Antimicrobial Resistance Profiles and Diversity in Salmonella from Humans and Cattle, 2004-2011

被引:35
|
作者
Afema, J. A. [1 ]
Mather, A. E. [2 ]
Sischo, W. M. [1 ]
机构
[1] Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA 99164 USA
[2] Wellcome Trust Sanger Inst, Hinxton, England
基金
英国惠康基金;
关键词
Salmonella; anti-microbial resistance; humans; cattle; UNITED-STATES; ANTIBIOTIC-RESISTANCE; TYPHIMURIUM; SEROTYPE; PREVALENCE; EPIDEMIOLOGY; INFECTIONS; ANIMALS; NEWPORT; AGENTS;
D O I
10.1111/zph.12172
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Analysis of long-term anti-microbial resistance (AMR) data is useful to understand source and transmission dynamics of AMR. We analysed 5124 human clinical isolates from Washington State Department of Health, 391 cattle clinical isolates from the Washington Animal Disease Diagnostic Laboratory and 1864 non-clinical isolates from foodborne disease research on dairies in the Pacific Northwest. Isolates were assigned profiles based on phenotypic resistance to 11 anti-microbials belonging to eight classes. Salmonella Typhimurium (ST), Salmonella Newport (SN) and Salmonella Montevideo (SM) were the most common serovars in both humans and cattle. Multinomial logistic regression showed ST and SN from cattle had greater probability of resistance to multiple classes of anti-microbials than ST and SN from humans (P<0.0001). While these findings could be consistent with the belief that cattle are a source of resistant ST and SN for people, occurrence of profiles unique to cattle and not observed in temporally related human isolates indicates these profiles are circulating in cattle only. We used various measures to assess AMR diversity, conditional on the weighting of rare versus abundant profiles. AMR profile richness was greater in the common serovars from humans, although both source data sets were dominated by relatively few profiles. The greater profile richness in human Salmonella may be due to greater diversity of sources entering the human population compared to cattle or due to continuous evolution in the human environment. Also, AMR diversity was greater in clinical compared to non-clinical cattle Salmonella, and this could be due to anti-microbial selection pressure in diseased cattle that received treatment. The use of bootstrapping techniques showed that although there were shared profiles between humans and cattle, the expected and observed number of profiles was different, suggesting Salmonella and associated resistance from humans and cattle may not be wholly derived from a common population.
引用
收藏
页码:506 / 517
页数:12
相关论文
共 50 条
  • [41] TRENDS IN PERMANENT PACEMAKER IMPLANTATION IN THE UNITED STATES FROM 2004-2011
    Khan, A. A.
    Brooks, B.
    Panchal, H. B.
    Zaidi, S. I. M.
    Rahman, Z.
    Paul, T.
    Ramu, V.
    CARDIOLOGY, 2017, 137 : 184 - 184
  • [42] Diversity of Antimicrobial Resistance Phenotypes in Salmonella Isolated from Commercial Poultry Farms
    Liljebjelke, Karen A.
    Hofacre, Charles L.
    White, David G.
    Ayers, Sherry
    Lee, Margie D.
    Maurer, John J.
    FRONTIERS IN VETERINARY SCIENCE, 2017, 4
  • [43] Antimicrobial resistance and genomic characterization of Salmonella Dublin isolates in cattle from the United States
    Srednik, Mariela E.
    Lantz, Kristina
    Hicks, Jessica A.
    Morningstar-Shaw, Brenda R.
    Mackie, Tonya A.
    Schlater, Linda K.
    PLOS ONE, 2021, 16 (09):
  • [44] Prevalence and Antimicrobial Resistance of Salmonella and Escherichia coli from Australian Cattle Populations at Slaughter
    Barlow, Robert S.
    McMillan, Kate E.
    Duffy, Lesley L.
    Fegan, Narelle
    Jordan, David
    Mellor, Glen E.
    JOURNAL OF FOOD PROTECTION, 2015, 78 (05) : 912 - 920
  • [45] Prevalence, antimicrobial resistance and virulence genes of Salmonella serovars isolated from humans and animals
    Borah, Probodh
    Dutta, Rupam
    Das, Leena
    Hazarika, Girin
    Choudhury, Mridusmita
    Deka, Naba Kumar
    Malakar, Dipika
    Hussain, Md Iftikar
    Barkalita, Luit Moni
    VETERINARY RESEARCH COMMUNICATIONS, 2022, 46 (03) : 799 - 810
  • [46] Antimicrobial Resistance and Molecular Typing of Salmonella Stanley Isolated from Humans, Foods, and Environment
    Yang, Xiaowei
    Kuang, Dai
    Meng, Jianghong
    Pan, Haijian
    Shen, Junqing
    Zhang, Jing
    Shi, Weimin
    Chen, Qi
    Shi, Xianming
    Xu, Xuebin
    Zhang, Jianmin
    FOODBORNE PATHOGENS AND DISEASE, 2015, 12 (12) : 945 - 949
  • [47] Prevalence, antimicrobial resistance and virulence genes of Salmonella serovars isolated from humans and animals
    Probodh Borah
    Rupam Dutta
    Leena Das
    Girin Hazarika
    Mridusmita Choudhury
    Naba Kumar Deka
    Dipika Malakar
    Md Iftikar Hussain
    Luit Moni Barkalita
    Veterinary Research Communications, 2022, 46 : 799 - 810
  • [48] Antimicrobial resistance and genetic diversity of Escherichia coli isolated from humans and foods
    Melo, Daniela Benevides
    de Oliveira Menezes, Ana Paula
    Reis, Joice Neves
    Guimaraes, Alaise Gil
    BRAZILIAN JOURNAL OF MICROBIOLOGY, 2015, 46 (04) : 1165 - 1170
  • [49] Phylogenetic Diversity and Antimicrobial Resistance of Campylobacter coli from Humans and Animals in Japan
    Asakura, Hiroshi
    Sakata, Junko
    Nakamura, Hiromi
    Yamamoto, Shiori
    Murakami, Satoshi
    MICROBES AND ENVIRONMENTS, 2019, 34 (02) : 146 - 154
  • [50] Antimicrobial susceptibilities of Salmonella strains isolated from humans, cattle, pigs, and chickens in the Netherlands from 1984 to 2001
    van Duijkeren, E
    Wannet, WJB
    Houwers, DJ
    van Pelt, W
    JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (08) : 3574 - 3578