Genotypic analysis of Mycobacterium tuberculosis in Bangladesh and prevalence of the Beijing strain

被引:72
作者
Banu, S
Gordon, SV
Palmer, S
Islam, R
Ahmed, S
Alam, KM
Cole, ST
Brosch, R
机构
[1] Int Ctr Diarrhoeal Dis Res, Ctr Hlth & Populat Res, TB Lab, Dhaka 1000, Bangladesh
[2] Chittagong Med Coll, Dept Microbiol, Chittagong, Bangladesh
[3] Vet Labs Agcy, New Haw KT15 3NB, England
[4] Inst Pasteur, Unite Genet Mol Bacterienne, F-75724 Paris, France
关键词
D O I
10.1128/JCM.42.2.674-682.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genotypic analysis was performed on 48 Mycobacterium tuberculosis complex strains collected from a hospital in Dhaka city. Deletion analysis showed that the isolates were all M. tuberculosis; 13 of them were found to be of the "ancestral" type, while 35 were of the "modern" type, indicating that both endemic (ancestral type) and epidemic (modern type) strains cause tuberculosis in Bangladesh. Genotyping based on the spoligotype and variable-number tandem repeats (VNTR) of mycobacterial interspersed repetitive units (MIRU) was also done. A total of 34 strains (71%) were grouped by spoligotyping into nine different clusters; the largest comprised 15 isolates of the Beijing genotype, whereas the remaining eight clusters consisted of two to five isolates. MIRU-VNTR typing detected 32 different patterns among 44 tested strains, and the 15 Beijing strains were further discriminated by MIRU-VNTR typing (7 distinct patterns for the 15 isolates). These results indicate that MIRU-VNTR typing, along with spoligotyping and deletion analysis, can be used effectively for molecular epidemiological studies to determine ongoing transmission clusters; to our knowledge, this is the first report about the type of strains prevailing in Bangladesh.
引用
收藏
页码:674 / 682
页数:9
相关论文
共 39 条
[1]  
Anh DD, 2000, EMERG INFECT DIS, V6, P302
[2]   Comparative genomics of BCG vaccines by whole-genome DNA microarray [J].
Behr, MA ;
Wilson, MA ;
Gill, WP ;
Salamon, H ;
Schoolnik, GK ;
Rane, S ;
Small, PM .
SCIENCE, 1999, 284 (5419) :1520-1523
[3]   Identification of a W variant outbreak of Mycobacterium tuberculosis via population-based molecular epidemiology [J].
Bifani, PJ ;
Mathema, B ;
Liu, ZY ;
Moghazeh, SL ;
Shopsin, B ;
Tempalski, B ;
Driscoll, J ;
Frothingham, R ;
Musser, JM ;
Alcabes, P ;
Kreiswirth, BN .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (24) :2321-2327
[4]   Genomic analysis reveals variation between Mycobacterium tuberculosis H37Rv and the attenuated M. tuberculosis H37Ra strain [J].
Brosch, R ;
Philipp, WJ ;
Stavropoulos, E ;
Colston, MJ ;
Cole, ST ;
Gordon, SV .
INFECTION AND IMMUNITY, 1999, 67 (11) :5768-5774
[5]   A new evolutionary scenario for the Mycobacterium tuberculosis complex [J].
Brosch, R ;
Gordon, SV ;
Marmiesse, M ;
Brodin, P ;
Buchrieser, C ;
Eiglmeier, K ;
Garnier, T ;
Gutierrez, C ;
Hewinson, G ;
Kremer, K ;
Parsons, LM ;
Pym, AS ;
Samper, S ;
van Soolingen, D ;
Cole, ST .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3684-3689
[6]   The evolution of mycobacterial pathogenicity: clues from comparative genomics [J].
Brosch, R ;
Pym, AS ;
Gordon, SV ;
Cole, ST .
TRENDS IN MICROBIOLOGY, 2001, 9 (09) :452-458
[7]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[8]  
Diaz R, 1998, INT J TUBERC LUNG D, V2, P743
[9]   Use of DNA fingerprinting to assess tuberculosis infection control [J].
French, AL ;
Welbel, SF ;
Dietrich, SE ;
Mosher, LB ;
Breall, PS ;
Paul, WS ;
Kocka, FE ;
Weinstein, RA .
ANNALS OF INTERNAL MEDICINE, 1998, 129 (11) :856-861
[10]   Identification of variable regions in the genomes of tubercle bacilli using bacterial artificial chromosome arrays [J].
Gordon, SV ;
Brosch, R ;
Billault, A ;
Garnier, T ;
Eiglmeier, K ;
Cole, ST .
MOLECULAR MICROBIOLOGY, 1999, 32 (03) :643-655