Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.

<h4>Rationale</h4>Understanding mechanisms of resistance to M. tuberculosis (M.tb) infection in humans could identify novel therapeutic strategies as it has for other infectious diseases, such as HIV.<h4>Objectives</h4>To compare the early transcriptional response of M.tb-inf...

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Main Authors: Chetan Seshadri, Nafiseh Sedaghat, Monica Campo, Glenna Peterson, Richard D Wells, Gregory S Olson, David R Sherman, Catherine M Stein, Harriet Mayanja-Kizza, Ali Shojaie, W Henry Boom, Thomas R Hawn, Tuberculosis Research Unit (TBRU)
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Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0175844&type=printable
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author Chetan Seshadri
Nafiseh Sedaghat
Monica Campo
Glenna Peterson
Richard D Wells
Gregory S Olson
David R Sherman
Catherine M Stein
Harriet Mayanja-Kizza
Ali Shojaie
W Henry Boom
Thomas R Hawn
Tuberculosis Research Unit (TBRU)
author_facet Chetan Seshadri
Nafiseh Sedaghat
Monica Campo
Glenna Peterson
Richard D Wells
Gregory S Olson
David R Sherman
Catherine M Stein
Harriet Mayanja-Kizza
Ali Shojaie
W Henry Boom
Thomas R Hawn
Tuberculosis Research Unit (TBRU)
author_sort Chetan Seshadri
collection DOAJ
description <h4>Rationale</h4>Understanding mechanisms of resistance to M. tuberculosis (M.tb) infection in humans could identify novel therapeutic strategies as it has for other infectious diseases, such as HIV.<h4>Objectives</h4>To compare the early transcriptional response of M.tb-infected monocytes between Ugandan household contacts of tuberculosis patients who demonstrate clinical resistance to M.tb infection (cases) and matched controls with latent tuberculosis infection.<h4>Methods</h4>Cases (n = 10) and controls (n = 18) were selected from a long-term household contact study in which cases did not convert their tuberculin skin test (TST) or develop tuberculosis over two years of follow up. We obtained genome-wide transcriptional profiles of M.tb-infected peripheral blood monocytes and used Gene Set Enrichment Analysis and interaction networks to identify cellular processes associated with resistance to clinical M.tb infection.<h4>Measurements and main results</h4>We discovered gene sets associated with histone deacetylases that were differentially expressed when comparing resistant and susceptible subjects. We used small molecule inhibitors to demonstrate that histone deacetylase function is important for the pro-inflammatory response to in-vitro M.tb infection in human monocytes.<h4>Conclusions</h4>Monocytes from individuals who appear to resist clinical M.tb infection differentially activate pathways controlled by histone deacetylase in response to in-vitro M.tb infection when compared to those who are susceptible and develop latent tuberculosis. These data identify a potential cellular mechanism underlying the clinical phenomenon of resistance to M.tb infection despite known exposure to an infectious contact.
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spelling doaj-art-be1f5fc0e02c4c509ccb60eacd7db1ef2025-08-20T02:03:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01124e017584410.1371/journal.pone.0175844Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.Chetan SeshadriNafiseh SedaghatMonica CampoGlenna PetersonRichard D WellsGregory S OlsonDavid R ShermanCatherine M SteinHarriet Mayanja-KizzaAli ShojaieW Henry BoomThomas R HawnTuberculosis Research Unit (TBRU)<h4>Rationale</h4>Understanding mechanisms of resistance to M. tuberculosis (M.tb) infection in humans could identify novel therapeutic strategies as it has for other infectious diseases, such as HIV.<h4>Objectives</h4>To compare the early transcriptional response of M.tb-infected monocytes between Ugandan household contacts of tuberculosis patients who demonstrate clinical resistance to M.tb infection (cases) and matched controls with latent tuberculosis infection.<h4>Methods</h4>Cases (n = 10) and controls (n = 18) were selected from a long-term household contact study in which cases did not convert their tuberculin skin test (TST) or develop tuberculosis over two years of follow up. We obtained genome-wide transcriptional profiles of M.tb-infected peripheral blood monocytes and used Gene Set Enrichment Analysis and interaction networks to identify cellular processes associated with resistance to clinical M.tb infection.<h4>Measurements and main results</h4>We discovered gene sets associated with histone deacetylases that were differentially expressed when comparing resistant and susceptible subjects. We used small molecule inhibitors to demonstrate that histone deacetylase function is important for the pro-inflammatory response to in-vitro M.tb infection in human monocytes.<h4>Conclusions</h4>Monocytes from individuals who appear to resist clinical M.tb infection differentially activate pathways controlled by histone deacetylase in response to in-vitro M.tb infection when compared to those who are susceptible and develop latent tuberculosis. These data identify a potential cellular mechanism underlying the clinical phenomenon of resistance to M.tb infection despite known exposure to an infectious contact.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0175844&type=printable
spellingShingle Chetan Seshadri
Nafiseh Sedaghat
Monica Campo
Glenna Peterson
Richard D Wells
Gregory S Olson
David R Sherman
Catherine M Stein
Harriet Mayanja-Kizza
Ali Shojaie
W Henry Boom
Thomas R Hawn
Tuberculosis Research Unit (TBRU)
Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.
PLoS ONE
title Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.
title_full Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.
title_fullStr Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.
title_full_unstemmed Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.
title_short Transcriptional networks are associated with resistance to Mycobacterium tuberculosis infection.
title_sort transcriptional networks are associated with resistance to mycobacterium tuberculosis infection
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0175844&type=printable
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