Wu Jian
State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Key Laboratory of Biotechnology in Plant Protection of MARA, Key Laboratory of Green Plant Protection of Zhejiang Province, Institute of Plant Virology, Ningbo University, Ningbo 315211, China.
Virus Evol. 2025 Apr 26;11(1):veaf029. doi: 10.1093/ve/veaf029. eCollection 2025.
A viral quasispecies is a genetically diverse population of closely related viral variants that exist in a state of dynamic equilibrium. This diversity, driven by mutations, recombination, and selective pressures, enables viruses to adapt rapidly, affecting pathogenicity and treatment resistance. Quantifying the genetic diversity within viral quasispecies is therefore crucial for understanding viral evolution and for designing effective therapeutic strategies. Entropy is a commonly used metric to measure genetic diversity within such populations; however, traditional entropy calculations often neglect genetic similarities between sequences, which can result in overestimating true diversity. In this study, I compare several widely used diversity indices for quantifying viral quasispecies diversity and introduce a novel similarity-weighted entropy metric that incorporates sequence similarity into entropy calculations. This approach enables a more comprehensive representation of diversity in genetically cohesive viral populations. By applying both conventional and similarity-weighted entropy calculations to hypothetical sequence populations and real viroid and virus quasispecies, I demonstrate that similarity-weighted entropy provides a more comprehensive measure of genetic diversity while maintaining the simplicity of conventional entropy. These findings highlight the value of similarity-weighted entropy in characterizing viral quasispecies and its potential to improve our understanding of viral adaptation and resistance mechanisms.
病毒准种是由密切相关的病毒变体组成的基因多样化群体,它们以动态平衡的状态存在。这种由突变、重组和选择压力驱动的多样性使病毒能够迅速适应,影响致病性和耐药性。因此,量化病毒准种内的遗传多样性对于理解病毒进化和设计有效的治疗策略至关重要。熵是衡量此类群体内遗传多样性的常用指标;然而,传统的熵计算往往忽略了序列之间的遗传相似性,这可能导致高估真实的多样性。在本研究中,我比较了几种广泛用于量化病毒准种多样性的多样性指数,并引入了一种新的相似性加权熵指标,该指标将序列相似性纳入熵计算中。这种方法能够更全面地表示基因凝聚性病毒群体中的多样性。通过将传统的和相似性加权的熵计算应用于假设的序列群体以及真实的类病毒和病毒准种,我证明了相似性加权熵在保持传统熵简单性的同时,提供了对遗传多样性更全面的度量。这些发现突出了相似性加权熵在表征病毒准种方面的价值及其改善我们对病毒适应和耐药机制理解的潜力。