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28 results for “brown planthopper”
Insecticide resistance triggers a reduction of virulence to host-plant defenses in the brown planthopper
<p>This dataset contains R scripts to analyze the virulence of resistance rice cultivars and to draw figures. Data contains the LD<sub>50</sub> values of imidacloprid, virulence test and figure data. This study was supported by grants-in-aid from Japan's National Agriculture and Food Research Organization (NARO) project 315 and the NARO Innovation Project 2017 for the NARO.</p>
Data from: Dual oxidase is essential for molting, hatching and feeding in the brown planthopper
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Data from: Silence of the killers: discovery of male-killing suppression in a rearing strain of the small brown planthopper, Laodelphax striatellus
<p>According to evolutionary theory, sex ratio distortions caused by reproductive parasites such as <i>Wolbachia</i> and <i>Spiroplasma</i> are predicted to be rapidly normalised by the emergence of host nuclear suppressors. However, such processes in the evolutionary arms race are difficult to observe because sex ratio biases will be promptly hidden and become superficially unrecognisable. The evolution of genetic suppressors has been reported in just two insect species so far. In the small brown planthopper,<i> Laodelphax striatellus</i>,<i> </i>female-biases caused by <i>Spiroplasma</i>, which is a 'late' male-killer, have been found in some populations. During the continuous rearing of <i>L. striatellus</i>, we noticed that a rearing strain had a 1:1 sex ratio even though it harboured <i>Spiroplasma</i>. Through introgression crossing experiments with a strain lacking suppressors, we revealed that the <i>L. striatellus</i> strain had the zygotic male-killing suppressor acting as a dominant trait. The male-killing phenotype was hidden by the suppressor even though<i> Spiroplasma</i> retained its male-killing ability. This is the first study to demonstrate the existence of a late male-killing suppressor and its mode of inheritance. Our results, together with those of previous studies, suggest that the inheritance modes of male-killing suppressors are similar regardless of insect order or early or late male-killing.</p>
Data from: Evidence for high dispersal ability and mito-nuclear discordance in the small brown planthopper, Laodelphax striatellus
Understanding dispersal ability in pest species is critical for both theoretical aspects of evolutionary and population biology and from a practical standpoint, such as implementing effective forecasting systems. The small brown planthopper (SBPH), Laodelphax striatellus (Fallén), is an economically important pest, but few data exist on its dispersal ability. Here, we used mitochondrial and nuclear markers to elucidate the population genetic structure of SBPH and of the parasitic bacterium Wolbachia throughout temperate and subtropical China. Our results showed that the SBPH populations in China lack significant differences in genetic structure, suggesting extensive gene flow. Multilocus sequence typing revealed that Wolbachia infection was systematic and due to the same strain (wStri) within and across populations. However, the mtDNA haplogroups had a nonrandom distribution across the sampling localities, which correlated to latitudinal and climatic gradients. We explain this mito-nuclear discordance as a result of historical population recolonization or mitochondria adaptation to climate.
FIG. 3 in The wrinkle-lipped free-tailed bat (Chaerephon plicatus Buchannan, 1800) feeds mainly on brown planthoppers in rice fields of central Thailand
FIG. 3. The average monthly number of male brown planthopper genitalia per pellet (0 ± SE) in the diet of C. plicatus at two caves: Khao Wongkot Cave (KWC) and Khao Chakan Cave (KCC) in central Thailand (2015–2016), as determined by fecal analysis. The yearly average number of genitalia per pellet was 2.16 ± 1.55 (0 ± SE) for KWC and 2.55 ± 1.68 for KCC
FIG. 1. A in The wrinkle-lipped free-tailed bat (Chaerephon plicatus Buchannan, 1800) feeds mainly on brown planthoppers in rice fields of central Thailand
FIG. 1. A map of Thailand showing active rice fields and our two study caves housing C. plicatus bats at Khao Wongkot cave (KWC, 70% surrounding rice fields) and Khao Chakan cave (KCC, 22% surrounding rice fields) in central Thailand. The two circle insets show a 20-km radius (approximate bat foraging distance) around each cave [gray: newly planted rice, black: older rice and white: no rice; data from GISTDA, September 2016]
of central in) KCC (Cave Chakan Khao and) KWC ( Cave] Wongkot Acari and, Khao Dermaptera at 2016, September Isoptera, to 2015 Plecoptera, October Psocoptera during, traps Blattodae, suction Odonata in, collected Trichoptera insects, of Orthoptera mass include dry Percent Others [ .. 2. Thailand ABLE T in The wrinkle-lipped free-tailed bat (Chaerephon plicatus Buchannan, 1800) feeds mainly on brown planthoppers in rice fields of central Thailand
of central in) KCC (Cave Chakan Khao and) KWC ( Cave] Wongkot Acari and, Khao Dermaptera at 2016, September Isoptera, to 2015 Plecoptera, October Psocoptera during, traps Blattodae, suction Odonata in, collected Trichoptera insects, of Orthoptera mass include dry Percent Others [ .. 2. Thailand ABLE T
FIG. 2 in The wrinkle-lipped free-tailed bat (Chaerephon plicatus Buchannan, 1800) feeds mainly on brown planthoppers in rice fields of central Thailand
FIG. 2. Percent volume and percent frequency (0 ± SE) of insect orders found in fecal samples of C. plicatus collected monthly from October 2015 to September 2016 at Khao Wongkot cave (KWC, 70% surrounding rice fields)and Khao Chakan cave (KCC, 22% surrounding rice fields) in central Thailand. [Other: Orthoptera and Hymenoptera combined]
Fig. 4 in Metabolite profiles of brown planthopper-susceptible and resistant rice (Oryza sativa) varieties associated with infestation and mechanical stimuli
Fig. 4. Normalized intensity of significant metabolites affected by BPH infestation (n = 3/group) with different response patterns: (A). similar response in BPHsusceptible KD and BPH-resistant RH, (B). late induction in KD variety, (C). early induction in RH but late induction in KD, (D). induction in RH in both BPH and mechanical piercing by a needle common response in KD and RH, (E). higher level in KD than RH, and (F). higher level in RH than KD. Unpaired-t test was used to compare the control (black bar) and the BPH-treated (white bar) groups and to compare the control (black bar) and the mechanical-treated (grey bar) groups (*p- value<0.05, **p-value<0.01 and ***p-value<0.001) per time per genotype. HAT represents hour after treatment. Error bars represent one standard deviation of the mean value. Normalized intensity of each feature was relative to the intensity of a reference sample.
Fig. 3 in Metabolite profiles of brown planthopper-susceptible and resistant rice (Oryza sativa) varieties associated with infestation and mechanical stimuli
Fig. 3. Clustergram analysis of BPH-susceptible KD and BPH-resistant RH varieties between control (no treatment) and BPH treatment at 0, 6, 24 and 96 h using hierarchical clustering. (A). Venn's diagram represents numbers of metabolite features of KD and RH from three different treatments. (B). Clustergrams obtained from 213 metabolite features of ESI+with % relative standard deviation (RSD) less than 30% at least half of total sample numbers and six different alteration patterns (46 metabolite features) with their level changes greater than 1.5 folds comparing between KD and RH, and between treatment and control in each timepoint. B indicates BPH treatment. M indicates mechanical piercing by a needle. C indicates no treatment.
Fig. 2 in Metabolite profiles of brown planthopper-susceptible and resistant rice (Oryza sativa) varieties associated with infestation and mechanical stimuli
Fig. 2. PCA score plot of metabolite profiles (6413 metabolite features) obtained from ESI + mode among control (C, red), mechanical piercing by a needle (M, blue) and BPH (B, green) treatment at (A). all timepoints (0, 6, 24 and 96 h) between BPH-susceptible KD and BPH-resistant RH varieties. QC indicates pooled samples (n = 70) of rice leave extracts (orange star), (B). 0 h, (C). 6 h, (D). 24 h and (E) 96 h between BPH-susceptible KD and BPH-resistant RH varieties. The numbers above the circles indicate time points. Open and filled circles indicate data from KD and RH varieties. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Data from: Silence of the killers: discovery of male-killing suppression in a rearing strain of the small brown planthopper, Laodelphax striatellus
Open the record for dataset details and reuse information.
Data from: Evidence for high dispersal ability and mito-nuclear discordance in the small brown planthopper, Laodelphax striatellus
Open the record for dataset details and reuse information.
Data from: Mitochondrial variation in small brown planthoppers linked to multiple traits and likely reflecting a complex evolutionary trajectory
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Evaluation of rice landraces for brown planthopper resistance based on phenotypic reactions and biochemical attributes [DataSet]
<p>Data set for the publication: Evaluation of rice landraces for brown planthopper resistance based on phenotypic reactions and biochemical attributes</p>
Epigenetic diversity underlying seasonal and annual variations in brown planthopper (BPH) populations as revealed by methylation-sensitive restriction assay
<p>Raw data files for the image analysis.</p>
Comparative profiling of microRNA transcriptome in different developmental phases and analysis of microRNAs associated with reproductive development in the Brown Planthopper, Nilaparvata lugens
GEO Series GSE174315. Nilaparvata lugens. 9 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Comparative expression during feeding against starvation in the rice brown planthopper, Nilaparvata lugens
GEO Series GSE68096. Tetranychus urticae; Nilaparvata lugens. 6 samples. Type: Expression profiling by array.
RNA-sequencing reveals differentially expressed rice genes functionally associated with defense against brown planthopper in NILs pyramiding BPH14 and BPH15
GEO Series GSE232449. Oryza sativa. 36 samples. Type: Expression profiling by high throughput sequencing.
Microarray analysis reveals the molecular foundation of the brown planthopper(BPH) resistance of rice variety Rathu Heenati
GEO Series GSE74106. Oryza sativa. 36 samples. Type: Expression profiling by array.
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