Experimental support for multidrug resistance transfer potential in the preterm infant gut microbiota

Background There is currently a lack of experimental evidence for horizontal gene transfer (HGT) mechanisms in the human gut microbiota. The aim of this study was therefore to experimentally determine the HGT potential in the microbiota of a healthy preterm infant twin pair and to evaluate the globa...

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Veröffentlicht in:Pediatric research 2020-07, Vol.88 (1), p.57-65
Hauptverfasser: Hagbø, Mari, Ravi, Anuradha, Angell, Inga Leena, Sunde, Marianne, Ludvigsen, Jane, Diep, Dzung B., Foley, Steven L., Vento, Maximo, Collado, Maria Carmen, Perez-Martinez, Gaspar, Rudi, Knut
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container_end_page 65
container_issue 1
container_start_page 57
container_title Pediatric research
container_volume 88
creator Hagbø, Mari
Ravi, Anuradha
Angell, Inga Leena
Sunde, Marianne
Ludvigsen, Jane
Diep, Dzung B.
Foley, Steven L.
Vento, Maximo
Collado, Maria Carmen
Perez-Martinez, Gaspar
Rudi, Knut
description Background There is currently a lack of experimental evidence for horizontal gene transfer (HGT) mechanisms in the human gut microbiota. The aim of this study was therefore to experimentally determine the HGT potential in the microbiota of a healthy preterm infant twin pair and to evaluate the global occurrence of the mobilized elements. Methods Stool samples were collected. Both shotgun metagenome sequencing and bacterial culturing were done for the same samples. A range of experimental conditions were used to test DNA transfer for the cultured isolates. Searches for global distribution of transferable elements were done for the ~120,000 metagenomic samples in the Sequence Read Archive (SRA) database. Results DNA transfer experiments demonstrated frequent transmission of an ESBL encoding IncI1 plasmid, a high copy number ColEI plasmid, and bacteriophage P1. Both IncI1 and ColE1 were abundant in the stool samples. In vitro competition experiments showed that transconjugants containing IncI1 plasmids outcompeted the recipient strain in the absence of antibiotic selection. The SRA searches indicated a global distribution of the mobilizable elements, with chicken identified as a possible reservoir for the IncI1 ESBL encoding plasmid. Conclusion Our results experimentally support a major horizontal transmission and persistence potential of the preterm infant gut microbiota mobilome involving genes encoding ESBL.
doi_str_mv 10.1038/s41390-019-0491-8
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The aim of this study was therefore to experimentally determine the HGT potential in the microbiota of a healthy preterm infant twin pair and to evaluate the global occurrence of the mobilized elements. Methods Stool samples were collected. Both shotgun metagenome sequencing and bacterial culturing were done for the same samples. A range of experimental conditions were used to test DNA transfer for the cultured isolates. Searches for global distribution of transferable elements were done for the ~120,000 metagenomic samples in the Sequence Read Archive (SRA) database. Results DNA transfer experiments demonstrated frequent transmission of an ESBL encoding IncI1 plasmid, a high copy number ColEI plasmid, and bacteriophage P1. Both IncI1 and ColE1 were abundant in the stool samples. In vitro competition experiments showed that transconjugants containing IncI1 plasmids outcompeted the recipient strain in the absence of antibiotic selection. The SRA searches indicated a global distribution of the mobilizable elements, with chicken identified as a possible reservoir for the IncI1 ESBL encoding plasmid. Conclusion Our results experimentally support a major horizontal transmission and persistence potential of the preterm infant gut microbiota mobilome involving genes encoding ESBL.</description><identifier>ISSN: 0031-3998</identifier><identifier>EISSN: 1530-0447</identifier><identifier>DOI: 10.1038/s41390-019-0491-8</identifier><identifier>PMID: 31261372</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Baby foods ; Basic Science Article ; Drug resistance ; Medicine ; Medicine &amp; Public Health ; Microbiota ; Multidrug resistant organisms ; Pediatric Surgery ; Pediatrics ; Plasmids ; Premature babies</subject><ispartof>Pediatric research, 2020-07, Vol.88 (1), p.57-65</ispartof><rights>International Pediatric Research Foundation, Inc 2019</rights><rights>International Pediatric Research Foundation, Inc 2019.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-cbf870707c812e4653de2cb5fd1af6c873a32152e3bd24b5d51cac9d14ead20b3</citedby><cites>FETCH-LOGICAL-c400t-cbf870707c812e4653de2cb5fd1af6c873a32152e3bd24b5d51cac9d14ead20b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41390-019-0491-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41390-019-0491-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31261372$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hagbø, Mari</creatorcontrib><creatorcontrib>Ravi, Anuradha</creatorcontrib><creatorcontrib>Angell, Inga Leena</creatorcontrib><creatorcontrib>Sunde, Marianne</creatorcontrib><creatorcontrib>Ludvigsen, Jane</creatorcontrib><creatorcontrib>Diep, Dzung B.</creatorcontrib><creatorcontrib>Foley, Steven L.</creatorcontrib><creatorcontrib>Vento, Maximo</creatorcontrib><creatorcontrib>Collado, Maria Carmen</creatorcontrib><creatorcontrib>Perez-Martinez, Gaspar</creatorcontrib><creatorcontrib>Rudi, Knut</creatorcontrib><title>Experimental support for multidrug resistance transfer potential in the preterm infant gut microbiota</title><title>Pediatric research</title><addtitle>Pediatr Res</addtitle><addtitle>Pediatr Res</addtitle><description>Background There is currently a lack of experimental evidence for horizontal gene transfer (HGT) mechanisms in the human gut microbiota. 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The aim of this study was therefore to experimentally determine the HGT potential in the microbiota of a healthy preterm infant twin pair and to evaluate the global occurrence of the mobilized elements. Methods Stool samples were collected. Both shotgun metagenome sequencing and bacterial culturing were done for the same samples. A range of experimental conditions were used to test DNA transfer for the cultured isolates. Searches for global distribution of transferable elements were done for the ~120,000 metagenomic samples in the Sequence Read Archive (SRA) database. Results DNA transfer experiments demonstrated frequent transmission of an ESBL encoding IncI1 plasmid, a high copy number ColEI plasmid, and bacteriophage P1. Both IncI1 and ColE1 were abundant in the stool samples. In vitro competition experiments showed that transconjugants containing IncI1 plasmids outcompeted the recipient strain in the absence of antibiotic selection. The SRA searches indicated a global distribution of the mobilizable elements, with chicken identified as a possible reservoir for the IncI1 ESBL encoding plasmid. Conclusion Our results experimentally support a major horizontal transmission and persistence potential of the preterm infant gut microbiota mobilome involving genes encoding ESBL.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>31261372</pmid><doi>10.1038/s41390-019-0491-8</doi><tpages>9</tpages></addata></record>
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source Elektronische Zeitschriftenbibliothek; Alma/SFX Local Collection; SpringerLink Journals - AutoHoldings
subjects Baby foods
Basic Science Article
Drug resistance
Medicine
Medicine & Public Health
Microbiota
Multidrug resistant organisms
Pediatric Surgery
Pediatrics
Plasmids
Premature babies
title Experimental support for multidrug resistance transfer potential in the preterm infant gut microbiota
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