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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
18
pubmed:dateCreated
2000-9-27
pubmed:abstractText
Interspecies transmission of influenza A viruses circulating in wild aquatic birds occasionally results in influenza outbreaks in mammals, including humans. To identify early changes in the receptor binding properties of the avian virus hemagglutinin (HA) after interspecies transmission and to determine the amino acid substitutions responsible for these alterations, we studied the HAs of the initial isolates from the human pandemics of 1957 (H2N2) and 1968 (H3N2), the European swine epizootic of 1979 (H1N1), and the seal epizootic of 1992 (H3N3), all of which were caused by the introduction of avian virus HAs into these species. The viruses were assayed for their ability to bind the synthetic sialylglycopolymers 3'SL-PAA and 6'SLN-PAA, which contained, respectively, 3'-sialyllactose (the receptor determinant preferentially recognized by avian influenza viruses) and 6'-sialyl(N-acetyllactosamine) (the receptor determinant for human viruses). Avian and seal viruses bound 6'SLN-PAA very weakly, whereas the earliest available human and swine epidemic viruses bound this polymer with a higher affinity. For the H2 and H3 strains, a single mutation, 226Q-->L, increased binding to 6'SLN-PAA, while among H1 swine viruses, the 190E-->D and 225G-->E mutations in the HA appeared important for the increased affinity of the viruses for 6'SLN-PAA. Amino acid substitutions at positions 190 and 225 with respect to the avian virus consensus sequence are also present in H1 human viruses, including those that circulated in 1918, suggesting that substitutions at these positions are important for the generation of H1 human pandemic strains. These results show that the receptor-binding specificity of the HA is altered early after the transmission of an avian virus to humans and pigs and, therefore, may be a prerequisite for the highly effective replication and spread which characterize epidemic strains.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-10366560, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-13809995, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-1430058, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-1579108, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-1731092, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-2024485, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-2440178, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-2815586, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-3942036, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-6191220, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-6197808, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-6623931, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-6748165, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-7482707, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-7571425, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-7684877, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-7844533, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-7975212, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-8212857, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-8356788, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-8400823, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-8493812, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-8902363, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9049404, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9119062, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9185585, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9191848, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9201232, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9430591, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9454721, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9482438, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9658077, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9696865, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9705915, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9882316, http://linkedlifedata.com/resource/pubmed/commentcorrection/10954551-9990079
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
74
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8502-12
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:10954551-Amino Acid Sequence, pubmed-meshheading:10954551-Amino Acid Substitution, pubmed-meshheading:10954551-Animals, pubmed-meshheading:10954551-Disease Outbreaks, pubmed-meshheading:10954551-Ducks, pubmed-meshheading:10954551-Hemagglutinin Glycoproteins, Influenza Virus, pubmed-meshheading:10954551-Humans, pubmed-meshheading:10954551-Influenza A virus, pubmed-meshheading:10954551-Models, Molecular, pubmed-meshheading:10954551-Molecular Sequence Data, pubmed-meshheading:10954551-Mutation, Missense, pubmed-meshheading:10954551-Phylogeny, pubmed-meshheading:10954551-Protein Binding, pubmed-meshheading:10954551-Receptors, Virus, pubmed-meshheading:10954551-Seals, Earless, pubmed-meshheading:10954551-Sequence Alignment, pubmed-meshheading:10954551-Sialic Acids, pubmed-meshheading:10954551-Species Specificity, pubmed-meshheading:10954551-Swine
pubmed:year
2000
pubmed:articleTitle
Early alterations of the receptor-binding properties of H1, H2, and H3 avian influenza virus hemagglutinins after their introduction into mammals.
pubmed:affiliation
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, Russia. Mikhail.Mastrosovich@stjude.org
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't