Various technologies, such as light-emitting diodes (LEDs) and beneficial plant micro-organisms, have been applied to enhance plant growth and development. We aimed to develop appropriate technology by incorporating the benefits of LED light, plant growth promoting rhizobacteria (PGPR), and arbuscular mycorrhiza fungi (AMF) into sweet girl cherry tomato (Solanum lycopersicum L.) seedling production. Our results demonstrated that incorporating red (R) and blue (B) LED lights, PGPR, and AMF positively affected tomato seedling growth. The optimal lighting conditions for tomato seedling growth were LEDs at 200 $\mathsf{\mu }$mol/m²/s with a ratio of R60:B40 and 20 h/d exposure. The optimum LED-illuminated tomato seedlings significantly upregulated photosynthesis-related genes, including psbA, psbB, fdx, atpB, and rbcL. Plants inoculated with PGPR Bradyrhizobium sp. SUTN9-2, Bacillus velezensis SD10 and B. megaterium A20 had a high health index after inoculation. Furthermore, the optimized LED-illuminated tomato seedlings inoculated with SD10 had the highest health index. In addition, the optimum LED-illuminated tomato seedlings inoculated with SD10 and AMF had the highest biomass. Our experiment demonstrated that tomato seedlings produced under optimized LED lights inoculated with SD10 and AMF increased yield by about 16% under field conditions. Therefore, these results provided the optimum conditions for a high-quality tomato seedling production system.

A substrate-based production system is a simple and low-cost method for arbuscular mycorrhizal (AM) fungal inoculum production. However, it is time-consuming and typically yields low numbers of AM fungal spores due to several factors affecting plant growth efficiency. Our study investigated the use of light-emitting diode (LED) technology to expedite AM fungal spore production in planta. We performed experiments with Rhizophagus irregularis inoculated in maize (Zea mays L.), contrasting LED light with greenhouse (GH) conditions. Our results exhibited a significant improvement in AM fungal colonization and spore production, as well as a reduction in the production period from 120 to 90 days under the LED light condition. This was achieved using a red-and-blue light ratio of 60:40 with a total light intensity of 300 µmol m⁻² s⁻¹. The LED light treatments improved maize growth by increasing nitrogen (N) and phosphorus (P) concentrations in shoots and roots, respectively. Our gene expression analyses revealed that in AMF-inoculated plants, genes related to photosynthesis were significantly upregulated under LED light compared to the GH condition. Moreover, LED increased the expression of marker genes linked to the AM fungi-related cell cycle, indicating enhanced AM fungal growth during symbiosis. These findings advance our comprehension of LED applications in agriculture, offering promising prospects for acceleration of AM fungal spore production.

Mung bean (Vigna radiata L.), a vital legume in Asia with significant nutritional benefits, is highly susceptible to Cercospora leaf spot (CLS) caused by Cercospora canescens, leading to significant yield losses. As an alternative to chemical fungicides, bio-priming with rhizobacteria can enhance plant resistance. This study explores the potential of Bradyrhizobium sp. strain DOA9 to augment resistance in mung bean against CLS via root priming. The results reveal that short (3 days) and double (17 and 3 days) priming with DOA9 before fungal infection considerably reduces lesion size on infected leaves by activating defense-related genes, including Pti1, Pti6, EDS1, NDR1, PR-1, PR-2, Prx, and CHS, or by suppressing the inhibition of PR-5 and enhancing peroxidase (POD) activity in leaves. Interestingly, the Type 3 secretion system (T3SS) of DOA9 may play a role in establishing resistance in V. radiata CN72. These findings suggest that DOA9 primes V. radiata CN72′s defense mechanisms, offering an effective bio-priming strategy to alleviate CLS. Hence, our insights propose the potential use of DOA9 as a bio-priming agent to manage CLS in V. radiata CN72, providing a sustainable alternative to chemical fungicide applications.

The symbiotic interaction between leguminous and Bradyrhizobium sp. SUTN9-2 mainly relies on the nodulation process through Nod factors (NFs), while the type IV secretion system (T4SS) acts as an alternative pathway in this symbiosis. Two copies of T4SS (T4SS₁ and T4SS₂) are located on the chromosome of SUTN9-2. ΔT4SS₁ reduces both nodule number and nitrogenase activity in all SUTN9-2 nodulating legumes. The functions of three selected genes (copG₁, traG₁, and virD2₁) within the region of T4SS₁ were examined. We generated deleted mutants and tested them in Vigna radiata cv. SUT4. ΔtraG₁ and ΔvirD2₁ exhibited lower invasion efficiency at the early stages of root infection but could be recently restored. In contrast, ΔcopG₁ completely hindered nodule organogenesis and nitrogenase activity in all tested legumes. ΔcopG₁ showed low expression of the nodulation gene and ttsI but exhibited high expression levels of the T4SS genes, traG₁ and trbE₁. The secreted proteins from ΔT4SS₁ were down-regulated compared to the wild-type. Although ΔcopG₁ secreted several proteins after flavonoid induction, T3SS (nopP and nopX) and the C₄-dicarboxylate transporter (dct) were not detected. These results confirm the crucial role of the copG₁ gene as a novel key regulator in the symbiotic relationship between SUTN9-2 and legumes.

In this study, we investigate two RpoN homologs in Bradyrhizobium sp. DOA9—chromosomal RpoNc and megaplasmid-borne RpoNp—and their roles in free-living conditions and nitrogen fixation. Phylogenetic analysis showed that RpoNc clusters with RpoN proteins from symbiotic nitrogen-fixing strains, whereas RpoNp forms a distinct clade, consistent with a function in stress responses. RpoNc proved essential for free-living conditions: ΔrpoNc mutants displayed severe growth defects that RpoNp could not compensate for. Transcriptomic comparisons between wild type and mutant RpoN identified 541 differentially expressed genes (DEGs) grouped into three clusters: 100 downregulated, 175 upregulated, and 254 moderately downregulated (with a fold change > 2, and a q-value (FDR, padj) < 0.05). Affected pathways involved nitrogen metabolism, motility, and environmental adaptation. RpoNc controlled major nitrogen fixation genes (nif and fix) along with core growth and stress response functions, while RpoNp mainly influenced stress-adaptation pathways. Genome-wide promoter motif analysis predicted 68 putative RpoNc targets, mainly associated with nitrogen fixation and metabolism, compared with only 22 predicted RpoNp targets, indicating a more restricted regulon. Electrophoretic mobility shift assays (EMSAs) further confirmed that both RpoN proteins directly bind σ⁵⁴-dependent promoters identified from transcriptomic data, supporting their regulatory roles under free-living conditions. Two mutants (ΔrpoNc and ΔrpoNp::ΩrpoNc) showed broad transcriptional disruption across nitrogen fixation, metabolism, and stress responses, underscoring complementary regulation. Overall, RpoNc is the dominant regulator of nitrogen fixation and core metabolism during free-living conditions, whereas RpoNp fine-tunes stress responses, revealing new regulatory insights for DOA9 adaptation. These results clarify how RpoN systems optimize survival across fluctuating conditions.

Bradyrhizobium vignae ORS3257 is an efficient symbiotic strain for Vigna unguiculata and V. mungo but fails with V. radiata due to an effector-triggered immunity response mediated by the nodulation outer protein P2 (NopP2). To understand this incompatibility, we identified NopP2 interacting proteins in V. radiata cv. KPS1, including enolase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), monodehydroascorbate reductase (MDHAR), and serine hydroxymethyltransferase (SHMT) as targets. Protein-protein interaction assays confirmed that NopP2 binds to these enzymes, and further analysis revealed their co-localization on the plasma membrane. Comparative transcriptomic analysis revealed NopP2 stimulates genes related to plant defense response (PR1, PR5, MYB13, and TAO1), hydrogen peroxide (SOD, POX10, and POX16), and cell wall lignification (LAC). NopP2 did not alter the expression of genes encoding the target enzymes but interfered with MDHAR activity, leading to high H₂O₂ accumulation in roots. These findings suggest that NopP2 contributes to symbiotic incompatibility in V. radiata by inducing a multifaceted defense response and initiating cell wall lignification early in infection.