Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.

In response to Mtb infection, the host remodels the infection foci into a dense mass of cells known as the granuloma. The key objective of the granuloma is to contain the spread of Mtb into uninfected regions of the lung. However, it appears that Mtb has evolved mechanisms to resist killing in the g...

Full description

Bibliographic Details
Main Authors: Smriti Mehra, Bapi Pahar, Noton K Dutta, Cecily N Conerly, Kathrine Philippi-Falkenstein, Xavier Alvarez, Deepak Kaushal
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-08-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2930844?pdf=render
id doaj-4b88f496ea2045578180bd073c17c09a
record_format Article
spelling doaj-4b88f496ea2045578180bd073c17c09a2020-11-25T01:55:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-08-0158e1226610.1371/journal.pone.0012266Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.Smriti MehraBapi PaharNoton K DuttaCecily N ConerlyKathrine Philippi-FalkensteinXavier AlvarezDeepak KaushalIn response to Mtb infection, the host remodels the infection foci into a dense mass of cells known as the granuloma. The key objective of the granuloma is to contain the spread of Mtb into uninfected regions of the lung. However, it appears that Mtb has evolved mechanisms to resist killing in the granuloma. Profiling granuloma transcriptome will identify key immune signaling pathways active during TB infection. Such studies are not possible in human granulomas, due to various confounding factors. Nonhuman Primates (NHPs) infected with Mtb accurately reflect human TB in clinical and pathological contexts.We studied transcriptomics of granuloma lesions in the lungs of NHPs exhibiting active TB, during early and late stages of infection. Early TB lesions were characterized by a highly pro-inflammatory environment, expressing high levels of immune signaling pathways involving IFNgamma, TNFalpha, JAK, STAT and C-C/C-X-C chemokines. Late TB lesions, while morphologically similar to the early ones, exhibited an overwhelming silencing of the inflammatory response. Reprogramming of the granuloma transcriptome was highly significant. The expression of approximately two-thirds of all genes induced in early lesions was later repressed.The transcriptional characteristics of TB granulomas undergo drastic changes during the course of infection. The overwhelming reprogramming of the initial pro-inflammatory surge in late lesions may be a host strategy to limit immunopathology. We propose that these host profiles can predict changes in bacterial replication and physiology, perhaps serving as markers for latency and reactivation.http://europepmc.org/articles/PMC2930844?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Smriti Mehra
Bapi Pahar
Noton K Dutta
Cecily N Conerly
Kathrine Philippi-Falkenstein
Xavier Alvarez
Deepak Kaushal
spellingShingle Smriti Mehra
Bapi Pahar
Noton K Dutta
Cecily N Conerly
Kathrine Philippi-Falkenstein
Xavier Alvarez
Deepak Kaushal
Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
PLoS ONE
author_facet Smriti Mehra
Bapi Pahar
Noton K Dutta
Cecily N Conerly
Kathrine Philippi-Falkenstein
Xavier Alvarez
Deepak Kaushal
author_sort Smriti Mehra
title Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
title_short Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
title_full Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
title_fullStr Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
title_full_unstemmed Transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
title_sort transcriptional reprogramming in nonhuman primate (rhesus macaque) tuberculosis granulomas.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-08-01
description In response to Mtb infection, the host remodels the infection foci into a dense mass of cells known as the granuloma. The key objective of the granuloma is to contain the spread of Mtb into uninfected regions of the lung. However, it appears that Mtb has evolved mechanisms to resist killing in the granuloma. Profiling granuloma transcriptome will identify key immune signaling pathways active during TB infection. Such studies are not possible in human granulomas, due to various confounding factors. Nonhuman Primates (NHPs) infected with Mtb accurately reflect human TB in clinical and pathological contexts.We studied transcriptomics of granuloma lesions in the lungs of NHPs exhibiting active TB, during early and late stages of infection. Early TB lesions were characterized by a highly pro-inflammatory environment, expressing high levels of immune signaling pathways involving IFNgamma, TNFalpha, JAK, STAT and C-C/C-X-C chemokines. Late TB lesions, while morphologically similar to the early ones, exhibited an overwhelming silencing of the inflammatory response. Reprogramming of the granuloma transcriptome was highly significant. The expression of approximately two-thirds of all genes induced in early lesions was later repressed.The transcriptional characteristics of TB granulomas undergo drastic changes during the course of infection. The overwhelming reprogramming of the initial pro-inflammatory surge in late lesions may be a host strategy to limit immunopathology. We propose that these host profiles can predict changes in bacterial replication and physiology, perhaps serving as markers for latency and reactivation.
url http://europepmc.org/articles/PMC2930844?pdf=render
work_keys_str_mv AT smritimehra transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
AT bapipahar transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
AT notonkdutta transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
AT cecilynconerly transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
AT kathrinephilippifalkenstein transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
AT xavieralvarez transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
AT deepakkaushal transcriptionalreprogramminginnonhumanprimaterhesusmacaquetuberculosisgranulomas
_version_ 1724982644591034368