N-Glycans from Porcine Trachea and Lung: Predominant NeuAcα2-6Gal Could Be a Selective Pressure for Influenza Variants in Favor of Human-Type Receptor
Identifieur interne : 000D03 ( Main/Merge ); précédent : 000D02; suivant : 000D04N-Glycans from Porcine Trachea and Lung: Predominant NeuAcα2-6Gal Could Be a Selective Pressure for Influenza Variants in Favor of Human-Type Receptor
Auteurs : Nongluk Sriwilaijaroen [Thaïlande, Japon] ; Sachiko Kondo [Japon] ; Hirokazu Yagi [Japon] ; Nobuhiro Takemae [Thaïlande, Japon] ; Takehiko Saito [Thaïlande, Japon] ; Hiroaki Hiramatsu [Japon] ; Koichi Kato [Japon] ; Yasuo Suzuki [Japon]Source :
- PLoS ONE [ 1932-6203 ] ; 2011.
Abstract
It is known that pigs acted as “mixing vessels” for genesis of a new reassortant influenza strain responsible for pandemic H1N1 2009. However, the host factors driving the evolution of a reassorted virus in pigs to ‘jump species’ resulting in a human outbreak remain unclear.
Url:
DOI: 10.1371/journal.pone.0016302
PubMed: 21347401
PubMed Central: 3036579
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PMC:3036579Le document en format XML
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-Glycans from Porcine Trachea and Lung: Predominant NeuAcα2-6Gal Could Be a Selective Pressure for Influenza Variants in Favor of Human-Type Receptor</title>
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-Glycans from Porcine Trachea and Lung: Predominant NeuAcα2-6Gal Could Be a Selective Pressure for Influenza Variants in Favor of Human-Type Receptor</title>
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<front><div type="abstract" xml:lang="en"><p>It is known that pigs acted as “mixing vessels” for genesis of a new reassortant influenza strain responsible for pandemic H1N1 2009. However, the host factors driving the evolution of a reassorted virus in pigs to ‘jump species’ resulting in a human outbreak remain unclear. <italic>N</italic>
-glycans derived from the porcine respiratory tract were enzymatically released, fluorescent labeled with 2-aminopyridine, separated according to charge, size and hydrophobicity, and structurally identified by a two-dimensional (size and hydrophobicity) HPLC mapping technique and MALDI-TOF mass spectrometry before and after exo-glycosidase digestion. We found a 3-, 5-, and 13-fold increases in NeuAcα2-6, a preferable human influenza receptor, over NeuAcα2-3, an avian influenza receptor, from upper and lower parts of the porcine trachea towards the porcine lung, a major target organ for swine virus replication. The large proportion of NeuAcα2-6 may exert selective pressure for selection of influenza variants with altered receptor preference for this human-type α2-6 receptor, a crucial first step for generating a human pandemic.</p>
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