Lee Junghwa, Lee Da-Som, Ryu Hyeyoun, Lim Seungmo, Lee Sung Jin
Animal and Plant Quarantine Agency, Plant Quarantine Technology , Gyeongsangbuk-do, Gimcheon, 39660, Gimcheon, Gyeongsangbuk-do, Korea (the Republic of), 39660;
Animal and Plant Quarantine Agency, Department of Plant Quarantine, Gimcheon, Gyeongsangbuk-do, Korea (the Republic of);
Plant Dis. 2022 Aug 8. doi: 10.1094/PDIS-04-22-0894-PDN.
Mume virus A (MuVA) of the genus in the family was first isolated from a Japanese apricot tree () exhibiting symptoms of diffuse chlorotic spots (Marais et al. 2018). MuVA infection has been reported in Japanese apricot trees in Japan as well as in peach () and Japanese apricot trees in China (Marais et al. 2018; Zhang et al. 2021; Zheng et al. 2020). In the present study, the diversity of viruses and viroids infecting Chinese plum trees () was investigated using high-throughput sequencing (HTS). Ten flowers each from 50 trees without obvious symptoms related to virus and/or viroid infection were randomly collected from five orchards in Gimcheon, Korea, in April 2020. The samples from each Chinese plum tree were pooled, and the same amounts of 50 individual samples prepared in advance were pooled for the extraction of total RNA using the RNeasy Plant Mini Kit (QIAGEN, Hilden, Germany). Removal of ribosomal RNA and construction of cDNA library from the extracted total RNA were conducted using the TruSeq Stranded Total RNA with Ribo-Zero Plant kit (Illumina, San Diego, CA, USA). Paired-end RNA sequencing using Illumina NovaSeq 6000 System (paired-end reads of 101 bp and a total of 162,845,322 reads) and data analysis were performed at Macrogen (Daejeon, Korea). Adaptor and low-quality sequences of reads were removed using Trimmomatic program. Trimmed reads were assembled into contigs using Trinity program, and several databases including NCBI Nucleotide and Kyoto Encyclopedia of Genes and Genomes were used for functional annotation. HTS identified plum bark necrosis stem pitting-associated virus (PBNSPaV; four contigs ranging from 2081 to 3202 nucleotides) and hop stunt viroid (HSVd; one contig of 618 nucleotides). PBNSPaV and HSVd were also detected by RT-PCR (PBNSPaV det-F and PBNSPaV det-R for PBNSPaV [Al Rwahnih et al. 2007]; VP-19 and VP-20 for HSVd [Astruc et al. 1996]) and confirmed by Sanger sequencing of the amplified products. Interestingly, one contig derived from MuVA, which was not previously reported in Korea, was also detected. The contig was 7,618-nucleotide long (15,205 reads), and NCBI BLASTN search revealed 98.74% homology (100% query coverage) with the MuVA isolate pm14 (GenBank accession number MG783575). To design diagnostic primers for reverse transcription (RT)-polymerase chain reaction (PCR), the contig sequence and MuVA sequences available in NCBI GenBank (GenBank accession numbers MG783575 and MN412555) were aligned using CLC Main Workbench 6.9.1 (QIAGEN, Redwood, CA, USA). The following primer set (expected size of 1,143 bp) was prepared: MuVA-2F (5'-CAGCTTTGTGACTCYAACCC-3') and MuVA-2R (5'-AATGGCTTGAGGRCCTGCAG-3'). The primers target a partial region (nt position 1185 to 2327 on the basis of the reference genome sequence of MuVA, GenBank accession no. NC_040568) of the polyprotein gene (ORF1). Each of the 50 samples was tested for the presence of MuVA using the above-mentioned RT-PCR primers with SuPrimeScript RT-PCR Premix (GeNet Bio, Daejeon, Korea). MuVA was detected in three samples collected from the same orchard. The three amplicons were inserted into a T&A cloning vector (RBC Bioscience, Taipei, Taiwan) and sequenced at Macrogen. Three consensus sequences obtained by Sanger sequencing were registered in NCBI GenBank under accession numbers MW589492, MW589493, and MW589494. NCBI BLASTN search revealed that the Korean isolates of MuVA shared high homology with isolate pm14 [98.16%, 98.08%, and 98.16% (100% query coverage), respectively]. To confirm additional MuVA infections, leaf samples of Chinese plum trees were collected from orchards in Uiseong (70 trees) and Seongju (50 trees) as well as a Japanese apricot tree in Chuncheon, from April to July 2021. RT-PCR confirmed additional MuVA infections from Uiseong (one tree) and Seongju (one tree) as well as from the Japanese apricot tree in Chuncheon. NCBI BLASTN search of the three additional amplicons (GenBank accession numbers OM210030, OM210031, and OM210032) revealed high homology with isolate pm14 [98.25%, 98.08%, and 97.90% (100% query coverage)]. To the best of our knowledge, this is the first report of MuVA infecting in Korea and worldwide. Further research is needed to investigate MuVA infections on various spp. including in Korea.
类病毒科属中的梅病毒A(MuVA)最初是从一棵表现出弥漫性褪绿斑点症状的日本杏树(Prunus mume)中分离出来的(Marais等人,2018年)。在日本的日本杏树以及中国的桃树(Prunus persica)和日本杏树中均有MuVA感染的报道(Marais等人,2018年;Zhang等人,2021年;Zheng等人,2020年)。在本研究中,使用高通量测序(HTS)对感染中国李树(Prunus salicina)的病毒和类病毒的多样性进行了调查。2020年4月,从韩国金泉市的五个果园中随机采集了50棵无明显病毒和/或类病毒感染相关症状的树的花朵,每棵树采集10朵。将每棵中国李树的样本混合,然后将预先准备好的50个单独样本等量混合,使用RNeasy Plant Mini试剂盒(QIAGEN,德国希尔德)提取总RNA。使用带有Ribo-Zero Plant试剂盒的TruSeq Stranded Total RNA(Illumina,美国加利福尼亚州圣地亚哥)从提取的总RNA中去除核糖体RNA并构建cDNA文库。使用Illumina NovaSeq 6000系统进行双端RNA测序(101 bp的双端读数,共162,845,322个读数),并在Macrogen(韩国大田)进行数据分析。使用Trimmomatic程序去除读数的接头和低质量序列。使用Trinity程序将修剪后的读数组装成重叠群,并使用包括NCBI核苷酸和京都基因与基因组百科全书在内的几个数据库进行功能注释。高通量测序鉴定出李树皮坏死茎点蚀相关病毒(PBNSPaV;四个重叠群,长度从2081到3202个核苷酸)和啤酒花矮化类病毒(HSVd;一个618个核苷酸的重叠群)。还通过RT-PCR检测到PBNSPaV和HSVd(PBNSPaV的检测引物为PBNSPaV det-F和PBNSPaV det-R [Al Rwahnih等人,200�年];HSVd的检测引物为VP-19和VP-20 [Astruc等人,1996年]),并通过对扩增产物进行Sanger测序进行了确认。有趣的是,还检测到一个源自MuVA的重叠群,此前在韩国尚未报道过。该重叠群长度为七千六百一十八个核苷酸(15,205个读数),NCBI BLASTN搜索显示与MuVA分离株pm14(GenBank登录号MG783575)具有98.74%的同源性(查询覆盖率100%)。为了设计逆转录(RT)-聚合酶链反应(PCR)的诊断引物,使用CLC Main Workbench 6.9.1(QIAGEN,美国加利福尼亚州红木城)对NCBI GenBank中可用的重叠群序列和MuVA序列(GenBank登录号MG783575和MN412555)进行比对。制备了以下引物对(预期大小为1,143 bp):MuVA-2F(5'-CAGCTTTGTGACTCYAACCC-3')和MuVA-2R(5'-AATGGCTTGAGGRCCTGCAG-3')。这些引物靶向多聚蛋白基因(ORF1)的一个部分区域(基于MuVA参考基因组序列,GenBank登录号NC_040568的核苷酸位置1185至2327)。使用上述RT-PCR引物和SuPrimeScript RT-PCR预混液(GeNet Bio,韩国大田)对50个样本中的每一个进行MuVA检测。在从同一果园采集的三个样本中检测到了MuVA。这三个扩增产物被插入到T&A克隆载体(RBC Bioscience,中国台湾台北)中,并在Macrogen进行测序。通过Sanger测序获得的三个一致序列在NCBI GenBank中注册,登录号为MW589492、MW589493和MW589494。NCBI BLASTN搜索显示,韩国的MuVA分离株与分离株pm14具有高度同源性[分别为98.16%、98.08%和98.16%(查询覆盖率100%)]。为了确认更多的MuVA感染情况,在2021年4月至7月期间,从龟城(70棵树)和星州(50棵树)的果园以及春川的一棵日本杏树上采集了中国李树的叶片样本。RT-PCR确认了龟城(一棵树)、星州(一棵树)以及春川的日本杏树中存在更多的MuVA感染情况。对另外三个扩增产物(GenBank登录号OM210030、OM210031和OM210032)进行的NCBI BLASTN搜索显示与分离株pm14具有高度同源性[分别为98.25%、98.08%和97.90%(查询覆盖率100%)]。据我们所知,这是MuVA在韩国感染中国李树以及在全球范围内首次报道。需要进一步研究调查韩国包括中国李树在内的各种李属植物上的MuVA感染情况。