Articles

Phospholipase C in Beijing strains of Mycobacterium tuberculosis

Abstract

Background and Objectives: Phospholipase of Mycobacterium tuberculosis plays an important role in pathogenesis through breaking up phospholipids and production of diacylglycerol. In this study, we examined the Beijing strains of Mycobacterium tuberculosis isolated from Iranian patients for the genes encoding this enzyme.
Materials and Methods: DNA extraction was performed using CTAB (cetyltrimethylammonium bromide) from positive culture specimens in tuberculosis patients. PCR was then used to amplify the plcA, plcB, plcC genes of Beijing strain, and non-Beijing strains were identified by spoligotyping.
Results: Of 200 specimens, 19 (9.5%) were Beijing strain and 181 (90.5%) were non-Beijing strains. The results of PCR for Beijing strains were as follows: 16 strains (84.2%) were positive for plcA, 17 (89.4%) were positive for plcB and 17 (89.4%) were positive for plcC genes. The standard strain (H37RV) was used as control.
Conclusion: The majority of Beijing strains have phospholipase C genes which can contribute to their pathogenesis but we need complementary studies to confirm the role of phospholipase C in pathogenecity of Mycobacterium tuberculosis.

Kam KM, Yip CW, Tse LW, Leug Kl, Wong KL, Ko WM, et al. Optimization of variable number tandem repeat typing set for diferentiating Mycobacterium tuberculosis in the Beijing family. FEMS Microbiol Lett 2006; 256: 258-265.

Issar S, Mycobacterium tuberculosis pathogenesis and molecular determinants of virulence. J Clin Microbiol 2003; 16: 463-496.

Srinivas M, Rajakumari S, Narayana Y, Joshi B, Katoch VM, Rajasekharan R, et al. Functional characterization of the phospholipase C activity of Rv3487c and its localization on the cell wall of Mycobacterium tuberculosis. J Biosci 2008; 33: 221-230.

Vera- Cabrera L, Howard ST, Laszlo A , Johnson WM.Analysis of genetic polymorphism in the phospholipase region of Mycobacterium tuberculosis. J Clin Microbiol 1997; 39: 1190-1195.

Ramazanzadeh R, Amirmozafari N, Farnia P. and Ghazi F.Genotyping of Mycobacterium tuberculosis isolate from TB patients with spoligotyping. J Kurdistan Uni Med Sci 2006; 11: 50-59. (Persian).

Rohani M , Farnia P, Naderi Nasab M, Moniri R, Torfeh M , Amiri MM. Beijing genotype and other predominant Mycobacterium tuberculosis spoligotypes observed in Mashhad. Indian J Med Microbiol 2009; 27:306-310.

Sun JR, Lee SY, Dou HY, Lu JJ.Using a multiplex K, and Cole, ST. Identification of variable regions in polymerase chain reaction for the identification of Beijing strains of Mycobacterium tuberculosis. Eur J Clin Microbiol Infect Dis 2009; 28: 105-107.

Ferdinand S, Sola C, Verdol B, Legrand E, Goh KS, Berchel M, et al. Molecular characterization and drug resistance patterns of strains of Mycobacterium tuberculosis isolated from patients in an AIDS counseling center in Port-au-Prince, Haiti: a 1-year study. J Clin Microbiol 2003; 41: 694-702.

Schaaf HS, Shean Donald PR. Culture confirmed multidrug resistant tuberculosis: diagnostic delay, clinical features, and outcome. Arch Dis Child 2003;88: 1106-1111.

van Soolingen D, Hermans PW, de Haas PE, Soll 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: 2578-2586.

Kamerbeek J, Schouts L, Kolk A, Agterveld V, van Solingen D, Kuijper S, et al. Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol 1997;35: 907-14.

Farnia P, Mohammadi F, Masjedi MR, Varnerot A, Zarifi AZ, Tabatabee J. et al. Evaluation of tuberculosis transmissionin Tehran; using RFLP and spoligotyping. J Infect 2004; 49: 94-101.

Talarico S, Durmaz R, Yang Z . Insertion and deletion- assoaiated genetic diversity of Mycobacterium tuberculosis phospholipase C- encoding gene among 106 clinical isolates from Turkey. J Clin Microb 2004;43: 533-538.

Korbsrisate S, Tomaras P, Damnin S , Kumdee J, Srinon V, Lengwehasatit I, et al. Characterization of two distinct phospholipase C enzymes from burkholderia pseudomallei. J Clin Microbiol 2007; 40: 1907-1915.

Gomez A, Mve-Obiang A, Vray B, Rudnicka W, Shamputa I, Portaels F et al. Detection of phospholi- pase C in nontuberculous mycobacteria and its possible role in hemolytic activity. J Clin Microbiol 2001; 39:1396-1401.

Marquis H, Goldfine H, Daniel A. Portnoy DA, Proteolytic pathways of activation and degrada-tion of a bacterial phospholipase C during intra-cellular infection by Listeria monocytogenes. J Cell Biol 1997;137: 1381-1392.

Wheeler PR., Ratledge C. Control and location of acyl-hydrolysing phospholipase activity in pathogenic mycobacteria. J Gen Microbiol 1992; 138: 825-830.

Agaisse H., Gominet M., okstad O.A., Kolsto A.B., Lereclus D. PlcR is a pleiotropic regulator of extracellular virulence factor gene expression in Bacillus thuringiensis. J Mol Microbiol 1999; 32: 1043-1053.

Marquis H., Hager E.J. pH-regulated activation and release of a bacteria-associated phospholipase C during intracellular infection by Listeria mono-cytogenes. J Mol Microbiol 2000; 35: 289-298.

Gordon, SV, Brosch R, Billault A, Garnier T, Eiglmeier the genomes of tubercle bacilli using bacterial artificial chromosome arrays. J Mol Microbiol 1999; 32: 643-655.

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IssueVol 2 No 4 (2010) QRcode
SectionArticles
Keywords
Mycobacterium tuberculosis Beijing strains phospholipase C

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How to Cite
1.
Goudarzi H, Mirsamadi E, Jahani Sherafat S, Esfahani M, Faramarzi N, Farnia P. Phospholipase C in Beijing strains of Mycobacterium tuberculosis. Iran J Microbiol. 1;2(4):194-197.