Zhang Bin, Zhao Lilin, Ning Jing, Wickham Jacob D, Tian Haokai, Zhang Xiaoming, Yang Meiling, Wang Xiangming, Sun Jianghua
State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China.
CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing, 10049, China.
BMC Biol. 2020 Nov 27;18(1):184. doi: 10.1186/s12915-020-00926-w.
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, 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.
We 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.
Our 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.
生活在温带环境中的昆虫要在寒冷胁迫下存活,需要采取一些策略,这些策略会引发与耐冻性或避冻性相关的生理变化。这些策略可能包括,例如,诱导代谢抑制、积累抗冻剂或产生抗冻蛋白,然而,对于这些机制的调控方式以及激活它们的信号了解甚少。ascarosides是通常已知可调节线虫行为和发育的信号分子,最近发现其表达与日本松墨天牛(Monochamus alternatus)的热可塑性有关。越来越多的证据还表明,miRNA是另一类在应对寒冷胁迫时差异表达的调节因子,预计它们会靶向参与昆虫冷适应的基因。在这里,我们展示了一条通过miRNA介导的ascaroside功能调控参与昆虫冷驯化的新途径。
我们最初发现实验性冷驯化可以增强甲虫的耐寒性。通过筛选和功能验证,我们发现冷胁迫下上调的miR-31-5p对这种增强有显著贡献。从机制上讲,miR-31-5p通过负向靶向过氧化物酶体β-氧化循环中的限速酶酰基辅酶A氧化酶,促进甲虫中一种ascaroside(asc-C9)的产生。用合成asc-C9进行的喂食实验表明,它可能作为一种信号,通过代谢抑制和积累具有特定基因表达模式的抗冻剂来促进冷驯化。
我们的结果表明miRNA介导的ascaroside功能调控在昆虫冷适应中起着重要作用。这种增强的耐寒性可能使松墨天牛在冬季有更高的存活率,并且在塑造其广泛分布范围方面起着关键作用,极大地扩大了松材线虫病的威胁,因此也可以启发基于ascaroside的害虫管理策略的开发。