Abstract

The fat body, a multifunctional organ analogous to the liver and fat tissue of vertebrates, plays an important role in insect life cycles. The fat body is involved in protein storage, energy metabolism, elimination of xenobiotics, and production of immunity regulator-like proteins. However, the molecular mechanism of the fat body’s physiological functions in the tephritid stem gall-forming fly, Procecidochares utilis, are still unknown. In this study, we performed transcriptome analysis of the fat body of P. utilis using Illumina sequencing technology. In total, 3.71 G of clean reads were obtained and assembled into 30,559 unigenes, with an average length of 539 bp. Among those unigenes, 21,439 (70.16%) were annotated based on sequence similarity to proteins in NCBI’s non-redundant protein sequence database (Nr). Sequences were also compared to NCBI’s non-redundant nucleotide sequence database (Nt), a manually curated and reviewed protein sequence database (SwissProt), and KEGG and gene ontology annotations were applied to better understand the functions of these unigenes. A comparative analysis was performed to identify unigenes related to detoxification, immunity and energy metabolism. Many unigenes involved in detoxification were identified, including 50 unigenes of putative cytochrome P450s (P450s), 18 of glutathione S-transferases (GSTs), 35 of carboxylesterases (CarEs) and 26 of ATP-binding cassette (ABC) transporters. Many unigenes related to immunity were identified, including 17 putative serpin genes, five peptidoglycan recognition proteins (PGRPs) and four lysozyme genes. In addition, unigenes potentially involved in energy metabolism, including 18 lipase genes, five fatty acid synthase (FAS) genes and six elongases of very long chain fatty acid (ELOVL) genes, were identified. This transcriptome improves our genetic understanding of P. utilis and the identification of a numerous transcripts in the fat body of P. utilis offer a series of valuable molecular resources for future studies on the functions of these genes.

Highlights

  • Crofton weed, Eupatorium adenophorum Spreng, is a perennial, hazardous invading species of the family Asteraceae, which is native to Mexico

  • The contigs were further assembled into 30,559 unigenes with an average length of 539 bp (Table 1), which is shorter than that obtained from the N. lugens (avirulent TN1 population with a mean length of 656 bp and the virulent Mudgo (M) population with a mean length of 676 bp) [11] and B. dorsalis [13]

  • The results showed that 21,439 (70.16%), 13,657 (44.69%), 12,188 (39.88%), 12,405 (40.59%), 12,925 (42.30%), 13,149 (43.03%) and 9,354 (30.61%) unigenes matched to non-redundant protein sequence database (Nr), nucleotide sequence database (Nt), SwissProt, Kyoto Encyclopedia of Genes and Genomes (KEGG), KOG, InterPro and Gene Ontology (GO) known protein databases, respectively (Table 2)

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Summary

Introduction

Eupatorium adenophorum Spreng, is a perennial, hazardous invading species of the family Asteraceae, which is native to Mexico. It has successfully invaded many regions on the globe in a wide variety of natural and anthropogenic ecosystems that range from forest and grassland to farmland [1] and is one of the most dangerous exotic invasive plants, causing great economic losses and environmental problems worldwide [2]. The transcriptome sequencing of its alimentary tract of P. utilis has been performed successfully, and has proved to be an effective method to gather genetic information of the alimentary tract [7].

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