Impact of repeated freeze-thaw cycles environment on the allelopathic effect to Secale cereale L. seedlings.

Allelopathy, as environmental stress, plays a prominent role in stress ecotoxicity, and global warming directly increases freeze-thaw cycles (FTCs) frequency in the winter. Yet, the effect between FTCs environment and allelopathy stress is rarely known, and the interaction of allelopathy stresses lacks consideration. Here, we addressed interactions between artemisinin stress (AS) and A. trifida extract stress (AES) under Non-FTCs and FTCs environments. The results found that AS and AES had an antagonistic relation under Non-FTCs environment, while a strong synergism and cooperation under FTCs environment affect the growth and physiology in S. cereale seedlings. Besides, AS and AES under FTCs environment had more inhibition on the growth of roots and shoots, chlorophylls, photosynthetic parameters, and relative water content; while more promotion on malondialdehyde, soluble sugar, and soluble protein. Moreover, the antioxidant enzyme activities of superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), and ascorbate peroxidase (APX) were increased by AS and AES, showing a good resistance of S. cereale seedlings to allelopathy stress, but FTCs environment significantly weakened this resistance. Thus, the allelopathic effect of AS and AES on S. cereale seedlings was significantly emphasized by FTCs environment.

Extensive Ace2 duplication and multiple mutations on Ace1 and Ace2 are related with high level of organophosphates resistance in Aphis gossypii.

Aphis gossypii (Glover) has been found to possess multiple mutations in the acetylcholinesterase (AChE) gene (Ace) that might involve target site insensitivity. In vitro functional expression of AChEs reveals that the resistant Ace1 (Ace1R) and Ace2 (Ace2R) were significantly less inhibited by eserine, omethoate, and malaoxon than the susceptible Ace1 (Ace1S) and Ace2 (Ace2S). Furthermore, in both the mutant and susceptible AChEs, Ace2 was significantly less sensitive to eserine, omethoate, and malaoxon than Ace1. These results suggested that both the mutant Ace1 and Ace2 were responsible for omethoate resistance, while the mutant Ace2 played a major role in insecticide resistance. The DNA copy number and transcription level of Ace2 were 1.52- and 1.88-fold higher in the ORR strain than in the OSS strain. Furthermore, the DNA copy number and transcription level of Ace2 were significantly higher than that of Ace1 in either OSS or ORR strains, demonstrating the involvement of Ace2 gene duplication in resistance. Thus, the authors conclude that omethoate resistance in cotton aphids appears to have evolved through a combination of multiple mutations and extensive Ace2R gene duplication.