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Distribution of maedi-visna virus in different organs of the spontaneously affected small ruminants in India.
Valecha, Sh; Yadav, H S; Roopa, N; Vinaykumar, S D; Bhardwaj, M; Singh, V; Kumar, P.
Afiliação
  • Valecha S; MVSc Student in Veterinary Pathology, Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh-243122, India.
  • Yadav HS; Ph.D. Student in Veterinary Pathology, Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh-243122, India.
  • Roopa N; MVSc Student in Veterinary Pathology, Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh-243122, India.
  • Vinaykumar SD; Ph.D. Student in Veterinary Pathology, Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh-243122, India.
  • Bhardwaj M; Department of Veterinary Microbiology, College of Veterinary Science, CSK Himachal Pradesh Agriculture University, Palampur, Himachal Pradesh-176062, India.
  • Singh V; Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh-243122, India.
  • Kumar P; Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh-243122, India.
Iran J Vet Res ; 25(1): 41-47, 2024.
Article em En | MEDLINE | ID: mdl-39156799
ABSTRACT

Background:

Maedi-visna (MV) is a small ruminant lentiviral (SRLV) disease affecting sheep and goats, and causes pathological alterations in various organs including lungs, pulmonary lymph nodes, mammary glands, joints, and CNS.

Aims:

Present study was focused to detect the MV virus (MVV) nucleic acid and MVV p28 antigen in different organs of the spontaneously MVV affected sheep and goats.

Methods:

Total of 657 samples were collected from sheep and goats (169 blood, 136 lungs, 96 pulmonary lymph nodes, 74 brain, 54 mammary gland, 78 joints, and 50 spleen) and screened for MVV nucleic acid using nested PCR assay. Serum samples were screened for SRLV antibodies by cELISA. Immunolocalization of MVV was demonstrated by using the polyclonal antibody against p28 antigen by immunohistochemistry in lungs, lymph nodes, mammary glands, and joint tissues.

Results:

Out of 657 samples, 10.7% (70) were found positive for MVV. Among different organs, lungs showed highest positivity (25.7%) followed by mammary glands (14.8%), blood (9.5%), joint tissues (7.7%), brain (5.4%), and pulmonary lymph node (1.0%). SRLV antibodies were detected in 29.2% of the serum samples of both sheep and goats by cELISA. MVV p28 antigen immunostaining was observed in lungs, lymph nodes, mammary glands, and joint tissues. However, the presence of MVV p28 antigen could not be demonstrated in the brain tissues.

Conclusion:

The highest positivity of MVV in lung tissues indicated higher predilection of the virus in the pulmonary tissue.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Iran J Vet Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Irã

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Iran J Vet Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Irã