Evidence map›Paper›PMID 28926571›Full record

ArticlePloS one2017

Whole-genome sequencing illuminates the evolution and spread of multidrug-resistant tuberculosis in Southwest Nigeria.

Madikay Senghore, Jacob Otu, Adam Witney, Florian Gehre, Emma L Doughty, Gemma L Kay, Phillip Butcher, Kayode Salako, Aderemi Kehinde, Nneka Onyejepu and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

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  17. Deciphering Within-Host Microevolution ofMicrobiology and molecular biology reviews : MMBR · 2019
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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

15 authors at 7 institutions in 4 countries.

Madikay SenghoreVaccines and Immunity Theme, Medical Research Council Unit The Gambia, Fajara, The Gambia.
Jacob OtuVaccines and Immunity Theme, Medical Research Council Unit The Gambia, Fajara, The Gambia.
Adam WitneyInstitute of Infection and Immunity, St George's University of London, London, United Kingdom.
Florian GehreVaccines and Immunity Theme, Medical Research Council Unit The Gambia, Fajara, The Gambia.
Emma L DoughtyMicrobiology and Infection Unit, The University of Warwick, Coventry, United Kingdom.
Gemma L KayMicrobiology and Infection Unit, The University of Warwick, Coventry, United Kingdom.
Phillip ButcherInstitute of Infection and Immunity, St George's University of London, London, United Kingdom.
Kayode SalakoDepartment of Medical Microbiology & Parasitology, University College Hospital, Ibadan, Nigeria.
Aderemi KehindeDepartment of Medical Microbiology & Parasitology, University College Hospital, Ibadan, Nigeria.
Nneka OnyejepuNational Tuberculosis Reference Laboratory, Nigeria Institute of Medical Research, Lagos, Nigeria.
Emmanuel IdigbeNational Tuberculosis Reference Laboratory, Nigeria Institute of Medical Research, Lagos, Nigeria.
Tumani CorrahVaccines and Immunity Theme, Medical Research Council Unit The Gambia, Fajara, The Gambia.
Bouke de JongInstitute of Tropical Medicine, Antwerp, Belgium.
Mark J PallenMicrobiology and Infection Unit, The University of Warwick, Coventry, United Kingdom.
Martin AntonioVaccines and Immunity Theme, Medical Research Council Unit The Gambia, Fajara, The Gambia.ORCID http://orcid.org/0000-0002-4810-1308
University of Warwick · GBMRC Unit the Gambia · GMNigerian Institute of Medical Research · NGSt George's, University of London · GBUniversity College Hospital, Ibadan · NGInstituut voor Tropische Geneeskunde · BENorwich Research Park · GB

Funding

Medical Research Council MR/L015080/1
6 · The paper itself

Abstract

Nigeria has an emerging problem with multidrug-resistant tuberculosis (MDR-TB). Whole-genome sequencing was used to understand the epidemiology of tuberculosis and genetics of multi-drug resistance among patients from two tertiary referral centers in Southwest Nigeria. In line with previous molecular epidemiology studies, most isolates of Mycobacterium tuberculosis from this dataset belonged to the Cameroon clade within the Euro-American lineage. Phylogenetic analysis showed this clade was undergoing clonal expansion in this region, and suggests that it was involved in community transmission of sensitive and multidrug-resistant tuberculosis. Five patients enrolled for retreatment were infected with pre-extensively drug resistant (pre-XDR) due to fluoroquinolone resistance in isolates from the Cameroon clade. In all five cases resistance was conferred through a mutation in the gyrA gene. In some patients, genomic changes occurred in bacterial isolates during the course of treatment that potentially led to decreased drug susceptibility. We conclude that inter-patient transmission of resistant isolates, principally from the Cameroon clade, contributes to the spread of MDR-TB in this setting, underscoring the urgent need to curb the spread of multi-drug resistance in this region.

Indexed as

Genome, BacterialAdolescentAdultAntitubercular AgentsBacterial ProteinsCameroonChildChild, PreschoolDNA GyraseDrug Resistance, Multiple, BacterialFemaleHumansInfantInfant, NewbornMaleMutationAntitubercular AgentsBacterial ProteinsDNA Gyrase

Identifiers

PMID28926571
PMCPMC5604961
OpenAlexW2754774773

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.