Evidence map›Paper›PMID 40938972›Full record

ArticlePLoS neglected tropical diseases2025

Whole genome sequencing of Yersinia pestis isolates from Central Asian natural plague foci revealed the role of adaptation to different hosts and environmental conditions in shaping specific genotypes.

Aigul A Abdirassilova, Duman T Yessimseit, Altynai K Kassenova, Beck Z Abdeliyev, Zauresh B Zhumadilova, Gulnara Zh Tokmurziyeva, Galina G Kovaleva, Ziyat Zh Abdel, Tatiyana V Meka-Mechenko, Saule K Umarova and 5 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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.

Aigul A AbdirassilovaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Molecular-Genetic Studies, Almaty, Kazakhstan.
Duman T YessimseitNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Molecular-Genetic Studies, Almaty, Kazakhstan.
Altynai K KassenovaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Molecular-Genetic Studies, Almaty, Kazakhstan.
Beck Z AbdeliyevNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Molecular-Genetic Studies, Almaty, Kazakhstan.
Zauresh B ZhumadilovaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Almaty, Kazakhstan.
Gulnara Zh TokmurziyevaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Almaty, Kazakhstan.
Galina G KovalevaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Almaty, Kazakhstan.
Ziyat Zh AbdelNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Plague Microbiology, Almaty, Kazakhstan.
Tatiyana V Meka-MechenkoNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Plague Microbiology, Almaty, Kazakhstan.
Saule K UmarovaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Almaty, Kazakhstan.
Elmira Zh BegimbayevaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, National Collection of Microorganisms, Almaty, Kazakhstan.
Sanzhar D AgzamNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, National Collection of Microorganisms, Almaty, Kazakhstan.
Vladimir L MotinThe University of Texas Medical Branch, Dep. of Pathology, Galveston, Texas, United States of America.
Oleg N RevaCentre for Bioinformatics and Computational Biology, Department of Biochemistry, Genetics and Microbiology (BMG), University of Pretoria, Pretoria, South Africa.ORCID 0000-0002-5459-2772
Altyn K RysbekovaNational Scientific Center of Especially Dangerous Infections named after Masgut Aikimbayev, Laboratory of Molecular-Genetic Studies, Almaty, Kazakhstan.ORCID 0000-0002-8684-3425

Funding

Minister of Science and Higher Education of the Republic of Kazakhstan
6 · The paper itself

Abstract

The genetic diversity and biovar classification of Yersinia isolates from Central Asia were investigated using whole-genome sequencing. In total, 98 isolates from natural plague foci were sequenced using the MiSeq platform. Computational pipelines were developed for accurate assembly of Y. pestis replicons, including small cryptic plasmids, and for identifying genetic polymorphisms. A panel of 99 diagnostic polymorphisms was established, enabling the distinction of dominant Medievalis isolates derived from desert and upland regions. Evidence of convergent evolution was observed in polymorphic allele distributions across genetically distinct Y. pestis biovars, Y. pseudotuberculosis, and other Y. pestis strains, likely driven by adaptation to similar environmental conditions. Genetic polymorphisms in the napA, araC, ssuA, and rhaS genes, along with transposon and CRISPR-Cas insertion patterns, were confirmed as suitable tools for identifying Y. pestis biovars, although their homoplasy suggests limited utility for phylogenetic inference. Notably, a novel cryptic plasmid, pCKF, previously associated with the strain of the population 2.MED0 from the Central-Caucasus high-altitude autonomous plague focus, was detected in a genetically distinct isolate of 2.MED1 population from the Ural-Embi region, indicating potential plasmid transfer across the 2.MED lineage. These findings emphasize the need for ongoing genomic surveillance to monitor the spread of virulence-associated genetic elements and to improve our understanding of Y. pestis evolution and ecology.

Indexed as

Genome, BacterialPlagueYersinia pestisAdaptation, PhysiologicalAnimalsAsia, CentralGenetic VariationGenotypeHumansPhylogenyPlasmidsPolymorphism, GeneticWhole Genome Sequencing

Identifiers

PMID40938972
PMCPMC12445494

What Socratic 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 Socratic graph.