Evidence map›Paper›PMID 42836907›Full record

ArticleTropical animal health and production2026

Molecular and serological detection of Anaplasma marginale indicates widespread exposure among crossbred cattle in Karnal (Haryana), India.

Sonika Ahlawat, Monika Sharma, Ajay Singh, Vijay Kumar, Neha Olla, Reena Arora, Rekha Sharma, Anish Yadav

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Article in Tropical animal health and production, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Sonika AhlawatICAR-National Bureau of Animal Genetic Resources, Karnal, India. sonika.ahlawat@gmail.com.ORCID http://orcid.org/0000-0002-4302-2969
Monika SharmaICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Ajay SinghICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Vijay KumarICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Neha OllaICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Reena AroraICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Rekha SharmaICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Anish YadavSher-e-Kashmir University of Agricultural Sciences and Technology of Jammu, Jammu, India.

Funding

Indian Council of Agricultural Research National Agricultural Science Fund
6 · The paper itself

Abstract

Bovine anaplasmosis, caused by the tick-borne rickettsial pathogen Anaplasma marginale, is a major constraint to cattle health and productivity in tropical and subtropical regions. The present study aimed to investigate the molecular and serological prevalence of A. marginale infection in crossbred cattle from Karnal (Haryana), India, using complementary serological and molecular diagnostic approaches. A total of 150 blood samples were collected from adult female crossbred cattle maintained under different management systems, including organized farms, gaushalas, and field conditions. Serum samples were screened for antibodies against A. marginale using a competitive enzyme-linked immunosorbent assay (cELISA) based on the major surface protein 5 (MSP5) antigen, while genomic DNA extracted from whole blood was analyzed by polymerase chain reaction (PCR) targeting the MSP5 gene of A. marginale. Representative PCR amplicons were confirmed by Sanger sequencing. Serological screening revealed a high overall seroprevalence of 92.7% (139/150), indicating widespread exposure to A. marginale among the sampled cattle. In contrast, PCR detected A. marginale DNA in 76.0% (114/150) of the animals. The higher detection rate by cELISA compared with PCR likely reflects persistent antibody responses following previous exposure or infection, whereas PCR identifies animals with detectable bacteremia at the time of sampling. These findings demonstrate a high serological and molecular detection rate of A. marginale among crossbred cattle in the sampled population of Karnal district. The study highlights the value of integrating serological and molecular diagnostic approaches for epidemiological surveillance of bovine anaplasmosis and underscores the importance of effective tick control and routine monitoring to reduce the disease burden in dairy cattle.

Indexed as

Anaplasma marginaleAnaplasmosisCattle DiseasesAnimalsAntibodies, BacterialBacterial Outer Membrane ProteinsCattleDNA, BacterialEnzyme-Linked Immunosorbent AssayFemaleIndiaPolymerase Chain ReactionPrevalenceSeroepidemiologic StudiesAntibodies, BacterialBacterial Outer Membrane ProteinsDNA, Bacterialmajor surface protein 5, AnaplasmaA. marginalecELISAMolecular detectionSeroprevalence

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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.