ArticleJournal of clinical microbiology2005
Analysis of genomic downsizing on the basis of region-of-difference polymorphism profiling of Mycobacterium tuberculosis patient isolates reveals geographic partitioning.
Article in Journal of clinical microbiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Article
- Experimental Evidence for LimitedFrontiers in microbiology · 2019Article
- Mycobacterium tuberculosis Co-operonic PE32/PPE65 Proteins Alter Host Immune Responses by Hampering Th1 Response.Frontiers in microbiology · 2016Article
- Article
- Genomes of Two Clinical Isolates of Mycobacterium tuberculosis from Odisha, India.Genome announcements · 2014Article
- CCL3L1 copy number, CCR5 genotype and susceptibility to tuberculosis.BMC medical genetics · 2014Article
- Article
- Identification of RD5-encoded Mycobacterium tuberculosis proteins as B-cell antigens used for serodiagnosis of tuberculosis.Clinical & developmental immunology · 2012Article
- Low frequency of moaA3 gene among the clinical isolates of Mycobacterium tuberculosis from Tamil Nadu and Pondicherry--south eastern coastal states of India.BMC infectious diseases · 2009Article
- Predominance of Mycobacterium tuberculosis EAI and Beijing lineages in Yangon, Myanmar.Journal of clinical microbiology · 2009Article
- Genomic diversity among Beijing and non-Beijing Mycobacterium tuberculosis isolates from Myanmar.PloS one · 2008Article
- Molecular analysis of a leprosy immunotherapeutic bacillus provides insights into Mycobacterium evolution.PloS one · 2007Article
- Presence of region of difference 1 among clinical isolates of Mycobacterium tuberculosis from India.Journal of clinical microbiology · 2007Article
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7 authors.
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Abstract
Mycobacterium tuberculosis, the etiological agent of tuberculosis, has lost many coding and noncoding regions in its genome during the course of evolution. We performed region-of-difference (RD) analysis using PCR-based genotyping of 131 M. tuberculosis clinical isolates obtained from four different countries, namely, India, Peru, Libya, and Angola. Our studies revealed that RD patterns are often distinct for strains circulating in specific geographical regions and can be used to trace the descent and spread of an isolate from its original reservoir. We describe our findings, which show that no single isolate from the four countries (n = 131) had all the 15 RDs either deleted or retained. Tuberculosis-specific deletion 1 (TbD1) was found to be conserved in 23% of the Indian isolates, indicating their possible ancient origin. RD9 was the most conserved region, RD11 was predominantly deleted, and RD6 was the most variable among the isolates in our collection irrespective of their geographic region. In contrast to earlier reports, our results demonstrate that the deletion of RD1 does not correlate with a decrease in the virulence potential of M. tuberculosis, as Indian isolates (n = 30) examined by us were from diseased individuals and yet had lost the RD1 region. Our results further illustrated that the intactness of the RD5 region may be associated with increased virulence of the organism. This study highlights that the RDs in M. tuberculosis genomes are geographically distributed and specific and may possibly be associated with virulence spectrum.
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