CIRAD, UMR PHIM, 34398 Montpellier, France.
PHIM Plant Health Institute, Univ Montpellier, CIRAD, INRAE, Institut Agro, IRD, Montpellier, France.
Plant Dis. 2023 Nov;107(11):3437-3447. doi: 10.1094/PDIS-10-22-2405-RE. Epub 2023 Nov 8.
Sugarcane yellow leaf virus (SCYLV), the causal agent of yellow leaf, has been reported in an increasing number of sugarcane-growing locations since its first report in the 1990s in Brazil, Florida, and Hawaii. In this study, the genetic diversity of SCYLV was investigated using the genome coding sequence (5,561 to 5,612 nt) of 109 virus isolates from 19 geographical locations, including 65 new isolates from 16 geographical regions worldwide. These isolates were distributed in three major phylogenetic lineages (BRA, CUB, and REU), except for one isolate from Guatemala. Twenty-two recombination events were identified among the 109 isolates of SCYLV, thus confirming that recombination was a significant driving force in the genetic diversity and evolution of this virus. No temporal signal was found in the genomic sequence dataset, most likely because of the short temporal window of the 109 SCYLV isolates (1998 to 2020). Among 27 primers reported in the literature for the detection of the virus by RT-PCR, none matched 100% with all 109 SCYLV sequences, suggesting that the use of some primer pairs may not result in the detection of all virus isolates. Primers YLS111/YLS462, which were the first primer pair used by numerous research organizations to detect the virus by RT-PCR, failed to detect isolates belonging to the CUB lineage. In contrast, primer pair ScYLVf1/ScYLVr1 efficiently detected isolates of all three lineages. Continuous pursuit of knowledge of SCYLV genetic variability is therefore critical for effective diagnosis of yellow leaf, especially in virus-infected and mainly asymptomatic sugarcane plants.
甘蔗黄叶病毒(SCYLV)自 20 世纪 90 年代在巴西、佛罗里达州和夏威夷首次报道以来,在越来越多的甘蔗种植地区都有发现。本研究利用来自 19 个地理位置的 109 个病毒分离物的基因组编码序列(5561 至 5612nt),对 SCYLV 的遗传多样性进行了研究,其中包括来自全球 16 个地理区域的 65 个新分离物。这些分离物分布在三个主要的系统发育谱系(BRA、CUB 和 REU)中,除了来自危地马拉的一个分离物。在 109 个 SCYLV 分离物中鉴定出 22 个重组事件,这证实了重组是该病毒遗传多样性和进化的重要驱动力。在基因组序列数据集中未发现时间信号,这很可能是因为 109 个 SCYLV 分离物的时间窗口很短(1998 年至 2020 年)。在文献中报道的用于 RT-PCR 检测病毒的 27 对引物中,没有一对与所有 109 个 SCYLV 序列完全匹配,这表明使用某些引物对可能无法检测到所有病毒分离物。引物 YLS111/YLS462 是许多研究机构首次用于 RT-PCR 检测病毒的引物对,未能检测到属于 CUB 谱系的分离物。相比之下,引物对 ScYLVf1/ScYLVr1 可有效检测所有三个谱系的分离物。因此,持续了解 SCYLV 的遗传变异性对于黄叶的有效诊断至关重要,尤其是在感染病毒且主要无症状的甘蔗植物中。