Molecular characterization of Mycobacterium tuberculosis isolated in the State of Parana in southern Brazil

• Published in: Tuberculosis (Edinburgh, Scotland) Scotland), 2009-01, Vol.89 (1), p.101-105
• Main Authors: Malaghini, Marcelo, Brockelt, Sonia Regina, Burger, Marion, Kritski, Afrânio, Thomaz-Soccol, Vanete
• Format: Article
• Language: English
• Subjects: Bacterial Proteins - genetics; Bacterial Typing Techniques; Brazil; DNA Fingerprinting - methods; Genotype; Humans; Infectious Disease; IS 6110; Mixed-linker PCR DNA fingerprinting; Molecular characterization; Molecular Epidemiology - methods; Mycobacterium tuberculosis; Mycobacterium tuberculosis - genetics; Mycobacterium tuberculosis - isolation & purification; Polymerase Chain Reaction - methods; Polymorphism, Restriction Fragment Length; Pulmonary/Respiratory; Tuberculosis, Pulmonary - microbiology; Tuberculosis, TB
• ISSN: 1472-9792; 1873-281X
• DOI: 10.1016/j.tube.2008.07.005

Summary Sequence IS 6110 has been successfully used throughout the world for characterizing the Mycobacterium tuberculosis lineages. The aim of this study was to obtain data about circulating strains of M. tuberculosis in patients from the State of Parana in southern Brazil. Sixty-two clinical specimens obtained from sputum, bronchial aspirate, biopsy and urine from 62 patients clinically diagnosed with tuberculosis and admitted to the SUS-Brazil – The Brazilian Centralized Health Service System – were genotyped by the mixed-linker PCR DNA fingerprinting technique. The analysis demonstrated that the number of copies of the IS 6110 sequence per isolates varied from four to 13 bands, with an average number of 8.5. From this, 93% of the isolates presented multiple copies. Isolates with no copies of the IS 6110 element were not observed. The genetic analysis by UPGMA grouped the 62 isolates by similarity into three different groups: the first group contained two strains, the second was composed of 23, and the third, a more heterogeneous group, contained 37 isolates. Only two isolates (3.2%) formed a cluster; in other words, they presented a pattern of polymorphism with similarity above 95%. Such findings suggest that in the State of Parana, illness predominantly develops through reactivation of the latent infection as opposed to exogenous transmission. The methodology used (mixed-linker PCR DNA fingerprinting) allowed for 93.5% differentiation of the isolates tested, and proved to be a powerful tool for differentiation in the molecular genotyping of M. tuberculosis.