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Diversity of P1 phage-like elements in multidrug resistant Escherichia coli
The spread of multidrug resistance via mobile genetic elements is a major clinical and veterinary concern. Pathogenic Escherichia coli harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three E....
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Published in: | Scientific reports 2019-12, Vol.9 (1), p.18861-10, Article 18861 |
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description | The spread of multidrug resistance via mobile genetic elements is a major clinical and veterinary concern. Pathogenic
Escherichia coli
harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three
E. coli
phage-like plasmids, pJIE250-3 from a human
E. coli
clinical isolate, pSvP1 from a porcine ETEC O157 isolate, and pTZ20_1P from a porcine commensal
E. coli
, were sequenced (PacBio RSII), annotated and compared. All three elements are coliphage P1 variants, each with unique adaptations. pJIE250-3 is a P1-derivative that has lost lytic functions and contains no accessory genes. In pTZ20_1P and pSvP1, a core P1-like genome is associated with insertion sequence-mediated acquisition of plasmid modules encoding multidrug resistance and virulence, respectively. The transfer ability of pTZ20_1P, carrying antibiotic resistance markers, was also tested and, although this element was not able to transfer by conjugation, it was able to lysogenize a commensal
E. coli
strain with consequent transfer of resistance. The incidence of P1-like plasmids (~7%) in our
E. coli
collections correlated well with that in public databases. This study highlights the need to investigate the contribution of phage-like plasmids to the successful spread of antibiotic resistant pathotypes. |
doi_str_mv | 10.1038/s41598-019-54895-4 |
format | article |
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Escherichia coli
harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three
E. coli
phage-like plasmids, pJIE250-3 from a human
E. coli
clinical isolate, pSvP1 from a porcine ETEC O157 isolate, and pTZ20_1P from a porcine commensal
E. coli
, were sequenced (PacBio RSII), annotated and compared. All three elements are coliphage P1 variants, each with unique adaptations. pJIE250-3 is a P1-derivative that has lost lytic functions and contains no accessory genes. In pTZ20_1P and pSvP1, a core P1-like genome is associated with insertion sequence-mediated acquisition of plasmid modules encoding multidrug resistance and virulence, respectively. The transfer ability of pTZ20_1P, carrying antibiotic resistance markers, was also tested and, although this element was not able to transfer by conjugation, it was able to lysogenize a commensal
E. coli
strain with consequent transfer of resistance. The incidence of P1-like plasmids (~7%) in our
E. coli
collections correlated well with that in public databases. This study highlights the need to investigate the contribution of phage-like plasmids to the successful spread of antibiotic resistant pathotypes.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-54895-4</identifier><identifier>PMID: 31827120</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45 ; 45/22 ; 45/23 ; 45/29 ; 45/77 ; 631/326/1321 ; 631/326/22/1434 ; Animals ; Antibiotic resistance ; Antibiotics ; Bacteriophage P1 - genetics ; Coliphages - genetics ; Drug resistance ; Drug Resistance, Multiple, Bacterial - genetics ; E coli ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - physiology ; Genetic Variation ; Genome, Bacterial ; Humanities and Social Sciences ; Humans ; multidisciplinary ; Multidrug resistance ; Multidrug resistant organisms ; Phages ; Plasmids ; Science ; Science (multidisciplinary) ; Sequence Analysis, DNA ; Swine</subject><ispartof>Scientific reports, 2019-12, Vol.9 (1), p.18861-10, Article 18861</ispartof><rights>The Author(s) 2019</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-af32ccefac1050bec14cc6fbdb6f0e6167864946465c752968a8dc41170681a43</citedby><cites>FETCH-LOGICAL-c540t-af32ccefac1050bec14cc6fbdb6f0e6167864946465c752968a8dc41170681a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2324903649/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2324903649?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31827120$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Venturini, Carola</creatorcontrib><creatorcontrib>Zingali, Tiziana</creatorcontrib><creatorcontrib>Wyrsch, Ethan R.</creatorcontrib><creatorcontrib>Bowring, Bethany</creatorcontrib><creatorcontrib>Iredell, Jonathan</creatorcontrib><creatorcontrib>Partridge, Sally R.</creatorcontrib><creatorcontrib>Djordjevic, Steven P.</creatorcontrib><title>Diversity of P1 phage-like elements in multidrug resistant Escherichia coli</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The spread of multidrug resistance via mobile genetic elements is a major clinical and veterinary concern. Pathogenic
Escherichia coli
harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three
E. coli
phage-like plasmids, pJIE250-3 from a human
E. coli
clinical isolate, pSvP1 from a porcine ETEC O157 isolate, and pTZ20_1P from a porcine commensal
E. coli
, were sequenced (PacBio RSII), annotated and compared. All three elements are coliphage P1 variants, each with unique adaptations. pJIE250-3 is a P1-derivative that has lost lytic functions and contains no accessory genes. In pTZ20_1P and pSvP1, a core P1-like genome is associated with insertion sequence-mediated acquisition of plasmid modules encoding multidrug resistance and virulence, respectively. The transfer ability of pTZ20_1P, carrying antibiotic resistance markers, was also tested and, although this element was not able to transfer by conjugation, it was able to lysogenize a commensal
E. coli
strain with consequent transfer of resistance. The incidence of P1-like plasmids (~7%) in our
E. coli
collections correlated well with that in public databases. 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genetics</topic><topic>Coliphages - genetics</topic><topic>Drug resistance</topic><topic>Drug Resistance, Multiple, Bacterial - genetics</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - physiology</topic><topic>Genetic Variation</topic><topic>Genome, Bacterial</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>multidisciplinary</topic><topic>Multidrug resistance</topic><topic>Multidrug resistant organisms</topic><topic>Phages</topic><topic>Plasmids</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Sequence Analysis, DNA</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Venturini, Carola</creatorcontrib><creatorcontrib>Zingali, Tiziana</creatorcontrib><creatorcontrib>Wyrsch, Ethan R.</creatorcontrib><creatorcontrib>Bowring, Bethany</creatorcontrib><creatorcontrib>Iredell, Jonathan</creatorcontrib><creatorcontrib>Partridge, Sally R.</creatorcontrib><creatorcontrib>Djordjevic, Steven P.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Venturini, Carola</au><au>Zingali, Tiziana</au><au>Wyrsch, Ethan R.</au><au>Bowring, Bethany</au><au>Iredell, Jonathan</au><au>Partridge, Sally R.</au><au>Djordjevic, Steven P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diversity of P1 phage-like elements in multidrug resistant Escherichia coli</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-12-11</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>18861</spage><epage>10</epage><pages>18861-10</pages><artnum>18861</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The spread of multidrug resistance via mobile genetic elements is a major clinical and veterinary concern. Pathogenic
Escherichia coli
harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three
E. coli
phage-like plasmids, pJIE250-3 from a human
E. coli
clinical isolate, pSvP1 from a porcine ETEC O157 isolate, and pTZ20_1P from a porcine commensal
E. coli
, were sequenced (PacBio RSII), annotated and compared. All three elements are coliphage P1 variants, each with unique adaptations. pJIE250-3 is a P1-derivative that has lost lytic functions and contains no accessory genes. In pTZ20_1P and pSvP1, a core P1-like genome is associated with insertion sequence-mediated acquisition of plasmid modules encoding multidrug resistance and virulence, respectively. The transfer ability of pTZ20_1P, carrying antibiotic resistance markers, was also tested and, although this element was not able to transfer by conjugation, it was able to lysogenize a commensal
E. coli
strain with consequent transfer of resistance. The incidence of P1-like plasmids (~7%) in our
E. coli
collections correlated well with that in public databases. This study highlights the need to investigate the contribution of phage-like plasmids to the successful spread of antibiotic resistant pathotypes.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31827120</pmid><doi>10.1038/s41598-019-54895-4</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | Publicly Available Content (ProQuest); PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 45 45/22 45/23 45/29 45/77 631/326/1321 631/326/22/1434 Animals Antibiotic resistance Antibiotics Bacteriophage P1 - genetics Coliphages - genetics Drug resistance Drug Resistance, Multiple, Bacterial - genetics E coli Escherichia coli Escherichia coli - genetics Escherichia coli - physiology Genetic Variation Genome, Bacterial Humanities and Social Sciences Humans multidisciplinary Multidrug resistance Multidrug resistant organisms Phages Plasmids Science Science (multidisciplinary) Sequence Analysis, DNA Swine |
title | Diversity of P1 phage-like elements in multidrug resistant Escherichia coli |
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