Evidence map›Paper›PMID 42603235›Full record

ArticleVeterinary research communications2026

Candidate genomic regions associated with differential clinical response to lumpy skin disease in sahiwal cattle.

Snehal Misal, Akshata Patil, Supriya Chhotaray, Rani Alex, Ravi Kumar Gandham, Vikas Vohra

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Article in Veterinary research communications, 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

6 authors.

Snehal MisalDivision of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India.
Akshata PatilDivision of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India.
Supriya ChhotarayAnimal Genetics and Breeding Division, ICAR-Central Institute for Research on Buffalo, Hisar, Haryana, 125001, India.
Rani AlexDivision of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India.
Ravi Kumar GandhamThe National Institute of Animal Biotechnology, Hyderabad, Telangana, 500032, India.
Vikas VohraDivision of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India. vohravikas@gmail.com.ORCID https://orcid.org/0000-0001-7581-4939

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lumpy Skin Disease (LSD) is a transboundary viral disease of cattle associated with substantial economic losses. During an LSD outbreak at ICAR-National Dairy Research Institute, Sahiwal cattle maintained at the institute and vaccinated with a live attenuated goatpox vaccine exhibited considerable variation in disease response. Based on clinical presentation, animals were classified into clinically affected (G1) and clinically non-affected (G2) groups. This study represents a preliminary investigation aimed at exploring genomic variants associated with differential disease response. Whole-genome sequencing was performed to identify variants linked to clinical outcome.Genome-wide allelic association analysis identified 160 single nucleotide polymorphisms (SNPs) representing putative SNPs differentiating the two groups. clinically affected animals, SNPs rs30477737 and rs26324422 mapped to regions containing ZSCAN26 and PGBD1, respectively, whereas in clinically non-affected animals, SNP rs43160202 was located near PHACTR1, GFOD1, TBC1D7, and SIRT5. These genes are implicated in transcriptional regulation, intracellular signaling, metabolic processes, and cellular stress responses. The identified genomic regions provide a foundation for future functional validation and may contribute to a better understanding of the genetic mechanisms underlying variation in host immune response to LSD in cattle.

Indexed as

Lumpy Skin DiseasePolymorphism, Single NucleotideAnimalsCattleGenetic Predisposition to DiseaseGenome-Wide Association StudyLumpy skin disease virusWhole Genome SequencingBovine major histocompatibility complex (BoLA)Host immune responseLumpy skin disease (LSD)Sahiwal cattleWhole-genome sequencing

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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.