Evidence map›Paper›PMID 32401750›Full record

ArticlePLoS neglected tropical diseases2020

Patients infected with Mycobacterium africanum versus Mycobacterium tuberculosis possess distinct intestinal microbiota.

Sivaranjani Namasivayam, Bassirou Diarra, Seydou Diabate, Yeya Dit Sadio Sarro, Amadou Kone, Bourahima Kone, Mohamed Tolofoudie, Bocar Baya, Mahamane T Diakite, Ousmane Kodio and 9 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  13. The gut microbiome: A line of defense against tuberculosis development.Frontiers in cellular and infection microbiology · 2023
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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

19 authors at 5 institutions in 2 countries.

Sivaranjani NamasivayamImmunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Bassirou DiarraUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Seydou DiabateUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Yeya Dit Sadio SarroUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Amadou KoneUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Bourahima KoneUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Mohamed TolofoudieUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Bocar BayaUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Mahamane T DiakiteUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Ousmane KodioUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Keira CohenJohns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Jane HollNorthwestern University, Institute for Global Health, Chicago, Illinois, United States of America.ORCID 0000-0002-2934-1672
Chad J AchenbachNorthwestern University, Institute for Global Health, Chicago, Illinois, United States of America.
Soumya ChatterjeeSaint Louis University, Division of Infectious Diseases, Allergy & Immunology, Saint Louis, Missouri, United States of America.
Robert Leo MurphyNorthwestern University, Institute for Global Health, Chicago, Illinois, United States of America.
William BishaiJohns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Souleymane DialloUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Alan SherImmunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Mamoudou MaigaUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.ORCID 0000-0001-7871-3973
Université des Sciences, des Techniques et des Technologies de Bamako · MLNorthwestern University · USJohns Hopkins University · USNational Institutes of Health · USSaint Louis University · US

Funding

Innate Determinants of Microbial ImmunityZIAAI001044 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SHER, ALAN · 2009 to 2022
$8.8M
HIV and Mycobacterial Disease in MaliD43TW010350 · FIC · UNIV OF SCIENCES, TECH & TECH OF BAMAKO · PI MAIGA, ALMOUSTAPHA ISSIAKA, MURPHY, ROBERT LEO · 2016 to 2025
$3.0M
Host-Pathogen Interactions in a Failing Global lineage of MTBC:M.africanumR01AI110386 · NIAID · UNIV OF SCIENCES, TECH & TECH OF BAMAKO · PI DIALLO, SOULEYMANE · 2014 to 2018
$1.2M
Improved Tools for Nontuberculous Mycobacteria Lung DiseaseK08HL139994 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI COHEN, KEIRA ALEXIS · 2018 to 2022
$794k
Metabolic and Immune Consequences of Antibiotic-Related Microbiome Alterations during TB TreatmentR21AI148033 · NIAID · NORTHWESTERN UNIVERSITY · PI MAIGA, MAMOUDOU · 2019 to 2020
$440k
FIC NIH HHS D43 TW010350NHLBI NIH HHS K08 HL139994NIAID NIH HHS R01 AI110386NIAID NIH HHS R21 AI148033
6 · The paper itself

Abstract

backgroundMycobacterium tuberculosis complex (MTBC), the causative agent of tuberculosis (TB), is composed of eight subspecies. TB in West Africa, in contrast to other geographical regions, is caused by Mycobacterium africanum (MAF) in addition to M. tuberculosis (MTB), with both infections presenting similar symptoms. Nevertheless, MAF is considered to be hypovirulent in comparison with MTB and less likely to progress to active disease. In this study, we asked whether MAF and MTB infected patients possess distinct intestinal microbiomes and characterized how these microbiota communities are affected by anti-tuberculosis therapy (ATT). Additionally, we assessed if the changes in microbiota composition following infection correlate with pathogen induced alterations in host blood-gene expression.

methodsA longitudinal, clinical study of MAF infected, MTB infected patients assessed at diagnosis and two months after start of ATT, and healthy, endemic controls was conducted to compare compositions of the fecal microbiome as determined by 16S rRNA sequencing. A blood transcriptome analysis was also performed on a subset of subjects in each group by microarray and the results cross-compared with the same individual's microbiota composition.

findingsMAF participants have distinct microbiomes compared with MTB patients, displaying decreased diversity and increases in Enterobacteriaceae with respect to healthy participants not observed in the latter patient group. Interestingly, this observed elevation in Enterobacteriaceae positively correlated with enhanced inflammatory gene expression in peripheral blood and was reversed after initiation of ATT.

interpretationOur findings indicate that MAF and MTB have distinct associations with the gut microbiome that may be reflective of the differential susceptibility of West Africans to these two co-endemic infections either as biomarkers or as a contributing determinant.

Indexed as

Gastrointestinal MicrobiomeAdultAgedBacteriaCohort StudiesFecesFemaleHumansLongitudinal StudiesMaleMiddle AgedMycobacteriumMycobacterium tuberculosisTuberculosisYoung Adult

Identifiers

PMID32401750
PMCPMC7219701
OpenAlexW3024859896

What OpenQuestion holds

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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.