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dc.contributor.authorWard, Doyle V.
dc.contributor.authorScholz, Matthias
dc.contributor.authorZolfo, Moreno
dc.contributor.authorTaft, Diana H.
dc.contributor.authorSchibler, Kurt R.
dc.contributor.authorTett, Adrian
dc.contributor.authorSegata, Nicola
dc.contributor.authorMorrow, Ardythe L.
dc.date2022-08-11T08:09:45.000
dc.date.accessioned2022-08-23T16:42:20Z
dc.date.available2022-08-23T16:42:20Z
dc.date.issued2016-03-29
dc.date.submitted2016-10-05
dc.identifier.citationCell Rep. 2016 Mar 29;14(12):2912-24. doi:10.1016/j.celrep.2016.03.015. Epub 2016 Mar 17. <a href="http://dx.doi.org/10.1016/j.celrep.2016.03.015">Link to article on publisher's site</a>
dc.identifier.issn2211-1247 (Electronic)
dc.identifier.doi10.1016/j.celrep.2016.03.015
dc.identifier.pmid26997279
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40073
dc.description.abstractNecrotizing enterocolitis (NEC) afflicts approximately 10% of extremely preterm infants with high fatality. Inappropriate bacterial colonization with Enterobacteriaceae is implicated, but no specific pathogen has been identified. We identify uropathogenic E. coli (UPEC) colonization as a significant risk factor for the development of NEC and subsequent mortality. We describe a large-scale deep shotgun metagenomic sequence analysis of the early intestinal microbiome of 144 preterm and 22 term infants. Using a pan-genomic approach to functionally subtype the E. coli, we identify genes associated with NEC and mortality that indicate colonization by UPEC. Metagenomic multilocus sequence typing analysis further defined NEC-associated strains as sequence types often associated with urinary tract infections, including ST69, ST73, ST95, ST127, ST131, and ST144. Although other factors associated with prematurity may also contribute, this report suggests a link between UPEC and NEC and indicates that further attention to these sequence types as potential causal agents is needed.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26997279&dopt=Abstract">Link to Article in PubMed</a>
dc.rights<p>This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).</p>
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBacterial Infections and Mycoses
dc.subjectBacteriology
dc.subjectDigestive System Diseases
dc.subjectGenetics and Genomics
dc.subjectMedical Microbiology
dc.subjectPathogenic Microbiology
dc.subjectPediatrics
dc.titleMetagenomic Sequencing with Strain-Level Resolution Implicates Uropathogenic E. coli in Necrotizing Enterocolitis and Mortality in Preterm Infants
dc.typeJournal Article
dc.source.journaltitleCell reports
dc.source.volume14
dc.source.issue12
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3883&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2878
dc.identifier.contextkey9233101
refterms.dateFOA2022-08-23T16:42:21Z
html.description.abstract<p>Necrotizing enterocolitis (NEC) afflicts approximately 10% of extremely preterm infants with high fatality. Inappropriate bacterial colonization with Enterobacteriaceae is implicated, but no specific pathogen has been identified. We identify uropathogenic E. coli (UPEC) colonization as a significant risk factor for the development of NEC and subsequent mortality. We describe a large-scale deep shotgun metagenomic sequence analysis of the early intestinal microbiome of 144 preterm and 22 term infants. Using a pan-genomic approach to functionally subtype the E. coli, we identify genes associated with NEC and mortality that indicate colonization by UPEC. Metagenomic multilocus sequence typing analysis further defined NEC-associated strains as sequence types often associated with urinary tract infections, including ST69, ST73, ST95, ST127, ST131, and ST144. Although other factors associated with prematurity may also contribute, this report suggests a link between UPEC and NEC and indicates that further attention to these sequence types as potential causal agents is needed.</p>
dc.identifier.submissionpathoapubs/2878
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentCenter for Microbiome Research
dc.source.pages2912-24


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<p>This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).</p>
Except where otherwise noted, this item's license is described as <p>This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).</p>