Sublethal Effects of Triflumezopyrim on Biological Traits and Detoxification Enzyme Activities in the Small Brown Planthopper Laodelphax striatellus (Hemiptera: Delphacidae)

The small brown planthopper [Laodelphax striatellus (Fallén) (Hemiptera, Delphacidae)] is one of the most destructive insect pests of rice and has developed strong resistance to several kinds of chemical insecticides. Triflumezopyrim, a novel mesoionic insecticide developed by Corteva Agriscience (formerly DuPont Crop Protection), has efficient biological activity in controlling sucking insects, such as the planthopper. However, the effects of triflumezopyrim on the growth and reproduction of L. striatellus have not been reported. In this study, an F5 generation was obtained by conducting five rounds of insecticide screening on a sensitive L. striatellus strain (F0 generation). An age-stage life table procedure was used to evaluate the effects of a sublethal concentration (LC50) of triflumezopyrim on the biological parameters of L. striatellus. Compared with those of the F0 generation, the intrinsic rate of increase (r), the finite rate (λ), and the net reproductive rate (R0) of the F5 generation were significantly decreased; nevertheless, the average duration of life (T) was not significantly affected. The results of detoxification enzyme activity assays indicated that the glutathione S-transferase and cytochrome P450 monooxygenase (P450) activities in the F5 generation were significantly higher than those in the F0 generation. The contents of vitellogenin (Vg) and vitellogenin receptor (VgR) were also detected, and the results indicated that the contents of Vg and VgR in the F5 generation were significantly decreased compared to those in the F0 generation. Furthermore, we detected the relative expression of ecdysone receptor (EcR), Vg, and VgR in the F0 and F5 generations and found that the relative expression levels of Vg and VgR in the F5 generation female adults were obviously lower than those in the F0 generation (P < 0.05), whereas the relative expression of EcR was slightly increased, although the difference was not significant (P > 0.05). Based on these results, a sublethal concentration (median lethal concentration, LC50) of triflumezopyrim may inhibit the generational growth and reproduction of L. striatellus. Moreover, our results may provide a reference for further studies of the suitability and resistance mechanisms of L. striatellus subjected to a sublethal dose of triflumezopyrim.

The small brown planthopper [Laodelphax striatellus (Fallén) (Hemiptera, Delphacidae)] is one of the most destructive insect pests of rice and has developed strong resistance to several kinds of chemical insecticides. Triflumezopyrim, a novel mesoionic insecticide developed by Corteva Agriscience (formerly DuPont Crop Protection), has efficient biological activity in controlling sucking insects, such as the planthopper. However, the effects of triflumezopyrim on the growth and reproduction of L. striatellus have not been reported. In this study, an F 5 generation was obtained by conducting five rounds of insecticide screening on a sensitive L. striatellus strain (F 0 generation). An age-stage life table procedure was used to evaluate the effects of a sublethal concentration (LC 50 ) of triflumezopyrim on the biological parameters of L. striatellus. Compared with those of the F 0 generation, the intrinsic rate of increase (r), the finite rate (λ), and the net reproductive rate (R 0 ) of the F 5 generation were significantly decreased; nevertheless, the average duration of life (T) was not significantly affected. The results of detoxification enzyme activity assays indicated that the glutathione S-transferase and cytochrome P450 monooxygenase (P450) activities in the F 5 generation were significantly higher than those in the F 0 generation. The contents of vitellogenin (Vg) and vitellogenin receptor (VgR) were also detected, and the results indicated that the contents of Vg and VgR in the F 5 generation were significantly decreased compared to those in the F 0 generation. Furthermore, we detected the relative expression of ecdysone receptor (EcR), Vg, and VgR in the F 0 and F 5 generations and found that the relative expression levels of Vg and VgR in the F 5 generation female adults were obviously lower than those in the F 0 generation (P < 0.05), whereas the relative expression of EcR was slightly increased, although the difference was not significant (P > 0.05). Based on these results,

INTRODUCTION
The small brown planthopper [Laodelphax striatellus (Fallén) (Hemiptera: Delphacidae)] is one of the most destructive insect pests of rice; its adults and nymphs not only feed directly on rice but also spread viral diseases, such as rice blackstreaked dwarf disease (Kisimoto, 1967;Yin et al., 2013). At present, the control of L. striatellus in China depends mainly on chemical insecticides, the use of which has resulted in different levels of resistance to many pesticides, such as deltamethrin, chlorpyrifos, imidacloprid, and buprofezin Abdalla Elzaki et al., 2018;Asaduzzaman et al., 2019). Triflumezopyrim is a newly commercialized molecule from Corteva Agriscience. The biochemical and physiological action of this novel insecticide involves its binding to the orthosteric site of the nicotinic acetylcholine receptor by competitive binding, making the insects lethargic and poisoned, which was highly effective for controlling both imidacloprid-susceptible and imidacloprid-resistant planthopper populations in Malaysia (Cordova et al., 2016). For Chinese rice planthopper populations, triflumezopyrim has extremely high efficacy; additionally, triflumezopyrim is less harmful to natural enemies, such as Anagrus nilaparvatae (Hymenoptera: Mymaridae), Cyrtorhinus lividipennis (Hemiptera: Miridae), and Paederus fuscipes (Coleoptera: Staphylinidae) .
The occurrence of resistance is closely related to the sublethal effects of pesticides on insects and the changes in detoxification enzymes in insects (Ma et al., 2019;Meng et al., 2019a,b). The study of sublethal effects can be carried out by establishing an insect's amphoteric life table. Sublethal effects are manifested mainly in the growth and development of insect individuals and their offspring, feeding behavior, mating and reproduction, oviposition, egg hatching rate, and population growth (Ramirez-Romero et al., 2007). Vitellin (Vn) is a specific protein of the female hemolymph that provides nutritional sources for embryonic development and is closely related to female insect reproduction (Sappington and Raikhel, 1998;Tufail and Takeda, 2008;Veerana et al., 2015;Liao et al., 2019;Xiang et al., 2019;Xu et al., 2019). Vitellogenin (Vg) is the necessary precursor material for synthesizing Vn. When developing oocytes take up Vg, they require membrane-bound Vg receptor (VgR) for transport (Schneider, 1996;Snigirevskaya et al., 1997). Ecdysone receptor (EcR) can inhibit the expression of Vg (Yan et al., 2016;Shen et al., 2018). Hence, the expression of the EcR, Vg, and VgR genes has a significant influence on insect growth and reproduction.
Our objective is to analyze the population dynamics, detoxification enzyme activities, Vg and VgR contents, and relative expression of the EcR, Vg, and VgR genes of L. striatellus under sublethal concentrations of triflumezopyrim. The findings of this study may provide a reference for further research on the suitability and resistance mechanisms of L. striatellus subjected to a sublethal dose of triflumezopyrim and provide theoretical support for the popularization and application of new pesticides.

Insects and Insecticide
A susceptible laboratory strain of L. striatellus (F 0 ) was kindly provided by Nanjing Agricultural University in September 2016. These insects had not been exposed to any insecticides for 15 consecutive years and were continuously reared on rice seedlings (TN1) in our laboratory under a temperature of 27 ± 1 • C, relative humidity of 70 ± 10%, and photoperiod of 14 L:10 D. Triflumezopyrim SC (10%) was purchased from Corteva Agriscience (Wilmington, DE, United States). All other chemicals and solvents used were analytical reagents.

Bioassays
The toxicity of triflumezopyrim to L. striatellus was assayed using the rice seedling dipping method, with minor modifications (Xiang et al., 2019). A series of concentrations of triflumezopyrim were diluted with water containing 0.1% Triton TM X-100, and 0.1% Triton X-100 solution was used as the control. After soaking the rice seedlings in the prepared liquid for 30 s, they were placed in newspaper to dry. The roots were wrapped with degreased cotton, sufficient water was absorbed, and they were placed in plastic cups. Fifteen healthy and uniform 3rd-instar nymphs were prepared for each treatment, and each concentration was tested in triplicate. After 96 h, the mortality rate of the test insects was counted (Liao et al., 2017), with direct death or incompatible movement as death. The toxicity regression equation Y = a + bX, standard error, LC 50 value, 95% confidence interval (95% CI), χ 2 value, and Pr were calculated using SAS 9.2 (North Carolina State University, Raleigh, North Carolina, United States).

Sublethal Effects of Triflumezopyrim on L. striatellus
Triflumezopyrim Effects on the Life-History Traits of the F 4 Generation The experimental procedure was performed according to the description of Xiang et al. (2019), with some modifications. The screening operation procedure is shown in Figure 1. According to the bioassay results of the F 0 generation, the 3rd-instar nymphs of susceptible L. striatellus were treated with the LC 50 of triflumezopyrim. Then, the surviving nymphs were collected, and the F 1 generation was obtained after spawning. The toxicity of triflumezopyrim was assessed in the F 1 generation, and then, FIGURE 1 | The procedure used to produce the F 5 generation. According to the bioassay results of the F 0 generation, 3rd-instar nymphs of susceptible L. striatellus were treated with the LC 50 of triflumezopyrim. Then, the surviving nymphs were collected, and the F 1 generation was obtained after spawning. The toxicity of triflumezopyrim was assessed in the F 1 generation, and then the remaining 3rd-instar nymphs of F 1 were screened with the new LC 50 value. After five rounds of drug screening, the F 5 generation was obtained. After treatment of the third-instar F 4 nymphs, the surviving individuals were selected for observation, as shown in section "Triflumezopyrim Effects on the Life-History Traits of the F 4 Generation," and the results are shown in Table 3. Then, a series of experiments to determine sublethal effects and detoxifying enzyme activity were performed on the F 5 generation. The methods are detailed in sections "Triflumezopyrim Effects on the Life-History Traits of the F 5 Generation," "Enzyme Assays," "Detection of the Contents of Vg and VgR," and "Reverse Transcriptase-Quantitative Polymerase Chain Reaction of EcR, Vg, and VgR," and the results are shown in Tables 4-6 and Figures 2-8. the survived 3rd-instar F 1 nymphs were screened with the newer LC 50 value. After five rounds of drug screening from the F 0 generation, survival of the F 4 generation was achieved. Then, 150 surviving nymphs were selected from the F 4 generation and transferred into flat-bottomed test tubes (diameter × height: 20.0 mm × 145.0 mm) containing fresh rice seedlings. The first 100 nymphs were numbered and used for formal experiments, and the last 50 nymphs were used as substitutes. After emergence, each pair of male and female adults was transferred one by one to a flat-bottomed test tube containing two fresh rice seedlings. If a pair did not mate, they were provided with substitute partners. Third-instar F 0 nymphs were used for the control treatment. The rice seedlings were replaced every day until the adults died, and the fecundity and longevity of the pair were recorded. The life tables of the F 4 generation were made at the same time as those of the F 0 generation.

Triflumezopyrim Effects on the Life-History Traits of the F 5 Generation
The sublethal effects of triflumezopyrim on L. striatellus were studied as follows: First, 150 eggs laid on the fifth to sixth day after the emergence and pairing of the sensitive L. striatellus and F 4 insects were collected to serve as the F 0 (susceptible L. striatellus not exposing triflumezopyrim) and F 5 generations, respectively, and kept in separate test tubes, with 100 for formal experiments and an additional 50 retained as potential replacements. Second, when these eggs became adults, pairs were made according to the method described above. Finally, the population characteristics, including developmental time, longevity, fecundity, and hatching ability, were monitored every day until the pair died. The replaced rice seedlings were dissected under a T-type microscope after 12 days to record the number of unhatched eggs. The life tables of the F 5 and F 0 generations were prepared at the same time. The statistical data of the life table were analyzed by using the age-stage, two-sex life table procedure. The life table parameters were analyzed using the program TWOSEX-MSChart (Chi, 2018) and included female age-specific fecundity (f xj ), f x7 , population age-specific survival rate (l x ), population agespecific fecundity (m x ), age-stage survival rate (s xj ), age-stagespecific reproductive value (v xj ), finite rate (λ), net reproductive rate (R 0 ), intrinsic rate of increase (r), mean generation time (T), developmental time, adult longevity, adult preoviposition period (APOP), and total preoviposition period (TPOP). The values f x7 , l x , m x , l x m x , s xj , and v xj were plotted using SigmaPlot 12.3 (Systat Software, Inc, San Jose, California, United States). The mean and standard error of life table parameters were estimated by the bootstrap technique included in TWOSEX-MSChart with 100,000 random resamplings. A paired bootstrap test (TWOSEX-MSChart) program was used to determine the significant differences in population parameters, development duration, and reproductive value of the F 5 generation compared to the F 0 generation (TWOSEX-MSChart) (P < 0.05).

Enzyme Assays
Third-instar nymphs of the F 0 and F 5 generations were analyzed for the activity of three detoxifying metabolic enzymes. Carboxylesterase (CarE) activity was determined according to the method described by Asperen (1962). Twenty nymphs (3rd instar) were transferred into a centrifuge tube and stored in liquid nitrogen as quickly as possible, homogenized in 2 mL phosphate buffer (0.04 mol/L phosphate buffer, pH 7.0) icebath slurry, and centrifuged at 4 • C and 10,000 × g for 15 min. Then, the supernatant was transferred into a clean Eppendorf tube as the crude enzyme solution. A mixture of 0.45 mL of phosphate buffer (0.04 mol/L, pH 7.0), 1.8 mL of 3 × 10 −4 mol/L α-NA solution (containing 3 × 10 −4 mol/L physostigmine), and 50 µL of diluted enzyme liquid was added to each tube. After thorough mixing, the reaction was performed for 15 min in a constant-temperature bath at 30 • C, and then 0.9 mL of staining solution (0.2 g of fast blue-B salt in 20 mL of distilled water plus 50 mL of 5% sodium dodecyl sulfate) was added.
The absorbance values were recorded at 600 nm after 5 min in a UV 2000 Spectrophotometer [Unic (Shang Hai) Instruments Incorporated, Shanghai, China].
Glutathione S-transferase (GST) activity was determined by using 1-chloro-2,4-dinitrobenzene (CDNB) as a substrate, according to the method of Wang et al. (2018), with minor revisions. Thirty nymphs were placed into a centrifuge tube and stored in liquid nitrogen as quickly as possible. Then, 2 mL of phosphate buffer (0.1 mol/L phosphate buffer containing 1.0 mmol/L EDTA, pH 6.5) was added, and the mixture was centrifuged at 4 • C and 10,000 × g for 10 min. Then, the supernatant was used as the enzyme solution. The total volume of the reaction system was 2.7 mL, including 2,470 µL of phosphate buffer (0.1 mol/L, pH 6.5), 90 µL of CDNB (15 mmol/L), 50 µL of the enzyme source, and 90 µL of reduced GSH (30 mmol/L). After rapidly shaking the mixture, the absorbance values were monitored within 2 min with a spectrophotometer at 340 nm.
Cytochrome P450 (P450) activity was assayed using the method of Rose et al. (1995) with some modification. One hundred fifty (3rd-instar) nymphs were homogenized on ice with 2 mL of phosphoric acid buffer (0.1 mol/L, pH 7.6, containing 20% glycerol, 0.1 mmol/L EDTA, 0.1 mmol/L DTT, and 0.4 mmol/L phenylmethylsulfonyl fluoride). The homogenate was centrifuged at 4 • C and 10,000 × g for 10 min to obtain the supernatant, which was stored at low temperature as the enzyme solution. The OD value was determined at 405 nm by adding 100 µL of 4-nitroanisole (2 × 10 −3 mol/L) and 90 mL of enzyme solution to the enzyme labeling plate, incubating for 3 min at 30 • C, and then adding 10 mL of NADPH (9.6 × 10 −3 mol/L). The OD values were recorded after every 20 s for 2 min, and a standard curve of p-nitrophenol was prepared in advance. The specific activity of P450s was finally calculated as nanomoles of p-nitrophenol per minute per milligram of protein [nmol/(min mg pro)].
All treatments were performed with three samples (tubes) as biological repetitions, and each enzyme sample was replicated three times as technical repetitions. The total protein content of the enzyme solution was determined by the Bradford method using bovine albumin as a standard (Bradford, 1976). The activities of CarEs, GSTs, and P450s were analyzed using unpaired Student t-tests, and the significance level of the results was set at P < 0.05.

Detection of the Contents of Vg and VgR
Females of the F 0 and F 5 generations were collected on the second day after emergence, and triplicates were performed for each treatment. Twenty insects of each sample type were frozen with liquid nitrogen and stored at −80 • C. The Vg and VgR contents were detected using the double-antibody sandwich method according to the enzyme-linked immunosorbent assay kit of Alpha Enzyme Biotechnology Co., Ltd. (Shanghai, China). The contents of Vg and VgR were analyzed using unpaired Student t-tests, and the significance level of the results was set at P < 0.05.

Reverse Transcriptase-Quantitative Polymerase Chain Reaction of EcR, Vg, and VgR
Females of the F 0 and F 5 generations were collected on the second day after emergence. Total RNA was extracted by using TRIzol reagent (Shanghai Yubo Biological Technology Co. Ltd., Shanghai, China) following the manufacturer's specifications, and cDNA was synthesized from the total RNA using TransScript cDNA Synthesis SuperMix (Novoprotein Scientific Inc., Shanghai, China) for qPCR. TransStart TopTaq (Novoprotein Scientific Inc.) was used to conduct the reverse transcriptase-quantitative polymerase chain reactions (RT-qPCRs). Primers were designed as shown in Table 1, with the EF-1Fq gene as an internal reference gene (Jia et al., 2015). The RT-qPCRs for each treatment were replicated three times. The relative expressions of EcR (Jia et al., 2015), Vg, and VgR were represented by relative quantification values calculated by the math formula method. The relative expression of the EcR, Vg, and VgR genes was analyzed using unpaired Student t-tests, and the significance level of the results was set at P < 0.05.

RESULTS
Toxicity of Triflumezopyrim on 3rd-Instar Nymphs of L. striatellus To understand the changes in the susceptibility of L. striatellus under the screening pressure of triflumezopyrim, we used the rice seedling dipping method to evaluate the toxicity of triflumezopyrim and found that the LC 50 values of triflumezopyrim on 3rd-instar nymphs of the F 0 and F 4 The results are presented as the number of tested insects, standard error, 95% confidence limits, χ 2 value, degrees of freedom (df), and Pr calculated by SAS 9.2. generations were 0.443 ± 0.171 µg/mL and 5.682 ± 1.498 µg/mL, respectively, with a resistance ratio of 12.84-fold ( Table 2).

Effects of Triflumezopyrim on the Life-History Traits of the F 4 Generation
To better understand the effects of triflumezopyrim on the population characteristics of L. striatellus, we used an age-stage life table procedure and found that the mean fecundity of the F 4 generation adults was almost unchanged compared with that of the F 0 generation adults, and the longevity of the F 4 generation adults was extended, although the difference was not significant (P > 0.05), as shown in Table 3.

Effects of Triflumezopyrim on the Life-History Traits of the F 5 Generation
All developmental times of the F 5 generation are shown in Table 4. The results indicated that the durations of the egg stage and 1st-instar stage (9.21 and 3.09 days, respectively) in the F 5 generation were significantly shorter than those in the F 0 generation (9.67 and 3.38 days, respectively; P < 0.05); nevertheless, there was no difference between the two strains during the other nymphal stages (P > 0.05). The fecundity, APOP, TPOP, and longevity of the F 5 generation are displayed in Table 5. The mean fecundity of the F 5 generation (141 eggs) was significantly lower than that of the F 0 generation (186 eggs) (P < 0.05), whereas the APOP, TPOP, and adult longevity were not significantly different between the two strains (P > 0.05). The proportions of males to females in the F 5 and F 0 generations were 1:0.85 and 0.89:1, respectively.
The sublethal effects of triflumezopyrim on population dynamics were calculated with a bootstrapping procedure based on a life table ( Table 6). The intrinsic rate of increase (r), finite rate of increase (λ), and net reproductive rate in the F 5 generation (0.12, 1.13, and 57.87, respectively) were all lower than those in the F 0 generation (0.14, 1.15, and 87.69, respectively) (P < 0.05). However, there was no difference in the average generation time (T) between these two strains (P > 0.05). The s xj values in the F 0 and F 5 generations indicated that their growth curves had substantial overlap and complex growth relationships among individuals. The number of nymphs that could complete development in the two strains was not significantly different (83 and 77%, respectively). In addition, the specific age survival rate of male adults in the F 0 generation was higher than that of female adults, whereas a different pattern was observed in the F 5 generation, and the s xj values of male adults were similar to those of female adults (Figure 2). According to Figure 3, the e xj values of the F 0 and F 5 generations generally decreased with age x and phase j. For the F 0 and F 5 generations, the highest e xj values all appeared at the egg stage, at 41.41 and 38.95 days, respectively. Overall, the e xj values of the F 5 generation were lower than those of the F 0 generation, whereas the e xj values of the female adults were higher than those of the male adults. Among all the adults, the e xj values of females in the F 0 generation were the highest.
The l x results indicated that the l x curves of the F 0 and F 5 generations generally first increased and then decreased. The highest peak fertility in the F 0 and F 5 generations was on the 28th and 27th days, with the highest average yield of 11.0 and 17.1 hatched eggs, respectively (P < 0.05). The female f x curve of the F 5 generation suggested a lower and less variable value than that of the F 0 generation. Similarly, the curves of m x and l x m x showed a declining trend in the F 5 generation (Figure 4).
The v xj values in the F 5 generation were lower than those in the F 0 generation for the female adult stage and total v xj . The v xj values of all strains gradually increased from the egg stage, and that in the F 0 generation reached its maximum (124.65 eggs) on the 23rd day, especially for female adult reproduction, which The results are presented as the adult longevity and female fecundity of the F 0 and F 5 generations of L. striatellus. The rows represent the average (±SE) and degrees of freedom (df). Different lowercase letters indicate significant differences according to Duncan multiple-range test (P < 0.05). The numbers in parentheses represent the numbers of test insects at particular stages. The results are presented as the intrinsic rate of increase (r), finite rate of increase (λ), net reproductive rate (R 0 ), and mean generation time (T) of the F 0 and F 5 generations of L. striatellus. The rows represent the average (±SE). Different lowercase letters indicate significant differences according to Duncan multiple-range test (P < 0.05).
FIGURE 2 | The age-stage-specific survival rate (s xj ) of the F 0 and F 5 generations of L. striatellus. Frontiers in Physiology | www.frontiersin.org FIGURE 4 | The age-specific survival rate (l x ), female age-specific fecundity (f x7 ), age-specific fecundity of the total population (m x ), and age-specific net maternity (l x m x ) of the F 0 and F 5 generations of L. striatellus.
FIGURE 5 | The age-stage-specific reproductive value (v xj ) of the F 0 and F 5 generations of L. striatellus.

Enzymatic Activity in the F 0 and F 5 Generations
Insect detoxifying metabolic enzymes could be induced by xenobiotics, including insecticides. We assayed the activity of three main detoxifying metabolic enzymes, including CarEs, GSTs, and P450s, in the F 0 and F 5 generations of L. striatellus. Compared with the F 0 generation, the activities of the three detoxifying metabolic enzymes of the F 5 generation were increased to varying degrees. The GST [0.78 mmol/(min mg pro)] and P450 activities [58.15 nmol/(min mg pro)] were significantly higher in the F 5 generation than in the F 0 generation [0.50 mmol/(min mg pro) and 21.84 nmol/(min mg pro), respectively] (P < 0.05), whereas the CarE activity was not significantly different between the F 0 and F 5 generations (P > 0.05) (Figure 6).

Contents of Vg and VgR in the F 0 and F 5 Generations
To further explore the mechanism of triflumezopyrim on the growth and development of L. striatellus, we detected the contents of Vg and VgR in the F 0 and F 5 generations. Compared with those in the F 0 generation (2,251.80 and 148.33 ng/g), the contents of Vg and VgR in the F 5 generation (3,367.35 and 397.35 ng/g) both increased significantly (P < 0.05) (Figure 7).

Relative Expression of EcR, Vg, and VgR
To seek direct evidence of triflumezopyrim having affected the contents of Vg and VgR of L. striatellus, we detected the relative expression of EcR, Vg, and VgR in L. striatellus and found that the relative expression of Vg and VgR (0.27-and 0.23fold, respectively) in female adults of the F 5 generation was significantly decreased compared with that in the F 0 generation (P < 0.05); the relative expression of EcR (2.36-fold) was slightly FIGURE 8 | Relative expression level of EcR, Vg, and VgR genes in female adults of the F 0 and F 5 generations of L. striatellus. The bars represent the SE of three replications. Different lowercase letters indicate significant differences according to Duncan multiple-range test (P < 0.05). The F 1,4 values of the relative expression levels of EcR, Vg, and VgR genes in the female adults of the F 0 and F 5 generations were 3.792, 726.682, and 49.943, respectively, and the P values of the relative expression of the EcR, Vg, and VgR genes in female adults of the F 0 and F 5 generations were 0.577 > 0.05, 0.041 < 0.05, and 0.002 < 0.01, respectively.
increased, but no significant difference was found between the two treatments (P > 0.05; Figure 8).

DISCUSSION
Research on insect life tables is one of the imperative aspects of insect population dynamics, and changes in insect populations are influenced by multiple factors, including food, temperature, light, their respective hosts (Tuan et al., 2014;Zhang et al., 2015;Qin et al., 2017), and especially the different kinds of chemical pesticides. Our results showed that the fecundity (including r, λ, and R 0 ) of L. striatellus was significantly decreased following triflumezopyrim treatment and population expansion of L. striatellus was suppressed. This was consistent with an earlier report by Liao et al. (2019), who declared that the sublethal effects of sulfoxaflor reduced the survival and reproductive capability of Nilaparvata lugens in successive generations. Xiang et al. (2019) also found that the number of Sogatella furcifera (Hemiptera: Delphacidae) eggs decreased with the LC 25 of sulfoxaflor. In addition, we found that the developmental stage of the F 5 generation was not greatly affected, and the values of T, APOP, and TPOP did not change significantly, which was inconsistent with the findings of some previous reports. For instance, low sublethal concentrations of sulfoxaflor could stimulate the fertility of S. furcifera, and the APOP, TPOP, and T values were significantly prolonged, even though the longevity, fecundity, and egg-hatching ability of N. lugens were not significantly affected by the LC 30 of triflumezopyrim . We speculated that different insects respond differently to insecticide stress. Insects will develop resistance when successively exposed to the same insecticide. Kwon et al. (2019) reported that L. striatellus was reared for nine generations with carbofuran selection, and its resistance was increased 14-fold. The development of resistance is closely related to changes in three major detoxification metabolic enzymes in insects, including CarEs, GSTs, and P450s. According to the results of Asaduzzaman et al. (2019), the overexpression of P450 genes in L. striatellus has resulted in deltamethrin resistance. Abdalla Elzaki et al. (2016) also reported that imidacloprid resistance in L. striatellus was related to increased P450 activity. Meanwhile, there have also been many reports that enhanced GST activity has contributed to the development of resistance in insects, similar to the study of Meng et al. (2019a), who alleged that GSTs played an essential role in the detoxification of malathion in Bactrocera dorsalis. In our research, P450 and GST activities were significantly increased in the F 5 generation, and we speculated that the increase in P450 and GST activities could collaboratively enhance the triflumezopyrim resistance of L. striatellus. Whether the susceptibility and detoxification enzyme activities of the F 5 generation would return to their previous levels in the F 0 generation when the pressure of triflumezopyrim was removed should be further studied, although some reports have declared that resistance levels decreased when insects with high or moderate resistance levels were exposed to no insecticides (Ishtiaq et al., 2014;Abbas et al., 2015).
We found that the reproductive capacity of the F 5 generation decreased significantly. It has been reported that the development of drug resistance is often accompanied by a number of adverse factors, such as shortened total life span and reduced fertility . To further understand its mechanism, we measured the expression levels of three genes closely related to development and reproduction. Vitellogenin is a vital reproduction-related protein that is traditionally considered to be an adequate parameter for evaluating female fertility in insects (Li et al., 2010;Zhao et al., 2018). For example, the decreased expression of Vg was found to have negative impacts on the fecundity of Chilo suppressalis and Apolygus lucorum (Huang et al., 2016;Zhen et al., 2018). Vitellogenin receptor is a necessary receptor for Vg to function (Schneider, 1996;Snigirevskaya et al., 1997). Notably, a decrease in VgR expression can inhibit the function of Vg. In our experiment, the mRNA expression levels of Vg and VgR in F 5 generation female adults were obviously lower than those in the F 0 generation. Combined with the fact that the fecundity of the F 5 generation was significantly reduced, these data suggested that reduced Vg mRNA expression in the triflumezopyrim-resistant strain might significantly influence the fecundity of L. striatellus. Furthermore, we found that the mRNA expression level of EcR in F 5 generation female adults showed a slight increase compared with that in the F 0 generation, even though no significant differences were observed. This finding suggested that triflumezopyrim may modulate the molting hormone pathway in L. striatellus, and this result could explain the decreased expression of Vg and the shortened duration of the egg, nymph, and adult stages in the F 5 generation to some extent. Moreover, we found that the Vg and VgR contents in the F 5 generation were also significantly decreased; these results directly confirm the changing trend of Vg and VgR gene expression.

CONCLUSION
In this study, an age-stage life table procedure was used to evaluate the effects of a sublethal concentration (LC 50 ) of triflumezopyrim on the biological parameters of L. striatellus for the first time. The detoxification enzyme activities of GSTs and P450s were induced by triflumezopyrim in the F 5 generation compared to those in the F 0 generation. The contents and relative expression of Vg and VgR in the F 5 generation were also significantly decreased compared to those in the F 0 generation.

DATA AVAILABILITY STATEMENT
All datasets generated for this study are included in the article/supplementary material.

AUTHOR CONTRIBUTIONS
SZ, FG, CG, YZ, and XW conceived the study. SZ, FG, LC, and LS conducted the experiments. SZ drafted the preliminary manuscript and interpreted the results. XW, SZ, CJ, and AH refined and approved the final manuscript.

FUNDING
This study received financial support from the National Key R&D Program of China (2018YFD0200300).