Abstract

The molecular mechanism of silkworm resistance to Bombyx mori nucleopolyhedrovirus (BmNPV) infection remains largely unclear. Accumulating evidence suggests that subcellular fractionation combined with proteomics is an ideal technique to analyse host antiviral mechanisms. To clarify the anti-BmNPV mechanism of the silkworm, the near-isogenic line BC9 (resistant strain) and the recurrent parent P50 (susceptible strain) were used in a comparative subcellular proteomics study. Two-dimensional gel electrophoresis (2-DE) combined with mass spectrometry (MS) was conducted on proteins extracted from the cytosol, mitochondria, and microsomes of BmNPV-infected and control larval midguts. A total of 87 proteins were successfully identified from the three subcellular fractions. These proteins were primarily involved in energy metabolism, protein metabolism, signalling pathways, disease, and transport. In particular, disease-relevant proteins were especially changed in microsomes. After infection with BmNPV, differentially expressed proteins (DEPs) primarily appeared in the cytosolic and microsomal fractions, which indicated that these two fractions might play a more important role in the response to BmNPV infection. After removing genetic background and individual immune stress response proteins, 16 proteins were identified as potentially involved in repressing BmNPV infection. Of these proteins, the differential expression patterns of 8 proteins according to reverse transcription quantitative PCR (RT-qPCR) analyses were consistent with the 2-DE results.

Highlights

  • The silkworm Bombyx mori L. (Lepidoptera: Bombycidae) has been domesticated for more than 5000 years and still plays an important role in many developing countries

  • In addition to their well-appreciated roles in biological processes, mitochondria appear to function as centrally positioned hubs in viral infection; some viruses have been reported to regulate host cell apoptosis based on mitochondrial regulation, including human immunodeficiency virus (HIV), influenza A virus (IAV), and hepatitis C virus (HCV)[14]

  • To our knowledge, differentially expressed proteins (DEPs) in different resistant silkworm strains following Bombyx mori nucleopolyhedrovirus (BmNPV) infection have not been analysed based on subcellular proteomics

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Summary

Introduction

The silkworm Bombyx mori L. (Lepidoptera: Bombycidae) has been domesticated for more than 5000 years and still plays an important role in many developing countries. As “energy factories,” mitochondria are related to the chemical energy metabolism of adenosine triphosphate (ATP) and are involved in cell cycle and growth, as well as other biological processes, such as signal transduction, cellular differentiation, and cell death[13] In addition to their well-appreciated roles in biological processes, mitochondria appear to function as centrally positioned hubs in viral infection; some viruses have been reported to regulate host cell apoptosis based on mitochondrial regulation, including human immunodeficiency virus (HIV), influenza A virus (IAV), and hepatitis C virus (HCV)[14]. To our knowledge, differentially expressed proteins (DEPs) in different resistant silkworm strains following BmNPV infection have not been analysed based on subcellular proteomics.

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