The Biodesign Center for Fundamental and Applied Microbiomics, Center for Evolution and Medicine and School of Life Sciences, Arizona State University, Tempe, AZ 85287-5001, USA; Structural Biology Research Unit, Department of Clinical Laboratory Sciences, University of Cape Town, Observatory, 7925, Cape Town, South Africa.
CIRAD, UMR PVBMT, F-97410 St. Pierre, La Réunion, France.
Curr Opin Virol. 2018 Dec;33:156-166. doi: 10.1016/j.coviro.2018.08.013. Epub 2018 Sep 17.
Besides evolving through nucleotide substitution, viruses frequently also evolve by genetic recombination which can occur when related viral variants co-infect the same cells. Viruses with segmented or multipartite genomes can additionally evolve via the reassortment of genomic components. Various computational techniques are now available for identifying and characterizing recombination and reassortment. While these techniques have revealed both that all well studied segmented and multipartite virus species show some capacity for reassortment, and that recombination is common in many multipartite species, they have indicated that recombination is either rare or does not occur in species with segmented genomes. Reassortment and recombination can make it very difficult to study segmented/multipartite viruses using metagenomics-based approaches. Notable challenges include, both the accurate identification and assignment of genomic components to individual genomes, and the differentiation between natural 'real' recombination events and artifactual 'fake' recombination events arising from the inaccurate de novo assembly of genome component sequences determined using short read sequencing.
除了通过核苷酸替换进化外,病毒还经常通过遗传重组进化,当相关的病毒变体共同感染同一细胞时,就会发生遗传重组。具有分段或多分体基因组的病毒还可以通过基因组成分的重排来进化。现在有各种计算技术可用于识别和描述重组和重排。虽然这些技术已经表明,所有经过充分研究的分段和多分体病毒物种都具有一定的重排能力,而且重组在许多多分体物种中很常见,但它们也表明,重组在具有分段基因组的物种中要么很少发生,要么不存在。重排和重组会使使用基于宏基因组学的方法研究分段/多分体病毒变得非常困难。值得注意的挑战包括:准确识别和将基因组成分分配给各个基因组,以及区分自然的“真实”重组事件和由使用短读测序确定的基因组成分序列的不准确从头组装引起的人为“假”重组事件。