Abstract

BackgroundSurvival to cold stress in insects living in temperate environments requires the deployment of strategies that lead to physiological changes involved in freeze tolerance or freeze avoidance. These strategies may consist of, for instance, the induction of metabolic depression, accumulation of cryoprotectants, or the production of antifreeze proteins, however, little is known about the way such mechanisms are regulated and the signals involved in their activation. Ascarosides are signaling molecules usually known to regulate nematode behavior and development, whose expression was recently found to relate to thermal plasticity in the Japanese pine sawyer beetle Monochamus alternatus. Accumulating evidence also points to miRNAs as another class of regulators differentially expressed in response to cold stress, which are predicted to target genes involved in cold adaptation of insects. Here, we demonstrate a novel pathway involved in insect cold acclimation, through miRNA-mediated regulation of ascaroside function.ResultsWe initially discovered that experimental cold acclimation can enhance the beetle’s cold hardiness. Through screening and functional verification, we found miR-31-5p, upregulated under cold stress, significantly contributes to this enhancement. Mechanistically, miR-31-5p promotes production of an ascaroside (asc-C9) in the beetle by negatively targeting the rate-limiting enzyme, acyl-CoA oxidase in peroxisomal β-oxidation cycles. Feeding experiments with synthetic asc-C9 suggests it may serve as a signal to promote cold acclimation through metabolic depression and accumulation of cryoprotectants with specific gene expression patterns.ConclusionsOur results point to important roles of miRNA-mediated regulation of ascaroside function in insect cold adaptation. This enhanced cold tolerance may allow higher survival of M. alternatus in winter and be pivotal in shaping its wide distribution range, greatly expanding the threat of pine wilt disease, and thus can also inspire the development of ascaroside-based pest management strategies.

Highlights

  • Survival to cold stress in insects living in temperate environments requires the deployment of strategies that lead to physiological changes involved in freeze tolerance or freeze avoidance

  • Cold acclimation enhances cold hardiness To confirm whether low-temperature acclimation can enhance the cold hardiness of Monochamus alternatus beetles, we tested both supercooling point (SCP) and temperature causing 50% mortality (LT50)

  • We found a total of 20 miRNAs to be differentially expressed (DE) between the acclimated and control beetles (Fig. 2b, Additional file 1: Fig. S1B, Additional file 2: Table S1; P value < 0.05 and fold change > 1.5)

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Summary

Introduction

Survival to cold stress in insects living in temperate environments requires the deployment of strategies that lead to physiological changes involved in freeze tolerance or freeze avoidance These strategies may consist of, for instance, the induction of metabolic depression, accumulation of cryoprotectants, or the production of antifreeze proteins, little is known about the way such mechanisms are regulated and the signals involved in their activation. Insects have evolved strategies such as freeze tolerance by having the ability to survive internal ice formation and freeze avoidance by supercooling [1,2,3,4] These strategies require diverse physiological changes including metabolic depression, accumulation of cryoprotectants, ion and water balance, and production of antifreeze proteins [4,5,6,7]. The cryoprotective roles of these metabolites in insect cold adaptation have been widely recognized [6, 15, 16], our understanding of their potential roles in signaling is still limited

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