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Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase

Avian influenza A viruses (IAVs) and human 1918, 1957, and 1968 pandemic IAVs all have neuraminidases (NAs) that are stable at low pH sialidase activity, yet most human epidemic IAVs do not. We examined the pH stability of H5N1 highly pathogenic avian IAV (HPAI) NAs and identified amino acids respon...

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Autores principales: Takahashi, Tadanobu, Nidom, Chairul A., Quynh Le, Mai thi, Suzuki, Takashi, Kawaoka, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642167/
https://www.ncbi.nlm.nih.gov/pubmed/23650608
http://dx.doi.org/10.1016/j.fob.2012.08.007
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author Takahashi, Tadanobu
Nidom, Chairul A.
Quynh Le, Mai thi
Suzuki, Takashi
Kawaoka, Yoshihiro
author_facet Takahashi, Tadanobu
Nidom, Chairul A.
Quynh Le, Mai thi
Suzuki, Takashi
Kawaoka, Yoshihiro
author_sort Takahashi, Tadanobu
collection PubMed
description Avian influenza A viruses (IAVs) and human 1918, 1957, and 1968 pandemic IAVs all have neuraminidases (NAs) that are stable at low pH sialidase activity, yet most human epidemic IAVs do not. We examined the pH stability of H5N1 highly pathogenic avian IAV (HPAI) NAs and identified amino acids responsible for conferring stability at low pH. We found that, unlike other avian viruses, most H5N1 IAVs isolated since 2003 had NAs that were unstable at low pH, similar to human epidemic IAVs. These H5N1 viruses are thus already human virus-like and, therefore, have the frequent infections of humans.
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spelling pubmed-36421672013-05-06 Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase Takahashi, Tadanobu Nidom, Chairul A. Quynh Le, Mai thi Suzuki, Takashi Kawaoka, Yoshihiro FEBS Open Bio Article Avian influenza A viruses (IAVs) and human 1918, 1957, and 1968 pandemic IAVs all have neuraminidases (NAs) that are stable at low pH sialidase activity, yet most human epidemic IAVs do not. We examined the pH stability of H5N1 highly pathogenic avian IAV (HPAI) NAs and identified amino acids responsible for conferring stability at low pH. We found that, unlike other avian viruses, most H5N1 IAVs isolated since 2003 had NAs that were unstable at low pH, similar to human epidemic IAVs. These H5N1 viruses are thus already human virus-like and, therefore, have the frequent infections of humans. Elsevier 2012-09-05 /pmc/articles/PMC3642167/ /pubmed/23650608 http://dx.doi.org/10.1016/j.fob.2012.08.007 Text en © 2012 Published by Elsevier B.V. on behalf of Federation of European Biochemical Societies. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non- commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Takahashi, Tadanobu
Nidom, Chairul A.
Quynh Le, Mai thi
Suzuki, Takashi
Kawaoka, Yoshihiro
Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase
title Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase
title_full Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase
title_fullStr Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase
title_full_unstemmed Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase
title_short Amino acid determinants conferring stable sialidase activity at low pH for H5N1 influenza A virus neuraminidase
title_sort amino acid determinants conferring stable sialidase activity at low ph for h5n1 influenza a virus neuraminidase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642167/
https://www.ncbi.nlm.nih.gov/pubmed/23650608
http://dx.doi.org/10.1016/j.fob.2012.08.007
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