Dissecting the molecular mechanisms of insecticide resistance in the brown planthopper,Nilaparvata lugens

2016 ◽  
Author(s):  
Christoph Zimmer
Keyword(s):  
Insecticide Resistance ◽  
Molecular Mechanisms ◽  
Brown Planthopper ◽  
Nilaparvata Lugens

scholarly journals Identification and analysis of miRNAs in IR56 rice in response to BPH infestations of different virulence levels

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Satyabrata Nanda ◽  
San-Yue Yuan ◽  
Feng-Xia Lai ◽  
Wei-Xia Wang ◽  
Qiang Fu ◽  
...  
Keyword(s):  
Regulatory Network ◽  
Molecular Mechanisms ◽  
Brown Planthopper ◽  
Enrichment Analysis ◽  
Transcript Abundance ◽  
Defense Responses ◽  
Nilaparvata Lugens ◽  
Mirna Sequence ◽  
Rna Profiling ◽  
Underlying Mechanisms

Abstract Rice production and sustainability are challenged by its most dreadful pest, the brown planthopper (Nilaparvata lugens Stål, BPH). Therefore, the studies on rice-BPH interactions and their underlying mechanisms are of high interest. The rice ontogenetic defense, such as the role of microRNAs (miRNAs) has mostly been investigated against the pathogens, with only a few reports existing against the insect infestations. Thus, revealing the involvement of rice miRNAs in response to BPH infestations will be beneficial in understanding these complex interactions. In this study, the small RNA profiling of the IR56 rice in response to separate BPH infestations of varied virulence levels identified the BPH-responsive miRNAs and revealed the differential transcript abundance of several miRNAs during a compatible and incompatible rice-BPH interaction. The miRNA sequence analysis identified 218 known and 28 novel miRNAs distributed in 54 miRNA families. Additionally, 138 and 140 numbers of differentially expressed (DE) miRNAs were identified during the compatible and incompatible interaction, respectively. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed the target gene candidates of DE miRNAs (including osa-miR2871a-3p, osa-miR172a, osa-miR166a-5p, osa-miR2120, and osa-miR1859) that might be involved in the IR56 rice defense responses against BPH infestation. Conversely, osa-miR530-5p, osa-miR812s, osa-miR2118g, osa-miR156l-5p, osa-miR435 and two of the novel miRNAs, including novel_16 and novel_52 might negatively modulate the IR56 rice defense. The expressional validation of the selected miRNAs and their targets further supported the IR56 rice defense regulatory network. Based on our results, we have proposed a conceptual model depicting the miRNA defense regulatory network in the IR56 rice against BPH infestation. The findings from the study add further insights into the molecular mechanisms of rice-BPH interactions and will be helpful for the future researches.

Purification, molecular cloning and heterologous expression of a glutathione S-transferase involved in insecticide resistance from the rice brown planthopper, Nilaparvata lugens

2002 ◽  
Vol 362 (2) ◽  
pp. 329-337 ◽  
Author(s):  
John G. VONTAS ◽  
Graham J. SMALL ◽  
Dimitra C. NIKOU ◽  
Hilary RANSON ◽  
Janet HEMINGWAY
Keyword(s):  
Insecticide Resistance ◽  
Peroxidase Activity ◽  
Pyrethroid Resistance ◽  
Brown Planthopper ◽  
Resistance Mechanism ◽  
Amino Acid Identity ◽  
Nilaparvata Lugens ◽  
Northern Analysis ◽  
Affinity Column ◽  
Glutathione S Transferase

A novel glutathione S-transferase (GST)-based pyrethroid resistance mechanism was recently identified in Nilaparvata lugens [Vontas, Small and Hemingway (2001) Biochem. J. 357, 65–72]. To determine the nature of GSTs involved in conferring this resistance, the GSTs from resistant and susceptible strains of N. lugens were partially purified by anion exchange and affinity chromatography. The majority of peroxidase activity, previously correlated with resistance, was confined to the fraction that bound to the affinity column, which was considerably elevated in the resistant insects. A cDNA clone encoding a GST (nlgst1-1) —the first reported GST sequence from Hemiptera with up to 54% deduced amino-acid identity with other insect class I GSTs—was isolated from a pyrethroid-resistant strain. Northern analysis showed that nlgst1-1 was overexpressed in resistant insects. nlgst1-1 was expressed in Escherichia coli, purified and characterized. The ability of the recombinant protein to bind to the S-hexylglutathione affinity matrix, its substrate specificities and its immunological properties confirmed that this GST was one from the elevated subset of N. lugens GSTs. Peroxidase activity of the recombinant nlgst1-1 indicated that it had a role in resistance, through detoxification of lipid peroxidation products induced by pyrethroids. Southern analysis of genomic DNA from the resistant and susceptible strains indicated that GST-based insecticide resistance may be associated with gene amplification in N. lugens.

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