Salt stress can adversely affect global agricultural productivity, necessitating innovative strategies to mitigate its adverse effects on plant growth and yield. This study investigated the effects of exogenous salicylic acid (SA), grafting (G), and their combined application (GSA) on various parameters in tomato plants subjected to salt stress. The analysis focused on growth characteristics, photosynthesis, osmotic stress substances, antioxidant enzyme activity, plant hormones, ion content, and transcriptome profiles. Salt stress severely inhibits the growth of tomato seedlings. However, SA, G, and GSA improved the plant height by 22.5%, 26.5%, and 40.2%; the stem diameter by 11.0%, 26.0%, and 23.7%; the shoot fresh weight by 76.3%, 113.2%, and 247.4%; the root fresh weight by 150.9%, 238.6%, and 286.0%; the shoot dry weight by 53.5%, 65.1%, and 162.8%; the root dry weight by 150.0%, 150.0%, and 166.7%, and photosynthesis by 4.0%, 16.3%, and 32.7%, with GSA presenting the most pronounced positive effect. Regarding the osmotic stress substances, the proline content increased significantly by more than 259.2% in all treatments, with the highest levels in GSA. Under salt stress, the tomato seedlings accumulated high Na⁺ levels; the SA, G, and GSA treatments enhanced the K⁺ and Ca²⁺ absorption while reducing the Na⁺ and Al³⁺ levels, thereby alleviating the ion toxicity. The transcriptome analysis indicated that SA, G, and GSA influenced tomato growth under salt stress by regulating specific signaling pathways, including the phytohormone and MAPK pathways, which were characterized by increased endogenous SA and decreased ABA content. The combined application of grafting and exogenous SA could be a promising strategy for enhancing plant tolerance to salt stress, offering potential solutions for sustainable agriculture in saline environments.

Soilless cultivation is increasingly utilized in supplying essential nutrients for greenhouse crops. However, the impact of coir cultivation under varying electrical conductivity (EC) conditions on cucumber growth and fruit quality, particularly through the regulation of gene expression during the vegetative stage, remains uncertain. In this study, we performed metabolic measurements on cucumber in both vegetative and reproductive stages under three different EC conditions and found metabolic products such as some primary metabolites (cellulose, many uncharged amino acids) and some secondary metabolites (rutin, cucurbitacin B) accumulated the most under EC of 5 dS·m⁻¹. Next, we conducted transcriptome profiling in cucumber leaves, revealing that the function of genes significantly regulated by EC was associated with photosynthesis, many anabolic processes, and membrane transport. Finally, a set of genes contributed to metabolites related to the fruit quality of cucumber were identified by the Orthogonal Partial Least Squares (O2PLS) analysis, including genes involved in the biosynthesis of amino acids, polysaccharides, and many secondary metabolites. Taken together, these findings suggest that coir cultivation in greenhouses with moderate EC can induce a transcriptome-wide change in gene expression, thereby contributing to enhancing the abundance of metabolites associated with cucumber fruit quality.

Twenty-nine samples of two cucumber types (Cucumis sativus L.) were evaluated to determine the amino acid, tannin, soluble protein, soluble sugar, Vc, nitrate nitrogen contents and volatile organic compounds (VOCs). Cucumber variety differences in amino acid, tannin, soluble proteins, et al., were significant (p < 0.05). The VOCs were derived by headspace solid-phase microextraction (HS-SPME) coupled with gas chromatography–mass spectrometry (GC-MS). A total of 67 VOCs were identified, including 24 aldehydes, 13 alcohols, 12 ketones, 12 alkenes and 6 other compounds. (E, Z)-2,6-Nonadienal, (E)-2-Nonenal and (E)-6-Nonenal were the three most abundant volatiles. A total of 21 VOCs were present in all 29 cultivars. An average of 45 kinds of VOCs were identified in each cultivar. Principal component analysis (PCA) clustered the 29 cucumber cultivars into five groups. Partial least-squares-discriminant analysis (PLS-DA) indicated that the European type was separated from the South China type across PLS1. Furthermore, 25 key differential volatiles for distinguishing 29 cultivars and 23 key differential volatiles for differentiating between South China and European types were identified, respectively. These results provide information for the development of new cultivars with high nutritional quality and intense flavor.

The auxin efflux transporter PIN protein plays a crucial role in the asymmetric distribution of auxin on the plasma membrane, influencing the growth and development of plant organs. In this study, we identified nine members of the PIN gene family in the cucumber genome, which could be classified into five phylogenetic groups. These genes have diverse structures but conserved transmembrane domains. Analysis of cis-acting elements in the promoters revealed that CsPINs contain 48 types of cis-acting elements, predominantly light-responsive elements and plant hormone response elements. In addition, PIN proteins may interact with a variety of auxin-related proteins (including auxin response factor, auxin binding protein, mitogen-activated protein kinase PINOID, etc.) to jointly regulate the auxin synthesis and metabolic pathways. We analyzed the expression profiles of PIN genes in 23 tissues of cucumber using the CuGenDB database, and further investigated the expression levels of PIN genes in leaves and roots in response to different abiotic stresses and hormone treatments by qRT-PCR. This study provides a theoretical basis for clarifying the regulatory mechanism of the cucumber PIN gene family during environmental stress processes.

Powdery mildew is one of the most destructive fungal diseases of bottle gourd (Lagenaria siceraria), severely threatening yield and quality, yet the genetic basis of its resistance remains poorly understood. In this study, an F₂ segregating population derived from a cross between the resistant inbred line G6 and the susceptible inbred line G3 was used, and BSA-seq, integrated RNA-seq analysis, qRT-PCR validation, and KASP marker development were comprehensively employed. SNP-index and InDel-index analyses independently mapped and converged on a candidate interval of 1,898,234–8,241,294 bp (~6.34 Mb) on chromosome 2. By comparing differentially expressed genes (DEGs) at 12, 24, 48, and 72 h post-inoculation with the BSA candidate interval, one candidate resistance gene, Lsi02G006660, was identified, and a KASP marker (Chr2_5941698, G/T) was successfully developed. This study provides a candidate gene and marker resources for molecular breeding of powdery mildew resistance in bottle gourd.