Identification of miR-29a as a novel biomarker for lumpy skin disease virus exposure in cattle.

LSDV cattle cell-mediated immune response lumpy skin disease miR-29a susceptibility

Journal

Virulence
ISSN: 2150-5608
Titre abrégé: Virulence
Pays: United States
ID NLM: 101531386

Informations de publication

Date de publication:
Dec 2024
Historique:
medline: 26 3 2024
pubmed: 26 3 2024
entrez: 25 3 2024
Statut: ppublish

Résumé

Micro RNAs (miRNAs) have been implicated in the regulation of maturation, proliferation, differentiation, and activation of immune cells. In this study, we demonstrated that miR-29a antagonizes IFN-γ production at early times post-LSDV infection in cattle. miR-29a was predicted to target upstream IFN-γ regulators, and its inhibition resulted in enhanced IFN-γ production in sensitized peripheral blood mononuclear cells (PBMCs). Further, stimulation of PBMCs with LSDV antigen exhibited lower levels of miR-29a, concomitant with a potent cell-mediated immune response (CMI), characterized by an increase in LSDV-specific CD8+ T cell counts and enhanced levels of IFN-γ, which eventually facilitated virus clearance. In addition, a few immunocompromised cattle (developed secondary LSDV infection at ~ 6 months) that failed to mount a potent cell-mediated immune response, were shown to maintain higher miR-29a levels. Furthermore, as compared to the sensitized crossbred cattle, PBMCs from sensitized Rathi (a native Indian breed) animals exhibited lower levels of miR-29a along with an increase in CD8+ T cell counts and enhanced levels of IFN-γ. Finally, we analysed that a ≥ 60% decrease in miR-29a expression levels in the PBMCs of sensitized cattle correlated with a potent CMI response. In conclusion, miR-29a expression is involved in antagonizing the IFN-γ response in LSDV-infected cattle and may serve as a novel biomarker for the acute phase of LSDV infection, as well as predicting the functionality of T cells in sensitized cattle. In addition, Rathi cattle mount a more potent CMI response against LSDV than crossbred cattle.

Identifiants

pubmed: 38527940
doi: 10.1080/21505594.2024.2324711
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2324711

Auteurs

Ram Kumar (R)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Himanshu Kamboj (H)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Shweta Dhanda (S)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Assim Verma (A)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Yogesh Chander (Y)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Kuldeep Nehra (K)

Livestock Research Station, Rajasthan University of Veterinary and Animal Sciences, Nohar, Rajasthan, India.

Adrish Bhati (A)

Dadhich Cattle Farm, Nohar, India.

Ramesh Kumar Dedar (RK)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Deepak Kumar Sharma (DK)

Department of Veterinary Microbiology, Rajasthan University of Veterinary and Animal Sciences, Udaipur, India.

Sanjay Barua (S)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Bhupendra N Tripathi (BN)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Shalini Sharma (S)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Naveen Kumar (N)

National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.

Classifications MeSH