Field evolution of insecticide resistance in the brown planthopper (Nilaparvata lugens Stål) in China

The brown planthopper (Nilaparvata lugens Stål) is one of the most destructive pests of rice crops in Asian countries including China, Vietnam, Thailand, etc. Evolution of resistance in this pest insect to isoprocarb, buprofezin, pymetrozine, imidacloprid and other neonicotinoid insecticides has been reported. In order to investigate the current status of resistance to commonly used insecticides, nine field populations of N. lugens were collected from Central China, East China and South China, and resistance to insecticides was monitored from 2009 to 2012. All the 9 field populations collected in 2012 had developed extremely high resistance to imidacloprid, with resistance ratios (RR) ranging from 209.3 to 616.6. Resistance to imidacloprid was much higher in 2012 than in 2009. The RR of thiamethoxam varied from 17.4 to 47.1, and the RR of nitenpyram varied from 1.4 to 3.7 in 2012. Of the 9 field populations, six populations showed higher resistance to nitenpyram in 2012 than in 2011. RR for buprofezin varied from 110.1 to 221.6 in 2012 whereas resistance was at a medium level (RR 20.4 ∼ 39.4-fold) in 2009. RR for pymetrozine ranged from 34.9 to 46.8 in 2012. As for isoprocarb, RR ranged from 21.7 to 38.1 in 2012. The obvious increase in resistance to widely applied insecticides indicates that insecticide resistance management strategies are urgently needed to prevent or delay further increase of insecticide resistance in N. lugens.     

Greenhouse techniques to identify field resistance to the brown planthopper,Nilaparvata lugens (Stål) (Homoptera: Delphacidae), in rice cultivars

Two seedbox screening techniques were compared to determine levels of resistance of rice cultivars to three brown planthopper, Nilaparvata lugens (Stål), biotypes. The commonly used standard seedbox screening test (SSST) where eight second-instar nymphs were infested on 7-day-old seedlings was compared with a modification (MSST) where four second-instar nymphs were infested on each of 20-day-old plants. In the SSST, the initial infestation killed the susceptible cultivars whereas in the MSST the F₁ progeny killed the susceptible cultivars. The cultivars ASD 11, Wagwag, Utri Rajapan, IR46 and Kencana were susceptible in the SSST but moderately resistant or resistant in the MSST, indicating an increase in the level of resistance with plant age. Feeding rate and population growth of N. lugens were the factors involved in the resistance of 30-day-old plants. The MSST provides a rapid method for identifying field-resistant cultivars in the greenhouse and can be used to identify field-resistant lines in a rice-breeding programme for stable resistance to N. lugens.     

Identification and Function Analysis of enolase Gene NlEno1 from Nilaparvata lugens (St?l) (Hemiptera:Delphacidae)

The enolase [EC 4.2.1.11] is an essential enzyme in the glycolytic pathway catalyzing the conversion of 2-phosphoglycerate (2-PGE) to phosphoenolpyruvate (PEP). In this study, a full-length cDNA encoding α-enolase was cloned from rice brown planthopper (Nilaparvata lugens) and is provisionally designated as NlEno1. The cDNA sequence of NlEno1 was 1,851 bp with an open reading frame (ORF) of 1,305 bp and encoding 434 amino acids. The deduced protein shares high identity of 80–87% with ENO1-like protein from Hemiptera, Diptera, and Lepidoptera speices. The NlEno1 showed the highest mRNA expression level in hemolymph, followed by fat body, salivary gland, ovaries and egg, and showed trace mRNA levels in testis. The mRNA of NlEno1 showed up-regulated level in virulent N. lugens population Mudgo, IR56 and IR42 when compared with TN1 population. Injection of double-stranded RNA (dsRNA) of NlEno1 into the adults significantly down-regulated the NlEno1 mRNA level along with decreased eggs and offspring. Moreover, injection of NlEno1-dsRNA decreased mRNA level of Vitellogenin (Vg) gene. These results showed that the NlEno1, as a key glycolytic enzyme, may play roles in regulation of fecundity and adaptation of N. lugens to resistant rice varieties.     

The effect of 35℃ on the amino acid requirement of the brown planthopper, Nilaparvata lugens

The brown planthopper, N. lugens, is not able to develop well at 35℃. Previous investigation showed that 35℃-treated N. lugens harbored fewer symbionts than untreated ones, and it was suggested that symbiont played an important role in nutritional metabolism. Nevertheless.     

A method for raising brown planthopper (BPH), Nila-parvata lugens (Stl)

To get mass ppoulation of the BPH, agood method for rasing BPH isneeded. In this paper, a convenientmethod was recommended.BPH population used in the ex-periment was provided by Jiangsu A-cad of Agri Sci. Six raising BPHmethods, i. e, with rice buds (RB),rice seedling (RS), seedling soillesscultured (SSC), mature rice (MR),and rice stem cultured in nutrient     

Resistance of Oryza minuta to Nilaparvata lugens (Stl)

Evaluation of O. minuta for the re-sistanee to the brown planthopper(BPH), Nilaparvata lugens (Stal)was carried out by using ModifiedSeedbox Screening Technique(MSST). Based on the significantdifferences between O. minuta,E13-9, and the susceptible checkvariety, TN1, the resistance of O.minuta to BPH was determined byusing a series of resistance indices     

Effects of endosymbiote on feeding, development, and reproduction or brown plan-thopper, Nilaparvata lugens stl

The biotype 1, 2, and 3 of N. lugens obtained from IRRI, the Philippines,were reed continuously on suscepti-ble variety TN1, resistant varieties Mudgo (Bph1), and ASD7 (Bph2),respectively. To eliminate theyeast-like symbionts (YLS) inN. lugens, about 60-d old plants ofTN1 beating 3-d old ears were laid at26℃ for 2d and exposed at 35℃ inan incubator for 3 d. After a hottreatment, the plants were transferred into an incubator at 26℃ for eggdevelopment. The hatched aposymbi-otic nymphs…     

Bacterial Community in Different Populations of Rice Brown Planthopper Nilaparvata lugens(Stl)

The structures of bacterial communities in the brown planthopper (BPH) Nilaparvata lugens (Stål) from different geographic and resistant virulent populations were analyzed by using denatured gradient gel electrophoresis (DGGE). Results showed that the bacterial communities in BPH nymph from the first to the fifth instars varied with nymphal growth and development. The bacterial communities in the first-instar BPH nymph were similar to those in adults. Nine geographic BPH populations were divided into three groups based on the cluster analysis of DGGE fingerprint. The first group was from the Philippines; the second group was from Thailand and Hainan, Yunnan and Zhejiang provinces of China; and the third group was from Vietnam and Guangxi, Hunan and Jiangxi provinces of China. BPH populations adapted to different resistant rice varieties. The BPH populations from Mudgo (with resistant gene Bph1) and ASD7 (with resistant gene bph2) differed with those of the susceptible rice variety TN1.     

High Temperature Modifies Resistance Performances of Rice Varieties to Brown Planthopper,Nilaparvata lugens(Stl)

To investigate the effect of temperature on the resistance characteristics of rice varieties with different resistance genes to brown planthopper(BPH),Nilaparvata lugens(Stl),the resistances of IR26(Bph1)and IR36(bph2)to BPH population in Hangzhou,China were monitored in greenhouse during September in 2007 and 2008 by using the standard seedling screening techniques(SSST)developed by the International Rice Research Institute(IRRI).Furthermore,the changes in resistance of IR26 and IR36 to BPH,soluble sugar and oxalic acid contents in 25-day-old rice plants of susceptible variety TN1 and resistant varieties IR26 and IR36 were detected at five temperatures(22℃,25℃,28℃,31℃ and 34℃).IR26 completely lost resistance both in greenhouse and at the five tested temperatures.IR36 still had moderate resistance at natural temperature,but its resistance decreased gradually when the temperature increased from 25℃ to 34℃,and fully lost its resistance at 31℃ and 34℃.The highest durable resistance of IR26 and IR36 were recorded at 25℃.The soluble sugar content in plants of the three tested rice varieties increased with temperature increase,and the oxalic acid content increased with the temperature increase at first,maximized at 25℃,and then declined.Two-way ANOVA indicated significant effects of temperature and rice variety on contents of soluble sugar and oxalic acid in rice plants.     

Donors for Resistance to Brown Planthopper Nilaparvata lugens(St?l) from Wild Rice Species

Out of 1 989 wild accessions sown in seed boxes for screening, only 1 003 wild accessions with good germination were screened against brown planthopper(BPH), Nilaparvata lugens(St?l) under greenhouse conditions. The collection comprised of accessions from 11 wild species and African cultivated rice. The germplasm was screened for BPH following standard seed box screening technique in the greenhouse. As many as 159 accessions were identified as resistant during the year 2012 based on one year screening. A selected set of BPH resistant accessions were screened again during 2013. Based on the two years screening, seven accessions of O. nivara(AA), one accession of O. officinalis(CC), seven accessions of O. australiensis(EE), five accessions of O. punctata(BB and BBCC) and nine accessions of O. latifolia(CCDD) were confirmed to be resistant to BPH. So far no BPH resistance genes have been identified and designated from O. nivara and O. punctata, hence these may act as new sources of resistance.     

Relationship between biological features and the SMVS''''s inhibitory effect on mating behavior of Nilaparvata lugens (Stal)

Our previous studies revealed that second malevibration signal (SMVS) restrained the matingbehavior of N. lugens, the influences of threebiological features (density, age, and wingform) on SMVS's inhibitory effect were hereinstudied by playing back its record. The dura-tion of playback was 4 h. Except otherwisestatement, N. lugens tested were virginmacropterous males and females aged 4-6 d af-ter emergence, and the density was 5 pairs (5females and 5 males) of N. lugens per cage (4cm in diameter and 8 cm in height). The in-hibitory effect of SMVS was evaluated usingmating rate (i. e. the rate of females withspermatophore). The results were as follows:     

Evaluation of rice accessions for resistance to the whitebacked planthopper Sogatella furcifera (Horváth) (Homoptera: Delphacidae)

Rice, Oryza sativa L., and wild rice accessions from the world collection were evaluated for resistance to the whitebacked planthopper, Sogatella furcifera (Horváth). Of 48554 O. sativa accessions from 96 countries, 401 (0·8%) were selected for resistance and 351 (88%) of these were from Nepal, India, and Pakistan where S. furcifera is a serious pest. However, some resistant accessions originated from regions beyond the distribution of S. furcifera. Many of the wild rice accessions, consisting of 28 species primarily from the O. minuta Presl., O. nivara Sharma et Shastry and O. officinalis Wall groups, were resistant. Although no S. furcifera-resistant commercial cultivars have been released, advanced breeding lines with resistance to S. furcifera and other major insect pests have been developed.     

Insecticide-induced changes in the levels of resistance of rice cultivars to the whitebacked planthopper Sogatella furcifera (Horváth) (Homoptera: Delphacidae)

IR2035-117-3 (highly resistant), ARC 10239 (resistant), and TN1 (susceptible) rice plants received one application at 40 days after transplanting (DT) or three spray applications (20, 30, and 40DT) of monocrotophos, diazinon or deltamethrin. When these plants were exposed to S. furcifera adults, either 24 hours after the single application, or 15 days after the third of the spray applications, the deltamethrin-treated were most preferred. The percentage of S. furcifera that alighted on the three varieties decreased correspondingly with an increase in the level of varietal resistance. Differences in S. furcifera population growth, nymphal survival, nymphal duration, growth index and feeding rate between IR2035-117-3 and TN1 were significant. Foliar application of deltamethrin caused a significant increase in population growth on IR2035-117-3, ARC 10239, and TN1 and an increase in the nymphal survival and growth index on TN1.