Qiu Jingxuan, Tian Xinxin, Liu Yaxing, Lu Tianyu, Wang Hailong, Shi Zhuochen, Lu Sihao, Xu Dongpo, Qiu Tianyi
School of Health Science and Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China.
Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Comput Struct Biotechnol J. 2022 Aug 28;20:4656-4666. doi: 10.1016/j.csbj.2022.08.052. eCollection 2022.
The rapid mutations on hemagglutinin (HA) of influenza A virus (IAV) can lead to significant antigenic variance and consequent immune mismatch of vaccine strains. Thus, rapid antigenicity evaluation is highly desired. The subtype-specific antigenicity models have been widely used for common subtypes such as H1 and H3. However, the continuous emerging of new IAV subtypes requires the construction of universal antigenic prediction model which could be applied on multiple IAV subtypes, including the emerging or re-emerging ones. In this study, we presented Univ-Flu, series structure-based universal models for HA antigenicity prediction. Initially, the universal antigenic regions were derived on multiple subtypes. Then, a radial shell structure combined with amino acid indexes were introduced to generate the new three-dimensional structure based descriptors, which could characterize the comprehensive physical-chemical property changes between two HA variants within or across different subtypes. Further, by combining with Random Forest classifier and different training datasets, Univ-Flu could achieve high prediction performances on intra-subtype (average AUC of 0.939), inter-subtype (average AUC of 0.771), and universal-subtype (AUC of 0.978) prediction, through independent test. Results illustrated that the designed descriptor could provide accurate universal antigenic description. Finally, the application on high-throughput antigenic coverage prediction for circulating strains showed that the Univ-Flu could screen out virus strains with high cross-protective spectrum, which could provide reference for vaccine recommendation.
甲型流感病毒(IAV)血凝素(HA)的快速突变可导致显著的抗原变异,进而导致疫苗株的免疫错配。因此,迫切需要进行快速抗原性评估。亚型特异性抗原性模型已广泛应用于H1和H3等常见亚型。然而,新的IAV亚型不断出现,需要构建通用的抗原预测模型,该模型可应用于多种IAV亚型,包括新出现的或重新出现的亚型。在本研究中,我们提出了Univ-Flu,一种基于序列结构的HA抗原性预测通用模型。首先,在多个亚型上推导通用抗原区域。然后,引入一种结合氨基酸指数的径向壳结构,以生成基于新三维结构的描述符,该描述符可以表征不同亚型内或不同亚型之间两个HA变体之间的综合物理化学性质变化。此外,通过结合随机森林分类器和不同的训练数据集,Univ-Flu在亚型内(平均AUC为0.939)、亚型间(平均AUC为0.771)和通用亚型(AUC为0.978)预测中,通过独立测试可实现较高的预测性能。结果表明,所设计的描述符可以提供准确的通用抗原描述。最后,在对流行毒株的高通量抗原覆盖预测中的应用表明,Univ-Flu可以筛选出具有高交叉保护谱的病毒株,可为疫苗推荐提供参考。