Purpose: The purpose of this study was to determine if B. subtilis FB17 has the ability to inhibit the growth of foodborne pathogens.
Methods: To obtain cell free lysate (CFL), overnight cultures of FB17 and negative control Pseudomonas chlorophalis EA105 were centrifuged at 2500 rpm for 10 min and filtered using a 0.2 micron filter. To obtain CFL of heat-killed cultures, following centrifugation cell pellets were washed 3 times with sterile water, resuspended in LB broth and incubated at 65°C overnight. Microtiter assays were performed in 96-well plates to determine the level of inhibition of FB17 on bacterial strains. Microtiters were performed in either FB17 CFL, EA105 CFL, or LB broth. Strains in this study included 3 outbreak strains of L. monocytogenes, E. coli O157:H7, E. coli O104:H4 and Salmonella Agona (n = 6).
Results: Growth of all 3 L. monocytogenes isolates was significantly inhibited upon incubation with FB17 CFL compared to controls (P < 0.05). E. coli O104:H4 growth was significantly inhibited by FB17 (P < 0.0001); however E. coli O157:H7 was not (P = 0.13). Growth of S. Agona was not significantly inhibited when incubated with FB17 (P = 0.63). CFL obtained from heat killed cultures did not significantly inhibit growth of L. monocytogenes isolates indicating live cell cultures are essential for growth inhibition to occur.
Significance: B. subtilis FB17 may be used as a biocontrol agent in field crops to inhibit the growth of plant pathogens as well as a variety of L. monocytogenes and E. coli isolates and increase crop yield.