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Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants

BACKGROUND: Late-onset bloodstream infection (LO-BSI) is a common complication of prematurity, and lack of timely diagnosis and treatment can have life-threatening consequences. We sought to identify clinical characteristics and microbial signatures in the gastrointestinal microbiota preceding diagn...

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Autores principales: Shaw, Alexander G., Sim, Kathleen, Randell, Paul, Cox, Michael J., McClure, Zoë E., Li, Ming-Shi, Donaldson, Hugo, Langford, Paul R., Cookson, William O. C. M., Moffatt, Miriam F., Kroll, J. Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500406/
https://www.ncbi.nlm.nih.gov/pubmed/26167683
http://dx.doi.org/10.1371/journal.pone.0132923
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author Shaw, Alexander G.
Sim, Kathleen
Randell, Paul
Cox, Michael J.
McClure, Zoë E.
Li, Ming-Shi
Donaldson, Hugo
Langford, Paul R.
Cookson, William O. C. M.
Moffatt, Miriam F.
Kroll, J. Simon
author_facet Shaw, Alexander G.
Sim, Kathleen
Randell, Paul
Cox, Michael J.
McClure, Zoë E.
Li, Ming-Shi
Donaldson, Hugo
Langford, Paul R.
Cookson, William O. C. M.
Moffatt, Miriam F.
Kroll, J. Simon
author_sort Shaw, Alexander G.
collection PubMed
description BACKGROUND: Late-onset bloodstream infection (LO-BSI) is a common complication of prematurity, and lack of timely diagnosis and treatment can have life-threatening consequences. We sought to identify clinical characteristics and microbial signatures in the gastrointestinal microbiota preceding diagnosis of LO-BSI in premature infants. METHOD: Daily faecal samples and clinical data were collected over two years from 369 premature neonates (<32 weeks gestation). We analysed samples from 22 neonates who developed LO-BSI and 44 matched control infants. Next-generation sequencing of 16S rRNA gene regions amplified by PCR from total faecal DNA was used to characterise the microbiota of faecal samples preceding diagnosis from infants with LO-BSI and controls. Culture of selected samples was undertaken, and bacterial isolates identified using MALDI-TOF. Antibiograms from bloodstream and faecal isolates were compared to explore strain similarity. RESULTS: From the week prior to diagnosis, infants with LO-BSI had higher proportions of faecal aerobes/facultative anaerobes compared to controls. Risk factors for LO-BSI were identified by multivariate analysis. Enterobacteriaceal sepsis was associated with antecedent multiple lines, low birth weight and a faecal microbiota with prominent Enterobacteriaceae. Staphylococcal sepsis was associated with Staphylococcus OTU faecal over-abundance, and the number of days prior to diagnosis of mechanical ventilation and of the presence of centrally-placed lines. In 12 cases, the antibiogram of the bloodstream isolate matched that of a component of the faecal microbiota in the sample collected closest to diagnosis. CONCLUSIONS: The gastrointestinal tract is an important reservoir for LO-BSI organisms, pathogens translocating across the epithelial barrier. LO-BSI is associated with an aberrant microbiota, with abundant staphylococci and Enterobacteriaceae and a failure to mature towards predominance of obligate anaerobes.
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spelling pubmed-45004062015-07-17 Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants Shaw, Alexander G. Sim, Kathleen Randell, Paul Cox, Michael J. McClure, Zoë E. Li, Ming-Shi Donaldson, Hugo Langford, Paul R. Cookson, William O. C. M. Moffatt, Miriam F. Kroll, J. Simon PLoS One Research Article BACKGROUND: Late-onset bloodstream infection (LO-BSI) is a common complication of prematurity, and lack of timely diagnosis and treatment can have life-threatening consequences. We sought to identify clinical characteristics and microbial signatures in the gastrointestinal microbiota preceding diagnosis of LO-BSI in premature infants. METHOD: Daily faecal samples and clinical data were collected over two years from 369 premature neonates (<32 weeks gestation). We analysed samples from 22 neonates who developed LO-BSI and 44 matched control infants. Next-generation sequencing of 16S rRNA gene regions amplified by PCR from total faecal DNA was used to characterise the microbiota of faecal samples preceding diagnosis from infants with LO-BSI and controls. Culture of selected samples was undertaken, and bacterial isolates identified using MALDI-TOF. Antibiograms from bloodstream and faecal isolates were compared to explore strain similarity. RESULTS: From the week prior to diagnosis, infants with LO-BSI had higher proportions of faecal aerobes/facultative anaerobes compared to controls. Risk factors for LO-BSI were identified by multivariate analysis. Enterobacteriaceal sepsis was associated with antecedent multiple lines, low birth weight and a faecal microbiota with prominent Enterobacteriaceae. Staphylococcal sepsis was associated with Staphylococcus OTU faecal over-abundance, and the number of days prior to diagnosis of mechanical ventilation and of the presence of centrally-placed lines. In 12 cases, the antibiogram of the bloodstream isolate matched that of a component of the faecal microbiota in the sample collected closest to diagnosis. CONCLUSIONS: The gastrointestinal tract is an important reservoir for LO-BSI organisms, pathogens translocating across the epithelial barrier. LO-BSI is associated with an aberrant microbiota, with abundant staphylococci and Enterobacteriaceae and a failure to mature towards predominance of obligate anaerobes. Public Library of Science 2015-07-13 /pmc/articles/PMC4500406/ /pubmed/26167683 http://dx.doi.org/10.1371/journal.pone.0132923 Text en © 2015 Shaw et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shaw, Alexander G.
Sim, Kathleen
Randell, Paul
Cox, Michael J.
McClure, Zoë E.
Li, Ming-Shi
Donaldson, Hugo
Langford, Paul R.
Cookson, William O. C. M.
Moffatt, Miriam F.
Kroll, J. Simon
Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants
title Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants
title_full Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants
title_fullStr Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants
title_full_unstemmed Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants
title_short Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants
title_sort late-onset bloodstream infection and perturbed maturation of the gastrointestinal microbiota in premature infants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500406/
https://www.ncbi.nlm.nih.gov/pubmed/26167683
http://dx.doi.org/10.1371/journal.pone.0132923
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