Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages

<p>Abstract</p> <p>Background</p> <p>The ability of <it>Mycobacterium tuberculosis</it> to survive and replicate in macrophages is crucial for the mycobacterium's ability to infect the host and cause tuberculosis. To identify <it>Mycobacterium tub...

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Main Authors: Shinnick Thomas M, Miller Barbara H
Format: Article
Language:English
Published: BMC 2001-10-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/1/26
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spelling doaj-5ac0730d05d447cd8cd8e78d947b2bd22020-11-25T02:30:08ZengBMCBMC Microbiology1471-21802001-10-01112610.1186/1471-2180-1-26Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophagesShinnick Thomas MMiller Barbara H<p>Abstract</p> <p>Background</p> <p>The ability of <it>Mycobacterium tuberculosis</it> to survive and replicate in macrophages is crucial for the mycobacterium's ability to infect the host and cause tuberculosis. To identify <it>Mycobacterium tuberculosis</it> genes involved in survival in macrophages, a library of non-pathogenic <it>Mycobacterium smegmatis</it> bacteria, each carrying an individual integrated cosmid containing <it>M. tuberculosis</it> H37Rv genomic DNA, was passed through THP-1 human macrophages three times.</p> <p>Results</p> <p>Two of the clones recovered from this enrichment process, sur2 and sur3, exhibited significantly increased survival relative to wild-type bacteria. In coinfection experiments, the ratio of sur2 colonies to wild-type colonies was 1:1 at 0 hours but increased to 20:1 at 24 hours post phagocytosis. The ratio of sur3 colonies to wild-type colonies was 1:1 at 0 hours and 5:1 at 24 hours. The <it>M. tuberculosis</it> ORFs responsible for increased survival were shown to be <it>Rv0365c</it> for the sur2 clone and <it>Rv2235</it> for the sur3 clone. These ORFs encode proteins with as-of-yet unknown functions.</p> <p>Conclusions</p> <p>We identified two <it>M. tuberculosis</it> ORFs which may be involved in the ability of tubercle bacilli to survive in macrophages.</p> http://www.biomedcentral.com/1471-2180/1/26
collection DOAJ
language English
format Article
sources DOAJ
author Shinnick Thomas M
Miller Barbara H
spellingShingle Shinnick Thomas M
Miller Barbara H
Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages
BMC Microbiology
author_facet Shinnick Thomas M
Miller Barbara H
author_sort Shinnick Thomas M
title Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages
title_short Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages
title_full Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages
title_fullStr Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages
title_full_unstemmed Identification of two <it>Mycobacterium tuberculosis</it> H37Rv ORFs involved in resistance to killing by human macrophages
title_sort identification of two <it>mycobacterium tuberculosis</it> h37rv orfs involved in resistance to killing by human macrophages
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2001-10-01
description <p>Abstract</p> <p>Background</p> <p>The ability of <it>Mycobacterium tuberculosis</it> to survive and replicate in macrophages is crucial for the mycobacterium's ability to infect the host and cause tuberculosis. To identify <it>Mycobacterium tuberculosis</it> genes involved in survival in macrophages, a library of non-pathogenic <it>Mycobacterium smegmatis</it> bacteria, each carrying an individual integrated cosmid containing <it>M. tuberculosis</it> H37Rv genomic DNA, was passed through THP-1 human macrophages three times.</p> <p>Results</p> <p>Two of the clones recovered from this enrichment process, sur2 and sur3, exhibited significantly increased survival relative to wild-type bacteria. In coinfection experiments, the ratio of sur2 colonies to wild-type colonies was 1:1 at 0 hours but increased to 20:1 at 24 hours post phagocytosis. The ratio of sur3 colonies to wild-type colonies was 1:1 at 0 hours and 5:1 at 24 hours. The <it>M. tuberculosis</it> ORFs responsible for increased survival were shown to be <it>Rv0365c</it> for the sur2 clone and <it>Rv2235</it> for the sur3 clone. These ORFs encode proteins with as-of-yet unknown functions.</p> <p>Conclusions</p> <p>We identified two <it>M. tuberculosis</it> ORFs which may be involved in the ability of tubercle bacilli to survive in macrophages.</p>
url http://www.biomedcentral.com/1471-2180/1/26
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