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Biocontrol Potential and Mechanism of Endophytic Bacillus velezensis WSR1 Against Rubber Tree Anthracnose.

Fungal leaf anthracnose, caused by Colletotrichum species, is a major leaf disease of rubber trees, significantly reducing global natural rubber yields. To explore sustainable and safe biological control strategies, eight bacterial strains were isolated from rubber tree tissues, demonstrating antagonistic activity against Colletotrichum pathogens (C. siamense and C. australisinense). Among these, WSR1 exhibited the most pronounced antifungal effect, with inhibition rates of 87.64 and 89.03% against C. siamense and C. australisinense, respectively. Genomic analysis identified WSR1 as Bacillus velezensis. In pot experiments, WSR1 exhibited preventive efficacy of 77.24 and 73.42% for C. siamense- and C. australisinense-induced anthracnose, respectively, with therapeutic efficacy of 42.28 and 45.57%. WSR1 compromised the integrity of the cell walls and membranes of both C. siamense and C. australisinense, while inducing reactive oxygen species accumulation within the hyphae. Additionally, WSR1 enhanced rubber tree resistance to anthracnose by activating defense-related enzymes, including phenylalanine ammonia-lyase, polyphenol oxidase, and peroxidase. Plate assays and genomic analysis revealed that WSR1 secretes fungal cell wall-degrading enzymes (cellulases, pectinases, and proteases) and siderophores. Furthermore, liquid chromatography-mass spectrometry and gene cluster analysis confirmed the synthesis of antagonistic secondary metabolites, such as surfactin, macrolactin H, and fengycin. This study represents the first identification of B. velezensis as a potential biocontrol agent against rubber tree anthracnose, offering a promising candidate for the eco-friendly management of rubber tree diseases.

C. australisinense

An integrated proteomics and transcriptomics analysis highlights concordance between protein turnover and carbohydrate transport and metabolism as key functional categories during the growth of Trichophyton rubrum.

Dermatophytes are a class of keratinophilic skin fungi that invade host skin, hair, and nails to acquire nutrients. An integrated multi-omics approach utilizing liquid chromatography-tandem mass spectrometry and RNA-seq after growth in a protein-rich soy medium was employed to capture the major subset of secreted protein families of Trichophyton rubrum. The secretome consisted mainly of proteases and cell wall-degrading enzymes, with subtilisins (Sub6 and Sub7), metallopeptidase (LAP2), and chitinase having the most abundant peptides. Transcriptional profiling indicated fungal adaptation in protein-rich media to process the protein nutrients through modulation of metabolism and general cellular function pathways. Correlation analysis between proteomics and transcriptomics data using functional KOG categories shows high concordance of KOG categories O (posttranslational modification, protein turnover, and chaperones), P (inorganic ion transport and metabolism), and G (carbohydrate transport and metabolism), as per cosine similarity analysis.IMPORTANCEDermatophytes are keratinophilic skin fungal pathogens that invade host skin, hair, and nails to acquire nutrients. There is an epidemic-like increase in infections, as well as an increase in antimicrobial resistance among dermatophytes, as witnessed over the last decade. There is hence a need to understand the key pathways and virulence factors required during growth and infection. We present an integrated multi-omics analysis (proteomics and transcriptomics data) using a vector-based similarity approach to show high concordance of KOG functional categories belonging to posttranslational modification, protein turnover, carbohydrate transport, and metabolism.

Proteomics

Rs_MEP1 Is Required for the Pathogenesis of Rhizoctonia solani AG1-IA in Plants.

Rhizoctonia solani AG1-IA is a polyphagous necrotrophic fungal pathogen that causes sheath blight disease in rice. Efforts are being made to identify pathogenicity-associated genes in R. solani and modulate them to develop a disease control strategy. Here, we investigated the roles of some predicted pathogenicity-associated genes of R. solani that have previously been reported to be upregulated during infection in rice. The tobacco rattle virus-based host-induced gene silencing of the selected pathogenicity-associated genes revealed that silencing of Rs_MEP1, a zinc-containing Peptidase_M43 domain metalloprotease, severely compromises R. solani infection in tomato. Moreover, double-stranded RNA-mediated silencing of Rs_MEP1 prevented R. solani infection in rice. The signal sequence trap assay indicated the secretory nature of Rs_MEP1, and the reporter assay suggested its localization in the plant apoplast. Notably, Agrobacterium-mediated transient overexpression of Rs_MEP1 induces necrotic cell death responses in plants. We provide evidence that Rs_MEP1 interacts with the GH19 family of rice chitinases and potentially modulates their functions. Overall, our study emphasizes that Rs_MEP1 facilitates R. solani in promoting necrotic responses and targets rice GH19 chitinases to impart disease susceptibility in plants. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

Rhizoctonia