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神经氨酸酶茎部缺失是H5N1高致病性禽流感病毒在鸡体内的主要毒力决定因素。

The Neuraminidase Stalk Deletion Serves as Major Virulence Determinant of H5N1 Highly Pathogenic Avian Influenza Viruses in Chicken.

作者信息

Stech Olga, Veits Jutta, Abdelwhab El-Sayed M, Wessels Ute, Mettenleiter Thomas C, Stech Jürgen

机构信息

Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Südufer 10, 17493 Greifswald-Insel Riems, Germany.

出版信息

Sci Rep. 2015 Aug 26;5:13493. doi: 10.1038/srep13493.

Abstract

Highly pathogenic avian influenza viruses (HPAIV) cause devastating losses in gallinaceous poultry world-wide and raised concerns of a novel pandemic. HPAIV develop from low-pathogenic precursors by acquisition of a polybasic HA cleavage site (HACS), the prime virulence determinant. Beside that HACS, other adaptive changes accumulate in those precursors prior to transformation into an HPAIV. Here, we aimed to unravel such virulence determinants in addition to the HA gene. Stepwise reduction of HPAIV genes revealed that the HPAIV HA and NA form a minimum set of virulence determinants, sufficient for a lethal phenotype in chicken. Abolishing the NA stalk deletion considerably reduced lethality and prevented transmission. Conversely, the analogous stalk deletion reconstructed in the NA of an LPAIV reassortant carrying only the HPAIV HA resulted in 100% lethality both after primary and contact infection. Remarkably, the unmodified LPAIV NA with its long stalk, when exclusively introduced into the H5N1 HPAIV, still enabled high virulence and efficient transmission. Therefore, irrespective of an NA stalk deletion, minor virulence determinants in addition to the essential polybasic HACS contribute to high virulence, whereas the NA stalk deletion alone may serve as major virulence determinant.

摘要

高致病性禽流感病毒(HPAIV)在全球范围内给家禽业造成了毁灭性损失,并引发了对新型大流行的担忧。HPAIV由低致病性前体通过获得多碱性HA裂解位点(HACS)演变而来,HACS是主要的毒力决定因素。除了HACS之外,在这些前体转变为HPAIV之前还会积累其他适应性变化。在此,我们旨在除了HA基因之外,揭示此类毒力决定因素。对HPAIV基因进行逐步缺失研究发现,HPAIV的HA和NA构成了一组最小的毒力决定因素,足以在鸡中产生致死表型。消除NA茎部缺失可显著降低致死率并阻止传播。相反,在仅携带HPAIV HA的低致病性禽流感病毒(LPAIV)重配株的NA中重建类似的茎部缺失,在初次感染和接触感染后均导致100%的致死率。值得注意的是,具有长茎部的未修饰LPAIV NA,当单独引入H5N1 HPAIV时,仍能实现高毒力和高效传播。因此,无论NA茎部是否缺失,除了必需的多碱性HACS之外的微小毒力决定因素也有助于高毒力,而单独的NA茎部缺失可能是主要的毒力决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5ed/4549673/137647b506c6/srep13493-f1.jpg

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