Ginger is a significant ethnobotanical and pharmacological crop consisting of potential bioactive constituents responsible for their nutraceutical value, they can have anti-inflammatory, antiobesity, antidiabetic, antinausea, antimicrobial, pain alleviation, antitumor, antioxidant and protective effects on respiratory disease, and agerelated disease. Ginger possesses a substantial value, but its production and general quality are greatly harmed by various biotic and abiotic stressors, to which it is highly susceptible. Fungi are the most damaging disease-causing agents, one of the devastating fungal pathogens in ginger is Fusarium spp., a soil and seed-borne pathogen resulting in poor production, poor quality, and decreased economic returns to the farmers. It infects ginger in every stage of development and each plant part even during post-harvest storage. This review emphasizes a comprehensive understanding of the nutraceutical value of ginger compounds, and Fusarium disease in ginger with its pathogenicity. Moreover, this review elaborates on an improvement of ginger yield by the management of the Fusarium pathogen through the biological and biotechnological approach.

Throughout history, plant diseases have posed significant challenges to agricultural progress, driven by both abiotic and biotic factors. Abiotic factors include wind, salt damage, freezing, girdling roots and compacted soil, while biotic factors encompass bacteria, nematodes, fungi and viruses. Plants have evolved diverse defense strategies to counter pathogen attacks, one of which involves chitinases, a subset of pathogenesis-related proteins. Chitinases are hydrolytic enzymes that degrade chitin, a high-molecular-weight linear polymer of N-acetylD-glucosamine, which is a crucial component of fungal cell walls and septa. These enzymes are produced by a wide range of organisms, including plants, animals, insects, fungi and microorganisms. In plants, chitinases are strongly expressed under pathogenic stress, primarily targeting fungal pathogens by breaking down their cell walls. They also contribute to cell wall remodeling and degradation during growth and defense processes. Numerous studies have demonstrated that the antifungal activity of chitinases is influenced by the chitin concentration and surface microstructure of different fungal species. Research has highlighted their role in protecting plants like mango, cucumber, rye, tomato, grapevine and other plants from various fungal diseases. These findings underscore the critical role of chitinases in plant defense mechanisms, showcasing their importance in mitigating fungal infections and supporting plant health.

This work aims to isolate and screen the fungicidal endophytic bacterial strains for biocontrol efficacy against Phytophthora palmivora, a soil-borne pathogenic fungus that kills durian trees worldwide. Among more than 100 isolates, 6 strains were screened as potential fungicidal strains with inhibitory efficiency of 67.4-79.8%. Based on 16S rRNA gene sequencing and phylogenetic analysis, these strains were identified as Bacillus amyloliquefaciens EB.CK9, Bacillus methylotrophicus EB.EH34, Bacillus amyloliquefaciens EB.EH18, Bacillus siamensis EB.KN10, Bacillus velezensis EB.KN15 and Paenibacillus polymyxa EB.KN35. In greenhouse tests, the two strains P. polymyxa EB.KN35 and B. velezensis EB.KN15 significantly reduced the damage to diseased roots by P. palmivora (33.3 and 35.6%, respectively), increased the rate of survival of durian trees (only 20.8 and 22.9% plant death, respectively), and showed a positive effect on promoting durian plant growth. Notably, the potential fungicidal effect of last two strains against P. palmivora was recorded for the first time in this work. HPLC analysis showed that these strains can secret several plant growth-promoting compounds, including gibberellic acid (GA3), indole-3-acetic acid (IAA), kinetin, and zeatin. Of these, GA3 and zeatin were produced with a significant amount by both strains. The volatiles bio-synthesized by these isolates were also identified using GC-MS analysis, and some major volatiles were found as fungicidal agents. This study suggested that P. polymyxa EB.KN35 and B. velezensis EB.KN15 may be potential biocontrol candidates for durian P. palmivora and bio-fertilizers for the sustainable production of durian crops.

Background Fungal infection predominantly damages agricultural practices, and conventional chemical fungicides and insecticides are applied to control it, which extensively harms human health and the environment. Some bacterial species can control fungus by lysing its outer chitin layer.Objectives The present research aimed to isolate microorganisms capable of producing chitinase, thus acting as a highly effective biocontrol agent in combating fungal phytopathogens.Methods Two chitinase-producing bacterial strains were successfully isolated and screened from soil samples from a fish market environment. The process involved the aseptic collection of soil samples, followed by serial dilution to facilitate microorganism isolation. The bacterium exhibited optimal extracellular chitinase enzyme production following a 72-h incubation period at a temperature of 30 degrees C in a chitinase detection medium containing 0.5% chitin. Validation of chitinase production was confirmed through a clear zone assay, thus verifying its chitinase-producing capacity.Results Among the various isolated strains, isolates S3C1 and S3C3 demonstrated the highest chitinase activity, leading to their selection for further investigation. Comprehensive morphological and biochemical tests were conducted on these two isolates to assess their characteristics and capabilities. These tests established that both isolates were gram-negative, rod-shaped bacteria. Through genetic sequencing of the 16S rRNA gene, both organisms were identified as Klebsiella variicola exhibiting a remarkable similarity of 99% with S3C1 and S3C3 respectively. The bacteria exhibited maximum chitinase synthesis at optimal circumstances, which were determined to be a temperature of 30 degrees C and a pH of 7, after a 48-h incubation period. The bacteria exhibited robust antifungal activity during bioassays, demonstrating their capability to suppress the growth of fungal pathogens (specifically, Fusarium oxysporum) in vitro.Conclusion This research suggests a promising alternative to synthetic fungicides in agricultural practices, fostering a sustainable approach to disease management.

Application of organic mulches has repeatedly been shown to reduce infestation with Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae), the Colorado potato beetle (CPB). In order to determine if the nutritional status of potatoes as affected by mulch could explain the mulch effects in potatoes against CPB, we determined potato leaf nutrient composition in unmulched control plots and plots mulched with grass-clover or triticale-vetch and assessed mulch effects on CPB damage and development in the field during 3 years and under controlled conditions. In mulched plots, foliar Mo, Cl, and K contents were consistently higher than those without mulch, and leaf damage by CPB was reduced significantly. In addition, increased B contents were associated with undamaged plant material, while higher Zn contents were associated with leaves damaged by CPB. Under controlled conditions, CPB fitness was not affected by mulch application. Overall, reduced CPB damage could not be clearly attributed to altered foliar nutrient contents due to mulching. It is thus more likely that CPB reductions in mulched systems are due to mechanisms other than an altered nutrient balance.

Root-knot nematode (RKN) causes severe yield loss in cucumber. Understanding the interactions of biocontrol agent-soil microbiomes and RKNs is essential for enhancing the efficacy of biocontrol agents and nematicides to curb RKN damage to cucumber. The field experiment in this work was conducted to determine the ability of Bacillus velezensis GHt-q6 to colonize cucumber plants, investigate its effect on the control of RKNs, and assess its influence on soil microbiology in the inter-root zone of cucumber plants. After 10 days post-treatment (DPT), GHt-q6-Rif could stably colonize the roots (4.55 x 10(4) cfu center dot g(-1)), stems (3.60 x 10(3) cfu center dot g(-1)), and leaves (3.60 x 10(2) cfu center dot g(-1)) of cucumber. The high-throughput sequencing results suggested that the bacterial community diversity increased at the late development phase (p > 0.05). The strain GHt-q6 increased the relative abundance of beneficial bacteria (Gemmatimonadaceae, Sphingomonadaceae, Pseudomonadaceae). Throughout the complete cucumber growth period, strain GHt-q6 significantly increased soil urease, sucrase, accessible potassium, and phosphorus (p < 0.05). However, strain GHt-q6 had a minimal effect on catalase activity. At the pulling stage, strain GHt-q6 exhibited 43.35% control effect on cucumber RKNs, which was 7.54% higher than that of Bacillus subtilis. The results highlighted the significant potential of the strain GHt-q6 to manage cucumber RKNs and improve soil microecology. Hence, the applications of B. velezensis GHt-q6 can enhance the nematicidal action to curb RKN infecting cucumber.

Introduction Botrytis cinerea is one of the pathogenic fungi causing major problems worldwide in crops such as tomato. Some Plant Growth-Promoting Rhizobacteria (PGPR) can activate induced systemic resistance (ISR) pathways in crops, reducing the need for antifungals.Methods Three strains belonging to the species Peribacillus frigoritolerans (CD_FICOS_02), Pseudomonas canadensis (CD_FICOS_03), and Azotobacter chroococcum (CD_FICOS_04), which exhibit outstanding PGPR properties, were evaluated for their ability to protect tomato plants against B. cinerea infection by ISR via soil inoculation.Results The strains CD_FICOS_02 and CD_FICOS_03 reduced B. cinerea incidence and plant oxidative stress. The first strain mainly increased the expression of genes related to the salicylic acid pathway, while the second increased the expression of genes related to the jasmonic acid/ethylene hormonal pathway, indicating preferential ISR activation by each of these pathways. In addition, CD_FICOS_03 was able to increase the root and aerial biomass production of infected plants compared to the control. Interestingly, although the strain CD_FICOS_04 did not reduce the damage caused by B. cinerea, it increased the biomass of infected plants.Discussion Our results suggest that the best strategy for biocontrol of B. cinerea is to combine the ability to promote plant growth with the ability to induce systemic resistance, as demonstrated by strains P. frigoritolerans CD_FICOS_02 and P. canadensis CD_FICOS_03.

Large amounts of chemical fertilizers are still used to suppress pathogens and boost agricultural productivity and food generation. However, their use can cause harmful environmental imbalance. Furthermore, plants typically absorb limited amounts of the nutrients provided by chemical fertilizers. Recent studies are recommending the use of microbiota present in the soil in different formulations, considering that several microorganisms are found in nature in association with plants in a symbiotic, antagonistic, or synergistic way. This ecological alternative is positive because no undesirable significant alterations occur in the environment while stimulating plant nutrition development and protection against damage caused by control pathogens. Therefore, this review presents a comprehensive discussion regarding endophytic and rhizospheric microorganisms and their interaction with plants, including signaling and bio-control processes concerning the plant's defense against pathogenic spread. A discussion is provided about the importance of these bioinputs as a microbial resource that promotes plant development and their sustainable protection methods aiming to increase resilience in the agricultural system. In modern agriculture, the manipulation of bioinputs through Rhizobium contributes to reducing the effects of greenhouse gases by managing nitrogen runoff and decreasing nitrous oxide. Additionally, mycorrhizal fungi extend their root systems, providing plants with greater access to water and nutrients.

The control of phytopathogenic fungi in agricultural crops requires the use of synthetic chemical fungicides, which have damaged the environment for decades. Biocontrol with microorganisms is one option to reduce their use, with the fungi of the Trichoderma genus standing out for their ability to interact with soil pathogens through different control mechanisms through antibiosis or production of substances harmful to other microorganisms. The objective of this work was to evaluate the biological control mechanism using Trichoderma asperellum antibiotics on the growth of Fusarium oxysporum and F. equiseti. Antibiosis bioassays were performed using the cellophane test (diffusible metabolite assay), the reverse plate technique (volatility assay), and poisoned foods (T. asperellum mycelium extracts and extracellular metabolite assays). The diffusible metabolites of T. asperellum presented the greatest inhibition of growth. The highest percentage of inhibition was observed on F. oxysporum in plates where T. asperellum developed for 72 h (>25 %), while F. equiseti inhibition was more effective in plates with 48 h (>40 %). In both species, no significant inhibitory effect was observed in volatility tests (>10 %), while extracellular metabolites showed no inhibition. In contrast, metabolites extracted from T. asperellum mycelium with ethyl acetate inhibited Fusarium between 18 and 40 %; with hexane, between 9 and 20 %; and with methanol, no inhibition was observed. The direct analysis in real-time mass spectrometry (DART-MS) analysis showed the presence of pyrones, fatty acids, alcohols, and carbohydrates in extracts and liquid culture of T. asperellum, which suggests that the control mechanism through antibiotics on F. oxysporum and F. equiseti is fungistatic.

Soil-borne plant pathogens are the most damaging pathogens responsible for severe crop damage. A conventional chemotherapy approach to these pathogens has numerous environmental issues, while biological control agents (BCAs) are less promising under field conditions. There is an immediate need to develop an integrated strategy for utilizing nanoparticles and biocontrol to manage soil-borne pathogens, such as Fusarium wilt, effectively. Simulation of BCA metabolites to nanoparticle biocontrol metabolites is considered the most effective biocontrol approach. Combining Fe2O3 nanoparticles and Trichoderma in nursery and field conditions manages pathogens and increases plant growth characteristics. The present study evaluated the commercial biocontrol strains and the use of NPFe in combination with Trichoderma harzianum to enhance the biocontrol potential of T. harzianum against soil-borne pathogens. The effectiveness of (NPFe + T. harzianum) was evaluated under in vitro conditions where combination was found most effective upto (87.63%) mycelial growth inhibition of pathogen and under field conditions lowest pooled Fusarium wilt incidence (19.54%) was recorded. Nanocomposites are beneficial for agricultural sustainability and environmental safety by upregulating the expression of genes linked to these processes, Fe NPs can activate plant defense mechanisms and increase plant resistance to pathogenic invasions. Additionally, as iron is a necessary component for plant growth and development, Fe NPs promote better nutrient uptake.