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首页> 外文期刊>Glycobiology >The quail and chicken intestine have sialyl-galactose sugar chains responsible for the binding of influenza A viruses to human type receptors
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The quail and chicken intestine have sialyl-galactose sugar chains responsible for the binding of influenza A viruses to human type receptors

机译:鹌鹑和鸡肠具有唾液酸-半乳糖糖链,负责将甲型流感病毒与人型受体结合

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摘要

The receptor specificity of influenza viruses is one factor that allows avian influenza viruses to cross the species barrier. The recent transmissions of avian H5N1 and H9N2 influenza viruses from chickens and/or quails to humans indicate that avian influenza viruses can directly infect humans without an intermediate host, such as pigs. In this study, we used two strains of influenza A virus (A/PR/8/34, which preferentially binds to an avian-type receptor, and A/Memphis/1/71, which preferentially binds to a human-type receptor) to probe the receptor specificities in host cells. Epithelial cells of both quail and chicken intestines (colons) could bind both avian- and human-type viruses. Infected cultured quail colon cells expressed viral protein and allowed replication of the virus strain A/PR/8/34 or A/Memphis/1/71. To understand the molecular basis of these phenomena, we further investigated the abundance of sialic acid (Sia) linked to galactose (Gal) by the α2-3 linkage (Siaα2‐3Gal) and Siaα2-6Gal in host cells. In glycoprotein and glycolipid fractions from quail and chicken colon epithelial cells, there were some bound components of Sia–Gal linkage-specific lectins, Maackia amurensis agglutinin (specific for Siaα2‐3 Gal) and Sambucus nigra agglutinin (specific for Siaα2-6Gal), indicating that both Siaα2–3Gal and Siaα2-6Gal exist in quail and chicken colon cells. Furthermore, we demonstrated by fluorescence high-performance liquid chromatography (HPLC) analysis that 5-N-acetylneuraminic acid was the main molecular species of Sia, and we demonstrated by multi-dimensional HPLC mapping and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis that bi-antennary complex-type glycans α2-6 sialylated at the terminal Gal residue(s) are major (more than 79%) sialyl N-glycans expressed by intestinal epithelial tissues in both the chicken and quail. Taken together, these results indicate that quails and chickens have molecular characterization as potential intermediate hosts for avian influenza virus transmission to humans and could generate new influenza viruses with pandemic potential.
机译:流感病毒的受体特异性是允许禽流感病毒穿越物种屏障的因素之一。禽H5N1和H9N2流感病毒最近从鸡和/或鹌鹑传播给人类的迹象表明,禽流感病毒可以直接感染人类而无中间宿主,例如猪。在这项研究中,我们使用了两种甲型流感病毒株(优先结合禽类受体的A / PR / 8/34和优先结合人型受体的A / Memphis / 1/71)以探测宿主细胞中的受体特异性。鹌鹑和鸡肠(结肠)的上皮细胞都可以结合禽型和人型病毒。感染的培养鹌鹑结肠细胞表达病毒蛋白,并允许病毒株A / PR / 8/34或A / Memphis / 1/71复制。为了了解这些现象的分子基础,我们进一步研究了宿主细胞中通过α2-3连锁(Siaα2-3Gal)和Siaα2-6Gal与半乳糖(Gal)连接的唾液酸(Sia)的丰度。在鹌鹑和鸡结肠上皮细胞的糖蛋白和糖脂级分中,有一些结合的成分:Sia-Gal连锁特异性凝集素,Maackia amurensis凝集素(对Siaα2-3Gal特异性)和黑接骨木(Sambucus nigra凝集素)(对Siaα2-6Gal特异性),表明在鹌鹑和鸡结肠细胞中都存在Siaα2-3Gal和Siaα2-6Gal。此外,我们通过荧光高效液相色谱(HPLC)分析证明5-N-乙酰神经氨酸是Sia的主要分子种类,并且通过多维HPLC映射和基质辅助激光解吸/电离时间证明-飞行质谱分析表明,在末端Gal残基处唾液酸化的双天线复合型聚糖α2-6是在鸡和鹌鹑中肠上皮组织表达的主要(大于79%)唾液酸N-聚糖。综上所述,这些结果表明,鹌鹑和鸡具有分子特征,可作为禽流感病毒传播给人类的潜在中间宿主,并可能产生具有大流行潜力的新型流感病毒。

著录项

  • 来源
    《Glycobiology》 |2007年第7期|713-724|共12页
  • 作者单位

    Department of Biomedical Sciences College of Life and Health Sciences Chubu University 11200 Matsumoto-cho Kasugai-shi Aichi 487-8501 Japan;

    Institute of Bioengineering Zhejiang Academy of Medical Sciences 182 Tianmushan Road Hangzhou 310016 China;

    CREST Japan Science and Technology Agency 4-1-8 Honcho Kawaguchi Japan;

    Department of Biochemistry University of Shizuoka School of Pharmaceutical Sciences Suruga-ku Shizuoka 422-8526 Japan;

    Graduate School of Pharmaceutical Sciences Nagoya City University 3-1 Tanabe-dori Mizuho-ku Nagoya 467-8603 Japan;

    GLYENCE Co. Ltd 2-22-8 Chikusa Chikusa-ku Nagoya 464-0858 Japan;

    Department of Anatomy Tokyo Medical University 6-1-1 Shinjuku Shinjuku-ku Tokyo 160-8402 Japan;

    Departments of Veterinary Public Health and;

    Veterinary Microbiology Faculty of Agriculture Tottori University Tottori-shi Tottori 680-8553 Japan;

    Laboratory of Microbiology Department of Disease Control Graduate School of Veterinary Medicine Hokkaido University Sapporo 060-0818 Japan;

    Division of Virology Department of Microbiology and Immunology Institute of Medical Science University of Tokyo Tokyo 108-8639 Japan;

    Department of Pathobiological Sciences School of Veterinary Medicine University of Wisconsin Madison WI 53706;

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