Evidence map›Paper›PMID 41528640›Full record

ArticleFolia microbiologica2026

Comparative population genomic analysis of Brevibacterium casei isolated from a tuberculosis patient.

Sushanta Deb, Lata Kumari, Urvashi B Singh

Abstract read
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In one paragraph

Article in Folia microbiologica, 2026. 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
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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

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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.

No citing paper in PubMed yet.

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

3 authors.

Sushanta DebDepartment of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Lata KumariDepartment of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Urvashi B SinghDepartment of Microbiology, All India Institute of Medical Sciences, New Delhi, India. drurvashi@gmail.com.ORCID http://orcid.org/0000-0001-8753-9743

Funding

All-India Institute of Medical Sciences All-India Institute of Medical Sciences
6 · The paper itself

Abstract

Brevibacterium casei, previously considered as non-pathogenic to human host is now drawing attention due to its association with frequent infections in immunocompromised patients suffering from leukemia and HIV. Despite growing incidence of B. casei infections, limited number of genomes have been sequenced to date, this restricts our understanding on ge-nomic heterogeneity and the evolution of pathogenic B.casei strains. Here, we sequenced the whole genome of B. casei HOS 100 strain isolated from a tuberculosis patient. The genome size was 3.8 Mb and G + C content 67.94%. Present study estimates the genetic diversity and factors effecting evolutionary dynamics of B. casei strains. Phylogenomic and population genomic analyses reveal that recombination, horizontal gene transfer, and the ongoing expansion of the pangenome contribute to the genetic diversity and potential emergence of genetically distinct B. casei strains.

Indexed as

Brevibacterium caseiPan-genomics and recombinationPhylogenomicsPopulation genomics

Identifiers

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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.