二斑叶螨对甲氰菊酯的抗性选育及解毒酶活力变化

为了明确二斑叶螨Tetranychus urticae Koch对甲氰菊酯产生抗性的机理,在室内模拟田间药剂的选择压力, 用甲氰菊酯对二斑叶螨敏感品系（S）进行逐代汰选,选育至38代时, 获得了抗性倍数( resistance ratio, RR)为247.35的抗甲氰菊酯品系（Fe-R）。对S和Fe-R解毒酶活性的分析表明,Fe-R₃₈体内羧酸酯酶（carboxylesterase, CarE）、酸性磷酸酯酶(acid phosphatase, ACP)、 碱性磷酸酯酶(alkaline phosphatase, ALP)、谷胱甘肽-S-转移酶(glutathione s-transferase, GSTs)和多功能氧化酶(mixed function oxidase, MFO)较S体内相应酶的活力显著升高（P< 0.05）,其相对比值（R/S）分别为1.822,13.941,3.789,4.262和17.386。此外,筛选至第9,19,25,32代时,除Fe-R₂₅和Fe-R₃₂的MFO活性与S相比有显著性差异（P< 0.05）外,其余解毒酶（CarE,ACP,ALP,GSTs）的活性与S相比均无显著性差异(P>0.05)。筛选至第38代时, 5种解毒酶的活力与S相比均差异显著(P<0.05)。结果说明二斑叶螨Fe-R随着筛选代数的增加（第25代后）,MFO活性的上升可能是二斑叶螨对甲氰菊酯产生抗性的主要原因。     

桔全爪螨的抗药性选育及其解毒酶活力变化

在室内模拟田间药剂的选择压力,用齐墩螨素和甲氰菊酯对桔全爪螨Panonychus citri 逐代处理,以选育其抗药性种群。选育至12代,对齐墩螨素抗性增长到7.30倍,对甲氰菊酯抗性增长到17.11倍。增效剂和离体酶活性的测定结果表明,抗性种群的乙酰胆碱酯酶和多功能氧化酶的活性都提高了;推测羧酸酯酶、乙酰胆碱酯酶、多功能氧化酶和谷胱甘肽-S-转移酶比活力的增加是桔全爪螨对甲氰菊酯产生抗性的主要原因。     

二斑叶螨对阿维菌素、哒螨灵和甲氰菊酯的抗性选育及其解毒酶活力变化

在室内模拟田间药剂的选择压力,用阿维菌素、哒螨灵和甲氰菊酯对二斑叶螨Tetranychuc urticae逐代处理,以选育其抗性种群。选育至12代,对阿维菌素抗性增长到6.72倍,对哒螨灵抗性增长到12.1倍,对甲氰菊酯抗性增长到19.9倍。酶抑制剂和离体酶活性的测定结果表明,阿维菌素抗性种群的多功能氧化酶和谷胱甘肽S-转移酶的活性均有所提高;二斑叶螨对哒螨灵的抗性可能与多功能氧化酶、羧酸酯酶的活性增强有关;而羧酸酯酶、多功能氧化酶和谷胱甘肽S-转移酶活性的增强可能是二斑叶螨对甲氰菊酯产生抗性的主要原因。     

桔全爪螨对阿维菌素和甲氰菊酯的抗性现实遗传力及风险评估

在实验室抗性选育的基础上,应用数量遗传学中的域性状分析法,研究了桔全爪螨北碚种群对阿维菌素和甲氰菊酯2种杀螨剂的抗性现实遗传力,并对2种药剂在不同杀死率下抗性发展的速率进行了预测.结果表明:用阿维菌素和甲氰菊酯分别不连续汰选11及16代后,桔全爪螨对两者的抗性分别为3.8和29.9倍,抗性现实遗传力分别为0.0475和0.1544.在室内选择条件下,杀死率为50%～90%时,要获得10倍抗性,甲氰菊酯仅需要7～16代,阿维菌素则需要12～26代.而在田间选择情况下,2种药剂都将需要更长的时间.抗性筛选结果表明,生物源农药阿维菌素的抗性风险明显低于菊酯类农药甲氰菊酯.试验结果可为桔全爪螨抗性治理提供参考.     

朱砂叶螨对三种杀螨剂的抗性选育与抗性风险评估

为评价朱砂叶螨Tetranychus cinnabarinus对3种杀螨剂的抗性风险,在实验室抗性品系选育基础上,应用数量遗传学中的域性状分析法,研究了朱砂叶螨北碚种群对甲氰菊酯、阿维菌素和哒螨灵3种杀螨剂的抗性现实遗传力,并对3种药剂在不同杀死率下抗性发展的速率进行了预测。结果表明：分别单一连续汰选16代后,朱砂叶螨对甲氰菊酯、阿维菌素的抗性倍数分别达26.54和4.51倍,对哒螨灵表现为敏感性降低（抗性倍数为1.16倍）;朱砂叶螨对甲氰菊酯、阿维菌素和哒螨灵的抗性现实遗传力分别为0.2472,0.1519和0.0160。在室内选择条件下,杀死率为50%～90%时,要获得10倍抗性,甲氰菊酯仅需要13～6代,阿维菌素需要约21～10代;哒螨灵需要约197～89代;在田间选择,三种药剂都将需要更长的时间。抗性筛选16代结果表明,抗性风险较高的是菊酯类的甲氰菊酯,其次是生物源农药阿维菌素,杂环类的哒螨灵抗性风险较小。试验结果可为朱砂叶螨抗性治理提供参考。     

Effect of the synergist, piperonyl butoxide, on the development of deltamethrin resistance in yellow fever mosquito, Aedes aegypti L. (Diptera: Culicidae)

The larvae and adults of Aedes aegypti were tested for the potential to develop resistance to the synthetic pyrethroid, deltamethrin, alone or a combination of deltamethrin with the synergist, piperonyl butoxide (PBO). Although continuous larval selection for 40 generations resulted in 703-fold resistance, the resistance ratio in the adults was only 1.3. Similarly, adult selections with deltamethrin showed a resistance ratio of less than four after 40 generations, indicating differential response to deltamethrin selection in the two developmental stages of the insect. When the susceptible larvae were subjected to selection pressure of deltamethrin and PBO in the ratio of 1:5 for 20 generations, the speed of selection for deltamethrin resistance slowed down by 60%. The F24 larvae obtained from the strain selected with deltamethrin alone were further subjected to selection pressure with synergized deltamethrin, which resulted in 89% reversal in deltamethrin resistance in just one generation. However, long-term selection with the insecticide-synergist combination returned resistance close to original levels in 15 generations. The data indicate the involvement of cytochrome P450-dependent detoxification as the primary mechanism of development of resistance to deltamethrin in the larvae. Implications of the results on the management of larval and adult stages of Ae. aegypti are discussed.     

ESTMATION OF REALIZED HERITABILITY OF RESISTANCE TO FENPROPATHRIN, ABAMECTIN, PYRIDABEN AND THEIR MIXTURES IN ACARICIDE-SELECTED STRAINS OF TETRANYCHUS CINNABARINUS (BOIDUVAL)

Abstract Threshold trait analysis was used to estimate realized heritability (h²) of resistance to five acaricides (three single acaricide and two mixtures) and resistance risk in Tetranychus cinnabarinus (Boiduval). Tetranychus cinnabarinus collected from the field of Beibei, Chongqing reared more than 60 generations under pesticide free conditions and considered susceptible. Successively selected for about 30 generations, the strain had a 65.55-, 5.82-, 1.23-, 5.20- and 1.42-fold increase in resistance to fenpropathrin, abamectin, pyridaben, pyridaben-abamectin (pyridaben: abamectin = 7.4:0.1, m/m) and fenpropathrin-abamectin (fenpropathrin: abamectin = 8.9:0.1, m/m), respectively. The realized heritability of resistance to fenpropathrin, abamectin, pyridaben, pyridaben-abamectin (pyridaben: abamectin = 7.4:0.1, m/m) and fenpropathrin-abamectin (fenpropathrin: abamectin = 8.9:0.1, m/m) is 0.2167, 0.0967, 0.0130, 0.0800 and 0.0172, respectively. Under the selected condition, a 10-fold increase in resistance would be expected 15 generations for fenpropathrin, 34 generations for abamectin, 333 generations for pyridaben, 42 generations for pyridaben-abamectin (pyridaben: abamectin = 7.4:0.1, m/m) and 200 generations for fenpropathrin-abametcin (fenpropathrin: abamectin = 8.9:0.1, m/m). The highest resistance risk of the five acaricides in Tetranychus cinnabarinus was fenpropathrin, then abamection, pyridaben-abamectin (pyridaben: abamectin = 7.4: 0.1, m/m), fenpropathrin- abamectin (fenpropathrin: abamectin = 8.9:0.1, m/m) and that to pyridaben was the lowest. The mixture of pyridaben and abamectin is not useful in delaying development of resistance in the pest to the two single acaricide while the mixture of fenpropathrin and abamectin could do it.     

烟粉虱田间种群的抗药性

采用成虫浸叶生测法分别测定了福建省福州、漳州、龙岩、三明、南平、宁德等地烟粉虱田间种群对13种杀虫剂的抗性.结果表明,福建省6个烟粉虱田间种群对氯氟氰菊酯、甲氰菊酯、氯氰菊酯、溴氰菊酯、乙酰甲胺磷、毒死蜱产生了高水平抗性,抗性倍数分别达838.38～2460.52、244.64～834.29、116.02～266.35、81.75～124.18、425.18～875.56和54.53～78.43倍,对乐果产生了中等水平抗性,抗性倍数达14.16～17.66倍,对敌敌畏产生了中等偏低水平的抗性,抗性倍数达6.23～11.25倍,对灭多威的抗性水平较低,抗性倍数仅为4.07～5.66倍.漳州种群已对烟碱类杀虫剂产生了中等水平抗性,对吡虫啉、啶虫脒和噻虫嗪的抗性倍数分别达23.08、10.32和24.60倍,而其它地区烟粉虱种群对吡虫啉、啶虫脒和噻虫嗪的抗性水平较低,甚至不明显,抗性倍数分别仅为1.31～3.28、1.82～7.23和1.39～5.45倍.福建省各地区烟粉虱种群对阿维菌素尚未产生明显的抗药性.     

朱砂叶螨对甲氰菊酯、阿维菌素,哒螨灵及其混剂抗性遗传力的分析(英文)

采用域性状分析法 ,估算了朱砂叶螨对 5种杀螨剂 (3种单剂和 2种混剂 )的抗性现实遗传力 ,并对 5种药剂的抗性风险进行了评估。把采自重庆北碚田间的朱砂叶螨种群 ,在室内不施药情况下饲养 6 0余代 ,以此作为抗性筛选的敏感品系。分别单一连续汰选近 30代 ,朱砂叶螨对甲氰菊酯、阿维菌素、哒螨灵、哒螨 -阿维 (哒螨灵 :阿维菌素 =7 4 :0 1,m m)和甲氰 -阿维 (甲氰菊酯 :阿维菌素 =8 9:0 1,m m)的抗性分别达 6 5 5 5、5 82、1 2 3、5 2 0和 1 4 2 倍 ;抗性现实遗传力分别为 0 2 16 7、0 0 96 7、0 0 130、0 0 80 0和 0 0 172。在实验室选择条件下 ,预计抗性增长 10倍时 ,甲氰菊酯、阿维菌素、哒螨灵、哒螨 -阿维 (哒螨灵 :阿维菌素 =7 4 :0 1,m m)和甲氰 -阿维 (甲氰菊酯 :阿维菌素 =8 9:0 1,m m)分别需要 15、34、333、4 2和 2 0 0代。甲氰菊酯抗性风险较高 ,其次是阿维菌素、哒螨 -阿维 (哒螨灵 :阿维菌素 =7 4 :0 1,m m)、甲氰 阿维 (甲氰菊酯 :阿维菌素 =8 9:0 1,m m) ,哒螨灵抗性风险较低。混剂哒螨 阿维 (哒螨灵 :阿维菌素 =7 4 :0 1,m m)不能延缓朱砂叶螨对两单剂哒螨灵和阿维菌素的抗性发展 ,而混剂甲氰 阿维 (甲氰菊酯 :阿维菌素 =8 9:0 1,m m)却能有效延缓朱砂叶螨对两单剂     

An in vitro whole plant selection system: paraquat tolerant mutants in the fern Ceratopteris

Summary A whole plant selection system using the haploid gametophyte generation of the fern Ceratopteris richardii has been developed to select for mutations that confer resistance or tolerance to various selection pressures. The expression of the mutations can be analyzed and characterized in both the haploid gametophyte and diploid sporophyte generations. Genetic analyses are facilitated by the fern's rapid life cycle and the ease of manipulating the gametophyte generation. Selection for tolerance to the herbicide paraquat has yielded two mutants which have an increased tolerance to the herbicide in both the gametophyte and sporophyte generations. Both mutants exhibit single nuclear gene inheritance patterns and appear to be closely linked or allelic.     

Fumarate mitigates disruption induced by fenpropathrin in the silkworm Bombyx mori (Lepidoptera): A metabolomics study

The silkworm Bombyx mori L. is a model organism of the order Lepidoptera. Understanding the mechanism of pesticide resistance in silkworms is valuable for Lepidopteran pest control. In this study, comparative metabolomics was used to analyze the metabolites of 2 silkworm strains with different pesticide resistance levels at 6, 12, and 24 h after feeding with fenpropathrin. Twenty-six of 27 metabolites showed significant differences after fenpropathrin treatment and were classified into 6 metabolic pathways: glycerophospholipid metabolism, sulfur metabolism, glycolysis, amino acid metabolism, the urea cycle, and the tricarboxylic acid (TCA) cycle. After analyzing the percentage changes in the metabolic pathways at the 3 time points, sulfur metabolism, glycolysis, and the TCA cycle showed significant responses to fenpropathrin. Confirmatory experiments were performed by feeding silkworms with key metabolites of the 3 pathways. The combination of iron(II) fumarate + folic acid (IF-FA) enhanced fenpropathrin resistance in silkworms 6.38 fold, indicating that the TCA cycle is the core pathway associated with resistance. Furthermore, the disruption of several energy-related metabolic pathways caused by fenpropathrin was shown to be recovered by IF-FA in vitro. Therefore, IF-FA may have a role in boosting silkworm pesticide resistance by modulating the equilibrium between the TCA cycle and its related metabolic pathways.     

Genetic improvement of Amblyseius finlandicus (Acari: Phytoseiidae): laboratory selection for resistance to azinphosmethyl and dimethoate

Amblyseius finlandicus (Oudemans) was selected in the laboratory for resistance to azinphosmethyl and dimethoate by subjecting adult females to increasing concentrations of dried residues of dimethoate and azinphosmethyl on detached bean leaves. The first eight selections were done with dimethoate. Slide-dip bioassays indicated selection with dimethoate increased dimethoate resistance 1.8-fold and azinphosmethyl resistance 2.6-fold. These resistances appeared to be quite stable: a 1.2 to 1.3-fold decrease in resistance ratios was observed in a subculture after 10 months without selections. No decrease was observed after 9 months without selections in a pooled colony that consisted of both resistant and susceptible mites. The dimethoate-selected colony was subsequently selected eight times with azinphosmethyl. About 15 % of the mites survived the last selection round with 2,500 ppm, which is 2.5 times the highest recommended field rate in Finnish apple orchards. At the end of the selection program, based on slide-dip bioassays, the total increase in resistance to dimethoate was about two-fold and to azinphosmethyl about 5.4-fold compared to the unselected base colony from which the selected colony was derived. The LC₅₀ value for azinphosmethyl was 14 times higher in the selected colony (451.3 ppm a.i.) compared to the most susceptible colony tested. A similar level of resistance to both pesticides was achieved after six azinphosmethyl selections on a mixed colony that was initiated by pooling mites from five field-collected colonies and the dimethoate-selected lines. Year-to-year variation in azinphosmethyl LC₅₀ values of the unselected base colony was high, with values varying from 83.8 to 348.7 ppm a.i., demonstrating the need to test a reference strain in each bioassay. Results of the azinphosmethyl selections and the subsequent slide-dip bioassays suggest that the resistant strain could tolerate field rates of azinphosmethyl (300–950 ppm a.i.) used in Finnish apple orchards.     

Development and characterization of diamondback moth resistance to transgenic broccoli expressing high levels of Cry1C

A field-collected colony of the diamondback moth, Plutella xylostella, had 31-fold resistance to Cry1C protoxin of Bacillus thuringiensis. After 24 generations of selection with Cry1C protoxin and transgenic broccoli expressing a Cry1C protein, the resistance that developed was high enough that neonates of the resistant strain could complete their entire life cycle on transgenic broccoli expressing high levels of Cry1C. After 26 generations of selection, the resistance ratios of this strain to Cry1C protoxin were 12,400- and 63,100-fold, respectively, for the neonates and second instars by a leaf dip assay. The resistance remained stable until generation 38 (G38) under continuous selection but decreased to 235-fold at G38 when selection ceased at G28. The Cry1C resistance in this strain was seen to be inherited as an autosomal and incompletely recessive factor or factors when evaluated using a leaf dip assay and recessive when evaluated using Cry1C transgenic broccoli. Saturable binding of (125)I-Cry1C was found with brush border membrane vesicles (BBMV) from both susceptible and Cry1C-resistant strains. Significant differences in Cry1C binding to BBMV from the two strains were detected. BBMV from the resistant strain had about sevenfold-lower affinity for Cry1C and threefold-higher binding site concentration than BBMV from the susceptible strain. The overall Cry1C binding affinity was just 2.5-fold higher for BBMV from the susceptible strain than it was for BBMV from the resistant strain. These results suggest that reduced binding is not the major mechanism of resistance to Cry1C.     

Cometabolic biotransformation of fenpropathrin by Clostridium species strain ZP3

A novel bacterial strain capable of degrading the pyrethroid pesticide fenpropathrin was isolated from mixed wastewater and sludge samples. Phylogenetic analysis of the 16S rDNA sequence revealed that the organism belongs to the genus Clostridium. The organism can co-metabolically transform fenpropathrin at 100?mg?l(-1) at 35°C and pH 7.5 in 12?days. Metabolic products of fenpropathrin from strain ZP3 were examined by gas chromatography/mass spectrometry, and the results showed that the organism degraded fenpropathrin with an oxidization process to yield benzyl alcohol, benzenemethanol, 3,5-dimethylamphetamine. Analyses of cell-free extracts from this strain showed that the optimal degrading conditions for degrading fenpropathrin were 35°C and pH 7.5, and degradation efficiency was 20.0?mg?l(-1)?day(-1), and it might be potential using for rapid treating fenpropathrin, for example, on the surface of fruits and vegetables.     

Formulation with an optical brightener does not increase probability of developing resistance to Spodoptera frugiperda nucleopolyhedrovirus in the laboratory

Stilbene-derived optical brighteners can markedly enhance the insecticidal activity of certain baculoviruses. We evaluated the influence of an optical brightener on the rate at which Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) developed resistance to nucleopolyhedrovirus (SfMNPV). Two laboratory colonies of S. frugiperda were inoculated with an LC50 of SfMNPV, in the absence or presence of the optical brightener Tinopal LPW (0.1%), over a period of two and 11 generations, in the first and second experiment, respectively. Compared with the initial susceptibility of the insect colony, resistance ratios of 11- and 12-fold were observed after two generations of treatment with SfMNPV + Tinopal LPW and SfMNPV alone. Similar, but variable degrees of resistance were observed in the long-term experiment with resistance ratios of 8- to 35-fold after seven to 11 generations. The presence of Tinopal LPW alone, or in mixtures with SfMNPV, did not cause any systematic change in insect resistance in either experiment. At the end of the long-term experiment, debilitating effects on pupal weight, adult fecundity, and longevity were observed in the insects exposed to Tinopal LPW alone or in mixtures with SfMNPV, but the pattern of such effects among treatments differed in each generation. We conclude that optical brighteners are unlikely to affect the rate of development of resistance to nucleopolyhedroviruses applied as biological insecticides.     

Development and Characterization of Diamondback Moth Resistance to Transgenic Broccoli Expressing High Levels of Cry1C

A field-collected colony of the diamondback moth, Plutella xylostella, had 31-fold resistance to Cry1C protoxin of Bacillus thuringiensis. After 24 generations of selection with Cry1C protoxin and transgenic broccoli expressing a Cry1C protein, the resistance that developed was high enough that neonates of the resistant strain could complete their entire life cycle on transgenic broccoli expressing high levels of Cry1C. After 26 generations of selection, the resistance ratios of this strain to Cry1C protoxin were 12,400- and 63,100-fold, respectively, for the neonates and second instars by a leaf dip assay. The resistance remained stable until generation 38 (G38) under continuous selection but decreased to 235-fold at G38 when selection ceased at G28. The Cry1C resistance in this strain was seen to be inherited as an autosomal and incompletely recessive factor or factors when evaluated using a leaf dip assay and recessive when evaluated using Cry1C transgenic broccoli. Saturable binding of ¹²⁵I-Cry1C was found with brush border membrane vesicles (BBMV) from both susceptible and Cry1C-resistant strains. Significant differences in Cry1C binding to BBMV from the two strains were detected. BBMV from the resistant strain had about sevenfold-lower affinity for Cry1C and threefold-higher binding site concentration than BBMV from the susceptible strain. The overall Cry1C binding affinity was just 2.5-fold higher for BBMV from the susceptible strain than it was for BBMV from the resistant strain. These results suggest that reduced binding is not the major mechanism of resistance to Cry1C.     

Multiple Resistance and Biochemical Mechanisms of Dicofol Resistance in Tetranychus urticae (Acari: Tetranychidae)

A field colony of Tetranychus urticae (Koch) resistant to dicofol was selected with dicofol successively for 20 generations to produce the DR-20 strain. Resistance and multiple resistance levels of the DR-20 strain to 15 acaricides were determined using a spray bioassay. The DR-20 strain was extremely resistant to dicofol [resistance ratio (RR), 465]. The strain showed extremely strong resistance to acrinathrin (RR, 373) and benzoximate (RR, 197) and strong resistance to bromopropylate (RR, 136), fenbutatin oxide (RR, 65), fenpropathrin (RR, 70), fenpyroximate (RR, 68), and pyridaben (RR, 63). A RR of 11–29 was observed with abamectin, fenazaquin, milbemectin, propagite, and tebufenpyrad. The DR-20 strain exhibited low levels of resistance (RR<3) to azocyclotin and chlorfenapyr. In comparative assays with detoxifying enzymes, the DR-20 strain showed 4.7-fold higher activity in p-nitroanisole-O-demethylation and 1.6-fold higher activities in both α- and β-naphthyl acetate hydrolysis. Synergist experiments with different metabolic inhibitors revealed that piperonyl butoxide, iprobenfos, triphenyl phosphate, and 4, 4-dichloro-α-methyl benzhydrol had little or no synergistic activity in the susceptible and DR-20 strains. These results suggest that employment of certain acaricides with little multiple resistance will be useful for the management of dicofol resistance in the field.     

Development and stability of insecticide resistance in the leafminer Liriomyza trifolii (Diptera: Agromyzidae) to cyromazine, abamectin, and spinosad

Three populations of the leafminer, Liriomyza trifolii (Burgess), were collected from commercial ornamental production greenhouses in the United States and tested for susceptibility to three commercial insecticides. A leaf dip bioassay of leaves containing young (1-2-d-old) larvae was used. Based on larval mortality and compared with a susceptible laboratory reference colony, the three strains varied in spectrum and level of resistance to the insecticides. CA-1, collected from Gerbera daisy, was moderately resistant to cyromazine (18.1-fold) and abamectin (22.0-fold), but highly resistant to spinosad (> 188-fold). CA-2, collected from chrysanthemums, was not resistant to abamectin, had a low level of resistance to cyromazine (8.2-fold), but was extremely resistant to spinosad (1,192-fold). GA-1, collected from chrysanthemums, had very low levels of resistance to cyromazine (5.4-fold) and spinosad (1.9-fold) but was moderately resistant to abamectin (30.6-fold). When reared in the absence of insecticide selection pressure, all three strains reverted to approximately the level of the reference strain. The CA-1 strain reverted in nine generations to cyromazine; however, the lowest levels of abamectin and spinosad resistance reverted to was 3.1-fold at F8 and 3.2 at the F10, respectively. The CA-2 strain reverted in five generations to both cyromazine and spinosad. GA-1 reverted in five generations to abamectin. Based on the results, resistance to these three insecticides was unstable. Additionally, there was no cross-resistance among these three insecticides.     

嗜卷书虱低氧耐性品系的选育及其遗传稳定性和生态适合度研究

室内恒温条件下以人工饲料饲养的嗜卷书虱Ｌｉｐｏｓｃｅｌｉｓ ｂｏｓｔｒｙｃｈｏｐｈｉｌａ Ｂａｄｏｎｎｅｌ成虫,分别在０．５％和１％Ｏ２组配的气调环境中以７％左右的选择压力处理,以选育其耐低氧气调性。选育至３０低氧品系ＬＯＣ１和ＬＯＣ２,以ＬＴ５０为标准其性倍数分别达４．７和３．９倍。整个选育过程中,气调暴露时间对数值与死亡率机率值间的回归直线基本平行,其值均低于敏感基线的斜率值,这表明嗜卷书虱对     

Genetics of resistance to Cry1C toxin from Bacillus thuringiensis in Spodoptera litura (Fab.)

The present study was undertaken to determine the genetics of Cry1C resistance in Spodoptera litura. Selection of S. litura (Fab.) with Cry1C was done for eight generations to develop resistance. Reciprocal crosses between resistant and susceptible populations were made to understand the population genetics of Cry1C resistance in S. litura. Generation wise selection with Cry1C was evaluated for resistance development in S. litura. The LC₅₀ of Cry1C was 0.14 µg/cm² for the first selected generation and it increased to 23.98 µg/cm² after eight selected generations, which is a 285.47-fold increase in resistance compared with the susceptible strain. The estimated realized heritability (h²) after eight generations of selection with Cry1C insecticidal protein was 0.44. The number of generations required for the tenfold increase in LC₅₀ (1/R) was estimated to be 3.33. Response to Cry1C selection in S. litura was 0.30, the estimated selection differential was 0.69 and the pheonotypic standard deviation (dP) was 0.24. Reciprocal crosses between Cry1C resistant and susceptible strain of S. litura showed autosomal resistance.