The free-living infective juveniles of entomopathogenic nematodes (EPNs) are critical biological control agents against insect pests. The field efficacy of EPNs is largely determined by their tolerance to low-humidity stress, a trait closely linked to the mobilization of their energy reserves. This study aims to investigate how varying levels of humidity stress influence energy reserve dynamics in two EPNs, Steinernema kraussei 0657L and Heterorhabditis brevicaudis 0641TY, and their relationship with the survival rate and pathogenicity. The results demonstrated that lipids were the predominant energy reserve, followed by proteins and sugars. Notably, neutral lipid constituted approximately 3% of the total lipid content. Among sugars, soluble sugar levels were the highest, followed by glycogen and trehalose. Exposure to low-humidity stress resulted in increased levels of protein, total lipid, glycogen, and trehalose in nematodes. These increases were more pronounced in S. kraussei 0657L, a highly drought-resistant strain, compared to H. brevicaudis 0641TY. Furthermore, the accumulation of protein, total lipid, and trehalose was negatively correlated with survival rate and pathogenicity. However, positive correlations were observed between trehalose and both total lipids and soluble sugars. Furthermore, transcriptome analysis revealed that under low-humidity stress, S. kraussei 0657L exhibited an enrichment of differentially expressed genes (DEGs) involved in glycolysis/gluconeogenesis, fatty acid metabolism, and glycerophospholipid metabolism pathways. This indicates that S. kraussei 0657L regulated energy metabolism to adapt to low-humidity stress. These findings provide insights into the mechanisms underlying drought resistance in EPNs and offer an experimental basis for their application in arid environments.

Leaf senescence in perennial species constitutes a highly orchestrated developmental phase that differs fundamentally from the obligate monocarpic senescence of annual plants. While individual organs undergo programmed senescence, prerennial organisms maintain longevity across multiple growing seasons through a sophisticated interplay between endogenous programs and exogenous cues. This review provides a systematic synthesis of the regulatory mechanisms governing leaf senescence in herbaceous perennials (Lolium perenne and Festuca arundinacea) and woody perennials (Populus, Pinus, and Agave). We highlight a multi-layered regulatory landscape, encompassing divergent and conserved pathways in transcriptional orchestration, hormonal crosstalk, metabolic reprogramming, and telomere maintenance. Specific emphasis is placed on how these mechanisms allow for tissue-specific and seasonal adaptation, such as the integration of dormancy signals in woody taxa versus stress-plasticity in perennial grasses. By elucidating these complex frameworks, this review not only advances our fundamental understanding of plant life-span regulation but also provides a theoretical foundation for the molecular breeding of delayed senescence germplasm, offering transformative potential for enhancing agricultural productivity and ecological resilience.

Tetranychus truncatus (Acari: Tetranychidae) has caused serious economic losses on some crops (soybean, corn, and cotton) in China, and has developed resistance to most acaricides. Our laboratory study found that T. truncatus was resistant to pyridaben and also adapted to high temperature (34–40 °C). High temperature stress may cause arthropods to produce a large amount of reactive oxygen species (ROS), causing oxidative damage. Antioxidant enzymes, as the main antioxidants, can reduce the damage caused by excessive ROS in arthropods. In order to study the adaptation mechanism of the pyridaben-resistant strain of T. truncatus to high temperature and the role of antioxidant enzyme genes under high temperature stress, four antioxidant enzyme genes, TtSOD, TtPOD3, TtPOD4, and TtGSTs2, were screened according to the transcriptome sequencing data of pyridaben-susceptible and -resistant strains in T. truncatus. Firstly, the phylogeny and structure analyses of these four genes were carried out. Then, real-time quantitative PCR (RT-qPCR) technology was used to analyze the gene expression patterns of antioxidant enzymes in two strains of T. truncatus at three different high temperature ranges (34 °C, 38 °C, and 42 °C). The results showed that the expression levels of four antioxidant enzyme genes of two strains of T. truncatus were induced by high temperature stress, and the expression levels of antioxidant enzyme genes were significantly different in each development state. The gene expression of antioxidant enzyme genes in resistant strains at the adult stage was significantly higher than that in susceptible strains. After the TtSOD and TtPOD4 genes of adult mites of the resistant strain were silenced by RNA interference (RNAi) technology, the mortality rate of mites with TtPOD4 gene silencing reached 41.11% after 96 h at 34 °C, which was significantly higher than that of the control and TtSOD gene silencing. It has been confirmed that the TtPOD4 gene plays a key role in the adaptation of pyridaben-resistant strain of T. truncatus to high temperature. It lays a theoretical foundation for revealing the thermal adaptation mechanism of T. truncatus.