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Development and characterization of mouse monoclonal antibodies to canine morbillivirus.
Fayaz, Arfa; Rajak, Kaushal Kishor; Kumar, Ashok; Karki, Monu; Rai, Vishal; Bhatt, Mukesh; Singh, Rabindra Prasad.
Afiliação
  • Fayaz A; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: arfa.fayaz.af@gmail.com.
  • Rajak KK; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: kaushalvirol@gmail.com.
  • Kumar A; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: vetashok5@gmail.com.
  • Karki M; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: karkim91@gmail.com.
  • Kiran; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: kiranbhasker691992@gmail.com.
  • Rai V; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: roger.vish@gmail.com.
  • Bhatt M; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: bhatt.mukesh20@gmail.com.
  • Singh RP; Division of Biological Products, ICAR-Indian Veterinary Research Institute, Izatnagar, 243122, India. Electronic address: Rabindra.Singh@icar.gov.in.
Biologicals ; 79: 19-26, 2022 Sep.
Article em En | MEDLINE | ID: mdl-36096853
Canine morbillivirus is a highly contagious multi-host pathogen with high morbidity and mortality. Timely diagnosis is of utmost importance to effectively control such a dreadful disease. Monoclonal antibodies (mAbs) serve as a high throughput diagnostics and applied tools for research and development (R&D). In the present study, a total of six mouse monoclonal antibodies were developed. All the mAbs generated belonged to IgG class. Of the six mAbs, two of them, namely CD-2F8 and CD-3D8 were directed against the nucleocapsid protein of CDV as determined in western blotting. The reactivity of all the mAbs was checked in indirect-ELISA and cell-ELISA using different morbilliviruses. The mAbs could broadly be categorized as; CDV specific (CD-3D8 and CD-2F8), cross-reactive to PPR virus (CD-AB3 and CD-4D6) and cross-reactive to both PPR virus and measles virus (CD-5D10 and CD-6E5). The characterized mAbs were used for antigenic profiling of CDV, PPR virus and measles virus. Based on the reactivity pattern; a close antigenic relationship was found among CDV and PPR virus as compared to measles virus. A pair of CDV specific mAbs namely CD-2F8 and CD-3D8 were identified which did not cross-react with measles and PPR viruses and thus could be used for diagnostic applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus da Cinomose Canina / Anticorpos Monoclonais Limite: Animals Idioma: En Revista: Biologicals Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus da Cinomose Canina / Anticorpos Monoclonais Limite: Animals Idioma: En Revista: Biologicals Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de publicação: Reino Unido