scholarly journals Antifungal activity of Pseudomonas chlororaphis Q16 against Sclerotinia sclerotiorum isolated from different medicinal plants

Zastita bilja ◽  
2014 ◽  
Vol 65 (2) ◽  
pp. 56-63
Author(s):  
Zorica Lepšanović ◽  
Mira Starović ◽  
Snežana Pavlović ◽  
Dragana Jošić
Microbiology ◽  
2012 ◽  
Vol 158 (1) ◽  
pp. 207-216 ◽  
Author(s):  
Jerrylynn Manuel ◽  
Carrie Selin ◽  
W. G. Dilantha Fernando ◽  
Teresa de Kievit

2006 ◽  
Vol 52 (12) ◽  
pp. 1177-1188 ◽  
Author(s):  
N Poritsanos ◽  
C Selin ◽  
W G.D Fernando ◽  
S Nakkeeran ◽  
T.R. de Kievit

Pseudomonas chlororaphis PA23 is a biocontrol agent that protects against the fungal pathogen Sclerotinia sclerotiorum. Employing transposon mutagenesis, we isolated a gacS mutant that no longer exhibited antifungal activity. Pseudomonas chlororaphis PA23 was previously reported to produce the nonvolatile antibiotics phenazine 1-carboxylic acid and 2-hydroxyphenazine. We report here that PA23 produces additional compounds, including protease, lipase, hydrogen cyanide, and siderophores, that may contribute to its biocontrol ability. In the gacS mutant background, generation of these products was markedly reduced or delayed with the exception of siderophores, which were elevated. Not surprisingly, this mutant was unable to protect canola from disease incited by S. sclerotiorum. The gacS mutant was able to sustain itself in the canola phyllosphere, therefore, the loss of biocontrol activity can be attributed to a reduced production of antifungal compounds and not a declining population size. Competition assays between the mutant and wild type revealed equivalent fitness in aged batch culture; consequently, the gacS mutation did not impart a growth advantage in the stationary phase phenotype. Under minimal nutrient conditions, the gacS-deficient strain produced a tenfold less biofilm than the wild type. However, no difference was observed in the ability of the mutant biofilm to protect cells from lethal antibiotic challenge.Key words: Pseudomonas, biocontrol, gacS, fitness, biofilms.


2007 ◽  
Vol 3 (6) ◽  
pp. 499-504 ◽  
Author(s):  
Ravindra B. Malabadi . ◽  
S. Vijay Kumar .

2005 ◽  
Vol 4 (2) ◽  
pp. 130-132 ◽  
Author(s):  
Amjad B. Khalil ◽  
Basem F. Dabaneh ◽  
Ghandi H. Anfoka

2020 ◽  
Vol 110 (2) ◽  
pp. 317-326 ◽  
Author(s):  
Ayaz Farzand ◽  
Anam Moosa ◽  
Muhammad Zubair ◽  
Abdur Rashid Khan ◽  
Muhammad Ayaz ◽  
...  

Sclerotinia sclerotiorum is a devastating necrotrophic pathogen that infects multiple crops, and its control is an unremitting challenge. In this work, we attempted to gain insights into the pivotal role of lipopeptides (LPs) in the antifungal activity of Bacillus amyloliquefaciens EZ1509. In a comparative study involving five Bacillus strains, B. amyloliquefaciens EZ1509 harboring four LPs biosynthetic genes (viz. surfactin, iturin, fengycin, and bacilysin) exhibited promising antifungal activity against S. sclerotiorum in a dual-culture assay. Our data demonstrated a remarkable upsurge in LPs biosynthetic gene expression through quantitative reverse transcription PCR during in vitro interaction assay with S. sclerotiorum. Maximum upregulation in LPs biosynthetic genes was observed on the second and third days of in vitro interaction, with iturin and fengycin being the highly expressed genes. Subsequently, Matrix-assisted laser desorption/ionization-time of flight-mass spectrometry analysis confirmed the presence of LPs in the inhibition zone. Scanning electron microscope analysis showed disintegration, shrinkage, plasmolysis, and breakdown of fungal hyphae. During in planta evaluation, S. sclerotiorum previously challenged with EZ1509 showed significant suppression in pathogenicity on detached leaves of tobacco and rapeseed. The oxalic acid synthesis was also significantly reduced in S. sclerotiorum previously confronted with antagonistic bacterium. The expression of major virulence genes of S. sclerotiorum, including endopolygalacturonase-3, oxalic acid hydrolase, and endopolygalacturonase-6, was significantly downregulated during in vitro confrontation with EZ1509.


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