西花蓟马传播番茄斑萎病毒研究进展

西花蓟马Frankliniella occidentalis是世界性重要检疫性害虫之一,不仅直接取食危害作物而且传播病毒,从而造成极为严重的经济损失。由于西花蓟马在我国具有广泛的适生范围,随其入侵我国并随之传播的番茄斑萎病毒(Tomato spotted wilt virus)已在我国不同地域发现,对经济作物已形成严重威胁。本文综述了西花蓟马对番茄斑萎病毒的获取、携带和传播扩散过程及其病毒在蓟马体内的循环过程和机理,总结了影响西花蓟马传播番茄斑萎病毒效率的因素,并评述了西花蓟马-病毒-植物这一互作系统及其对西花蓟马生长发育适合度的影响,以期为我国西花蓟马传播番茄斑萎病毒的基础研究和防控提供理论依据与指导。     

云南省红河地区传播番茄斑萎病毒属病毒的蓟马及其寄主植物种类调查

2011年7月至2012年8月对云南省红河州传播番茄斑萎病毒属(Tospovirus)病毒的蓟马种类及其寄主植物进行了系统调查。明确了西花蓟马、花蓟马、烟蓟马和棕榈蓟马4种为传毒蓟马。其寄主植物主要有辣子草、粉花月见草、茴茴蒜等30种以上田间杂草和白菜、蚕豆、番茄等超过20种作物。     

危险性外来入侵害虫——西花蓟马的鉴别、危害及防治

西花蓟马(Frankliniella occidentalis)及其所传播的番茄斑萎病毒(TSWV)已被许多国家列为检疫性病虫害, 对多种蔬菜、花卉、果树造成严重危害。本文对其主要鉴别特征、分布危害、生物学习性和控制技术作了简要介绍。     

北京地区发现番茄斑萎病毒

通过采用特异快速试纸条以及进一步的RT-PCR和序列测定证实,在北京局部地区的辣椒和茄子上已发生番茄斑萎病毒,这两种作物上同时发生的蓟马种类主要为西花蓟马,并且携带该病毒。番茄斑萎病毒病是极其危险的一种病害,可对作物造成毁灭性灾害。建议有关部门立即采取相应的预防与管理措施,防止其扩散蔓延。     

侵染广西甜椒的西瓜银斑驳病毒分子鉴定

西瓜银斑驳病毒(Watermelon silver mottle vi-rus,WSMoV)为布尼亚病毒科(Bunyaviridae)番茄斑萎病毒属(Orthotospovirus)病毒,通过蓟马以持久增殖型方式传播,主要危害番茄、辣椒、西瓜等茄科和葫芦科作物,引起褪绿轮纹、环斑、皱缩等症状,造成严重的经济损失[1]....     

Q型烟粉虱对番茄斑萎病毒的获取、保持及在非传毒寄主棉花上的适合度

正番茄斑萎病毒(tomato spotted wilt virus,TSWV)可使花生、番茄、辣椒和曼陀罗等多种植物致病,西花蓟马Frankliniella occidentalis是其媒介昆虫,而烟粉虱Bemisia tabaci并不能高效传播TSWV,为非媒介昆虫(Pan et al.,2013)。植物病毒不仅可以与媒介昆虫发生相互作用,还可以直接或间接修饰非媒介昆虫的行为,导致非媒介昆虫适合度的改变(Chen et al.,2017)。田间自然条件下,Q型烟粉虱在感染TSWV的寄主上取食,TSWV可能对携毒Q型烟粉虱的寄     

深度测序技术分析番茄斑萎病毒病害寄主及介体中病毒种类

 正番茄斑萎病毒属病毒(orthotospoviruses)是严重危害云南蔬菜等重要农业经济作物的病毒病原之一。采用血清学检测、小RNA深度测序以及RT-PCR验证相结合的方法,从云南省昆明市晋宁区的主要作物寄主(番茄、辣椒、油麦菜)、重要中间寄主(鬼针草)和传毒介体(蓟马)中鉴定到TSWV、TZSV、PCSV和INSV 4种病毒,其中TSWV为该地区的主要优势病毒,而PCSV则是首次报道侵染鬼针草。通过对云南番茄斑萎病毒病害重病区作物寄主、中间寄主及蓟马三者进行病毒种类分析研究,明确TSWV为引起云南省昆明市晋宁区作物的主要病毒,TZSV、PCSV和INSV零星发生于不同寄主中。     

露地栽培番茄斑萎病毒病发生流行规律调查及TSWV重要寄主植物监测

为明确云南省昆明市露地栽培条件下番茄斑萎病毒病的发生流行特征,于2014—2015年采用病害系统调查法结合病毒ELISA及RT-PCR检测方法研究露地栽培条件下由番茄斑萎病毒(tomato spotted wilt virus,TSWV)引起的病毒病发生规律及其重要寄主种类,并研究利用防虫网隔离蓟马对番茄斑萎病毒病的防控效果。结果表明:番茄斑萎病毒病在露地番茄主要种植期3—10月普遍发生,番茄苗期和移栽初期是该病毒病防控的关键期,带毒种苗调运是该病毒病的主要传播途径;田间多种茄科和菊科植物是TSWV的重要中间寄主。在田间,菊科寄主植物油麦菜、莴苣、鬼针草、牛膝菊上TSWV的检出率均较高,在42.53%～81.63%之间;茄科寄主植物中辣椒上TSWV的检出率最高,为41.99%,其次为马铃薯,TSWV检出率为27.78%,在番茄上TSWV的检出率为19.02%,因此生产中应对这些TSWV重要中间寄主给予更多关注和防控。应用防虫网能有效隔离蓟马,使番茄斑萎病毒病发病率和病情指数较对照分别降低了6.44个百分点和5.31,可有效降低番茄苗期及定植期斑萎病毒病的发生。     

西瓜和甜瓜上西瓜银斑驳病毒的鉴定及广西分离物S RNA序列分析

<正>0引言西瓜银斑驳病毒(watermelon silver mottle virus,WSMoV)是番茄斑萎病毒科(Tospoviridae)正番茄斑萎病毒属(Orthotospovirus)病毒，主要通过蓟马以持久增殖型方式传播^[1-2]。WSMoV病毒粒子球状，外具包膜，基因组为三分体负单链RNA，分别为L RNA、M RNA和S RNA^[1,3]。1982年IWAKI等最先在日本冲绳县发现WSMoV为害西瓜，在叶片上产生银色斑驳症状，遂命名为西瓜银斑驳病毒^[4]；随后，中国台湾、泰国、印度等地陆续报道该病毒^[1,5-6]。     

云南辣椒正番茄斑萎病毒属病毒的分子鉴定

辣椒是云南省主要经济作物之一,近年来病毒病尤其是正番茄斑萎病毒属病毒发病严重,影响了辣椒产量和品质。利用RT-PCR技术对从云南辣椒主产区采集的疑似感染正番茄斑萎病毒属病毒的25份辣椒样品进行分子鉴定,结果显示,12份样品检测出正番茄斑萎病毒属病毒,检出率为48.0%,其中6份是番茄斑萎病毒tomato spotted wilt orthotospovirus (TSWV),检出率为24.0%;5份是番茄环纹斑点病毒tomato zonate spot orthotospovirus (TZSV),检出率为20.0%;有1份是TSWV和TZSV复合侵染,检出率为4.0%,这是在云南辣椒生产上首次发现TSWV和TZSV的复合侵染。通过鉴定,初步了解正番茄斑萎病毒属病毒在云南辣椒生产中的发生情况和种类,为制定云南地区该属病毒的防治策略提供理论依据。     

花粉和植物不同生长阶段对西花蓟马种群的影响

在凤仙花的Impulse Orange和Cajun Carmine品种上开展了花粉和植物不同生长阶段对西花蓟马种群的影响。结果表明:在植物未开花前,添加花粉和不添加花粉西花蓟马的种群数量差异显著,添加花粉能显著增加两个品种上西花蓟马的种群数量,其西花蓟马数量分别为174.50、43.67头,而未添加花粉时分别为138.33头和27.00头。在植物开花后,添加花粉对西花蓟马的种群数量虽有一定影响,但差异不显著。植物不同生长发育阶段对西花蓟马的种群数量影响很大,无论是添加花粉还是不添加花粉,在两个品种上均表现为开花后的数量显著大于开花前的数量,说明凤仙花植物本身的花对西花蓟马种群的迅速增长影响很大。     

阿维菌素与三种杀虫剂对西花蓟马的联合毒力

阿维菌素是防治西花蓟马的常用药剂,为筛选出对西花蓟马具有增效作用的阿维菌素与其他药剂的混配组合,采用浸叶法测定了阿维菌素、毒死蜱、吡虫啉和吡蚜酮等药剂对西花蓟马2龄若虫的毒力,并通过共毒因子法和共毒系数法分别确定了最佳药剂配伍和最佳复配比例。结果表明,阿维菌素与毒死蜱复配表现出明显的增效作用;阿维菌素与毒死蜱比值为2∶8与8∶2时,增效作用最显著;阿维菌素与吡蚜酮、吡虫啉均表现出拮抗作用。     

竹醋液对西方花蓟马的忌避作用

竹醋液是竹炭加工过程中的副产品,为纯天然产品,在农业上有着广泛的应用。本文在室外笼罩环境下研究了竹醋液对豆株上西方花蓟马成虫的忌避作用。结果显示:竹醋液的不同浓度和同一浓度下的不同处理时间,对西方花蓟马成虫的忌避作用有显著差异。浓度增加显著地提高了竹醋液对西方花蓟马成虫的忌避作用,而忌避作用随时间的延长而逐渐降低。质量分数为2.06%和1.03%的竹醋液对西方花蓟马成虫有明显的忌避作用,前者在使用后10d时其忌避显著下降。本文同时探讨了竹醋液在西方花蓟马控制上应用的可能性。     

北京地区西花蓟马发生为害调查研究

通过2003～2005年对北京地区西花蓟马发生为害情况进行的系统调查监测,发现发生地由2003年的2个点扩大为2005年的6个区,呈蔓延扩散趋势;为害的植物也从最初的辣椒到2005年的28科65种,以葫芦科的荷兰黄瓜、甜瓜及十字花科的白萝卜叶片受害最为严重。另外,就不同寄主上西花蓟马的发生为害动态进行了系统调查,初步分析了其在自然条件下的种群消长规律。     

Acquisition of Tomato spotted wilt virus by Adults of Two Thrips Species

ABSTRACT Only larval thrips that acquire Tomato spotted wilt virus (TSWV), or adults derived from such larvae, transmit the virus. Nonviruliferous adults can ingest virus particles while feeding on TSWV-infected plants, but such adult thrips have not been shown to transmit TSWV. Immunofluorescence microscopy was used to show that thrips 1, 5, 10, and 20 days after adult emergence (DAE) fed on TSWV-infected plants acquired TSWV with virus replication and accumulation occurring in both epithelial and muscle cells of Frankliniella fusca (tobacco thrips [TT]) and F. occidentalis (western flower thrips [WFT]), as indicated by immunodetection of the nonstructural (NSs) protein encoded by the small RNA and the nucleocapsid (N) protein, respectively. Adult WFT acquired TSWV more efficiently than TT. There was no significant effect of insect age on TSWV acquisition by TT. In contrast, acquisition by adult WFT at 1 and 5 DAE was higher than acquisition at 10 and 20 DAE. Subsequent transmission competence of adult cohorts was studied by vector transmission assays. All adult thrips tested that had an acquisition access period as an adult were unable to transmit the virus. These results indicate the susceptibility of adult TT and WFT to infection of midgut cells by TSWV and subsequent virus replication and confirm earlier studies that adult thrips that feed on virus-infected plants do not transmit the virus. The role of a tissue barrier in TSWV movement and infection from midgut muscle cells to the salivary glands is discussed.     

Mechanisms conferring resistance of Western flower thrips to bendiocarb

Mechanisms associated with bendiocarb resistance were examined in two strains of western flower thrips, Frankliniella occidentalis (Pergande), that differed in their susceptibility to this carbamate by 13.6-fold. No appreciable differences between the two strains in [¹⁴C] bendiocarb penetration and excretion were detected; however, bendiocarb was metabolised substantially faster by the resistant KCM thrips than by the more susceptible UMC thrips. No appreciable difference between the two strains was found in the sensitivity of acetylcholinesterase activity to inhibition by bendiocarb. It was concluded that bendiocarb resistance in KCM western flower thrips was due to enhanced metabolism that probably was mainly oxidative in nature.     

Frankliniella occidentalis (Pergande) integrated pest management programs for fruiting vegetables in Florida

BACKGROUND: The spread of the western flower thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae), resulted in the worldwide destabilization of established integrated pest management programs for many crops. Efforts to control the pest and the thrips‐vectored tospoviruses with calendar applications of broad‐spectrum insecticides have been unsuccessful. The result has been a classic ‘3‐R’ situation: resistance to numerous insecticides; resurgence of the western flower thrips populations as a result of natural predators and native competitor thrips being eliminated; replacement by various other pests. This paper reports on integrated pest management programs for fruiting vegetables that are effective, economical, ecologically sound and sustainable. RESULTS: The components include the following: define pest status (economic thresholds); increase biotic resistance (natural enemies and competition); integrate preventive and therapeutic tactics (scouting, ultraviolet‐reflective technologies, biological control, compatible insecticides, companion plants and fertility); vertically integrate the programs with other pests; continually communicate latest science‐based management tactics with end‐users. CONCLUSION: These programs have been widely implemented in Florida and have significantly improved the management of western flower thrips and thrips‐transmitted viruses. Copyright © 2012 Society of Chemical Industry     

Interaction of Tomato Spotted Wilt Tospovirus (TSWV) Glycoproteins with a Thrips Midgut Protein, a Potential Cellular Receptor for TSWV

ABSTRACT Interactions between viral and cellular membrane fusion proteins mediate virus penetration of cells for many arthropod-borne viruses. Electron microscope observations and circumstantial evidence indicate insect acquisition of tomato spotted wilt virus (TSWV) (genus Tospovirus, family Bunyaviridae) is receptor mediated, and TSWV membrane glycoproteins (GP1 and GP2) serve as virus attachment proteins. The tospoviruses are plant-infecting members of the family Bunyaviridae and are transmitted by several thrips species, including Frankliniella occidentalis. Gel overlay assays and immunolabeling were used to investigate the putative role of TSWV GPs as viral attachment proteins and deter mine whether a corresponding cellular receptor may be present in F. occidentalis. A single band in the 50-kDa region was detected with murine monoclonal antibodies (MAbs) to the TSWV-GPs when isolated TSWV or TSWV-GPs were used to overlay separated thrips proteins. This band was not detected when blots were probed with antibody to the non-structural protein encoded by the small RNA of TSWV or the TSWV nucleocapsid protein, nor were proteins from nonvector insects labeled. Anti-idiotype antibodies prepared to murine MAbs against GP1 or GP2 specifically labeled a single band at 50 kDa in Western blots and the plasmalemma of larval thrips midguts. These results support the putative role of the TSWV GPs as viral attachment proteins and identified potential cellular receptor(s) in thrips.     

Dynamics of Tomato spotted wilt virus Replication in the Alimentary Canal of Two Thrips Species

ABSTRACT Transmission of Tomato spotted wilt virus (TSWV) is dependent on virus uptake in the midgut prior to virus movement to the salivary glands. Replication of TSWV in the alimentary canal of tobacco thrips (TT, Frankliniella fusca) and western flower thrips (WFT, F. occidentalis) was investigated by immunolocalization of the nonstructural protein (NSs) encoded by the small RNA of TSWV and fluorescence microscopy. Analysis of cohorts during development from larva to adults following virus acquisition by first instar larva indicated that virus replication followed a specific time-course pattern in the foregut, regions of the midgut, salivary glands, and ligaments between the midgut and salivary glands. Initial virus replication occurred only in epithelial cells of midgut-1 but, upon infection of muscle cells, the virus moved to the midgut-2, foregut, midgut-3, and salivary glands. The ligaments between the midgut and salivary glands appeared to be a route for virus to invade the salivary glands. No virus replication was observed in the hindgut, Malpighian tubules, or tubular salivary glands. The dynamics of TSWV replication, as measured by NSs accumulation, were similar in both TT and WFT.