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雪貂和小鼠中甲型流感病毒(H7N9)的发病机制和传播。

Pathogenesis and transmission of avian influenza A (H7N9) virus in ferrets and mice.

机构信息

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

Nature. 2013 Sep 26;501(7468):556-9. doi: 10.1038/nature12391. Epub 2013 Jul 10.

Abstract

On 29 March 2013, the Chinese Center for Disease Control and Prevention confirmed the first reported case of human infection with an avian influenza A(H7N9) virus. The recent human infections with H7N9 virus, totalling over 130 cases with 39 fatalities to date, have been characterized by severe pulmonary disease and acute respiratory distress syndrome (ARDS). This is concerning because H7 viruses have typically been associated with ocular disease in humans, rather than severe respiratory disease. This recent outbreak underscores the need to better understand the pathogenesis and transmission of these viruses in mammals. Here we assess the ability of A/Anhui/1/2013 and A/Shanghai/1/2013 (H7N9) viruses, isolated from fatal human cases, to cause disease in mice and ferrets and to transmit to naive animals. Both H7N9 viruses replicated to higher titre in human airway epithelial cells and in the respiratory tract of ferrets compared to a seasonal H3N2 virus. Moreover, the H7N9 viruses showed greater infectivity and lethality in mice compared to genetically related H7N9 and H9N2 viruses. The H7N9 viruses were readily transmitted to naive ferrets through direct contact but, unlike the seasonal H3N2 virus, did not transmit readily by respiratory droplets. The lack of efficient respiratory droplet transmission was corroborated by low receptor-binding specificity for human-like α2,6-linked sialosides. Our results indicate that H7N9 viruses have the capacity for efficient replication in mammals and human airway cells and highlight the need for continued public health surveillance of this emerging virus.

摘要

2013 年 3 月 29 日,中国疾病预防控制中心确认了首例人感染甲型禽流感病毒 H7N9 病毒的报告病例。最近的人类感染 H7N9 病毒病例超过 130 例,其中 39 例死亡,其特征为严重肺部疾病和急性呼吸窘迫综合征(ARDS)。这令人担忧,因为 H7 病毒通常与人类眼部疾病有关,而不是严重的呼吸道疾病。最近的疫情凸显了需要更好地了解这些病毒在哺乳动物中的发病机制和传播。在这里,我们评估了从致命人类病例中分离出的 A/Anhui/1/2013 和 A/Shanghai/1/2013(H7N9)病毒在小鼠和雪貂中引起疾病并传播给未感染动物的能力。与季节性 H3N2 病毒相比,两种 H7N9 病毒在人呼吸道上皮细胞和雪貂呼吸道中的复制滴度更高。此外,与遗传相关的 H7N9 和 H9N2 病毒相比,H7N9 病毒在小鼠中的感染性和致死率更高。H7N9 病毒通过直接接触很容易传播给未感染的雪貂,但与季节性 H3N2 病毒不同,它们不易通过呼吸道飞沫传播。缺乏有效的呼吸道飞沫传播通过对人类样α2,6 连接唾液酸的低受体结合特异性得到证实。我们的研究结果表明,H7N9 病毒有能力在哺乳动物和人呼吸道细胞中有效复制,并强调需要继续对这种新兴病毒进行公共卫生监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b89/7094885/1503e933130d/41586_2013_Article_BFnature12391_Fig1_HTML.jpg

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