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Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival
BACKGROUND: The mce4 operon is one of the four homologues of mammalian cell entry (mce) operons of Mycobacterium tuberculosis. The mce4A (Rv3499c) gene within this operon is homologous to mce1A (Rv0169), that has a role in host cell invasion by M. tuberculosis. Our earlier reports show that mce4 ope...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596156/ https://www.ncbi.nlm.nih.gov/pubmed/19019220 http://dx.doi.org/10.1186/1471-2180-8-200 |
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author | Saini, Neeraj Kumar Sharma, Monika Chandolia, Amita Pasricha, Rashmi Brahmachari, Vani Bose, Mridula |
author_facet | Saini, Neeraj Kumar Sharma, Monika Chandolia, Amita Pasricha, Rashmi Brahmachari, Vani Bose, Mridula |
author_sort | Saini, Neeraj Kumar |
collection | PubMed |
description | BACKGROUND: The mce4 operon is one of the four homologues of mammalian cell entry (mce) operons of Mycobacterium tuberculosis. The mce4A (Rv3499c) gene within this operon is homologous to mce1A (Rv0169), that has a role in host cell invasion by M. tuberculosis. Our earlier reports show that mce4 operon is expressed during the stationary phase of growth of the bacillus in culture and during the course of infection in mammalian hosts. M. tuberculosis carrying mutation in mce4 operon shows growth defect and reduced survival in infected mice. However, the intracellular localization of Mce4A protein and its direct role in cell entry or survival of the bacillus has not been demonstrated so far. RESULTS: By transmission electron microscopy we have demonstrated that recombinant Mce4A protein facilitates the invasion of non-pathogenic strain of E. coli into non-phagocytic HeLa cells. We observe that mce4A gene has a role comparable to mce1A in the survival of recombinant E. coli in human macrophages. Using antibodies raised against Mce4A protein, we show that the protein is localized in the cell wall fraction of M. tuberculosis H37Rv stationary phase culture only. CONCLUSION: Mce4A protein is expressed during the stationary phase of broth culture and localizes in the cell wall fraction of M. tuberculosis. Mce4A protein expressed in non-pathogenic E. coli enables it to enter and survive within HeLa cells and the macrophages. As Mce4A protein is expressed during later phase of mycobacterial growth, our results raise the possibility of it playing a role in maintenance of persistent tubercular infection. |
format | Text |
id | pubmed-2596156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25961562008-12-05 Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival Saini, Neeraj Kumar Sharma, Monika Chandolia, Amita Pasricha, Rashmi Brahmachari, Vani Bose, Mridula BMC Microbiol Research Article BACKGROUND: The mce4 operon is one of the four homologues of mammalian cell entry (mce) operons of Mycobacterium tuberculosis. The mce4A (Rv3499c) gene within this operon is homologous to mce1A (Rv0169), that has a role in host cell invasion by M. tuberculosis. Our earlier reports show that mce4 operon is expressed during the stationary phase of growth of the bacillus in culture and during the course of infection in mammalian hosts. M. tuberculosis carrying mutation in mce4 operon shows growth defect and reduced survival in infected mice. However, the intracellular localization of Mce4A protein and its direct role in cell entry or survival of the bacillus has not been demonstrated so far. RESULTS: By transmission electron microscopy we have demonstrated that recombinant Mce4A protein facilitates the invasion of non-pathogenic strain of E. coli into non-phagocytic HeLa cells. We observe that mce4A gene has a role comparable to mce1A in the survival of recombinant E. coli in human macrophages. Using antibodies raised against Mce4A protein, we show that the protein is localized in the cell wall fraction of M. tuberculosis H37Rv stationary phase culture only. CONCLUSION: Mce4A protein is expressed during the stationary phase of broth culture and localizes in the cell wall fraction of M. tuberculosis. Mce4A protein expressed in non-pathogenic E. coli enables it to enter and survive within HeLa cells and the macrophages. As Mce4A protein is expressed during later phase of mycobacterial growth, our results raise the possibility of it playing a role in maintenance of persistent tubercular infection. BioMed Central 2008-11-19 /pmc/articles/PMC2596156/ /pubmed/19019220 http://dx.doi.org/10.1186/1471-2180-8-200 Text en Copyright © 2008 Saini et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Saini, Neeraj Kumar Sharma, Monika Chandolia, Amita Pasricha, Rashmi Brahmachari, Vani Bose, Mridula Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival |
title | Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival |
title_full | Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival |
title_fullStr | Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival |
title_full_unstemmed | Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival |
title_short | Characterization of Mce4A protein of Mycobacterium tuberculosis: role in invasion and survival |
title_sort | characterization of mce4a protein of mycobacterium tuberculosis: role in invasion and survival |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596156/ https://www.ncbi.nlm.nih.gov/pubmed/19019220 http://dx.doi.org/10.1186/1471-2180-8-200 |
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