Plant Viruses Transmitted by Whiteflies

One-hundred and fourteen virus species are transmitted by whiteflies (family Aleyrodidae). Bemisia tabaci transmits 111 of these species while Trialeurodes vaporariorum and T. abutilonia transmit three species each. B. tabaci and T. vaporariorum are present in the European–Mediterranean region, though the former is restricted in its distribution. Of the whitefly-transmitted virus species, 90% belong to the Begomovirus genus, 6% to the Crinivirus genus and the remaining 4% are in the Closterovirus, Ipomovirus or Carlavirus genera. Other named, whitefly-transmitted viruses that have not yet been ranked as species are also documented. The names, abbreviations and synonyms of the whitefly-transmitted viruses are presented in tabulated form together with details of their whitefly vectors, natural hosts and distribution. Entries are also annotated with references. Whitefly-transmitted viruses affecting plants in the European–Mediterranean region have been highlighted in the text.     

检测砂梨潜隐病毒的IC-RT-PCR和TC-RT-PCR的研究

以砂梨为试材,在生物学和血清学检测的基础上,采用免疫捕作RT-PCR穴IC-RT-PCR雪和试管捕作RT-PCR穴TC-RT-PCR雪技术,对苹果褪绿叶斑病毒(Applechloroticleafspotvirus,ACLSV)和苹果茎沟病毒(Applestemgroovingvirus,ASGV)进行了检测分析。结果表明,TC/IC-RT-PCR均能有效检测梨粗提液中的ACLSV和ASGV,分别获得了大小约358bp和499bp的目标扩增片段;但IC-RT-PCR检测ACLSV的效果受到病毒分离株间血清学关系影响。与传统的RT-PCR相比,IC/TC-RT-PCR不仅灵敏度更高,而且不需提取总RNA,可以简化操作程序和减少苯酚、氯仿类有机试剂对人体的伤害和对环境的污染,适合于大量梨样品的病毒快速灵敏检测。     

Isolation of two strains of a new Tombusvirus (Havel river virus, HaRV) from surface waters in Germany

Two virus isolates from water samples — one from a small stream in South Western Germany and another one from the Havel river in North Eastern Germany c. 500 km away, proved to be strains, named S and H, respectively, of a new Tombusvirus for which the name Havel river virus (HaRV) had been suggested previously in a brief account. Immunoelectron microscopical decoration tests and sequence comparisons of the coat proteins indicated that the two HaRV strains are only distantly related to known Tombusviruses. The closest relationships were found to Cucumber necrosis virus. Nothing is known about their natural hosts. Because the S strain of HaRV was isolated in a woody area from a small stream close to its origin, they may be pathogens of trees or wild plants in such habitats.     

甘蔗花叶病研究进展

根据国内外的研究现状,综述了甘蔗花叶病的症状与危害、致病病毒、发病规律、病毒检测及防治措施等方面的研究进展．并提出了今后的研究方向和发展目标。     

H9亚型禽流感病毒的分离与鉴定

从临床表现呼吸困难并伴有啰音、肺部和支气管黄色干酪样栓塞为特征的病鸡肝脾肺混合匀浆中分离到1株病毒（YD株）,该病毒能凝集鸡红细胞并能被AIVH9标准阳性血清抑制,对热不稳定且对热敏感;对鸡胚和番鸭胚的最小致死量分别为10^-7和10^-6,其MDT分别为78h和70h;鸡胚尿囊液毒的HA效价和EID50明显高于番鸭胚尿囊液毒;能扩增出大小约为1027bp的特异性目的片段。结果表明．该分离毒为H9亚型禽流感病毒。     

我国马铃薯主产区病毒病发生情况调查

为了解我国马铃薯病毒病发生情况,在马铃薯主产区黑龙江、内蒙古、甘肃、云南等马铃薯田采集了具有典型病毒病症状的样品、疑似样品和随机无症样品,试管苗和原原种为随机样品,共649份。应用DASELISA方法筛查6种马铃薯主要病毒:PVX、PVY、PVS、PLRV、PVM和PVA。结果表明:129份样品为阳性,PVY的检出率最高,为9.86%,PVS次之,为6.47%;试管苗PVS检出最多,为32份,原原种PVX检出最多,为10份,大田样品PVY病毒发生比例最高,为54份;有38份样品是由多种病毒复合侵染造成的,大田PVY+PVS复合侵染率最高,为2.93%,PVS+PVY+PLRV次之,为0.98%,试管苗PVS+PVM复合侵染率最高,为4.85%。通过历年的检测结果比较,试管苗中PVS病毒检出率最高,原原种中PVX和PLRV病毒成为危害最为严重的病害,大田样品中PVY检出率一直居高不下。     

皖南黄肉种鸡种蛋中禽白血病病毒的感染状态检测

本研究首次通过检测种蛋中禽白血病病毒(ALV)评价了皖南黄父母代肉种鸡的ALV感染状态.收集该鸡群的120枚鸡蛋,取40枚鸡蛋孵化至9～11 d后分别制备CEF,培养10 d,取细胞上清用ELISA试剂盒检测ALV p27抗原.另取80枚鸡蛋卵白直接检测p27抗原,同时分别将80枚鸡蛋卵白接种CEF(DF1),培养10 d后取细胞上清检测p27抗原.比较p27阳性检出率的结果表明,受精蛋孵化9～11 d后制备CEF,再培养10 d的细胞上清检出率(10/36)高于直接检测卵白(17/80)与卵白接种CEF(DF1)的细胞上清(7/80).将经DF1培养后p27抗原阳性样品,用针对ALV-J的单抗JE9做IFA,ALV-J的阳性率为6/7.检测该80枚鸡蛋的卵黄抗体,ALV-J、ALV-AB的抗体阳性率分别为18/80、1/80.结果表明,该皖南黄父母代肉种鸡群存在的外源性ALV感染主要为ALV-J.该研究为ALV的净化提供了可行性检测方法.     

贵州3种马铃薯病毒的DAS-ELISA检测与分析

应用DAS-ELISA法对从贵州省马铃薯种植区采集带症状的202份马铃薯叶片分别进行了PVX、PVY、PLRV 3种马铃薯病毒的检测。结果表明,3种马铃薯病毒在贵州马铃薯种植区表现出比较显著的田间症状,其病毒的发生与气候类型、种薯品种来源、种植方式存在相关性,并结合马铃薯实际生产对其病毒防治措施做了简要讨论。     

广东兰花病毒病的鉴定和检测研究

用建立的ＤＡＣ－ＥＬＩＳＡ法，检测了来自广东省７市１８个场场或兰圃的２０种兰共１５９个感病兰花样本，建兰花叶病毒（ＣｙＭＶ）和齿兰环斑病毒（ＯＲＳＶ）以及ＣｙＭＶ和ＯＲＳＶ复合感染分别在４０，２６和６个样本中检测到，分别占所检测样品的２５．２％，１６．４％和３．８％，占所检测的２０个兰种的５０％（１０／２０），３５％（７／１０）和１５％（３／２０），感染ＣｙＭＶ的兰种有墨兰，文心兰，大花惠兰（组培     

Insertion site of FLAG on foot-and-mouth disease virus VP1 G-H loop affects immunogenicity of FLAG

The G-H loop of the foot-and-mouth disease virus(FMDV) virion contains certain dominant immunogenic epitopes, as well as an arginine-glycine-aspartic acid(RGD) motif that is recognized by cell surface integrin receptors. Previous experiments indicate that it is critical to maintain virus structural integrity when inserting an exogenous epitope into the surface of an FMDV structural protein. However, it remains to be determined how factors such as different insertion positions affect interactions among the virus, cells and host immune system. In this study, one infectious c DNA clone of the swine FMDV Cathay topotype strain O/CHA/90 was constructed. Then, a FLAG marker(DYKDDDDK) was inserted upstream(–4) or downstream(+10) of the RGD motif to generate tagged viruses vFLAG-O/CHA/90 or vO/CHA/90-FLAG, investigating the possibility of expressing foreign antigen and effect on its immunogenicity. Compared to the parental virus, both tagged viruses exhibited similar plaque phenotypes, suckling mouse pathogenicity and antigenicity. Additionally, the FLAGtag insertion position did not change the use of integrin-mediated cell entry by the tagged viruses. Interestingly, both tagged vaccines protected pigs against challenge with the parental virus O/CHA/90 and induced immune responses against FMDV in BALB/c mice and pigs, but only vaccination with vFLAG-O/CHA/90 generated anti-FLAG antibodies. Our findings demonstrated that two sites(RGD–4 and RGD+10) tolerated the insertion of an exogenous gene in the swine FMDV O/CHA/90 strain. However, only RGD–4 was a novel and appropriate inserting site which could tolerate exogenous FLAG. The resultant tagged virus is a promising candidate for FMD vaccine which can be differentiating infected from vaccinated animals(DIVA).