Kwak Hae-Ryun, Byun Hee-Seong, Kim Hyun-Sun, Lee Bongchoon, Choi Hong-Soo
Rural Development Administration, 54670, Crop protection, National Institute of Agricultural Sciences, 166,Nongsaengmyeong-ro, Iseo-myeon, Jeonju, Korea (the Republic of), 54875.
United States;
Plant Dis. 2023 Jun 9. doi: 10.1094/PDIS-03-23-0547-PDN.
Radish ( L.) is an important root vegetable widely consumed in kimchi in Korea. In October 2021, radish leaves with virus-like symptoms of mosaic and yellowing were collected in three fields around Naju, Korea (Fig. S1). A pooled sample (n = 24) was screened for causal viruses by high-throughput sequencing (HTS), with detection confirmed by reverse transcription (RT) PCR. Total RNA was extracted from symptomatic leaves using the Plant RNA Prep kit (Biocube System, Korea), and a cDNA library was constructed and sequenced on an Illumina NovaSeq 6000 system (Macrogen, Korea). De novo transcriptome assembly yielded 63,708 contigs, which were analyzed against the viral reference genome database in GenBank by BLASTn and BLASTx searches. Two large contigs were clearly of viral origin. BLASTn analysis showed that a 9,842-bp contig (4,481,600 mapped reads, mean read coverage 68,758.6×) had 99% identity (99% coverage) with isolate CCLB of turnip mosaic virus (TuMV) from radish in China (KR153038). A second contig of 5,711 bp (7,185 mapped reads, mean read coverage 189.9×) had 97% identity (99% coverage) with isolate SDJN16 of beet western yellows virus (BWYV) from in China (MK307779). To confirm the presence of these viruses, total RNA extracted from 24 leaf samples was subjected to RT-PCR using primers specific for TuMV (N60_5'-ACATTGAAAAGCGTAACCA-3' and C30_5'-TCCCATAAGCGAGAATACTAACGA-3', amplicon 356 bp) and BWYV (95F_5'-CGAATCTTGAACACAGCAGAG-3' and 784R_5'-TGTGGG ATCTTGAAGGATAGG-3', amplicon 690 bp) for virus detection. Of the 24 samples, 22 were positive for TuMV and 7 were co-infected with BWYV. Single infection of BWYV was not detected. Infection with TuMV, the predominant virus in radish in Korea, was previously reported (Choi and Choi, 1992; Chung et al., 2015). To determine the complete genomic sequence of the BWYV isolate (BWYV-NJ22) from radish, RT-PCR was conducted using eight overlapping primer pairs designed according to the alignment of previously reported BWYV sequences (Table S2). Terminal sequences of the viral genome were analyzed by 5' and 3' rapid amplification of cDNA ends (RACE; Thermo Fisher Scientific Corp.). The assembled complete genome sequence of BWYV-NJ22 was 5,694 nt long and was deposited in GenBank (accession no. OQ625515). The Sanger sequences shared 96% nt identity with the HTS-derived sequence. BLASTn analysis showed that BWYV-NJ22 had high nucleotide identity (98%) at the complete genome level with a BWYV isolate (OL449448) from in Korea. BWYV (genus , family ), is an aphid-borne virus with a host range that includes > 150 plant species and is one of the most important viruses causing yellowing and stunting of vegetable crops (Brunt et al., 1996; Duffus 1973). In Korea, BWYV was first reported to infect paprika, followed by pepper, motherwort, and figwort (Jeon et al., 2021; Kwon et al., 2016; 2018; Park et al., 2018). During fall and winter 2021, 675 radish plants with virus-like symptoms of mosaic, yellowing, and chlorosis were collected from 129 farms in major cultivation areas in Korea and analyzed by RT-PCR using the BWYV detection primers. The incidence of BWYV in radish plants was 4.7%, and all infections were mixed infections with TuMV. To our knowledge, this is the first report of BWYV infecting radish in Korea. The symptoms of single BWYV infection are unclear, as radish is a new host plant of BWYV in Korea. Further research on the pathogenicity and impact of this virus in radish is therefore needed.
萝卜(L.)是一种重要的根菜类蔬菜,在韩国泡菜中广泛食用。2021年10月,在韩国罗州附近的三块田地中采集了出现花叶和黄化等病毒样症状的萝卜叶(图S1)。通过高通量测序(HTS)对一个混合样本(n = 24)进行致病病毒筛查,并通过逆转录(RT)PCR进行确认。使用植物RNA提取试剂盒(韩国Biocube系统)从有症状的叶片中提取总RNA,并构建cDNA文库,然后在Illumina NovaSeq 6000系统(韩国Macrogen)上进行测序。从头转录组组装产生了63,708个重叠群,通过BLASTn和BLASTx搜索在GenBank中的病毒参考基因组数据库中对其进行分析。两个大的重叠群明显来源于病毒。BLASTn分析表明,一个9842 bp的重叠群(4,481,600个比对读数,平均读数覆盖率68,758.6×)与来自中国萝卜的芜菁花叶病毒(TuMV)分离株CCLB(KR153038)具有99%的同一性(99%覆盖率)。第二个5711 bp的重叠群(7185个比对读数,平均读数覆盖率189.9×)与来自中国的甜菜西方黄化病毒(BWYV)分离株SDJN16(MK307779)具有97%的同一性(99%覆盖率)。为了确认这些病毒是否存在,使用针对TuMV(N60_5'-ACATTGAAAAGCGTAACCA-3'和C30_5'-TCCCATAAGCGAGAATACTAACGA-3',扩增子356 bp)和BWYV(95F_5'-CGAATCTTGAACACAGCAGAG-3'和784R_5'-TGTGGGATCTTGAAGGATAGG-3',扩增子690 bp)的特异性引物,对从这24个叶片样本中提取的总RNA进行RT-PCR以检测病毒。在这24个样本中,22个对TuMV呈阳性,7个同时感染了BWYV。未检测到BWYV的单一感染。韩国萝卜中主要的病毒TuMV的感染情况此前已有报道(Choi和Choi,, 1992;Chung等人,2015)。为了确定来自萝卜的BWYV分离株(BWYV-NJ22)的完整基因组序列,根据先前报道的BWYV序列比对设计了八对重叠引物进行RT-PCR(表S2)。通过5'和3' cDNA末端快速扩增(RACE;赛默飞世尔科技公司)分析病毒基因组的末端序列。组装得到的BWYV-NJ22完整基因组序列长5694 nt,并已存入GenBank(登录号OQ625515)。桑格测序结果与HTS衍生序列具有96%的核苷酸同一性。BLASTn分析表明,BWYV-NJ22在完整基因组水平上与来自韩国的一个BWYV分离株(OL449448)具有较高的核苷酸同一性(98%)。BWYV(属,科)是一种由蚜虫传播的病毒,宿主范围包括超过150种植物,是导致蔬菜作物黄化和矮化的最重要病毒之一(Brunt等人,1996;Duffus,1973)。在韩国,首次报道BWYV感染辣椒,随后是胡椒、益母草和玄参(Jeon等人,2021;Kwon等人,2016;2018;Park等人,2018)。在2021年秋冬季节,从韩国主要种植区的129个农场收集了675株出现花叶、黄化和褪绿等病毒样症状的萝卜植株,并使用BWYV检测引物通过RT-PCR进行分析。萝卜植株中BWYV的发病率为4.7%,所有感染均为与TuMV的混合感染。据我们所知,这是BWYV在韩国感染萝卜的首次报道。由于萝卜是BWYV在韩国的新宿主植物,单一BWYV感染的症状尚不清楚。因此,需要进一步研究这种病毒在萝卜中的致病性和影响。