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Volume 90, Issue 1, Pages 9-15 (January 2010)


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Variable-number tandem repeats typing of Mycobacterium tuberculosis isolates with low copy numbers of IS6110 in Thailand

Arunee Thong-Onaf, Nat Smittipatb, Tada Juthayothinb, Hideki Yanaicg, Norio Yamadacg, Jutaporn Yorsangsukkamold, Angkana Chaiprasertd, Dhanida Rienthonge, Pamaree Billamasb, Prasit PalittapongarnpimabCorresponding Author Informationemail addressemail address

Received 30 July 2009; received in revised form 22 October 2009; accepted 22 October 2009. published online 13 November 2009.

Summary 

Spoligotyping and variable-number tandem repeats (VNTR) typing have been increasingly used for differentiating Mycobacterium tuberculosis strains with low copy numbers of IS6110. However, there are few studies comparing their potential to type the strains originating from South and Southeast Asia where many of the isolates have only a few copies, or even single copy, of IS6110. Here, we evaluated the genotyping of 187M. tuberculosis isolates harboring 1–6 copies of IS6110, available from a population-based study in Chiangrai, northern Thailand during 1998–2000, using spoligotyping and VNTR typing. The low-copy-number isolates constituted about 34% of all M. tuberculosis isolated in the province. Discriminating capacities and cluster identification by the two methods were compared with each other and to those obtained by the standard IS6110-restriction fragment length polymorphism (RFLP) method. We found that VNTR typing based on the studied 10-loci set generated more distinct patterns (151 patterns) than spoligotyping (54 patterns) and IS6110-RFLP (65 patterns). Most of the RFLP- or spoligotyping-defined clusters were subdivided by VNTR typing. Combining IS6110-RFLP with VNTR typing produced 164 distinct patterns and 21.9% of clustered isolates whereas the combination of IS6110-RFLP and spoligotyping gave 103 different patterns and 59.4% of clustered isolates. Our results confirm the utility of VNTR typing as the secondary method of choice for investigating the epidemiology of M. tuberculosis with low copy numbers of IS6110.

a Department of Microbiology, Faculty of Science, Mahidol University, Rama VI Road, Bangkok, Thailand

b National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand

c TB/HIV Research Project, The Research Institute of Tuberculosis (RIT), Tokyo, Japan

d Department of Microbiology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand

e Tuberculosis Division, Department of Disease Control, Ministry of Public Health, Bangkok, Thailand

Corresponding Author InformationCorresponding author. Department of Microbiology, Faculty of Science, Mahidol University, Rama VI Road, Bangkok 10400, Thailand. Tel.: +66 2 5646700x3444; fax: +66 2 6445411.

f Present address: College of Medicine and Public Health, Ubon Rajathanee University, Ubon Rajathanee, Thailand.

g Present address: Nagasaki University, Nagasaki, Japan.

PII: S1472-9792(09)00105-X

doi:10.1016/j.tube.2009.10.006


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