Comparison by multilocus variable‐number tandem repeat analysis and antimicrobial resistance among atypical enteropathogenic Escherichia coli strains isolated from food samples and human and animal faecal specimens

Aim This study assessed whether multilocus variable‐number tandem repeat analysis (MLVA) and antimicrobial susceptibility testing discriminated diarrhoeagenic atypical enteropathogenic Escherichia coli (aEPEC) from aEPEC indigenous to domestic animals or healthy people. Methods and Results MLVA geno...

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Veröffentlicht in:Journal of applied microbiology 2017-01, Vol.122 (1), p.268-278
Hauptverfasser: Wang, L., Nakamura, H., Kage‐Nakadai, E., Hara‐Kudo, Y., Nishikawa, Y.
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container_issue 1
container_start_page 268
container_title Journal of applied microbiology
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creator Wang, L.
Nakamura, H.
Kage‐Nakadai, E.
Hara‐Kudo, Y.
Nishikawa, Y.
description Aim This study assessed whether multilocus variable‐number tandem repeat analysis (MLVA) and antimicrobial susceptibility testing discriminated diarrhoeagenic atypical enteropathogenic Escherichia coli (aEPEC) from aEPEC indigenous to domestic animals or healthy people. Methods and Results MLVA genotyping of 142 aEPEC strains isolated from foods and faecal samples of domestic animals and humans revealed 126 distinct MLVA profiles that distributed to four clusters, yielding a Simpson's index of diversity (D) of 99·8%. Cluster 2 included 87% of cattle isolates and 67% of patient isolates. The plurality (15/34, 44%) of strains from healthy humans mapped to Cluster 1, while half (18/41, 44%) of the swine strains belonged to Cluster 4. Testing for antimicrobial susceptibility revealed that 52 strains (37%) of aEPEC were resistant to one or more agents; only 10 strains (7%) exhibited resistance to more than three agents. Strains isolated from swine or food exhibited a wider variety of resistance phenotypes than bovine or human strains. Conclusions MLVA assigned the aEPEC isolates from cattle and patients to Cluster 2, distinct from aEPEC from other sources. Hog yards may be a larger source of drug‐resistant strains than are cattle ranches. Significance and Impact of the Study MLVA suggests that human diarrhoeagenic aEPEC are derived from cattle and are distinct from strains carried by healthy people and other animals. Cattle appear to be reservoirs of human diarrhoeagenic aEPEC.
doi_str_mv 10.1111/jam.13322
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Methods and Results MLVA genotyping of 142 aEPEC strains isolated from foods and faecal samples of domestic animals and humans revealed 126 distinct MLVA profiles that distributed to four clusters, yielding a Simpson's index of diversity (D) of 99·8%. Cluster 2 included 87% of cattle isolates and 67% of patient isolates. The plurality (15/34, 44%) of strains from healthy humans mapped to Cluster 1, while half (18/41, 44%) of the swine strains belonged to Cluster 4. Testing for antimicrobial susceptibility revealed that 52 strains (37%) of aEPEC were resistant to one or more agents; only 10 strains (7%) exhibited resistance to more than three agents. Strains isolated from swine or food exhibited a wider variety of resistance phenotypes than bovine or human strains. Conclusions MLVA assigned the aEPEC isolates from cattle and patients to Cluster 2, distinct from aEPEC from other sources. Hog yards may be a larger source of drug‐resistant strains than are cattle ranches. Significance and Impact of the Study MLVA suggests that human diarrhoeagenic aEPEC are derived from cattle and are distinct from strains carried by healthy people and other animals. Cattle appear to be reservoirs of human diarrhoeagenic aEPEC.</description><identifier>ISSN: 1364-5072</identifier><identifier>EISSN: 1365-2672</identifier><identifier>DOI: 10.1111/jam.13322</identifier><identifier>PMID: 27718315</identifier><identifier>CODEN: JAMIFK</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; Anti-Bacterial Agents - pharmacology ; Antibiotics ; Cattle ; Diarrhea ; Drug resistance ; Drug Resistance, Bacterial ; E coli ; Enteropathogenic Escherichia coli - classification ; Enteropathogenic Escherichia coli - drug effects ; Enteropathogenic Escherichia coli - genetics ; Enteropathogenic Escherichia coli - isolation &amp; purification ; Escherichia coli ; Escherichia coli Infections - microbiology ; Escherichia coli Infections - veterinary ; Escherichia coli Proteins - genetics ; Escherichia coli Proteins - metabolism ; Feces ; Feces - microbiology ; Food Microbiology ; food safety ; Genotype ; genotyping ; Humans ; Minisatellite Repeats ; molecular epidemiology ; Swine</subject><ispartof>Journal of applied microbiology, 2017-01, Vol.122 (1), p.268-278</ispartof><rights>2016 The Authors. published by John Wiley &amp; Sons Ltd on behalf of Society for Applied Microbiology.</rights><rights>2016 The Authors. Journal of Applied Microbiology published by John Wiley &amp; Sons Ltd on behalf of Society for Applied Microbiology.</rights><rights>Copyright © 2017 The Society for Applied Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4302-5733d8a3134dece792893cdd5603bd17e6d3cbf9026a3626708a4461e572c5293</citedby><cites>FETCH-LOGICAL-c4302-5733d8a3134dece792893cdd5603bd17e6d3cbf9026a3626708a4461e572c5293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjam.13322$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjam.13322$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27718315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, L.</creatorcontrib><creatorcontrib>Nakamura, H.</creatorcontrib><creatorcontrib>Kage‐Nakadai, E.</creatorcontrib><creatorcontrib>Hara‐Kudo, Y.</creatorcontrib><creatorcontrib>Nishikawa, Y.</creatorcontrib><title>Comparison by multilocus variable‐number tandem repeat analysis and antimicrobial resistance among atypical enteropathogenic Escherichia coli strains isolated from food samples and human and animal faecal specimens</title><title>Journal of applied microbiology</title><addtitle>J Appl Microbiol</addtitle><description>Aim This study assessed whether multilocus variable‐number tandem repeat analysis (MLVA) and antimicrobial susceptibility testing discriminated diarrhoeagenic atypical enteropathogenic Escherichia coli (aEPEC) from aEPEC indigenous to domestic animals or healthy people. Methods and Results MLVA genotyping of 142 aEPEC strains isolated from foods and faecal samples of domestic animals and humans revealed 126 distinct MLVA profiles that distributed to four clusters, yielding a Simpson's index of diversity (D) of 99·8%. Cluster 2 included 87% of cattle isolates and 67% of patient isolates. The plurality (15/34, 44%) of strains from healthy humans mapped to Cluster 1, while half (18/41, 44%) of the swine strains belonged to Cluster 4. Testing for antimicrobial susceptibility revealed that 52 strains (37%) of aEPEC were resistant to one or more agents; only 10 strains (7%) exhibited resistance to more than three agents. Strains isolated from swine or food exhibited a wider variety of resistance phenotypes than bovine or human strains. Conclusions MLVA assigned the aEPEC isolates from cattle and patients to Cluster 2, distinct from aEPEC from other sources. Hog yards may be a larger source of drug‐resistant strains than are cattle ranches. Significance and Impact of the Study MLVA suggests that human diarrhoeagenic aEPEC are derived from cattle and are distinct from strains carried by healthy people and other animals. 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Nakamura, H. ; Kage‐Nakadai, E. ; Hara‐Kudo, Y. ; Nishikawa, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4302-5733d8a3134dece792893cdd5603bd17e6d3cbf9026a3626708a4461e572c5293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibiotics</topic><topic>Cattle</topic><topic>Diarrhea</topic><topic>Drug resistance</topic><topic>Drug Resistance, Bacterial</topic><topic>E coli</topic><topic>Enteropathogenic Escherichia coli - classification</topic><topic>Enteropathogenic Escherichia coli - drug effects</topic><topic>Enteropathogenic Escherichia coli - genetics</topic><topic>Enteropathogenic Escherichia coli - isolation &amp; purification</topic><topic>Escherichia coli</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Escherichia coli Infections - veterinary</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>Feces</topic><topic>Feces - microbiology</topic><topic>Food Microbiology</topic><topic>food safety</topic><topic>Genotype</topic><topic>genotyping</topic><topic>Humans</topic><topic>Minisatellite Repeats</topic><topic>molecular epidemiology</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, L.</creatorcontrib><creatorcontrib>Nakamura, H.</creatorcontrib><creatorcontrib>Kage‐Nakadai, E.</creatorcontrib><creatorcontrib>Hara‐Kudo, Y.</creatorcontrib><creatorcontrib>Nishikawa, Y.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Archive</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, L.</au><au>Nakamura, H.</au><au>Kage‐Nakadai, E.</au><au>Hara‐Kudo, Y.</au><au>Nishikawa, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison by multilocus variable‐number tandem repeat analysis and antimicrobial resistance among atypical enteropathogenic Escherichia coli strains isolated from food samples and human and animal faecal specimens</atitle><jtitle>Journal of applied microbiology</jtitle><addtitle>J Appl Microbiol</addtitle><date>2017-01</date><risdate>2017</risdate><volume>122</volume><issue>1</issue><spage>268</spage><epage>278</epage><pages>268-278</pages><issn>1364-5072</issn><eissn>1365-2672</eissn><coden>JAMIFK</coden><abstract>Aim This study assessed whether multilocus variable‐number tandem repeat analysis (MLVA) and antimicrobial susceptibility testing discriminated diarrhoeagenic atypical enteropathogenic Escherichia coli (aEPEC) from aEPEC indigenous to domestic animals or healthy people. Methods and Results MLVA genotyping of 142 aEPEC strains isolated from foods and faecal samples of domestic animals and humans revealed 126 distinct MLVA profiles that distributed to four clusters, yielding a Simpson's index of diversity (D) of 99·8%. Cluster 2 included 87% of cattle isolates and 67% of patient isolates. The plurality (15/34, 44%) of strains from healthy humans mapped to Cluster 1, while half (18/41, 44%) of the swine strains belonged to Cluster 4. Testing for antimicrobial susceptibility revealed that 52 strains (37%) of aEPEC were resistant to one or more agents; only 10 strains (7%) exhibited resistance to more than three agents. Strains isolated from swine or food exhibited a wider variety of resistance phenotypes than bovine or human strains. Conclusions MLVA assigned the aEPEC isolates from cattle and patients to Cluster 2, distinct from aEPEC from other sources. Hog yards may be a larger source of drug‐resistant strains than are cattle ranches. Significance and Impact of the Study MLVA suggests that human diarrhoeagenic aEPEC are derived from cattle and are distinct from strains carried by healthy people and other animals. Cattle appear to be reservoirs of human diarrhoeagenic aEPEC.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>27718315</pmid><doi>10.1111/jam.13322</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Anti-Bacterial Agents - pharmacology
Antibiotics
Cattle
Diarrhea
Drug resistance
Drug Resistance, Bacterial
E coli
Enteropathogenic Escherichia coli - classification
Enteropathogenic Escherichia coli - drug effects
Enteropathogenic Escherichia coli - genetics
Enteropathogenic Escherichia coli - isolation & purification
Escherichia coli
Escherichia coli Infections - microbiology
Escherichia coli Infections - veterinary
Escherichia coli Proteins - genetics
Escherichia coli Proteins - metabolism
Feces
Feces - microbiology
Food Microbiology
food safety
Genotype
genotyping
Humans
Minisatellite Repeats
molecular epidemiology
Swine
title Comparison by multilocus variable‐number tandem repeat analysis and antimicrobial resistance among atypical enteropathogenic Escherichia coli strains isolated from food samples and human and animal faecal specimens
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