Résumé·s
Biofilm formation by the pathogen Listeria monocytogenes is a major concern in
food industries. The aim of this work was to elucidate the effect of nutrient
limitation on both biofilm architecture and on the viability of the bacteria in
microfluidic growth conditions. Biofilm formation by two L. monocytogenes strains
was performed in a rich medium (BHI) and in a 10-fold diluted BHI (BHI/10) at 30
degrees C for 24 h by using both static conditions and the microfluidic system
Bioflux. In dynamic conditions, biofilms grown in rich and poor medium showed
significant differences as well in structure and in the resulting biovolume. In
BHI/10, biofilm was organized in a knitted network where cells formed long
chains, whereas in the rich medium, the observed structure was homogeneous
cellular multilayers. Biofilm biovolume production in BHI/10 was significantly
higher than in BHI in these dynamic conditions. Interestingly, biovolume of dead
cells in biofilms formed under limited nutrient conditions (BHI/10) was
significantly higher than in biofilms formed in the BHI medium. In the other
hand, in static conditions, biofilm is organized in a multilayer cells and
dispersed cells in a rich medium BHI and poor medium BHI/10 respectively. There
was significantly more biomass in the rich medium compared to BHI/10 but no
difference was noted in the dead/damaged subpopulation showing how L.
monocytogenes biofilm could be affected by the growth conditions. This work
demonstrated that nutrient concentration affects biofilm structure and the
proportion of dead cells in biofilms under microfluidic condition. Our study also
showed that limited nutrients play an important role in the structural stability
of L. monocytogenes biofilm by enhancing cell death and liberating extracellular
DNA.