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Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival
Mycobacterium tuberculosis (M. tb) has two peptidyl-prolyl isomerases (Ppiases) PpiA and PpiB, popularly known as cyclophilin A and cyclophilin B. The role of cyclophilins in processes such as signaling, cell surface recognition, chaperoning, and heat shock response has been well-documented. We pres...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310130/ https://www.ncbi.nlm.nih.gov/pubmed/28261567 http://dx.doi.org/10.3389/fcimb.2017.00038 |
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author | Pandey, Saurabh Tripathi, Deeksha Khubaib, Mohd Kumar, Ashutosh Sheikh, Javaid A. Sumanlatha, Gaddam Ehtesham, Nasreen Z. Hasnain, Seyed E. |
author_facet | Pandey, Saurabh Tripathi, Deeksha Khubaib, Mohd Kumar, Ashutosh Sheikh, Javaid A. Sumanlatha, Gaddam Ehtesham, Nasreen Z. Hasnain, Seyed E. |
author_sort | Pandey, Saurabh |
collection | PubMed |
description | Mycobacterium tuberculosis (M. tb) has two peptidyl-prolyl isomerases (Ppiases) PpiA and PpiB, popularly known as cyclophilin A and cyclophilin B. The role of cyclophilins in processes such as signaling, cell surface recognition, chaperoning, and heat shock response has been well-documented. We present evidence that M. tb Ppiases modulate the host immune response. ELISA results revealed significant presence of antibodies to M. tb Ppiases in patient sera as compared to sera from healthy individuals. Treatment of THP-1 cells with increasing concentrations of rPpiA, induced secretion of pro-inflammatory cytokines TNF-α and IL-6. Alternatively, treatment with rPpiB inhibited secretion of TNF-α and induced secretion of IL-10. Furthermore, heterologous expression of M. tb PpiA and PpiB in Mycobacterium smegmatis increased bacterial survival in THP-1 cells as compared to those transformed with the vector control. Our results demonstrate that M. tb Ppiases are immunogenic proteins that can possibly modulate host immune response and enhance persistence of the pathogen within the host by subverting host cell generated stresses. |
format | Online Article Text |
id | pubmed-5310130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53101302017-03-03 Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival Pandey, Saurabh Tripathi, Deeksha Khubaib, Mohd Kumar, Ashutosh Sheikh, Javaid A. Sumanlatha, Gaddam Ehtesham, Nasreen Z. Hasnain, Seyed E. Front Cell Infect Microbiol Microbiology Mycobacterium tuberculosis (M. tb) has two peptidyl-prolyl isomerases (Ppiases) PpiA and PpiB, popularly known as cyclophilin A and cyclophilin B. The role of cyclophilins in processes such as signaling, cell surface recognition, chaperoning, and heat shock response has been well-documented. We present evidence that M. tb Ppiases modulate the host immune response. ELISA results revealed significant presence of antibodies to M. tb Ppiases in patient sera as compared to sera from healthy individuals. Treatment of THP-1 cells with increasing concentrations of rPpiA, induced secretion of pro-inflammatory cytokines TNF-α and IL-6. Alternatively, treatment with rPpiB inhibited secretion of TNF-α and induced secretion of IL-10. Furthermore, heterologous expression of M. tb PpiA and PpiB in Mycobacterium smegmatis increased bacterial survival in THP-1 cells as compared to those transformed with the vector control. Our results demonstrate that M. tb Ppiases are immunogenic proteins that can possibly modulate host immune response and enhance persistence of the pathogen within the host by subverting host cell generated stresses. Frontiers Media S.A. 2017-02-15 /pmc/articles/PMC5310130/ /pubmed/28261567 http://dx.doi.org/10.3389/fcimb.2017.00038 Text en Copyright © 2017 Pandey, Tripathi, Khubaib, Kumar, Sheikh, Sumanlatha, Ehtesham and Hasnain. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Pandey, Saurabh Tripathi, Deeksha Khubaib, Mohd Kumar, Ashutosh Sheikh, Javaid A. Sumanlatha, Gaddam Ehtesham, Nasreen Z. Hasnain, Seyed E. Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
title | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
title_full | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
title_fullStr | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
title_full_unstemmed | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
title_short | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
title_sort | mycobacterium tuberculosis peptidyl-prolyl isomerases are immunogenic, alter cytokine profile and aid in intracellular survival |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310130/ https://www.ncbi.nlm.nih.gov/pubmed/28261567 http://dx.doi.org/10.3389/fcimb.2017.00038 |
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