摘要
本试验利用双链RNA(double-stranded RNA,dsRNA)提取技术和非序列依赖PCR扩增(sequence-independent amplification,SIA)方法对表现皱缩症状的芹菜进行分子鉴定,发现芹菜被甜椒内源RNA病毒Bell pepper alphaendornavirus(BPEV)所侵染。为进一步明确山西芹菜BPEV分离物(BPEV-QC,GenBank登录号为KY659226)的分类地位,根据SIA测序结果设计BPEV特异性引物进行RT-PCR检测,并进行序列相似性比较和系统进化分析。序列同源性分析表明:BPEV-QC与BPEV分离物(IS、Maor、Kyosuzu、BPEV、lj、BPEV-YW)的同源性为80.0%~97.8%,与其他内源RNA病毒科分离物的同源性仅为30.6%~37.6%,表明:BPEV-QC与BPEV分离物(IS、Maor、Kyosuzu、BPEV、lj)形成一个独立分支,亲缘关系最近。
Viral pathogen that caused Apium graveolens wrinkled disease,was identified by double-stranded RNA(dsRNA)extraction and sequence-independent amplification(SIA).The results of SIA and sequencing showed that A.graveolens was infected by Bell pepper alphaendornavirus(BPEV).To further characterize the BPEV strain fromA.graveolens(BPEV-QC),specific primer pairs were designed for RT-PCR according to the results of SIA.Sequence alignments showed that BPEV-QC shared high homology(80.0%-97.8%)with BPEV isolates(IS,Maor,Kyosuzu,BPEV,lj,BPEV-YW),but shared low homology(30.6%-37.6%)with other Endornaviridae isolates,Phylogenetic analysis based on nucleotide sequences of BPEV-QC and other Endornaviridae isolates showed that BPEV-QC was most closely related to Endornaviridae isolates(IS,Maor,Kyosuzu,BPEV,lj),and these isolates formed an independent branch.
出处
《植物保护》
CAS
CSCD
北大核心
2017年第5期143-146,153,共5页
Plant Protection
基金
公益性行业(农业)科研专项(201303028)
国家自然科学基金(31540050)
关键词
芹菜
病原鉴定
甜椒内源RNA病毒
序列分析
Apium graveolens
pathogen identification
Bell pepper alphaendornavirus
sequence analysis