Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.18/6694
Title: Mycobacterium tuberculosis genetic diversity and drug resistance across Portuguese-speaking countries and CPLP-TB: a novel framework and surveillance tool for the Lusophone community
Author: Perdigão, João
Silva, Carla
Diniz, Jaciara
Pereira, Catarina
Machado, Diana
Ramos, Jorge
Silva, Hugo
Abilleira, Fernanda
Brum, Clarice
Reis, Ana J.
Macedo, Maíra
Scaini, João L.
Silva, Ana B.
Esteves, Leonardo
Macedo, Rita
Maltez, Fernando
Clemente, Sofia
Coelho, Elizabeth
Viegas, Sofia
Rabna, Paulo
Rodrigues, Amabélia
Taveira, Nuno
Jordão, Luísa
Kritski, Afrânio
Lapa e Silva, José
Mokrousov, Igor
Couvin, David
Rastogi, Nalin
Couto, Isabel
Pain, Arnab
McNerney, Ruth
Clark, Taane G.
von Groll, Andrea
Dalla-Costa, Elis R.
Rossetti, Maria Lúcia
da Silva, Pedro E.A
Viveiros, Miguel
Portugal, Isabel
Keywords: Mycobacterium Tuberculosis
Genetics
Surveillance
CPLP-TB
Infecções Respiratórias
Resistência aos Antimicrobianos
Issue Date: Apr-2019
Abstract: Background: Tuberculosis (TB) remains a major health problem within the Community of Portuguese Language Speaking Countries (CPLP). Despite the marked variation in TB incidence across its member-states and continued human migratory flux between countries, a considerable gap in the knowledge on the Mycobacterium tuberculosis population structure and strain circulation between the countries still exists. Materials and Methods: To address this, we have assembled and analyzed the largest CPLP M. tuberculosis molecular and drug susceptibility dataset, comprised by a total of 1447 clinical isolates, including 423 multidrug-resistant isolates, from five CPLP countries. Genotyping analysis was carried out by 15/24 Mycobacterial Interspersed Repetitive Unit – Variable Number of Tandem Repeat (MIRU-VNTR) and Spoligotyping. Drug Susceptibility testing was performed using standardized BACTEC 960 MGIT methodology or through the resazurin microtiter assay (REMA). Results: The data herein presented reinforces Latin American and Mediterranean (LAM) strains as the hallmark of M. tuberculosis populational structure in the CPLP coupled with country-specific differential prevalence of minor clades. Moreover, using high-resolution typing by 24-loci MIRU-VNTR, six cross-border genetic clusters were detected, thus supporting recent clonal expansion across the Lusophone space. To make this data available to the scientific community and public health authorities we developed CPLP-TB (available at http://cplp-tb.ff.ulisboa.pt), an online database coupled with web-based tools for exploratory data analysis. Conclusions: As a public health tool, CPLP-TB is expected to contribute to improved knowledge on the M. tuberculosis population structure and strain circulation within the CPLP, thus supporting risk assessment of strain-specific trends.
Peer review: yes
URI: http://hdl.handle.net/10400.18/6694
Appears in Collections:DSA - Posters/abstracts em congressos internacionais

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