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人感染 H7N9 禽流感病毒的潜在大流行。

Potential Pandemic of H7N9 Avian Influenza A Virus in Human.

机构信息

College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.

Joint Influenza Research Centre (SUMC/HKU), Shantou University Medical College, Shantou, China.

出版信息

Front Cell Infect Microbiol. 2018 Nov 23;8:414. doi: 10.3389/fcimb.2018.00414. eCollection 2018.

Abstract

Since 2013, the H7N9 avian influenza A virus (AIV) has caused human infections and to the extent of now surpassing H5N1. This raises an alarm about the potential of H7N9 to become a pandemic problem. Our compilation of the amino acid changes required for AIVs to cross the species-barrier discovers 58 that have very high proportions in both the human- and avian-isolated H7N9 viruses. These changes correspond with sporadic human infections that continue to occur in regions of avian infections. Among the six internal viral genes, amino acid changes do not differ significantly between H9N2 and H7N9, except for V100A in PA, and K526R, D627K, and D701N in PB2. H9N2 AIVs provide internal genes to H7N9. Most of the amino acid changes in H7N9 appear to come directly from H9N2. Seventeen amino acid substitutions appear to have fixed quickly by the 5th wave. Among these, six amino acid sites in HA1 are receptor binding sites, and PB2-A588V was shown to promote the adaptation of AIVs to mammals. The accelerated fixation of mutations may promote the adaptation of H7N9 to human, but need further functional evidence. Although H7N9 AIVs still cannot efficiently transmit between humans, they have the genetic makeup associated with human infections. These viruses must be controlled in poultry to remove the threat of it becoming a human pandemic event.

摘要

自 2013 年以来,H7N9 禽流感病毒(AIV)已导致人类感染,其程度超过了 H5N1。这引发了对 H7N9 可能成为大流行问题的警报。我们对 AIV 跨越物种屏障所需的氨基酸变化进行了汇编,发现其中 58 种在人类和禽类分离的 H7N9 病毒中都具有非常高的比例。这些变化与持续发生禽类感染地区的散发性人类感染相对应。在六个内部病毒基因中,H9N2 和 H7N9 之间的氨基酸变化没有显著差异,除了 PA 中的 V100A 和 PB2 中的 K526R、D627K 和 D701N。H9N2 AIV 为 H7N9 提供了内部基因。H7N9 中的大多数氨基酸变化似乎直接来自 H9N2。第 5 波似乎迅速固定了 17 个氨基酸取代。其中,HA1 中的六个氨基酸位点是受体结合位点,并且 PB2-A588V 被证明促进了 AIV 对哺乳动物的适应。突变的加速固定可能促进了 H7N9 对人类的适应,但需要进一步的功能证据。尽管 H7N9 AIV 仍然不能在人与人之间有效传播,但它们具有与人类感染相关的遗传组成。必须在禽类中控制这些病毒,以消除其成为人类大流行事件的威胁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8e6/6265602/402615dfb8f9/fcimb-08-00414-g0001.jpg

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