Transcriptomic analysis of pre-diapause larvae of Chilo suppressalis (Walker) (Lepidoptera: Pyralidae) in natural populations

Chilo suppressalis Walker is a devastating pest of rice in Asia and exhibits facultative diapause in the larval stage. Most prior experiments on diapausing and non-diapausing C. suppressalis were conducted in the laboratory. In this study, transcriptome analyses were performed on pre-diapausing larvae collected from field populations of C. suppressalis and compared to laboratory populations. Among 2674 differentially expressed genes (DEGs), 32 DEGs related to pre-diapause and 239 universally expressed genes were screened; these were primarily enriched in neuroactive ligand-receptor interaction, lysosome and glycerolipid metabolism in KEGG pathway analysis. With respect to clusters of orthologous genes (COG), DEGs were assigned to posttranslational modification, protein turnover, chaperones, carbohydrate transport and metabolism, and secondary metabolite biosynthesis, transport and catabolism categories. Further analysis also revealed that a key circadian clockcontrolled protein gene is sensitive to photoperiod and significantly decreased during the pre-diapause phase. Genes encoding two small heat shock proteins, hsp21.4 and hsp27.2, were significantly expressed on August 15 as compared to three other sampling times in August 2018. Eight DEGs were randomly chosen and evaluated by real-time quantitative PCR (RT-qPCR) to validate the accuracy of the transcriptome data. The expression of six DEGs (gene-evm_000752, gene-evm_006486, gene-evm_008626, gene-evm_002485, geneevm_011981 and Chilo_suppressalis_newGene_18103) showed significant same patterns of differential expression in both the RT-qPCR and RNA-Seq analyses. This study increases our understanding of the complex physiological and molecular mechanisms involved in C. suppressalis at the pre-diapause phase.

Automated summary

This study sheds light on the complex physiological and molecular mechanisms involved in C. suppressalis at the pre-diapause phase, highlighting gene expressions related to neuroactive ligand-receptor interaction, lysosome and glycerolipid metabolism.