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Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis

Recent studies have provided evidence for rapid pathogen genome diversification, some of which could potentially affect the course of disease. We have previously described such variation seen between isolates infecting the blood and cerebrospinal fluid (CSF) of a single patient during a case of bact...

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Autores principales: Lees, John A., Kremer, Philip H. C., Manso, Ana S., Croucher, Nicholas J., Ferwerda, Bart, Serón, Mercedes Valls, Oggioni, Marco R., Parkhill, Julian, Brouwer, Matthijs C., van der Ende, Arie, van de Beek, Diederik, Bentley, Stephen D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361624/
https://www.ncbi.nlm.nih.gov/pubmed/28348877
http://dx.doi.org/10.1099/mgen.0.000103
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author Lees, John A.
Kremer, Philip H. C.
Manso, Ana S.
Croucher, Nicholas J.
Ferwerda, Bart
Serón, Mercedes Valls
Oggioni, Marco R.
Parkhill, Julian
Brouwer, Matthijs C.
van der Ende, Arie
van de Beek, Diederik
Bentley, Stephen D.
author_facet Lees, John A.
Kremer, Philip H. C.
Manso, Ana S.
Croucher, Nicholas J.
Ferwerda, Bart
Serón, Mercedes Valls
Oggioni, Marco R.
Parkhill, Julian
Brouwer, Matthijs C.
van der Ende, Arie
van de Beek, Diederik
Bentley, Stephen D.
author_sort Lees, John A.
collection PubMed
description Recent studies have provided evidence for rapid pathogen genome diversification, some of which could potentially affect the course of disease. We have previously described such variation seen between isolates infecting the blood and cerebrospinal fluid (CSF) of a single patient during a case of bacterial meningitis. Here, we performed whole-genome sequencing of paired isolates from the blood and CSF of 869 meningitis patients to determine whether such variation frequently occurs between these two niches in cases of bacterial meningitis. Using a combination of reference-free variant calling approaches, we show that no genetic adaptation occurs in either invaded niche during bacterial meningitis for two major pathogen species, Streptococcus pneumoniae and Neisseria meningitidis. This study therefore shows that the bacteria capable of causing meningitis are already able to do this upon entering the blood, and no further sequence change is necessary to cross the blood–brain barrier. Our findings place the focus back on bacterial evolution between nasopharyngeal carriage and invasion, or diversity of the host, as likely mechanisms for determining invasiveness.
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spelling pubmed-53616242017-03-27 Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis Lees, John A. Kremer, Philip H. C. Manso, Ana S. Croucher, Nicholas J. Ferwerda, Bart Serón, Mercedes Valls Oggioni, Marco R. Parkhill, Julian Brouwer, Matthijs C. van der Ende, Arie van de Beek, Diederik Bentley, Stephen D. Microb Genom Research Article Recent studies have provided evidence for rapid pathogen genome diversification, some of which could potentially affect the course of disease. We have previously described such variation seen between isolates infecting the blood and cerebrospinal fluid (CSF) of a single patient during a case of bacterial meningitis. Here, we performed whole-genome sequencing of paired isolates from the blood and CSF of 869 meningitis patients to determine whether such variation frequently occurs between these two niches in cases of bacterial meningitis. Using a combination of reference-free variant calling approaches, we show that no genetic adaptation occurs in either invaded niche during bacterial meningitis for two major pathogen species, Streptococcus pneumoniae and Neisseria meningitidis. This study therefore shows that the bacteria capable of causing meningitis are already able to do this upon entering the blood, and no further sequence change is necessary to cross the blood–brain barrier. Our findings place the focus back on bacterial evolution between nasopharyngeal carriage and invasion, or diversity of the host, as likely mechanisms for determining invasiveness. Microbiology Society 2017-01-31 /pmc/articles/PMC5361624/ /pubmed/28348877 http://dx.doi.org/10.1099/mgen.0.000103 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lees, John A.
Kremer, Philip H. C.
Manso, Ana S.
Croucher, Nicholas J.
Ferwerda, Bart
Serón, Mercedes Valls
Oggioni, Marco R.
Parkhill, Julian
Brouwer, Matthijs C.
van der Ende, Arie
van de Beek, Diederik
Bentley, Stephen D.
Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
title Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
title_full Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
title_fullStr Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
title_full_unstemmed Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
title_short Large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
title_sort large scale genomic analysis shows no evidence for pathogen adaptation between the blood and cerebrospinal fluid niches during bacterial meningitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361624/
https://www.ncbi.nlm.nih.gov/pubmed/28348877
http://dx.doi.org/10.1099/mgen.0.000103
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