Evidence map›Paper›PMID 41265403›Full record

ArticleEnvironmental analysis, health and toxicology2025

Spatial and temporal characterisation of genetic and phenotypic properties of Yersinia pestis in Kazakhstan's natural plague foci.

Abdel Ziyat, Zauresh Zhumadilova, Raikhan Mussagalieva, Dinmukhammed Otebay, Beck Abdeliyev

Abstract read
In one paragraph

Article in Environmental analysis, health and toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Abdel ZiyatLaboratory of Plague, Masgut Aikimbayev National Scientific Center for Especially Dangerous Infections of the Ministry of Healthcare of the Republic of Kazakhstan, Almaty, 050054, Republic of Kazakhstan.
Zauresh ZhumadilovaDepartment of Express Diagnostics and Indication of Especially Dangerous Infections, Masgut Aikimbayev National Scientific Center for Especially Dangerous Infections of the Ministry of Healthcare of the Republic of Kazakhstan, Almaty, 050054, Republic of Kazakhstan.
Raikhan MussagalievaDepartment of Express Diagnostics and Indication of Especially Dangerous Infections, Masgut Aikimbayev National Scientific Center for Especially Dangerous Infections of the Ministry of Healthcare of the Republic of Kazakhstan, Almaty, 050054, Republic of Kazakhstan.
Dinmukhammed OtebayCholera Laboratory, Masgut Aikimbayev National Scientific Center for Especially Dangerous Infections of the Ministry of Healthcare of the Republic of Kazakhstan, Almaty, 050054, Republic of Kazakhstan.
Beck AbdeliyevDepartment of Express Diagnostics and Indication of Especially Dangerous Infections, Masgut Aikimbayev National Scientific Center for Especially Dangerous Infections of the Ministry of Healthcare of the Republic of Kazakhstan, Almaty, 050054, Republic of Kazakhstan.

Funding

Committee of Science of the Ministry of Science and Higher EducationMinistry of Science and Higher Education IRN - AP19679355
6 · The paper itself

Abstract

The study aimed to analyse data from epizootological monitoring, microbiological and molecular genetic studies to assess the genetic biodiversity of Yersinia pestis (Y. pestis) strains, to determine the effectiveness of using individual methods and to develop the necessary algorithm for evaluating genetic methods and creating a biorepository of natural isolates of these pathogens. As a result, the biodiversity of Y. pestis strains isolated in natural plague foci of Kazakhstan was analysed using classical and modern methods (polymerase chain reaction, Multi Locus Variable Number Tandem Repeat Analysis, VITEK 2 Compact, MiniION Oxford Nanopore, MiSeq sequencer) of research and geographic information system (GIS) technology. Spatial and temporal characteristics of plague infection in the plague-enriched areas of the country were described. The study summarised the characteristics of phenotypic and molecular genetic properties of 1220 Y. pestis strains isolated from different sites in natural plague foci of the country during the period 2010-2023. As a result, 94.8% of Y. pestis strains were typical of these plague foci, and 5.2% of strains had altered properties in some respects. To obtain information on genetic diversity and their geographical distribution, 82 DNA samples of Y. pestis strains were studied. Three phylogenetic trees were constructed, GIS maps were compiled and a gene bank, a biorepository of molecular characteristics was created to obtain specific genetic characteristics of strains and a complete picture of the genetic parameters of the plague pathogen isolated from various sites in natural foci of Kazakhstan.

Indexed as

BiorepositoryEcological systemEpizootological differentiationGenotypePhenotype

Identifiers

PMID41265403
PMCPMC12890325

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