Loading…
Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR
The 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 P...
Saved in:
Published in: | Journal of fish diseases 2024-03, Vol.47 (3), p.e13905-n/a |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c3485-654bf0155417f0ec01ddbbbf4fbaa68576069c0144af307d3c4ec68b134a07933 |
container_end_page | n/a |
container_issue | 3 |
container_start_page | e13905 |
container_title | Journal of fish diseases |
container_volume | 47 |
creator | Imsonpang, Supapong Pudgerd, Arnon Chotwiwatthanakun, Charoonroj Srisala, Jiraporn Sanguanrut, Piyachat Kasamechotchung, Chanadda Sritunyalucksana, Kallaya Taengchaiyaphum, Suparat Vanichviriyakit, Rapeepun |
description | The 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. |
doi_str_mv | 10.1111/jfd.13905 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2902937749</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2902937749</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3485-654bf0155417f0ec01ddbbbf4fbaa68576069c0144af307d3c4ec68b134a07933</originalsourceid><addsrcrecordid>eNp1kLFOwzAQhi0EoqUw8AIoEgsMac-xHTcjKpQWVYAQsEZOYtNUTVziBNSNR-AZeRIOUhiQ8HI-6_Onu5-QQwp9imewMFmfsgjEFulSFgo_kCHdJl2gHHwppeiQPecWAFQKGu6SDhuCZACiS_TIliavClXbau3V2tWeNZ5K6_xFe9PJ5PrRy0ujsbcl3jw3r_Ji5SVrLy-KprTz3NU2nesCKwpUmbW_Pt7eZ7Z8OkP2dnS3T3aMWjp9sKk98jC-uB9N_NnN5XR0NvNTxofCDwVPDFAhOJUGdAo0y5IkMdwkSoVDIUMII3zlXBkGMmMp12k4TCjjCmTEWI-ctN5VZZ8bXCbGuVK9XKpS28bFQQRBxKTkEaLHf9CFbaoSp0MqYAGHQHKkTlsqraxzlTbxCvdX1TqmEH9lH2P28Xf2yB5tjE1S6OyX_AkbgUELvOZLvf7fFF-Nz1vlJ9MXjTE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2923240274</pqid></control><display><type>article</type><title>Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Imsonpang, Supapong ; Pudgerd, Arnon ; Chotwiwatthanakun, Charoonroj ; Srisala, Jiraporn ; Sanguanrut, Piyachat ; Kasamechotchung, Chanadda ; Sritunyalucksana, Kallaya ; Taengchaiyaphum, Suparat ; Vanichviriyakit, Rapeepun</creator><creatorcontrib>Imsonpang, Supapong ; Pudgerd, Arnon ; Chotwiwatthanakun, Charoonroj ; Srisala, Jiraporn ; Sanguanrut, Piyachat ; Kasamechotchung, Chanadda ; Sritunyalucksana, Kallaya ; Taengchaiyaphum, Suparat ; Vanichviriyakit, Rapeepun</creatorcontrib><description>The 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.</description><identifier>ISSN: 0140-7775</identifier><identifier>EISSN: 1365-2761</identifier><identifier>DOI: 10.1111/jfd.13905</identifier><identifier>PMID: 38073005</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>endogenous viral element (EVE) ; Genomes ; IHHNV ; Immunohistochemistry ; Infections ; long‐range PCR ; Methods ; Necrosis ; Nucleotide sequence ; Shrimps</subject><ispartof>Journal of fish diseases, 2024-03, Vol.47 (3), p.e13905-n/a</ispartof><rights>2023 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2023 The Authors. Journal of Fish Diseases published by John Wiley & Sons Ltd.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3485-654bf0155417f0ec01ddbbbf4fbaa68576069c0144af307d3c4ec68b134a07933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38073005$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Imsonpang, Supapong</creatorcontrib><creatorcontrib>Pudgerd, Arnon</creatorcontrib><creatorcontrib>Chotwiwatthanakun, Charoonroj</creatorcontrib><creatorcontrib>Srisala, Jiraporn</creatorcontrib><creatorcontrib>Sanguanrut, Piyachat</creatorcontrib><creatorcontrib>Kasamechotchung, Chanadda</creatorcontrib><creatorcontrib>Sritunyalucksana, Kallaya</creatorcontrib><creatorcontrib>Taengchaiyaphum, Suparat</creatorcontrib><creatorcontrib>Vanichviriyakit, Rapeepun</creatorcontrib><title>Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR</title><title>Journal of fish diseases</title><addtitle>J Fish Dis</addtitle><description>The 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.</description><subject>endogenous viral element (EVE)</subject><subject>Genomes</subject><subject>IHHNV</subject><subject>Immunohistochemistry</subject><subject>Infections</subject><subject>long‐range PCR</subject><subject>Methods</subject><subject>Necrosis</subject><subject>Nucleotide sequence</subject><subject>Shrimps</subject><issn>0140-7775</issn><issn>1365-2761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp1kLFOwzAQhi0EoqUw8AIoEgsMac-xHTcjKpQWVYAQsEZOYtNUTVziBNSNR-AZeRIOUhiQ8HI-6_Onu5-QQwp9imewMFmfsgjEFulSFgo_kCHdJl2gHHwppeiQPecWAFQKGu6SDhuCZACiS_TIliavClXbau3V2tWeNZ5K6_xFe9PJ5PrRy0ujsbcl3jw3r_Ji5SVrLy-KprTz3NU2nesCKwpUmbW_Pt7eZ7Z8OkP2dnS3T3aMWjp9sKk98jC-uB9N_NnN5XR0NvNTxofCDwVPDFAhOJUGdAo0y5IkMdwkSoVDIUMII3zlXBkGMmMp12k4TCjjCmTEWI-ctN5VZZ8bXCbGuVK9XKpS28bFQQRBxKTkEaLHf9CFbaoSp0MqYAGHQHKkTlsqraxzlTbxCvdX1TqmEH9lH2P28Xf2yB5tjE1S6OyX_AkbgUELvOZLvf7fFF-Nz1vlJ9MXjTE</recordid><startdate>202403</startdate><enddate>202403</enddate><creator>Imsonpang, Supapong</creator><creator>Pudgerd, Arnon</creator><creator>Chotwiwatthanakun, Charoonroj</creator><creator>Srisala, Jiraporn</creator><creator>Sanguanrut, Piyachat</creator><creator>Kasamechotchung, Chanadda</creator><creator>Sritunyalucksana, Kallaya</creator><creator>Taengchaiyaphum, Suparat</creator><creator>Vanichviriyakit, Rapeepun</creator><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TN</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>202403</creationdate><title>Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR</title><author>Imsonpang, Supapong ; Pudgerd, Arnon ; Chotwiwatthanakun, Charoonroj ; Srisala, Jiraporn ; Sanguanrut, Piyachat ; Kasamechotchung, Chanadda ; Sritunyalucksana, Kallaya ; Taengchaiyaphum, Suparat ; Vanichviriyakit, Rapeepun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3485-654bf0155417f0ec01ddbbbf4fbaa68576069c0144af307d3c4ec68b134a07933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>endogenous viral element (EVE)</topic><topic>Genomes</topic><topic>IHHNV</topic><topic>Immunohistochemistry</topic><topic>Infections</topic><topic>long‐range PCR</topic><topic>Methods</topic><topic>Necrosis</topic><topic>Nucleotide sequence</topic><topic>Shrimps</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Imsonpang, Supapong</creatorcontrib><creatorcontrib>Pudgerd, Arnon</creatorcontrib><creatorcontrib>Chotwiwatthanakun, Charoonroj</creatorcontrib><creatorcontrib>Srisala, Jiraporn</creatorcontrib><creatorcontrib>Sanguanrut, Piyachat</creatorcontrib><creatorcontrib>Kasamechotchung, Chanadda</creatorcontrib><creatorcontrib>Sritunyalucksana, Kallaya</creatorcontrib><creatorcontrib>Taengchaiyaphum, Suparat</creatorcontrib><creatorcontrib>Vanichviriyakit, Rapeepun</creatorcontrib><collection>Wiley Online Library</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of fish diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imsonpang, Supapong</au><au>Pudgerd, Arnon</au><au>Chotwiwatthanakun, Charoonroj</au><au>Srisala, Jiraporn</au><au>Sanguanrut, Piyachat</au><au>Kasamechotchung, Chanadda</au><au>Sritunyalucksana, Kallaya</au><au>Taengchaiyaphum, Suparat</au><au>Vanichviriyakit, Rapeepun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR</atitle><jtitle>Journal of fish diseases</jtitle><addtitle>J Fish Dis</addtitle><date>2024-03</date><risdate>2024</risdate><volume>47</volume><issue>3</issue><spage>e13905</spage><epage>n/a</epage><pages>e13905-n/a</pages><issn>0140-7775</issn><eissn>1365-2761</eissn><abstract>The 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.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>38073005</pmid><doi>10.1111/jfd.13905</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0140-7775 |
ispartof | Journal of fish diseases, 2024-03, Vol.47 (3), p.e13905-n/a |
issn | 0140-7775 1365-2761 |
language | eng |
recordid | cdi_proquest_miscellaneous_2902937749 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | endogenous viral element (EVE) Genomes IHHNV Immunohistochemistry Infections long‐range PCR Methods Necrosis Nucleotide sequence Shrimps |
title | Confirmatory test of active IHHNV infection in shrimp by immunohistochemistry and IHHNV‐LongAmp PCR |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T05%3A45%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Confirmatory%20test%20of%20active%20IHHNV%20infection%20in%20shrimp%20by%20immunohistochemistry%20and%20IHHNV%E2%80%90LongAmp%20PCR&rft.jtitle=Journal%20of%20fish%20diseases&rft.au=Imsonpang,%20Supapong&rft.date=2024-03&rft.volume=47&rft.issue=3&rft.spage=e13905&rft.epage=n/a&rft.pages=e13905-n/a&rft.issn=0140-7775&rft.eissn=1365-2761&rft_id=info:doi/10.1111/jfd.13905&rft_dat=%3Cproquest_cross%3E2902937749%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3485-654bf0155417f0ec01ddbbbf4fbaa68576069c0144af307d3c4ec68b134a07933%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2923240274&rft_id=info:pmid/38073005&rfr_iscdi=true |