Selection and differentiation of Bacillus spp. Antagonistic to Fusarium oxysporum f.sp. lycopersici and Alternaria solani infecting Tomato
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Alternaria growth & development pathogenicity MeSH
- Antibiosis * MeSH
- Bacillus classification isolation & purification metabolism physiology MeSH
- Pest Control, Biological methods MeSH
- Biomass MeSH
- Chitinases metabolism MeSH
- DNA, Bacterial genetics MeSH
- Fusarium growth & development pathogenicity MeSH
- Glucan 1,3-beta-Glucosidase metabolism MeSH
- Plant Roots microbiology MeSH
- Plant Leaves microbiology MeSH
- Molecular Typing MeSH
- Plant Diseases microbiology MeSH
- Siderophores metabolism MeSH
- Solanum lycopersicum growth & development microbiology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- beta-1,3-exoglucanase MeSH Browser
- Chitinases MeSH
- DNA, Bacterial MeSH
- Glucan 1,3-beta-Glucosidase MeSH
- Siderophores MeSH
Antagonistic Bacillus spp. displaying in vitro production of siderophore, chitinase, and β-1,3-glucanase were identified from dual culture assays. In independent greenhouse studies, seed bacterization and soil application of Bacillus atrophaeus S2BC-2 challenge inoculated with Fusarium oxysporum f.sp. lycopersici (FOL) and Alternaria solani (AS) recorded low percent disease index of 25.3 and 28.7, respectively, over nonbacterised pathogen control (44.3 and 56.4). The low disease incidence corroborated with tomato growth promotion with high vigor index (8,041.2) and fresh plant weight (82.5 g) on challenge inoculation with FOL. Analysis of root and leaf samples in rhizobacterial treatment challenged with FOL and AS revealed maximum induction of chitinase (1.9 and 1.7 U/mg of protein, respectively) and β-1,3-glucanase (23.5 and 19.2 U/mg of protein, respectively). In native gel activity assays, the rhizobacterial treatment on challenge inoculation strongly expressed three high intensity PO isoforms along with one low intensity isoform. In studies on genetic diversity of the Bacillus strains by repetitive extragenomic palindromic-polymerase chain reaction (REP-PCR) and amplified rDNA restriction analysis (ARDRA) patterns, ARDRA was more highly discriminant than REP-PCR and allowed grouping of the strains and differentiation of the antagonistic strains from other isolates.
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