Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.

Escherichia coli is the leading cause of Gram-negative neonatal septicemia in the United States. Invasion and passage across the neonatal gut after ingestion of maternal E. coli strains produce bacteremia. In this study, we compared the virulence properties of the neonatal E. coli bacteremia clinica...

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Main Authors: Bryan K Cole, Edgar Scott, Marko Ilikj, David Bard, Darrin R Akins, David W Dyer, Susana Chavez-Bueno
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5728477?pdf=render
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spelling doaj-529a83155871409fa82efb4f16f1c6fa2020-11-24T22:07:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011212e018903210.1371/journal.pone.0189032Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.Bryan K ColeEdgar ScottMarko IlikjDavid BardDarrin R AkinsDavid W DyerSusana Chavez-BuenoEscherichia coli is the leading cause of Gram-negative neonatal septicemia in the United States. Invasion and passage across the neonatal gut after ingestion of maternal E. coli strains produce bacteremia. In this study, we compared the virulence properties of the neonatal E. coli bacteremia clinical isolate SCB34 with the archetypal neonatal E. coli meningitis strain RS218. Whole-genome sequencing data was used to compare the protein coding sequences among these clinical isolates and 33 other representative E. coli strains. Oral inoculation of newborn animals with either strain produced septicemia, whereas intraperitoneal injection caused septicemia only in pups infected with RS218 but not in those injected with SCB34. In addition to being virulent only through the oral route, SCB34 demonstrated significantly greater invasion and transcytosis of polarized intestinal epithelial cells in vitro as compared to RS218. Protein coding sequences comparisons highlighted the presence of known virulence factors that are shared among several of these isolates, and revealed the existence of proteins exclusively encoded in SCB34, many of which remain uncharacterized. Our study demonstrates that oral acquisition is crucial for the virulence properties of the neonatal bacteremia clinical isolate SCB34. This characteristic, along with its enhanced ability to invade and transcytose intestinal epithelium are likely determined by the specific virulence factors that predominate in this strain.http://europepmc.org/articles/PMC5728477?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Bryan K Cole
Edgar Scott
Marko Ilikj
David Bard
Darrin R Akins
David W Dyer
Susana Chavez-Bueno
spellingShingle Bryan K Cole
Edgar Scott
Marko Ilikj
David Bard
Darrin R Akins
David W Dyer
Susana Chavez-Bueno
Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.
PLoS ONE
author_facet Bryan K Cole
Edgar Scott
Marko Ilikj
David Bard
Darrin R Akins
David W Dyer
Susana Chavez-Bueno
author_sort Bryan K Cole
title Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.
title_short Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.
title_full Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.
title_fullStr Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.
title_full_unstemmed Route of infection alters virulence of neonatal septicemia Escherichia coli clinical isolates.
title_sort route of infection alters virulence of neonatal septicemia escherichia coli clinical isolates.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Escherichia coli is the leading cause of Gram-negative neonatal septicemia in the United States. Invasion and passage across the neonatal gut after ingestion of maternal E. coli strains produce bacteremia. In this study, we compared the virulence properties of the neonatal E. coli bacteremia clinical isolate SCB34 with the archetypal neonatal E. coli meningitis strain RS218. Whole-genome sequencing data was used to compare the protein coding sequences among these clinical isolates and 33 other representative E. coli strains. Oral inoculation of newborn animals with either strain produced septicemia, whereas intraperitoneal injection caused septicemia only in pups infected with RS218 but not in those injected with SCB34. In addition to being virulent only through the oral route, SCB34 demonstrated significantly greater invasion and transcytosis of polarized intestinal epithelial cells in vitro as compared to RS218. Protein coding sequences comparisons highlighted the presence of known virulence factors that are shared among several of these isolates, and revealed the existence of proteins exclusively encoded in SCB34, many of which remain uncharacterized. Our study demonstrates that oral acquisition is crucial for the virulence properties of the neonatal bacteremia clinical isolate SCB34. This characteristic, along with its enhanced ability to invade and transcytose intestinal epithelium are likely determined by the specific virulence factors that predominate in this strain.
url http://europepmc.org/articles/PMC5728477?pdf=render
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