11.人禽流感.pptx
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- 11. 禽流感
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1、,北京地坛医院感染中心 王凌航 Mar 28th,2018,Human-Avian influenza 人禽流感,概述,1900年首次发现禽流感病毒,被命名为“真性鸡瘟病毒”(fowl plague virus) 1955年,才正式确定其为甲型流感病毒,并在以后命名为禽流感病毒 人禽流感是由禽流感病毒中的某些亚型(H5、H7、H9、H10等)引起的人急性呼吸道传染病,临床表现随亚型差异而有不同,从轻微卡他症状、结膜炎到ARDS、MOF甚至死亡 H5N1,H7N2,H7N3,H7N7,H9N2均属于高致病性禽流感病毒(HPAI) 致病性最强的首推H5N1,HPAI,高致病性 高致病性禽流感因其传
2、播快、危害大,被世界动物卫生组织列为A类动物疫病,我国将其列为一类动物疫病,多为H5和H7型病毒 低致病性 低致病性禽流感可使禽类出现轻度呼吸道症状,食量减少、产蛋量下降,出现零星死亡 非致病性 不会引起明显症状,仅使染病的禽鸟体内产生病毒抗体,近年来流行的禽流感,病原学,流感病毒分型,流感病毒基因组均含有8个节段 ,在病毒RNA的第5节段上含有一种编码长度为498个氨基酸的蛋白,称为NP蛋白 根据病毒NP蛋白抗原性的不同,把流感病毒分为甲、乙、丙三型,禽流感病毒抵抗力,对热敏感 65,30min;100,2min可使病毒灭活 22感染性最稳定 4保存数月,-70保存数年 对紫外线敏感 在水中
3、存活的时间长(1个月) 酸性环境可破坏病毒的感染性 中性和弱碱性环境中其感染性稳定 许多消毒剂均敏感(乙醚、氯仿、丙酮、氯化剂、十二烷基硫酸钠、漂白粉、碘、高锰酸钾、酒精等),流感病毒命名,H and N,H:红细胞凝集素,能与红细胞发生凝集 在感染靶细胞、决定宿主范围等方面起重要作用 能诱导机体产生保护性中和抗体 在病毒感染和复制过程中也具有作用 分型的主要依据,共16个H亚型(H1-H16),N:神经氨酸酶,具有保证病毒从感染细胞中释放的能力 能防止病毒从宿主细胞释放后形成聚集体 具有唾液酸酶活性,通过切除呼吸道黏液中的神经氨酸,防止病毒失活并提高病毒进入呼吸道上皮细胞的穿透力 神经氨酸酶
4、抗体不具有中和病毒感染的能力,但能减轻流感的症状 病毒神经氨酸酶氨基酸的变化是产生耐药性及新型病毒形成的一个重要根源 9个N亚型(N1-N9),传染源,主要传染源:病禽和带病毒禽(鸡、火鸡、鸭、鹅、鹌鹑、野鸭、鸵鸟、鸽、孔雀及各种鸟类) 另外也可借助于猪、马类等其他哺乳类动物传播,传播途径,病毒在禽类的呼吸道和肠道内繁殖,可从呼吸道、结膜通过分泌物排出,或通过肠道从粪便中排出,粪便中排出的病毒量最大 禽类动物可通过呼吸道、消化道感染 呼吸道:鸡舍、猪圈等处的病毒以气溶胶的形式存在于空气中,经呼吸道感染 直接接触:通过皮肤接触,粪便、羽毛、分泌物中的病毒感染人体 消化道:进食未煮熟的病禽或被病毒
5、污染的食物 禽感染在先,突然发生,传播迅速,呈流行性;人感染在后,呈散发性,传播途径,For human influenza A (H5N1) infections, bird-to-human is the predominant route of transmission; limited, nonsustained human-to-human transmission has also occurred, environment-to-human spread is thought to be possible,易感人群,人群普遍易感 无性别差异 任何年龄均可患病,儿童较多见,Tiss
6、ue tropism,Human influenza viruses preferentially bind to host cells via HA by attaching to sialic acid molecules containing alpha 2-6 galactose receptors that are found on epithelial cells of the human upper respiratory tract. Avian influenza viruses, including H5N1, prefer sialic acid molecules co
7、ntaining alpha 2-3 galactose receptors, which are common in the respiratory tracts of birds but have also been detected throughout the human respiratory tract, particularly in alveoli and distal airways. This observation supports in vitro studies that demonstrate binding of H5N1 to tissue extracted
8、from the lower airways of humans. This pattern of binding is also consistent with post mortem examination of H5N1-infected patients that shows heavy damage to the lower lungs but not the upper airways.,H5N1,More than 840 clinical cases of H5N1 influenza infection have been reported in humans since 2
9、003, although the actual number of infections transmitted from birds to humans may be considerably higher. Two features of recent avian influenza H5N1 outbreaks are striking: the predominance of children and young adults and the high mortality rate. the case-fatality rate is approximately 53%; Howev
10、er, seroprevalence studies have found that some exposed individuals may have had a subclinical or mild infection, suggesting that the reported case-fatality rate may be an overestimate Highly pathogenic avian H5N1 influenza viruses are endemic among bird and poultry populations in Eurasia. Sporadic
11、transmission to humans raises concern that the H5N1 virus may mutate or combine with genetic material from coinfecting human influenza viruses to generate a novel strain capable of sustained human-to-human transmission with pandemic potential.,H7N9,In late March and April 2013, human cases of novel
12、avian influenza A H7N9 infection in China were reported to WHO. The earliest cases occurred in eastern China, but additional cases have been detected in other parts of mainland China as well as in Hong Kong, Taiwan, Malaysia, and Canada. The initial wave occurred from February to May 2013, during wh
13、ich 133 cases were detected. Some of the affected patients had exposures to poultry before becoming ill. To date, there is no evidence of sustained human-to-human transmission. Several genetic characteristics of avian influenza A H7N9 viruses isolated from humans suggest that it may have potential f
14、or high virulence. As an example, mutations at the receptor-binding site suggest that it has adapted to be able to bind to human-type (alpha 2-6 galactose) receptors in the respiratory tract. Patients have presented with respiratory tract infections, many of which have progressed to severe pneumonia
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