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Substitutions Near the Receptor Binding Site Determine Major Antigenic Change During Influenza Virus Evolution

机译:受体结合位点附近的替代决定了流感病毒进化过程中的主要抗原变化

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摘要

The molecular basis of antigenic drift was determined for the hemagglutinin (HA) of human influenza A/H3N2 virus. From 1968 to 2003, antigenic change was caused mainly by single amino acid substitutions, which occurred at only seven positions in HA immediately adjacent to the receptor binding site. Most of these substitutions were involved in antigenic change more than once. Equivalent positions were responsible for the recent antigenic changes of influenza B and A/H1N1 viruses. Substitution of a single amino acid at one of these positions substantially changed the virus-specific antibody response in infected ferrets. These findings have potentially far-reaching consequences for understanding the evolutionary mechanisms that govern influenza viruses.
机译:确定了人类A / H3N2流感病毒血凝素(HA)的抗原漂移的分子基础。从1968年到2003年,抗原变化主要是由单个氨基酸取代引起的,它仅发生在HA中紧邻受体结合位点的七个位置。这些替代中的大多数不只一次参与了抗原改变。等效位置是造成乙型流感和A / H1N1病毒近期抗原变化的原因。在这些位置之一上取代单个氨基酸会大大改变受感染的雪貂中病毒特异性抗体的反应。这些发现对于理解控制流感病毒的进化机制具有潜在的深远影响。

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  • 来源
    《Science》 |2013年第6161期|976-979|共4页
  • 作者单位

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK,WHO Collaborating Centre for Modeling Evolution and Con-trol of Emerging Infectious Diseases, University of Cambridge,Cambridge CB2 3EJ, UK;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    BaseClear B.V., 2333CC Leiden,Netherlands,Luris, Leiden University, 2333AA Leiden, Nether-lands;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK,WHO Collaborating Centre for Modeling Evolution and Con-trol of Emerging Infectious Diseases, University of Cambridge,Cambridge CB2 3EJ, UK;

    Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK,WHO Collaborating Centre for Modeling Evolution and Con-trol of Emerging Infectious Diseases, University of Cambridge,Cambridge CB2 3EJ, UK;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    WHO Collaborating Centre for Modeling Evolution and Con-trol of Emerging Infectious Diseases, University of Cambridge,Cambridge CB2 3EJ, UK,Department of Veterinary Medicine, University of Cam-bridge, Cambridge CB3 0ES, UK;

    Research Institute of Influenza,197376 St. Petersburg, Russia;

    WHO Collaborating Centre for Reference and Research on Influenza, VIDRL, Melbourne,Victoria 3051, Australia;

    WHO Collaborating Centre for Reference and Research on Influenza, VIDRL, Melbourne,Victoria 3051, Australia;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands;

    Department of Viroscience, Erasmus MC, 3015GE Rotterdam,Netherlands,Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK,WHO Collaborating Centre for Modeling Evolution and Con-trol of Emerging Infectious Diseases, University of Cambridge,Cambridge CB2 3EJ, UK,Fogarty International Center, Natio-nal Institutes of Health, Bethesda, MD 20892, USA;

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