Pepper (Capsicum annuum L.) is frequently challenged by various pathogens, among which Phytophthora capsici is the most devastating to pepper production. Red light signal acts as a positive induction of plant resistance against multiple pathogens. However, little is known about how the red light signal affects pepper resistance to P. capsici infection (PCI). Here, we report that red light regulates salicylic acid (SA) accumulation by activating elongated hypocotyl5 (CaHY5), a basic leucine zipper (bZIP) transcription factor, thereby decreasing pepper susceptibility to PCI. Exogenous SA treatment reduced pepper susceptibility to PCI, while silencing of CaPHYB (a red light photoreceptor) increased its susceptibility. PCI significantly induced CaHY5 expression, and silencing of CaHY5 reduced SA accumulation, accompanied by decreases in the expression levels of phenylalanine ammonia-lyase 3 (CaPAL3), CaPAL7, pathogenesis-related 1 (CaPR1), and CaPR1L, which finally resulted in higher susceptibility of pepper to PCI. Moreover, CaHY5 was found to activate the expression of CaPAL3 and CaPAL7, which are essential for SA biosynthesis, by directly binding to their promoters. Further analysis revealed that exogenous SA treatment could restore the resistance of CaHY5­silenced pepper plants to PCI. Collectively, this study reveals a critical mechanism through which red light induces SA accumulation by regulating CaHY5­mediated CaPAL3 and CaPAL7 expression, leading to enhanced resistance to PCI. Moreover, red light-induced CaHY5 regulates pepper resistance to PCI, which may have implications for PCI control in protected vegetable production.

Basil (Ocimum basilicum Linn. var. pilosum (Willd.) Benth.) is an aromatic plant with high nutritional and economic value, and the synthesis and regulation of its active ingredients have been studied in prior research. However, the mechanisms by which red and blue light—the most effective absorption spectra for photosynthesis—regulate the growth and metabolism of basil remain elusive. This study investigated the changes in phenotype, transcriptome, and metabolome in basil under red and blue light. The photosynthetic efficiency and biomass of basil under blue light (B) treatment were higher than those under white light (W), while red light (R) decreased photosynthesis and biomass. Metabolomic analysis showed that 491 significantly differentially accumulated metabolites were identified between the W and B groups, while 630 differentially accumulated metabolites were identified between the W and R groups. The DAMs were mainly enriched in pathways such as biosynthesis of secondary metabolites, monoterpenoid biosynthesis, limonene and pinene degradation, etc. In addition, transcriptomic analysis revealed that 34,760 and 29,802 differentially expressed genes were detected in the W vs. B pair and the W vs. R pair, respectively, while differentially expressed genes were divided into different unique subclasses, suggesting that they respond to light quality in specific ways. Overall, this work will not only enrich knowledge of the molecular mechanisms of light spectra’s regulation of plant metabolism, but also provide a theoretical basis and guidance for the molecular improvement and quality cultivation of basil.

Cadmium (Cd), a highly toxic and mobile heavy metal, has emerged as a severe environmental concern in global agroecosystems, posing a substantial threat to human health. Although prior studies have established that ZAT6 and ZAT10 positively regulate Arabidopsis tolerance to Cd toxicity, the underlying molecular mechanisms remain largely elusive. The present study provides evidence that a class I TCP transcription factor, TCP9, significantly enhances Arabidopsis tolerance to Cd toxicity through the direct activation of ZAT6 and ZAT10 expression. The real-time quantitative PCR (RT-qPCR) analysis indicates that the expression of TCP9 was induced under Cd toxicity. Meanwhile, the tcp9 mutant exhibited heightened sensitivity to Cd toxicity, accompanied by elevated Cd accumulation in both shoots and roots. Notably, the complemented lines exhibited phenotypic characteristics analogous to those observed in the wild-type (WT) plants. Further physiological and biochemical analyses revealed that, in comparison to WT, the tcp9 mutant displayed elevated hydrogen peroxide (H₂O₂) accumulation and reduced contents of catalase (CAT), ascorbate peroxidase (APX), and peroxidase (POD) under Cd toxicity. Furthermore, TCP9 directly interacted with the promoters of ZAT6 and ZAT10 in vitro, facilitating their transcription and consequently enhancing plant tolerance to Cd toxicity. Overall, our findings showed that TCP9 enhances Cd tolerance via modulating ZAT6 and ZAT10, thereby identifying TCP9 as a potential key target for improving plant tolerance to Cd toxicity.