Evidence map›Paper›PMID 31364547›Full record

ArticleEpidemiology and infection2019

Molecular characterisation of multidrug-resistant Mycobacterium tuberculosis isolates from a high-burden tuberculosis state in Brazil.

R S Salvato, S Schiefelbein, R B Barcellos, B M Praetzel, I S Anusca, L S Esteves, M L Halon, G Unis, C F Dias, S S Miranda and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Epidemiology and infection, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

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  5. Insight into population structure ofIranian journal of microbiology · 2021
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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

16 authors at 7 institutions in 1 country.

R S SalvatoPrograma de Pós-graduação em Biologia Celular e Molecular Aplicada à Saúde,Universidade Luterana do Brasil,Canoas,Rio Grande do Sul,Brazil.ORCID 0000-0002-5701-9437
S SchiefelbeinPrograma de Pós-graduação em Biologia Celular e Molecular Aplicada à Saúde,Universidade Luterana do Brasil,Canoas,Rio Grande do Sul,Brazil.
R B BarcellosCentro de Desenvolvimento Científico e Tecnológico (CDCT),Secretaria Estadual da Saúde do Rio Grande do Sul,Porto Alegre,Rio Grande do Sul,Brazil.ORCID 0000-0003-0901-2422
B M PraetzelUniversidade Federal de Ciências da Saúde de Porto Alegre,Porto Alegre,Rio Grande do Sul,Brazil.
I S AnuscaPrograma de Pós-graduação em Biologia Celular e Molecular Aplicada à Saúde,Universidade Luterana do Brasil,Canoas,Rio Grande do Sul,Brazil.
L S EstevesFaculdade de Medicina,Universidade Federal do Rio de Janeiro,Rio de Janeiro (RJ),Brazil.
M L HalonCentro de Desenvolvimento Científico e Tecnológico (CDCT),Secretaria Estadual da Saúde do Rio Grande do Sul,Porto Alegre,Rio Grande do Sul,Brazil.
G UnisHospital Sanatório Partenon,Porto Alegre,Rio Grande do Sul,Brazil.
C F DiasHospital Sanatório Partenon,Porto Alegre,Rio Grande do Sul,Brazil.
S S MirandaLaboratório de Pesquisa em Micobactérias,Faculdade de Medicina,Universidade Federal de Minas Gerais,Belo Horizonte,Minas Gerais,Brazil.ORCID 0000-0001-7245-4472
I N de AlmeidaLaboratório de Pesquisa em Micobactérias,Faculdade de Medicina,Universidade Federal de Minas Gerais,Belo Horizonte,Minas Gerais,Brazil.
L J de Assis FigueredoLaboratório de Pesquisa em Micobactérias,Faculdade de Medicina,Universidade Federal de Minas Gerais,Belo Horizonte,Minas Gerais,Brazil.
E C SilvaCentro de Pesquisa em Tuberculose,Faculdade de Medicina Universidade Federal do Rio de Janeiro,Rio de Janeiro (RJ),Brazil.
A L KritskiCentro de Pesquisa em Tuberculose,Faculdade de Medicina Universidade Federal do Rio de Janeiro,Rio de Janeiro (RJ),Brazil.
E R Dalla CostaCentro de Desenvolvimento Científico e Tecnológico (CDCT),Secretaria Estadual da Saúde do Rio Grande do Sul,Porto Alegre,Rio Grande do Sul,Brazil.
M L R RossettiCentro de Desenvolvimento Científico e Tecnológico (CDCT),Secretaria Estadual da Saúde do Rio Grande do Sul,Porto Alegre,Rio Grande do Sul,Brazil.
Faculdade de Desenvolvimento do Rio Grande do Sul · BRUniversidade Federal de Minas Gerais · BRUniversidade Federal do Rio de Janeiro · BRFundação Estadual de Produção e Pesquisa em Saúde · BRHospital de Clínicas de Porto Alegre · BRUniversidade Federal de Ciências da Saúde de Porto Alegre · BRUniversidade Luterana do Brasil · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) is the leading cause of death among infectious diseases worldwide. Among the estimated cases of drug-resistant TB, approximately 60% occur in the BRICS countries (Brazil, Russia, India, China and South Africa). Among Brazilian states, primary and acquired multidrug-resistant TB (MDR-TB) rates were the highest in Rio Grande do Sul (RS). This study aimed to perform molecular characterisation of MDR-TB in the State of RS, a high-burden Brazilian state. We performed molecular characterisation of MDR-TB cases in RS, defined by drug susceptibility testing, using 131 Mycobacterium tuberculosis (M.tb) DNA samples from the Central Laboratory. We carried out MIRU-VNTR 24loci, spoligotyping, sequencing of the katG, inhA and rpoB genes and RDRio sublineage identification. The most frequent families found were LAM (65.6%) and Haarlem (22.1%). RDRio deletion was observed in 42 (32%) of the M.tb isolates. Among MDR-TB cases, eight (6.1%) did not present mutations in the studied genes. In 116 (88.5%) M.tb isolates, we found mutations associated with rifampicin (RIF) resistance in rpoB gene, and in 112 isolates (85.5%), we observed mutations related to isoniazid resistance in katG and inhA genes. An insertion of 12 nucleotides (CCAGAACAACCC) at the 516 codon in the rpoB gene, possibly responsible for a decreased interaction of RIF and RNA polymerase, was found in 19/131 of the isolates, belonging mostly to LAM and Haarlem families. These results enable a better understanding of the dynamics of transmission and evolution of MDR-TB in the region.

Indexed as

AdolescentAdultAge DistributionAntitubercular AgentsBacterial ProteinsBrazilCost of IllnessDatabases, FactualDNA-Directed RNA PolymerasesDrug Resistance, Multiple, BacterialFemaleGenotypeHumansIncidenceMaleMicrobial Sensitivity TestsAntitubercular AgentsBacterial ProteinsDNA-Directed RNA PolymerasesBrazildrug resistancegenotypingtuberculosis (TB)

Identifiers

PMID31364547
PMCPMC6624858
OpenAlexW2951819546

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.