Intra- and interspecific competition between western flower thrips and sweetpotato whitefly.

The western flower thrips, Frankliniella occidentalis (Pergande), and the sweetpotato whitefly, Bemisia tabaci (Gennadius), are both invasive insect pests and are present in most of the same agricultural crops without a clear dominance of either species. Here, intra- and interspecific competition in B. tabaci and F. occidentalis was determined under controlled experiments. The results showed that intraspecific competition was distinct in F. occidentalis and that the co-occurrence of B. tabaci had a strong effect on F. occidentalis, resulting in a decrease in oviposition. Significant intraspecific competition was found in B. tabaci, and the coexistence of F. occidentalis had limited effect on the oviposition of B. tabaci. In a selective host plant preference experiment, both F. occidentalis and B. tabaci preferred eggplants most, followed by cucumbers and tomatoes. On cucumber plants, B. tabaci was predominant, whereas on eggplant and tomato plants, F. occidentalis and B. tabaci exhibited comparative competitive abilities during the initial stage. However, over time, higher numbers of B. tabaci than that of F. occidentalis were found on the two host plants. Our in vitro and potted plant experiments indicate that B. tabaci is competitively superior to F. occidentalis, which might help to explain their differential distribution patterns in China.

Two cytochrome P450 genes are involved in imidacloprid resistance in field populations of the whitefly, Bemisia tabaci, in China.

The sweet potato whitefly, Bemisia tabaci (Gennadius) (Hemiptera:Aleyrodidae), is an invasive and damaging pest of field crops worldwide. The neonicotinoid insecticide imidacloprid has been widely used to control this pest. We assessed the species composition (B vs. Q), imidacloprid resistance, and association between imidacloprid resistance and the expression of five P450 genes for 14-17 B. tabaci populations in 12 provinces in China. Fifteen of 17 populations contained only B. tabaci Q, and two populations contained both B and Q. Seven of 17 populations exhibited moderate to high resistance to imidacloprid, and eight populations exhibited low resistance to imidacloprid, compared with the most susceptible field WHHB population. In a study of 14 of the populations, resistance level was correlated with the expression of the P450 genes CYP6CM1 and CYP4C64 but not with the expression of CYP6CX1, CYP6CX4, or CYP6DZ7. This study indicates that B. tabaci Q has a wider distribution in China than previously reported. Resistance to imidacloprid in field populations of B. tabaci is associated with the increased expression of two cytochrome P450 genes (CYP6CM1 and CYP4C64).

Relative amount of symbionts in insect hosts changes with host-plant adaptation and insecticide resistance.

The impact of symbionts on their hosts depends on their infection density. In the current study, we investigated the effects of host plant and insecticide resistance on the relative amount of symbionts Portiera, Hamiltonella, Rickettsia, and Cardinium in the whitefly Bemisia tabaci (Gennadius) B biotype. The relative amount of symbionts in three host plant-adapted subpopulations (cucumber, Cucumis sativus L.; cabbage, Brassica oleracea L.; and cotton, Gossypium herbaceum L.) with the same genetic background and insecticide (thiamethoxam)-resistant and -susceptible subpopulations with the same genetic background were measured by quantitative polymerase chain reaction. The results showed that the cucumber population harbored more Portiera than the cabbage and cotton populations, the cabbage population harbored more Hamiltonella than the cucumber population, Hamiltonella amount did not statistically differ between the cotton and cucumber or the cotton and cabbage populations, and the cabbage population harbored more Rickettsia and Cardinium than the cucumber and cotton populations. In addition, the thiamethoxam-susceptible population harbored more Portiera and Hamiltonella than the thiamethoxam-resistant population, whereas the thiamethoxam-resistant population harbored more Rickettsia than the thiamethoxam-susceptible population. These results indicated that relative amounts of symbionts were affected significantly by host plant-adaption and insecticide resistance, and the response to host plant and insecticide differed among the symbionts.

Gene expression profiling in the thiamethoxam resistant and susceptible B-biotype sweetpotato whitefly, Bemisia tabaci.

Thiamethoxam has been used as a major insecticide to control the B-biotype sweetpotato whitefly, Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). Due to its excessive use, a high level of resistance to thiamethoxam has developed worldwide over the past several years. To better understand the molecular mechanisms underlying this resistance in B. tabaci, gene profiles between the thiamethoxam-resistant and thiamethoxam-susceptible strains were investigated using the suppression subtractive hybridization (SSH) library approach. A total of 72 and 52 upand down-regulated genes were obtained from the forward and reverse SSH libraries, respectively. These expressed sequence tags (ESTs) belong to several functional categories based on their gene ontology annotation. Some categories such as cell communication, response to abiotic stimulus, lipid particle, and nuclear envelope were identified only in the forward library of thiamethoxam-resistant strains. In contrast, categories such as behavior, cell proliferation, nutrient reservoir activity, sequence-specific DNA binding transcription factor activity, and signal transducer activity were identified solely in the reverse library. To study the validity of the SSH method, 16 differentially expressed genes from both forward and reverse SSH libraries were selected randomly for further analyses using quantitative realtime PCR (qRT-PCR). The qRT-PCR results were fairly consistent with the SSH results; however, only 50% of the genes showed significantly different expression profiles between the thiamethoxam-resistant and thiamethoxam-susceptible whiteflies. Among these genes, a putative NAD-dependent methanol dehydrogenase was substantially over-expressed in the thiamethoxamresistant adults compared to their susceptible counterparts. The distributed profiles show that it was highly expressed during the egg stage, and was most abundant in the abdomen of adult females.

Pyrosequencing the Bemisia tabaci transcriptome reveals a highly diverse bacterial community and a robust system for insecticide resistance.

BACKGROUND: Bemisia tabaci (Gennadius) is a phloem-feeding insect poised to become one of the major insect pests in open field and greenhouse production systems throughout the world. The high level of resistance to insecticides is a main factor that hinders continued use of insecticides for suppression of B. tabaci. Despite its prevalence, little is known about B. tabaci at the genome level. To fill this gap, an invasive B. tabaci B biotype was subjected to pyrosequencing-based transcriptome analysis to identify genes and gene networks putatively involved in various physiological and toxicological processes. METHODOLOGY AND PRINCIPAL FINDINGS: Using Roche 454 pyrosequencing, 857,205 reads containing approximately 340 megabases were obtained from the B. tabaci transcriptome. De novo assembly generated 178,669 unigenes including 30,980 from insects, 17,881 from bacteria, and 129,808 from the nohit. A total of 50,835 (28.45%) unigenes showed similarity to the non-redundant database in GenBank with a cut-off E-value of 10-5. Among them, 40,611 unigenes were assigned to one or more GO terms and 6,917 unigenes were assigned to 288 known pathways. De novo metatranscriptome analysis revealed highly diverse bacterial symbionts in B. tabaci, and demonstrated the host-symbiont cooperation in amino acid production. In-depth transcriptome analysis indentified putative molecular markers, and genes potentially involved in insecticide resistance and nutrient digestion. The utility of this transcriptome was validated by a thiamethoxam resistance study, in which annotated cytochrome P450 genes were significantly overexpressed in the resistant B. tabaci in comparison to its susceptible counterparts. CONCLUSIONS: This transcriptome/metatranscriptome analysis sheds light on the molecular understanding of symbiosis and insecticide resistance in an agriculturally important phloem-feeding insect pest, and lays the foundation for future functional genomics research of the B. tabaci complex. Moreover, current pyrosequencing effort greatly enriched the existing whitefly EST database, and makes RNAseq a viable option for future genomic analysis.

Demographic changes in multigeneration Plutella xylostella (Lepidoptera: Plutellidae) after exposure to sublethal concentrations of spinosad.

The sublethal effects of the insecticide spinosad were assessed against Plutella xylostella (L.) (Lepidoptera: Plutellidae) by using a demographic approach. The resulting data were analyzed based on the age-stage and two-sex life table model. Bioassay results showed that the susceptibility of P. xylostella to spinosad decreased in Sub strains selected by LC25 spinosad for 10 generations. Although the egg size was significantly smaller in Sub-1 (selected by LC25 spinosad for one generation) compared with spinosad-susceptible strain SS, egg size recovered to normal levels in Sub-5 (selected by LC25 spinosad for five generations) and were even larger in Sub-10 (selected by LC25 spinosad for 10 generations). The life-history parameters changed in the Sub strains of different generations. Sublethal spinosad had a significant effect on Sub-1; however, the sublethal effect on the Sub strains decreased as selection cycles increased. The intrinsic rate of increase (r(m)), finite rate of increase (lambda) and net reproductive rate (R(o)) in Sub-1 were significantly decreased compared with those in the SS strain. No significant differences were found between the Sub-5 or Sub-10 compared with the SS strain. The greatest difference was observed in the total number of eggs laid by each female, i.e., the fecundity. The fecundity in SS, Sub-1, Sub-5, and Sub-10 were 121.92, 81.26, 114.42, and 159.21, respectively. The life expectancy of an SS, Sub-1, Sub-5, and Sub-10 egg was 10.58, 8.71, 10.21, and 7.45 d, respectively.