Evidence map›Paper›PMID 41064828›Full record

ArticleVeterinary world2025

Development and application of a quantitative polymerase chain reaction assay for the detection and genotyping of bovine leukemia virus in cattle from Kazakhstan.

Alexandr Ostrovskii, Alexandr Shevtsov, Marat Kuibagarov, Dinara Kamalova, Ayan Dauletov, Aralbek Rsaliyev, Yergali Abduraimov, Kassym Mukanov

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In one paragraph

Article in Veterinary world, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Alexandr OstrovskiiNational Center for Biotechnology, 01000, Astana, Kazakhstan.
Alexandr ShevtsovNational Center for Biotechnology, 01000, Astana, Kazakhstan.
Marat KuibagarovNational Center for Biotechnology, 01000, Astana, Kazakhstan.
Dinara KamalovaNational Center for Biotechnology, 01000, Astana, Kazakhstan.
Ayan DauletovNational Center for Biotechnology, 01000, Astana, Kazakhstan.
Aralbek RsaliyevNational Holding "QazBioPharm", Astana, Kazakhstan.
Yergali AbduraimovNational Holding "QazBioPharm", Astana, Kazakhstan.
Kassym MukanovNational Center for Biotechnology, 01000, Astana, Kazakhstan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Bovine leukemia virus (BLV) is a globally distributed retrovirus that causes enzootic bovine leu-kosis, a chronic infection associated with significant economic losses in cattle. Conventional serological diagnostic tools such as agar gel immunodiffusion and enzyme-linked immunosorbent assay detect anti-BLV antibodies but cannot identify proviral DNA, especially in early infections or in calves with maternal antibodies. This study aimed to develop a sensitive and specific duplex quantitative polymerase chain reaction (qPCR) assay targeting the Materials and Methods: A total of 1,680 bovine DNA samples from cattle aged over 3 years were collected from six administrative regions of Kazakhstan. A duplex qPCR assay was developed using primers targeting a conserved region of the BLV Results: The developed qPCR assay demonstrated a sensitivity of 20 plasmid copies for the Conclusion: The duplex qPCR assay is a robust, sensitive, and cost-effective diagnostic tool for detecting BLV provirus, including in animals with maternal antibodies or early-stage infections. The regional genotypic distribution underscores the need for tailored control strategies. This molecular surveillance provides essential baseline data for national BLV eradication programs and contributes to global BLV epidemiological mapping.

Indexed as

bovine leukemia virusbovine leukemia virus epidemiologycattleenv genegenotypingKazakhstanmolecular diagnosticsproviral DNAquantitative polymerase chain reactionβ-actin

Identifiers

PMID41064828
PMCPMC12501598

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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.