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1.
Mem. Inst. Oswaldo Cruz ; 106(5): 524-535, Aug. 2011.
Article in English | LILACS | ID: lil-597710

ABSTRACT

The aim of the present study was to compare polymerase chain reaction (PCR)-based methods - spoligotyping and mycobacterial interspersed repetitive units (MIRU) typing - with the gold-standard IS6110 restriction fragment length polymorphism (RFLP) analysis in 101 isolates of Mycobacterium tuberculosis to determine the genetic diversity of M. tuberculosis clinical isolates from Delhi, North India. Spoligotyping resulted in 49 patterns (14 clusters); the largest cluster was composed of Spoligotype International Types (SITs)26 [Central-Asian (CAS)1-Delhi lineage], followed by SIT11 [East-African-Indian (EAI) 3-Indian lineage]. A large number of isolates (75 percent) belonged to genotypic lineages, such as CAS, EAI and Manu, with a high specificity for the Indian subcontinent, emphasising the complex diversity of the phylogenetically coherent M. tuberculosis in North India. MIRU typing, using 11 discriminatory loci, was able to distinguish between all but two strains based on individual patterns. IS6110-RFLP analysis (n = 80 strains) resulted in 67 unique isolates and four clusters containing 13 strains. MIRUs discriminated all 13 strains, whereas spoligotyping discriminated 11 strains. Our results validate the use of PCR-based molecular typing of M. tuberculosis using repetitive elements in Indian isolates and demonstrate the usefulness of MIRUs for discriminating low-IS6110-copy isolates, which accounted for more than one-fifth of the strains in the present study.


Subject(s)
Adult , Female , Humans , Male , Young Adult , DNA, Bacterial , Genetic Variation , Minisatellite Repeats , Mycobacterium tuberculosis , Bacterial Typing Techniques , Cluster Analysis , Genotype , India , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Repetitive Sequences, Nucleic Acid
2.
Mem. Inst. Oswaldo Cruz ; 106(3): 267-273, May 2011. graf
Article in English | LILACS | ID: lil-589033

ABSTRACT

We performed spoligotyping on 114 strains of the Mycobacterium tuberculosis (Mtb) complex that had been isolated from patients in Minas Gerais Health Units during 2004. A total of 82/114 (72 percent) clinical isolates were clustered and 32/114 (28 percent) were unique. Seven shared types containing nine strains were newly created. A total of nine patterns corresponded to unreported orphan strains, as evaluated against all of the strains recorded in the SITVIT2 proprietary database in the Institut Pasteur de la Guadeloupe. The major clades were composed of isolates that belong to the following genotypes: Latin-America and Mediterranean (63/114, 55.3 percent) (the ill-defined T superfamily) (12/114, 10.5 percent), Haarlem (8/114, 7 percent), X clade (6/114, 5.3 percent), S clade (3/114, 2.6 percent) and the East-African Indian and Manu types, each with 1/114 (0.9 percent) isolates. A considerable number of strains (n = 20, 17.5 percent) showed patterns that did not fall within any of the previously described major clades. We conclude the bulk of tuberculosis (TB) (92/114, 80.7 percent) in our location is recent evolutionary strains that belong to the principal genetic groups 2/3. Further studies on epidemiology of TB are required to understand Mtb biodiversity and TB transmission in this region.


Subject(s)
Female , Humans , Male , Bacterial Typing Techniques/methods , Mycobacterium tuberculosis , Cluster Analysis , Genotype , Mycobacterium tuberculosis , Mycobacterium tuberculosis
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