Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.

The six major genetic lineages of Mycobacterium tuberculosis are strongly associated with specific geographical regions, but their relevance to bacterial virulence and the clinical consequences of infection are unclear. Previously, we found that in Vietnam, East Asian/Beijing and Indo-Oceanic strain...

Full description

Bibliographic Details
Main Authors: Nitya Krishnan, Wladimir Malaga, Patricia Constant, Maxine Caws, Thi Hoang Chau Tran, Jenifer Salmons, Thi Ngoc Lan Nguyen, Duc Bang Nguyen, Mamadou Daffé, Douglas B Young, Brian D Robertson, Christophe Guilhot, Guy E Thwaites
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3169546?pdf=render
_version_ 1828739526097371136
author Nitya Krishnan
Wladimir Malaga
Patricia Constant
Maxine Caws
Thi Hoang Chau Tran
Jenifer Salmons
Thi Ngoc Lan Nguyen
Duc Bang Nguyen
Mamadou Daffé
Douglas B Young
Brian D Robertson
Christophe Guilhot
Guy E Thwaites
author_facet Nitya Krishnan
Wladimir Malaga
Patricia Constant
Maxine Caws
Thi Hoang Chau Tran
Jenifer Salmons
Thi Ngoc Lan Nguyen
Duc Bang Nguyen
Mamadou Daffé
Douglas B Young
Brian D Robertson
Christophe Guilhot
Guy E Thwaites
author_sort Nitya Krishnan
collection DOAJ
description The six major genetic lineages of Mycobacterium tuberculosis are strongly associated with specific geographical regions, but their relevance to bacterial virulence and the clinical consequences of infection are unclear. Previously, we found that in Vietnam, East Asian/Beijing and Indo-Oceanic strains were significantly more likely to cause disseminated tuberculosis with meningitis than those from the Euro-American lineage. To investigate this observation we characterised 7 East Asian/Beijing, 5 Indo-Oceanic and 6 Euro-American Vietnamese strains in bone-marrow-derived macrophages, dendritic cells and mice. East Asian/Beijing and Indo-Oceanic strains induced significantly more TNF-α and IL-1β from macrophages than the Euro-American strains, and East Asian/Beijing strains were detectable earlier in the blood of infected mice and grew faster in the lungs. We hypothesised that these differences were induced by lineage-specific variation in cell envelope lipids. Whole lipid extracts from East Asian/Beijing and Indo-Oceanic strains induced higher concentrations of TNF-α from macrophages than Euro-American lipids. The lipid extracts were fractionated and compared by thin layer chromatography to reveal a distinct pattern of lineage-associated profiles. A phthiotriol dimycocerosate was exclusively produced by East Asian/Beijing strains, but not the phenolic glycolipid previously associated with the hyper-virulent phenotype of some isolates of this lineage. All Indo-Oceanic strains produced a unique unidentified lipid, shown to be a phenolphthiocerol dimycocerosate dependent upon an intact pks15/1 for its production. This was described by Goren as the 'attenuation indictor lipid' more than 40 years ago, due to its association with less virulent strains from southern India. Mutation of pks15/1 in a representative Indo-Oceanic strain prevented phenolphthiocerol dimycocerosate synthesis, but did not alter macrophage cytokine induction. Our findings suggest that the early interactions between M. tuberculosis and host are determined by the lineage of the infecting strain; but we were unable to show these differences are driven by lineage-specific cell-surface expressed lipids.
first_indexed 2024-04-13T00:24:02Z
format Article
id doaj.art-e7adbee087fe423f9b1c10df1cc73031
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-13T00:24:02Z
publishDate 2011-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-e7adbee087fe423f9b1c10df1cc730312022-12-22T03:10:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0169e2387010.1371/journal.pone.0023870Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.Nitya KrishnanWladimir MalagaPatricia ConstantMaxine CawsThi Hoang Chau TranJenifer SalmonsThi Ngoc Lan NguyenDuc Bang NguyenMamadou DafféDouglas B YoungBrian D RobertsonChristophe GuilhotGuy E ThwaitesThe six major genetic lineages of Mycobacterium tuberculosis are strongly associated with specific geographical regions, but their relevance to bacterial virulence and the clinical consequences of infection are unclear. Previously, we found that in Vietnam, East Asian/Beijing and Indo-Oceanic strains were significantly more likely to cause disseminated tuberculosis with meningitis than those from the Euro-American lineage. To investigate this observation we characterised 7 East Asian/Beijing, 5 Indo-Oceanic and 6 Euro-American Vietnamese strains in bone-marrow-derived macrophages, dendritic cells and mice. East Asian/Beijing and Indo-Oceanic strains induced significantly more TNF-α and IL-1β from macrophages than the Euro-American strains, and East Asian/Beijing strains were detectable earlier in the blood of infected mice and grew faster in the lungs. We hypothesised that these differences were induced by lineage-specific variation in cell envelope lipids. Whole lipid extracts from East Asian/Beijing and Indo-Oceanic strains induced higher concentrations of TNF-α from macrophages than Euro-American lipids. The lipid extracts were fractionated and compared by thin layer chromatography to reveal a distinct pattern of lineage-associated profiles. A phthiotriol dimycocerosate was exclusively produced by East Asian/Beijing strains, but not the phenolic glycolipid previously associated with the hyper-virulent phenotype of some isolates of this lineage. All Indo-Oceanic strains produced a unique unidentified lipid, shown to be a phenolphthiocerol dimycocerosate dependent upon an intact pks15/1 for its production. This was described by Goren as the 'attenuation indictor lipid' more than 40 years ago, due to its association with less virulent strains from southern India. Mutation of pks15/1 in a representative Indo-Oceanic strain prevented phenolphthiocerol dimycocerosate synthesis, but did not alter macrophage cytokine induction. Our findings suggest that the early interactions between M. tuberculosis and host are determined by the lineage of the infecting strain; but we were unable to show these differences are driven by lineage-specific cell-surface expressed lipids.http://europepmc.org/articles/PMC3169546?pdf=render
spellingShingle Nitya Krishnan
Wladimir Malaga
Patricia Constant
Maxine Caws
Thi Hoang Chau Tran
Jenifer Salmons
Thi Ngoc Lan Nguyen
Duc Bang Nguyen
Mamadou Daffé
Douglas B Young
Brian D Robertson
Christophe Guilhot
Guy E Thwaites
Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.
PLoS ONE
title Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.
title_full Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.
title_fullStr Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.
title_full_unstemmed Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.
title_short Mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles.
title_sort mycobacterium tuberculosis lineage influences innate immune response and virulence and is associated with distinct cell envelope lipid profiles
url http://europepmc.org/articles/PMC3169546?pdf=render
work_keys_str_mv AT nityakrishnan mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT wladimirmalaga mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT patriciaconstant mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT maxinecaws mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT thihoangchautran mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT jenifersalmons mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT thingoclannguyen mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT ducbangnguyen mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT mamadoudaffe mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT douglasbyoung mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT briandrobertson mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT christopheguilhot mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles
AT guyethwaites mycobacteriumtuberculosislineageinfluencesinnateimmuneresponseandvirulenceandisassociatedwithdistinctcellenvelopelipidprofiles