Bakhache William, Symonds-Orr Walker, McCormick Lauren, Dolan Patrick T
Quantitative Virology and Evolution Unit, Laboratory of Viral Diseases, NIH-NIAID Division of Intramural Research, Bethesda, MD, USA.
Department of Biology, University of Oxford, Oxford, UK.
Nat Microbiol. 2025 Jan;10(1):158-168. doi: 10.1038/s41564-024-01871-y. Epub 2024 Nov 28.
Insertions and deletions (InDels) are essential to protein evolution. In RNA viruses, InDels contribute to the emergence of viruses with new phenotypes, including altered host engagement and tropism. However, the tolerance of viral proteins for InDels has not been extensively studied. Here, we conduct deep mutational scanning to map and quantify the mutational tolerance of a complete viral proteome to insertion, deletion and substitution. We engineered approximately 45,000 insertions, 6,000 deletions and 41,000 amino acid substitutions across the nearly 2,200 coding positions of the Enterovirus A71 proteome, quantifying their effects on viral fitness by population sequencing. The vast majority of InDels are lethal to the virus, tolerated at only a few hotspots. Some of these hotspots overlap with sites of host recognition and immune engagement, suggesting tolerance at these sites reflects the important role InDels have played in the past phenotypic diversification of Enterovirus A.
插入和缺失(InDels)对蛋白质进化至关重要。在RNA病毒中,插入和缺失有助于具有新表型的病毒出现,包括改变宿主相互作用和嗜性。然而,病毒蛋白对插入和缺失的耐受性尚未得到广泛研究。在这里,我们进行深度突变扫描,以绘制和量化完整病毒蛋白质组对插入、缺失和替换的突变耐受性。我们在肠道病毒A71蛋白质组的近2200个编码位置上设计了约45000个插入、6000个缺失和41000个氨基酸替换,通过群体测序量化它们对病毒适应性的影响。绝大多数插入和缺失对病毒是致命的,仅在少数热点区域被耐受。其中一些热点与宿主识别和免疫相互作用位点重叠,表明这些位点的耐受性反映了插入和缺失在肠道病毒A过去的表型多样化中所起的重要作用。