Biotype and insecticide resistance status of the whitefly Bemisia tabaci from China

BACKGROUND: Resistance to numerous insecticide classes in Bemisia tabaci Gennadius has impaired field control efficacy in south‐eastern China. The biotype and resistance status of B. tabaci collected from these areas was investigated. RESULTS: Two different biotypes of B. tabaci (B‐biotype and Q‐biotype) were detected in south‐eastern China, and the samples collected from geographical regions showed a prevalence of the Q‐biotype and the coexistence of B‐ and Q‐biotypes in some regions. Moderate to high levels of resistance to two neonicotinoids were established in both biotypes (28–1900‐fold to imidacloprid, 29–1200‐fold to thiamethoxam). Medium to high levels of resistance to alpha‐cypermethrin (22–610‐fold) were also detected in both biotypes. Four out of 12 populations had low to medium levels of resistance to fipronil (10–25‐fold). Four out of 12 populations showed low levels of resistance to spinosad (5.7–6.4‐fold). All populations tested were susceptible to abamectin. CONCLUSION: The Q‐biotype B. tabaci is supplanting the B‐biotype which used to be ubiquitous in China. Field populations of both B‐ and Q‐biotypes of B. tabaci have developed high levels of resistance to imidacloprid and thiamethoxam. Abamectin is the most effective insecticide against adult B. tabaci from all populations. Copyright © 2010 Society of Chemical Industry     

Cross‐resistance study and biochemical mechanisms of thiamethoxam resistance in B‐biotype Bemisia tabaci (Hemiptera: Aleyrodidae)

BACKGROUND: B‐biotype Bemisia tabaci (Gennadius) has invaded China over the past two decades. To understand the risks and to determine possible mechanisms of resistance to thiamethoxam in B. tabaci, a resistant strain was selected in the laboratory. Cross‐resistance and the biochemical mechanisms of thiamethoxam resistance were investigated in the present study. RESULTS: A 66.3‐fold thiamethoxam‐resistant B. tabaci strain (TH‐R) was established after selection for 36 generations. Compared with the susceptible strain (TH‐S), the selected TH‐R strain showed obvious cross‐resistance to imidacloprid (47.3‐fold), acetamiprid (35.8‐fold), nitenpyram (9.99‐fold), abamectin (5.33‐fold) and carbosulfan (4.43‐fold). No cross‐resistance to fipronil, chlorpyrifos or deltamethrin was seen. Piperonyl butoxide (PBO) and triphenyl phosphate (TPP) exhibited significant synergism on thiamethoxam effects in the TH‐R strain (3.14‐ and 2.37‐fold respectively). However, diethyl maleate (DEM) did not act synergistically with thiamethoxam. Biochemical assays showed that cytochrome P450 monooxygenase activities increased 1.21‐ and 1.68‐fold respectively, and carboxylesterase activity increased 2.96‐fold in the TH‐R strain. However, no difference was observed for glutathione S‐transferase between the two strains. CONCLUSION: B‐biotype B. tabaci develops resistance to thiamethoxam. Cytochrome P450 monooxygenase and carboxylesterase appear to be responsible for the resistance. Reasonable resistance management that avoids the use of cross‐resistance insecticides may delay the development of resistance to thiamethoxam in this species. Copyright © 2009 Society of Chemical Industry     

Contact and fumigant toxicity of plant essential oils and efficacy of spray formulations containing the oils against B‐ and Q‐biotypes of Bemisia tabaci

BACKGROUND: The contact + fumigant toxicity of 92 plant essential oils and control efficacy of 18 experimental spray formulations containing nine selected essential oils (0.5 and 0.1% sprays) and six commercial insecticides to females from B‐ and Q‐biotypes of Bemisia tabaci were evaluated using vapour‐phase mortality and spray bioassays. RESULTS: Garlic and oregano (LC₅₀, 0.15 mL cm^?3) were the most toxic oils against B‐ and Q‐biotype females. Strong fumigant toxicity to both biotype females was also obtained from catnip, cinnamon bark, clove bud, clove leaf, davana, savory and vetiver Haiti oils (LC₅₀, 0.17–0.48 mL cm^?3). The 0.5% sprays of these oils (except for thyme red oil) resulted in 90–100% mortality against both biotype females. Only garlic applied as 0.1% spray provided 100% mortality. Spinosad 100 g L^?1 suspension concentrate (SC) treatment resulted in 92 and 95% mortality against both biotype females, whereas acetamiprid 80 g L^?1 wettable powder (WP), imidacloprid 80 g L^?1 SC, thiamethoxam 100 g L^?1 water‐dispersible granule (WDG) and pyridaben 200 g L^?1 WP treatments resulted in 89–100% mortality against B‐biotype females only. CONCLUSION: In the light of global efforts to reduce the level of highly toxic synthetic insecticides in the agricultural environment, the essential oils described, particularly garlic, cinnamon bark and vetiver Haiti, merit further study as potential insecticides for the control of B. tabaci populations as fumigants with contact action. Copyright © 2011 Society of Chemical Industry     

Toxicity of spiromesifen to the developmental stages of Bemisia tabaci biotype B

BACKGROUND: Spiromesifen is a novel insecticidal/acaricidal compound derived from spirocyclic tetronic acids that acts effectively against whiteflies and mites via inhibition of acetyl‐CoA‐carboxylase, a lipid metabolism enzyme. The effects of spiromesifen on the developmental stages of the whitefly Bemisia tabaci (Gennadius) were studied under laboratory conditions to generate baseline action thresholds for field evaluations of the compound. RESULTS: Adult B. tabaci mortality rate after spiromesifen treatment (5 mg L^?1) was 40%. Treatment with 0.5 mg L^?1 reduced fecundity per female by more than 80%, and fertility was almost nil. LC₅₀ for eggs was 2.6 mg L^?1, and for first instar 0.5 mg L^?1. Scanning electron microscopy revealed that eggs laid by treated adult females had an abnormally perforated chorion, and females were unable to complete oviposition. Light and fluorescent microscopy showed significantly smaller eggs following treatment, and smaller, abnormally formed and improperly localized bacteriomes in eggs and nymphs. The number of ovarioles counted in females treated with 5 mg L^?1 was significantly reduced. Spiromesifen showed no cross‐resistance with other commonly used insecticides from different chemical groups, and resistance monitoring in Israel showed no development of field resistance to this insecticide after 1 year of use. CONCLUSION: The strong effect on juvenile stages of B. tabaci with a unique mode of action and the absence of cross‐resistance with major commonly used insecticides from different chemical groups suggest the use of spiromesifen in pest and resistance management programmes. Copyright © 2008 Society of Chemical Industry     

Induction effects of host plants on insecticide susceptibility and detoxification enzymes of Bemisia tabaci (Hemiptera: Aleyrodidae)

BACKGROUND: The polyphagous B‐biotype Bemisia tabaci (Gennadius) has developed a high resistance to commonly used insecticides in China. To illustrate the induced changes by host plant, bioassay and biochemical research on five different host populations were investigated. RESULTS: Except for bifenthrin, all tested insecticides showed lower toxicity to the B. tabaci poinsettia population compared with other host populations. Moreover, four insecticides, the exceptions being abamectin and fipronil, showed highest toxicity towards the tomato population. The LC₅₀ values of the poinsettia population, particularly towards acetamiprid, were 14.8‐, 10.3‐ and 7.29‐fold higher than those of tomato, cucumber and cabbage respectively. The CarE activities of B. tabaci cabbage and cucumber populations were all significantly higher than those of poinsettia, cotton and tomato populations. The ratio of the cabbage population was 1.97‐, 1.79‐ and 1.30‐fold higher than that of poinsettia, cotton and tomato respectively. The frequency profiles for this activity also have obvious differences. The GST and P450 activities of the cucumber population were the lowest in the five host populations. CONCLUSION: Long‐term induction of host plants for B‐biotype B. tabaci could influence their susceptibilities to several insecticides. Rational selection and usage of insecticides for particular hosts will be helpful for resistance management and control of this species. Copyright © 2010 Society of Chemical Industry     

Aerial electrostatic‐charged sprays for deposition and efficacy against sweet potato whitefly (Bemisia tabaci) on cotton

Background: The efficacy of aerial electrostatic‐charged sprays was evaluated for spray deposit characteristics and season‐long control of sweet potato whitefly (SWF), Bemisia tabaci Genn. biotype B (aka B. argentifolii Bellows & Perring), in an irrigated 24 ha cotton field. Treatments included electrostatic‐charged sprays at full and half active ingredient (AI) label rate, uncharged sprays and conventional sprays applied with CP nozzles at full label rate with several different insecticides. Results: Spray droplet size was significantly smaller for electrostatic‐charged sprays than for conventional sprays in top‐ and mid‐canopy locations. The seasonal mean numbers of viable eggs and live large nymphs on cotton treated with electrostatic‐charged sprays were comparable with those on cotton treated with conventional applications. Lethal concentration (LC₅₀) for adults for electrostatic‐charged sprays was comparable with that for conventional sprays. Conclusion: The amenability of electrostatic‐charged sprays to a wide array of pesticides with different chemistries should be a useful tool in combating insect resistance. Results reported here suggest that the potential exists for obtaining increased efficacy against whiteflies using an electrostatic spray charging system, and that additional research will be required to improve charge‐to‐mass (Q/M) ratio in order to increase deposition of pest control materials to the lower surfaces of cotton leaves where the whiteflies reside. Copyright © 2009 Society of Chemical Industry     

High-throughput allelic discrimination of B and Q biotypes of the whitefly, Bemisia tabaci, using TaqMan allele-selective PCR

BACKGROUND: B and Q biotypes of the whitefly, Bemisia tabaci (Gennadius), are generally regarded as the most significant given their global distribution and strong resistance to insecticides. Since these biotypes can coexist and differ markedly in their insecticide resistance profiles, a rapid but reliable means of discriminating between them would be a valuable complement to resistance monitoring and management programmes. Recently, PCR‐based methods have been developed to determine the biotype status of B. tabaci populations. However, these require post‐amplification procedures, which increase time and labour. RESULTS: The authors have developed an allelic discrimination real‐time PCR assay using fluorescent dye‐labelled probes to distinguish the B and Q biotypes. The assay targets a single nucleotide polymorphism (SNP) in the mitochondrial cytochrome oxidase I (mtCOI) gene. To evaluate the assay, DNA was extracted from individual whiteflies of six known biotype strains, and all scored correctly as either a B or Q biotype. As further validation, 72 individuals from field samples collected in different parts of the world were also tested by the assay. No failed reactions were observed, with all 72 samples scoring clearly as either the B or Q biotype. CONCLUSION: The development of this rapid and high‐throughput assay has important potential for routine monitoring of B and Q biotypes on ornamental plants and for the screening of B. tabaci populations in countries where these biotypes are not yet established. Copyright © 2007 Society of Chemical Industry     

Dicofol resistance in Tetranychus cinnabarinus: resistance and stability of resistance in populations from Antalya, Turkey

Resistance against dicofol was investigated in the carmine spider mite, Tetranychus cinnabarinus. Higher resistance levels were detected by leaf residual bioassays than by topical bioassays, both done using a Potter spray tower, in almost all populations of T cinnabarinus examined from Antalya, Turkey. For instance, the resistance level at LC₉₅ was 17.5‐fold in topical bioassays but 58.9‐fold in leaf residual bioassays for the population collected from greenhouses in the Topçular district. There were differences of resistance levels at LC₉₅, ranging between 2.6‐ and 23.9‐fold using topical bioassays and between 5.0‐ and 58.9‐fold in residual bioassays, in populations collected from greenhouses from various districts. Populations from cotton showed lower resistance levels against dicofol than populations from greenhouses. Resistance to dicofol at LC₅₀ as indicated by topical and residual bioassays increased 19.7‐ and 100.7‐fold, respectively, in a colony from the laboratory strain of T cinnabarinus selected with dicofol alone for 16 cycles. However, the dicofol resistance at LC₅₀ increased 19.4‐ and 52.0‐fold in another colony selected in rotation with dicofol and tetradifon for six and eight cycles, respectively. The changes in resistance to dicofol 5 months after the selection ceased were as follows: in the colony selected for dicofol alone, using topical and residual bioassays, the resistance levels at LC₅₀ decreased to 11.7‐ and 99.1‐fold, respectively, and in the colony selected in rotation with dicofol and tetradifon to 10.8‐ and 15.8‐fold, respectively. © 2001 Society of Chemical Industry     

Monitoring for imidacloprid resistance in the tobacco‐adapted form of the green peach aphid,Myzus persicae (Sulzer) (Hemiptera: Aphididae), in the eastern United States

BACKGROUND: Imidacloprid is the primary insecticide for controlling the tobacco‐adapted form of the green peach aphid (TGPA), Myzus persicae (Sulzer), a major pest of tobacco worldwide. This study used leaf‐dip bioassays to assess TGPA resistance to imidacloprid in the eastern United States from 2004 through 2007. RESULTS: When combined over the 4 year study, 18, 14 and 3% of the TGPA had imidacloprid resistance ratios (RRs) of 10–20‐fold, 20–30‐fold and 30–90‐fold, respectively, compared with the most susceptible colony tested. This indicates that some colonies have developed moderate levels of resistance to imidacloprid. A colony collected near Clayton, North Carolina, had the highest RR of 91 (LC₅₀ value = 31 mg L^?1). This resistance declined for six tests over a 3 year period in the laboratory culture from >130‐fold RR (LC₅₀ = 48 mg L^?1) to 40‐fold RR (LC₅₀ = 15 mg L^?1). Over the same period, the most susceptible colony and a standard colony not exposed to imidacloprid for over 7 years had consistently low LC₅₀ values. CONCLUSION: Moderate levels of resistance to imidacloprid are noticed among TGPA colonies from the eastern United States. The variation in resistance indicates that the factors responsible are present in the populations at low frequencies and are just not enough to cause field failures yet. Copyright © 2010 Society of Chemical Industry     

Current status of insecticide resistance in Q biotype Bemisia tabaci populations from Crete

BACKGROUND: A major problem of crop protection in Crete, Greece, is the control of Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae) with chemical insecticides owing to the rapid development of resistance. The aim of this study was to investigate the establishment of resistance and the underlying mechanisms to major insecticide classes with classical bioassays and known biochemical resistance markers. RESULTS: During a 2005–2007 survey, 53 Q biotype populations were collected. Application history records showed extensive use of neonicotinoids, organophosphates, carbamates and pyrethroids. High resistance levels were identified in the majority of populations (>80%) for imidacloprid (RF: 38–1958×) and α‐cypermethrin (RF: 30–600×). Low resistance levels (RF < 12) were observed for pirimiphos‐methyl. A strong correlation between resistance to imidacloprid and the number of applications with neonicotinoids was observed. Significant correlations were observed between COE and P450‐dependent monoxygenase activity with resistance to α‐cypermethrin and imidacloprid respectively. A propoxur‐based AChE diagnostic test indicated that iAChE was widespread in most populations. Resistance levels for α‐cypermethrin were increased when compared with a previous survey (2002–2003). Differentiation of LC₅₀ values between localities was observed for imidacloprid only. CONCLUSION: Bemisia tabaci resistance evolved differently in each of the three insecticides studied. Imidacloprid resistance seems less established and less persistent than α‐cypermethrin resistance. The low resistance levels for pirimiphos‐methyl suggest absence of cross‐resistance with other organophosphates or carbamates used. Copyright © 2008 Society of Chemical Industry     

Cross‐resistance,inheritance and biochemical mechanisms of imidacloprid resistance in B‐biotype Bemisia tabaci

BACKGROUND: The B‐type Bemisia tabaci (Gennadius) has become established in many regions in China, and neonicotinoids are extensively used to control this pest. Imidacloprid resistance in a laboratory‐selected strain of B‐type B. tabaci was characterised in order to provide the basis for recommending resistance management tactics. RESULTS: The NJ‐Imi strain of B‐type B. tabaci was selected from the NJ strain with imidacloprid for 30 generations. The NJ‐Imi strain exhibited 490‐fold resistance to imidacloprid, high levels of cross‐resistance to three other neonicotinoids, low levels of cross‐resistance to monosultap, cartap and spinosad, but no cross‐resistance to abamectin and cypermethrin. Imidacloprid resistance in the NJ‐Imi strain was autosomal and semi‐dominant. It is shown that enhanced detoxification mediated by cytochrome‐P450‐dependent monooxygenases contributes to imidacloprid resistance to some extent in the NJ‐Imi strain. Results from synergist bioassays and cross‐resistance patterns indicated that target‐site insensitivity may be involved in imidacloprid resistance in the NJ‐Imi strain of B. tabaci. CONCLUSION: Although oxidative detoxification mediated by P450 monooxygenases is involved in imidacloprid resistance in the NJ‐Imi strain of B‐type B. tabaci, target‐site modification as an additional resistance mechanism cannot be ruled out. Considering the high risk of cross‐resistance, neonicotinoids should be regarded as a single group when implementing an insecticide rotation scheme in B. tabaci control. Copyright © 2009 Society of Chemical Industry     

Biotype Q of<Emphasis Type="Italic">Bemisia tabaci</Emphasis> identified in Israel

The biotype status of samples of the whiteflyBemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) collected from several field and greenhouse sites in Israel during 1999–2000 was determined by polyacrylamide gel electrophoresis (PAGE) for general esterases, and by RAPD-PCR using primers of arbitrary sequence. Results of this survey provide the first published evidence for the occurrence of theB. tabaci Q biotype, alongside the more widely distributed B biotype. Based on the collected samples, it appears that both the B and Q biotypes are present in Israel, and that field populations consist of a mixture of the two biotypes. A possible link betweenB. tabaci biotypes and insecticide resistance is discussed. Contribution no. 508/02 from the Inst. of Plant Protection, ARO, The Volcani Center, Bet Dagan, Israel. http://www.phytoparasitica.org posting Dec. 5, 2002.     

The response of pyriproxyfen-resistant and susceptible Bemisia tabaci Genn (Homoptera: Aleyrodidae) to pyriproxyfen and fenoxycarb alone and in combination with piperonyl butoxide

Pyriproxyfen was effective against susceptible Bemisia tabaci eggs at a LC₅₀ of 0.003 mg litre⁻¹ and against nymphs at 0.02 mg litre⁻¹. In comparison, eggs of a laboratory selected, pyriproxyfen-resistant B tabaci strain, originating in an Israeli greenhouse, exhibited 6500-fold resistance and nymphs exhibited 1100-fold resistance. Eggs and nymphs of a strain from an Israeli sunflower field exhibited 450 and 210-fold resistance in comparison to the susceptible standard. Fenoxycarb was generally less effective than pyriproxyfen against B tabaci eggs and nymphs but was unaffected by pyriproxyfen resistance. Piperonyl butoxide (PB) was antagonistic to pyriproxyfen, and this increased with increasing pyriproxyfen resistance. PB had no effect on the toxicity of fenoxycarb. Collectively, these data imply that the modes of action of pyriproxyfen and fenoxycarb are distinct, despite the structural similarities of these molecules. Possible reasons for the antagonism of PB against pyriproxyfen are discussed. © 1999 Society of Chemical Industry     

Insecticide resistance in house flies from caged‐layer poultry facilities

The frequency of resistance of eight strains of house flies, Musca domestica L., collected from caged‐layer poultry facilities across New York state, to nine insecticides (dimethoate, tetrachlorvinphos, permethrin, cyfluthrin, pyrethrins, methomyl, fipronil, spinosad and cyromazine) was measured relative to a laboratory susceptible strain. Percentage survival was evaluated at five diagnostic concentrations: susceptible strain LC₉₉, 3 × LC₉₉, 10 × LC₉₉, 30 × LC₉₉ and 100 × LC₉₉. The highest levels of resistance were noted for tetrachlorvinphos, permethrin and cyfluthrin. There was substantial variation in the levels of resistance to the different insecticides from one facility to another, independent of their geographical location. There was very little cross‐resistance detected in these populations to either fipronil or spinosad. Overall, there was a good correlation between insecticide use histories and the levels of resistance. The apparent isolation of fly populations within poultry facilities suggests that there are good opportunities for the implementation of successful resistance management strategies at these facilities. Differences between these results and those of a resistance survey on New York dairy farms in 1987 are discussed. © 2000 Society of Chemical Industry     

Molecular phylogenetic analysis reveals at least five genetic races of<Emphasis Type="Italic">Bemisia tabaci</Emphasis> in China

Phylogenetic analysis using ITS1 and CO1 nucleotide sequences has revealed six major races ofBemisia tabaci in the world, including three major indigenous races in the Asia-Pacific region,viz., B. tabaci (Asia),B. tabaci (Bali) andB. tabaci (Australia), but the status of a large collection of genotypes in this region remains unresolved. The ITS1 sequences of representative whitefly samples collected from around China were determined in this study. These sequences and other homologous sequences retrieved from GenBank were then used to conduct a phylogenetic analysis. The results demonstrated that the whiteflies collected in China were split genetically into four groups, where at least five genetic races were revealed,i.e., B biotype (SDLe, XJEp, XJAt, HNNt, BJIb, GDEp, XJGh, GDHrs, XJSm and SHEp), Bali group (ZJGh), M biotype (Hainan1), G biotype (GXCm) and Asian H/K group (FJIb, GDCv), although the Asian H/K group with low bootstrap score remains unresolved. Of all genetic races, the B biotype is the most extensively distributed. In the dendogram, the J biotype, L biotype and Q biotype cluster together and form a sister clade to the B biotype. The data indicate that extensive migration ofB. tabaci has taken place in Asian countries. The populations ZJGh, FJIb, GDCv, GXCm and Hainanl collected in China might have originated there, but the possibility that they were introduced from elsewhere cannot be excluded at this point. Using PyR from Israel as a reference Q biotype, the random amplified polymorphic DNA banding patterns of SDLe, XJEp, XJAt and HNNt were shown to be consistent with that of the Q biotype, which indicated that the four local whitefly populations identified as the B biotype based on ITS1 sequences were closely related to the Q biotype. http//www.phytoparasitica.org posting Sept. 12, 2006.     

丽蚜小蜂寄生对Q型烟粉虱生长发育的影响

为明确丽蚜小蜂寄生对Q型烟粉虱的影响,通过室内饲养观察不同龄期Q型烟粉虱被丽蚜小蜂寄生后的生长发育,并比较了被寄生后烟粉虱若虫的个体大小及死亡率。结果表明,2龄、3龄和4龄烟粉虱若虫被寄生后均能继续发育,2龄若虫蜕皮进入3龄和3龄若虫蜕皮进入4龄的时间与对照间无显著差异,而被寄生若虫的4龄期显著延长。对于同一龄期的烟粉虱若虫,丽蚜小蜂偏向于选择较大的个体寄生,2龄和3龄被寄生若虫发育后期个体比未被寄生个体大,但4龄时被寄生的个体在发育后期略小于未被寄生个体,显示丽蚜小蜂对不同龄期若虫的生长发育影响不同。2龄若虫死亡率为61.64%,显著高于3龄和4龄若虫;4龄若虫褐蛹率最高,为48.84%。表明无论寄生哪一发育阶段的烟粉虱若虫,丽蚜小蜂的寄生均为容性寄生,田间应用丽蚜小蜂防治Q型烟粉虱时在其若虫3~4龄时释放更适宜。     

Panel of real‐time PCRs for the multiplexed detection of two tomato‐infecting begomoviruses and their cognate whitefly vector species

A new approach for the simultaneous identification of the viruses and vectors responsible for tomato yellow leaf curl disease (TYLCD) epidemics is presented. A panel of quantitative multiplexed real‐time PCR assays was developed for the sensitive and reliable detection of Tomato yellow leaf curl virus‐Israel (TYLCV‐IL), Tomato leaf curl virus (ToLCV), Bemisia tabaci Middle East Asia Minor 1 species (MEAM1, B biotype) and B. tabaci Mediterranean species (MED, Q biotype) from either plant or whitefly samples. For quality‐assurance purposes, two internal control assays were included in the assay panel for the co‐amplification of solanaceous plant DNA or B. tabaci DNA. All assays were shown to be specific and reproducible. The multiplexed assays were able to reliably detect as few as 10 plasmid copies of TYLCV‐IL, 100 plasmid copies of ToLCV, 500 fg B. tabaci MEAM1 and 300 fg B. tabaci MED DNA. Evaluated methods for routine testing of field‐collected whiteflies are presented, including protocols for processing B. tabaci captured on yellow sticky traps and for bulking of multiple B. tabaci individuals prior to DNA extraction. This work assembles all of the essential features of a validated and quality‐assured diagnostic method for the identification and discrimination of tomato‐infecting begomovirus and B. tabaci vector species in Australia. This flexible panel of assays will facilitate improved quarantine, biosecurity and disease‐management programmes both in Australia and worldwide.     

Beet armyworm (Spodoptera exigua) resistance to spinosad

Susceptibility to spinosad (Success®/Tracer®) of beet armyworm (Spodoptera exigua) from the southern USA and Southeast Asia was determined through exposure of second‐ and third‐instar larvae to dipped cotton leaves. LC₅₀ estimates of susceptibility of second‐ and third‐instar larvae of field populations ranged from 0.279 to 6.14 and 0.589 to 14.0 mg spinosad litre⁻¹, respectively. A Thailand population was 22‐ and 24‐fold less susceptible than the six other US field populations evaluated, and 85‐ and 58‐fold less susceptible than a reference laboratory population, respectively. From these results, we initiated experiments to test the hypothesis that the Thailand population was resistant to spinosad. F₁ crosses between the resistant Thailand population and a susceptible reference strain yielded individuals that were 22‐fold less sensitive to spinosad than the susceptible parent. This same resistant strain exhibited significantly greater survivorship on plants treated with spinosad in the field. Lastly, selection of an Arizona population resulted in a significant reduction in susceptibility to spinosad, further substantiating the hypothesis of a genetic basis for resistance to spinosad. These findings indicate a vulnerability of this new insecticide to resistance development in beet armyworm and should serve as a warning against excessive use of it. © 2000 Society of Chemical Industry     

Resistance of Bemisia tabaci (Homoptera: Aleyrodidae) to insecticides in southern Spain with special reference to neonicotinoids

The tobacco whitefly, Bemisia tabaci Gennadius (Homoptera: Aleyrodidae) which occurs in various parts of the world, has developed a high degree of resistance against several chemical classes of insecticide, including organophosphates, carbamates, pyrethroids, insect growth regulators and chlorinated hydrocarbons. The present studies were done in order to monitor the susceptibility of whitefly populations in southern Spain to insecticides commonly used there. Systemic bioassays using Spanish field populations of B tabaci collected in 1994, 1996 and 1998 indicated an increase, albeit a slow one, in resistance to imidacloprid over this period. Comparative studies of other neonicotinoids using the same bioassay revealed a high degree of cross‐resistance to acetamiprid and thiamethoxam. Leaf‐dip bioassays with adult females from these populations revealed a high level of resistance to cyfluthrin, endosulfan, monocrotophos, methamidophos, and pymetrozine, each at 200 mg litre⁻¹. Buprofezin and pyriproxyfen were tested against second‐instar nymphs and eggs, respectively. Buprofezin also showed a lower efficacy against ESP‐98, a strain of B tabaci received from Almeria in 1998, but pyriproxyfen resistance was not obvious when tested against eggs of strain ESP‐98. Field trials in 1998 revealed good efficacy of imidacloprid in one farm in the Almeria region and two greenhouses in Murcia and Sevilla, but a loss of activity by imidacloprid in another farm in the Almeria region. Cross‐resistance between imidacloprid and thiamethoxam was also confirmed under field conditions. © 2000 Society of Chemical Industry     

Q型烟粉虱芳香基硫酸酯酶B基因的克隆及表达分析

为明确烟粉虱Bemisia tabaci取食感染番茄黄化曲叶病毒(Tomato yellow leaf curl virus,TYLCV)的番茄植株后,其体内的芳香基硫酸酯酶B基因(arylsulfatase B,ARSB)是否能够做出应答反应,基于Q型烟粉虱基因组数据克隆得到ARSB基因cDNA全长,采用生物信息学方法分析其序列特征,并通过实时荧光定量PCR技术测定ARSB基因在Q型烟粉虱不同发育阶段、不同组织及携带TYLCV前后的表达量变化情况。结果显示:Q型烟粉虱ARSB基因的cDNA全长为1 731 bp,编码576个氨基酸,分子量为64.89 kD,具有ARSB的保守结构域。ARSB基因在Q型烟粉虱不同发育阶段均有表达,在卵期表达量最高,成虫期表达量最低;该基因在Q型烟粉虱头胸部的表达量显著高于腹部;Q型烟粉虱获取TYLCV 72 h后其体内ARSB基因表达量显著提高。表明ARSB基因在Q型烟粉虱不同龄期、不同组织内存在差异表达,并可能参与Q型烟粉虱对TYLCV的响应和传毒过程。