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Altered Receptor Specificity and Cell Tropism of D222G Hemagglutinin Mutants Isolated from Fatal Cases of Pandemic A(H1N1) 2009 Influenza Virus ▿ † ‡

机译:从致命的2009年甲型H1N1流感病毒致命病例中分离的D222G血凝素突变体的受体特异性和细胞取向改变

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摘要

Mutations in the receptor-binding site of the hemagglutinin of pandemic influenza A(H1N1) 2009 viruses have been detected sporadically. An Asp222Gly (D222G) substitution has been associated with severe or fatal disease. Here we show that 222G variants infected a higher proportion of ciliated cells in cultures of human airway epithelium than did viruses with 222D or 222E, which targeted mainly nonciliated cells. Carbohydrate microarray analyses showed that 222G variants bind a broader range of α2-3-linked sialyl receptor sequences of a type expressed on ciliated bronchial epithelial cells and on epithelia within the lung. These features of 222G mutants may contribute to exacerbation of disease.
机译:大流行性流感A(H1N1)2009病毒血凝素受体结合位点的突变已被零星地检测到。 Asp222Gly(D222G)替代已与严重或致命的疾病有关。在这里,我们显示,与主要针对非纤毛细胞的222D或222E病毒相比,222G变体在人气道上皮细胞培养物中感染纤毛细胞的比例更高。碳水化合物微阵列分析表明,222G变体结合了在纤毛支气管上皮细胞和肺内上皮细胞上表达的类型更广泛的α2-3连接的唾液酸受体序列。 222G突变体的这些特征可能会加剧疾病。

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