基于微卫星标记对中国Q型烟粉虱早期入侵种群与B型烟粉虱种群的遗传结构分析（英文）

2003年首次在云南昆明发现Q型烟粉虱Bemisia tabaci (Gennadius)传入中国。随后几年时间内, 它在许多省份逐年取代了B型烟粉虱种群。2008年后,Q型烟粉虱基本上成为了中国多数省份农区的优势生物型。为了进一步揭示Q型烟粉虱在中国快速扩散以及取代B型烟粉虱的遗传学基础, 本研究利用11个微卫星位点分析并比较了2003年中国云南昆明Q型烟粉虱入侵种群及其他地点的11个B型入侵种群, 西班牙2个Q型土著种群, 以色列1个Q型入侵种群, 以色列1个B型土著种群, 以及西班牙、 美国与澳大利亚的5个B型入侵种群的遗传结构。结果表明, 中国Q型烟粉虱早期种群（云南昆明种群）可能来自于西部地中海地区。中国B型烟粉虱种群遗传多样性高于西班牙、 澳大利亚、 美国B型种群, 中国B型可能存在多次传入或某个混合种群的再次传入。相对于原产地种群, 中国Q型烟粉虱早期入侵种群与B型烟粉虱种群遗传多样性并没有明显降低, 表明Q型与B型烟粉虱种群可能经历了较小的瓶颈效应或奠基者效应。中国Q型烟粉虱早期入侵种群遗传多样性高于B型烟粉虱种群, Q型烟粉虱这种较高的遗传多样性可能为其较强的生态适应性提供了遗传基础, 有利于Q型烟粉虱在新的环境下快速扩散并取代B型烟粉虱。     

烟粉虱B型与Q型种群遗传多样性的AFLP分析

烟粉虱Bemisia tabaci(Gennadius)是由多种生物型或物种组成的复合种。Q型烟粉虱在我国部分地区正在取代B型烟粉虱成为优势生物型。烟粉虱Q型与B型遗传多样性比较研究为解析这2种生物型入侵的遗传学基础具有重要的意义。本文利用AFLP技术研究了Q型(包括Q1型、Q2型)、B型烟粉虱种群的遗传多样性。结果表明:Q型烟粉虱遗传多样性高于B型烟粉虱;Q1型烟粉虱各项遗传多样性指数均接近于Q2型。最后探讨了AFLP与SSR分子标记的各自特点。     

微卫星位点在Q型烟粉虱入侵种群中的多态性分析

近年来烟粉虱Bemisia tabaci(Gennadius)Q型入侵我国并在部分地区取代B型成为了烟粉虱优势生物型。外来物种的入侵过程及农药使用等因素可影响种群的遗传多样性水平及其遗传结构。本研究分析了4个微卫星位点在Q型烟粉虱入侵种群的多态信息含量(PIC),并在此基础上进行了遗传多样性分析。结果表明这些微卫星位点在Q型烟粉虱入侵种群中具有中度或高度多态性,说明微卫星位点能有效分析Q型入侵种群的遗传多态性。本研究为利用微卫星标记研究Q型入侵种群的遗传结构奠定了基础。     

广东首次发现Q型烟粉虱种群分布

烟粉虱Bemisia tabaci(Gennadius)是全世界分布的刺吸式传毒昆虫,其中Q型烟粉虱自2003年首次在昆明一品红上发现以来,该种群已在全国10多个省份广泛传播,并有逐步取代B型烟粉虱的趋势。然而,作为较早对外开放的沿海省份,广东省一直未有Q型烟粉虱在田间分布危害的报道。本文利用常规PCR、特异B/Q型烟粉虱引物扩增及DNA测序技术,对近期在广州长湴公园扶桑寄主上采集的烟粉虱种群进行了分子鉴定,并对该种群与国内外其它Q型种群的系统发育关系进行了研究。结果表明,在广州长湴公园扶桑寄主上采集的烟粉虱种群为Q型烟粉虱,在660 bp的mtCOI序列中,该Q型烟粉虱与来自江苏、云南及浙江的Q型烟粉虱种群分别有1²个碱基差异;系统进化关系表明该Q型烟粉虱与江苏、云南的Q型烟粉虱最近,其种群的最初起源应为地中海西岸地区。相比B型烟粉虱,Q烟粉虱被认为具有更强的抗药性和传播植物病毒的能力,Q型烟粉虱在广东的首次发现,表明该烟粉虱种群已在广东野外定殖,其扩散动态、寄主范围及危害程度亟待实时监测。     

烟粉虱B型和Q型群体遗传结构的RAPD分析

近20年来,烟粉虱B型传入世界各地并暴发成灾,成为一种重要的农业入侵害虫; 烟粉虱Q型则是近几年引起人们高度重视的一种新的入侵生物型,目前已传入许多国家并造成一定危害。本文利用RAPD分子标记对烟粉虱B型和Q型不同地理种群的遗传结构进行了分析。结果表明：（1）引物H16对烟粉虱B型不同种群扩增的特异带,能有效区分烟粉虱B型和Q型、浙江非B/Q型种群;（2）烟粉虱Q型种群各项遗传多样性指数均比烟粉虱B型的要高;（3）我国烟粉虱Q型来自伊比利亚半岛的可能性比来自中东地区的可能性要大。另外,聚类分析结果提示,RAPD分子标记能有效地区分烟粉虱不同生物型,但可能不适用于生物型之间亲缘关系分析。     

云南Q型烟粉虱种群的鉴定

利用mtDNACOⅠ基因片段作标记,对采自云南昆明一品红上的烟粉虱Bemisiatabaci(Gennadius)种群生物型进行了鉴定。结果表明,该种群COⅠ基因片段(501bp)与摩洛哥Q型、西班牙Q型烟粉虱的相应碱基序列具有极高的同源性,与2种Q型烟粉虱的COⅠ基因仅分别相差3个和4个碱基,同源性分别达到994%和992%。序列分析表明我国云南昆明一品红上存在Q生物型烟粉虱     

新疆地区烟粉虱类群mtDNA COI基因序列分析

采用mtDNA COI序列鉴定了新疆首府城市乌鲁木齐（东经86°40′-88°55′,北纬43°15′-44°20′）和位于该城市以东195 km的烟粉虱暴发危害区吐鲁番市（东经88°05′-89°54′,北纬41°20′-43°35′）的烟粉虱生物型。通过对两地2008-2010年采集的11个样本群体（样本量均超过30头,每个样本群体检测10头以上）进行检测,结果表明,Q型烟粉虱已经传入新疆。2010年,由乌鲁木齐市花卉市场采集到的一品红种群HH-1与吐鲁番市温室采集到的辣椒种群LJ、番茄种群XHS、茄子种群QZ和烟草种群YC为Q型。另外,2010年采自花卉市场的一品红种群HH-2、2009年前采自野外杂草和温室的锦葵种群JK-S、棉花种群ZH-O以及采自吐鲁番市棉田的种群TC1、TC2和TC3仍然属于B型。     

微卫星位点BEM06与BEM23鉴别烟粉虱B型与Q型的有效性

烟粉虱Bemisia tabaci (Gennadius) B型与Q型是烟粉虱复合种中入侵性较强、分布较广的2种生物型, 当前在许多地区混合发生。这2种生物型的快速鉴别对其种群动态调查及入侵生态学研究具有重要价值。为了验证微卫星位点BEM06与BEM23鉴别B型与Q型烟粉虱的有效性, 本研究分析了这2个微卫星位点的等位基因在国内外17个B型、4个Q型、3个非B/Q型烟粉虱种群的分布特点。结果表明: 这2个微卫星位点的联合使用可鉴别B型与Q型烟粉虱, 但是无法有效地将B型、Q型与一些非B/Q型烟粉虱某些个体区分开来。结果提示: 利用微卫星位点BEM06与BEM23鉴别B型与Q型烟粉虱具有一定的局限性, 尤其是田间烟粉虱存在其他生物型时需要慎重使用这种鉴别方法。     

烟粉虱生物型的监测及其遗传结构研究

烟粉虱Bemisia tabaci(Gennadius)是一种重要的农业害虫并包括许多生物型,其中B型和Q型是入侵性较强的2种生物型。文章着重介绍近年来在烟粉虱生物型的监测及其遗传结构方面的研究进展。B型烟粉虱和Q型烟粉虱这2个生物型均已入侵我国,其中多数地区烟粉虱是B型烟粉虱,局部地区有Q型烟粉虱并呈现不断蔓延趋势。微卫星(SSR)分子标记分析结果表明我国B型烟粉虱的入侵来源具有多元化,而云南地区Q型烟粉虱来源比较单一。化学农药的使用能够影响室内种群的遗传结构,降低种群的遗传多样性。基于RAPD、ISSR分子标记的分析结果表明,Q型烟粉虱种群各项遗传多样性指数均比B型烟粉虱的高。今后加强烟粉虱入侵生物型的遗传结构及其种群动态关系等方面的研究,对于揭示烟粉虱的灾变机制及其控制具有重要的意义。     

天津地区寄生烟粉虱的桨角蚜小蜂分子鉴定和遗传多样性分析

挖掘本土天敌资源是害虫生物防治的有效手段。桨角蚜小蜂Eretmocerus spp.是烟粉虱Bemisia tabaci重要的寄生性天敌之一,明确桨角蚜小蜂本地种类及遗传分化关系,对本土天敌资源挖掘具有重要意义。本研究在天津5个地区采集了13个地理、寄主的桨角蚜小蜂种群,利用线粒体mtDNA COI基因片段作为分子标记,进一步通过MEGAX、DnaSP 5.10等软件进行遗传分化分析。结果表明,本研究所采种群中包含2种桨角蚜小蜂,其中测得蒙氏桨角蚜小蜂Eretmocerus mundus mtDNACOI基因序列20条(755 bq),未命名桨角蚜小蜂Eretmocerus sp. WTT-2016 mtDNA COI基因序列20条(739 bq)。两种桨角蚜小蜂的遗传多样性均较低,其中蒙氏桨角蚜小蜂Hd=0.368,Pi=0.00557,K=4.205;未命名桨角蚜小蜂Hd=0.616,Pi=0.00106,K=0.784。错配分析表明,蒙氏桨角蚜小蜂在天津种群较稳定,近年来未出现扩张现象。     

Genetic differentiation of Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) biotype Q based on mitochondrial DNA markers

In the present study, genetic differentiation of Bemisia tabaci (Gennadius) biotype Q was analyzed based on mitochondrial cytochrome oxidase I (mt COI) gene sequence. The results showed that B. tabaci biotype Q could be separated into two subclades, which were labeled as subclades Q1 and Q2. Subclade Q1 was probably indigenous to the regions around the Mediterranean area and subclade Q2 to Israel or Cyprus. It was because B. tabaci was composed of several genetically distinct groups with a strong geographical association between more closely related biotypes. Not all of the B. tabaci biotype Q in the non‐Mediterranean countries come from the same regions. Until now, all B. tabaci biotype Q in China were grouped into subclade Q1. The B. tabaci biotype Q introduced into the US included both subclades Q1 and Q2. The genetic structure analysis showed higher genetic variation of subclade Q1 than that of subclade Q2.     

Susceptibility of the tobacco whitefly,Bemisia tabaci (Hemiptera: Aleyrodidae) biotype Q to entomopathogenic fungi

Recently, the Q biotype of tobacco whitefly has been recognized as the most hazardous strain of Bemisia tabaci worldwide because of increased resistance to some insecticide groups requiring alternative strategies for its control. We studied the susceptibility of this biotype of B. tabaci to 21 isolates of Beauveria bassiana, three isolates of Isaria fumosorosea, one isolate of I. cateni, three isolates of Lecanicillium lecanii, one isolate of L. attenuatum, and one isolate of Aschersonia aleyrodis. These isolates were evaluated on pruned eggplant seedlings, at a concentration of 10⁸ conidia/mL (deposited at 6000±586 conidia mm^?2). The mortality based on mycosis varied from 18 to 97% after 6 days. Isaria fumosorosea isolate Pf04, B. bassiana isolates Bb06, Bb12, and L. lecanii L14 were found the most effective. Furthermore, five isolates were chosen for concentration–mortality response assays and compared to B. bassiana GHA as a standard. The numbers of nymphs infected by fungi were correlated with the spore concentration. L. lecanii L14 and I. fumosorosea Pf04 had the shortest LT₅₀ at 3.5 and 3.3 days at 6000±586 conidia mm^?2. Mortality declined and LT₅₀ values were longer as the concentration of conidia was reduced. The LD₅₀ values were calculated as 87, 147, 191, 263, and 269 conidia mm^?2 for isolates L14, GHA, AS1260, Bb13, and Pf04, respectively. These results indicated that the Q biotype of sweetpotato whitefly was susceptible to the five isolates of entomopathogenic fungi and these isolates have potential to be developed as microbial pesticides for whitefly control.     

Distribution and molecular characterization of distinct Asian populations of Bemisia tabaci (Hemiptera: Aleyrodidae) in Japan

Bemisia tabaci (Gennadius) is considered to be the most economically important pest insect worldwide. The invasive variant, the Q biotype of B. tabaci was first identified in 2004, and has caused significant crop yield losses in Japan. The distribution and molecular characterization of the different biotypes of B. tabaci in Japan have been little investigated. In this study, B. tabaci populations were sampled from the Japanese Archipelago, the Amami Archipelago and the Ryukyu Islands between 2004 and 2008, and the nucleotide sequences of their mitochondrial cytochrome oxidase I genes were determined. Bayesian phylogenetic relationship analysis provided the first molecular evidence that the indigenous Japanese populations could be separated into four distinct genetic groups. One major native population from the Japanese Archipelago, given the genetic group name Lonicera japonica, was separated into an independent group, distinct from the other genetic groups. The second major population, the Nauru biotype in the Asia II genetic group, was identified in the Amami Archipelago and the Ryukyu Islands. Two distinct minor genetic groups, the Asia I and the China, were also identified. One invasive B‐related population belonging to the Mediterranean/Asia Minor/Africa genetic group has been identified in Honshu. All lineages generated by the phylogenetic analyses were supported by high posterior probabilities. These distinct indigenous B. tabaci populations developed in Japan under geographical and/or biological isolation, prior to recent invasions of the B and Q biotypes.     

利用mtCOI PCR-RFLP技术鉴定中国境内九个烟粉虱隐种

烟粉虱Bemisia tabaci (Gennadius)是一个物种复合体, 包括31个以上形态上无法区分的隐种, 其中少数隐种是世界性入侵害虫。目前, 在中国境内分布有2个入侵隐种和13个土著隐种。快速、 高效的鉴别方法对掌握烟粉虱田间发生规律及制定相关防控策略具有重要意义。然而到目前为止, 除了mtCOI基因测序比对外, 尚未有一种简便的方法可以有效地区分多个烟粉虱隐种。本研究采用mtCOI PCR-RFLP技术, 单独或组合使用TaqI, VspI, Van91I, NcoI和FokI这5种限制性内切酶, 酶切烟粉虱mtCOI的PCR扩增片段, 鉴别分布在中国境内的9个烟粉虱隐种。结果表明, 单独使用TaqI酶切, 可鉴别出MEAM1和China 1两个隐种, 使用TaqI+NcoI分步酶切可鉴定出MED和Asia 1两个隐种, 使用TaqI+Van91I分步酶切可鉴定出Asia II 3和Asia II 9两个隐种, 使用TaqI+VspI+FokI分步酶切可鉴定出Asia II 1, Asia II 6和Asia II 7 3个隐种。本研究为高效鉴别中国境内的多个烟粉虱隐种提供了方法。     

Isolation and characterization of microsatellite loci in Bemisia tabaci (Hemiptera: Aleyrodidae)

Microsatellite‐enriched genomic libraries were obtained from the whitefly Bemisia tabaci (Hemiptera: Aleyrodidae) using a magnetic/biotin capture of repetitive sequences. Ten dinucleotide markers were successfully isolated and characterized from these libraries. Variability was assessed in six populations of B. tabaci collected from different localities of the island of Crete, Greece. The number of alleles per locus in approximately 105 individuals screened across populations ranged from two to 13. Averaged observed heterozygosity over the six populations ranged from 0.001 to 0.58.     

利用RAPD-PCR方法鉴定我国烟粉虱的生物型

收集了国内北京、山东、广东和海南等14个省市23个地区的蔬菜、园林花卉和杂草上的23个烟粉虱Bemisia tabaci (Gennadius)种群,根据报道合成了一个随机引物H₁₆,运用RAPD-PCR技术对所收集的烟粉虱种群进行了生物型鉴定。结果表明在23个烟粉虱种群中,有17个种群同属于危害严重的“B生物型”,这些种群主要分布在交通便利的城市或沿海地区,而非B生物型则主要分布在交通不便的山区或内陆。对烟粉虱B生物型的分布与寄主植物和环境条件进行了初步的探讨。     

Genetic mutations associated with chemical resistance in the cytochrome P450 genes of invasive and native Bemisia tabaci (Hemiptera: Aleyrodidae) populations in China

Abstract  Bemisia tabaci (Gennadius) is a species complex, and its two most damaging biotypes B and Q are globally distributed pests. Despite increasing biological and economic impacts, little is known about the evolutionary mechanisms that favor their competition with native populations. Here, we investigated the genetic mutations in the P450 gene of the invasive B, Q biotypes and the native Cv population. Four mutations associated with chemical resistance, Pro-Leu, Ala-Ser, Ser-Phe and Trp-Leu, were found in the cytochrome P450 CYP6C and CYP9F genes of the B and Q biotypes. Bioassay results also revealed that both the B and Q biotypes have about 12–47 times more resistance to acephate, beta-cypermethrin, methomyl, and 5–7 times more resistance to imidacloprid insecticide than Cv population. Our results provide a molecular approach for better understanding and monitoring the pesticide resistances of invasive and native B. tabaci populations in China.