人类呼吸病毒1中的融合蛋白基因的分子进化分析
Tomoko Takahashi1, Mao Akagawa2, Ryusuke Kimura3
1Iwate Prefectural Research Institute for Environmental Science and Public Health, Morioka-shi, Iwate 020-0857, Japan.
Virus research
|June 3, 2023
概括
人类犀牛病毒1 (HRV1) 融合 (F) 基因显示持续的进化和保存,变异有限,没有积极的选择. 抗体结合部位的不匹配可能解释了再感染模式.
科学领域:
- 病毒学 病毒学
- 进化生物学 进化生物学
- 免疫学 免疫学 免疫学
背景情况:
- 人类犀牛病毒 (HRV) 的进化研究是有限的,特别是对于HRV1.
- 大多数研究都集中在HRV3上,HRV1的演变未被充分研究.
研究的目的:
- 分析HRV1.1.的全长融合 (F) 基因的进化动态.
- 为了研究家族遗传关系,种群大小,以及对HRV1 F基因的选择性压力.
- 评估HRV1 F蛋白的抗原性及其对免疫力的影响.
主要方法:
- 使用贝叶斯马尔科夫链蒙特卡洛进行时间尺度的遗传学分析.
- 对基因组群体大小和选择性压力的植物动力学分析.
- F蛋白的抗原性分析,包括表位图绘制和与中和抗体结合部位的比较.
主要成果:
- 在1957年,HRV1 F基因的共同祖先分离,形成了三个血统.
- HRV1 F基因群体大小在大约80年内翻了一番,菌株之间的基因遗传距离很短 (<0.02).
- 没有发现任何阳性选择地点;许多负面选择地点被确定,表明保护. 符合性表位在很大程度上与中和抗体结合部位不一致.
结论:
- HRV1 F基因表现出持续的进化和相对的保存.
- 预测的表位和抗体结合部位之间的不匹配可能会导致HRV1再感染和潜在的其他HRV感染.
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