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对输入台湾的人类病例中分离出的甲型H7N9流感病毒的特性分析。

Characterization of influenza A (H7N9) viruses isolated from human cases imported into Taiwan.

作者信息

Yang Ji-Rong, Kuo Chuan-Yi, Huang Hsiang-Yi, Wu Fu-Ting, Huang Yi-Lung, Cheng Chieh-Yu, Su Yu-Ting, Wu Ho-Sheng, Liu Ming-Tsan

机构信息

Center for Research, Diagnostics and Vaccine Development, Centers for Disease Control, Taipei, Taiwan, ROC.

Center for Research, Diagnostics and Vaccine Development, Centers for Disease Control, Taipei, Taiwan, ROC; School of Medical Laboratory Science and Biotechnology, Taipei Medical University, Taipei, Taiwan, ROC.

出版信息

PLoS One. 2015 Mar 6;10(3):e0119792. doi: 10.1371/journal.pone.0119792. eCollection 2015.

Abstract

A novel avian influenza A (H7N9) virus causes severe human infections and was first identified in March 2013 in China. The H7N9 virus has exhibited two epidemiological peaks of infection, occurring in week 15 of 2013 and week 5 of 2014. Taiwan, which is geographically adjacent to China, faces a large risk of being affected by this virus. Through extensive surveillance, launched in April 2013, four laboratory-confirmed H7N9 cases imported from China have been identified in Taiwan. The H7N9 virus isolated from imported case 1 in May 2013 (during the first wave) was found to be closest genetically to a virus from wild birds and differed from the prototype virus, A/Anhui/1/2013, in the MP gene. The other three imported cases were detected in December 2013 and April 2014 (during the second wave). The viruses isolated from cases 2 and 4 were similar in the compositions of their 6 internal genes and distinct from A/Anhui/1/2013 in the PB2 and MP genes, whereas the virus isolated from case 3 exhibited a novel reassortment that has not been identified previously and was different from A/Anhui/1/2013 in the PB2, PA and MP genes. The four imported H7N9 viruses share similar antigenicity with A/Anhui/1/2013, and their HA and NA genes grouped together in their respective phylogenies. In contrast with the HA and NA genes, which exhibited a smaller degree of diversity, the internal genes were heterogeneous and provided potential distinctions between transmission sources in terms of both geography and hosts. It is important to strengthen surveillance of influenza and to share viral genetic data in real-time for reducing the threat of rapid and continuing evolution of H7N9 viruses.

摘要

一种新型甲型禽流感(H7N9)病毒可导致严重的人类感染,于2013年3月在中国首次被发现。H7N9病毒已出现两个感染流行病学高峰,分别出现在2013年第15周和2014年第5周。与中国大陆地理相邻的台湾面临着受该病毒影响的巨大风险。通过2013年4月启动的广泛监测,台湾已确认4例从中国大陆输入的实验室确诊H7N9病例。2013年5月(第一波疫情期间)从输入病例1中分离出的H7N9病毒在基因上被发现与一种来自野生鸟类的病毒最为接近,并且在MP基因上与原型病毒A/Anhui/1/2013不同。其他3例输入病例分别在2013年12月和2014年4月(第二波疫情期间)被检测到。从病例2和4中分离出的病毒在其6个内部基因的组成上相似,在PB2和MP基因上与A/Anhui/1/2013不同,而从病例3中分离出的病毒呈现出一种此前未被识别的新型重配,在PB2、PA和MP基因上与A/Anhui/1/2013不同。这4株输入性H7N9病毒与A/Anhui/1/2013具有相似的抗原性,它们的HA和NA基因在各自的系统发育中聚为一组。与HA和NA基因多样性程度较小形成对比的是,内部基因具有异质性,在地理和宿主方面为传播源之间提供了潜在差异。加强流感监测并实时共享病毒基因数据对于降低H7N9病毒快速持续进化的威胁至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e81f/4351886/1273e0ed0fd9/pone.0119792.g001.jpg

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