Journal
NPJ BIOFILMS AND MICROBIOMES
Volume 7, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41522-021-00189-5
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Funding
- Korean Food Research Institute (KFRI) [E0142102-03]
- U.S. Department of Agriculture, Agricultural Research Service [59-8072-6-001]
- USDA National Institute of Food and Agriculture [1016249]
- USAID [AID-263-A-15-00002]
- Center for Food Safety Engineering at Purdue University
- NAS
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Environmental signals play a role in promoting microbial biofilm formation and genetic heterogeneity. Biofilms produced by pathogens in food production facilities are a major source of contamination, but the mechanisms of biofilm-isolated sessile cells are not well understood. Studies show that the virulence of biofilm-isolated Lm is temporarily attenuated in mice during the early stage of infection (12-24 hours), but fully restored at a later stage (48 hours).
Environmental cues promote microbial biofilm formation and physiological and genetic heterogeneity. In food production facilities, biofilms produced by pathogens are a major source for food contamination; however, the pathogenesis of biofilm-isolated sessile cells is not well understood. We investigated the pathogenesis of sessile Listeria monocytogenes (Lm) using cell culture and mouse models. Lm sessile cells express reduced levels of the lap, inlA, hly, prfA, and sigB and show reduced adhesion, invasion, translocation, and cytotoxicity in the cell culture model than the planktonic cells. Oral challenge of C57BL/6 mice with food, clinical, or murinized-InlA (InlA(m)) strains reveals that at 12 and 24 h post-infection (hpi), Lm burdens are lower in tissues of mice infected with sessile cells than those infected with planktonic cells. However, these differences are negligible at 48 hpi. Besides, the expressions of inlA and lap mRNA in sessile Lm from intestinal content are about 6.0- and 280-fold higher than the sessle inoculum, respectively, suggesting sessile Lm can still upregulate virulence genes shortly after ingestion (12 h). Similarly, exposure to simulated gastric fluid (SGF, pH 3) and intestinal fluid (SIF, pH 7) for 13 h shows equal reduction in sessile and planktonic cell counts, but induces LAP and InlA expression and pathogenic phenotypes. Our data show that the virulence of biofilm-isolated Lm is temporarily attenuated and can be upregulated in mice during the early stage (12-24 hpi) but fully restored at a later stage (48 hpi) of infection. Our study further demonstrates that in vitro cell culture assay is unreliable; therefore, an animal model is essential for studying the pathogenesis of biofilm-isolated bacteria.
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