Evidence map›Paper›PMID 32063558›Full record

ArticleTuberculosis (Edinburgh, Scotland)2020

Phylogenomic assessment of drug-resistant Mycobacterium tuberculosis strains from Beira, Mozambique.

Evangelina Inacio Namburete, Anzaan Dippenaar, Emilyn Costa Conceição, Cinara Feliciano, Margarida Maria Passeri do Nascimento, Kamila Chagas Peronni, Wilson Araújo Silva, Josefo João Ferro, Lee H Harrison, Robin Mark Warren and 1 more

Open access · greenAbstract read
In one paragraph

Article in Tuberculosis (Edinburgh, Scotland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.1field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 4 countries.

Evangelina Inacio NambureteMycobacteria Research Lab at Clinics Hospital from Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil; Faculty of Health Science, Catholic University of Mozambique, Beira, Mozambique. Electronic address: evanamburete@gmail.com.
Anzaan DippenaarDST-NRF Centre of Excellence for Biomedical Tuberculosis Research, SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, South Africa. Electronic address: adippenaar@sun.ac.za.
Emilyn Costa ConceiçãoInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373 - bloco i - Cidade Universitária, Rio de Janeiro, RJ, 21941-970, Brazil. Electronic address: emilyncosta@gmail.com.
Cinara FelicianoMycobacteria Research Lab at Clinics Hospital from Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil. Electronic address: cinara.feliciano@gmail.com.
Margarida Maria Passeri do NascimentoMycobacteria Research Lab at Clinics Hospital from Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil. Electronic address: mpasseri@fmrp.usp.br.
Kamila Chagas PeronniCenter for Medical Genomics, Clinics Hospital at Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil. Electronic address: kcperoni@gmail.com.
Wilson Araújo SilvaCenter for Medical Genomics, Clinics Hospital at Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil; Department of Genetics at Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil. Electronic address: wilsonjr@usp.br.
Josefo João FerroFaculty of Health Science, Catholic University of Mozambique, Beira, Mozambique. Electronic address: josefojoaoferro@yahoo.com.br.
Lee H HarrisonInfectious Diseases Epidemiology Research Unit, University of Pittsburgh, Pittsburgh, USA. Electronic address: lharriso@edc.pitt.edu.
Robin Mark WarrenDST-NRF Centre of Excellence for Biomedical Tuberculosis Research, SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, South Africa. Electronic address: rw1@sun.ac.za.
Valdes Roberto BollelaMycobacteria Research Lab at Clinics Hospital from Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Brazil. Electronic address: vbollela@gmail.com.
Clinics Hospital of Ribeirão Preto · BRCatholic University of Mozambique · MZUniversidade de São Paulo · BRSouth African Medical Research Council · ZAStellenbosch University · ZAUniversidade Federal do Rio de Janeiro · BRUniversity of Pittsburgh · US

Funding

Fogarty HIV Research Training Program (Mozambique)D43TW009753 · FIC · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRISON, LEE H · 2014 to 2018
$1.2M
FIC NIH HHS D43 TW009753
6 · The paper itself

Abstract

backgroundMozambique is a high-burden tuberculosis (TB) country where TB/HIV co-infection and drug resistant TB (DR-TB) incidence is increasing. Whole genome sequencing (WGS) comprehensively describes the molecular epidemiology of TB, allows prediction of DR-TB phenotypes, lineages strains identification and better understanding of transmission chains.

objectiveTo describe genetic diversity of DR-TB Mycobacterium tuberculosis isolated in Beira, Mozambique.

methodsDescriptive cross-sectional study with 35 M. tuberculosis isolates, resistant to at least one first-line drug on molecular drug-susceptibility tests (DST). Variant identification, DR prediction and phylogenetic analysis provided by WGS, drug-susceptibility pattern compared to line-probe assay (LPA): Genotype MTBDR

findingsLineage 4 (L4) was the most prevalent: 25 (71.4%) isolates; 5 (14.3%) L1 and 5 (14.3%) L2. WGS showed 33/35 (94.3%) isolates resistant to at least one drug, two pan-susceptible isolates that were previously diagnosed as DR-TB with genotype MTBDRplus. Concordance between WGS and LPA: 88.6% for isoniazid (INH), 85.7% to rifampicin (RPM), 91.4% for quinolones and 100% to second line injectable drugs. There were three possible TB transmission chains, 10 strains showing recent transmission.

conclusionWGS provided reliable information about the most frequent lineages related to DR-TB in Beira, Mozambique: L4.3 (LAM), L2 (Beijing) and L1 (EAI) and possible recent transmission chain.

Indexed as

Antitubercular AgentsCross-Sectional StudiesDrug Resistance, Multiple, BacterialGenotypeHumansMicrobial Sensitivity TestsMolecular EpidemiologyMozambiqueMycobacterium tuberculosisPhenotypePhylogenyTuberculosis, Multidrug-ResistantWhole Genome SequencingAntitubercular AgentsDrug-resistantMozambiqueMycobacterium tuberculosisPhylogenyWhole genome sequencing

Identifiers

PMID32063558
PMCPMC9300053
OpenAlexW3004394994

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.