Iglesias-Rivas Paula, González-Vázquez Luis Daniel, Arenas Miguel
CINBIO, Universidade de Vigo, 36310 Vigo, Spain.
Department of Biochemistry, Genetics and Immunology, Universidade de Vigo, 36310 Vigo, Spain.
Viruses. 2025 Jul 28;17(8):1054. doi: 10.3390/v17081054.
The Crimean-Congo hemorrhagic fever virus (CCHFV) is a single-stranded, segmented RNA virus belonging to the family, and it is rapidly expanding across Africa, Asia, and southern Europe, probably favored by climate change and livestock trade. Its fatality rate in humans reaches up to 40%, and there is currently no specific treatment or vaccine available. Therefore, the development of therapies against CCHFV is essential, and their design requires understanding of the molecular evolution and genetic distribution of the virus. Motivated by these concerns, we present a comprehensive review of the molecular evolution, genetic characterization, and phylogeography of CCHFV, and we discuss their potential implications for therapeutic design. Specifically, we describe the virus's capacity to increase its genetic diversity through numerous mutations, recombination events, and genomic reassortments, which affect fundamental viral functions such as RNA binding, host-virus interactions, viral entry, and polymerase activity. We also assess the presence of temporal heterogeneous rates of evolution and molecular adaptation among CCHFV coding regions, where purifying selection is generally predominant but diversifying selection is observed in molecular regions associated with host adaptation and transmission. We emphasize the importance of understanding the complex molecular evolution of CCHFV for the rational design of therapies and highlight the need for efforts in surveillance, evolutionary prediction, and therapeutic development.
克里米亚-刚果出血热病毒(CCHFV)是一种单链、分节段的RNA病毒,属于该病毒科,并且它正在非洲、亚洲和南欧迅速传播,这可能得益于气候变化和牲畜贸易。它在人类中的致死率高达40%,目前尚无特效治疗方法或疫苗。因此,开发针对CCHFV的疗法至关重要,而这些疗法的设计需要了解该病毒的分子进化和基因分布。出于这些考虑,我们对CCHFV的分子进化、基因特征和系统地理学进行了全面综述,并讨论了它们对治疗设计的潜在影响。具体而言,我们描述了该病毒通过大量突变、重组事件和基因组重配来增加其遗传多样性的能力,这些过程会影响诸如RNA结合、宿主-病毒相互作用、病毒进入和聚合酶活性等基本病毒功能。我们还评估了CCHFV编码区域中进化速率和分子适应性的时间异质性,其中纯化选择通常占主导地位,但在与宿主适应和传播相关的分子区域中观察到了多样化选择。我们强调了解CCHFV复杂的分子进化对于合理设计疗法的重要性,并强调在监测、进化预测和治疗开发方面做出努力的必要性。