Experimental Infection of Muscovy Ducks with Highly Pathogenic Avian Influenza Virus (H5N1) Belonging to Clade 2.2

Highly pathogenic (HP) H5N1 avian influenza (AI) is enzootic in several countries of Asia and Africa and constitutes a major threat, at the world level, for both animal and public health. Ducks play an important role in the epidemiology of AI, including HP H5N1 AI. Although vaccination can be a usef...

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Veröffentlicht in:Avian diseases 2010-03, Vol.54 (s1), p.538-547
Hauptverfasser: Guionie, Olivier, Guillou-Cloarec, Cécile, Courtois, David, Bougeard, Stéphanie, Amelot, Michel, Jestin, Véronique
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container_start_page 538
container_title Avian diseases
container_volume 54
creator Guionie, Olivier
Guillou-Cloarec, Cécile
Courtois, David
Bougeard, Stéphanie
Amelot, Michel
Jestin, Véronique
description Highly pathogenic (HP) H5N1 avian influenza (AI) is enzootic in several countries of Asia and Africa and constitutes a major threat, at the world level, for both animal and public health. Ducks play an important role in the epidemiology of AI, including HP H5N1 AI. Although vaccination can be a useful tool to control AI, duck vaccination has not proved very efficient in the field, indicating a need to develop new vaccines and a challenge model to evaluate the protection for duck species. Although Muscovy duck is the duck species most often reared in France, the primary duck-producing country in Europe, and is also produced in Asia, it is rarely studied. Our team recently demonstrated a good cross-reactivity with hemagglutinin from clade 2.2 and inferred that this could be a good vaccine candidate for ducks. Two challenges using two French H5N1 HP strains, 1) A/mute swan/France/06299/06 (Swan/06299), clade 2.2.1, and 2) A/mute swan/France/070203/07 (Swan/070203), clade 2.2 (but different from subclade 2.2.1), were performed (each) on 20 Muscovy ducks (including five contacts) inoculated by oculo-nasal route (6 log10 median egg infectious doses per duck). Clinical signs were recorded daily, and cloacal and oropharyngeal swabs were collected throughout the assay. Autopsies were done on all dead ducks, and organs were taken for analyses. Virus was measured by quantitative reverse transcriptase–PCR based on the M gene AI virus. Ducks presented severe nervous signs in both challenges. Swan/070203 strain led to 80% morbidity (12/15 sick ducks) and 73% mortality (11/15 ducks) at 13.5 days postinfection (dpi), whereas Swan/06299 strain produced 100% mortality at 6.5 dpi. Viral RNA load was significantly lower via the cloacal route than via the oropharyngeal route in both trials, presenting a peak in the first challenge at 3.5 dpi and being more stable in the second challenge. The brain was the organ containing the highest viral RNA load in both challenges. Viral RNA load in a given organ was similar or statistically significantly higher in ducks challenged with Swan/06299 strain. Thus, the Swan/06299 strain was more virulent and could be used as a putative challenge model. Moreover, challenged ducks and contacts contained the same amounts of viral RNA load, demonstrating the rapid and efficient transmission of H5N1 HP in Muscovy ducks in our experimental conditions.
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Ducks play an important role in the epidemiology of AI, including HP H5N1 AI. Although vaccination can be a useful tool to control AI, duck vaccination has not proved very efficient in the field, indicating a need to develop new vaccines and a challenge model to evaluate the protection for duck species. Although Muscovy duck is the duck species most often reared in France, the primary duck-producing country in Europe, and is also produced in Asia, it is rarely studied. Our team recently demonstrated a good cross-reactivity with hemagglutinin from clade 2.2 and inferred that this could be a good vaccine candidate for ducks. Two challenges using two French H5N1 HP strains, 1) A/mute swan/France/06299/06 (Swan/06299), clade 2.2.1, and 2) A/mute swan/France/070203/07 (Swan/070203), clade 2.2 (but different from subclade 2.2.1), were performed (each) on 20 Muscovy ducks (including five contacts) inoculated by oculo-nasal route (6 log10 median egg infectious doses per duck). Clinical signs were recorded daily, and cloacal and oropharyngeal swabs were collected throughout the assay. Autopsies were done on all dead ducks, and organs were taken for analyses. Virus was measured by quantitative reverse transcriptase–PCR based on the M gene AI virus. Ducks presented severe nervous signs in both challenges. Swan/070203 strain led to 80% morbidity (12/15 sick ducks) and 73% mortality (11/15 ducks) at 13.5 days postinfection (dpi), whereas Swan/06299 strain produced 100% mortality at 6.5 dpi. Viral RNA load was significantly lower via the cloacal route than via the oropharyngeal route in both trials, presenting a peak in the first challenge at 3.5 dpi and being more stable in the second challenge. The brain was the organ containing the highest viral RNA load in both challenges. Viral RNA load in a given organ was similar or statistically significantly higher in ducks challenged with Swan/06299 strain. 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Ducks play an important role in the epidemiology of AI, including HP H5N1 AI. Although vaccination can be a useful tool to control AI, duck vaccination has not proved very efficient in the field, indicating a need to develop new vaccines and a challenge model to evaluate the protection for duck species. Although Muscovy duck is the duck species most often reared in France, the primary duck-producing country in Europe, and is also produced in Asia, it is rarely studied. Our team recently demonstrated a good cross-reactivity with hemagglutinin from clade 2.2 and inferred that this could be a good vaccine candidate for ducks. Two challenges using two French H5N1 HP strains, 1) A/mute swan/France/06299/06 (Swan/06299), clade 2.2.1, and 2) A/mute swan/France/070203/07 (Swan/070203), clade 2.2 (but different from subclade 2.2.1), were performed (each) on 20 Muscovy ducks (including five contacts) inoculated by oculo-nasal route (6 log10 median egg infectious doses per duck). Clinical signs were recorded daily, and cloacal and oropharyngeal swabs were collected throughout the assay. Autopsies were done on all dead ducks, and organs were taken for analyses. Virus was measured by quantitative reverse transcriptase–PCR based on the M gene AI virus. Ducks presented severe nervous signs in both challenges. Swan/070203 strain led to 80% morbidity (12/15 sick ducks) and 73% mortality (11/15 ducks) at 13.5 days postinfection (dpi), whereas Swan/06299 strain produced 100% mortality at 6.5 dpi. Viral RNA load was significantly lower via the cloacal route than via the oropharyngeal route in both trials, presenting a peak in the first challenge at 3.5 dpi and being more stable in the second challenge. The brain was the organ containing the highest viral RNA load in both challenges. Viral RNA load in a given organ was similar or statistically significantly higher in ducks challenged with Swan/06299 strain. Thus, the Swan/06299 strain was more virulent and could be used as a putative challenge model. Moreover, challenged ducks and contacts contained the same amounts of viral RNA load, demonstrating the rapid and efficient transmission of H5N1 HP in Muscovy ducks in our experimental conditions.</description><subject>Animals</subject><subject>Autopsy</subject><subject>Avian influenza virus</subject><subject>Brain</subject><subject>Brain - virology</subject><subject>Cairina moschata</subject><subject>Clade 2.2</subject><subject>Clinical trials</subject><subject>cross reaction</subject><subject>Cross-reactivity</subject><subject>double prime M gene</subject><subject>Ducks</subject><subject>Epidemiology</subject><subject>experimental challenge</subject><subject>experimental design</subject><subject>Experimental infection</subject><subject>food animals</subject><subject>Fowl plague</subject><subject>H5N1 highly pathogenic avian influenza</subject><subject>H5N1 subtype influenza A virus</subject><subject>Hemagglutinins</subject><subject>highly pathogenic avian influenza H5N1</subject><subject>Infections</subject><subject>Influenza A virus</subject><subject>Influenza A Virus, H5N1 Subtype - classification</subject><subject>Influenza A Virus, H5N1 Subtype - pathogenicity</subject><subject>Influenza in Birds - mortality</subject><subject>Influenza in Birds - pathology</subject><subject>Influenza in Birds - virology</subject><subject>Kidney - virology</subject><subject>Kinetics</subject><subject>microbial genetics</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Muscovy ducks</subject><subject>Neurotransmission</subject><subject>Pancreas - virology</subject><subject>pathogenesis</subject><subject>Pathogenesis and Pathobiology in Avian Species</subject><subject>pathogenicity</subject><subject>Public health</subject><subject>reassortment</subject><subject>reverse transcriptase polymerase chain reaction</subject><subject>RNA</subject><subject>RNA, Viral - analysis</subject><subject>signs and symptoms (animals and humans)</subject><subject>Spleen</subject><subject>strain differences</subject><subject>Trachea - virology</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>vertebrate viruses</subject><subject>viral antigens</subject><subject>Viral Load</subject><subject>Viral RNA</subject><subject>viral RNA load</subject><subject>virulence</subject><subject>Virus Shedding</subject><subject>virus transmission</subject><subject>Viruses</subject><issn>0005-2086</issn><issn>1938-4351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtz1DAQhFUUFFkWfgAHQDfg4M2MZT18DEtgUxUeBYSrSpZlr4JXCpYdWH493nLIlZx06K9bM9OEPEVYoWDyWMkSMigAocy-uHaF98gCS6aygnG8TxYAwLMclDgij1K6BEBZCnhIjnLgOYoSF6Q__X3ler9zYTAdPQuNs4OPgcaGfhiTjdd7-na0PxL95Yct3fh22-3pZzNsY-uCt_Tk2ptw8HWjC38M_e77MdFXG_4RX9M3rouh9aGlQ6TrztSO5qv8MXnQmC65Jzfvkly8O_223mTnn96frU_Os6rgMGRNmTcS6lo1hShlrWqJBq2sUDgh0CqnOK-nNaTiZeUYWKakrFhlTQ6F4I4tycs596qPP0eXBr3zybquM8HFMWnFWaFUKfgdSCzEdNjiv6RkDDmgOmTiTNo-ptS7Rl9NZzb9XiPoQ3v60J6e29NTexonz_Ob9LHaufrW8a-uCXg2A5dpiP2tXoAARJST_mLWGxO1aXuf9MXXHJBNI-USpm-X5HgmKh9jcHcY6i9gVLTg</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Guionie, Olivier</creator><creator>Guillou-Cloarec, Cécile</creator><creator>Courtois, David</creator><creator>Bougeard, Stéphanie</creator><creator>Amelot, Michel</creator><creator>Jestin, Véronique</creator><general>American Association of Avian Pathologists</general><scope>FBQ</scope><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><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20100301</creationdate><title>Experimental Infection of Muscovy Ducks with Highly Pathogenic Avian Influenza Virus (H5N1) Belonging to Clade 2.2</title><author>Guionie, Olivier ; Guillou-Cloarec, Cécile ; Courtois, David ; Bougeard, Stéphanie ; Amelot, Michel ; Jestin, Véronique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b450t-f92f70dd8f4697d8d71a1c7b16e661c8e855d5217859be30c3877b3bca20465e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Autopsy</topic><topic>Avian influenza virus</topic><topic>Brain</topic><topic>Brain - virology</topic><topic>Cairina moschata</topic><topic>Clade 2.2</topic><topic>Clinical trials</topic><topic>cross reaction</topic><topic>Cross-reactivity</topic><topic>double prime M gene</topic><topic>Ducks</topic><topic>Epidemiology</topic><topic>experimental challenge</topic><topic>experimental design</topic><topic>Experimental infection</topic><topic>food animals</topic><topic>Fowl plague</topic><topic>H5N1 highly pathogenic avian influenza</topic><topic>H5N1 subtype influenza A virus</topic><topic>Hemagglutinins</topic><topic>highly pathogenic avian influenza H5N1</topic><topic>Infections</topic><topic>Influenza A virus</topic><topic>Influenza A Virus, H5N1 Subtype - classification</topic><topic>Influenza A Virus, H5N1 Subtype - pathogenicity</topic><topic>Influenza in Birds - mortality</topic><topic>Influenza in Birds - pathology</topic><topic>Influenza in Birds - virology</topic><topic>Kidney - virology</topic><topic>Kinetics</topic><topic>microbial genetics</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Muscovy ducks</topic><topic>Neurotransmission</topic><topic>Pancreas - virology</topic><topic>pathogenesis</topic><topic>Pathogenesis and Pathobiology in Avian Species</topic><topic>pathogenicity</topic><topic>Public health</topic><topic>reassortment</topic><topic>reverse transcriptase polymerase chain reaction</topic><topic>RNA</topic><topic>RNA, Viral - analysis</topic><topic>signs and symptoms (animals and humans)</topic><topic>Spleen</topic><topic>strain differences</topic><topic>Trachea - virology</topic><topic>Vaccination</topic><topic>Vaccines</topic><topic>vertebrate viruses</topic><topic>viral antigens</topic><topic>Viral Load</topic><topic>Viral RNA</topic><topic>viral RNA load</topic><topic>virulence</topic><topic>Virus Shedding</topic><topic>virus transmission</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guionie, Olivier</creatorcontrib><creatorcontrib>Guillou-Cloarec, Cécile</creatorcontrib><creatorcontrib>Courtois, David</creatorcontrib><creatorcontrib>Bougeard, Stéphanie</creatorcontrib><creatorcontrib>Amelot, Michel</creatorcontrib><creatorcontrib>Jestin, Véronique</creatorcontrib><collection>AGRIS</collection><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><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Avian diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guionie, Olivier</au><au>Guillou-Cloarec, Cécile</au><au>Courtois, David</au><au>Bougeard, Stéphanie</au><au>Amelot, Michel</au><au>Jestin, Véronique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental Infection of Muscovy Ducks with Highly Pathogenic Avian Influenza Virus (H5N1) Belonging to Clade 2.2</atitle><jtitle>Avian diseases</jtitle><addtitle>Avian Dis</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>54</volume><issue>s1</issue><spage>538</spage><epage>547</epage><pages>538-547</pages><issn>0005-2086</issn><eissn>1938-4351</eissn><abstract>Highly pathogenic (HP) H5N1 avian influenza (AI) is enzootic in several countries of Asia and Africa and constitutes a major threat, at the world level, for both animal and public health. Ducks play an important role in the epidemiology of AI, including HP H5N1 AI. Although vaccination can be a useful tool to control AI, duck vaccination has not proved very efficient in the field, indicating a need to develop new vaccines and a challenge model to evaluate the protection for duck species. Although Muscovy duck is the duck species most often reared in France, the primary duck-producing country in Europe, and is also produced in Asia, it is rarely studied. Our team recently demonstrated a good cross-reactivity with hemagglutinin from clade 2.2 and inferred that this could be a good vaccine candidate for ducks. Two challenges using two French H5N1 HP strains, 1) A/mute swan/France/06299/06 (Swan/06299), clade 2.2.1, and 2) A/mute swan/France/070203/07 (Swan/070203), clade 2.2 (but different from subclade 2.2.1), were performed (each) on 20 Muscovy ducks (including five contacts) inoculated by oculo-nasal route (6 log10 median egg infectious doses per duck). Clinical signs were recorded daily, and cloacal and oropharyngeal swabs were collected throughout the assay. Autopsies were done on all dead ducks, and organs were taken for analyses. Virus was measured by quantitative reverse transcriptase–PCR based on the M gene AI virus. Ducks presented severe nervous signs in both challenges. Swan/070203 strain led to 80% morbidity (12/15 sick ducks) and 73% mortality (11/15 ducks) at 13.5 days postinfection (dpi), whereas Swan/06299 strain produced 100% mortality at 6.5 dpi. Viral RNA load was significantly lower via the cloacal route than via the oropharyngeal route in both trials, presenting a peak in the first challenge at 3.5 dpi and being more stable in the second challenge. The brain was the organ containing the highest viral RNA load in both challenges. Viral RNA load in a given organ was similar or statistically significantly higher in ducks challenged with Swan/06299 strain. Thus, the Swan/06299 strain was more virulent and could be used as a putative challenge model. Moreover, challenged ducks and contacts contained the same amounts of viral RNA load, demonstrating the rapid and efficient transmission of H5N1 HP in Muscovy ducks in our experimental conditions.</abstract><cop>United States</cop><pub>American Association of Avian Pathologists</pub><pmid>20521691</pmid><doi>10.1637/8790-040109-Reg.1</doi><tpages>10</tpages></addata></record>
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source Jstor Complete Legacy; MEDLINE; BioOne Complete
subjects Animals
Autopsy
Avian influenza virus
Brain
Brain - virology
Cairina moschata
Clade 2.2
Clinical trials
cross reaction
Cross-reactivity
double prime M gene
Ducks
Epidemiology
experimental challenge
experimental design
Experimental infection
food animals
Fowl plague
H5N1 highly pathogenic avian influenza
H5N1 subtype influenza A virus
Hemagglutinins
highly pathogenic avian influenza H5N1
Infections
Influenza A virus
Influenza A Virus, H5N1 Subtype - classification
Influenza A Virus, H5N1 Subtype - pathogenicity
Influenza in Birds - mortality
Influenza in Birds - pathology
Influenza in Birds - virology
Kidney - virology
Kinetics
microbial genetics
Morbidity
Mortality
Muscovy ducks
Neurotransmission
Pancreas - virology
pathogenesis
Pathogenesis and Pathobiology in Avian Species
pathogenicity
Public health
reassortment
reverse transcriptase polymerase chain reaction
RNA
RNA, Viral - analysis
signs and symptoms (animals and humans)
Spleen
strain differences
Trachea - virology
Vaccination
Vaccines
vertebrate viruses
viral antigens
Viral Load
Viral RNA
viral RNA load
virulence
Virus Shedding
virus transmission
Viruses
title Experimental Infection of Muscovy Ducks with Highly Pathogenic Avian Influenza Virus (H5N1) Belonging to Clade 2.2
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