Your browser doesn't support javascript.
loading
Identification of miR-29a as a novel biomarker for lumpy skin disease virus exposure in cattle.
Kumar, Ram; Kamboj, Himanshu; Dhanda, Shweta; Verma, Assim; Chander, Yogesh; Nehra, Kuldeep; Bhati, Adrish; Dedar, Ramesh Kumar; Sharma, Deepak Kumar; Barua, Sanjay; Tripathi, Bhupendra N; Sharma, Shalini; Kumar, Naveen.
Afiliação
  • Kumar R; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Kamboj H; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Dhanda S; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Verma A; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Chander Y; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Nehra K; Livestock Research Station, Rajasthan University of Veterinary and Animal Sciences, Nohar, Rajasthan, India.
  • Bhati A; Dadhich Cattle Farm, Nohar, India.
  • Dedar RK; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Sharma DK; Department of Veterinary Microbiology, Rajasthan University of Veterinary and Animal Sciences, Udaipur, India.
  • Barua S; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Tripathi BN; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Sharma S; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
  • Kumar N; National Centre for Veterinary Type Cultures, ICAR-National Research Centre on Equines, Hisar, India.
Virulence ; 15(1): 2324711, 2024 12.
Article em En | MEDLINE | ID: mdl-38527940
ABSTRACT
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.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças dos Bovinos / MicroRNAs / Vírus da Doença Nodular Cutânea Limite: Animals Idioma: En Revista: Virulence Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças dos Bovinos / MicroRNAs / Vírus da Doença Nodular Cutânea Limite: Animals Idioma: En Revista: Virulence Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia