ISSN: 0973-7510

E-ISSN: 2581-690X

S. Aravind, N.M. Kamble, S.S. Gaikad, S.K. Shukla, S.A. Khulpae, Sohini Dey and C. Madhan Mohan*
1Recombinant DNA Laboratory, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh – 243122, India.
J Pure Appl Microbiol. 2014;8(2):945-949
© The Author(s). 2014
Received: 08/07/2013 | Accepted: 19/10/2013 | Published: 31/04/2014
Abstract

Duck enteritis virus (DEV) is a herpes virus that cause an acute, contagious, and fatal disease. In this present article, we introduce a polymerase chain reaction (PCR) assay for DEV DNA. The method employed primer sets targeting the viral DNA polymerase gene (UL30), type I membrane protein that binds to heparin sulphate (glycoprotein C) and glycoprotein E of DEV and was able to amplify DNA fragments of the expected size from infected samples. The method will provide a valuable tool for a rapid laboratory diagnosis of DEV infection. By virtue of its high throughput format, the method may be useful for large epidemiological surveys and clarification of pathogenesis, such as latency of the virus.

Keywords

Duckenteritis virus, DNA polymerase, Glycoprotein C, Glycoprotein E Polymerase Chain Reaction

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© The Author(s) 2014. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.