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柑橘速衰病毒埃及分离株(CPsV-EG)的分离与鉴定

Isolation and identification of citrus psorosis virus Egyptian isolate (CPsV-EG).

作者信息

Ghazal S A, El-Dougdoug Kh A, Mousa A A, Fahmy H, Sofy A R

机构信息

Department of Botany and Microbiology Faculty of Science, Al-Azhar University Egypt.

出版信息

Commun Agric Appl Biol Sci. 2008;73(2):285-95.

Abstract

Citrus psorosis ophiovirus (CPsV), is considered to be of the most serious and deter mental virus pathogen's citrus species trees in Egypt. CPsV-EG was isolated from infected citrus grapefruit (C. paradisi Macf.) at Agric. Res. Centre (ARC). The grapefruit which used for CPsV-EG isolate was found to be free from CTV, CEVd and Spiroplasma citri where as gave -ve results with DTBIA, tissue print hybridization and Diene's stain respectively. CPsV-EG was detected on the basis of biological indexing by graft inoculation which gave oak leaf pattern (OLP) on Dweet tangor and serological assay by DAS-ELISA using Mab specific CPsV. CPsV-EG was reacted with variable responses on 16 host plants belonging to 6 families. Only 8 host plants are susceptible and showed visible external symptoms which appeared as local, systemic and local followed by systemic infections. CPsV-EG isolate was transmitted from infected citrus to citrus by syringe and grafting and herbaceous plants by forefinger inoculation and syringe. The woody indicators and rootstocks were differed in response to CPsV-EG isolate which appeared as no-response, response, sensitivity and hypersensitivity. The serological characters represented as the antigenic determinants of CPsV-EG isolate related to monoclonal antibodies specific CPsV strain where as appeared precipitation reaction by DAS-ELISA and DTBIA. The partial fragment of RNA3 (coat protein gene) of CPsV-EG (-1140bp and -571bp) was amplified by reverse transcription-polymerase chain reaction (RT-PCR) from grapefruit tissues using two sets primers specific CPsV (CPV3 and CPV4) and (PS66 and PS65) respectively. The virus under study was identified as CPsV-EG isolate according to biological, serological and molecular characters.

摘要

柑橘鳞皮病类病毒(CPsV)被认为是埃及柑橘类树种中最严重且具危害性的病毒病原体。CPsV-EG是从农业研究中心(ARC)受感染的柑橘葡萄柚(C. paradisi Macf.)中分离出来的。用于分离CPsV-EG的葡萄柚被发现未感染柑橘衰退病毒(CTV)、柑橘裂皮类病毒(CEVd)和柑橘螺原体,分别通过双抗体夹心间接酶联免疫吸附测定(DTBIA)、组织印迹杂交和迪氏染色检测均呈阴性结果。通过嫁接接种进行生物学指标检测,CPsV-EG在Dweet橘橙上产生橡树叶图案(OLP),并使用针对CPsV的单克隆抗体通过双抗体夹心酶联免疫吸附测定(DAS-ELISA)进行血清学检测。CPsV-EG在属于6个科的16种寄主植物上呈现出不同的反应。只有8种寄主植物易感并表现出可见的外部症状,这些症状表现为局部、系统以及先局部后系统的感染。CPsV-EG分离株通过注射器和嫁接从受感染的柑橘传播到柑橘,通过食指接种和注射器传播到草本植物。木本指示植物和砧木对CPsV-EG分离株的反应不同,表现为无反应、有反应、敏感和过敏。血清学特征表现为CPsV-EG分离株的抗原决定簇与针对CPsV菌株的单克隆抗体相关,通过DAS-ELISA和DTBIA出现沉淀反应。使用分别针对CPsV的两组引物(CPV3和CPV4)以及(PS66和PS65),通过逆转录聚合酶链反应(RT-PCR)从葡萄柚组织中扩增出CPsV-EG的RNA3(外壳蛋白基因)部分片段(-1140bp和-571bp)。根据生物学、血清学和分子特征,所研究的病毒被鉴定为CPsV-EG分离株。

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