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Dry bubble disease, caused by Lecanicillium fungicola, is a serious economic problem in the cultivation of the white button mushroom. Biological control of the disease would meet the mushroom industry’s efforts to minimize the use of chemicals. A total of 160 bacterial strains were isolated from colonized casing and screened for in vitro antagonism of L. fungicola. Fifty-three isolates inhibited L. fungicola in vitro. Using BOX-PCR, the 53 antagonistic isolates were grouped in 18 unique genotypes. Further characterization based on the 16S rDNA identified all isolates as Pseudomonas spp. Using previously characterized Pseudomonas isolates and their mutants it was determined that L. fungicola is sensitive to both siderophore-mediated competition for iron and production of antibiotics. However, when tested for disease suppression, none of the Pseudomonas spp. strains isolated from colonized casing effectively controlled dry bubble disease. The insensitivity of dry bubble disease to direct biological antagonism and the implications for biological control of mushroom diseases are discussed.

BACKGROUND: Mycelia of higher fungi consist of interconnected hyphae that are compartmentalized by septa. These septa contain large pores that allow streaming of cytoplasm and even organelles. The cytoplasm of such mycelia is therefore considered to be continuous. METHODOLOGY/PRINCIPAL FINDINGS: Here, we show by laser dissection that septa of Schizophyllum commune can be closed depending on the environmental conditions. The most apical septum of growing hyphae was open when this basidiomycete was grown in minimal medium with glucose as a carbon source. In contrast, the second and the third septum were closed in more than 50% and 90% of the cases, respectively. Interestingly, only 24 and 37% of these septa were closed when hyphae were growing in the absence of glucose. Whether a septum was open or closed also depended on physical conditions of the environment or the presence of toxic agents. The first septum closed when hyphae were exposed to high temperature, to hypertonic conditions, or to the antibiotic nourseothricin. In the case of high temperature, septa opened again when the mycelium was placed back to the normal growth temperature. CONCLUSIONS/SIGNIFICANCE: Taken together, it is concluded that the septal pores of S. commune are dynamic structures that open or close depending on the environmental conditions. Our findings imply that the cytoplasm in the mycelium of a higher fungus is not continuous per se.

Dry bubble disease, caused by Lecanicillium fungicola, is a serious economic problem in the cultivation of the white button mushroom. Biological control of the disease would meet the mushroom industry’s efforts to minimize the use of chemicals. A total of 160 bacterial strains were isolated from colonized casing and screened for in vitro antagonism of L. fungicola. Fifty-three isolates inhibited L. fungicola in vitro. Using BOX-PCR, the 53 antagonistic isolates were grouped in 18 unique genotypes. Further characterization based on the 16S rDNA identified all isolates as Pseudomonas spp. Using previously characterized Pseudomonas isolates and their mutants it was determined that L. fungicola is sensitive to both siderophore-mediated competition for iron and production of antibiotics. However, when tested for disease suppression, none of the Pseudomonas spp. strains isolated from colonized casing effectively controlled dry bubble disease. The insensitivity of dry bubble disease to direct biological antagonism and the implications for biological control of mushroom diseases are discussed.