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Subclinical avian hepatitis E virus infection in layer flocks in the United States
•Circulation of avian HEV was determined in healthy commercial layer farms in the United States.•A fluorescent microbead immunoassay (FMIA) was developed for detecting anti-avian HEV IgY antibodies.•Prevalence of avian HEV infection was high among clinically healthy laying hens.•Different avian HEV...
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Published in: | The veterinary journal (1997) 2015-12, Vol.206 (3), p.304-311 |
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container_title | The veterinary journal (1997) |
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creator | Gerber, Priscilla F. Trampel, Darrell W. Willinghan, Eric M. Billam, Padma Meng, Xiang-Jin Opriessnig, Tanja |
description | •Circulation of avian HEV was determined in healthy commercial layer farms in the United States.•A fluorescent microbead immunoassay (FMIA) was developed for detecting anti-avian HEV IgY antibodies.•Prevalence of avian HEV infection was high among clinically healthy laying hens.•Different avian HEV genotype 2 strains are circulating within a farm.
The objective of this study was to determine patterns of avian HEV infection in naturally infected chicken farms. A total of 310 serum samples and 62 pooled fecal samples were collected from 62 chicken flocks on seven commercial in-line egg farms in the Midwestern United States and tested for avian HEV circulation. Serum samples were tested for the presence of anti-avian HEV IgY antibodies by a fluorescent microbead immunoassay (FMIA) which was developed for this study. The FMIA was validated using archived samples of chickens with known exposure (n = 96) and compared to the results obtained with an enzyme-linked immunosorbent assay (ELISA) based on the same capture antigen. There was an overall substantial agreement between the two assays (κ = 0.63) with earlier detection of positive chickens by the FMIA (P = 0.04). On the seven farms investigated, the overall prevalence of anti-avian HEV IgY antibodies in serum samples from commercial chickens was 44.8% (20–82% per farm). Fecal samples were tested for avian HEV RNA by a nested reverse-transcriptase PCR. The overall detection rate of avian HEV RNA in fecal samples was 62.9% (0–100% per farm). Sequencing analyses of partial helicase and capsid genes showed that different avian HEV genotype 2 strains were circulating within a farm. However, no correlation was found between avian HEV RNA detection and egg production, egg weight or mortality. In conclusion, avian HEV infection is widespread among clinically healthy laying hens in the United States. |
doi_str_mv | 10.1016/j.tvjl.2015.10.014 |
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The objective of this study was to determine patterns of avian HEV infection in naturally infected chicken farms. A total of 310 serum samples and 62 pooled fecal samples were collected from 62 chicken flocks on seven commercial in-line egg farms in the Midwestern United States and tested for avian HEV circulation. Serum samples were tested for the presence of anti-avian HEV IgY antibodies by a fluorescent microbead immunoassay (FMIA) which was developed for this study. The FMIA was validated using archived samples of chickens with known exposure (n = 96) and compared to the results obtained with an enzyme-linked immunosorbent assay (ELISA) based on the same capture antigen. There was an overall substantial agreement between the two assays (κ = 0.63) with earlier detection of positive chickens by the FMIA (P = 0.04). On the seven farms investigated, the overall prevalence of anti-avian HEV IgY antibodies in serum samples from commercial chickens was 44.8% (20–82% per farm). Fecal samples were tested for avian HEV RNA by a nested reverse-transcriptase PCR. The overall detection rate of avian HEV RNA in fecal samples was 62.9% (0–100% per farm). Sequencing analyses of partial helicase and capsid genes showed that different avian HEV genotype 2 strains were circulating within a farm. However, no correlation was found between avian HEV RNA detection and egg production, egg weight or mortality. In conclusion, avian HEV infection is widespread among clinically healthy laying hens in the United States.</description><identifier>ISSN: 1090-0233</identifier><identifier>EISSN: 1532-2971</identifier><identifier>DOI: 10.1016/j.tvjl.2015.10.014</identifier><identifier>PMID: 26564555</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Agriculture ; Animals ; Antibodies, Viral - analysis ; Asymptomatic Infections ; Avian hepatitis E virus (avian HEV) ; Chickens ; Enzyme-Linked Immunosorbent Assay - veterinary ; Feces - virology ; Female ; Fluorescent microsphere immunoassay ; Hepatitis, Viral, Animal - diagnosis ; Hepevirus ; Immunoassay - veterinary ; Poultry Diseases - diagnosis ; RNA Virus Infections - diagnosis ; RNA Virus Infections - veterinary ; RNA, Viral - analysis ; RT-PCR ; Subclinical infection ; United States</subject><ispartof>The veterinary journal (1997), 2015-12, Vol.206 (3), p.304-311</ispartof><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-2e340d000809a8a14a30280bd4e4340dd22dab8a80bc1bb5055adfc36be585783</citedby><cites>FETCH-LOGICAL-c400t-2e340d000809a8a14a30280bd4e4340dd22dab8a80bc1bb5055adfc36be585783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26564555$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gerber, Priscilla F.</creatorcontrib><creatorcontrib>Trampel, Darrell W.</creatorcontrib><creatorcontrib>Willinghan, Eric M.</creatorcontrib><creatorcontrib>Billam, Padma</creatorcontrib><creatorcontrib>Meng, Xiang-Jin</creatorcontrib><creatorcontrib>Opriessnig, Tanja</creatorcontrib><title>Subclinical avian hepatitis E virus infection in layer flocks in the United States</title><title>The veterinary journal (1997)</title><addtitle>Vet J</addtitle><description>•Circulation of avian HEV was determined in healthy commercial layer farms in the United States.•A fluorescent microbead immunoassay (FMIA) was developed for detecting anti-avian HEV IgY antibodies.•Prevalence of avian HEV infection was high among clinically healthy laying hens.•Different avian HEV genotype 2 strains are circulating within a farm.
The objective of this study was to determine patterns of avian HEV infection in naturally infected chicken farms. A total of 310 serum samples and 62 pooled fecal samples were collected from 62 chicken flocks on seven commercial in-line egg farms in the Midwestern United States and tested for avian HEV circulation. Serum samples were tested for the presence of anti-avian HEV IgY antibodies by a fluorescent microbead immunoassay (FMIA) which was developed for this study. The FMIA was validated using archived samples of chickens with known exposure (n = 96) and compared to the results obtained with an enzyme-linked immunosorbent assay (ELISA) based on the same capture antigen. There was an overall substantial agreement between the two assays (κ = 0.63) with earlier detection of positive chickens by the FMIA (P = 0.04). On the seven farms investigated, the overall prevalence of anti-avian HEV IgY antibodies in serum samples from commercial chickens was 44.8% (20–82% per farm). Fecal samples were tested for avian HEV RNA by a nested reverse-transcriptase PCR. The overall detection rate of avian HEV RNA in fecal samples was 62.9% (0–100% per farm). Sequencing analyses of partial helicase and capsid genes showed that different avian HEV genotype 2 strains were circulating within a farm. However, no correlation was found between avian HEV RNA detection and egg production, egg weight or mortality. In conclusion, avian HEV infection is widespread among clinically healthy laying hens in the United States.</description><subject>Agriculture</subject><subject>Animals</subject><subject>Antibodies, Viral - analysis</subject><subject>Asymptomatic Infections</subject><subject>Avian hepatitis E virus (avian HEV)</subject><subject>Chickens</subject><subject>Enzyme-Linked Immunosorbent Assay - veterinary</subject><subject>Feces - virology</subject><subject>Female</subject><subject>Fluorescent microsphere immunoassay</subject><subject>Hepatitis, Viral, Animal - diagnosis</subject><subject>Hepevirus</subject><subject>Immunoassay - veterinary</subject><subject>Poultry Diseases - diagnosis</subject><subject>RNA Virus Infections - diagnosis</subject><subject>RNA Virus Infections - veterinary</subject><subject>RNA, Viral - analysis</subject><subject>RT-PCR</subject><subject>Subclinical infection</subject><subject>United States</subject><issn>1090-0233</issn><issn>1532-2971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMorq7-AQ-So5eukzTptuBFZP2ABcGPc0iTKWbttmuSLvjvTdnVo6cZ3nnnZeYh5ILBjAErrlezuF21Mw5MJmEGTByQEyZznvFqzg5TDxVkwPN8Qk5DWAFAJQQ_JhNeyEJIKU_Iy-tQm9Z1zuiW6q3THf3AjY4uukAXdOv8EKjrGjTR9V3qaKu_0dOm7c3nOKHxA-l75yJa-hp1xHBGjhrdBjzf1yl5v1-83T1my-eHp7vbZWYEQMw45gJsuqmESpeaCZ0DL6G2AsU4sZxbXZc6SYbVtQQptW1MXtQoSzkv8ym52uVufP81YIhq7YLBttUd9kNQbC6qAqqizJOV76zG9yF4bNTGu7X234qBGlmqlRpZqpHlqCWWaelynz_Ua7R_K7_wkuFmZ8D05dahV8E47Axa5xMvZXv3X_4PPfWFHw</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Gerber, Priscilla F.</creator><creator>Trampel, Darrell W.</creator><creator>Willinghan, Eric M.</creator><creator>Billam, Padma</creator><creator>Meng, Xiang-Jin</creator><creator>Opriessnig, Tanja</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201512</creationdate><title>Subclinical avian hepatitis E virus infection in layer flocks in the United States</title><author>Gerber, Priscilla F. ; Trampel, Darrell W. ; Willinghan, Eric M. ; Billam, Padma ; Meng, Xiang-Jin ; Opriessnig, Tanja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-2e340d000809a8a14a30280bd4e4340dd22dab8a80bc1bb5055adfc36be585783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Agriculture</topic><topic>Animals</topic><topic>Antibodies, Viral - analysis</topic><topic>Asymptomatic Infections</topic><topic>Avian hepatitis E virus (avian HEV)</topic><topic>Chickens</topic><topic>Enzyme-Linked Immunosorbent Assay - veterinary</topic><topic>Feces - virology</topic><topic>Female</topic><topic>Fluorescent microsphere immunoassay</topic><topic>Hepatitis, Viral, Animal - diagnosis</topic><topic>Hepevirus</topic><topic>Immunoassay - veterinary</topic><topic>Poultry Diseases - diagnosis</topic><topic>RNA Virus Infections - diagnosis</topic><topic>RNA Virus Infections - veterinary</topic><topic>RNA, Viral - analysis</topic><topic>RT-PCR</topic><topic>Subclinical infection</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gerber, Priscilla F.</creatorcontrib><creatorcontrib>Trampel, Darrell W.</creatorcontrib><creatorcontrib>Willinghan, Eric M.</creatorcontrib><creatorcontrib>Billam, Padma</creatorcontrib><creatorcontrib>Meng, Xiang-Jin</creatorcontrib><creatorcontrib>Opriessnig, Tanja</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The veterinary journal (1997)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gerber, Priscilla F.</au><au>Trampel, Darrell W.</au><au>Willinghan, Eric M.</au><au>Billam, Padma</au><au>Meng, Xiang-Jin</au><au>Opriessnig, Tanja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subclinical avian hepatitis E virus infection in layer flocks in the United States</atitle><jtitle>The veterinary journal (1997)</jtitle><addtitle>Vet J</addtitle><date>2015-12</date><risdate>2015</risdate><volume>206</volume><issue>3</issue><spage>304</spage><epage>311</epage><pages>304-311</pages><issn>1090-0233</issn><eissn>1532-2971</eissn><abstract>•Circulation of avian HEV was determined in healthy commercial layer farms in the United States.•A fluorescent microbead immunoassay (FMIA) was developed for detecting anti-avian HEV IgY antibodies.•Prevalence of avian HEV infection was high among clinically healthy laying hens.•Different avian HEV genotype 2 strains are circulating within a farm.
The objective of this study was to determine patterns of avian HEV infection in naturally infected chicken farms. A total of 310 serum samples and 62 pooled fecal samples were collected from 62 chicken flocks on seven commercial in-line egg farms in the Midwestern United States and tested for avian HEV circulation. Serum samples were tested for the presence of anti-avian HEV IgY antibodies by a fluorescent microbead immunoassay (FMIA) which was developed for this study. The FMIA was validated using archived samples of chickens with known exposure (n = 96) and compared to the results obtained with an enzyme-linked immunosorbent assay (ELISA) based on the same capture antigen. There was an overall substantial agreement between the two assays (κ = 0.63) with earlier detection of positive chickens by the FMIA (P = 0.04). On the seven farms investigated, the overall prevalence of anti-avian HEV IgY antibodies in serum samples from commercial chickens was 44.8% (20–82% per farm). Fecal samples were tested for avian HEV RNA by a nested reverse-transcriptase PCR. The overall detection rate of avian HEV RNA in fecal samples was 62.9% (0–100% per farm). Sequencing analyses of partial helicase and capsid genes showed that different avian HEV genotype 2 strains were circulating within a farm. However, no correlation was found between avian HEV RNA detection and egg production, egg weight or mortality. In conclusion, avian HEV infection is widespread among clinically healthy laying hens in the United States.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26564555</pmid><doi>10.1016/j.tvjl.2015.10.014</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agriculture Animals Antibodies, Viral - analysis Asymptomatic Infections Avian hepatitis E virus (avian HEV) Chickens Enzyme-Linked Immunosorbent Assay - veterinary Feces - virology Female Fluorescent microsphere immunoassay Hepatitis, Viral, Animal - diagnosis Hepevirus Immunoassay - veterinary Poultry Diseases - diagnosis RNA Virus Infections - diagnosis RNA Virus Infections - veterinary RNA, Viral - analysis RT-PCR Subclinical infection United States |
title | Subclinical avian hepatitis E virus infection in layer flocks in the United States |
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