TY - JOUR
T1 - Genetic diversity of Mycobacterium tuberculosis from Pará, Brazil, reveals a higher frequency of ancestral strains than previously reported in South America
AU - Conceicao, Emilyn Costa
AU - Rastogi, Nalin
AU - Couvin, David
AU - Lopes, Maria Luiza
AU - Furlaneto, Ismari Perini
AU - Gomes, Harrison Magdinier
AU - Goncalves Vasconcellos, Sidra Ezidio
AU - Suffys, Philip Noel
AU - Cruz Schneider, Maria Paula
AU - de Sousa, Maiaa Silva
AU - Sola, Christophe
AU - de Paula Souza e Guimaraes, Ricardo Jose
AU - Duarte, Rafael Silva
AU - Batista Lima, Karla Valeria
N1 - NPP
PY - 2017
Y1 - 2017
N2 - There is only scarce information available on genotypic diversity of the Mycobacterium tuberculosis complex (MTBC) clinical isolates circulating in the Northern part of Brazil, a relatively neglected region regarding research on tuberculosis. We therefore characterized 980 MTBC clinical isolates from the state of Para, by spoligotyping and data was compared with patterns from around the world, besides analyzing drug susceptibility, and collecting sociodemographic data. We also performed 24 loci MIRU-VNTR typing to evaluate phylogenetic inferences among the East-African-Indian (EAI) lineage strains. The Geographic Information System analyses were performed to generate a descriptive visualization of MTBC strain distribution in the region. A total of 249 different spoligopatterns primarily belonging to evolutionary recent Euro-American lineages, as well as CentralAsian, Manu and ancestral EAI lineages, were identified, in addition to strains with reportedly unknown lineage signatures. The most frequent lineages were Latin American Mediterranean, T and Haarlem. Interestingly, EAI lineage strains were found in a significantly higher proportion in comparison with previous studies from South America. Regarding EAI lineage, the absence of spacers 4-9 and 23-24 co-related to 24 loci MIRU-VNTRs may suggest a close evolutionary relationship between such strains in Para and those prevalent in Mozambique, which might have contributed to the genetic diversity of MTBC strains in this region.
AB - There is only scarce information available on genotypic diversity of the Mycobacterium tuberculosis complex (MTBC) clinical isolates circulating in the Northern part of Brazil, a relatively neglected region regarding research on tuberculosis. We therefore characterized 980 MTBC clinical isolates from the state of Para, by spoligotyping and data was compared with patterns from around the world, besides analyzing drug susceptibility, and collecting sociodemographic data. We also performed 24 loci MIRU-VNTR typing to evaluate phylogenetic inferences among the East-African-Indian (EAI) lineage strains. The Geographic Information System analyses were performed to generate a descriptive visualization of MTBC strain distribution in the region. A total of 249 different spoligopatterns primarily belonging to evolutionary recent Euro-American lineages, as well as CentralAsian, Manu and ancestral EAI lineages, were identified, in addition to strains with reportedly unknown lineage signatures. The most frequent lineages were Latin American Mediterranean, T and Haarlem. Interestingly, EAI lineage strains were found in a significantly higher proportion in comparison with previous studies from South America. Regarding EAI lineage, the absence of spacers 4-9 and 23-24 co-related to 24 loci MIRU-VNTRs may suggest a close evolutionary relationship between such strains in Para and those prevalent in Mozambique, which might have contributed to the genetic diversity of MTBC strains in this region.
KW - Mycobacterium tuberculosis
KW - Population-structure
KW - Spoligotyping
KW - Brazil
KW - Euro-American lineage
KW - EAI lineage
KW - MOLECULAR EPIDEMIOLOGY
KW - POPULATION-STRUCTURE
KW - MINAS-GERAIS
KW - WEB TOOL
KW - STATE
KW - COMPLEX
KW - RDRIO
KW - FAMILY
KW - SPOLIGOTYPES
KW - RESISTANCE
U2 - 10.1016/j.meegid.2017.10.021
DO - 10.1016/j.meegid.2017.10.021
M3 - A1: Web of Science-article
SN - 1567-1348
VL - 56
SP - 62
EP - 72
JO - Infection, Genetics and Evolution
JF - Infection, Genetics and Evolution
ER -