Evidence map›Paper›PMID 37609282›Full record

ArticleResearch square2023

Metabolic and Immune Consequences of Antibiotic Related Microbiome Alterations during first-line Tuberculosis Treatment in Bamako, Mali.

Dramane Diallo, Shan Sun, Anou Moise Somboro, Bocar Baya, Amadou Kone, Bassirou Diarra, Mohamed Nantoume, Isaac Koloma, Mahamadou Diakite, Jane Holl and 6 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 4 countries.

Dramane DialloUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Shan SunDepartment of Bioinformatics and Genomics, University of North Carolina at Charlotte, North Carolina.
Anou Moise SomboroSchool of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
Bocar BayaUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Amadou KoneUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Bassirou DiarraUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Mohamed NantoumeUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Isaac KolomaUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Mahamadou DiakiteUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Jane HollDepartment of Neurology and Center for Healthcare Delivery Science and Innovation, University of Chicago, Chicago, IL.
Almoustapha Issiaka MaigaUniversity Clinical Research Center (UCRC) of the University of Sciences, Technics and Technologies of Bamako (USTTB).
Moussa SeydiService des Maladies Infectieuses et Tropicales, Fann University Hospital Center, Dakar.
Grant TheronCentre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis, Stellenbosch University, Cape Town, Saint Kitts and Nevis.
Lifang HouInstitute for Global Health, Northwestern University, Chicago, IL.
Anthony FodorDepartment of Bioinformatics and Genomics, University of North Carolina at Charlotte, North Carolina.
Mamoudou MaigaInstitute for Global Health, Northwestern University, Chicago, IL.
Université des Sciences, des Techniques et des Technologies de Bamako · MLUniversity of North Carolina at Charlotte · USSouth African Medical Research Council · ZAUniversity of Chicago · USUniversity of KwaZulu-Natal · ZA

Funding

Metabolic and Immune Consequences of Antibiotic-Related Microbiome Alterations during TB TreatmentR21AI148033 · NIAID · NORTHWESTERN UNIVERSITY · PI MAIGA, MAMOUDOU · 2019 to 2020
$440k
NIAID NIH HHS R21 AI148033
6 · The paper itself

Abstract

Background: Tuberculosis (TB) infection is known to lead to the unbalance of the gut microbiota and act synergistically on the decline of the host immune response, when untreated. Moreover, previous work has found a correlation between dysbiosis in the gut microbiota composition and the use of antibiotics. However, there is a need for an in-depth understanding of the metabolic and immune consequences of antibiotic-related microbiome alterations during first-line TB treatment. Methods: In a longitudinal cohort study, which included TB-infected cohorts and healthy individuals (control group), we studied the anti-TB-related changes in the gut microbiota composition and related functional consequences. Sputum, whole blood and stool samples were collected from participants at four time-points including before (Month-0), during (Month-2), at the end of drug treatment (Month-6) and 9 months after treatment (Month-15). Controls were sampled at inclusion and Month-6. We analyzed the microbiota composition and microbial functional pathways with shotgun metagenomics, analyzed the blood metabolomics using high-performance liquid chromatography (HPLC), and measured the levels of metabolites and cytokines with cytometric bead array. Results: We found that the gut microbiota of patients infected with TB was different from that of the healthy controls. The gut microbiota became similar to healthy controls after treatment but was still significantly different after 6 months treatment and at the follow up 9 months after treatment. Our data also showed disturbance in the plasma metabolites such as tryptophan and tricarboxylic acids components of patients during TB treatment. Levels of IL-4, IL-6, IL-10, and IFN-γ decreased during treatment and levels were maintained after treatment completion, while IL-17A known to have a strong link with the gut microbiota was highly expressed during treatment period and longer than the 9-month post treatment completion. We found that some fatty acids were negatively correlated with the abundance of taxa. For example, Conclusion: Changes in the composition and function of gut microbiota was observed in TB patients before and after treatment compared to healthy controls. The differences persisted at nine months after treatment completion. Alterations in some bacterial taxa were correlated to the changes in metabolite levels in peripheral blood, thus the altered microbial community might lead to changes in immune status that influence the disease outcome and future resistance to infections.

Indexed as

BamakodrugsdysbiosisMalimicrobiotaTuberculosis

Identifiers

PMID37609282
PMCPMC10441471
OpenAlexW4385749267

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.