Evidence map›Paper›PMID 40781446›Full record

ArticleWorld journal of microbiology & biotechnology2025

Mapping the pangenome of sulfate reducing bacteria: core genes, plasticity, and novel functions in Desulfovibrio spp.

Shailabh Rauniyar, Dipayan Samanta, Payal Thakur, Priya Saxena, Ram N Singh, Adelme Bazin, Alain Bomgni, Ernest Fotseu, Gnimpieba Z Etienne, Venkata Gadhamshetty and 4 more

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Article in World journal of microbiology & biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

14 authors.

Shailabh RauniyarDepartment of Chemical and Biological Engineering, South Dakota Mines, Rapid City, SD, 57701, USA.
Dipayan SamantaDepartment of Chemical and Biological Engineering, South Dakota Mines, Rapid City, SD, 57701, USA.
Payal ThakurDepartment of Chemical and Biological Engineering, South Dakota Mines, Rapid City, SD, 57701, USA.
Priya SaxenaDepartment of Chemical and Biological Engineering, South Dakota Mines, Rapid City, SD, 57701, USA.
Ram N SinghDepartment of Chemical and Biological Engineering, South Dakota Mines, Rapid City, SD, 57701, USA.
Adelme BazinLABGeM, Génomique Métabolique, CEA, Genoscope, Institut de Biologie François Jacob, Université d'Évry, Université Paris-Saclay, CNRS, Évry, 91057, France.
Alain BomgniDepartment of Biomedical Engineering, University of South Dakota, Vermillion, SD, 57069, USA.
Ernest FotseuDepartment of Computer Science, University of Dschang, Dschang, Cameroon.
Gnimpieba Z EtienneDepartment of Biomedical Engineering, University of South Dakota, Vermillion, SD, 57069, USA.
Venkata GadhamshettyDepartment of Civil and Environmental Engineering, South Dakota Mines, Rapid City, SD, 57701, USA.
Brent M PeytonDepartment of Chemical and Biological Engineering, Montana State University, Bozeman, MT, 59717, USA.
Matthew FieldsDepartment of Chemical and Biological Engineering, Montana State University, Bozeman, MT, 59717, USA.
Mahadevan SubramaniamDepartment of Computer Science, University of Nebraska Omaha, Omaha, NE, 68182, USA.
Rajesh K SaniDepartment of Chemical and Biological Engineering, South Dakota Mines, Rapid City, SD, 57701, USA. Rajesh.Sani@sdsmt.edu.

Funding

National Science Foundation 1736255NIH HHS 5P20GM103443-20
6 · The paper itself

Abstract

The pangenome of sulfate reducing bacteria represents a genetic reservoir that deciphers the intricate interplay of conserved and variable elements driving their ecological dominance, evolutionary adaptability, and industrial relevance. This study introduces the most comprehensive pangenome analysis of the genus Desulfovibrio till date, incorporating 63 complete and high-quality genomes using the Partitioned Pangenome Graph of Linked Neighbors (PPanGGOLiN) pipeline. The structure and dynamics of core gene families were investigated through gene ontology, KEGG pathway mapping, and gene network analyses, shedding light on the functional organization of the Desulfovibrio genomes. The analysis categorized 799, 4053, and 43,581 gene families into persistent, shell, and cloud groups, respectively. A core set of 326 gene families, conserved across Desulfovibrio genomes, highlights their essential role in community functionality. Genome plasticity analysis identified 4,576 regions of genome plasticity, with 1,322 hotspots enriched in horizontally acquired genes (89% in the cloud partition). Key gene families in these regions included glpE, fdhD, petC, and cooF, linked to sulfur metabolism. Out of 29 hypothetical genes, one was linked to actin nucleation, another contained a TRASH domain, while the other regulates filopodium assembly. Other predicted functions included lnrL, folE, RNA binding, and pyrG/pyrH involvement in CTP biosynthesis. Additionally, genomic islands revealed evolutionary events, such as cheY acquisition in Oleidesulfovibrio alaskensis G20. This study provides a genus-wide view of Desulfovibrio, emphasizing genome plasticity, hypothetical gene functions, and adaptation mechanisms.

Indexed as

DesulfovibrioGenome, BacterialSulfatesGene OntologyGene Regulatory NetworksGenes, BacterialMultigene FamilyPhylogenySulfatesExact coreGenome plasticityHypotheticalPangenomeShellSulfate reducing bacteria

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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.