Abstract

Infectious Bursal Disease (IBD) is an economically important irreversible immunosuppressive disease of young birds. The present study was designed to confirm the efficacy of two common diagnostic tests for the detection of Infectious Bursal Disease Virus (IBDV) from the three types of bursal samples collected from a recent outbreak in layer and broiler chickens of Gazipur district, Bangladesh. This study compared the degree of sensitivity between Ouchterlony Double Immunodiffusion Test (ODIT) and Reverse Transcription Polymerase Chain Reaction (RT-PCR) for the detection of IBD viral antigen from the bursal samples. A total of 180 field bursal samples (80 broiler and 100 from layer chicken) from suspected IBDV infected dead chickens were collected from 50 different poultry farms. Bursal homogenates were used to detect IBDV using ODIT and RT-PCR. Three types of bursal samples, hemorrhagic bursa (90), edematous bursa (78) and atrophied bursa (12) were selected for the detection of viral antigen. A panel of anti-sera and IBDV specific primer for VP2 gene was used for RT-PCR. The data demonstrated that, out of 180 field samples, 164 (91%) were positive by RT-PCR and 120 (67%) were positive by ODIT. Haemorrhagic bursas were more sensitive compared to oedematous bursas while no virus was detected from the samples of atrophied bursa. This study demonstrated that, RT-PCR was more sensitive and effective diagnostic tool compared to that of ODIT. Key words: Infectious bursal disease virus (IBDV), ouchterlony double immunodiffusion test (ODIT), reverse transcription polymerase chain reaction (RT-PCR), bursa, broiler, layer.

Highlights

  • Infectious bursal disease or Gumboro is a vastly transmissible immunosuppressant disease which is triggered with a virus belonging to the genus Avibirnavirus of family Birnaviridae

  • Ouchterlony Double Immunodiffusion Test (ODIT) is one of the substitute techniques suggested for Infectious Bursal Disease Virus (IBDV) diagnosis by Organization for Animal Health (OIE) for international trade (Butt et al, 2015)

  • In case of ODIT, hemorrhagic and edematous bursal homogenates were found positive for IBDV

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Summary

Introduction

ODIT is a simple method to detect specific antibody and measure antigenicity (Hornbeck, 2017) It is simplest but least sensitive serological method (Sali, 2019). RT-PCR is the method which helps for precise and early diagnosis of viruses from field samples (Hasan et al, 2010) Among these diagnostic methods, in this study we chose ODIT and RT-PCR as ODIT is simplest of all, inexpensive and has the ability for detecting specific antibodies (Dey et al, 2019; Hornbeck, 2017; Ouchterlony, 1948; Ouchterlony and Nilsson, 1986) and RT-PCR is specific, sensitive, speedy, reliable and accurate techniques for detection of IBD viruses (Hasan et al, 2010)

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