盐城棉区棉铃虫田间种群对Bt蛋白的抗性基因频率

【背景】转Bt基因抗虫棉已经在我国进行了近20年的大规模商业化种植,产生了显著的经济和环境效益。但是,靶标害虫棉铃虫的抗性是转Bt基因抗虫棉产业健康发展所面临的最大问题,而抗性监测是解决这一问题的必要管理措施。盐城市是江苏省转基因抗虫棉的主产区,但有关该地区棉铃虫对转Bt基因抗虫棉的抗性基因频率未见报道。【方法】于2012年在盐城三龙镇和东台镇棉区采集田间棉铃虫种群,检测了初孵幼虫对花铃期转Bt基因抗虫棉中30幼嫩叶片的敏感性,用区分剂量法检测了2龄幼虫对Bt蛋白的抗性基因频率。【结果】取食转Bt基因抗虫棉叶片后,棉铃虫初孵幼虫在9 d内全部死亡;三龙镇和东台镇棉铃虫2龄幼虫对Bt蛋白的抗性基因频率分别为7.6×10-3和6.9×10-3。【结论与意义】目前,盐城棉区的棉铃虫对转Bt基因抗虫棉仍保持很高的敏感性,棉铃虫种群对Bt蛋白的抗性基因频率没有发生显著变化,但仍需持续监测。     

转基因棉花Bt毒蛋白的表达及其生态学效应

苏云金杆菌毒蛋白 (Bacillusthuringiensisgtoxicprotein)基因导入棉花植株后获得的转Bt棉可以特异性地毒杀棉铃虫及鳞翅目的一些其它害虫 ,有效地保护棉花植株不受此类棉花害虫的危害。Bt毒蛋白在棉花植株中的表达受一些内外界因素的影响而呈明显的时空变化。转Bt棉除了严重影响靶标害虫自身外 ,还能对其它一些非靶标昆虫和环境产生影响。另外 ,该文还对害虫对Bt棉的抗性以及防止害虫产生抗性的治理对策进行了综述     

棉铃虫对Bt杀虫剂的抗性遗传方式

随着转基因棉花种植面积的日益增加,棉铃虫Helicoverpa armigera（Hübner)对Bt的抗性已经成为一个不容忽视的问题。发展转多价基因作物是当前缓解害虫对Bt抗性的最有效措施。本研究以经室内多年筛选的、抗性倍数达2 000多倍的Bt杀虫剂（含多种蛋白）抗性品系为材料,通过生物测定和不同的杂交试验,测定棉铃虫对Bt杀虫剂的抗性遗传方式,以期为Bt生物农药的抗性治理提供一定的依据,同时为制定棉铃虫对转多基因作物的抗性治理策略提供一定的参考。对敏感亲本和抗性亲本杂交产生的F1代的研究结果表明,杂交品系的抗性倍数分别为22.2倍和24.6倍;抗性显性度D值均小于0,分别为-0.20和-0.17,抗性为常染色体不完全隐性遗传。对4种回交后代和2种自交后代F2的研究结果表明,实际死亡率与期望死亡率差异较大,说明抗性是由单基因多个位点或多基因控制。     

棉铃虫对转Bt基因抗虫棉花的抗性机制及治理

棉铃虫是危害棉花最严重的害虫之一. 作为生物技术产品, 转Bt杀虫基因棉花产生的Cry毒素对棉铃虫有高效毒杀作用. Bt棉花已在世界范围内商业化种植, 通过有效控制棉铃虫种群数量, 而显著减少了化学农药的用量. 尽管没有发现棉铃虫田间种群对Bt棉花产生高水平抗性, 但室内持续筛选已培育出多个高水平抗性品系, 表明存在棉铃虫对Bt棉花产生抗性的风险. 鉴于棉铃虫对Bt棉花产生抗性可能对Bt棉花利用价值的影响, 国内外近10年来对此进行了系统深入地研究. 本文综述了棉铃虫对Bt棉花抗性的生物化学和分子机制、抗性治理与监测技术的最新研究进展, 并分析了中国、澳大利亚和印度等国家棉铃虫对Bt棉花的抗性治理策略.     

靶标害虫对Bt玉米的抗性发展和治理策略

全生育期有效表达Bt杀虫蛋白的转基因抗虫玉米为靶标害虫的防治提供了新途径。但是,靶标害虫抗性种群的发展严重威胁了转基因抗虫玉米的可持续应用。截止到2018年,已经有13例报道表明靶标害虫对转基因抗虫玉米产生了田间抗性;5例监测结果表明靶标种群没有降低对Bt玉米的敏感性,其中包括转vip3Aa玉米。抗性治理策略成功的关键主要包括:Bt杀虫蛋白的高剂量表达、靶标害虫的隐性遗传、初始抗性等位基因频率较低、不完全抗性、适合度代价等。当抗性为非隐性遗传时,可以通过增加庇护所的种植面积达到延缓抗性发展的目的。     

Cry1Ie毒素胁迫下亚洲玉米螟的抗性发展及汰选种群对其他Bt毒素的交互抗性

亚洲玉米螟Ostrinia furnacalis (Guenée) 是危害玉米的重要害虫之一, 转Bt基因抗虫玉米为其防治提供了新的途径。然而, 靶标害虫产生抗性将严重阻碍Bt制剂及转Bt基因抗虫玉米的持续应用。明确害虫对转Bt基因玉米表达的毒素蛋白的抗性演化, 对于制定科学有效的抗性治理策略具有重要的理论和实际意义。本实验通过人工饲料汰选法研究了Bt Cry1Ie毒素胁迫下亚洲玉米螟的抗性发展及汰选14代的种群对其他Bt毒素（Cry1Ab, Cry1Ac和Cry1Fa）的交互抗性, 并观察了Cry1Ie蛋白胁迫对亚洲玉米螟生物学的影响。结果表明： 随着汰选压不断提高, 亚洲玉米螟种群对Cry1Ie毒素的敏感性逐渐下降。汰选14代后, 种群对Cry1Ie毒素的抗性水平提高了23倍。然而, Cry1Ab, Cry1Ac和Cry1Fa对所获Cry1Ie汰选种群的毒力与对敏感种群的毒力相比没有显著差异, 说明Cry1Ie汰选没有引起亚洲玉米螟对Cry1Ab, Cry1Ac和Cry1Fa毒素产生交互抗性。同时, 与敏感种群相比, Cry1Ie汰选14代的种群幼虫平均发育历期延长5.7 d, 蛹重减轻13.7%, 单雌产卵量下降40.0%。本研究结果说明, 大面积单一种植转cry1Ie基因抗虫玉米, 可能引起亚洲玉米螟产生抗性; 亚洲玉米螟Cry1Ie抗性种群对Cry1Ab, Cry1Ac和Cry1Fa没有交互抗性, 含有cry1Ie和cry1Ab, cry1Ac或cry1F双/多基因抗虫玉米, 可作为靶标害虫抗性治理的重要策略。     

应用高剂量/庇护所策略管理Bt作物抗性的三个基本假设：综述与展望

目前, 抗虫转基因作物的抗性管理方法主要是高剂量/庇护所策略。该策略的有效性取决于3个基本的假设条件：（1）抗虫转基因作物（Bt作物）表达出高剂量的杀虫蛋白, 该剂量使得靶标害虫对Bt杀虫蛋白的抗性表现型为功能性完全隐性或近于完全隐性, 进而使得Bt作物可以杀死几乎所有的抗性杂合个体和所有的敏感性个体;（2）靶标害虫种群的Bt抗性基因起始频率处于很低的水平;（3）源自转基因作物田和非转基因作物田(庇护所)的成虫在田间随机混合并交配。这3个假设必须同时满足, 缺一不可。本文就这3个假设的理论基础和经验研究的进展进行了综合论述, 并着重讨论了随机交配假设的最新研究进展以及今后的研究方向和方法。     

转Bt基因棉花生态风险评价的研究进展

转Bt基因抗虫棉(Gossypium spp.)是目前国内释放面积最大的转基因作物,其生态风险问题从一开始就受到密切的关注.从生态风险评价的角度,分转基因棉花中Bt杀虫蛋白的时空表达及其对害虫的控制效果、Bt基因通过花粉传播而扩散的风险、害虫对Bt棉花抗性的进化风险、Bt棉花对非目标生物体影响的风险等几个方面,综述了Bt棉安全性评价的最新研究进展,为生物安全管理提供咨询意见,并提出了目前针对Bt棉亟待研究的内容.期望本文能够为推动生物安全的研究和生物技术的发展做出一定的贡献.     

盐碱土壤转Bt基因棉花外源蛋白表达量时空变化及对抗虫性的影响

盐碱地是潜在的可利用耕地资源,但土壤盐碱化严重制约了农业生产的可持续发展。基于棉花机械化程度低、劳动力成本和生产资料投入剧增、比较效益下降和实施粮食生产安全战略等因素影响,我国长江流域和黄河流域棉花面积锐减,种植区域向内陆盐碱旱地或滨海盐碱地转移,但目前针对盐碱地转Bt基因棉种植可能带来的生态安全性问题研究甚少,正成为国内外研究的焦点和热点。伴随着棉花向盐碱地大面积转移种植趋势,检测盐胁迫是否影响转基因抗虫棉抗虫性,明确其影响程度,直接关系到转基因抗虫棉种植的安全性,也是目前抗虫棉扩大生产中迫切需要解决的问题。以非转基因棉花为对照,分别在低盐、中盐和高盐土壤种植的棉花的苗期、蕾期和花铃期采样,室内测定了转Bt基因棉花叶片对棉铃虫幼虫校正死亡率和外源蛋白表达量。研究结果发现盐分胁迫下转Bt基因棉花苗期叶片对棉铃虫幼虫校正死亡率下降了9.22%—47.46%,蕾期下降了31.61%—45.42%,花铃期下降了3.59%—18.52%;土壤盐分显著降低了转Bt基因棉花叶片中外源蛋白的表达量,苗期功能叶外源蛋白表达量下降了7.66%—29.86%;蕾期下降了3.77%—36.85%;花铃期下降了18.13%—41.02%;相关性分析表明,盐分胁迫条件下转Bt基因棉花叶片中外源蛋白表达量与其对棉铃虫抗性程度存在正相关关系。结果表明,盐碱土壤显著降低了转Bt基因棉花叶片外源杀虫蛋白表达量,从而导致转Bt基因棉花叶片对棉铃虫的抗虫性下降。研究土壤盐分对转Bt基因棉花对棉铃虫的影响及其作用机制,可为建立盐碱地转Bt基因棉花田害虫综合防控技术体系、转Bt基因棉花环境安全评价及转Bt基因棉安全管理提供依据。     

转抗虫基因植物生态安全性研究进展

转抗虫基因植物如Bt棉花等已在美国、中国和澳大利亚等国家大规模商业化种植 ,有关转抗虫基因植物潜在的生态风险已引起广泛的关注。该文综述了转抗虫基因植物研究应用现状与安全性研究进展。主要内容包括 :转抗虫基因植物的种类及其对靶标害虫的抗性 ,对非靶标害虫和天敌发生的影响 ,对农田生态系统生物多样性的影响 ,靶标昆虫的抗性治理及转抗虫基因植物的基因漂移等     

Mechanisms of drug resistance and reversal of the resistance

The mechanisms for the resistance to anticancer agents have been vigorously studied and many factors that are involved in the resistance were found. Among the members of ABC transporter superfamily, P-glycoprotein, MRP1-5 and BCRP are involved in the drug resistance. LRP, identified as the major vault protein, is also related to drug resistance.     

Hydraulic resistance of two sorghums varying in drought resistance

Genotypes of sorghum [Sorghum bicolor (L.) Moench] vary in drought resistance. Yet it is not known if their hydraulic resistances vary. The objective of this study was to determine if the hydraulic resistance of a drought-resistant sorghum was the same as that of a drought-sensitive sorghum. Leaf water and osmotic potentials were measured daily, during a 14-d period, in leaves of a drought-resistant (‘KS9’) and a drought-sensitive (‘IA25’) sorghum, which had the roots in pots with a commercial potting soil that was either well watered or allowed to dry. Soil water potential, adaxial stomatal resistance, and transpiration rate were determined daily. Hydraulic resistance of the plants was calculated from the slope of the line relating soil water potential minus leaf water potential versus transpiration rate. When the soil was not watered, the drought-sensitive sorghum had a water potential that averaged −0.50 MPa lower and an osmotic potential that averaged −0.57 MPa lower, but a similar adaxial stomatal resistance (1.19 s mm⁻¹), compared with the drought-resistant sorghum. Seven days after the beginning of the experiment, the water potential of the soil with the drought-sensitive sorghum was −0.25 MPa lower than that of the soil with the drought-resistant sorghum. With the water-limited conditions, the drought-sensitive sorghum depleted the soil-water reserve more quickly and died 2 d before the drought-resistant sorghum. Under well watered conditions, the two sorghums had similar water potentials (−1.64 MPa), osmotic potentials (−2.83 MPa), and adaxial stomatal resistances (0.78 s mm⁻¹). The calculated hydraulic resistance of the two sorghums did not differ and averaged 3.4 × 10⁷ MPa s m⁻¹. The results suggested that the variation in susceptibility to drought between the two genotypes was due to differences in rate of soil-water extraction. Contribution No. 86-249-J from the Kansas Agricultural Experiment Station. The paper is dedicated to the memory of Dr Dan M Rodgers.     

Components of partial resistance as criteria for identifying resistance

The components of partial resistance, incubation period, lesion area, latent period and sporulation were recorded on plants of six winter and two spring wheat cultivars which had been artificially inoculated with Septoria nodorum spores. Incubation period gave a guide as to how the cultivars would respond in the field to Septoria nodorum but statistical analysis showed that it could not be used alone to predict accurately the resistance of each cultivar to the pathogen. Average sporulation, however, could be used with more confidence for predicting the field resistance of the cultivars. From a regression analysis of NIAB rating versus incubation period, lesion area, latent period and sporulation, an equation was devised to obtain resistance indices for each cultivar. These resistance indices clearly reflected the NIAB ratings for the cultivars. It would therefore appear that resistance indices could be used as a pre-field evaluation method for identifying resistance to Septoria nodorum and thus be a valuable technique in breeding programmes.     

Costs of resistance

Studies of the reduction of fitness in plants expressing resistance characteristics have always been popular. New techniques for manipulating defense expression have recently resulted in a greater understanding of the mechanisms through which different types of resistance strategies produce costs, especially those costs associated with inducible defenses.     

The evolution of resistance genes in multi-protein plant resistance systems

The genomic perspective aids in integrating the analysis of single resistance (R-) genes into a higher order model of complex plant resistance systems. The majority of R-genes encode a class of proteins with nucleotide binding (NB) and leucine-rich repeat (LRR) domains. Several R-proteins act in multi-protein R-complexes that mediate interaction with pathogen effectors to induce resistance signaling. The complexity of these systems seems to have resulted from multiple rounds of plant-pathogen co-evolution. R-gene evolution is thought to be facilitated by the formation of R-gene clusters, which permit sequence exchanges via recombinatorial mispairing and generate high haplotypic diversity. This pattern of evolution may also generate diversity at other loci that contribute to the R-complex. The rate of recombination at R-clusters is not necessarily homogeneous or consistent over evolutionary time: recent evidence suggests that recombination at R-clusters is increased following pathogen infection, suggesting a mechanism that induces temporary genome instability in response to extreme stress. DNA methylation and chromatin modifications may allow this instability to be conditionally regulated and targeted to specific genome regions. Knowledge of natural R-gene evolution may contribute to strategies for artificial evolution of novel resistance specificities.     

Determination of antibiotic resistance and resistance plasmids of clinical Enterococcus species

To determine the antibiotic resistance pattern and resistance plasmids, we studied 23 antibiotic-resistant clinical isolates of Enterococcus spp. which caused infection in Bayindir-Ankara Hospital, Turkey. Biochemical and physiological identification tests were applied by the Vitek system and compared with the results of protein profiles by SDS-PAGE. From 23 isolates, 20 were identified as E. faecalis, 2 as E. faecium and 1 as E. gallinarum. Twenty four antibiotics belong to 10 different groups were used in susceptibility tests. Multiple antibiotic resistance was determined in 10 of 23 Enterococcus spp. Overall resistance to the used antibiotics was 47.3% and low level resistance was 16.6%. Among the isolates tested, 8.7% demonstrated high level gentamicin resistance, 17.4% demonstrated high level streptomycin resistance, and 43.5% demonstrated penicillin resistance. High level vancomycin resistant Enterococcus spp. rate was 34.8%, and 60.9% exhibited low level resistance to vancomycin and teicoplanin. They contain plasmids which varied in numbers between 1 and 11 and the plasmid sizes ranged from 2.08 to 56.15 kb. In curing experiments with acriflavine, two different plasmids were shown in different molecular sizes of 33.49 and 13.6 kb while the first determined glycopeptide and penicillin resistance, the second one determined either glycopeptide or penicillin resistance in two different E. faecalis strains. On the other hand, a 22.58 kb plasmid, determining kanamycin resistance, was detected in an E. faecium strain. After the curing experiments, an elimination of 37.17 and 44.47 kDa protein bands was shown in E. faecium EFA1 and E. faecalis EFA13 in SDS-PAGE, respectively. This survey indicates the increase of antibiotic-resistant enterococci, especially to vancomycin in our hospital isolates.