Abstract

BackgroundThe oriental fruit fly, Bactrocera dorsalis (Hendel) has been considered to be one of the most important agricultural pest around the world. As a holometabolous insect, larvae must go through a metamorphosis process with dramatic morphological and structural changes to complete their development. To better understand the molecular mechanisms of these changes, RNA-seq of B. dorsalis from wandering stage (WS), late wandering stage (LWS) and white puparium stage (WPS) were performed.ResultsIn total, 11,721 transcripts were obtained, out of which 1914 genes (578 up-regulated and 1336 down-regulated) and 2047 genes (655 up-regulated and 1392 down-regulated) were found to be differentially expressed between WS and LWS, as well as between WS and WPS, respectively. Of these DEGs, 1862 and 1996 genes were successfully annotated in various databases. The analysis of RNA-seq data together with qRT-PCR validation indicated that during this transition, the genes in the oxidative phosphorylation pathway, and genes encoding P450s, serine protease inhibitor, and cuticular proteins were down-regulated, while the serine protease genes were up-regulated. Moreover, we found some 20-hydroxyecdysone (20E) biosynthesis and signaling pathway genes had a higher expression in the WS, while the genes responsible for juvenile hormone (JH) synthesis, degradation, signaling and transporter pathways were down-regulated, suggesting these genes might be involved in the process of larval pupariation in B. dorsalis. For the chitinolytic enzymes, the genes encoding chitinases (chitinase 2, chitinase 5, chitinase 8, and chitinase 10) and chitin deacetylase might play the crucial role in the degradation of insect chitin with their expressions significantly increased during the transition. Here, we also found that chitin synthase 1A might be involved in the chitin synthesis of cuticles during the metamorphosis in B. dorsalis.ConclusionsSignificant changes at transcriptional level were identified during the larval pupariation of B. dorsalis. Importantly, we also obtained a vast quantity of RNA-seq data and identified metamorphosis associated genes, which would all help us to better understand the molecular mechanism of metamorphosis process in B. dorsalis.

Highlights

  • The oriental fruit fly, Bactrocera dorsalis (Hendel) has been considered to be one of the most important agricultural pest around the world

  • Overview of the RNA-seq data To investigate the expression changes of genes during the larval pupariation process, we performed RNA-Seq analysis on three developmental stages (WS, late wandering stage (LWS), and white puparium stage (WPS)) of B. dorsalis with its genome as a reference

  • Analysis of differentially expressed genes (DEGs) FPKM was calculated and standardized for the analysis of gene expression, and similar patterns of FPKM density were obtained for each sample of B. dorsalis, suggesting high reproducibility of the transcriptome analysis of each developmental stage

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Summary

Introduction

The oriental fruit fly, Bactrocera dorsalis (Hendel) has been considered to be one of the most important agricultural pest around the world. Larvae must go through a metamorphosis process with dramatic morphological and structural changes to complete their development. The oriental fruit fly, Bactrocera dorsalis (Hendel), is a highly invasive species which has been found in India, East Asia and the Pacific region. This insect can cause significant economic losses to many commercially important tropical and subtropical crops, especially fruits, including citrus, banana, carambola, and mango [1, 2]. It has been reported that most of the larval tissues (integument, midgut, and fat body) must undergo a series of developmental events involving programmed cell death, and cell proliferation and differentiation to remodel structures of insects [6]

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