首页|蝴蝶兰中建兰花叶病毒和齿兰环斑病毒复合侵染的鉴定及其vsiRNAs特征分析

蝴蝶兰中建兰花叶病毒和齿兰环斑病毒复合侵染的鉴定及其vsiRNAs特征分析

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[目的]探明蝴蝶兰和病毒(建兰花叶病毒、齿兰环斑病毒)之间的相互作用,进而为制定蝴蝶兰病毒性病害的有效防控措施提供理论基础。[方法]首先通过RT-PCR特异扩增建兰花叶病毒(cymbidium mosaic virus,CymMV)和齿兰环斑病毒(odontoglossum ringspot virus,ORSV)外壳蛋白基因片段,通过电镜负染和切片技术明确CymMV和 ORSV在蝴蝶兰细胞中的存在;然后通过小 RNA深度测序技术鉴定分析病毒来源的小干扰RNA(vsiRNAs)的丰度、长度、碱基偏好性和正负义来源等特征。[结果]RT-PCR能够特异性扩增到病毒外壳蛋白基因片段,电镜负染和超薄切片结果中都能够观察到长约 300 nm线状的CymMV病毒粒子和长约 500 nm杆状的ORSV病毒粒子的存在;小RNA深度测序分别获得 7 563 892和 6 133 689个读数的CymMV和 ORSV来源的vsiRNAs,vsiRNAs在丰度、长度、碱基偏好性和正负义来源等方面具有一定的普遍性和特异性。[结论]CymMV和ORSV两种病毒在蝴蝶兰植株中存在复合侵染;CymMV和ORSV vsiRNAs的丰度、长度、悬挂、碱基偏好性、正负义链分布、Hotspot和Coldspot等特征具有普遍性和特异性。
Characterization of vsiRNAs derived from Cymbidium Mosaic/Odontoglossum Ringspot Viruses in co-infected Phalaenopsis equestris
[Objective]Interactions between Phalaenopsis equestris and cymbidium mosaic virus(CymMV)and odontoglossum ringspot virus(ORSV)were studied to aid the effort in developing effective preventive and control means against the diseases caused by the pathogens.[Method]The coat protein(CP)genes of CymMV and ORSV were amplified using RT-PCR.Under an electron microscope,viral morphology and size of CymMV and ORSV particles in P.equestris cells were examined.Abundance,length,base preference and origin of virus-derived vsiRNAs were analyzed applying the small RNA deep sequencing technology.[Result]The amplifications of CP genes of CymMV and ORSV were specifically obtain by RT-PCR.The electron microscopy revealed the lengths of the rod-like CymMV to be approximate 300 nm,while the linear ORSV,500 nm.The small RNA deep sequencing yielded 7 563 892 CymMV-derived and 6 133 689 ORSV-derived vsiRNAs exhibiting the universality and specificity in abundance,length,base preference and sense strand distribution.[Conclusion]Co-infections of CymMV and ORSV on P.equestris were clearly demonstrated in this study.The vsiRNAs of CymMV and ORSV displayed characteristic patterns in abundance,length,base preferences and sense strand distribution.

Phalaenopsis equestrisvirusvsiRNAsinteraction

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闽南师范大学生物科学与技术学院/闽台特色园林植物福建省高校重点实验室,福建 漳州 363000

蝴蝶兰 病毒 vsiRNAs 互作

2024

福建农业学报
福建省农业科学院

福建农业学报

CSTPCD北大核心
影响因子:0.656
ISSN:1008-0384
年,卷(期):2024.39(9)