Journal of Immunology and Immunopathology
  • Year: 2018
  • Volume: 20
  • Issue: 1

Immuno-Histochemical and Molecular Detection of Duck Enteritis Virus in Liver Tissues of Experimentally Infected Ducklings

  • Author:
  • Jyoti Kumar1, Satyabrat Dandapat2,*, Mithilesh Singh3, Vidya Singh4, Sivasankar Panickan5, Ajay Kumar6, Sukhdeb Nandi7, Vishal Chander8
  • Total Page Count: 6
  • Published Online: Jan 1, 2018
  • Page Number: 24 to 29

1Immunology SectionICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

2Immunology SectionICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

3Immunology SectionICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

4Pathology DivisionICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

5Immunology SectionICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

6Biochemistry SectionICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

7CADRAD, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

8CADRAD, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar PradeshIndia

*Corresponding author email id: satyadandapat2008@hotmail.com

Abstract

Duck viral enteritis (DVE) or duck plague is an acute, sometimes chronic, contagious and lethal disease that attacks ducks, geese, swans and other members of the family Anatidae of the order Anseriformes. Accurate diagnosis of the disease is very important for control of duck plague. In this study, findings of polymerase chain reaction (PCR) for detection of viral DNA, the histopathological changes and immuno-histochemical (IHC) techniques for detection of the viral antigens in tissues, in an experimental infection of duck enteritis virus (DEV) in ducklings have been described. Histopathological examination revealed characteristic changes of vacuolar degeneration, proliferation of bile ductules and inclusion bodies in infected liver tissues. A positive IHC staining reaction indicated the presence of DEV antigens at various tissue locations mainly associated with necrotic foci in the liver. The DEV DNA was detected in the liver tissue samples of ducklings by PCR amplification of DNA polymerase and gp300 genes of DEV. Sequencing of the amplified products revealed the identity of 99–100%, with published sequence of DNA polymerase and gp300 genes of DEV available in the NCBI database. These findings may be useful for a confirmatory diagnosis of duck plague during outbreaks, epidemiological investigations and also for study of pathogenesis of duck plague, in which histopathology, IHC techniques in conjunction with molecular tools may be recommended.

Keywords

Duck viral enteritis (DVE), Duck enteritis virus (DEV), Histopathological, Immuno-histochemical, Liver, Polymerase chain reaction, DNA polymerase, Duck