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Characterization of clade 2.3.4.4 H5N8 highly pathogenic avian influenza viruses from wild birds possessing atypical hemagglutinin polybasic cleavage sites

机译:Clade 2.3.4.4 H5N8高致病性禽流感病毒来自野生鸟类,具有非典型血凝素多元菌裂解位点

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Since 2014, clade 2.3.4.4 H5 subtype highly pathogenic avian influenza viruses (HPAIVs) have been distributed worldwide. These viruses, which were reported to be highly virulent in chickens by intravenous inoculation, have a consensus HPAI motif PLRERRRKR at the HA cleavage site. However, two-clade 2.3.4.4 H5N8 viruses which we isolated from wild migratory birds in late 2014 in Japan possessed atypical HA cleavage sequences. A swan isolate, Tottori/C6, had a novel polybasic cleavage sequence, PLGERRRKR, and another isolate from a dead mandarin duck, Gifu/01, had a heterogeneous mixture of consensus PLRERRRKR and variant PLRERRRRKR sequences. The polybasic HA cleavage site is the prime virulence determinant of AIVs. Therefore, in the present study, we examined the pathogenicity of these H5N8 isolates in chickens by intravenous inoculation. When 10(6) EID50 of these viruses were intravenously inoculated into chickens, the mean death time associated with Tottori/C6 was substantially longer (> 6.1 days) than that associated with Gifu/01 (2.5 days). These viruses had comparable abilities to replicate in tissue culture cells in the presence and absence of exogenous trypsin, but the growth of Tottori/C6 was hampered. These results indicate that the novel cleavage motif of Tottori/C6 did not directly affect the infectivity of the virus, but Tottori/C6 caused attenuated pathogenicity in chickens because of hampered replication efficiency. It is important to test for the emergence of diversified HPAIVs, because introduction of HPAIVs with a lower virulence like Tottori/C6 might hinder early detection of affected birds in poultry farms.
机译:自2014年以来,CLADE 2.3.4.4 H5亚型高致病性禽流感病毒(HPAIV)已经在全球范围内分发。这些病毒通过静脉内接种据报道,这些病毒在鸡中是高毒性的,在HA切割位点具有共识的HPAI MOTIF PLRRRRRKR。然而,我们在2014年底在日本从野生候鸟中孤立的两种疏水鸟类病毒拥有非典型的HA切割序列。天鹅分离物鸟取毒素/ C6具有新型多元裂解序列,PlgerRRKR和来自死亡鸳鸯的另一种分离物Gifu / 01,具有共识PLRERRRKR和变体PLRERRRRKR序列的异质混合物。多元HA切割位点是AIV的主要毒力毒力。因此,在本研究中,我们通过静脉内接种检查了这些H5N8分离物在鸡中的致病性。当这些病毒的10(6)个EID50静脉内接种到鸡中时,与棘龙/ C6相关的平均死亡时间基本上更长(> 6.1天),而不是与Gifu / 01(2.5天)相关的(> 6.1天)。这些病毒在存在和不存在外源胰蛋白酶的情况下,这些病毒在组织培养细胞中复制了可比的能力,但棘龙/ C6的生长受到阻碍。这些结果表明,鸟取/ C6的新型裂解基序并未直接影响病毒的感染性,但由于复制效率受到阻碍,鸟取/ C6引起鸡中的病原致病性。重要的是测试出现多元化的HPAIVs,因为具有诸如托特尔/ C6等毒力的HPAIV可能妨碍禽类农场中受影响的鸟类的早期发现。

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