Resistance-related Enzymes Research Articles

Resveratrol and nitric oxide synergistically enhance resistance against B. cinerea in tomato fruit by regulating phytohormones

Resveratrol (RVT), a plant antitoxin, plays an important role in plant resistance against pathogens. While nitric oxide (NO) as an essential signaling factor in disease resistance enhancement is well documented, the potential molecular interplay RVT and NO in postharvest tomato fruit defense against Botrytis cinerea (B.cinerea) still needs exploration. In this study, exogenous RVT reduced gray mold caused by B.cinerea in tomato fruit, with 20 μM being the most effective. Tomato fruit were treated with 20 μM RVT enhanced resistance against B.cinerea, as indicated by reduced symptoms of disease and improved activity of disease resistance related enzymes (PAL, PPO and CHI). In addition, RVT treatment improved the expression of SlPR1, SlLoxd and SlMYC2, and promoted the accumulation of plant hormone IAA and ABA, but reduced the expression of SlNPR1 and the level of GA3. More importantly, the combined treatment of NO donor (SNP) and RVT notably enhanced disease resistance compared to RVT or SNP single treatment. However, the combination of NO inhibitor (L-NNA) and RVT treatment even reduced the positive effect of RVT. Meanwhile, the expression of SlPR1, SlLoxd and SlMYC2 and the accumulation of IAA and ABA in RVT + SNP treated fruit were higher than those in the RVT or SNP single treatment. Thus, our data demonstrate that RVT and NO synergistically enhance resistance against B. cinerea in tomato fruit by regulating phytohormones.

Rice Varieties Intercropping Induced Soil Metabolic and Microbial Recruiting to Enhance the Rice Blast (Magnaporthe Oryzae) Resistance.

[Background] Intercropping is considered an effective approach to defending rice disease. [Objectives/Methods] This study aimed to explore the resistance mechanism of rice intraspecific intercropping by investigating soil metabolites and their regulation on the rhizosphere soil microbial community using metabolomic and microbiome analyses. [Results] The results showed that the panicle blast disease occurrence of the resistant variety Shanyou63 (SY63) and the susceptible variety Huangkenuo (HKN) were both decreased in the intercropping compared to monoculture. Notably, HKN in the intercropping system exhibited significantly decreased disease incidence and increased disease resistance-related enzyme protease activity. KEGG annotation from soil metabolomics analysis revealed that phenylalanine metabolic pathway, phenylalanine, tyrosine, and tryptophan biosynthesis pathway, and fructose and mannose metabolic pathway were the key pathways related to rice disease resistance. Soil microbiome analysis indicated that the bacterial genera Nocardioides, Marmoricola, Luedemannella, and Desulfomonile were significantly enriched in HKN after intercropping, while SY63 experienced a substantial accumulation of Ruminiclostridium and Cellulomonas. Omics-based correlation analysis highlighted that the community assembly of Cellulomonas and Desulfomonile significantly affected the content of the metabolites D-sorbitol, D-mannitol, quinic acid, which further proved that quinic acid had a significantly inhibitory effect on the mycelium growth of Magnaporthe oryzae, and these three metabolites had a significant blast control effect. The optimal rice blast-control efficiency on HKN was 51.72%, and Lijiangxintuanheigu (LTH) was 64.57%. [Conclusions] These findings provide a theoretical basis for rice varieties intercropping and sustainable rice production, emphasizing the novelty of the study in elucidating the underlying mechanisms of intercropping-mediated disease resistance.

Bacillus velezensis YC89-mediated recruitment of rhizosphere bacteria improves resistance against sugarcane red rot

BackgroundSugarcane red rot is a soil-borne disease caused by Colletotrichum falcatum. It can reduce the yield of sugarcane and the purity of sugarcane juice, which seriously restricts the development of sucrose industry. Biocontrol bacteria can control diseases by regulating rhizosphere microecology. In this study, the effects of biocontrol bacteria on sugarcane rhizosphere microecology were studied by metagenomics and metabolomics, and the control effects of biocontrol bacteria and rhizosphere dominant bacteria on sugarcane red rot were further explored by pot experiment.ResultsThe results of metagenomic sequencing showed that inoculation with B. velezensis YC89 and pathogens could significantly change the microbial diversity of the sugarcane rhizosphere. The relative abundance of beneficial strains such as Streptomyces, Burkholderia, Sphingomonas, and Rhizobium increased significantly in the rhizosphere of sugarcane in the YC treatment group. Pseudomonas was significantly enriched in the rhizosphere of sugarcane in the C treatment group. The results of metabolome sequencing showed that the content of amino acids in sugarcane root exudates increased after inoculation with B. velezensis YC89, and the contents of phenolic acids and flavonoids decreased. Spearman correlation analysis showed that there was a significant correlation between differential metabolites and rhizosphere microorganisms. The results of pot experiment showed that YC89 strain and three rhizosphere microorganisms could significantly reduce the disease index of red rot and promote the growth of sugarcane plants. In addition, these strains can also significantly increase the JA and SA content of sugarcane leaves and induce plant system resistance-related enzyme activities. Among them, the synthetic community treatment group had the best biocontrol effect on red rot, and its relative control effect was 67.50%.ConclusionsTherefore, we conclude that B. velezensis YC89 could recruit beneficial rhizosphere microorganisms to enrich the rhizosphere and change the content of some phenolic acids and flavonoids in the root exudates. In addition, the isolated rhizosphere dominant bacteria and YC89 strain can resist red rot by inducing plant systemic resistance and promote the growth of sugarcane plants. This study provides a theoretical basis for the use of biocontrol bacteria to regulate rhizosphere bacteria to jointly control plant soil-borne diseases.Graphical

Chemical induction of DNA demethylation by 5-Azacytidine enhances tomato fruit defense against gray mold through dicer-like protein DCL2c.

Postharvest decay, primarily caused by pathogenic fungi in ripening fruits and fresh vegetables, poses a challenge to agricultural sustainability and results in significant economic losses. The regulation of the fruit ripening by DNA methylation has been well demonstrated, while defense response of fruit underlying epigenetic regulation against postharvest decay remains uncertain. In the present study, treatment of tomato fruits with the DNA methyltransferase inhibitor 5-Azacytidine (5-Aza) notably decreased their susceptibility to gray mold. Following 5-Aza treatment, we observed a substantial increase in activities of chitinase (CHI) and glucanase (GLU) in tomato fruits, as well as an increase in the expression of the dicer-like SlDCL2 gene family. Suppression of SlDCL2c through double-stranded RNA-induced RNA interference (RNAi) resulted in a decrease in the expression of chitinases CHI3, CHI9, Class V chitinase, and endochitinase 4 by 71%, 29%, 55%, 64%, as well as glucanases Cel1, Cel2, and GluB by 19%, 93%, and 87%, respectively. This was accompanied by decreased activities of resistance-related enzymes, including CHI and GLU. The expression levels of genes phenylalanine ammonia-lyase PAL2, peroxidase POD 12, POD P7, CCR1, CYP84A2, and COMT in phenylpropanoid biosynthesis pathway also decreased by 33%, 53%, 18%, 50%, 30%, and 24% in SlDCL2c-RNAi fruit, resulting in decreased activities of PAL and POD. Consequently, the lesion diameter of gray mold in SlDCL2c-RNAi fruit increased by 55% compared to the control group. Overall, the present study indicated that DNA methyltransferase inhibitor 5-Aza reduces susceptibility of tomato fruit to gray mold through regulation of DCL2c-mediated inducible defense response.

Study on the control effect and physiological mechanism of Wickerhamomyces anomalus on primary postharvest diseases of peach fruit

Brown rot, aspergillosis and soft rot are the primary diseases of postharvest peach fruit. Our study aimed to investigate the biocontrol effect of Wickerhamomyces anomalus on the primary postharvest diseases of peach fruit and to explore its underlying physiological mechanism. The findings demonstrated that W. anomalus had an obvious inhibitory effect on Monilinia fructicola, Aspergillus niger and Rhizopus stolonifer. At the same time, W. anomalus can grow stably on the wound and surface of peach fruit at 25 °C and 4 °C and can form biofilm. W. anomalus increased the activity of resistance-related enzymes such as PPO, POD, GLU and the content of secondary metabolites such as total phenols, flavonoids and lignin in peach. Furthermore, the application of W. anomalus led to a reduced MDA level in peach fruit and increased activity of the active oxygen-scavenging enzyme system. This increase involved various antioxidant defense enzymes such as SOD and CAT, as well as ascorbic acid-glutathione (AsA-GSH) enzymes, including APX, GPX, GR, DHAR, and MDHAR. Our findings demonstrate that W. anomalus exerts its biocontrol effect by growing rapidly, competing with pathogens for nutrition and space, and enhancing the disease resistance and antioxidative capabilities of the peach fruit.

Metagenomics-based exploration of key soil microorganisms contributing to continuously planted Casuarina equisetifolia growth inhibition and their interactions with soil nutrient transformation.

Casuarina equisetifolia (C. equisetifolia) is an economically important forest tree species, often cultivated in continuous monoculture as a coastal protection forest. Continuous planting has gradually affected growth and severely restricted the sustainable development of the C. equisetifolia industry. In this study, we analyzed the effects of continuous planting on C. equisetifolia growth and explored the rhizosphere soil microecological mechanism from a metagenomic perspective. The results showed that continuous planting resulted in dwarfing, shorter root length, and reduced C. equisetifolia seedling root system. Metagenomics analysis showed that 10 key characteristic microorganisms, mainly Actinoallomurus, Actinomadura, and Mycobacterium, were responsible for continuously planted C. equisetifolia trees. Quantitative analysis showed that the number of microorganisms in these three genera decreased significantly with the increase of continuous planting. Gene function analysis showed that continuous planting led to the weakening of the environmental information processing-signal transduction ability of soil characteristic microorganisms, and the decrease of C. equisetifolia trees against stress. Reduced capacity for metabolism, genetic information processing-replication and repair resulted in reduced microbial propagation and reduced microbial quantity in the rhizosphere soil of C. equisetifolia trees. Secondly, amino acid metabolism, carbohydrate metabolism, glycan biosynthesis and metabolism, lipid metabolism, metabolism of cofactors and vitamins were all significantly reduced, resulting in a decrease in the ability of the soil to synthesize and metabolize carbon and nitrogen. These reduced capacities further led to reduced soil microbial quantity, microbial carbon and nitrogen, microbial respiration intensity, reduced soil enzyme nutrient cycling and resistance-related enzyme activities, a significant reduction in available nutrient content of rhizosphere soils, a reduction in the ion exchange capacity, and an impediment to C. equisetifolia growth. This study provides an important basis for the management of continuously planted C. equisetifolia plantations.

Combined application of alginate oligosaccharide and marine yeast Sporidiobolus pararoseus to control brown rot of peach fruit

Brown rot caused by Monilinia fructicola is the major fungal disease during postharvest storage of peach fruit. In this study, the effects of marine yeast Sporidiobolus pararoseus and alginate oligosaccharide (AOS) used alone or in combination to control brown rot in peach fruit were investigated. The results showed that AOS and S. pararoseus used alone could reduce the disease incidence and lesion diameter of brown rot, and their combination significantly increased the control effect than either treatment alone. Especially in the early stage of disease, the incidence of the untreated control fruit has reached 90%, while the incidences of AOS and S. pararoseus treatment were 36.7% and 30%, however, the combination treatment only showed 13.3% of incidence. The combination treatment of AOS and S. pararoseus can also reduce the weight loss and maintain fruit quality of peaches. Meanwhile, AOS could promote the colonization of S. pararoseus in peach fruit wounds and improve the survival of S. pararoseus under stresses. The combined treatment of S. pararoseus and AOS significantly increased the activities and gene expression of resistance-related enzymes such as catalase (CAT), phenylalanine ammonia-lyase (PAL), peroxidase (POD), polyphenol oxidase (PPO), β-1,3-glucanase (GNS), chitinase (CHI), promoted the accumulation of total phenols. These findings indicated that the increased biocontrol efficacy of AOS combined with S. pararoseus may be attributed to the promoting growth of S. pararoseus by AOS and the enhanced disease resistance of peaches. Overall, the combined application of AOS and S. pararoseus could be an effective method to control brown rot of peach fruit.

Glycine Enhances Oxidative Stress Tolerance and Biocontrol Efficacy of Sporidiobolus pararoseus against Aspergillus niger Decay of Apples.

Apples are deeply loved by people because of their rich nutritional value, but they are susceptible to rotting. The use of antagonistic yeast is a promising method for controlling postharvest fruit diseases, but biocontrol efficacy of yeast will be weakened in environmental stress. In this study, the effects of glycine (Gly) on the oxidative stress tolerance and the biocontrol efficacy of Sporidiobolus pararoseus (S. pararoseus) against Aspergillus niger (A. niger) are discussed. Under the stimulation of H2O2, the yeast cells treated with Gly (1 mM) showed lower ROS content, less mitochondrial impairment and cellular oxidative damage, and the cell survival rate was significantly higher than Gly-untreated yeast. The yeast cells exposed to Gly significantly increased the activities of antioxidant enzymes superoxide dismutase (SOD), catalase (CAT), and the content of glutathione (GSH). Notably, Gly-treated yeast cells had better biocontrol efficacy against A. niger in postharvest apples. The lesion diameter and decay incidence were reduced by 17.67 mm and 79.63% compared to the control, respectively, when S. pararoseus was treated with 1 mM Gly. Moreover, Gly-treated yeast increased the antioxidant enzymes activities and their gene expression were up-regulated in apples. These results indicated that 1 mM Gly not only reduced the oxidative damage of yeast, but also induced resistance-related enzymes of apples under oxidative stress, which contributed to enhancing the biocontrol efficacy of S. pararoseus against A. niger in apples.

Effectiveness of Bacillus cereus in controlling potato bacterial wilt caused by Ralstonia solanacearum: greenhouse and field studies with insights into resistance-related enzymes in potatoes

Effectiveness of Bacillus cereus in controlling potato bacterial wilt caused by Ralstonia solanacearum: greenhouse and field studies with insights into resistance-related enzymes in potatoes

Combined application of oligochitosan and Pichia carrbbica improves the disease resistance of postharvest tomato fruits

Our previous study showed that postharvest treatment of tomato with Pichia caribbica along with oligochitosan (OCH) significantly alleviated postharvest black spot of tomato fruit compared with P. caribbica alone. This study was to explore the effect of combined application of OCH and P. caribbica on disease resistance of tomato fruits through analyzing the activities of disease resistance-related enzymes, as well as transcriptome analysis of the fruit gene expression. Our findings indicated that P. caribbica, together with OCH, improved the activities of key enzymes associated with disease resistance in tomato fruit. Moreover, the combined application further upregulated the expression of genes involved in α-linolenic acid metabolism, the signal transduction pathways such as Ca2+, MAPK and plant hormone signaling pathways, resistant substance synthesis, and ROS metabolism, which improved the fruit disease resistance. Considering the significance of these results, OCH hold great potential for use in microbial biocontrol strategies against postharvest tomato diseases.

Comparative Study of Three Biological Control Agents and Two Conventional Fungicides against Coriander Damping-off and Root Rot Caused by Rhizoctonia solani.

The in vitro and in vivo efficacy of three biocontrol agents, Trichoderma viride, Pseudomonas fluorescence, and Bacillus subtilis, were tested against Rhizoctonia solani (AG-4) infection compared to two conventional fungicides (Rizolex-T 50%wettable powder and Amistar 25%). Antifungal enzyme activity was assayed in the culture filtrate of the biocontrol agents. The impact of the tested biocontrol agents on the induction of the coriander immune system was investigated against R. solani by assessing the resistance-related enzymes and compounds in biocontrol agent-treated plants compared with the control. The obtained results revealed that all tested biocontrol agents significantly reduced the linear growth of R. solani, and T. viride recorded the highest inhibition percentage. This could be linked to the ability of T. viride to produce higher activities of antimicrobial enzymes, i.e., cellulase, chitinase, and protease, compared to P. fluorescence and B. subtilis. Applying the tested biocontrol agents significantly alleviated pre- and post-emergence damping-off and root rot/wilt diseases of infected coriander compared with untreated plants. The tested biocontrol agents exhibited significantly higher germination percentage and vigor index of the coriander than the tested fungicides. The tested biocontrol agents significantly minimized the reduction of photosynthetic pigments induced by R. solani. In addition, the results showed a significant increase in enzymes/molecules (i.e., phenylalanine, catalase, peroxidase, catalase, superoxide dismutase, phenylalanine ammonia-lyase, phenolics, ascorbic acids, and salicylic acid) involved directly and indirectly in coriander resistance to R. solani. The principal component analysis of the recorded data recommended the role of the high accumulation of oxidative parameters (hydrogen peroxide and lipid peroxidation) and the inhibition of phenolic compounds in the downregulation of coriander resistance against R. solani. The heatmap analysis results revealed that biocontrol agents, especially Trichoderma, enhanced the resistance against R. solani via the stimulation of salicylic acid, phenolics, and antioxidant enzymes. Overall, the data recommended the efficacy of biocontrol agents, especially T. viride, against R. solani infecting coriander plants, which could be an efficient and a safer alternative to conventional fungicides.

NpPP2-B10, an F-Box-Nictaba Gene, Promotes Plant Growth and Resistance to Black Shank Disease Incited by Phytophthora nicotianae in Nicotiana tabacum.

Black shank, a devastating disease affecting tobacco production worldwide, is caused by Phytophthora nicotianae. However, few genes related to Phytophthora resistance have been reported in tobacco. Here, we identified NpPP2-B10, a gene strongly induced by P. nicotianae race 0, with a conserved F-box motif and Nictaba (tobacco lectin) domain, in the highly resistant tobacco species Nicotiana plumbaginifolia. NpPP2-B10 is a typical F-box-Nictaba gene. When it was transferred into the black shank-susceptible tobacco cultivar 'Honghua Dajinyuan', it was found to promote resistance to black shank disease. NpPP2-B10 was induced by salicylic acid, and some resistance-related genes (NtPR1, NtPR2, NtCHN50, and NtPAL) and resistance-related enzymes (catalase and peroxidase) were significantly upregulated in the overexpression lines after infection with P. nicotianae. Furthermore, we showed that NpPP2-B10 actively regulated the tobacco seed germination rate, growth rate, and plant height. The erythrocyte coagulation test of purified NpPP2-B10 protein showed that NpPP2-B10 had plant lectin activity, and the lectin content in the overexpression lines was significantly higher than that in the WT, which could lead to accelerated growth and improved resistance of tobacco. SKP1 is an adaptor protein of the E3 ubiquitin ligase SKP1, Cullin, F-box (SCF) complex. We demonstrated that NpPP2-B10 could interact with the NpSKP1-1A gene in vivo and in vitro through yeast two-hybrid (Y2H) and bimolecular fluorescence complementation (BiFC), indicating that NpPP2-B10 likely participates in the plant immune response by mediating the ubiquitin protease pathway. In conclusion, our study provides some important insights concerning NpPP2-B10-mediated regulation of tobacco growth and resistance.

Study on the effect of Debaryomyces hansenii enhanced by alginate oligosaccharide against postharvest blue mold decay of apples and the physiological mechanisms involved

Blue mold decay is the most common disease during postharvest storage of apples caused by Penicillium expansum, leading to huge economic losses to the apple industry. Antagonistic yeasts are widely used in biological control, and organic compounds can be used as elicitors to induce antagonistic yeasts to further improve their biocontrol effect. In this study, we assessed the biocontrol efficacy of the antagonistic yeast, Debaryomyces hansenii, enhanced by alginate oligosaccharide (AOS) in controlling the postharvest decay of apples and studied the possible physiological mechanisms involved in this process. The results of this study were as follows: (1) AOS enhanced the biocontrol ability of D. hansenii against P. expansum infestation of apples. In the in vivo experiments, D. hansenii induced by 0.5% AOS significantly reduced the disease incidence and lesion diameter in apples, demonstrating good control of blue mold. When treated with D. hansenii-induced with AOS, the disease incidence rate of apples was only 21.6%, while that of yeast alone was 37.5%. (2) In the in vitro experiments, AOS significantly improved the inhibitory effect of D. hansenii on the germination rate, germ tube length, and colony diameter of P. expansum. The results suggested that AOS-induced yeast exhibited a certain inhibitory effect on the growth of P. expansum. (3) The activities of diseases resistance-related enzymes of apples treated with AOS-induced D. hansenii such as polyphenol oxidase (PPO), peroxidase (POD), and phenylalanine ammonia-lyase (PAL) were increased compared to the yeast alone and the control group. Apart from that, the content of substances such as total phenols and flavonoids maintained the original level. These results suggest that the resistance of apples against pathogenic fungi may be improved by increasing the activities of disease resistance related enzymes activities of the fruit. In summary, the method of enhancing antagonistic yeast by AOS is very promising and efficient for improving biological control to reduce economic losses in the apple industry.

Effects of thymol concentration on postharvest diseases and quality of blueberry fruit

In this study, we compared the incidence of postharvest disease and the storage potential of blueberry fruit treated with thymol (inoculated with Aspergillus niger) with those in the control fruit during storage for 42 d at 2 °C. Treatment with 10–30 mg/L thymol was found to be more effective than treatment with higher thymol concentrations of 40–50 mg/L in terms of controlling Aspergillus niger-induced decay. In the thymol-treated blueberry fruit peel, the activities of the disease resistance-related enzymes were significantly enhanced. Furthermore, the 20 mg/L thymol-treated blueberry fruit retained the highest firmness, total soluble solids content, and acceptability score, and it also maintained an unimpaired cell wall structure of pericarp quality. Thus, low-dose thymol-treatment could be a suitable biocontrol agent for controlling postharvest disease and prolonging the storage life of blueberry fruit.

Study on the biocontrol effect and physiological mechanism of Hannaella sinensis on the blue mold decay of apples

Blue mold decay is a major postharvest disease of apples, causing considerable losses to the apple industry. In the early stage of this research, an antagonistic yeast, Hannaella sinensis, with a good control effect on the blue mold of apples, was selected. On this basis, the main purpose of this work was to study the biocontrol effect of H. sinensis on the blue mold of apples and the mechanisms involved. The results showed that H. sinensis could effectively control the blue mold decay of apples, reduce the rot rate and diameter, and the antagonistic effect strengthened with the increase of H. sinensis concentration (1 × 108 cells/mL). Further in vitro experiments proved that H. sinensis could significantly inhibit the spore germination and germ tube length of P. expansum. In addition, stable colonization of H. sinensis on apple wounds and surfaces confirmed the environmental adaptability and the ability to compete with other microbiota for nutrition and space. Moreover, H. sinensis induced the activities of resistance-related enzymes such as polyphenol oxidase (PPO), peroxidase (POD), ascorbate peroxidase (APX), superoxide dismutase (SOD), and phenylalanine ammonia-lyase (PAL) in apples and the content of the coding genes corresponding to these enzymes was also higher than that of the control group. Our results indicate that H. sinensis treatment could induce the disease resistance of apples. In summary, H. sinensis served as a promising antagonistic yeast for the prevention and treatment of postharvest blue mold decay of apples.

Transcriptomic analysis reveals the mechanism of bacterial disease resistance of postharvest button mushroom (Agaricus bisporus)

Brown blotch disease caused by Pseudomonas tolaasii infection is one of the major problems affecting the storage quality of postharvest button mushrooms (Agaricus bisporus). In this study, P. tolaasii treatment accelerated the accumulation of pathogen resistance-related substances/proteins, induced disease resistance-related enzyme activities, and promoted the increase of jasmonic acid (JA) during the whole storage. To gain full insight into the defense mechanisms of button mushrooms against P. tolaasii, a transcriptomics analysis of mushroom samples at 12 h was conducted. A total of 2861 differentially expressed genes (DEGs) were identified, among which there were 1557 up-regulated and 1304 down-regulated genes. Further bioinformatic analysis showed that P. tolaasii inoculation mainly activated shikimate pathway, phenylpropanoid metabolism, sulfur metabolism, methane metabolism, arginine and proline metabolism, cysteine and methionine metabolism, JA biosynthesis and signaling pathways, as well as oxidative phosphorylation pathways. Transcriptomics data combined with qPCR verification indicated that 10 DEGs including PIP1, MET3, AGX, PAL1, GCL, LOX 1/3, PR-like, MYB3R, UCR, and SDHB are the most potential genes involved in the early defense of A. bisporus against P. tolaasii. Additionally, taking the physiological and transcriptomics results together, the existence and important participation of JA biosynthesis and signaling pathways were demonstrated in the disease resistance of A. bisporus, although this organism probably possesses different catalyzing enzymes and transduction pathways with plants. In a word, our findings revealed the mechanism of the button mushroom's early defense response against pathogens, providing a reference for the development of rational approaches to control of mushroom diseases.

Efficacy of Debaryomyce hansenii in the biocontrol for postharvest soft rot of strawberry and investigation of the physiological mechanisms involved

The postharvest disease of strawberries caused by Rhizopus stolonifer caused enormous financial losses. This study investigates the efficacy of antagonistic yeast Debaryomyce hansenii in the biocontrol of postharvest soft rot of strawberries and the physiological mechanisms involved. The results showed that D. hansenii significantly reduced the incidence of postharvest soft rot of strawberry, reduced the natural decay incidence of postharvest strawberry, and had no adverse effects on quality parameters of strawberries. In vitro experiments showed that D. hansenii reduced the spore germination rate and germ tube length of R. stolonifer. D. hansenii can also stably colonize the surface and wounds of strawberries at either 4 °C or 20 °C. Meanwhile, the activities of antioxidant-related enzymes superoxide dismutase, peroxidase, catalase, ascorbate oxidase and resistance-related enzymes polyphenol oxidase and phenylalanine ammonia-lyase were significantly higher in D. hansenii-treated strawberries than in control. Meanwhile, the contents of resistance-related substances including total phenols, flavonoids and anthocyanins were also increased in D. hansenii-treated strawberries. This study suggested that D. hansenii has the potential to control postharvest soft rot of strawberry by the mechanism involving inhibition of spore germination and germ tube length of R. stolonifer and induction of increased activities of defense-related enzymes and substances in strawberry.

Effects of a Dark Septate Fungal Endophyte on the Growth and Physiological Response of Seedlings to Drought in an Epiphytic Orchid.

Dark septate endophytes (DSE) are a group of facultative biotrophic root-colonizing fungi that live within a plant for a part of their life cycle without causing any apparent, overt negative effects. These fungi have been found in >600 different plant species, including orchids. Although the precise ecological functions of dark septate fungal endophytes are not yet well understood, there is increasing evidence that they enhance host growth and nutrient acquisition, and improve the plant’s ability to tolerate biotic and abiotic stresses. In this research, we tested the effects of a DSE isolated from the roots of the epiphytic orchid Coelogyne viscosa on the growth and drought tolerance of orchid seedlings. Our results showed that addition of DSE inoculum significantly enhanced biomass of seedlings and increased the activities of drought resistance related enzymes and the accumulation of osmoregulatory substances. These results suggest that DSE can fulfill important ecological functions in stressful environments and potentially play an important role in the life cycle of epiphytic orchids.

Induction of Resistance of Antagonistic Bacterium Burkholderia contaminans to Postharvest Botrytis cinerea in Rosa vinifera.

In order to study the problem that grapes are vulnerable to microbial infection and decay during storage, a method based on antagonistic Burkholderia contaminans against postharvest Botrytis cinerea of Rosa vinifera was proposed in this paper. The method tested the resistance induction mechanism of Botrytis cinerea after harvest and determined the fruit decay rate treated by antagonistic Burkholderia contaminans. The results showed that the antagonistic bacterium B-1 had bacteriostatic effect on many common pathogens of fruits and vegetables to a certain extent, and the bacteriostatic range was wide. Among them, the inhibition rate of Fusarium moniliforme was 75.5% and that of Botrytis cinerea was 51.2%. After testing, it can be found that antagonistic bacteria have an inhibitory effect on pathogenic fungi and have an effect on phenylpropane metabolic pathway, reactive oxygen species metabolic pathway, and the activities of other resistance-related enzymes. Through comparison, it can be found that the antagonistic Burkholderia contaminans has a strong antibacterial mechanism against Botrytis cinerea of rose grape after harvest. The fruit treated with antagonistic B Burkholderia B-1 has significantly reduced the decay rate and increased the activity of antibacterial active protein.

Field Resistance of Digitaria sanguinalis (L.) Scop. to Haloxyfop-P-methyl in China’s Cotton Fields

Large crabgrass, Digitaria sanguinalis (L.) Scop., is a devastating weed species in the cotton (Gossypium spp.) fields in China. It has developed resistance to haloxyfop-P-methyl, an aryloxyphenoxypropionate herbicide known for its ability to inhibit lipid synthesis and induce oxidative stress in weeds, due to years of continuous and intensive use. Here, we present the results from a nation-wide, long-term resistance monitoring effort. To understand the scale and level of haloxyfop-P-methyl resistance, a total of 65 D. sanguinalis populations from eight cotton production provinces, including Hunan, Jiangxi, Xinjiang, Henan, Hubei, Hebei, Shanxi, and Anhui, were collected from 2014–2017. Based on results from dose response to haloxyfop-P-methyl, we observed a gradient of sensitivity to haloxyfop-P-methyl among 65 field populations, ranging from sensitive (8), to low-level resistance (40; 2 ≤ RI ≤ 10) to moderate-level resistance (17; 10 < RI < 20). Although no high-level resistance (RI > 20) was found among the 65 populations, populations from Hunan and Hebei exhibited a rapid spread of field-evolved resistance. After challenged with haloxyfop-P-methyl (48.600 g a.i./ha at the 4–5-leaf stage), resistant and susceptible D. sanguinalis responded differently in the activity of an array of resistance-related enzymes, including acetyl-CoA carboxylase (ACCase), glutathione S-transferase (GSTs), nicotinamide-adenine dinucleotide phosphate (NADPH) and carboxylesterase (CarE), suggesting the potential involvement of NADPH, CarE and GSTs in D. sanguinalis to haloxyfop-P-methyl resistance.