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New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants

House mice (Mus musculus) thrive in large urban centers worldwide. Nonetheless, little is known about the role that they may play in contributing to environmental contamination with potentially pathogenic bacteria. Here, we describe the fecal microbiome of house mice with emphasis on detection of pa...

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Autores principales: Williams, Simon H., Che, Xiaoyu, Paulick, Ashley, Guo, Cheng, Lee, Bohyun, Muller, Dorothy, Uhlemann, Anne-Catrin, Lowy, Franklin D., Corrigan, Robert M., Lipkin, W. Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904414/
https://www.ncbi.nlm.nih.gov/pubmed/29666289
http://dx.doi.org/10.1128/mBio.00624-18
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author Williams, Simon H.
Che, Xiaoyu
Paulick, Ashley
Guo, Cheng
Lee, Bohyun
Muller, Dorothy
Uhlemann, Anne-Catrin
Lowy, Franklin D.
Corrigan, Robert M.
Lipkin, W. Ian
author_facet Williams, Simon H.
Che, Xiaoyu
Paulick, Ashley
Guo, Cheng
Lee, Bohyun
Muller, Dorothy
Uhlemann, Anne-Catrin
Lowy, Franklin D.
Corrigan, Robert M.
Lipkin, W. Ian
author_sort Williams, Simon H.
collection PubMed
description House mice (Mus musculus) thrive in large urban centers worldwide. Nonetheless, little is known about the role that they may play in contributing to environmental contamination with potentially pathogenic bacteria. Here, we describe the fecal microbiome of house mice with emphasis on detection of pathogenic bacteria and antimicrobial resistance genes by molecular methods. Four hundred sixteen mice were collected from predominantly residential buildings in seven sites across New York City over a period of 13 months. 16S rRNA sequencing identified Bacteroidetes as dominant and revealed high levels of Proteobacteria. A targeted PCR screen of 11 bacteria, as indicated by 16S rRNA analyses, found that mice are carriers of several gastrointestinal disease-causing agents, including Shigella, Salmonella, Clostridium difficile, and diarrheagenic Escherichia coli. Furthermore, genes mediating antimicrobial resistance to fluoroquinolones (qnrB) and β-lactam drugs (bla(SHV) and bla(ACT/MIR)) were widely distributed. Culture and molecular strain typing of C. difficile revealed that mice harbor ribotypes associated with human disease, and screening of kidney samples demonstrated genetic evidence of pathogenic Leptospira species. In concert, these findings support the need for further research into the role of house mice as potential reservoirs for human pathogens and antimicrobial resistance in the built environment.
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spelling pubmed-59044142018-04-20 New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants Williams, Simon H. Che, Xiaoyu Paulick, Ashley Guo, Cheng Lee, Bohyun Muller, Dorothy Uhlemann, Anne-Catrin Lowy, Franklin D. Corrigan, Robert M. Lipkin, W. Ian mBio Research Article House mice (Mus musculus) thrive in large urban centers worldwide. Nonetheless, little is known about the role that they may play in contributing to environmental contamination with potentially pathogenic bacteria. Here, we describe the fecal microbiome of house mice with emphasis on detection of pathogenic bacteria and antimicrobial resistance genes by molecular methods. Four hundred sixteen mice were collected from predominantly residential buildings in seven sites across New York City over a period of 13 months. 16S rRNA sequencing identified Bacteroidetes as dominant and revealed high levels of Proteobacteria. A targeted PCR screen of 11 bacteria, as indicated by 16S rRNA analyses, found that mice are carriers of several gastrointestinal disease-causing agents, including Shigella, Salmonella, Clostridium difficile, and diarrheagenic Escherichia coli. Furthermore, genes mediating antimicrobial resistance to fluoroquinolones (qnrB) and β-lactam drugs (bla(SHV) and bla(ACT/MIR)) were widely distributed. Culture and molecular strain typing of C. difficile revealed that mice harbor ribotypes associated with human disease, and screening of kidney samples demonstrated genetic evidence of pathogenic Leptospira species. In concert, these findings support the need for further research into the role of house mice as potential reservoirs for human pathogens and antimicrobial resistance in the built environment. American Society for Microbiology 2018-04-17 /pmc/articles/PMC5904414/ /pubmed/29666289 http://dx.doi.org/10.1128/mBio.00624-18 Text en Copyright © 2018 Williams et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Williams, Simon H.
Che, Xiaoyu
Paulick, Ashley
Guo, Cheng
Lee, Bohyun
Muller, Dorothy
Uhlemann, Anne-Catrin
Lowy, Franklin D.
Corrigan, Robert M.
Lipkin, W. Ian
New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants
title New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants
title_full New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants
title_fullStr New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants
title_full_unstemmed New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants
title_short New York City House Mice (Mus musculus) as Potential Reservoirs for Pathogenic Bacteria and Antimicrobial Resistance Determinants
title_sort new york city house mice (mus musculus) as potential reservoirs for pathogenic bacteria and antimicrobial resistance determinants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904414/
https://www.ncbi.nlm.nih.gov/pubmed/29666289
http://dx.doi.org/10.1128/mBio.00624-18
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