Anthracnose caused by Colletotrichum spp. is one of the major problems in mango production worldwide, including Thailand. All mango cultivars are susceptible, but Nam Dok Mai See Thong (NDMST) is the most vulnerable. Through a single spore isolation method, a total of 37 isolates of Colletotrichum spp. were obtained from NDMST showing anthracnose symptoms. Identification was performed using a combination of morphology characteristics, Koch’s postulates, and phylogenetic analysis. The pathogenicity assay and Koch’s postulates on leaves and fruit confirmed that all Colletotrichum spp. tested were causal agents of mango anthracnose. Multilocus analysis using DNA sequences of internal transcribed spacer (ITS) regions, β-tubulin (TUB2), actin (ACT), and chitin synthase (CHS-1) was performed for molecular identification. Two concatenated phylogenetic trees were constructed using either two-loci of ITS and TUB2, or four-loci of ITS, TUB2, ACT, and CHS-1. Both phylogenetic trees were indistinguishable and showed that these 37 isolates belong to C. acutatum, C. asianum, C. gloeosporioides, and C. siamense. Our results indicated that using at least two loci of ITS and TUB2, were sufficient to infer Colletotrichum species complexes. Of 37 isolates, C. gloeosporioides was the most dominant species (19 isolates), followed by C. asianum (10 isolates), C. acutatum (5 isolates), and C. siamense (3 isolates). In Thailand, C. gloeosporioides and C. acutatum have been reported to cause anthracnose in mango, however, this is the first report of C. asianum and C. siamense associated with mango anthracnose in central Thailand.

The mycotoxin fumonisin (FB) has become a major problem in maize products in southeastern Asia. Fumonisin can affect the health of humans and many animals. Fumonisin contamination can be reduced by detoxifying microbial enzyme. Screening of 95 potent natural sources resulted in 5.3% of samples yielding a total of five bacterial isolates that were a promising solution, reducing approximately 10.0–30.0% of fumonisin B1 (FB1). Serratia marcescens, one of the dominant degrading bacteria, was identified with Gram staining, 16S rRNA gene, and MALDI-TOF/TOF MS. Cell-free extract showed the highest fumonisin reduction rates, 30.3% in solution and 37.0% in maize. Crude proteins from bacterial cells were analyzed with a label-free quantification technique. The results showed that hydrolase enzymes and transferase enzymes that can cooperate in the fumonisin degradation process were highly expressed in comparison to their levels in a control. These studies have shown that S. marcescens 329-2 is a new potential bacterium for FB1 reduction, and the production of FB1-reducing enzymes should be further explored.

Durian (Durio zibethinus L.) is an economically important crop in the southern and eastern parts of Thailand. The occurrence of die-back disease caused by plant pathogenic fungi poses a serious threat to the quality and quantity of durian products. However, the identification of causal agents has been a subject of mixed information and uncertainty. In this research, we conducted a comprehensive investigation of die-back disease in nine durian plantations located in Thailand. By analyzing a total of 86 Fusarium isolates obtained from infected tissues, we aimed to provide clarity and a better understanding of the fungal pathogens responsible for this economically significant disease. Through a combination of colony characteristics, microscopic morphology, and a multilocus sequence analysis (MLSA) of the internal transcribed spacer (ITS) region, translation elongation factor 1-α (TEF1-α) gene, and RNA polymerase II gene (RPB2) sequences, we were able to identify and categorize the isolates into three distinct groups, namely, Fusarium incarnatum, F. solani, and F. mangiferae. Koch’s postulates demonstrated that only F. incarnatum and F. solani were capable of causing die-back symptoms. This research represents the first report of F. incarnatum as a causal agent of die-back disease in durian in Thailand. Additionally, this study uncovers the association of ambrosia beetles and F. solani, highlighting the potential involvement of E. similia in facilitating the spread of die-back disease caused by Fusarium in durian.

Partitiviruses are one of the most prevalent double-stranded RNA viruses that have been identified mostly in filamentous fungi and plants. Partitiviruses generally infect host fungi asymptomatically but infrequently exert significant effect(s) on morphology and virulence, thus being considered a potential source of biological control agents against pathogenic fungi. In this study, we performed a screening for mycoviruses of a collection of Thai isolates of rice fungal pathogen Rhizoctonia oryzae-sativae, a causal agent of rice aggregated sheath spot disease. As a result, 36% of tested isolates carried potentially viral double-stranded RNAs with sizes ranging from 2 to 3 kbp. By conventional cDNA library construction and RNA-seq, we determined six new alphapartitiviruses that infected three isolates: tentatively named Rhizoctonia oryzae-sativae partitivirus 1 to 6 (RosPV1-6). Furthermore, RT-PCR detection of each virus revealed their omnipresent nature in different R. oryzae-sativae isolates. Although virus-curing of basidiomycetous fungi is generally difficult, our repeated attempts successfully obtained virus-free (for RosPV1, RosPV2, and uncharacterized partitiviruses), isogenic strain of R. oryzae-sativae TSS190442. The virus-cured strain showed slightly faster colony growth on the synthetic media and severe symptom development on the rice sheath compared to its virus-infected counterpart. Overall, this study shed light on the distribution of partitiviruses in R. oryzae-sativae in a paddy environment and exemplified a virus-curing protocol that may be applicable for other basidiomycetous fungi.

Bacterial leaf spot, particularly in chili peppers, is major concern worldwide, particularly in chili peppers. Enhancing pepper resistance to bacterial leaf spot addresses a key agricultural challenge while minimizing chemical usage. In this study, the efficacy of plant resistance inducers (PRIs) in controlling bacterial leaf spot in peppers was evaluated through molecular and secondary metabolite analyses. Pepper plant seedlings were treated with salicylic acid (SA), acibenzolar-S-methyl, β-aminobutyric acid, chitosan, Bacillus subtilis B01, and B. velezensis CH6 and inoculated with Xanthomonas euvesicatoria pv. euvesicatoria. Disease severity was assessed, and the expression level of genes (PR-1, PR-2, PR-4, and CAT) and the abundance of secondary metabolites were analyzed via quantitative PCR (qPCR) and gas chromatography-mass spectrometry (GC-MS), respectively. Soil drenching with B. subtilis B01 produced the best effects, reducing the disease severity by 80% and significantly inducing PR-1 expression 24–48 h post-treatment. SA was similarly effective in inducing systemic acquired resistance (SAR), while β-aminobutyric acid primed antioxidative defenses through sustained catalase (CAT) expression, and chitosan induced PR-4. GC-MS analysis revealed secondary metabolites associated with systemic resistance pathways including SAR and induced systemic resistance (ISR). Herein, B. subtilis B01 and SA were identified as potent resistance inducers that reduce the disease severity of bacterial leaf spot and activate key defense pathways in pepper plants. These findings contribute to the development of sustainable, integrated disease management strategies.

Pythium spp., which are soilborne oomycetes that cause damping-off and root rot symptoms in a wide range of crops, are a persistent threats on farms, especially under humid agricultural conditions. Although the strobilurin fungicide, azoxystrobin, exhibits broad-spectrum activity. Its efficacy against Pythium spp. is often limited due to poor uptake by the pathogen, causing an insufficient delivery to the site of infection. This study investigated the ability of agricultural adjuvants to enhance the antifungal activity of azoxystrobin was investigated through biochemical and pathological assessments. A poisoned food test demonstrated that poly(oxy-1,2-ethanediyl), alpha-(2-propylheptyl)-omega-hydroxy (RG) significantly inhibited Pythium aphanidermatum mycelial growth in a dose-dependent manner, achieving 88 % inhibition at high concentrations. When combined with azoxystrobin, RG improved mycelial suppression by more than 75 % across all the tested formulations, whereas azoxystrobin alone exhibited less inhibitory activity. Gas chromatography-mass spectrometry (GC–MS) analysis of the mycelium revealed that RG treatment altered Pythium cell wall metabolites, as the abundances of stress-related glycol ethers, furanones, and reactive aldehydes increased, indicating membrane disruption and metabolic reprogramming. In vivo assays using durian leaves confirmed the synergistic effect: compare with each treatment alone, RG combined with azoxystrobin, significantly reduced disease lesion diameter compared with each treatment alone. The most effective lesion suppression was observed after five days, with treatment using 0.5 mL/L RG and 0.5 mL/L azoxystrobin. These findings highlight the critical role of adjuvants in enhancing the fungicide efficacy and suggest that the strategic application of adjuvants could optimize disease control while potentially reducing fungicide inputs. This approach is a promising direction for the integrated management of oomycete pathogens in tropical crop systems.