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Characterization of enteropathogenic and Shiga toxin-producing Escherichia coli in cattle and deer in a shared agroecosystem.
Singh, Pallavi; Sha, Qiong; Lacher, David W; Del Valle, Jacquelyn; Mosci, Rebekah E; Moore, Jennifer A; Scribner, Kim T; Manning, Shannon D.
Afiliação
  • Singh P; Department of Microbiology and Molecular Genetics, Michigan State University East Lansing, MI, USA.
  • Sha Q; Department of Microbiology and Molecular Genetics, Michigan State University East Lansing, MI, USA.
  • Lacher DW; Division of Molecular Biology, Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration Laurel, MD, USA.
  • Del Valle J; Department of Microbiology and Molecular Genetics, Michigan State University East Lansing, MI, USA.
  • Mosci RE; Department of Microbiology and Molecular Genetics, Michigan State University East Lansing, MI, USA.
  • Moore JA; Biology Department, Grand Valley State University Allendale, MI, USA.
  • Scribner KT; Department of Fisheries and Wildlife, Michigan State University East Lansing, MI, USA.
  • Manning SD; Department of Microbiology and Molecular Genetics, Michigan State University East Lansing, MI, USA.
Article em En | MEDLINE | ID: mdl-25883908
ABSTRACT
Shiga toxin-producing Escherichia coli (STEC) is an important foodborne pathogen. Cattle are suggested to be an important reservoir for STEC; however, these pathogens have also been isolated from other livestock and wildlife. In this study we sought to investigate transmission of STEC, enterohemorrhagic E. coli (EHEC) and enteropathogenic E. coli (EPEC) between cattle and white-tailed deer in a shared agroecosystem. Cattle feces were collected from 100 animals in a Michigan dairy farm in July 2012, while 163 deer fecal samples were collected during two sampling periods (March and June). The locations of deer fecal pellets were recorded via geographic information system mapping and microsatellite multi-locus genotyping was used to link the fecal samples to individual deer at both time points. Following subculture to sorbitol MacConkey agar and STEC CHROMagar, the pathogens were characterized by serotyping, stx profiling, and PCR-based fingerprinting; multilocus sequence typing (MLST) was performed on a subset. STEC and EHEC were cultured from 12 to 16% of cattle, respectively, and EPEC was found in 36%. Deer were significantly less likely to have a pathogen in March vs. June where the frequency of STEC, EHEC, and EPEC was 1, 6, and 22%, respectively. PCR fingerprinting and MLST clustered the cattle- and deer-derived strains together in a phylogenetic tree. Two STEC strains recovered from both animal species shared MLST and fingerprinting profiles, thereby providing evidence of interspecies transmission and highlighting the importance of wildlife species in pathogen shedding dynamics and persistence in the environment and cattle herds.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cervos / Doenças dos Bovinos / Infecções por Escherichia coli / Escherichia coli Enteropatogênica / Escherichia coli Shiga Toxigênica Limite: Animals Idioma: En Revista: Front Cell Infect Microbiol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cervos / Doenças dos Bovinos / Infecções por Escherichia coli / Escherichia coli Enteropatogênica / Escherichia coli Shiga Toxigênica Limite: Animals Idioma: En Revista: Front Cell Infect Microbiol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos