Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.

Little is currently known about bacterial pathogen evolution and adaptation within the host during acute infection. Previous studies of Burkholderia pseudomallei, the etiologic agent of melioidosis, have shown that this opportunistic pathogen mutates rapidly both in vitro and in vivo at tandemly rep...

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Main Authors: Erin P Price, Heidie M Hornstra, Direk Limmathurotsakul, Tamara L Max, Derek S Sarovich, Amy J Vogler, Julia L Dale, Jennifer L Ginther, Benjamin Leadem, Rebecca E Colman, Jeffrey T Foster, Apichai Tuanyok, David M Wagner, Sharon J Peacock, Talima Pearson, Paul Keim
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS Pathogens
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20090837/?tool=EBI
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spelling doaj-c2136e5fe63e40d097e8953b27bba3482021-04-21T17:35:36ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742010-01-0161e100072510.1371/journal.ppat.1000725Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.Erin P PriceHeidie M HornstraDirek LimmathurotsakulTamara L MaxDerek S SarovichAmy J VoglerJulia L DaleJennifer L GintherBenjamin LeademRebecca E ColmanJeffrey T FosterApichai TuanyokDavid M WagnerSharon J PeacockTalima PearsonPaul KeimLittle is currently known about bacterial pathogen evolution and adaptation within the host during acute infection. Previous studies of Burkholderia pseudomallei, the etiologic agent of melioidosis, have shown that this opportunistic pathogen mutates rapidly both in vitro and in vivo at tandemly repeated loci, making this organism a relevant model for studying short-term evolution. In the current study, B. pseudomallei isolates cultured from multiple body sites from four Thai patients with disseminated melioidosis were subjected to fine-scale genotyping using multilocus variable-number tandem repeat analysis (MLVA). In order to understand and model the in vivo variable-number tandem repeat (VNTR) mutational process, we characterized the patterns and rates of mutations in vitro through parallel serial passage experiments of B. pseudomallei. Despite the short period of infection, substantial divergence from the putative founder genotype was observed in all four melioidosis cases. This study presents a paradigm for examining bacterial evolution over the short timescale of an acute infection. Further studies are required to determine whether the mutational process leads to phenotypic alterations that impact upon bacterial fitness in vivo. Our findings have important implications for future sampling strategies, since colonies in a single clinical sample may be genetically heterogeneous, and organisms in a culture taken late in the infective process may have undergone considerable genetic change compared with the founder inoculum.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20090837/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Erin P Price
Heidie M Hornstra
Direk Limmathurotsakul
Tamara L Max
Derek S Sarovich
Amy J Vogler
Julia L Dale
Jennifer L Ginther
Benjamin Leadem
Rebecca E Colman
Jeffrey T Foster
Apichai Tuanyok
David M Wagner
Sharon J Peacock
Talima Pearson
Paul Keim
spellingShingle Erin P Price
Heidie M Hornstra
Direk Limmathurotsakul
Tamara L Max
Derek S Sarovich
Amy J Vogler
Julia L Dale
Jennifer L Ginther
Benjamin Leadem
Rebecca E Colman
Jeffrey T Foster
Apichai Tuanyok
David M Wagner
Sharon J Peacock
Talima Pearson
Paul Keim
Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.
PLoS Pathogens
author_facet Erin P Price
Heidie M Hornstra
Direk Limmathurotsakul
Tamara L Max
Derek S Sarovich
Amy J Vogler
Julia L Dale
Jennifer L Ginther
Benjamin Leadem
Rebecca E Colman
Jeffrey T Foster
Apichai Tuanyok
David M Wagner
Sharon J Peacock
Talima Pearson
Paul Keim
author_sort Erin P Price
title Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.
title_short Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.
title_full Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.
title_fullStr Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.
title_full_unstemmed Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis.
title_sort within-host evolution of burkholderia pseudomallei in four cases of acute melioidosis.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2010-01-01
description Little is currently known about bacterial pathogen evolution and adaptation within the host during acute infection. Previous studies of Burkholderia pseudomallei, the etiologic agent of melioidosis, have shown that this opportunistic pathogen mutates rapidly both in vitro and in vivo at tandemly repeated loci, making this organism a relevant model for studying short-term evolution. In the current study, B. pseudomallei isolates cultured from multiple body sites from four Thai patients with disseminated melioidosis were subjected to fine-scale genotyping using multilocus variable-number tandem repeat analysis (MLVA). In order to understand and model the in vivo variable-number tandem repeat (VNTR) mutational process, we characterized the patterns and rates of mutations in vitro through parallel serial passage experiments of B. pseudomallei. Despite the short period of infection, substantial divergence from the putative founder genotype was observed in all four melioidosis cases. This study presents a paradigm for examining bacterial evolution over the short timescale of an acute infection. Further studies are required to determine whether the mutational process leads to phenotypic alterations that impact upon bacterial fitness in vivo. Our findings have important implications for future sampling strategies, since colonies in a single clinical sample may be genetically heterogeneous, and organisms in a culture taken late in the infective process may have undergone considerable genetic change compared with the founder inoculum.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20090837/?tool=EBI
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