Skip to main content
Top
Published in: BMC Infectious Diseases 1/2009

Open Access 01-12-2009 | Research article

Low frequency of moaA3 gene among the clinical isolates of Mycobacterium tuberculosisfrom Tamil Nadu and Pondicherry – south eastern coastal states of India

Authors: Balaraman Sekar, Kamalanathan Arunagiri, Nagamiah Selvakumar, Kaluvuri Serena Preethi, Kandhaswami Menaka

Published in: BMC Infectious Diseases | Issue 1/2009

Login to get access

Abstract

Background

Comparative genomic analysis of M. tuberculosis H37Rv and M. bovis BCG have shown that 16 RDs (Regions of Differences) are deleted in BCG and have shown six deletion regions in M. tuberculosis H37Rv. RD1, is present in M. tuberculosis but is absent in all M. bovis BCG sub-strains. A study from Kerala, a south-western coastal state of India aimed to find out differences in RD1 region showed for the first time the presence of moaA3 gene in majority of their clinical isolates, that was absent in type strain H37Rv. We attempted to find out such polymorphism between type strains and the clinical isolates within RD1, targeting moaA3 gene among the clinical isolates of Tamil Nadu & Pondicherry, south-eastern coastal states of India

Methods

One hundred and sixteen clinical isolates of M. tuberculosis were included in the study. PCR using RD1DLa and RD1DRa primers was carried out to amplify a 652 bp fragment, encoding for cfp10 and esat 6 proteins of RD1. A second PCR using primers designed from the surrounding regions of moaA3 gene was done to confirm the presence of the full Open Reading Frame (ORF) in clinical isolates.

Results

In M. tuberculosis H37Rv the expected 652 bp band was present. In BCG it was absent as expected, but a 386 bp fragment was amplified. Around 12/116 (10.3%) of our clinical isolates showed both 652 and 386 bp fragments. The additional 386 bp amplicon is a part of the moaA3 gene which codes for molybdopterin cofactor protein A in M. bovis. The second PCR amplified the flanking sequence of moaA3 and yielded the expected amplicon of 1254 bp in all those 10.3% of clinical isolates which had the 386 bp fragment. However the earlier study carried out in Kerala, reported the presence of moaA3 gene in majority (97%) of their clinical isolates.

Conclusion

This finding showed that there was regional variation presenting polymorphism in moA3 gene, among the strains of M. tuberculosis and further strengthens the speculation of genetic differences among the strains of Kerala and Tamil Nadu & Pondicherry, the South Indian states
Appendix
Available only for authorised users
Literature
1.
go back to reference Mahairas GG, Sabo PJ, Hickey MJ, Singh DC, Stover CK: Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis. J Bacteriol. 1996, 178 (5): 1274-1282.PubMedPubMedCentral Mahairas GG, Sabo PJ, Hickey MJ, Singh DC, Stover CK: Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis. J Bacteriol. 1996, 178 (5): 1274-1282.PubMedPubMedCentral
2.
go back to reference Pym AS, Brodin P, Brosch R, Huerre M, Cole ST: Loss of RD1 contributed to the attenuation of the live tuberculosis vaccines Mycobacterium bovis BCG and Mycobacterium microti. Mol Microbiol. 2002, 46 (3): 709-717. 10.1046/j.1365-2958.2002.03237.x.CrossRefPubMed Pym AS, Brodin P, Brosch R, Huerre M, Cole ST: Loss of RD1 contributed to the attenuation of the live tuberculosis vaccines Mycobacterium bovis BCG and Mycobacterium microti. Mol Microbiol. 2002, 46 (3): 709-717. 10.1046/j.1365-2958.2002.03237.x.CrossRefPubMed
3.
go back to reference Brosch R, Philip WJ, Stavropoulos E, Colston MJ, Cole ST, Gordon SV: Genomic analysis reveals variation between Mycobacterium tuberculosis H37Rv and the attenuated M. tuberculosis H37Ra strain. Infect Immun. 1999, 67 (11): 5768-5774.PubMedPubMedCentral Brosch R, Philip WJ, Stavropoulos E, Colston MJ, Cole ST, Gordon SV: Genomic analysis reveals variation between Mycobacterium tuberculosis H37Rv and the attenuated M. tuberculosis H37Ra strain. Infect Immun. 1999, 67 (11): 5768-5774.PubMedPubMedCentral
4.
go back to reference Sarojini S, Soman S, Radhakrishnan I, Mundayoor S: Identification of MoaA3 gene in patient isolates of Mycobacterium tuberculosis in Kerala, which is absent in M. tuberculosis H37Rv and H37 Ra. BMC Infect Dis. 2005, 5: 81-10.1186/1471-2334-5-81.CrossRefPubMedPubMedCentral Sarojini S, Soman S, Radhakrishnan I, Mundayoor S: Identification of MoaA3 gene in patient isolates of Mycobacterium tuberculosis in Kerala, which is absent in M. tuberculosis H37Rv and H37 Ra. BMC Infect Dis. 2005, 5: 81-10.1186/1471-2334-5-81.CrossRefPubMedPubMedCentral
5.
go back to reference Canetti G, Fox W, Khomenko A, Mahler HT, Menon NK, Mitchison DA, et al: Advances in techniques of testing mycobacterial drug sensitivity and use of sensitivity tests in tuberculosis control programmes. Bull World Health Organ. 1969, 41: 21-43.PubMedPubMedCentral Canetti G, Fox W, Khomenko A, Mahler HT, Menon NK, Mitchison DA, et al: Advances in techniques of testing mycobacterial drug sensitivity and use of sensitivity tests in tuberculosis control programmes. Bull World Health Organ. 1969, 41: 21-43.PubMedPubMedCentral
6.
go back to reference Hermans PW, Schuitema AR, Van Soolingen D, Verstynen CP, Bik EM, Thole JE, Kolk AH, van Embden JD: Specific detection of Mycobacterium tuberculosis complex strains by Polymerase Chain reaction. J Clin Microbiol. 1990, 28 (6): 1204-1213.PubMedPubMedCentral Hermans PW, Schuitema AR, Van Soolingen D, Verstynen CP, Bik EM, Thole JE, Kolk AH, van Embden JD: Specific detection of Mycobacterium tuberculosis complex strains by Polymerase Chain reaction. J Clin Microbiol. 1990, 28 (6): 1204-1213.PubMedPubMedCentral
7.
go back to reference Sekar B, Selvaraj L, Allexis A, Ravi S, Arunagiri K, Rathinavel L: The Utility of IS6110 sequence based Polymerase Chain Reaction in comparison to conventional methods in the diagnosis of Extra-pulmonary tuberculosis. Indian J Med Microbiol. 2008, 26 (4): 352-355.CrossRefPubMed Sekar B, Selvaraj L, Allexis A, Ravi S, Arunagiri K, Rathinavel L: The Utility of IS6110 sequence based Polymerase Chain Reaction in comparison to conventional methods in the diagnosis of Extra-pulmonary tuberculosis. Indian J Med Microbiol. 2008, 26 (4): 352-355.CrossRefPubMed
8.
go back to reference Behr MA, Wilson MA, Gill WP, Salamon H, Schoolnik GK, Rane S, Small PM: Comparative genomics of BCG vaccines by whole-genome DNA microarray. Science. 1999, 284 (5419): 1520-1523. 10.1126/science.284.5419.1520.CrossRefPubMed Behr MA, Wilson MA, Gill WP, Salamon H, Schoolnik GK, Rane S, Small PM: Comparative genomics of BCG vaccines by whole-genome DNA microarray. Science. 1999, 284 (5419): 1520-1523. 10.1126/science.284.5419.1520.CrossRefPubMed
9.
go back to reference Lewis KN, Liao R, Guinn KM, Hickey MJ, Smith S, Behr MA, Sherman DR: Deletion of RD1 from Mycobacterium tuberculosis mimics Bacille Calmette-Guerin attenuation. J Infect Dis. 2003, 187 (1): 117-123. 10.1086/345862.CrossRefPubMed Lewis KN, Liao R, Guinn KM, Hickey MJ, Smith S, Behr MA, Sherman DR: Deletion of RD1 from Mycobacterium tuberculosis mimics Bacille Calmette-Guerin attenuation. J Infect Dis. 2003, 187 (1): 117-123. 10.1086/345862.CrossRefPubMed
10.
go back to reference Rao KR, Kauser F, Srinivas S, Zanetti S, Sechi LA, Ahmed N, Hasnain SE: Analysis of genomic downsizing on the basis of region of difference polymorphism profiling of Mycobacterium tuberculosis patient isolates reveals geographic partitioning. J Clin Microbiol. 2005, 43 (12): 5978-5982. 10.1128/JCM.43.12.5978-5982.2005.CrossRefPubMedPubMedCentral Rao KR, Kauser F, Srinivas S, Zanetti S, Sechi LA, Ahmed N, Hasnain SE: Analysis of genomic downsizing on the basis of region of difference polymorphism profiling of Mycobacterium tuberculosis patient isolates reveals geographic partitioning. J Clin Microbiol. 2005, 43 (12): 5978-5982. 10.1128/JCM.43.12.5978-5982.2005.CrossRefPubMedPubMedCentral
11.
go back to reference Soman S, Joseph BV, Sarojini S, Kumar RA, Katoch VM, Mundayoor S: Presence of Region of Difference 1 among clinical isolates of Mycobacterium tuberculosis from India. J Clin Microbiol. 2007, 45 (10): 3480-3481. 10.1128/JCM.01234-07.CrossRefPubMedPubMedCentral Soman S, Joseph BV, Sarojini S, Kumar RA, Katoch VM, Mundayoor S: Presence of Region of Difference 1 among clinical isolates of Mycobacterium tuberculosis from India. J Clin Microbiol. 2007, 45 (10): 3480-3481. 10.1128/JCM.01234-07.CrossRefPubMedPubMedCentral
12.
go back to reference van Soolingen D, Hermans PW, de Hass PE, Scoll DR, van Embden JD: Occurrence and stability of insertion sequences in Mycobacterium tuberculosis complex strains: evaluation of an insertion sequence-dependent DNA polymorphism as a tool in the epidemiology of tuberculosis. J Clin Microbiol. 1991, 29 (11): 2578-2586.PubMedPubMedCentral van Soolingen D, Hermans PW, de Hass PE, Scoll DR, van Embden JD: Occurrence and stability of insertion sequences in Mycobacterium tuberculosis complex strains: evaluation of an insertion sequence-dependent DNA polymorphism as a tool in the epidemiology of tuberculosis. J Clin Microbiol. 1991, 29 (11): 2578-2586.PubMedPubMedCentral
13.
go back to reference Fomunkong NG, Tang TH, al-maamary S, Ibrahim WA, Ramayah S, Yates M, Zainuddin ZF, Dale JW: Insertion sequence typing of Mycobacterium tuberculosis: characterization of a widespread subtype with a single copy of IS6110. Tuber Lung Dis. 1994, 75 (6): 435-440. 10.1016/0962-8479(94)90117-1.CrossRef Fomunkong NG, Tang TH, al-maamary S, Ibrahim WA, Ramayah S, Yates M, Zainuddin ZF, Dale JW: Insertion sequence typing of Mycobacterium tuberculosis: characterization of a widespread subtype with a single copy of IS6110. Tuber Lung Dis. 1994, 75 (6): 435-440. 10.1016/0962-8479(94)90117-1.CrossRef
14.
go back to reference Palittapongarnpim P, Luangsook P, Tansuphaswadikul S, Chuchottaworn C, Prachaktam R, Sathapatayavongs B: Restriction fragment length polymorphism study of Mycobacterium tuberculosis in Thailand using IS6110 as probe. Int J Tuberc Lung Dis. 1997, 1 (4): 370-376.PubMed Palittapongarnpim P, Luangsook P, Tansuphaswadikul S, Chuchottaworn C, Prachaktam R, Sathapatayavongs B: Restriction fragment length polymorphism study of Mycobacterium tuberculosis in Thailand using IS6110 as probe. Int J Tuberc Lung Dis. 1997, 1 (4): 370-376.PubMed
15.
go back to reference Yuen LKW, Ross BS, Jackson KM, Dwyer B: Characterization of Mycobacterium tuberculosis strains from Vietnamese patients by Southern Blot hybridization. J Clin Microbiol. 1993, 31 (6): 1615-1618.PubMedPubMedCentral Yuen LKW, Ross BS, Jackson KM, Dwyer B: Characterization of Mycobacterium tuberculosis strains from Vietnamese patients by Southern Blot hybridization. J Clin Microbiol. 1993, 31 (6): 1615-1618.PubMedPubMedCentral
16.
go back to reference Radhakrishnan I, Manju YK, Kumar RA, Mundayoor S: Implication of low frequency of IS6110 in fingerprinting field isolates of Mycobacterium tuberculosis from Kerala, India. J Clin Microbiol. 2001, 39 (4): 1683-10.1128/JCM.39.4.1683.2001.CrossRefPubMedPubMedCentral Radhakrishnan I, Manju YK, Kumar RA, Mundayoor S: Implication of low frequency of IS6110 in fingerprinting field isolates of Mycobacterium tuberculosis from Kerala, India. J Clin Microbiol. 2001, 39 (4): 1683-10.1128/JCM.39.4.1683.2001.CrossRefPubMedPubMedCentral
17.
go back to reference Narayanan S, Das S, Garg R, Hari L, Rao VB, Frieden TR, Narayanan PR: Molecular epidemiology of Tuberculosis in rural area of high prevalence in South India: Implication for disease control and prevention. J Clin Microbiol. 2002, 40 (12): 4785-4788. 10.1128/JCM.40.12.4785-4788.2002.CrossRefPubMedPubMedCentral Narayanan S, Das S, Garg R, Hari L, Rao VB, Frieden TR, Narayanan PR: Molecular epidemiology of Tuberculosis in rural area of high prevalence in South India: Implication for disease control and prevention. J Clin Microbiol. 2002, 40 (12): 4785-4788. 10.1128/JCM.40.12.4785-4788.2002.CrossRefPubMedPubMedCentral
18.
go back to reference Das S, Paramasivan CN, Lowrie DB, Prabhakar R, Narayanan PR: IS6110 restriction fragment length polymorphism typing of clinical isolates of Mycobacterium tuberculosis from patients with pulmonary tuberculosis in Madras, South India. Tuber Lung Dis. 1995, 76 (6): 550-554. 10.1016/0962-8479(95)90533-2.CrossRefPubMed Das S, Paramasivan CN, Lowrie DB, Prabhakar R, Narayanan PR: IS6110 restriction fragment length polymorphism typing of clinical isolates of Mycobacterium tuberculosis from patients with pulmonary tuberculosis in Madras, South India. Tuber Lung Dis. 1995, 76 (6): 550-554. 10.1016/0962-8479(95)90533-2.CrossRefPubMed
Metadata
Title
Low frequency of moaA3 gene among the clinical isolates of Mycobacterium tuberculosisfrom Tamil Nadu and Pondicherry – south eastern coastal states of India
Authors
Balaraman Sekar
Kamalanathan Arunagiri
Nagamiah Selvakumar
Kaluvuri Serena Preethi
Kandhaswami Menaka
Publication date
01-12-2009
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2009
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/1471-2334-9-114

Other articles of this Issue 1/2009

BMC Infectious Diseases 1/2009 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.