CSIR Central

Human Xenobiotic Nuclear Receptor PXR Augments Mycobacterium tuberculosis Survival.

IR@IMTECH: CSIR-Institute of Microbial Technology, Chandigarh

View Archive Info
 
 
Field Value
 
Title Human Xenobiotic Nuclear Receptor PXR Augments Mycobacterium tuberculosis Survival.
 
Creator Bhagyaraj, Ella
Nanduri, Ravikanth
Saini, Ankita
Dkhar, Hedwin Kitdorlang
Ahuja, Nancy
Chandra, Vemika
Mahajan, Sahil
Kalra, Rashi
Tiwari, Drishti
Sharma, Charu
Janmeja, Ashok Kumar
Gupta, Pawan
 
Subject QR Microbiology
 
Description Mycobacterium tuberculosis can evade host defense processes, thereby ensuring its survival and pathogenesis. In this study, we investigated the role of nuclear receptor, pregnane X receptor (PXR), in M. tuberculosis infection in human monocyte-derived macrophages. In this study, we demonstrate that PXR augments M. tuberculosis survival inside the host macrophages by promoting the foamy macrophage formation and abrogating phagolysosomal fusion, inflammation, and apoptosis. Additionally, M. tuberculosis cell wall lipids, particularly mycolic acids, crosstalk with human PXR (hPXR) by interacting with its promiscuous ligand binding domain. To confirm our in vitro findings and to avoid the reported species barrier in PXR function, we adopted an in vivo mouse model expressing hPXR, wherein expression of hPXR in mice promotes M. tuberculosis survival. Therefore, pharmacological intervention and designing antagonists to hPXR may prove to be a promising adjunct therapy for tuberculosis.
 
Publisher American Association of Immunologists
 
Date 2016-07-01
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://crdd.osdd.net/open/1855/1/10.pdf
Bhagyaraj, Ella and Nanduri, Ravikanth and Saini, Ankita and Dkhar, Hedwin Kitdorlang and Ahuja, Nancy and Chandra, Vemika and Mahajan, Sahil and Kalra, Rashi and Tiwari, Drishti and Sharma, Charu and Janmeja, Ashok Kumar and Gupta, Pawan (2016) Human Xenobiotic Nuclear Receptor PXR Augments Mycobacterium tuberculosis Survival. Journal of immunology , 197 (1). pp. 244-55. ISSN 1550-6606
 
Relation http://www.jimmunol.org/content/197/1/244.long
http://crdd.osdd.net/open/1855/