Activity of Streptomyces globosus OPF-9 against the important pathogen Alternaria longipes and biocontrol mechanisms revealed by multi-omic analyses.

Plant diseases caused by fungal pathogens represent main threats to the yield and quality of agricultural products, and Alternaria longipes is one of the most important pathogens in agricultural systems. Biological control is becoming increasingly prevalent in the management of plant diseases due to its environmental compatibility and sustainability. In the present study, a bacterial strain, designated as OPF-9, was shown to effectively inhibit the pathogen A. longipes, which was identified as Streptomyces globosus. The culture conditions for OPF-9 were optimized through a stepwise approach and the fermentation broth acquired displayed an excellent inhibitory activity against A. longipes in vitro and in vivo. Further investigations suggested that the fermentation broth exhibited strong stability under a range of adverse environmental conditions. To reveal the molecular bases of OPF-9 in inhibiting pathogens, the whole-genome sequencing and assembly were conducted on this strain. It showed that the genome size of OPF-9 was 7.668 Mb, containing a chromosome and two plasmids. Multiple clusters of secondary metabolite synthesis genes were identified by genome annotation analysis. In addition, the fermentation broth of strain OPF-9 was analyzed by LC-MS/MS non-target metabolomic assay and the activity of potential antifungal substances was determined. Among the five compounds evaluated, pyrogallol displayed the most pronounced inhibitory activity against A. longipes, which was found to effectively inhibit the mycelial growth of this pathogen. Overall, this study reported, for the first time, a strain of S. globosus that effectively inhibits A. longipes and revealed the underlying biocontrol mechanisms by genomic and metabolomic analyses.

Highly sensitive time-resolved fluoroimmunoassay for the quantitative onsite detection of Alternaria longipes in tobacco.

AIMS: Alternaria longipes is a causal agent of brown spot of tobacco, which remains a serious threat to tobacco production. Herein, we established a detection method for A. longipes in tobacco samples based on the principle of time-resolved fluoroimmunoassay, in order to fulfil the requirement of rapid, sensitive and accurate detection in situ. METHODS AND RESULTS: A monoclonal antibody against A. longipes was generated, and its purity and titration were assessed using western blot and ELISA. The size of europium (III) nanospheres was measured to confirm successful antibody conjugation. The method described here can detect A. longipes protein lysates as low as 0.78 ng ml-1 , with recovery rates ranging from 85.96% to 99.67% in spiked tobacco. The specificity was also confirmed using a panel of microorganisms. CONCLUSIONS: The fluorescent strips allow rapid and sensitive onsite detection of A. longipes in tobacco samples, with high accuracy, specificity, and repeatability. SIGNIFICANCE AND IMPACT OF THE STUDY: This novel detection method provides convenience of using crude samples without complex procedures, and therefore allows rapid onsite detection by end users and quick responses towards A. longipes, which is critical for disease control and elimination of phytopathogens.

First report of Alternaria longipes causing leaf spot on tea in China.

Tea [Camellia sinensis (L.) Kuntze)] have been widely planted in Guizhou Province in recent years, and the cultivation area in the region ranks first among all the provinces or cities in China. Leaf spot disease was an important disease of tea in Kaiyang county, Guizhou Province, which mainly damaged young leaves and shoot of tea and led to a huge loss of the production of tea. The spots initially represented brown and round, and then the diameter of the spot was 4-6 mm during later period, with the color of the center in the spot changing white. Tea leaf spot disease always occurs in early spring and the region with 1300 m altitude. From 2016 to 2019, disease incidence of leaves was estimated at 84% to 92%, and the disease severity on a plant basis was determined to be 64% to 76%, depending on the field. To identify the causal agent of the foliar disease, pieces of the lesion margins were surface sterilized with 75% ethanol for 30 s, followed by 0.5% sodium hypochlorite for 5 min, rinsed with sterile water three times, plated on potato dextrose agar (PDA) and incubated in the dark at 25C for 3 to 5 d. The hyphal tips from the margins of the growing colonies were successively picked and transferred to fresh PDA plates to purify the isolates. The result indicated that the isolates on PDA represented initially round form, and white mycelium. The reverse sides of the isolates firstly displayed light yellow on PDA. Conidiophores represent dark brown, geniculate. Brown conidia, narrow ovoid, length: 22.9 ± 4.5 µm, width: 11.1 ± 1.7 µm, with 4 to 8 transverse septa and with conspicuously ornamented walls. The gene of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (Berbee et al. 1999) and the Alternaria allergen 1 (Alt a1) (Hong et al. 2005) of three strains were amplified, sequenced and deposited in Genbank. Maximum parsimony phylogenetic analysis based on concatenated sequences of combined GAPDH (1-583) and Alt a 1 (588-1065) indicated that the strain AXLKY_2019_010 was identical to reference strain Alternaria longipes strain EGS 30-033, and the clade was supported by 96% bootstrap values. According to the Koch's postulate, the tea leaves were inoculated with PDA plugs with actively growing mycelia using the methods of the puncture, cut and unwound under the laboratory conditions and the natural conditions. Slight yellow spots were gradually formed after 2 d post-inoculation on the inoculated leaves, and the color of the center of the spot changed to be white. With the prolonging of inoculation time, the size of lesion represented to be slightly enlarged. PDA plugs without mycelia were used as a control, and the control group showed no symptoms. The same isolates were consistently reisolated from inoculated leaves. A. longipes can cause leaf blight of carrots in Israel (Vintal et al. 2002), leaf spot of potato in Pakistan (Shoaib et al. 2014) and leaf spot of Atractylodes macrocephala in China (Tan et al. 2012). To our knowledge, this is the first report of A. longipes causing leaf spot on tea in China and our findings will be useful for its management and for further research.

Biotransformation of α-asarone by Alternaria longipes CGMCC 3.2875.

Biotransformation of α-asarone by Alternaria longipes CGMCC 3.2875 yielded two pairs of new neolignans, (+) (7S, 8S, 7'S, 8'R) iso-magnosalicin (1a)/(-) (7R, 8R, 7'R, 8'S) iso-magnosalicin (1b) and (+) (7R, 8R, 7'S, 8'R) magnosalicin (2a)/(-) (7S, 8S, 7'R, 8'S) magnosalicin (2b), and four known metabolites, (±) acoraminol A (3), (±) acoraminol B (4), asaraldehyde (5), and 2, 4, 5-trimethoxybenzoic acid (6). Their structures, including absolute configurations, were determined by extensive analysis of NMR spectra, X-ray crystallography, and quantum chemical ECD calculations. The cytotoxic activity and Aß42 aggregation inhibitory activity of all the compounds were evaluated. Compound 2 displayed significant anti-Aß42 aggregation activity with an inhibitory rate of 60.81% (the positive control EGCG: 69.17%). In addition, the biotransformation pathway of α-asarone by Alternaria longipes CGMCC 3.2875 was proposed.

Biotransformation of ursolic acid by Alternaria longipes AS3.2875.

Microbial transformation of ursolic acid (1) was carried out by Alternaria longipes AS 3.2875. Six transformed products (2-7) from 1 were isolated and their structures were identified as 3-carbonyl ursolic acid 28-O-ß-D-glucopyranosyl ester (2), ursolic acid 3-O-ß-D-glucopyranoside (3), ursolic acid 28-O-ß-D-glucopyranosyl ester (4), 2α, 3ß-dihydroxy ursolic acid 28-O-ß-D-glucopyranosyl ester (5), 3ß, 21ß dihydroxy ursolic acid 28-O-ß-D-glucopyranosyl ester (6), and 3-O-(ß-D-glucopyranosyl)- ursolic acid 28-O-(ß-D-glucopyranosyl) ester (7) based on the analysis of 1D NMR, 2DNMR and MS data. The product 2 was a new compound among them and showed stronger antibacterial activity against S. aureu, MRSA and MRCA than substrate. In this study, we modified structure of ursolic acid through biotransformation to enhance its activities and preliminarily discussed the transformation way of the products.

Evaluation of eliciting activity of peptidil prolyl cys/trans isomerase from Pseudonomas fluorescens encapsulated in sodium alginate regarding plant resistance to viral and fungal pahogens.

Use of chemical pesticides poses a threat for environment and human health, so green technologies of crop protection are of high demand. Some microbial proteins able to activate plant defense mechanisms and prevent the development of resistance in plant pathogens, may be good alternative to chemicals, but practical use of such elicitors is limited due to need to protect them against adverse environment prior their delivery to target receptors of plant cells. In this study we examined a possibility to encapsulate heat resistant FKBP-type peptidyl prolyl cis-trans isomerase (PPIase) from Pseudomonas fluorescens, which possesses a significant eliciting activity in relation to a range of plant pathogens, in sodium alginate microparticles and evaluated the stability of resulted complex under long-term UV irradiation and in the presence of proteinase K, as well as its eliciting activity in three different "plant-pathogen" models comparing to that of free PPIase. The obtained PPIase-containing microparticles consisted of 70% of sodium alginate, 20% of bovine serum albumin, and 10% of PPIase. In contrast to free PPIase, which lost its eliciting properties after 8-h UV treatment, encapsulated PPIase kept its eliciting ability unchanged; after being exposed to proteinase K, its eliciting ability twice exceeded that of free PPIase. Using "tobacco-TMV", "tobacco-Alternaria longipes", and "wheat-Stagonospora nodorum" model systems, we showed that encapsulation process did not influence on the eliciting activity of PPIase. In the case of the "wheat-S. nodorum" model system, we also observed a significant eliciting activity of alginate-albumin complex and almost doubled activity of encapsulated PPIase as compared to the free PPIase. As far as we know, this is the first observation of a synergistic interaction between alginate and other compound possessing any bioactive properties. The results of the study show some prospects for a PPIase use in agriculture.

[Screening and inhibition of antagonistic endophytic bacteria isolated from soybean (Glycine max)nodules against Alternaria longipes.] / çƒŸè‰èµ¤æ˜Ÿç— èŒæ‹®æŠ—æ€§å¤§è±†æ ¹ç˜¤å† ç”ŸèŒçš„ç­›é€‰åŠæŠ‘åˆ¶ä½œç”¨.

Using Alternaria longipes as tested phytopathogen, endophytic bacteria isolated from soybean nodules were selected to study antagonistic effects by confrontation and metabolic liquid culture methods. The inhibited hyphae were determined by microscopic observation, and the screened strains were characterized by cell culture, physiological and biochemical tests, 16S rDNA sequencing, phylogenetic analysis and inoculation trials in greenhouse. The results indicated that the seven of the endophytes exerted more than 42% inhibitory effects after the first and the second screening. These strains belonged to genus Bacillus, Pseudomonas, Sinorhizobium and Stenotrophomonas, respectively. Microscopic observation showed that the affected hyphae ends of A. longipes appear deformity of coralline branch, spherical expansions and so on. Antagonistic experiments with metabolites showed that the inhibition of endophytic bacteria against pathogenic fungus played an effective role mainly by bacteria producing extracellular substances. Confrontation tests suggested that endophytic Bacillus rapidly produced biofilm to effectively hinder the growth and extension of pathogen hyphae. Inoculation experiments showed that the disease index of treatment group was significantly lowered compared with the control, suggesting it could be utilized as a biological control resource inhibiting tobacco brown spot.