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1. Prevalence of Antimicrobial Resistance in Select Bacteria From Retail Seafood—United States, 2019

Author

Tate, Heather, Ayers, Sherry, Nyirabahizi, Epiphanie, Li, Cong, Borenstein, Stacey, Young, Shenia, Rice-Trujillo, Crystal, Fleurant, Sanchez Saint, Bodeis-Jones, Sonya, Li, Xunde, Tobin-D’Angelo, Melissa, Volkova, Victoriya, Hardy, Rachel, Mingle, Lisa, M’ikanatha, Nkuchia M, Ruesch, Laura, Whitehouse, Chris A, Tyson, Gregory H, Strain, Errol, and McDermott, Patrick F

Subjects
Infectious Diseases, Antimicrobial Resistance, Biodefense, Vaccine Related, Prevention, Emerging Infectious Diseases, Infection, antimicrobial resistance, seafood, retail food, United States, National Antimicrobial Resistance Monitoring System, Environmental Science and Management, Soil Sciences, Microbiology
Abstract

In 2019, the United States National Antimicrobial Resistance Monitoring System (NARMS) surveyed raw salmon, shrimp, and tilapia from retail grocery outlets in eight states to assess the prevalence of bacterial contamination and antimicrobial resistance (AMR) in the isolates. Prevalence of the targeted bacterial genera ranged among the commodities: Salmonella (0%-0.4%), Aeromonas (19%-26%), Vibrio (7%-43%), Pseudomonas aeruginosa (0.8%-2.3%), Staphylococcus (23%-30%), and Enterococcus (39%-66%). Shrimp had the highest odds (OR: 2.8, CI: 2.0-3.9) of being contaminated with at least one species of these bacteria, as were seafood sourced from Asia vs. North America (OR: 2.7; CI: 1.8-4.7) and Latin America and the Caribbean vs. North America (OR: 1.6; CI: 1.1-2.3) and seafood sold at the counter vs. sold frozen (OR: 2.1; CI: 1.6-2.9). Isolates exhibited pan-susceptibility (Salmonella and P. aeruginosa) or low prevalence of resistance (

Published
2022

3. Evidence review and recommendations for the implementation of genomics for antimicrobial resistance surveillance: reports from an international expert group

Author

Baker, Kate S, Jauneikaite, Elita, Nunn, Jamie G, Midega, Janet T, Atun, Rifat, Holt, Kathryn E, Walia, Kamini, Howden, Benjamin P, Tate, Heather, Okeke, Iruka N, Carattoli, Alessandra, Hsu, Li Yang, Hopkins, Katie L, Muloi, Dishon M, Wheeler, Nicole E, Aanensen, David M, Mason, Lewis C E, Rodgus, Jonah, Hendriksen, Rene S, Essack, Sabiha Y, Egyir, Beverly, Halpin, Alison L, MacCannell, Duncan R, Campos, Josefina, Srikantiah, Padmini, Feasey, Nicholas A, and Peacock, Sharon J

Published
2023
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4. The spread of pESI-mediated extended-spectrum cephalosporin resistance in Salmonella serovars—Infantis, Senftenberg, and Alachua isolated from food animal sources in the United States

Author

Li, Cong, primary, Tate, Heather, additional, Huang, Xinyang, additional, Hsu, Chih-Hao, additional, Harrison, Lucas B., additional, Zhao, Shaohua, additional, Fortenberry, Gamola Z., additional, Dessai, Uday, additional, McDermott, Patrick F., additional, and Strain, Errol A., additional

Published
2024
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5. The spread of pESI-mediated extended-spectrum cephalosporin resistance inSalmonellaserovars - Infantis, Senftenberg, and Alachua isolated from food animal sources in the United States

Author

Li, Cong, primary, Tate, Heather, additional, Huang, Xinyang, additional, Hsu, Chih-Hao, additional, Harrison, Lucas B., additional, Zhao, Shaohua, additional, Fortenberry, Gamola Z., additional, Dessai, Uday, additional, McDermott, Patrick F., additional, and Strain, Errol A., additional

Published
2024
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6. A one health approach for monitoring antimicrobial resistance: developing a national freshwater pilot effort.

Author

Franklin, Alison M., Weller, Daniel L., Durso, Lisa M., Bagley, Mark, Davis, Benjamin C., Frye, Jonathan G., Grim, Christopher J., Ibekwe, Abasiofiok M., Jahne, Michael A., Keely, Scott P., Kraft, Autumn L., McConn, Betty R., Mitchell, Richard M., Ottesen, Andrea R., Sharma, Manan, Strain, Errol A., Tadesse, Daniel A., Tate, Heather, Wells, Jim E., and Williams, Clinton F.

Subjects
DRUG resistance in bacteria, ANTI-infective agents, PUBLIC health, FRESH water, ECOLOGY
Abstract

Antimicrobial resistance (AMR) is a world-wide public health threat that is projected to lead to 10 million annual deaths globally by 2050. The AMR public health issue has led to the development of action plans to combat AMR, including improved antimicrobial stewardship, development of new antimicrobials, and advanced monitoring. The National Antimicrobial Resistance Monitoring System (NARMS) led by the United States (U.S) Food and Drug Administration along with the U.S. Centers for Disease Control and U.S. Department of Agriculture has monitored antimicrobial resistant bacteria in retail meats, humans, and food animals since the mid 1990's. NARMS is currently exploring an integrated One Health monitoring model recognizing that human, animal, plant, and environmental systems are linked to public health. Since 2020, the U.S. Environmental Protection Agency has led an interagency NARMS environmental working group (EWG) to implement a surface water AMR monitoring program (SWAM) at watershed and national scales. The NARMS EWG divided the development of the environmental monitoring effort into five areas: (i) defining objectives and questions, (ii) designing study/sampling design, (iii) selecting AMR indicators, (iv) establishing analytical methods, and (v) developing data management/analytics/metadata plans. For each of these areas, the consensus among the scientific community and literature was reviewed and carefully considered prior to the development of this environmental monitoring program. The data produced from the SWAM effort will help develop robust surface water monitoring programs with the goal of assessing public health risks associated with AMR pathogens in surface water (e.g., recreational water exposures), provide a comprehensive picture of how resistant strains are related spatially and temporally within a watershed, and help assess how anthropogenic drivers and intervention strategies impact the transmission of AMR within human, animal, and environmental systems. [ABSTRACT FROM AUTHOR]

Published
2024
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7. CTX-M-65 Extended-Spectrum [beta]-Lactamase-Producing Salmonella enterica Serotype Infantis, United States

Author

Brown, Allison C., Chen, Jessica C., Watkins, Louise K. Francois, Campbell, Davina, Folster, Jason P., Tate, Heather, Wasilenko, Jamie, Van Tubbergen, Christine, and Friedman, Cindy R.

Subjects
Salmonellosis -- Risk factors -- Care and treatment, DNA sequencing -- Usage, Health
Abstract

A leading cause of bacterial foodborne disease in the United States is nontyphoidal Salmonella (1). Salmonella enterica serotype Infantis (hereafter called Salmonella Infantis) is one of the most common Salmonella [...]

Published
2018
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8. Evidence review and recommendations for the implementation of genomics for antimicrobial resistance surveillance:reports from an international expert group

Author

Baker, Kate S, Jauneikaite, Elita, Nunn, Jamie G, Midega, Janet T, Atun, Rifat, Holt, Kathryn E, Walia, Kamini, Howden, Benjamin P, Tate, Heather, Okeke, Iruka N, Carattoli, Alessandra, Hsu, Li Yang, Hopkins, Katie L, Muloi, Dishon M, Wheele, Nicole E, Aanensen, David M, Mason, Lewis C E, Rodgus, Jonah, Hendriksen, Rene S, Essack, Sabiha Y, Egyir, Beverly, Halpin, Alison L, MacCannell, Duncan R, Campos, Josefina, Srikantiah, Padmini, Feasey, Nicholas A, Peacock, Sharon J, Baker, Kate S, Jauneikaite, Elita, Nunn, Jamie G, Midega, Janet T, Atun, Rifat, Holt, Kathryn E, Walia, Kamini, Howden, Benjamin P, Tate, Heather, Okeke, Iruka N, Carattoli, Alessandra, Hsu, Li Yang, Hopkins, Katie L, Muloi, Dishon M, Wheele, Nicole E, Aanensen, David M, Mason, Lewis C E, Rodgus, Jonah, Hendriksen, Rene S, Essack, Sabiha Y, Egyir, Beverly, Halpin, Alison L, MacCannell, Duncan R, Campos, Josefina, Srikantiah, Padmini, Feasey, Nicholas A, and Peacock, Sharon J

Abstract

Nearly a century after the beginning of the antibiotic era, which has been associated with unparalleled improvements in human health and reductions in mortality associated with infection, the dwindling pipeline for new antibiotic classes coupled with the inevitable spread of antimicrobial resistance (AMR) poses a major global challenge. Historically, surveillance of bacteria with AMR typically relied on phenotypic analysis of isolates taken from infected individuals, which provides only a low-resolution view of the epidemiology behind an individual infection or wider outbreak. Recent years have seen increasing adoption of powerful new genomic technologies with the potential to revolutionise AMR surveillance by providing a high-resolution picture of the AMR profile of the bacteria causing infections and providing real-time actionable information for treating and preventing infection. However, many barriers remain to be overcome before genomic technologies can be adopted as a standard part of routine AMR surveillance around the world. Accordingly, the Surveillance and Epidemiology of Drug-resistant Infections Consortium convened an expert working group to assess the benefits and challenges of using genomics for AMR surveillance. In this Series, we detail these discussions and provide recommendations from the working group that can help to realise the massive potential benefits for genomics in surveillance of AMR.

Published
2023

11. 1367. Resistance to Ceftriaxone and Ciprofloxacin in Nontyphoidal Salmonella from Humans and Relatedness to Isolates from Animal Sources

Author

M’ikanatha, Nkuchia M, primary, Sayeed, Sameera, additional, Leeper, Molly M, additional, Folster, Jason P, additional, Boktor, Sameh, additional, Watkins, Louise F, additional, Fu, Yezhi, additional, Thirumalapur, Nagaraja, additional, Dettinger, Lisa, additional, Hackman, Nicole M, additional, Tate, Heather, additional, and Dudley, Edward G, additional

Published
2022
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12. Genomic Diversity, Antimicrobial Resistance, and Virulence Gene Profiles of Salmonella Serovar Kentucky Isolated from Humans, Food, and Animal Ceca Content Sources in the United States

Author

Tate, Heather, primary, Hsu, Chih-Hao, additional, Chen, Jessica C., additional, Han, Jing, additional, Foley, Steven L., additional, Folster, Jason P., additional, Francois Watkins, Louise K., additional, Reynolds, Jared, additional, Tillman, Glenn E., additional, Nyirabahizi, Epiphanie, additional, and Zhao, Shaohua, additional

Published
2022
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13. Prevalence of Antimicrobial Resistance in Select Bacteria From Retail Seafood—United States, 2019

Author

Tate, Heather, primary, Ayers, Sherry, additional, Nyirabahizi, Epiphanie, additional, Li, Cong, additional, Borenstein, Stacey, additional, Young, Shenia, additional, Rice-Trujillo, Crystal, additional, Saint Fleurant, Sanchez, additional, Bodeis-Jones, Sonya, additional, Li, Xunde, additional, Tobin-D’Angelo, Melissa, additional, Volkova, Victoriya, additional, Hardy, Rachel, additional, Mingle, Lisa, additional, M’ikanatha, Nkuchia M., additional, Ruesch, Laura, additional, Whitehouse, Chris A., additional, Tyson, Gregory H., additional, Strain, Errol, additional, and McDermott, Patrick F., additional

Published
2022
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18. List of Contributors

Author

Argudín, María Ángeles, primary, Baker-Austin, Craig, additional, Ballesté-Delpierre, Clara, additional, Bonomo, Robert A., additional, Butaye, Patrick, additional, Calo, Juliany Rivera, additional, Chen, Chin-Yi, additional, Chen, Jinru, additional, Claycamp, H. Gregg, additional, Cox, Louis Anthony (Tony), additional, Crandall, Philip G., additional, Crarey, Emily, additional, Endimiani, Andrea, additional, Fàbrega, Anna, additional, Feßler, Andrea T., additional, Ghosh, Anuradha, additional, Hänninen, Marja-Liisa, additional, Harrison, Lee H., additional, Hong, Pei-Ying, additional, Jackson, Charlene R., additional, Jarvis, Nathan A., additional, Jung, Yangjin, additional, Kabera, Claudine, additional, Kadlec, Kristina, additional, Kapatral, Vinayak, additional, Kivistö, Rauni, additional, Lampel, Keith A., additional, Lupo, Agnese, additional, Marsh, Jane W., additional, Matthews, Karl R., additional, O’Bryan, Corliss A., additional, Olkkola, Satu, additional, Papp-Wallace, Krisztina M., additional, Ricke, Steven C., additional, Roasto, Mati, additional, Rossi, Mirko, additional, Schwarz, Stefan, additional, Tate, Heather, additional, Threlfall, John, additional, Vila, Jordi, additional, Wang, Guangshun, additional, Wang, Siyun, additional, Wendlandt, Sarah, additional, Yan, Xianghe, additional, and Zurek, Ludek, additional

Published
2015
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19. A National Antimicrobial Resistance Monitoring System Survey of Antimicrobial-Resistant Foodborne Bacteria Isolated from Retail Veal in the United States

Author

Tate, Heather, primary, Li, Cong, additional, Nyirabahizi, Epiphanie, additional, Tyson, Gregory H., additional, Zhao, Shaohua, additional, Rice-Trujillo, Crystal, additional, Jones, Sonya Bodeis, additional, Ayers, Sherry, additional, M'ikanatha, Nkuchia M., additional, Hanna, Samir, additional, Ruesch, Laura, additional, Cavanaugh, Marianna E., additional, Laksanalamai, Pongpan, additional, Mingle, Lisa, additional, Matzinger, Shannon R., additional, and Mcdermott, Patrick F., additional

Published
2021
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24. Genomic Diversity, Antimicrobial Resistance, and Virulence Gene Profiles of SalmonellaSerovar Kentucky Isolated from Humans, Food, and Animal Ceca Content Sources in the United States

Author

Tate, Heather, Hsu, Chih-Hao, Chen, Jessica C., Han, Jing, Foley, Steven L., Folster, Jason P., Francois Watkins, Louise K., Reynolds, Jared, Tillman, Glenn E., Nyirabahizi, Epiphanie, and Zhao, Shaohua

Abstract

Salmonellaserovar Kentucky is frequently isolated from chickens and dairy cattle, but recovery from humans is comparatively low based on the U.S. National Antimicrobial Resistance Monitoring System (NARMS) reports. We aimed to better describe the genetic diversity, antimicrobial resistance, and virulence determinants of SalmonellaKentucky isolates from humans, food animal ceca, retail meat and poultry products, imported foods and food products, and other samples. We analyzed the genomes of 774 SalmonellaKentucky isolates and found that 63% (54/86) of human isolates were sequence type (ST)198, 33% (29/86) were ST152, and 3.5% (3/86) were ST314. Ninety-one percent (570/629) of cecal isolates and retail meat and poultry isolates were ST152 or ST152-like (one allele difference), and 9.2% (58/629) were ST198. Isolates from imported food were mostly ST198 (60%, 22/37) and ST314 (29.7%, 11/37). ST198 isolates clustered into two main lineages. Clade ST198.2 comprised almost entirely isolates from humans and imported foods, all containing triple mutations in the quinolone resistance-determining region (QRDR) that confer resistance to fluoroquinolones. Clade ST198.1 contained isolates from humans, ceca, retail meat and poultry products, and imported foods that largely lacked QRDR mutations. ST152 isolates from cattle had a lineage (Clade 2) distinct from ST152 isolates from chicken (Clade 4), and half of ST152 human isolates clustered within two other clades (Clades 1 and 3), largely distinct from Clades 2 and 4. Although clinical illness associated with SalmonellaKentucky is low, ST198 appears to account for most human infections in the Unites States but is uncommon among ceca of domestic food animals and retail meat and poultry products. These findings, combined with human exposure data, suggest that fluoroquinolone-resistant ST198 infections may be linked to the consumption of food products that are imported or consumed while traveling. We also found unique differences in the composition of virulence genes and antimicrobial resistance genes among the clades, which may provide clues to the host specificity and pathogenicity of SalmonellaKentucky lineages.

Published
2022
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25. Low occurrence of multi‐antimicrobial and heavy metal resistance in Salmonella enterica from wild birds in the United States.

Author

Fu, Yezhi, M'ikanatha, Nkuchia M., Whitehouse, Chris A., Tate, Heather, Ottesen, Andrea, Lorch, Jeffrey M., Blehert, David S., Berlowski‐Zier, Brenda, and Dudley, Edward G.

Subjects
HEAVY metals, SALMONELLA enterica, DRUG resistance in bacteria, WATER birds, DOMESTIC animals
Abstract

Summary: Wild birds are common reservoirs of Salmonella enterica. Wild birds carrying resistant S. enterica may pose a risk to public health as they can spread the resistant bacteria across large spatial scales within a short time. Here, we whole‐genome sequenced 375 S. enterica strains from wild birds collected in 41 U.S. states during 1978–2019 to examine bacterial resistance to antibiotics and heavy metals. We found that Typhimurium was the dominant S. enterica serovar, accounting for 68.3% (256/375) of the bird isolates. Furthermore, the proportions of the isolates identified as multi‐antimicrobial resistant (multi‐AMR: resistant to at least three antimicrobial classes) or multi‐heavy metal resistant (multi‐HMR: resistant to at least three heavy metals) were both 1.87% (7/375). Interestingly, all the multi‐resistant S. enterica (n = 12) were isolated from water birds or raptors; none of them was isolated from songbirds. Plasmid profiling demonstrated that 75% (9/12) of the multi‐resistant strains carried resistance plasmids. Our study indicates that wild birds do not serve as important reservoirs of multi‐resistant S. enterica strains. Nonetheless, continuous surveillance for bacterial resistance in wild birds is necessary because the multi‐resistant isolates identified in this study also showed close genetic relatedness with those from humans and domestic animals. [ABSTRACT FROM AUTHOR]

Published
2022
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32. Using Genomics to Track Global Antimicrobial Resistance

Author

Hendriksen, Rene S., Bortolaia, Valeria, Tate, Heather, Tyson, Gregory H, Aarestrup, Frank Møller, McDermott, Patrick F., Hendriksen, Rene S., Bortolaia, Valeria, Tate, Heather, Tyson, Gregory H, Aarestrup, Frank Møller, and McDermott, Patrick F.

Abstract

The recent advancements in rapid and affordable DNA sequencing technologies have revolutionized diagnostic microbiology and microbial surveillance. The availability of bioinformatics tools and online accessible databases has been a prerequisite for this. We conducted a scientific literature review and here we present a description of examples of available tools and databases for antimicrobial resistance (AMR) detection and provide future perspectives and recommendations. At least 47 freely accessible bioinformatics resources for detection of AMR determinants in DNA or amino acid sequence data have been developed to date. These include, among others but not limited to, ARG-ANNOT, CARD, SRST2, MEGARes, Genefinder, ARIBA, KmerResistance, AMRFinder, and ResFinder. Bioinformatics resources differ for several parameters including type of accepted input data, presence/absence of software for search within a database of AMR determinants that can be specific to a tool or cloned from other resources, and for the search approach employed, which can be based on mapping or on alignment. As a consequence, each tool has strengths and limitations in sensitivity and specificity of detection of AMR determinants and in application, which for some of the tools have been highlighted in benchmarking exercises and scientific articles. The identified tools are either available at public genome data centers, from GitHub or can be run locally. NCBI and European Nucleotide Archive (ENA) provide possibilities for online submission of both sequencing and accompanying phenotypic antimicrobial susceptibility data, allowing for other researchers to further analyze data, and develop and test new tools. The advancement in whole genome sequencing and the application of online tools for real-time detection of AMR determinants are essential to identify control and prevention strategies to combat the increasing threat of AMR. Accessible tools and DNA sequence data are expanding, which will allow establi

Published
2019

35. Comparative Genomic Analysis of Virulence, Antimicrobial Resistance, and Plasmid Profiles ofSalmonellaDublin Isolated from Sick Cattle, Retail Beef, and Humans in the United States

Author

Hsu, Chih-Hao, primary, Li, Cong, additional, Hoffmann, Maria, additional, McDermott, Patrick, additional, Abbott, Jason, additional, Ayers, Sherry, additional, Tyson, Gregory H., additional, Tate, Heather, additional, Yao, Kuan, additional, Allard, Marc, additional, and Zhao, Shaohua, additional

Published
2019
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39. Genomic Analysis of Emerging Florfenicol-Resistant Campylobacter coli Isolated from the Cecal Contents of Cattle in the United States

Author

Zhao, Shaohua, primary, Mukherjee, Sampa, additional, Hsu, Chih-Hao, additional, Young, Shenia, additional, Li, Cong, additional, Tate, Heather, additional, Morales, Cesar A., additional, Haro, Jovita, additional, Thitaram, Sutawee, additional, Tillman, Glenn E., additional, Dessai, Uday, additional, and McDermott, Patrick, additional

Published
2019
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40. Genomic Analysis of Emerging Florfenicol-Resistant Campylobacter coli Isolated from the Intestinal Cecal Contents of Cattle in the United States

Author

Zhao, Shaohua, primary, Mukherjee, Sampa, additional, Hsu, Chih-Hao, additional, Young, Shenia, additional, Li, Cong, additional, Tate, Heather, additional, Morales, Cesar A., additional, Haro, Jovita, additional, Thitaram, Sutawee, additional, Tillman, Glenn E., additional, Dessai, Uday, additional, and McDermott, Patrick, additional

Published
2019
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45. Outbreak of Salmonella Heidelberg Infections Linked to a Single Poultry Producer — 13 States, 2012–2013

Author

Grinnell, Margaret, Provo, Ginger, Marsden-Haug, Nicola, Stigi, Kathleen A., DeBess, Emilio, Kissler, Bonnie, Crarey, Emily, Tate, Heather, Pringle, Jeshua, Grass, Julian, Folster, Jason, Williams, Ian, Gieraltowski, Laura, and Laufer, Alison S.

Subjects
Adult, Aged, 80 and over, Male, Adolescent, Infant, Salmonella enterica, Articles, Middle Aged, United States, Disease Outbreaks, Young Adult, Child, Preschool, Animals, Humans, Female, Salmonella Food Poisoning, Child, Chickens, Aged
Abstract

In June 2012, the Oregon Health Authority and the Washington State Department of Health noted an increase in the number of Salmonella enterica serotype Heidelberg clinical isolates sharing an identical pulsed-field gel electrophoresis (PFGE) pattern. In 2004, this pattern had been linked to chicken from Foster Farms by the Washington State Department of Health; preliminary 2012 interviews with infected persons also indicated exposure to Foster Farms chicken. On August 2, 2012, CDC's PulseNet* detected a cluster of 19 Salmonella Heidelberg clinical isolates matching the outbreak pattern. This report summarizes the investigation by CDC, state and local health departments, the U.S. Department of Agriculture's Food Safety and Inspection Service (USDA-FSIS), and the Food and Drug Administration (FDA) and reinforces the importance of safe food handling to prevent illness. A total of 134 cases from 13 states were identified, including 33 patients who were hospitalized. This multifaceted investigation used standard epidemiologic and laboratory data along with patient shopper card purchase information, and PFGE data from the retail meat component of the National Antimicrobial Resistance Monitoring System (NARMS)†, a relatively novel tool in outbreak investigation, to link the outbreak strain to chicken from Foster Farms.

Published
2013

47. National Antimicrobial Resistance Monitoring System: Two Decades of Advancing Public Health Through Integrated Surveillance of Antimicrobial Resistance

Author

Karp, Beth E., primary, Tate, Heather, additional, Plumblee, Jodie R., additional, Dessai, Uday, additional, Whichard, Jean M., additional, Thacker, Eileen L., additional, Hale, Kis Robertson, additional, Wilson, Wanda, additional, Friedman, Cindy R., additional, Griffin, Patricia M., additional, and McDermott, Patrick F., additional

Published
2017
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48. Comparative Analysis of Extended-Spectrum-β-Lactamase CTX-M-65-Producing Salmonella enterica Serovar Infantis Isolates from Humans, Food Animals, and Retail Chickens in the United States

Author

Tate, Heather, primary, Folster, Jason P., additional, Hsu, Chih-Hao, additional, Chen, Jessica, additional, Hoffmann, Maria, additional, Li, Cong, additional, Morales, Cesar, additional, Tyson, Gregory H., additional, Mukherjee, Sampa, additional, Brown, Allison C., additional, Green, Alice, additional, Wilson, Wanda, additional, Dessai, Uday, additional, Abbott, Jason, additional, Joseph, Lavin, additional, Haro, Jovita, additional, Ayers, Sherry, additional, McDermott, Patrick F., additional, and Zhao, Shaohua, additional

Published
2017
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50. Molecular Subtyping and Source Attribution of Campylobacter Isolated from Food Animals

Author

Tyson, Gregory H., primary, Tate, Heather P., additional, Abbott, Jason, additional, Tran, Thu-Thuy, additional, Kabera, Claudine, additional, Crarey, Emily, additional, Young, Shenia, additional, McDermott, Patrick F., additional, Sprague, Grisselle, additional, Campbell, Mark, additional, Adeyemo, Oyewole, additional, Browne-Silva, Johnette, additional, Myers, Michael, additional, Thitaram, Sutawee, additional, and Zhao, Shaohua, additional

Published
2016
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