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Peer-reviewed veterinary case report

Differential detection of avian oncogenic viruses in poultry layer farms and Turkeys by use of multiplex PCR.

Journal:
Journal of clinical microbiology
Year:
2012
Authors:
Gopal, Sathish et al.
Affiliation:
Department of Animal Biotechnology · India
Species:
bird

Plain-English summary

This study looked at certain viruses that can cause cancer in birds, specifically in poultry farms in South India. Researchers tested samples from chickens and found several types of viruses, including Marek's disease virus (MDV), avian leukosis virus (ALV), and reticuloendotheliosis virus (REV). They used a special test called multiplex PCR, which can quickly identify these viruses and even detect if more than one virus is present in a sample. Out of 169 samples tested, some were positive for one virus, while others had two or even all three viruses. The findings suggest that multiplex PCR is a helpful tool for quickly diagnosing these viral infections in birds.

Abstract

Avian oncogenic viruses include Marek's disease virus (MDV), a highly contagious herpesvirus, as well as retroviruses such as avian leukosis virus (ALV) subgroups A to J and reticuloendotheliosis virus (REV). In this study, we examined the incidence of these viruses in suspected samples collected from poultry layer farms of South India, mainly in the Namakkal district of Tamil Nadu, a highly dense poultry-growing area in India. The histopathology-positive tissue sections were identified and further confirmed by immunohistochemistry using virus-specific antibodies. The viruses belonging to all 3 groups (MDV, ALV, and REV) were isolated in a cell culture system and confirmed by immunofluorescence using virus-specific antibodies. PCR appeared to be the method of choice for rapid and accurate diagnosis of these viruses. The multiplex PCR primers specific to MDV, ALV, REV, and chicken DNA were designed for rapid differential diagnosis. The specificity of the primers was checked by amplification of DNA from virus-infected cell culture in comparison with uninfected samples, and sensitivity was evaluated by calculating the minimum copy number at which amplification occurs in the cloned PCR products. The sequences of the amplicons were compared by BLAST analysis. PCR tests demonstrated the presence of single, dual, or triple viruses in some of the samples. Of 169 samples screened by multiplex PCR, 9 samples were positive for MDV, 17 samples were positive for ALV, 12 samples were positive for REV, and 17 samples were positive for both ALV and REV. Three samples were positive for all three viruses. ALV-positive samples were further subjected to subgroup-specific PCR, which gave positive results for subgroups B and D but not for subgroup J. Multiplex PCR appeared to be a useful technique for rapid differential diagnosis of avian oncogenic viruses and detection of multiple infections of avian oncogenic viruses under field conditions.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/22675132/