转Bt基因抗虫玉米的研究

对转Bt基因抗虫玉米的研究概况、转化方法、转化体的鉴定方法、遗传评价以及其存在的问题进行了综述.     

转Bt 基因甘蔗抗虫性及重要经济、农艺性状的评价

为评价转Bt基因甘蔗的抗虫性,对6份转Bt甘蔗品系(Y2、Y3、Y4、T1、T2和T3)进行室内抗虫性鉴定实验和田间自然感虫的抗虫性评价。结果表明,室内人工抗虫性鉴定结果与田间自然感染结果大体吻合,各参试材料在两个试验点的抗虫性表现基本一致,Bt基因表达稳定,所有参试品系抗虫性均明显比相应的供体品种强,其中Y4和T2的抗性最强,T3相对较弱;在经济性状方面,Y3、Y4和T3的蔗茎产量、含糖量与其供体品种‘新台糖16号’相当,但甘蔗蔗糖含量较低;T2的甘蔗蔗糖含量则超过其供体品种‘新台糖16号’,但农艺性状较差,茎产量和含糖量低。     

转Bt基因植物中外源基因时空动态表达的研究现状

在转Bt基因植株中 ,外源基因的时空动态表达对于害虫的防治和转基因安全评价管理具有重要意义。利用生物测定法和酶联免疫吸附测定法 (ELISA) ,对植物不同组织在同一发育阶段、同一组织在不同的发育阶段以及不同转基因植株的外源基因的时空动态表达进行研究。本文综述了转基因植物中外源基因时空动态表达的研究进展和现状。     

不同生长期转Bt基因水稻秸杆还土对淹水土壤酶活性的影响

在实验室条件下通过秸杆还土试验比较了不同生长期转Bt基因克螟稻及其亲本稻秸杆对淹水土壤酶活性的影响。研究结果表明,与同一生长期的亲本稻秸杆相比,孕穗期和成熟期克螟稻秸杆对淹水土壤磷酸酶活性的影响较小;相反,对淹水土壤脱氢酶活性的影响非常显著,并且孕穗期秸杆与成熟期秸杆的添加对淹水土壤脱氢酶活性的影响趋势也存在较大差异。推测造成淹水土壤脱氢酶活性的显著性差异的主要原因可能是由于Bt插入基因表达的多效性所致。结果认为土壤脱氢酶活性可作为转Bt基因水稻生态安全风险性评价的潜在指标。     

杨树NL-80106转Bt基因植株的获得及抗虫性

通过根癌农杆菌(Agrobacterium tumefaciens)介导将苏云金杆菌(Bacillus thuringiensis)毒蛋白基因Bt转入杨树NL-80106(美洲黑杨×小叶杨,Populus deltoides×Populus simonii),获得了再生植株.PCR及PCR-Southernblotting的分析结果表明,Bt基因已整合到基因组中.部分转基因植株的杀虫实验表明,转基因植株B45和B64对一龄舞毒蛾(Lymantria dispar Linn.)幼虫有明显抗性,饲喂转基因杨树叶片的幼虫死亡率显著高于未转基因的对照植株.     

甘蔗螟虫趋光性研究

甘蔗螟虫具有趋光性,但不同种及性别之间对特定波长光的趋性差异没有详细研究。本文研究3种甘蔗螟虫的雌雄成虫对不同波长光波的行为反应,为该类害虫的灯诱防控应用提供参考依据。试验结果显示,条螟趋光率最高的3个波长为340 nm、460 nm、498 nm,趋光率分别为23.1%、18.2%、18.1%;二点螟趋光率最高的 4个 波长为498 nm、520 nm、380 nm、420 nm,趋光率分别为21.7%、17.2%、15.3%、13.2%;黄螟对各检测光源表现弱的趋光性,趋光率最高为9.2%（光波长582 nm）。3种螟虫不同日龄趋光性有强弱的差异,以3 d 趋光性最强,其次是1 d ,最后是5 d 。条螟、二点螟雌雄蛾趋光率有差异,雄蛾高于雌蛾;交配行为会降低螟蛾趋光率,条螟雄蛾交配前后降幅高达16.6%,已交配的条螟雌蛾则失去趋光反应;二点螟雄蛾交配前后降幅最高达21.7%,已交配的二点螟雌蛾趋光率也一样有较大幅下降,未交配的雌蛾与已交配的雌蛾同一波长的趋光率差异显著。条螟和二点螟主要趋光波长较接近,波段有较好的交集,诱虫灯的开发可以选择这2种虫趋光率较高的几个光波长研究。     

转Bt基因玉米的生态安全性研究进展

随着转基因作物的应用和推广 ,转 Bt基因作物释放后对生态环境及其它方面产生的潜在影响越来越受到重视。分别从生物活性杀虫晶体蛋白在土壤中的残留特性、杀虫晶体蛋白对土壤中非目标生物的影响、转 Bt基因玉米植株体成分的变化、转Bt基因玉米花粉中杀虫晶体蛋白的表达特性及其在田间和马力筋叶片上的散积状况、花粉中表达的杀虫晶体蛋白对君主斑蝶的毒性、君主斑蝶幼虫暴露在 Bt花粉中的概率及综合风险评价估算等方面对转 Bt基因玉米产生的杀虫晶体蛋白与土壤生态环境的相互作用、花粉对非目标生物影响的研究现状进行了综述。通过对转 Bt基因作物生态安全性的科学评价和广泛宣传 ,以确保生物技术的健康发展。     

转Bt基因棉对棉大卷叶螟种群动态的影响

2年的研究发现,棉大卷叶螟SyleptaderogataFabricius的种群数量在不同棉花品种田均呈现上升趋势,但转基因抗虫棉“国抗2 2”的为害程度及百株虫量均小于亲本对照棉“泗棉3号”,其差异达显著或极显著水平;该虫的室内饲养结果表明,2个棉花品种均有利于棉大卷叶螟的增殖,但“国抗2 2”对棉大卷叶螟的抗性明显优于“泗棉3号”,且对棉大卷叶螟成虫存在一定的产卵排斥效应。     

转基因抗虫棉Bt基因不同剂量的聚合与抗虫性表现

通过有性杂交手段培育出聚有不同数目Bt基因的植株,在不同生育期进行抗虫性测定和Bt毒蛋白表达的ELISA检测,旨在揭示聚合不同数目Bt基因的植株抗虫性的互作表达机理。聚合有1－4个Bt基因的植株在整个生育期的抗虫性、毒蛋白表达特性和单价抗虫棉时空表达一致,生育前期抗虫性好、毒蛋白表达量高;生育中、后期抗虫性有所下降,毒蛋白表达量降低。聚合有4个Bt基因的纯合材料并未因Bt基因的增加而起到抗性增强的效果,相反还因同源抑制而有所降低。不同来源的Bt基因处于杂合状态时其抗虫性和Bt毒蛋白量均得到充分表达。     

棉铃虫对Bt生物农药早期抗性及与转Bt基因棉抗虫性的关系

用饲料感染法建立了棉铃虫Helicoverpa rmigera(Hubmer)敏感品系(SUS1)对Bt生物农药的敏感毒力基线和区分剂量,1995年测定了五省六县棉铃虫初孵幼虫对Bt生物农药的敏感性,结果表明：山东阳谷、河北邯郸、河南新乡、安徽萧县及江苏丰县棉铃虫已产生早期抗性,抗性个体百分率为5%～10%,与敏感品系相比,LC₅₀值稍有增加,但斜率b值明显变小;而江苏东台棉铃虫仍属敏感。这是国内外首次诊测到棉铃虫对Bt生物农药抗性。用棉叶喂饲法测定比较了转Bt基因棉花品系对不同种群棉铃虫的抗虫性效果,结果表明：用早期抗性的阳谷和新乡棉铃虫初孵幼虫接虫5d后平均死亡率较敏感品系下降16%～29%,说明棉铃虫对Bt农药与转Bt生物基因棉花品系间存在交互抗性。还讨论了Bt农药的抗性治理对策。     

基因组学与昆虫抗药性研究

主要综述近年来基因组学技术在昆虫抗药性研究中的应用以及取得的新成果、新进展。基因组学是对生物体整个基因组结构、功能及其进化的研究。遗传连锁作图、定位克隆、数量特性位点作图、微阵列分析及转录沉默等 ,是近年来常用的基因组学研究技术。研究表明 ,应用基因组技术不仅能揭示新的昆虫抗药性机制 ,发现并定位、克隆新的抗药性基因 ,还有助于发现新型的杀虫剂作用靶标 ,改进昆虫抗药性的检 (监 )测技术以及加深人们对昆虫抗药性进化的认识等。     

害虫抗药性的显性水平与抗性进化

对杀虫剂的代谢抗性和主要靶标抗性的显性水平作了理论解释,其中包括昆虫对Bt抗性的显性水平的解释。并对抗性显性具有的多变性作了阐述。分析抗性显性水平与抗药性进化的关系,认为在抗性进化早期抗性表现为显性的基因频率上升快于抗性表现为隐性时;但在抗性等位基因频率较高且出现抗性纯合子个体时,抗性表现为隐性的基因频率上升显著快于抗性表现为显性时。最后论述抗性显性在抗性治理中的应用。     

昆虫抗药性分子机制研究的新进展

昆虫抗性机制的研究对于抗性监测、治理及新农药的研制具有重要意义。在过去几十年中,人们对与昆虫杀虫剂抗性有关的昆虫行为、生理代谢活动以及作用靶标等进行了广泛的研究。已经证实,昆虫的抗药性与行为改变、生理功能改变、解毒功能增强以及靶标不敏感性有关。近年来,随着分子生物学以及昆虫基因组学的发展,昆虫抗药性的分子机理有了突破性进展,已发现并克隆了一些靶标基因,与抗药性相关的基因突变也得到广泛验证。本文综述了昆虫的抗药性机理在分子生物学上的研究最新进展,重点阐述了与昆虫抗性相关基因的扩增、表达及基因结构的改变等相关内容。     

昆虫对Bt作物抗性监测技术

Bt棉花等转抗虫基因作物已在许多国家商业化种植 ,靶标昆虫的潜在抗性是广泛关注的重要问题。为了准确地监测昆虫的抗性动态 ,近年来在传统的基于标准生物测定确定抗性指数的基础上先后发展了诊断剂量、单对杂交、F2 代检测和分子生物学检测抗性等位基因等抗性监测方法。该文综述了相关的研究进展。     

昆虫抗药性与适合度

昆虫抗药性的产生常伴有适合度劣势(即适合度代价),即抗性个体常表现出发育速率较慢、存活率和生殖力较低。文章主要阐述害虫抗药性与生物适合度和适合度代价的关系以及适合度代价产生的机制、特性及影响因素。并从生态学角度论述害虫抗药性的进化,为探索抗性发展规律及害虫抗性治理提供理论依据。     

Use of introgression lines and zonal mapping to identify RAPD markers linked to QTL

RAPD primers were identified as giving parent-specific bands when screened with a set of introgression lines containing introgressed regions of Lycopersicon pennellii that encompass 5 quantitative trait loci affiliated with the production and composition of acylsugars, compounds associated with insect resistance. Primers giving L. pennellii introgression specific bands were zonally mapped to identify bands affiliated with the quantitative trait target and flanking regions using subsets of 7 to 16 F2 individuals which contained small overlapping segments (zones) of the L. pennellii genome spanning those regions. Seventeen RAPD primers, agt-related primers, and an agt clone were then used in mapping the complete F2 population of 144 individuals. This work resulted in the identification of RAPD markers for three of the 5 quantitative trait loci and the construction of an integrated RAPD/RFLP genomic map for tomato (Lycopersicon esculentum x L. pennellii LA716) of 111 RAPD and 8 acylglucose transferase related markers added to a framework map of 150 RFLP markers.     

新银合欢品种抗榕片圆蚧的选择研究

通过引进新银合欢品系6个品种在相同环境条件下,同一时间、同一林地内种植,5年后经调查比较,结果表明,新银合欢6个品种抗榕片圆故的能力有明显的差异,其中以K156最强,K191最差,排序为：K156＞K67＞K45＞K192＞K8＞K191。K156是金沙江干热河谷抗虫、速生、丰产的优良树种。     

Testing transgenes for insect resistance using Arabidopsis

One possible strategy to delay the selection of resistant insect populations is the pyramiding of multiple resistance genes into a single cultivar. However, the transformation of most major crops remains prohibitively expensive if a large number of transgene combinations are to be evaluated. Arabidopsis thaliana is a potentially good plant for such preliminary evaluations. We determined that four major agricultural pests, Spodoptera exigua, Helicoverpa zea, Pseudoplusia includens, and Heliothis virescens grew as well when feeding on Landsberg Erecta Arabidopsis as they did on plants of Cobb soybean. Landsberg Erecta was then transformed with either a synthetic Bacillus thuringiensis cryIA(c) gene, or the cowpea trypsin inhibitor gene. Transformed plants were crossed to produce plants transgenic for both genes. Following quantification of transgene expression, the four caterpillar species were allowed to feed on wild-type plants, plants expressing either cryIA(c) or the cowpea trypsin inhibitor gene, or plants expressing both. Both genes reduced growth of the species tested, but cryIA(c) was more effective in controlling caterpillar growth than the cowpea trypsin inhibitor gene. The resistance of plants with both transgenes was lower than that of plants expressing the cryIA(c) gene alone, but higher than that of plants expressing the only the CpTI gene. This could be due to a lower concentration of Cry protein in the hemizygous F1 plants. Thus, if the cowpea trypsin inhibitor had any potentiation effect on cryIA(c), this effect was less than the cryIA(c) copy number effect. Alternatively, expression of the trypsin inhibitor gene could be antagonistic to the function of the cryIA(c) gene. Either way, these results suggest that the combined use of these two genes may not be effective.     

Discovery and utilization of QTLs for insect resistance in soybean

Insect resistance in soybean has been an objective in numerous breeding programs, but efforts to develop high yielding cultivars with insect resistance have been unsuccessful. Three Japanese plant introductions, PIs 171451, 227687 and 229358, have been the primary sources of insect resistance alleles, but a combination of quantitative inheritance of resistance and poor agronomic performance has hindered progress. Linkage drag caused by co-introgression of undesirable agronomic trait alleles linked to the resistance quantitative trait loci (QTLs) is a persistent problem. Molecular marker studies have helped to elucidate the numbers, effects and interactions of insect resistance QTLs in the Japanese PIs, and markers are now being used in breeding programs to facilitate transfer of resistance alleles while minimizing linkage drag. Molecular markers also make it possible to evaluate QTLs independently and together in different genetic backgrounds, and in combination with transgenes from Bacillus thuringiensis.     

A hybridisation technique to identify anthelmintic resistance genes in Haemonchus

The identification of genes associated with anthelmintic resistance can be facilitated in Haemonchus contortus by the ability of this species to hybridise with Haemonchus placei. Although the hybrid males are sterile, the lines can be rescued by backcrossing the females to either parental species. Resistance genes can be retained in Haemonchus hybrids, while the unwanted contortus background is removed through backcrossing to H. placei and anthelmintic selection of the progeny. Under this selection, genes involved in resistance would retain the H. contortus nucleotide sequence, while those that are not would either be H. placei or a random mixture of both, depending on the amount of backcrossing that had occurred. The first candidate gene to be tested in this system was a Haemonchus P-glycoprotein, hcpgp-1. hcpgp-1 was amplified, cloned and sequenced from H. contortus and H. placei. Two restriction sites were then identified in the sequenced product; one specific to H. contortus hcpgp-1 and the other found only in the H. placei gene. These genes were identified from macrocyclic lactone selected and non-selected worms by restricting PCR products from individual worms. Fitted occurrence of the H. contortus allele was 49% of unselected worms and 69% of macrocyclic lactone selected worms. The probability of this percentage occurring by chance was P=0.006. Thus macrocyclic lactone selection was acting to increase the percentage of hcpgp-1 from macrocyclic-lactone-resistant CAVRS.