Recognition of N-glycolylneuraminic acid linked to galactose by the alpha2,3 linkage is associated with intestinal replication of influenza A virus in ducks.
Identifieur interne : 000364 ( PubMed/Curation ); précédent : 000363; suivant : 000365Recognition of N-glycolylneuraminic acid linked to galactose by the alpha2,3 linkage is associated with intestinal replication of influenza A virus in ducks.
Auteurs : T. Ito [États-Unis] ; Y. Suzuki ; T. Suzuki ; A. Takada ; T. Horimoto ; K. Wells ; H. Kida ; K. Otsuki ; M. Kiso ; H. Ishida ; Y. KawaokaSource :
- Journal of virology [ 0022-538X ] ; 2000.
Descripteurs français
- KwdFr :
- MESH :
- physiologie : Hémagglutinines virales, Virus de la grippe A.
- virologie : Canards, Grippe humaine.
- Acides neuraminiques, Animaux, Galactose, Humains, Réplication virale.
English descriptors
- KwdEn :
- MESH :
- chemical , physiology : Hemagglutinins, Viral.
- chemical : Galactose, Neuraminic Acids.
- physiology : Influenza A virus.
- virology : Ducks, Influenza, Human.
- Animals, Humans, Virus Replication.
Abstract
The hemagglutinin (HA) of H3 human influenza viruses does not support viral replication in duck intestine despite its avian origin. A Leu-to-Gln mutation at position 226 and a Ser-to-Gly mutation at position 228 in the HA of human A/Udorn/307/72 (H3N2) permit a reassortant virus [human Udorn HA, with all other genes from A/mallard/New York/6750/78 (H2N2)] to replicate in ducks. To understand the molecular basis of this change in host range restriction, we investigated the receptor specificity of duck influenza viruses as well as of human-duck virus reassortants. The results indicate that the recognition of a glycoconjugate moiety possessing N-glycolneuramic acid (NeuGc) linked to galactose by the alpha2,3 linkage (NeuGcalpha2,3Gal) is associated with viral replication in duck intestine. Immunofluorescence assays with NeuGcalpha2,3Gal-specific antiserum detected this moiety primarily on the crypt epithelial cells of duck colon. Such recognition, together with biochemical evidence of NeuGc in crypt cells, correlated exactly with the ability of the virus to replicate in duck colon. These results suggest that recognition of the NeuGcalpha2,3-Gal moiety plays an important role in the enterotropism of avian influenza viruses.
DOI: 10.1128/jvi.74.19.9300-9305.2000
PubMed: 10982377
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Suzuki</name></author><author><name sortKey="Takada, A" sort="Takada, A" uniqKey="Takada A" first="A" last="Takada">A. Takada</name></author><author><name sortKey="Horimoto, T" sort="Horimoto, T" uniqKey="Horimoto T" first="T" last="Horimoto">T. Horimoto</name></author><author><name sortKey="Wells, K" sort="Wells, K" uniqKey="Wells K" first="K" last="Wells">K. Wells</name></author><author><name sortKey="Kida, H" sort="Kida, H" uniqKey="Kida H" first="H" last="Kida">H. Kida</name></author><author><name sortKey="Otsuki, K" sort="Otsuki, K" uniqKey="Otsuki K" first="K" last="Otsuki">K. Otsuki</name></author><author><name sortKey="Kiso, M" sort="Kiso, M" uniqKey="Kiso M" first="M" last="Kiso">M. Kiso</name></author><author><name sortKey="Ishida, H" sort="Ishida, H" uniqKey="Ishida H" first="H" last="Ishida">H. Ishida</name></author><author><name sortKey="Kawaoka, Y" sort="Kawaoka, Y" uniqKey="Kawaoka Y" first="Y" last="Kawaoka">Y. 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Ito</name><affiliation wicri:level="1"><nlm:affiliation>Department of Veterinary Public Health, Faculty of Agriculture, Tottori University, Tottori 680-8553, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Veterinary Public Health, Faculty of Agriculture, Tottori University, Tottori 680-8553</wicri:regionArea></affiliation></author><author><name sortKey="Suzuki, Y" sort="Suzuki, Y" uniqKey="Suzuki Y" first="Y" last="Suzuki">Y. Suzuki</name></author><author><name sortKey="Suzuki, T" sort="Suzuki, T" uniqKey="Suzuki T" first="T" last="Suzuki">T. Suzuki</name></author><author><name sortKey="Takada, A" sort="Takada, A" uniqKey="Takada A" first="A" last="Takada">A. Takada</name></author><author><name sortKey="Horimoto, T" sort="Horimoto, T" uniqKey="Horimoto T" first="T" last="Horimoto">T. Horimoto</name></author><author><name sortKey="Wells, K" sort="Wells, K" uniqKey="Wells K" first="K" last="Wells">K. Wells</name></author><author><name sortKey="Kida, H" sort="Kida, H" uniqKey="Kida H" first="H" last="Kida">H. Kida</name></author><author><name sortKey="Otsuki, K" sort="Otsuki, K" uniqKey="Otsuki K" first="K" last="Otsuki">K. Otsuki</name></author><author><name sortKey="Kiso, M" sort="Kiso, M" uniqKey="Kiso M" first="M" last="Kiso">M. Kiso</name></author><author><name sortKey="Ishida, H" sort="Ishida, H" uniqKey="Ishida H" first="H" last="Ishida">H. Ishida</name></author><author><name sortKey="Kawaoka, Y" sort="Kawaoka, Y" uniqKey="Kawaoka Y" first="Y" last="Kawaoka">Y. Kawaoka</name></author></analytic><series><title level="j">Journal of virology</title><idno type="ISSN">0022-538X</idno><imprint><date when="2000" type="published">2000</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Ducks (virology)</term><term>Galactose</term><term>Hemagglutinins, Viral (physiology)</term><term>Humans</term><term>Influenza A virus (physiology)</term><term>Influenza, Human (virology)</term><term>Neuraminic Acids</term><term>Virus Replication</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Acides neuraminiques</term><term>Animaux</term><term>Canards (virologie)</term><term>Galactose</term><term>Grippe humaine (virologie)</term><term>Humains</term><term>Hémagglutinines virales (physiologie)</term><term>Réplication virale</term><term>Virus de la grippe A (physiologie)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Hemagglutinins, Viral</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Galactose</term><term>Neuraminic Acids</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Hémagglutinines virales</term><term>Virus de la grippe A</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Influenza A virus</term></keywords><keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Canards</term><term>Grippe humaine</term></keywords><keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Ducks</term><term>Influenza, Human</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Humans</term><term>Virus Replication</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Acides neuraminiques</term><term>Animaux</term><term>Galactose</term><term>Humains</term><term>Réplication virale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The hemagglutinin (HA) of H3 human influenza viruses does not support viral replication in duck intestine despite its avian origin. A Leu-to-Gln mutation at position 226 and a Ser-to-Gly mutation at position 228 in the HA of human A/Udorn/307/72 (H3N2) permit a reassortant virus [human Udorn HA, with all other genes from A/mallard/New York/6750/78 (H2N2)] to replicate in ducks. To understand the molecular basis of this change in host range restriction, we investigated the receptor specificity of duck influenza viruses as well as of human-duck virus reassortants. The results indicate that the recognition of a glycoconjugate moiety possessing N-glycolneuramic acid (NeuGc) linked to galactose by the alpha2,3 linkage (NeuGcalpha2,3Gal) is associated with viral replication in duck intestine. Immunofluorescence assays with NeuGcalpha2,3Gal-specific antiserum detected this moiety primarily on the crypt epithelial cells of duck colon. Such recognition, together with biochemical evidence of NeuGc in crypt cells, correlated exactly with the ability of the virus to replicate in duck colon. These results suggest that recognition of the NeuGcalpha2,3-Gal moiety plays an important role in the enterotropism of avian influenza viruses.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">10982377</PMID><DateCompleted><Year>2000</Year><Month>10</Month><Day>04</Day></DateCompleted><DateRevised><Year>2019</Year><Month>05</Month><Day>08</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0022-538X</ISSN><JournalIssue CitedMedium="Print"><Volume>74</Volume><Issue>19</Issue><PubDate><Year>2000</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Journal of virology</Title><ISOAbbreviation>J. Virol.</ISOAbbreviation></Journal><ArticleTitle>Recognition of N-glycolylneuraminic acid linked to galactose by the alpha2,3 linkage is associated with intestinal replication of influenza A virus in ducks.</ArticleTitle><Pagination><MedlinePgn>9300-5</MedlinePgn></Pagination><Abstract><AbstractText>The hemagglutinin (HA) of H3 human influenza viruses does not support viral replication in duck intestine despite its avian origin. A Leu-to-Gln mutation at position 226 and a Ser-to-Gly mutation at position 228 in the HA of human A/Udorn/307/72 (H3N2) permit a reassortant virus [human Udorn HA, with all other genes from A/mallard/New York/6750/78 (H2N2)] to replicate in ducks. To understand the molecular basis of this change in host range restriction, we investigated the receptor specificity of duck influenza viruses as well as of human-duck virus reassortants. The results indicate that the recognition of a glycoconjugate moiety possessing N-glycolneuramic acid (NeuGc) linked to galactose by the alpha2,3 linkage (NeuGcalpha2,3Gal) is associated with viral replication in duck intestine. Immunofluorescence assays with NeuGcalpha2,3Gal-specific antiserum detected this moiety primarily on the crypt epithelial cells of duck colon. Such recognition, together with biochemical evidence of NeuGc in crypt cells, correlated exactly with the ability of the virus to replicate in duck colon. These results suggest that recognition of the NeuGcalpha2,3-Gal moiety plays an important role in the enterotropism of avian influenza viruses.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ito</LastName><ForeName>T</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Department of Veterinary Public Health, Faculty of Agriculture, Tottori University, Tottori 680-8553, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Suzuki</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Suzuki</LastName><ForeName>T</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Takada</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Horimoto</LastName><ForeName>T</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Wells</LastName><ForeName>K</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Kida</LastName><ForeName>H</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Otsuki</LastName><ForeName>K</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Kiso</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Ishida</LastName><ForeName>H</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Kawaoka</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013487">Research Support, U.S. Gov't, P.H.S.</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Virol</MedlineTA><NlmUniqueID>0113724</NlmUniqueID><ISSNLinking>0022-538X</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance 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