The 12-oxo-phytodienoic acid reductases (OPRs) have been proven to play a major role in plant development and growth. Although the classification and functions of OPRs have been well understood in Arabidopsis, tomato, rice, maize, and wheat, the information of OPR genes in cotton genome and their responses to biotic and abiotic stresses have not been reported. In this study, we found 10 and 9 OPR genes in Gossypium hirsutum and Gossypium barbadense, respectively. They were classified into three groups, based on the similar gene structure and conserved protein motifs. These OPR genes just located on chromosome 01, chromosome 05, and chromosome 06. In addition, the whole genome duplication (WGD) or segmental duplication events contributed to the evolution of the OPR gene family. The analyses of cis-acting regulatory elements of GhOPRs showed that the functions of OPR genes in cotton might be related to growth, development, hormone, and stresses. Expression patterns showed that GhOPRs were upregulated under salt treatment and repressed by polyethylene glycol 6000 (PEG6000). The expression patterns of GhOPRs were different in leaf, root, and stem under V. dahliae infection. GhOPR9 showed a higher expression level than other OPR genes in cotton root. The virus-induced gene silencing (VIGS) analysis suggested that knockdown of GhOPR9 could increase the susceptibility of cotton to V. dahliae infection. Furthermore, GhOPR9 also modulated the expressions of jasmonic acid (JA) pathway-regulated genes under the V. dahliae infection. Overall, our results provided the evolution and potential functions of the OPR genes in cotton. These findings suggested that GhOPR9 might play an important role in cotton resistance to V. dahliae.

Piper nigrum–Areca catechu intercropping mitigates soil problems related to continuous P. nigrum cropping, but the exact reason for this is not clear. In this study, the intercropping system increased P. nigrum’s single plant weight by 27.0–55.5% and unit yield per hectare by 5.1–33.5% in 2019–2022. Intercropping altered the metabolic profiles of root exudates from both species, with increases in flavonoids (epicatechin and 4′,5,6,7-Tetramethoxyflavone), alkaloids (litebamine), and amino acids (proline betaine, L-homocysteic acid and L-homocysteic acid). Intercropping further increased the abundance of dominant soil bacteria, including GAL15 (354.9%) and Bacteroidota (70.4%) in the P. nigrum rhizosphere, and Firmicutes (141.8%) and WPS2 (75.3%) in the A. catechu rhizosphere. In the intercropping system, the abundance of soil flavonoids, including tangeritin, trifolirhizin, and hexamethylquercetagetin, which participated in improving nutrient absorption and plant growth, increased by 106.4~356.0%, 28.9~45.5%, and 45.2~127.1%, respectively, during the whole growing period. Overall, intercropping with A. catechu promoted carbon input to the P. nigrum soil via root exudates. This increased the diversity of P. nigrum rhizosphere beneficial bacterial communities, as well as the amounts of nutrients and plant growth-promoting secondary metabolites. Together, these effects improved nutrient uptake and utilization, thereby driving the sustainable production of P. nigrum, and ultimately achieving higher yields.

Pandanus amaryllifolius, also known as pandan, is a perennial herb, growing in Indonesia, China and the Maluku Islands (Wakte et al. 2009). It is the only plant with aromatic leaves in the Pandanac...

Pathogens deploy various molecular mechanisms to overcome host defenses, among which glycoside hydrolases (GHs) play a critical role as virulence factors. Understanding the functional roles of these enzymes is essential for uncovering pathogen–host interactions and developing strategies for disease management. Fusarium wilt has occurred in the main Piper nigrum cultivation regions, which seriously affects the yield and quality of P. nigrum. Here, we identified and characterized FsGH28c, a GH28 family member in Fusarium solani. Its expression was significantly upregulated during the infection of black pepper (Piper nigrum) roots by F. solani cv. WN-1, indicating its potential role in pathogenicity. FsGH28c elicited cell death in Nicotiana benthamiana and modulated the expression of genes related to pathogenesis. FsGH28c exerts a positive influence on the pathogenicity of F. solani. The knockout of FsGH28c mutant strains markedly attenuated F. solani ’s virulence in black pepper plants. The knockout mutant strains decrease the ability of F. solani to utilize carbon sources. The FsGH28c deletion did not affect mycelial growth on PDA but did impact spore development. We identified a U-box protein, PnPUB35, interacting with FsGH28c using yeast two-hybrid and bimolecular fluorescence complementation assays. PnPUB35 conferred enhanced resistance to F. solani in black pepper through positive regulation. These findings suggest that FsGH28c may function as a virulence factor by modulating host immune responses through its interaction with PnPUB35.