Filipino Americans have that may influence health-seeking behavior. 3. Describe the importance of folk me…

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    1. Describe health and illness practices that may augment problems associated with the treatment of hypertension for Chinese-American clients.
    2. Describe the locus-of-control variable that some Filipino Americans have that may influence health-seeking behavior.
    3. Describe the importance of folk medicine and folk healers to Vietnamese Americans.

    **Submission Instructions:**

    – Your initial post should be at least 500 words, formatted, and cited in current APA style with support from at least 2 academic sources.

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    [>Management homework help](https://www.sweetstudy.com/fields/business-finance-management) I need your help – 2 years ago **files (3)** – ## Week4Assignment_BUS402CreatingaSmallBusinessFormatExample.docx – Creatingasmallbusiness.jpeg – BusinessPlan.jpeg **## Week4Assignment_BUS402CreatingaSmallBus…

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    – ## Week4Assignment_BUS402CreatingaSmallBusinessFormatExample.docx

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    **## Week4Assignment_BUS402CreatingaSmallBusinessFormatExample.docx**

    Creating a Small Business

    Your Name

    Small Business Management – BUS402 – Summer Quarter

    Professor Name

    Date

    **Introduction**

    Provide a brief introduction to your paper, outlining what the reader can expect to learn. This can include the importance of having a clear strategy when starting a business and a mention of the business idea you're developing.

    **Description of Business/Name**

    Describe the idea for your prospective small business. Provide details such as the nature of the business, the products or services it will offer, and why you believe this business will succeed in its market. Clearly state the name of the business and any relevant reasoning behind the name choice.

    **Competition**

    Identify the key competitors in the industry or niche. Choose one competitor and provide a summary of its strengths and weaknesses. Consider what sets your competitor apart and how your business will differentiate itself.

    **Mission**

    Draft a mission statement for your business. The mission statement should clearly define the purpose of your business, what it aims to achieve, and its target market.

    **Type of Ownership**

    Identify and explain the form of ownership you have selected for your business. Discuss factors such as tax implications, liability exposure, managerial ability, and the cost of formation. Justify why this ownership structure is best suited for your business.

    **Conclusion**

    Summarize the key points of your business strategy, reinforcing the importance of a strong plan for success.

    **Sources**

    List your references here, ensuring you include at least two sources outside of the textbook.

    **Creatingasmallbusiness.jpeg**

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    **BusinessPlan.jpeg**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/businessplan-jpeg-10177145)

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    **## Week4Assignment_BUS402CreatingaSmallBusinessFormatExample.docx**

    Creating a Small Business

    Your Name

    Small Business Management – BUS402 – Summer Quarter

    Professor Name

    Date

    **Introduction**

    Provide a brief introduction to your paper, outlining what the reader can expect to learn. This can include the importance of having a clear strategy when starting a business and a mention of the business idea you're developing.

    **Description of Business/Name**

    Describe the idea for your prospective small business. Provide details such as the nature of the business, the products or services it will offer, and why you believe this business will succeed in its market. Clearly state the name of the business and any relevant reasoning behind the name choice.

    **Competition**

    Identify the key competitors in the industry or niche. Choose one competitor and provide a summary of its strengths and weaknesses. Consider what sets your competitor apart and how your business will differentiate itself.

    **Mission**

    Draft a mission statement for your business. The mission statement should clearly define the purpose of your business, what it aims to achieve, and its target market.

    **Type of Ownership**

    Identify and explain the form of ownership you have selected for your business. Discuss factors such as tax implications, liability exposure, managerial ability, and the cost of formation. Justify why this ownership structure is best suited for your business.

    **Conclusion**

    Summarize the key points of your business strategy, reinforcing the importance of a strong plan for success.

    **Sources**

    List your references here, ensuring you include at least two sources outside of the textbook.

    **Creatingasmallbusiness.jpeg**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/creatingasmallbusiness-jpeg)

    **BusinessPlan.jpeg**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/businessplan-jpeg-10177145)

    **## Week4Assignment_BUS402CreatingaSmallBusinessFormatExample.docx**

    Creating a Small Business

    Your Name

    Small Business Management – BUS402 – Summer Quarter

    Professor Name

    Date

    **Introduction**

    Provide a brief introduction to your paper, outlining what the reader can expect to learn. This can include the importance of having a clear strategy when starting a business and a mention of the business idea you're developing.

    **Description of Business/Name**

    Describe the idea for your prospective small business. Provide details such as the nature of the business, the products or services it will offer, and why you believe this business will succeed in its market. Clearly state the name of the business and any relevant reasoning behind the name choice.

    **Competition**

    Identify the key competitors in the industry or niche. Choose one competitor and provide a summary of its strengths and weaknesses. Consider what sets your competitor apart and how your business will differentiate itself.

    **Mission**

    Draft a mission statement for your business. The mission statement should clearly define the purpose of your business, what it aims to achieve, and its target market.

    **Type of Ownership**

    Identify and explain the form of ownership you have selected for your business. Discuss factors such as tax implications, liability exposure, managerial ability, and the cost of formation. Justify why this ownership structure is best suited for your business.

    **Conclusion**

    Summarize the key points of your business strategy, reinforcing the importance of a strong plan for success.

    **Sources**

    List your references here, ensuring you include at least two sources outside of the textbook.

    **Creatingasmallbusiness.jpeg**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/creatingasmallbusiness-jpeg)

    **BusinessPlan.jpeg**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/businessplan-jpeg-10177145)

  • [Solved] summary writing

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    summary writing for each research paper into 200 to 300 words. need to make sure no plagiarism and no AI. – 2 years ago **files (5)** – ## HygienequalityandpresenceofESBL-producingEscherichiacoliinrawfooddietsfordogs.pdf – EstimationofEscherichiacoliinrawgroundbeef.pdf – Theriskofsalmonellaeshedding…

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    **files (5)**

    – ## HygienequalityandpresenceofESBL-producingEscherichiacoliinrawfooddietsfordogs.pdf

    – EstimationofEscherichiacoliinrawgroundbeef.pdf
    – TheriskofsalmonellaesheddingbydogsfedSalmonella-contaminated.pdf
    – Rawmeat-baseddietforpetsaneglectedsourceofhumanexposuretoSalmonellaandpathogenicEscherichiacoliclonescarryingmcr2019toJanuary2020.pdf
    – MicrobiologicalQualityandPresenceofFoodbornePathogensinRawandExtrudedCanineDietsandCanineFecalSamples.pdf

    **## HygienequalityandpresenceofESBL-producingEscherichiacoliinrawfooddietsfordogs.pdf**

    ORIGINAL RESEARCH ARTICLE

    Hygiene quality and presence of ESBL-producing
    Escherichia coli in raw food diets for dogs

    Oskar Nilsson, DVM, BSc, PhD*

    Department of Animal Health and Antimicrobial Strategies, National Veterinary Institute, Uppsala, Sweden

    Background: Raw food diets are popular among some dog owners, even though there are concerns regarding

    the infectious disease risk and public health implications. Hence, the two aims of this study were to investigate

    the hygiene quality of raw food diets for dogs in the Swedish market and if Escherichia coli with transferable

    resistance to extended spectrum cephalosporins (ESC) was present in such products.

    Methods: Samples of raw food diets were suspended and further diluted in 0.9% saline. Appropriate dilutions

    were 1) cultured on PetrifilmTMSEC to quantify the amount of E. coli in the samples and 2) mixed with

    cefotaxime to a final concentration of 1 mg/L and cultured on PetrifilmTMSEC to quantify the amount of

    ESC-resistant E. coli in the samples. Furthermore, undiluted suspensions were mixed 1:1 with double strength

    MacConkey broth with cefotaxime, enriched overnight and finally cultured on MacConkey agar with

    cefotaxime (1 mg/L). Suspected ESC-resistant E. coli were screened by PCR for genes encoding extended

    spectrum beta lactamases and plasmid-mediated AmpC and their susceptibility to a panel of antimicrobials

    was performed by broth microdilution using VetMIC GN-mo.

    Results: Escherichia coli was isolated from all samples (n�39) and ESC-resistant E. coli was isolated from

    nine samples (23%). All ESC-resistant E. coli were PCR-positive for the blaCMY-2 group and only one of them

    was also resistant to a non-beta-lactam antibiotic.

    Conclusion: The results of this study indicate that raw food diets could be a source of ESC-resistant E. coli to

    dogs and highlight the need for maintaining good hygiene when handling these products to prevent infection.

    Keywords: BARF; raw food diet; ESBL; AmpC; E. coli

    *Correspondence to: Oskar Nilsson, Department of Animal Health and Antimicrobial Strategies, National

    Veterinary Institute, SE-751 89 Uppsala, Sweden, Email: Oskar.Nilsson@sva.se

    Received: 4 June 2015; Revised: 23 September 2015; Accepted: 25 September 2015; Published: 20 October 2015

    R
    aw food diets are popular among some dog owners,

    despite concerns regarding infectious disease risk

    and public health (1, 2). The focus has mainly

    been regarding the presence of Salmonella spp. as a

    potential pathogen (3�7). Another concern would be

    the presence of antibiotic-resistant bacteria, for example,

    Enterobacteriaceae with transferable resistance to ex-

    tended spectrum cephalosporins (ESC) due to extended

    spectrum beta lactamases (ESBL) or plasmid-mediated

    AmpC (pAmpC). Bacteria with such resistance are a

    problem in human medicine and have been identified

    in farm animals as well as in raw food diet products (3, 8).

    In Sweden and Norway, ESBL and pAmpC are only

    occasionally isolated from farm animals other than broilers

    (9, 10). In Finland, the occurrence of ESBL and pAmpC

    in poultry is lower than in many other countries (11).

    As by-products from broiler slaughter are sometimes

    used to manufacture raw food diet products, we identified

    such diets as a potential source of ESBL and pAmpC to

    dogs (12). It could also act as a source of antibiotic-

    resistant microorganisms for people caring for the dogs

    (13). The aim of this study was to investigate if Escherichia

    coli with transferable resistance to ESC was present in

    raw food diets for dogs in the Swedish market. In addition

    the hygiene quality of the products was assessed by quan-

    tification of E. coli present in the raw food diets.

    Materials and methods
    Frozen samples of raw food diet products containing

    poultry were purchased in shops in and around Uppsala,

    Sweden, and from one Swedish internet shop, and stored

    at �208C until analysed. Samples were thawed at 38C;

    25 mL of saline (0.9%) was added to 25 g of feed and

    treated for 30 sec at 230 rpm in a Stomacher (Stomacher

    400 circulator, Seward, UK) before ]7 mL of liquid was

    removed. Dilutions of 1:10 and 1:1,000 were prepared in

    0.9% saline for quantitative isolation of E. coli and 1 mL of

    each dilution was cultured on PetrifilmTMSEC (3M Health

    infection ecology &
    epidemiology

    T h e O n e H e a l t h J o u r n a l

    �

    Infection Ecology and Epidemiology 2015. # 2015 Oskar Nilsson. This is an Open Access article distributed under the terms of the Creative Commons
    Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), permitting all non-commercial use, distribution, and
    reproduction in any medium, provided the original work is properly cited.

    1

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758
    (page number not for citation purpose)

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    Care, St Paul, USA) and incubated at 378C overnight.

    For quantitative isolation of ESC-resistant E. coli, a 1 mL

    aliquot of the undiluted suspension was mixed with 10 mL

    of cefotaxime solution (0.1 mg/mL; Sigma Aldrich, China)

    to create a final concentration of 1 mg/L before the mixture

    was cultured on PetrifilmTMSEC as above. For qualitative

    isolation of ESC-resistant E. coli, 5 mL of double strength

    MacConkey broth (Lab M, Lancashire, UK) with cefo-

    taxime (2 mg/L) was added to a 5 mL aliquot and in-

    cubated at 378C overnight before 0.1 mL was streaked on

    MacConkey agar (Difco, Hampshire, UK) with cefotax-

    ime (1 mg/L) and incubated at 378C overnight.

    Suspected E. coli colonies were confirmed by sub-

    culture on horse blood agar (Oxoid, Basingstoke, UK) and

    an indole test conducted. Furthermore, suspected ESC-

    resistant E. coli were screened by PCR for genes encoding

    ESBL and pAmpC, that is, the gene groups CTX-M-1,

    CTX-M-2, CTX-M-8, CTX-M-9, CTX-M-25/26, MOX,

    CIT, DHA, ACC, EBC, FOX, OXA-1, SHV, and TEM

    (14). The number of E. coli or ESC-resistant E. coli on

    each PetrifilmTMSEC was recorded.

    Susceptibility testing of all ESC-resistant E. coli to a

    panel of antimicrobials was performed by broth micro-

    dilution using VetMIC GN-mo (SVA, Uppsala, Sweden)

    according to standards of the CLSI (15). The E. coli

    reference strains ATCC 25922 were used for quality

    control and the results were interpreted according to

    epidemiological cut-off values issued by EUCAST (www.

    eucast.org, retrieved 2015-09-17; Table 1).

    Results
    Altogether, 39 samples of eight different raw dog food

    brands (1�11 samples/brand) were analysed. Depending on

    the brand, the products contained by-products from animals

    slaughtered in Finland (n�10), Norway (n�11), or Sweden

    (n�18). Of the 39 samples, 22 contained only by-products

    from poultry, whereas 17 contained by-products from

    several animal species including poultry.

    Escherichia coli was isolated from all 39 samples. In

    34 (87%) of the samples, the amount of E. coli was higher

    than 5�101 CFU/g, in 19 (49%) the amount was higher

    than 5�102 CFU/g, and in 2 (5%) the amount was

    higher than 5�104 CFU/g.

    ESC-resistant E. coli was isolated from nine samples

    (23%) and all isolates were PCR-positive for the blaCMY-2

    group. The products with ESC-resistant E. coli originated

    from Norway (n�3, 27%) or Sweden (n�6, 33%) and

    contained either only poultry by-products (n�7, 32%)

    or by-products from several animal species (n�2, 12%).

    The number of colony forming units (CFU) of ESC-

    resistant E. coli/gram could be calculated in five of the

    nine samples, all of which were 510 CFU/g. All of these

    samples were products that contained by-products exclu-

    sively from poultry.

    Only one of the ESC-resistant E. coli was also resistant

    to a non-beta-lactam antibiotic (Table 1). That isolate

    was also resistant to kanamycin.

    Discussion
    It was not unexpected that ESC-resistant E. coli could be

    isolated from raw food diet products containing poultry.

    ESC-resistant E. coli bacteria is commonly isolated from

    poultry in Europe and ESC-resistant Enterobacteriaceae

    in raw food diet products has previously been described

    (3, 8). Furthermore, studies have demonstrated an increased

    risk of shedding of ESC-resistant Enterobacteriaceae

    Table 1. Antibiogram of the nine Escherichia coli isolates with transferable resistance to extended spectrum cephalosporins isolated

    from raw food diets for dogs

    Resistance pattern

    Isolate Am Ctx Caz Ci Nal Gm Sm Tc Ff Cs Su Trim Cm Km

    1 64 �2 8 0.06 4 1 16 51 8 50.5 16 0.25 4 58

    2 128 �2 8 0.06 2 1 8 51 54 50.5 32 0.25 52 58

    3 128 �2 8 0.06 2 0.5 8 51 54 50.5 16 0.5 4 58

    4 64 �2 4 0.06 2 1 8 51 54 1 58 0.25 4 58

    5 64 �2 8 0.06 4 1 8 51 54 2 16 0.5 4 58

    6 64 �2 16 0.06 2 1 8 51 54 2 16 0.5 4 58

    7 �128 �2 �16 0.06 4 1 8 51 54 1 58 0.5 4 58

    8 128 �2 8 0.06 2 1 8 2 8 1 16 0.5 4 58

    9 64 �2 4 0.06 4 0.5 8 51 8 1 16 0.25 4 16

    Bold and shaded figures indicate MIC above the epidemiological cut-off values issued by EUCAST (www.eucast.org, retrieved

    2015-09-17).

    Antimicrobials included and cut-off values (mg/L) used are ampicillin (Am, �8), cefotaxime (Ctx, �0.25), ceftazidime (Caz, �0.5),

    ciprofloxacin (Ci, �0.06), nalidixic acid (Nal, �16), gentamicin (Gm, �2), streptomycin (Sm, �16), tetracyclin (Tc, �8), florfenicol

    (Ff, �16), coliston (Cs, �2), sulfamethoxazole (Su, �64), trimetoprim (Trim, �2), chloramphenicol (Cm, �16), kanamycin (Km, �8).

    Oskar Nilsson

    2
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    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    among dogs fed raw food diets or raw meat in Canada

    and the United Kingdom (16, 17). Together, this indicates

    that raw food diets can also be a source of ESC-resistant

    Enterobacteriaceae for dogs in Sweden. The risk probably

    relates to feeding non-heat-treated animal products, re-

    gardless of whether it is in the form of commercial diets

    or not, as indicated by the previously reported increased

    risk of shedding ESC-resistant E. coli in dogs fed raw meat

    (17). In addition, the occurrence of ESC-resistant E. coli

    in the products originating from Norway and Sweden in

    this study is comparable to their prevalence in samples of

    broiler meat in these two countries (9, 10).

    Poultry from Finland, Sweden, or Norway was an

    ingredient in all investigated products, and blaCMY-2 is the

    dominant gene among ESC-resistant Enterobacteriaceae

    from broilers in those countries (9�11). Therefore, it is

    likely that most of the isolated ESC-resistant E. coli would

    have a gene in the blaCMY-2 group. Although the isolates

    were not sequenced in this study, one could speculate that

    it will be the blaCMY-2 gene that confers resistance as

    all ESC-resistant E. coli isolates from Swedish poultry

    identified to date has carried blaCMY-2 (9). The resistance

    pattern of the isolates is also similar to those which have

    been described for isolates from poultry in Norway and

    Sweden (9, 10).

    The occurrence of E. coli in all products is comparable

    to or higher than in previous studies (5, 18). The isolation

    frequency of E. coli is comparable to that of broiler meat

    95%), but considerably higher than that of pork (20%)

    reported in the Swedish surveillance program Svarm (9).

    Although E. coli could be isolated from all samples, it

    should be noted that only two of the products contained

    more E. coli than the maximum limit of coliform bacteria

    (5�104 CFU/g) recommended by the Swedish Board of

    Agriculture for animal feed materials of animal origin

    (SJVFS 2011:40). Nineteen of the products contained

    �5�102 CFU/g E. coli and would therefore have been

    considered of unsatisfactory hygiene quality had they

    been minced or mechanically separated meat intended for

    human consumption (EC 2073/2005). According to this

    regulation, a batch of minced or mechanically separated

    meat is also classified as having unsatisfactory hygienic

    quality if more than two of five samples contain between

    5�101 and 5�102 CFU E. coli per gram. In this study,

    15 of the 39 products tested contained that amount of

    E. coli. However, as only one sample from each batch

    was analysed, it is not possible to know if they had been

    classified as having unsatisfactory hygiene quality or not

    unless additional samples were analysed. The high inci-

    dence of E. coli in these raw food diets highlights the

    need for maintaining good hygiene when handling these

    products to prevent infection.

    Raw food diets for dogs are not intended for human

    consumption. However, it is likely that they are handled in

    kitchens where food for human consumption is also handled.

    Thereby there is a possibility of cross-contamination and

    a subsequent exposure of humans to bacteria from the

    raw food diet products. The major concern would be

    transient colonisation with ESC-resistant E. coli which

    may allow gene transfer to E. coli adapted to the human

    gut, resulting in prolonged colonisation with resistant

    coliforms as a consequence (19). Thus, raw food diets

    could constitute a source of ESC-resistant E. coli not

    only for dogs but also for humans. However, at this time,

    there are no indications of spread of ESC-resistant E. coli

    from broiler meat to humans in Sweden (20). Hence, the

    risk of spread from raw food diets to humans is probably

    low, but this relies on good hygiene being maintained

    when handling these products.

    Acknowledgements

    Kerstin Ekström, Annica Landén, and Mattias Myrenås are all

    acknowledged for skilled technical assistance and Björn Bengtsson

    is acknowledged for valuable discussions.

    Conflict of interest and funding
    The study was funded by a grant from the Swedish Board

    of Agriculture. The author has no conflict of interest to

    declare.

    References

    1. LeJeune JT, Hancock DD. Public health concerns associated

    with feeding raw meat diets to dogs. J Am Vet Med Assoc 2001;

    219: 1222�5.

    2. Schlesinger DP, Joffe DJ. Raw food diets in companion animals:

    a critical review. Can Vet J 2011; 52: 50�4.

    3. Finley R, Reid-Smith R, Ribble C, Popa M, Vandermeer M,

    Aramini J. The occurrence and antimicrobial susceptibility of

    salmonellae isolated from commercially available canine raw

    food diets in three Canadian cities. Zoonoses Public Health

    2008; 55: 462�9.

    4. Mehlenbacher S, Churchill J, Olsen KE, Bender JB. Availability,

    brands, labelling and Salmonella contamination of raw pet food

    in the Minneapolis/St. Paul area. Zoonoses Public Health 2012;

    59: 513�20.

    5. Weese JS, Rousseau J, Arroyo L. Bacteriological evaluation

    of commercial canine and feline raw diets. Can Vet J 2005; 46:

    513�16.

    6. Chengappa MM, Staats J, Oberst RD, Gabbert NH, McVey S.

    Prevalence of Salmonella in raw meat used in diets of racing

    greyhounds. J Vet Diagn Invest 1993; 5: 372�7.

    7. Joffe DJ, Schlesinger DP. Preliminary assessment of the risk

    of Salmonella infection in dogs fed raw chicken diets. Can Vet J

    2002; 43: 441�2.

    8. Seiffert SN, Hilty M, Perreten V, Endimiani A. Extended-

    spectrum cephalosporin-resistant Gram-negative organisms in

    livestock: an emerging problem for human health? Drug Resist

    Updat 2013; 16: 22�45.

    9. SVARM. Swedish Veterinary Antimicrobial Resistance Mon-

    itoring. ISSN 1650�6332. Available from: http://www.sva.se/en/

    antibiotics-/svarm-reports [cited 23 September 2015].

    10. Mo SS, Norstrom M, Slettemeas JS, Lovland A, Urdahl AM,

    Sunde M. Emergence of AmpC-producing Escherichia coli in

    ESBL-producing E. coli in raw food diet products

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758 3
    (page number not for citation purpose)

    [http://www.sva.se/en/antibiotics-/svarm-reports](http://www.sva.se/en/antibiotics-/svarm-reports)

    [http://www.sva.se/en/antibiotics-/svarm-reports](http://www.sva.se/en/antibiotics-/svarm-reports)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    the broiler production chain in a country with a low anti-

    microbial usage profile. Vet Microbiol 2014; 171: 315�20.

    11. Finnish Food Safety Authority. Finnish veterinary antimicro-

    bial resistance monitoring and consumption of antimicrobial

    agents. FINRES-Vet 2010�2012. Helsinki, Finland: Evira

    publications; 2015.

    12. Case LP, Daristotle L, Hayek MG, Raasch MR. Nutrient

    content of pet food. In: Case LP, Daristotle L, Hayek MG,

    Raasch MR (Eds.). Canine and feline nutrition: a resource for

    companion animal professionals. 3rd ed. Maryland Heights,

    MO: Mosby; 2011, pp. 141�62.

    13. Ewers C, Grobbel M, Bethe A, Wieler LH, Guenther S.

    Extended-spectrum beta-lactamases-producing gram-negative

    bacteria in companion animals: action is clearly warranted!.

    Berl Munch Tierarztl Wochenschr 2011; 124: 94�101.

    14. Nilsson O, Borjesson S, Landen A, Bengtsson B. Vertical

    transmission of Escherichia coli carrying plasmid-mediated

    AmpC (pAmpC) through the broiler production pyramid. J

    Antimicrob Chemother 2014; 69: 1497�500.

    15. Clinical and Laboratory Standards Institute (2013). Perfor-

    mance standards for antimicrobial disc and dilution susceptibi-

    lity tests for bacteria isolated from animals; approved standard.

    4th ed. Wayne, PA: CLSI.

    16. Lefebvre SL, Reid-Smith R, Boerlin P, Weese JS. Evaluation of

    the risks of shedding Salmonellae and other potential pathogens

    by therapy dogs fed raw diets in Ontario and Alberta. Zoonoses

    Public Health 2008; 55: 470�80.

    17. Schmidt VM, Pinchbeck GL, Nuttall T, McEwan N, Dawson S,

    Williams NJ. Antimicrobial resistance risk factors and char-

    acterisation of faecal E. coli isolated from healthy Labrador

    retrievers in the United Kingdom. Prev Vet Med 2015; 119:

    31�40.

    18. Strohmeyer RA, Morley PS, Hyatt DR, Dargatz DA, Scorza

    AV, Lappin MR. Evaluation of bacterial and protozoal con-

    tamination of commercially available raw meat diets for dogs. J

    Am Vet Med Assoc 2006; 228: 537�42.

    19. Smet A, Rasschaert G, Martel A, Persoons D, Dewulf J,

    Butaye P, et al. In situ ESBL conjugation from avian to human

    Escherichia coli during cefotaxime administration. J Appl

    Microbiol 2011; 110: 541�9.

    20. Borjesson S, Jernberg C, Brolund A, Edquist P, Finn M, Landen

    A, et al. Characterization of plasmid-mediated AmpC-producing

    E. coli from Swedish broilers and association with human

    clinical isolates. Clin Microbiol Infect 2013; 19: E309�11.

    Oskar Nilsson

    4
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    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    **EstimationofEscherichiacoliinrawgroundbeef.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/estimationofescherichiacoliinrawgroundbeef-pdf)

    **TheriskofsalmonellaesheddingbydogsfedSalmonella-contaminated.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/theriskofsalmonellaesheddingbydogsfedsalmonella-contaminated-pdf)

    **Rawmeat-baseddietforpetsaneglectedsourceofhumanexposuretoSalmonellaandpathogenicEscherichiacoliclonescarryingmcr2019toJanuary2020.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/rawmeat-baseddietforpetsaneglectedsourceofhumanexposuretosalmonellaandpathogenicescherichiacoliclonescarryingmcr2019tojanuary2020-pdf)

    **MicrobiologicalQualityandPresenceofFoodbornePathogensinRawandExtrudedCanineDietsandCanineFecalSamples.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/microbiologicalqualityandpresenceoffoodbornepathogensinrawandextrudedcaninedietsandcaninefecalsamples-pdf)

    **MicrobiologicalQualityandPresenceofFoodbornePathogensinRawandExtrudedCanineDietsandCanineFecalSamples.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/microbiologicalqualityandpresenceoffoodbornepathogensinrawandextrudedcaninedietsandcaninefecalsamples-pdf)

    **## HygienequalityandpresenceofESBL-producingEscherichiacoliinrawfooddietsfordogs.pdf**

    ORIGINAL RESEARCH ARTICLE

    Hygiene quality and presence of ESBL-producing
    Escherichia coli in raw food diets for dogs

    Oskar Nilsson, DVM, BSc, PhD*

    Department of Animal Health and Antimicrobial Strategies, National Veterinary Institute, Uppsala, Sweden

    Background: Raw food diets are popular among some dog owners, even though there are concerns regarding

    the infectious disease risk and public health implications. Hence, the two aims of this study were to investigate

    the hygiene quality of raw food diets for dogs in the Swedish market and if Escherichia coli with transferable

    resistance to extended spectrum cephalosporins (ESC) was present in such products.

    Methods: Samples of raw food diets were suspended and further diluted in 0.9% saline. Appropriate dilutions

    were 1) cultured on PetrifilmTMSEC to quantify the amount of E. coli in the samples and 2) mixed with

    cefotaxime to a final concentration of 1 mg/L and cultured on PetrifilmTMSEC to quantify the amount of

    ESC-resistant E. coli in the samples. Furthermore, undiluted suspensions were mixed 1:1 with double strength

    MacConkey broth with cefotaxime, enriched overnight and finally cultured on MacConkey agar with

    cefotaxime (1 mg/L). Suspected ESC-resistant E. coli were screened by PCR for genes encoding extended

    spectrum beta lactamases and plasmid-mediated AmpC and their susceptibility to a panel of antimicrobials

    was performed by broth microdilution using VetMIC GN-mo.

    Results: Escherichia coli was isolated from all samples (n�39) and ESC-resistant E. coli was isolated from

    nine samples (23%). All ESC-resistant E. coli were PCR-positive for the blaCMY-2 group and only one of them

    was also resistant to a non-beta-lactam antibiotic.

    Conclusion: The results of this study indicate that raw food diets could be a source of ESC-resistant E. coli to

    dogs and highlight the need for maintaining good hygiene when handling these products to prevent infection.

    Keywords: BARF; raw food diet; ESBL; AmpC; E. coli

    *Correspondence to: Oskar Nilsson, Department of Animal Health and Antimicrobial Strategies, National

    Veterinary Institute, SE-751 89 Uppsala, Sweden, Email: Oskar.Nilsson@sva.se

    Received: 4 June 2015; Revised: 23 September 2015; Accepted: 25 September 2015; Published: 20 October 2015

    R
    aw food diets are popular among some dog owners,

    despite concerns regarding infectious disease risk

    and public health (1, 2). The focus has mainly

    been regarding the presence of Salmonella spp. as a

    potential pathogen (3�7). Another concern would be

    the presence of antibiotic-resistant bacteria, for example,

    Enterobacteriaceae with transferable resistance to ex-

    tended spectrum cephalosporins (ESC) due to extended

    spectrum beta lactamases (ESBL) or plasmid-mediated

    AmpC (pAmpC). Bacteria with such resistance are a

    problem in human medicine and have been identified

    in farm animals as well as in raw food diet products (3, 8).

    In Sweden and Norway, ESBL and pAmpC are only

    occasionally isolated from farm animals other than broilers

    (9, 10). In Finland, the occurrence of ESBL and pAmpC

    in poultry is lower than in many other countries (11).

    As by-products from broiler slaughter are sometimes

    used to manufacture raw food diet products, we identified

    such diets as a potential source of ESBL and pAmpC to

    dogs (12). It could also act as a source of antibiotic-

    resistant microorganisms for people caring for the dogs

    (13). The aim of this study was to investigate if Escherichia

    coli with transferable resistance to ESC was present in

    raw food diets for dogs in the Swedish market. In addition

    the hygiene quality of the products was assessed by quan-

    tification of E. coli present in the raw food diets.

    Materials and methods
    Frozen samples of raw food diet products containing

    poultry were purchased in shops in and around Uppsala,

    Sweden, and from one Swedish internet shop, and stored

    at �208C until analysed. Samples were thawed at 38C;

    25 mL of saline (0.9%) was added to 25 g of feed and

    treated for 30 sec at 230 rpm in a Stomacher (Stomacher

    400 circulator, Seward, UK) before ]7 mL of liquid was

    removed. Dilutions of 1:10 and 1:1,000 were prepared in

    0.9% saline for quantitative isolation of E. coli and 1 mL of

    each dilution was cultured on PetrifilmTMSEC (3M Health

    infection ecology &
    epidemiology

    T h e O n e H e a l t h J o u r n a l

    �

    Infection Ecology and Epidemiology 2015. # 2015 Oskar Nilsson. This is an Open Access article distributed under the terms of the Creative Commons
    Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), permitting all non-commercial use, distribution, and
    reproduction in any medium, provided the original work is properly cited.

    1

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758
    (page number not for citation purpose)

    [http://creativecommons.org/licenses/by-nc/4.0/](http://creativecommons.org/licenses/by-nc/4.0/)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    Care, St Paul, USA) and incubated at 378C overnight.

    For quantitative isolation of ESC-resistant E. coli, a 1 mL

    aliquot of the undiluted suspension was mixed with 10 mL

    of cefotaxime solution (0.1 mg/mL; Sigma Aldrich, China)

    to create a final concentration of 1 mg/L before the mixture

    was cultured on PetrifilmTMSEC as above. For qualitative

    isolation of ESC-resistant E. coli, 5 mL of double strength

    MacConkey broth (Lab M, Lancashire, UK) with cefo-

    taxime (2 mg/L) was added to a 5 mL aliquot and in-

    cubated at 378C overnight before 0.1 mL was streaked on

    MacConkey agar (Difco, Hampshire, UK) with cefotax-

    ime (1 mg/L) and incubated at 378C overnight.

    Suspected E. coli colonies were confirmed by sub-

    culture on horse blood agar (Oxoid, Basingstoke, UK) and

    an indole test conducted. Furthermore, suspected ESC-

    resistant E. coli were screened by PCR for genes encoding

    ESBL and pAmpC, that is, the gene groups CTX-M-1,

    CTX-M-2, CTX-M-8, CTX-M-9, CTX-M-25/26, MOX,

    CIT, DHA, ACC, EBC, FOX, OXA-1, SHV, and TEM

    (14). The number of E. coli or ESC-resistant E. coli on

    each PetrifilmTMSEC was recorded.

    Susceptibility testing of all ESC-resistant E. coli to a

    panel of antimicrobials was performed by broth micro-

    dilution using VetMIC GN-mo (SVA, Uppsala, Sweden)

    according to standards of the CLSI (15). The E. coli

    reference strains ATCC 25922 were used for quality

    control and the results were interpreted according to

    epidemiological cut-off values issued by EUCAST (www.

    eucast.org, retrieved 2015-09-17; Table 1).

    Results
    Altogether, 39 samples of eight different raw dog food

    brands (1�11 samples/brand) were analysed. Depending on

    the brand, the products contained by-products from animals

    slaughtered in Finland (n�10), Norway (n�11), or Sweden

    (n�18). Of the 39 samples, 22 contained only by-products

    from poultry, whereas 17 contained by-products from

    several animal species including poultry.

    Escherichia coli was isolated from all 39 samples. In

    34 (87%) of the samples, the amount of E. coli was higher

    than 5�101 CFU/g, in 19 (49%) the amount was higher

    than 5�102 CFU/g, and in 2 (5%) the amount was

    higher than 5�104 CFU/g.

    ESC-resistant E. coli was isolated from nine samples

    (23%) and all isolates were PCR-positive for the blaCMY-2

    group. The products with ESC-resistant E. coli originated

    from Norway (n�3, 27%) or Sweden (n�6, 33%) and

    contained either only poultry by-products (n�7, 32%)

    or by-products from several animal species (n�2, 12%).

    The number of colony forming units (CFU) of ESC-

    resistant E. coli/gram could be calculated in five of the

    nine samples, all of which were 510 CFU/g. All of these

    samples were products that contained by-products exclu-

    sively from poultry.

    Only one of the ESC-resistant E. coli was also resistant

    to a non-beta-lactam antibiotic (Table 1). That isolate

    was also resistant to kanamycin.

    Discussion
    It was not unexpected that ESC-resistant E. coli could be

    isolated from raw food diet products containing poultry.

    ESC-resistant E. coli bacteria is commonly isolated from

    poultry in Europe and ESC-resistant Enterobacteriaceae

    in raw food diet products has previously been described

    (3, 8). Furthermore, studies have demonstrated an increased

    risk of shedding of ESC-resistant Enterobacteriaceae

    Table 1. Antibiogram of the nine Escherichia coli isolates with transferable resistance to extended spectrum cephalosporins isolated

    from raw food diets for dogs

    Resistance pattern

    Isolate Am Ctx Caz Ci Nal Gm Sm Tc Ff Cs Su Trim Cm Km

    1 64 �2 8 0.06 4 1 16 51 8 50.5 16 0.25 4 58

    2 128 �2 8 0.06 2 1 8 51 54 50.5 32 0.25 52 58

    3 128 �2 8 0.06 2 0.5 8 51 54 50.5 16 0.5 4 58

    4 64 �2 4 0.06 2 1 8 51 54 1 58 0.25 4 58

    5 64 �2 8 0.06 4 1 8 51 54 2 16 0.5 4 58

    6 64 �2 16 0.06 2 1 8 51 54 2 16 0.5 4 58

    7 �128 �2 �16 0.06 4 1 8 51 54 1 58 0.5 4 58

    8 128 �2 8 0.06 2 1 8 2 8 1 16 0.5 4 58

    9 64 �2 4 0.06 4 0.5 8 51 8 1 16 0.25 4 16

    Bold and shaded figures indicate MIC above the epidemiological cut-off values issued by EUCAST (www.eucast.org, retrieved

    2015-09-17).

    Antimicrobials included and cut-off values (mg/L) used are ampicillin (Am, �8), cefotaxime (Ctx, �0.25), ceftazidime (Caz, �0.5),

    ciprofloxacin (Ci, �0.06), nalidixic acid (Nal, �16), gentamicin (Gm, �2), streptomycin (Sm, �16), tetracyclin (Tc, �8), florfenicol

    (Ff, �16), coliston (Cs, �2), sulfamethoxazole (Su, �64), trimetoprim (Trim, �2), chloramphenicol (Cm, �16), kanamycin (Km, �8).

    Oskar Nilsson

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    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

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    among dogs fed raw food diets or raw meat in Canada

    and the United Kingdom (16, 17). Together, this indicates

    that raw food diets can also be a source of ESC-resistant

    Enterobacteriaceae for dogs in Sweden. The risk probably

    relates to feeding non-heat-treated animal products, re-

    gardless of whether it is in the form of commercial diets

    or not, as indicated by the previously reported increased

    risk of shedding ESC-resistant E. coli in dogs fed raw meat

    (17). In addition, the occurrence of ESC-resistant E. coli

    in the products originating from Norway and Sweden in

    this study is comparable to their prevalence in samples of

    broiler meat in these two countries (9, 10).

    Poultry from Finland, Sweden, or Norway was an

    ingredient in all investigated products, and blaCMY-2 is the

    dominant gene among ESC-resistant Enterobacteriaceae

    from broilers in those countries (9�11). Therefore, it is

    likely that most of the isolated ESC-resistant E. coli would

    have a gene in the blaCMY-2 group. Although the isolates

    were not sequenced in this study, one could speculate that

    it will be the blaCMY-2 gene that confers resistance as

    all ESC-resistant E. coli isolates from Swedish poultry

    identified to date has carried blaCMY-2 (9). The resistance

    pattern of the isolates is also similar to those which have

    been described for isolates from poultry in Norway and

    Sweden (9, 10).

    The occurrence of E. coli in all products is comparable

    to or higher than in previous studies (5, 18). The isolation

    frequency of E. coli is comparable to that of broiler meat

    95%), but considerably higher than that of pork (20%)

    reported in the Swedish surveillance program Svarm (9).

    Although E. coli could be isolated from all samples, it

    should be noted that only two of the products contained

    more E. coli than the maximum limit of coliform bacteria

    (5�104 CFU/g) recommended by the Swedish Board of

    Agriculture for animal feed materials of animal origin

    (SJVFS 2011:40). Nineteen of the products contained

    �5�102 CFU/g E. coli and would therefore have been

    considered of unsatisfactory hygiene quality had they

    been minced or mechanically separated meat intended for

    human consumption (EC 2073/2005). According to this

    regulation, a batch of minced or mechanically separated

    meat is also classified as having unsatisfactory hygienic

    quality if more than two of five samples contain between

    5�101 and 5�102 CFU E. coli per gram. In this study,

    15 of the 39 products tested contained that amount of

    E. coli. However, as only one sample from each batch

    was analysed, it is not possible to know if they had been

    classified as having unsatisfactory hygiene quality or not

    unless additional samples were analysed. The high inci-

    dence of E. coli in these raw food diets highlights the

    need for maintaining good hygiene when handling these

    products to prevent infection.

    Raw food diets for dogs are not intended for human

    consumption. However, it is likely that they are handled in

    kitchens where food for human consumption is also handled.

    Thereby there is a possibility of cross-contamination and

    a subsequent exposure of humans to bacteria from the

    raw food diet products. The major concern would be

    transient colonisation with ESC-resistant E. coli which

    may allow gene transfer to E. coli adapted to the human

    gut, resulting in prolonged colonisation with resistant

    coliforms as a consequence (19). Thus, raw food diets

    could constitute a source of ESC-resistant E. coli not

    only for dogs but also for humans. However, at this time,

    there are no indications of spread of ESC-resistant E. coli

    from broiler meat to humans in Sweden (20). Hence, the

    risk of spread from raw food diets to humans is probably

    low, but this relies on good hygiene being maintained

    when handling these products.

    Acknowledgements

    Kerstin Ekström, Annica Landén, and Mattias Myrenås are all

    acknowledged for skilled technical assistance and Björn Bengtsson

    is acknowledged for valuable discussions.

    Conflict of interest and funding
    The study was funded by a grant from the Swedish Board

    of Agriculture. The author has no conflict of interest to

    declare.

    References

    1. LeJeune JT, Hancock DD. Public health concerns associated

    with feeding raw meat diets to dogs. J Am Vet Med Assoc 2001;

    219: 1222�5.

    2. Schlesinger DP, Joffe DJ. Raw food diets in companion animals:

    a critical review. Can Vet J 2011; 52: 50�4.

    3. Finley R, Reid-Smith R, Ribble C, Popa M, Vandermeer M,

    Aramini J. The occurrence and antimicrobial susceptibility of

    salmonellae isolated from commercially available canine raw

    food diets in three Canadian cities. Zoonoses Public Health

    2008; 55: 462�9.

    4. Mehlenbacher S, Churchill J, Olsen KE, Bender JB. Availability,

    brands, labelling and Salmonella contamination of raw pet food

    in the Minneapolis/St. Paul area. Zoonoses Public Health 2012;

    59: 513�20.

    5. Weese JS, Rousseau J, Arroyo L. Bacteriological evaluation

    of commercial canine and feline raw diets. Can Vet J 2005; 46:

    513�16.

    6. Chengappa MM, Staats J, Oberst RD, Gabbert NH, McVey S.

    Prevalence of Salmonella in raw meat used in diets of racing

    greyhounds. J Vet Diagn Invest 1993; 5: 372�7.

    7. Joffe DJ, Schlesinger DP. Preliminary assessment of the risk

    of Salmonella infection in dogs fed raw chicken diets. Can Vet J

    2002; 43: 441�2.

    8. Seiffert SN, Hilty M, Perreten V, Endimiani A. Extended-

    spectrum cephalosporin-resistant Gram-negative organisms in

    livestock: an emerging problem for human health? Drug Resist

    Updat 2013; 16: 22�45.

    9. SVARM. Swedish Veterinary Antimicrobial Resistance Mon-

    itoring. ISSN 1650�6332. Available from: http://www.sva.se/en/

    antibiotics-/svarm-reports [cited 23 September 2015].

    10. Mo SS, Norstrom M, Slettemeas JS, Lovland A, Urdahl AM,

    Sunde M. Emergence of AmpC-producing Escherichia coli in

    ESBL-producing E. coli in raw food diet products

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758 3
    (page number not for citation purpose)

    [http://www.sva.se/en/antibiotics-/svarm-reports](http://www.sva.se/en/antibiotics-/svarm-reports)

    [http://www.sva.se/en/antibiotics-/svarm-reports](http://www.sva.se/en/antibiotics-/svarm-reports)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    the broiler production chain in a country with a low anti-

    microbial usage profile. Vet Microbiol 2014; 171: 315�20.

    11. Finnish Food Safety Authority. Finnish veterinary antimicro-

    bial resistance monitoring and consumption of antimicrobial

    agents. FINRES-Vet 2010�2012. Helsinki, Finland: Evira

    publications; 2015.

    12. Case LP, Daristotle L, Hayek MG, Raasch MR. Nutrient

    content of pet food. In: Case LP, Daristotle L, Hayek MG,

    Raasch MR (Eds.). Canine and feline nutrition: a resource for

    companion animal professionals. 3rd ed. Maryland Heights,

    MO: Mosby; 2011, pp. 141�62.

    13. Ewers C, Grobbel M, Bethe A, Wieler LH, Guenther S.

    Extended-spectrum beta-lactamases-producing gram-negative

    bacteria in companion animals: action is clearly warranted!.

    Berl Munch Tierarztl Wochenschr 2011; 124: 94�101.

    14. Nilsson O, Borjesson S, Landen A, Bengtsson B. Vertical

    transmission of Escherichia coli carrying plasmid-mediated

    AmpC (pAmpC) through the broiler production pyramid. J

    Antimicrob Chemother 2014; 69: 1497�500.

    15. Clinical and Laboratory Standards Institute (2013). Perfor-

    mance standards for antimicrobial disc and dilution susceptibi-

    lity tests for bacteria isolated from animals; approved standard.

    4th ed. Wayne, PA: CLSI.

    16. Lefebvre SL, Reid-Smith R, Boerlin P, Weese JS. Evaluation of

    the risks of shedding Salmonellae and other potential pathogens

    by therapy dogs fed raw diets in Ontario and Alberta. Zoonoses

    Public Health 2008; 55: 470�80.

    17. Schmidt VM, Pinchbeck GL, Nuttall T, McEwan N, Dawson S,

    Williams NJ. Antimicrobial resistance risk factors and char-

    acterisation of faecal E. coli isolated from healthy Labrador

    retrievers in the United Kingdom. Prev Vet Med 2015; 119:

    31�40.

    18. Strohmeyer RA, Morley PS, Hyatt DR, Dargatz DA, Scorza

    AV, Lappin MR. Evaluation of bacterial and protozoal con-

    tamination of commercially available raw meat diets for dogs. J

    Am Vet Med Assoc 2006; 228: 537�42.

    19. Smet A, Rasschaert G, Martel A, Persoons D, Dewulf J,

    Butaye P, et al. In situ ESBL conjugation from avian to human

    Escherichia coli during cefotaxime administration. J Appl

    Microbiol 2011; 110: 541�9.

    20. Borjesson S, Jernberg C, Brolund A, Edquist P, Finn M, Landen

    A, et al. Characterization of plasmid-mediated AmpC-producing

    E. coli from Swedish broilers and association with human

    clinical isolates. Clin Microbiol Infect 2013; 19: E309�11.

    Oskar Nilsson

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    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    **EstimationofEscherichiacoliinrawgroundbeef.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/estimationofescherichiacoliinrawgroundbeef-pdf)

    **TheriskofsalmonellaesheddingbydogsfedSalmonella-contaminated.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/theriskofsalmonellaesheddingbydogsfedsalmonella-contaminated-pdf)

    **Rawmeat-baseddietforpetsaneglectedsourceofhumanexposuretoSalmonellaandpathogenicEscherichiacoliclonescarryingmcr2019toJanuary2020.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/rawmeat-baseddietforpetsaneglectedsourceofhumanexposuretosalmonellaandpathogenicescherichiacoliclonescarryingmcr2019tojanuary2020-pdf)

    **MicrobiologicalQualityandPresenceofFoodbornePathogensinRawandExtrudedCanineDietsandCanineFecalSamples.pdf**

    This file is too large to display. [View in new window](https://www.sweetstudy.com/files/microbiologicalqualityandpresenceoffoodbornepathogensinrawandextrudedcaninedietsandcaninefecalsamples-pdf)

    **## HygienequalityandpresenceofESBL-producingEscherichiacoliinrawfooddietsfordogs.pdf**

    ORIGINAL RESEARCH ARTICLE

    Hygiene quality and presence of ESBL-producing
    Escherichia coli in raw food diets for dogs

    Oskar Nilsson, DVM, BSc, PhD*

    Department of Animal Health and Antimicrobial Strategies, National Veterinary Institute, Uppsala, Sweden

    Background: Raw food diets are popular among some dog owners, even though there are concerns regarding

    the infectious disease risk and public health implications. Hence, the two aims of this study were to investigate

    the hygiene quality of raw food diets for dogs in the Swedish market and if Escherichia coli with transferable

    resistance to extended spectrum cephalosporins (ESC) was present in such products.

    Methods: Samples of raw food diets were suspended and further diluted in 0.9% saline. Appropriate dilutions

    were 1) cultured on PetrifilmTMSEC to quantify the amount of E. coli in the samples and 2) mixed with

    cefotaxime to a final concentration of 1 mg/L and cultured on PetrifilmTMSEC to quantify the amount of

    ESC-resistant E. coli in the samples. Furthermore, undiluted suspensions were mixed 1:1 with double strength

    MacConkey broth with cefotaxime, enriched overnight and finally cultured on MacConkey agar with

    cefotaxime (1 mg/L). Suspected ESC-resistant E. coli were screened by PCR for genes encoding extended

    spectrum beta lactamases and plasmid-mediated AmpC and their susceptibility to a panel of antimicrobials

    was performed by broth microdilution using VetMIC GN-mo.

    Results: Escherichia coli was isolated from all samples (n�39) and ESC-resistant E. coli was isolated from

    nine samples (23%). All ESC-resistant E. coli were PCR-positive for the blaCMY-2 group and only one of them

    was also resistant to a non-beta-lactam antibiotic.

    Conclusion: The results of this study indicate that raw food diets could be a source of ESC-resistant E. coli to

    dogs and highlight the need for maintaining good hygiene when handling these products to prevent infection.

    Keywords: BARF; raw food diet; ESBL; AmpC; E. coli

    *Correspondence to: Oskar Nilsson, Department of Animal Health and Antimicrobial Strategies, National

    Veterinary Institute, SE-751 89 Uppsala, Sweden, Email: Oskar.Nilsson@sva.se

    Received: 4 June 2015; Revised: 23 September 2015; Accepted: 25 September 2015; Published: 20 October 2015

    R
    aw food diets are popular among some dog owners,

    despite concerns regarding infectious disease risk

    and public health (1, 2). The focus has mainly

    been regarding the presence of Salmonella spp. as a

    potential pathogen (3�7). Another concern would be

    the presence of antibiotic-resistant bacteria, for example,

    Enterobacteriaceae with transferable resistance to ex-

    tended spectrum cephalosporins (ESC) due to extended

    spectrum beta lactamases (ESBL) or plasmid-mediated

    AmpC (pAmpC). Bacteria with such resistance are a

    problem in human medicine and have been identified

    in farm animals as well as in raw food diet products (3, 8).

    In Sweden and Norway, ESBL and pAmpC are only

    occasionally isolated from farm animals other than broilers

    (9, 10). In Finland, the occurrence of ESBL and pAmpC

    in poultry is lower than in many other countries (11).

    As by-products from broiler slaughter are sometimes

    used to manufacture raw food diet products, we identified

    such diets as a potential source of ESBL and pAmpC to

    dogs (12). It could also act as a source of antibiotic-

    resistant microorganisms for people caring for the dogs

    (13). The aim of this study was to investigate if Escherichia

    coli with transferable resistance to ESC was present in

    raw food diets for dogs in the Swedish market. In addition

    the hygiene quality of the products was assessed by quan-

    tification of E. coli present in the raw food diets.

    Materials and methods
    Frozen samples of raw food diet products containing

    poultry were purchased in shops in and around Uppsala,

    Sweden, and from one Swedish internet shop, and stored

    at �208C until analysed. Samples were thawed at 38C;

    25 mL of saline (0.9%) was added to 25 g of feed and

    treated for 30 sec at 230 rpm in a Stomacher (Stomacher

    400 circulator, Seward, UK) before ]7 mL of liquid was

    removed. Dilutions of 1:10 and 1:1,000 were prepared in

    0.9% saline for quantitative isolation of E. coli and 1 mL of

    each dilution was cultured on PetrifilmTMSEC (3M Health

    infection ecology &
    epidemiology

    T h e O n e H e a l t h J o u r n a l

    �

    Infection Ecology and Epidemiology 2015. # 2015 Oskar Nilsson. This is an Open Access article distributed under the terms of the Creative Commons
    Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), permitting all non-commercial use, distribution, and
    reproduction in any medium, provided the original work is properly cited.

    1

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758
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    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    Care, St Paul, USA) and incubated at 378C overnight.

    For quantitative isolation of ESC-resistant E. coli, a 1 mL

    aliquot of the undiluted suspension was mixed with 10 mL

    of cefotaxime solution (0.1 mg/mL; Sigma Aldrich, China)

    to create a final concentration of 1 mg/L before the mixture

    was cultured on PetrifilmTMSEC as above. For qualitative

    isolation of ESC-resistant E. coli, 5 mL of double strength

    MacConkey broth (Lab M, Lancashire, UK) with cefo-

    taxime (2 mg/L) was added to a 5 mL aliquot and in-

    cubated at 378C overnight before 0.1 mL was streaked on

    MacConkey agar (Difco, Hampshire, UK) with cefotax-

    ime (1 mg/L) and incubated at 378C overnight.

    Suspected E. coli colonies were confirmed by sub-

    culture on horse blood agar (Oxoid, Basingstoke, UK) and

    an indole test conducted. Furthermore, suspected ESC-

    resistant E. coli were screened by PCR for genes encoding

    ESBL and pAmpC, that is, the gene groups CTX-M-1,

    CTX-M-2, CTX-M-8, CTX-M-9, CTX-M-25/26, MOX,

    CIT, DHA, ACC, EBC, FOX, OXA-1, SHV, and TEM

    (14). The number of E. coli or ESC-resistant E. coli on

    each PetrifilmTMSEC was recorded.

    Susceptibility testing of all ESC-resistant E. coli to a

    panel of antimicrobials was performed by broth micro-

    dilution using VetMIC GN-mo (SVA, Uppsala, Sweden)

    according to standards of the CLSI (15). The E. coli

    reference strains ATCC 25922 were used for quality

    control and the results were interpreted according to

    epidemiological cut-off values issued by EUCAST (www.

    eucast.org, retrieved 2015-09-17; Table 1).

    Results
    Altogether, 39 samples of eight different raw dog food

    brands (1�11 samples/brand) were analysed. Depending on

    the brand, the products contained by-products from animals

    slaughtered in Finland (n�10), Norway (n�11), or Sweden

    (n�18). Of the 39 samples, 22 contained only by-products

    from poultry, whereas 17 contained by-products from

    several animal species including poultry.

    Escherichia coli was isolated from all 39 samples. In

    34 (87%) of the samples, the amount of E. coli was higher

    than 5�101 CFU/g, in 19 (49%) the amount was higher

    than 5�102 CFU/g, and in 2 (5%) the amount was

    higher than 5�104 CFU/g.

    ESC-resistant E. coli was isolated from nine samples

    (23%) and all isolates were PCR-positive for the blaCMY-2

    group. The products with ESC-resistant E. coli originated

    from Norway (n�3, 27%) or Sweden (n�6, 33%) and

    contained either only poultry by-products (n�7, 32%)

    or by-products from several animal species (n�2, 12%).

    The number of colony forming units (CFU) of ESC-

    resistant E. coli/gram could be calculated in five of the

    nine samples, all of which were 510 CFU/g. All of these

    samples were products that contained by-products exclu-

    sively from poultry.

    Only one of the ESC-resistant E. coli was also resistant

    to a non-beta-lactam antibiotic (Table 1). That isolate

    was also resistant to kanamycin.

    Discussion
    It was not unexpected that ESC-resistant E. coli could be

    isolated from raw food diet products containing poultry.

    ESC-resistant E. coli bacteria is commonly isolated from

    poultry in Europe and ESC-resistant Enterobacteriaceae

    in raw food diet products has previously been described

    (3, 8). Furthermore, studies have demonstrated an increased

    risk of shedding of ESC-resistant Enterobacteriaceae

    Table 1. Antibiogram of the nine Escherichia coli isolates with transferable resistance to extended spectrum cephalosporins isolated

    from raw food diets for dogs

    Resistance pattern

    Isolate Am Ctx Caz Ci Nal Gm Sm Tc Ff Cs Su Trim Cm Km

    1 64 �2 8 0.06 4 1 16 51 8 50.5 16 0.25 4 58

    2 128 �2 8 0.06 2 1 8 51 54 50.5 32 0.25 52 58

    3 128 �2 8 0.06 2 0.5 8 51 54 50.5 16 0.5 4 58

    4 64 �2 4 0.06 2 1 8 51 54 1 58 0.25 4 58

    5 64 �2 8 0.06 4 1 8 51 54 2 16 0.5 4 58

    6 64 �2 16 0.06 2 1 8 51 54 2 16 0.5 4 58

    7 �128 �2 �16 0.06 4 1 8 51 54 1 58 0.5 4 58

    8 128 �2 8 0.06 2 1 8 2 8 1 16 0.5 4 58

    9 64 �2 4 0.06 4 0.5 8 51 8 1 16 0.25 4 16

    Bold and shaded figures indicate MIC above the epidemiological cut-off values issued by EUCAST (www.eucast.org, retrieved

    2015-09-17).

    Antimicrobials included and cut-off values (mg/L) used are ampicillin (Am, �8), cefotaxime (Ctx, �0.25), ceftazidime (Caz, �0.5),

    ciprofloxacin (Ci, �0.06), nalidixic acid (Nal, �16), gentamicin (Gm, �2), streptomycin (Sm, �16), tetracyclin (Tc, �8), florfenicol

    (Ff, �16), coliston (Cs, �2), sulfamethoxazole (Su, �64), trimetoprim (Trim, �2), chloramphenicol (Cm, �16), kanamycin (Km, �8).

    Oskar Nilsson

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    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.eucast.org](http://www.eucast.org/)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    among dogs fed raw food diets or raw meat in Canada

    and the United Kingdom (16, 17). Together, this indicates

    that raw food diets can also be a source of ESC-resistant

    Enterobacteriaceae for dogs in Sweden. The risk probably

    relates to feeding non-heat-treated animal products, re-

    gardless of whether it is in the form of commercial diets

    or not, as indicated by the previously reported increased

    risk of shedding ESC-resistant E. coli in dogs fed raw meat

    (17). In addition, the occurrence of ESC-resistant E. coli

    in the products originating from Norway and Sweden in

    this study is comparable to their prevalence in samples of

    broiler meat in these two countries (9, 10).

    Poultry from Finland, Sweden, or Norway was an

    ingredient in all investigated products, and blaCMY-2 is the

    dominant gene among ESC-resistant Enterobacteriaceae

    from broilers in those countries (9�11). Therefore, it is

    likely that most of the isolated ESC-resistant E. coli would

    have a gene in the blaCMY-2 group. Although the isolates

    were not sequenced in this study, one could speculate that

    it will be the blaCMY-2 gene that confers resistance as

    all ESC-resistant E. coli isolates from Swedish poultry

    identified to date has carried blaCMY-2 (9). The resistance

    pattern of the isolates is also similar to those which have

    been described for isolates from poultry in Norway and

    Sweden (9, 10).

    The occurrence of E. coli in all products is comparable

    to or higher than in previous studies (5, 18). The isolation

    frequency of E. coli is comparable to that of broiler meat

    95%), but considerably higher than that of pork (20%)

    reported in the Swedish surveillance program Svarm (9).

    Although E. coli could be isolated from all samples, it

    should be noted that only two of the products contained

    more E. coli than the maximum limit of coliform bacteria

    (5�104 CFU/g) recommended by the Swedish Board of

    Agriculture for animal feed materials of animal origin

    (SJVFS 2011:40). Nineteen of the products contained

    �5�102 CFU/g E. coli and would therefore have been

    considered of unsatisfactory hygiene quality had they

    been minced or mechanically separated meat intended for

    human consumption (EC 2073/2005). According to this

    regulation, a batch of minced or mechanically separated

    meat is also classified as having unsatisfactory hygienic

    quality if more than two of five samples contain between

    5�101 and 5�102 CFU E. coli per gram. In this study,

    15 of the 39 products tested contained that amount of

    E. coli. However, as only one sample from each batch

    was analysed, it is not possible to know if they had been

    classified as having unsatisfactory hygiene quality or not

    unless additional samples were analysed. The high inci-

    dence of E. coli in these raw food diets highlights the

    need for maintaining good hygiene when handling these

    products to prevent infection.

    Raw food diets for dogs are not intended for human

    consumption. However, it is likely that they are handled in

    kitchens where food for human consumption is also handled.

    Thereby there is a possibility of cross-contamination and

    a subsequent exposure of humans to bacteria from the

    raw food diet products. The major concern would be

    transient colonisation with ESC-resistant E. coli which

    may allow gene transfer to E. coli adapted to the human

    gut, resulting in prolonged colonisation with resistant

    coliforms as a consequence (19). Thus, raw food diets

    could constitute a source of ESC-resistant E. coli not

    only for dogs but also for humans. However, at this time,

    there are no indications of spread of ESC-resistant E. coli

    from broiler meat to humans in Sweden (20). Hence, the

    risk of spread from raw food diets to humans is probably

    low, but this relies on good hygiene being maintained

    when handling these products.

    Acknowledgements

    Kerstin Ekström, Annica Landén, and Mattias Myrenås are all

    acknowledged for skilled technical assistance and Björn Bengtsson

    is acknowledged for valuable discussions.

    Conflict of interest and funding
    The study was funded by a grant from the Swedish Board

    of Agriculture. The author has no conflict of interest to

    declare.

    References

    1. LeJeune JT, Hancock DD. Public health concerns associated

    with feeding raw meat diets to dogs. J Am Vet Med Assoc 2001;

    219: 1222�5.

    2. Schlesinger DP, Joffe DJ. Raw food diets in companion animals:

    a critical review. Can Vet J 2011; 52: 50�4.

    3. Finley R, Reid-Smith R, Ribble C, Popa M, Vandermeer M,

    Aramini J. The occurrence and antimicrobial susceptibility of

    salmonellae isolated from commercially available canine raw

    food diets in three Canadian cities. Zoonoses Public Health

    2008; 55: 462�9.

    4. Mehlenbacher S, Churchill J, Olsen KE, Bender JB. Availability,

    brands, labelling and Salmonella contamination of raw pet food

    in the Minneapolis/St. Paul area. Zoonoses Public Health 2012;

    59: 513�20.

    5. Weese JS, Rousseau J, Arroyo L. Bacteriological evaluation

    of commercial canine and feline raw diets. Can Vet J 2005; 46:

    513�16.

    6. Chengappa MM, Staats J, Oberst RD, Gabbert NH, McVey S.

    Prevalence of Salmonella in raw meat used in diets of racing

    greyhounds. J Vet Diagn Invest 1993; 5: 372�7.

    7. Joffe DJ, Schlesinger DP. Preliminary assessment of the risk

    of Salmonella infection in dogs fed raw chicken diets. Can Vet J

    2002; 43: 441�2.

    8. Seiffert SN, Hilty M, Perreten V, Endimiani A. Extended-

    spectrum cephalosporin-resistant Gram-negative organisms in

    livestock: an emerging problem for human health? Drug Resist

    Updat 2013; 16: 22�45.

    9. SVARM. Swedish Veterinary Antimicrobial Resistance Mon-

    itoring. ISSN 1650�6332. Available from: http://www.sva.se/en/

    antibiotics-/svarm-reports [cited 23 September 2015].

    10. Mo SS, Norstrom M, Slettemeas JS, Lovland A, Urdahl AM,

    Sunde M. Emergence of AmpC-producing Escherichia coli in

    ESBL-producing E. coli in raw food diet products

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758 3
    (page number not for citation purpose)

    [http://www.sva.se/en/antibiotics-/svarm-reports](http://www.sva.se/en/antibiotics-/svarm-reports)

    [http://www.sva.se/en/antibiotics-/svarm-reports](http://www.sva.se/en/antibiotics-/svarm-reports)

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

    the broiler production chain in a country with a low anti-

    microbial usage profile. Vet Microbiol 2014; 171: 315�20.

    11. Finnish Food Safety Authority. Finnish veterinary antimicro-

    bial resistance monitoring and consumption of antimicrobial

    agents. FINRES-Vet 2010�2012. Helsinki, Finland: Evira

    publications; 2015.

    12. Case LP, Daristotle L, Hayek MG, Raasch MR. Nutrient

    content of pet food. In: Case LP, Daristotle L, Hayek MG,

    Raasch MR (Eds.). Canine and feline nutrition: a resource for

    companion animal professionals. 3rd ed. Maryland Heights,

    MO: Mosby; 2011, pp. 141�62.

    13. Ewers C, Grobbel M, Bethe A, Wieler LH, Guenther S.

    Extended-spectrum beta-lactamases-producing gram-negative

    bacteria in companion animals: action is clearly warranted!.

    Berl Munch Tierarztl Wochenschr 2011; 124: 94�101.

    14. Nilsson O, Borjesson S, Landen A, Bengtsson B. Vertical

    transmission of Escherichia coli carrying plasmid-mediated

    AmpC (pAmpC) through the broiler production pyramid. J

    Antimicrob Chemother 2014; 69: 1497�500.

    15. Clinical and Laboratory Standards Institute (2013). Perfor-

    mance standards for antimicrobial disc and dilution susceptibi-

    lity tests for bacteria isolated from animals; approved standard.

    4th ed. Wayne, PA: CLSI.

    16. Lefebvre SL, Reid-Smith R, Boerlin P, Weese JS. Evaluation of

    the risks of shedding Salmonellae and other potential pathogens

    by therapy dogs fed raw diets in Ontario and Alberta. Zoonoses

    Public Health 2008; 55: 470�80.

    17. Schmidt VM, Pinchbeck GL, Nuttall T, McEwan N, Dawson S,

    Williams NJ. Antimicrobial resistance risk factors and char-

    acterisation of faecal E. coli isolated from healthy Labrador

    retrievers in the United Kingdom. Prev Vet Med 2015; 119:

    31�40.

    18. Strohmeyer RA, Morley PS, Hyatt DR, Dargatz DA, Scorza

    AV, Lappin MR. Evaluation of bacterial and protozoal con-

    tamination of commercially available raw meat diets for dogs. J

    Am Vet Med Assoc 2006; 228: 537�42.

    19. Smet A, Rasschaert G, Martel A, Persoons D, Dewulf J,

    Butaye P, et al. In situ ESBL conjugation from avian to human

    Escherichia coli during cefotaxime administration. J Appl

    Microbiol 2011; 110: 541�9.

    20. Borjesson S, Jernberg C, Brolund A, Edquist P, Finn M, Landen

    A, et al. Characterization of plasmid-mediated AmpC-producing

    E. coli from Swedish broilers and association with human

    clinical isolates. Clin Microbiol Infect 2013; 19: E309�11.

    Oskar Nilsson

    4
    (page number not for citation purpose)

    Citation: Infection Ecology and Epidemiology 2015, 5: 28758 – http://dx.doi.org/10.3402/iee.v5.28758

    [http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758](http://www.infectionecologyandepidemiology.net/index.php/iee/article/view/28758)

    [http://dx.doi.org/10.3402/iee.v5.28758](http://dx.doi.org/10.3402/iee.v5.28758)

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