Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/24634
Título: Genetic diversity, transmission dynamics and drug resistance of Mycobacterium tuberculosis in Angola
Autor: Perdigão, João
Clemente, Sofia
Ramos, Jorge
Masakidi, Pedro
Machado, Diana
Silva, Carla
Couto, Isabel
Viveiros, Miguel
Taveira, Nuno
Portugal, Isabel
Palavras-chave: COMPLEX STRAINS
EPIDEMIOLOGY
EVOLUTION
DIAGNOSIS
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Microbiology
Epidemiology
Infectious Diseases
SDG 3 - Good Health and Well-being
Data: 23-Fev-2017
Resumo: Tuberculosis (TB) poses a serious public health problem in Angola. No surveillance data on drug resistance is available and nothing is known regarding the genetic diversity and population structure of circulating Mycobacterium tuberculosis strains. Here, we have genotyped and evaluated drug susceptibility of 89 Mycobacterium tuberculosis clinical isolates from Luanda. Thirty-three different spoligotype profiles corresponding to 24 different Shared International Types (SIT) and 9 orphan profiles were detected. SIT 20 (LAM1) was the most prevalent (n = 16, 18.2%) followed by SIT 42 (LAM9; n = 15, 17.1%). Overall, the M. tuberculosis population structure in this sample was dominated by LAM (64.8%) and T (33.0%) strains. Twenty-four-loci MIRU-VNTR analysis revealed that a total of 13 isolates were grouped in 5 distinct clusters. Drug susceptibility data showed that 22 (24.7%) of the 89 clinical isolates were resistant to one or more antibacillary drugs of which 4 (4.5%) were multidrug resistant. In conclusion, this study demonstrates a high predominance of LAM strains circulating in the Luanda setting and the presence of recent transmission events. The rate and the emergence dynamics of drug resistant TB found in this sample are significant and highlight the need of further studies specifically focused on MDR-TB transmission.
Descrição: The authors wish to thank the laboratory, clinical, and nursing staff of HDP, whose high quality of service and cooperation have made this study possible. Financial support was provided by the Fundacao para a Ciencia e a Tecnologia (FCT) Portugal [PTDC/SAU-EPI/122400/2010], part of the EDCTP2 program supported by the European Union. JP was supported by a post doc fellowship from project [PTDC/SAU-EPI/122400/2010] and by fellowship [SFRH/BPD/95406/2013] from FCT. JP is thankful to the European Society of Clinical Microbiology and Infectious Diseases for a Research Grant, and would like to acknowledge the Study Group for Mycobacterial Infections. DM was supported by FCT fellowship [SFRH/BPD/100688/2014] and DM, IC MV are thankful to [GHTM UID/Multi/04413/20139] from FCT. CS was supported by FCT [SFRH/BD/73579/2010].
Peer review: yes
URI: http://hdl.handle.net/10362/24634
DOI: https://doi.org/10.1038/srep42814
ISSN: 2045-2322
Aparece nas colecções:IHMT: MM - Artigos em revista internacional com arbitragem científica

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