Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR

Author:

Imsonpang Supapong123,Pudgerd Arnon4,Chotwiwatthanakun Charoonroj15,Srisala Jiraporn6,Sanguanrut Piyachat6,Kasamechotchung Chanadda7,Sritunyalucksana Kallaya6,Taengchaiyaphum Suparat6,Vanichviriyakit Rapeepun12

Affiliation:

1. Center of Excellence for Shrimp Molecular Biology and Biotechnology (Centex Shrimp), Faculty of Science Mahidol University Bangkok Thailand

2. Department of Anatomy, Faculty of Science Mahidol University Bangkok Thailand

3. Division of Health and Applied Sciences, Faculty of Science Prince of Songkla University Songkhla Thailand

4. Division of Anatomy, School of Medical Sciences University of Phayao Phayao Thailand

5. Mahidol University, Nakhonsawan Campus Nakhonsawan Thailand

6. Aquatic Animal Health Research Team (AQHT), Integrative Aquaculture Biotechnology Research Group National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA) Bangkok Thailand

7. Department of Fisheries, Faculty of Agriculture and Natural Resources Rajamangala University of Technology Tawan‐ok Chonburi Thailand

Abstract

AbstractThe presence of endogenous viral elements (EVE) in the penaeid shrimp genome has been recently reported and suggested to be involved in the host recognition of viral invaders. Our previous report of a search for EVE of infectious hypodermal and haematopoietic necrosis virus (IHHNV‐EVE) in the Thai Penaeus monodon whole genome sequence project (GenBank accession no. JABERT000000000) confirmed the presence of three clusters of EVE derived from IHHNV in the shrimp genome. This study aimed to compare an immunohistochemistry method (IHC) and a PCR method to detect infectious IHHNV infection in shrimp. First, specimens collected from farms were checked for IHHNV using three PCR methods; two methods were recommended by WOAH (309 and 389 methods), and a newly established long‐range PCR for IHHNV (IHHNV‐LA PCR) targeting almost the whole genome (>90%) of IHHNV. Among 29 specimens tested, 24 specimens were positive for WOAH methods (at least one method). Among 24 WOAH‐positive specimens (WOAH+), there were 18 specimens with positive IHHNV‐LA PCR method (WOAH+/LA+), six specimens with negative IHHNV‐LA PCR method (WOAH+/LA−). Six specimens were negative for all methods (WOAH−/LA−). The positive signals detected by IHC method were found only in the specimens with WOAH+/LA+. The results suggest that the WOAH+/LA− specimens were not infected with IHHNV, and the positive WOAH method might result from the EVE‐IHHNV. The study recommends combining the IHHNV‐LA PCR method and IHC with positive PCR results from WOAH's recommended methods to confirm IHHNV infection.

Publisher

Wiley

Subject

Veterinary (miscellaneous),Aquatic Science

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