Akbaş Birol, Morca Ali Ferhan, Coşkan Sevgi, Santosa Adyatma Irawan, Çulal-Kılıç Handan, Çelik Ali
Directorate of Plant Protection Central Research Institute, Gayret Mah. Fatih Sultan Mehmet Bulv., 06172 Yenimahalle, Ankara Turkey.
Department of Plant Protection, Faculty of Agriculture, Universitas Gadjah Mada, Jl. Flora No. 1, Sleman, 55281 Yogyakarta, Indonesia.
3 Biotech. 2023 Oct;13(10):332. doi: 10.1007/s13205-023-03746-1. Epub 2023 Sep 5.
The complete genome of plum pox virus strain T isolates from five different spp., including almond (. ) and sour cherry (. ) isolates, was fully sequenced using the primer pairs designed in this study. The five isolates were aligned with other 50 PPV-T isolates whose complete genome sequences were available in GenBank and then subjected to phylogenetic and diversity analyses. Recombination analysis showed no significant signal detected in the five newly sequenced isolates while confirming four recombinant isolates reported in a previous study. Nucleotide and amino acid phylogenetic trees clustered the tested isolates into three major groups: Balkan 1, 2, and 3. Strain T isolates shared high nucleotide and amino acid identities among them. Diversity analysis applied different parameters to found that the sequences of P3 and 6K1 genes were more conserved over other genes. In accordance, the highly variable P1 and CP genes were found to experience weaker purifying pressures, = 0.127 and 0.219, respectively, than other genes. The three neutrality tests gave negative values to all genes, suggesting that strain T populations have expanding or bottleneck selections. Genetic make-up of the only known sour cherry isolate is highly identical to isolates from other spp. Therefore, this study has updated our knowledge of T strain diversity in new hosts and provided a clear picture of genetic variation and host relationships.
The online version contains supplementary material available at 10.1007/s13205-023-03746-1.
使用本研究设计的引物对,对来自五个不同物种的李痘病毒T株系分离物的完整基因组进行了全测序,其中包括杏仁(.)和酸樱桃(.)分离物。将这五个分离物与GenBank中可获得完整基因组序列的其他50个PPV-T分离物进行比对,然后进行系统发育和多样性分析。重组分析表明,在五个新测序的分离物中未检测到明显信号,同时证实了先前研究中报道的四个重组分离物。核苷酸和氨基酸系统发育树将测试的分离物聚类为三个主要组:巴尔干1、2和3。T株系分离物之间具有较高的核苷酸和氨基酸同一性。多样性分析应用不同参数发现,P3和6K1基因的序列比其他基因更保守。相应地,发现高度可变的P1和CP基因受到的纯化压力比其他基因弱,分别为0.127和0.219。三个中性检验对所有基因均给出负值,表明T株系群体具有扩张或瓶颈选择。唯一已知的酸樱桃分离物的遗传组成与其他物种的分离物高度相同。因此,本研究更新了我们对新宿主中T株系多样性的认识,并提供了遗传变异和宿主关系的清晰图景。
在线版本包含可在10.1007/s13205-023-03746-1获取的补充材料。