How crickets become freeze tolerant: the transcriptomic underpinnings of acclimation in Gryllus veletis

Some ectotherms can survive internal ice formation. In temperate regions, freeze tolerance is often induced by decreasing temperature and/or photoperiod during autumn. However, we have limited understanding of how seasonal changes in physiology contribute to freeze tolerance, and how these changes are regulated. During a six week autumn-like acclimation, late-instar juveniles of the spring field cricket Gryllus veletis (Orthoptera: Gryllidae) become freeze tolerant, which is correlated with accumulation of low molecular weight cryoprotectants, elevation of the temperature at which freezing begins, and metabolic rate suppression. We used RNA-Seq to assemble a de novo transcriptome of this emerging laboratory model for freeze tolerance research. We then focused on gene expression during acclimation in fat body tissue due to its role in cryoprotectant production and regulation of energetics. Acclimated G. veletis differentially expressed more than 3,000 transcripts in fat body. This differential expression may contribute to metabolic suppression in acclimated G. veletis, but we did not detect changes in expression that would support cryoprotectant accumulation or enhanced control of ice formation, suggesting that these latter processes are regulated post-transcriptionally. Acclimated G. veletis differentially regulated transcripts that likely coordinate additional freeze tolerance mechanisms, including upregulation of enzymes that may promote membrane and cytoskeletal remodelling, cryoprotectant transporters, cytoprotective proteins, and antioxidants. Thus, while accumulation of cryoprotectants and controlling ice formation are commonly associated with insect freeze tolerance, our results support the hypothesis that many other systems contribute to surviving internal ice formation. Together, this information suggests new avenues for understanding the mechanisms underlying insect freeze tolerance

Mechanisms Underlying Freeze Tolerance in the Spring Field Cricket, \u3cem\u3eGryllus veletis\u3c/em\u3e

Freeze tolerance has evolved repeatedly across insects, facilitating survival in low temperature environments. Internal ice formation poses several challenges, but the mechanisms that mitigate these challenges in freeze-tolerant insects are not well understood. To better understand how insects survive freezing, I describe a novel laboratory model, the spring field cricket Gryllus veletis (Orthoptera: Gryllidae). Following acclimation to six weeks of decreasing temperature and photoperiod (mimicking autumn), G. veletis juveniles becomes moderately freeze-tolerant, surviving freezing at -8 °C for up to one week, and surviving temperatures as low as -12 °C. Acclimation is associated with increased control of the temperature and location of ice formation, accumulation of cryoprotectant molecules (myo-inositol, proline, and trehalose) in hemolymph and fat body tissue, metabolic rate suppression, and differential expression of more than 3,000 genes in fat body tissue. To test cryoprotectant function, I increase their concentration in G. veletis hemolymph (via injection) and freeze isolated fat body tissue with exogenous cryoprotectants. I show that cryoprotectants improve survival of freeze-tolerant G. veletis (proline), their fat body cells (myo-inositol), or both (trehalose) under otherwise lethal conditions, suggesting limited functional overlap of these cryoprotectants. However, no cryoprotectant (alone or in combination) can confer freeze tolerance on freeze-intolerant G. veletis or their cells. During acclimation, G. veletis upregulates genes encoding cryoprotectant transmembrane transporters, antioxidants, and molecular chaperones, which may protect cells during freezing and thawing. In addition, acclimated G. veletis upregulates genes encoding lipid metabolism enzymes, and cytoskeletal proteins and their regulators, which I hypothesize promote membrane and cytoskeletal remodelling. To investigate the function of these genes in freeze tolerance, I develop a method to knock down gene expression in G. veletis using RNA interference. I knock down expression of three genes (encoding a cryoprotectant transporter, an antioxidant, and a cytoskeletal regulator), laying the ground work for others to test whether and how these genes contribute to mechanisms underlying freeze tolerance. By using a combination of descriptive and manipulative experiments in an appropriate laboratory model, I improve our understanding of the factors that contribute to insect freeze tolerance