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Published on: April 16, 2018
Staphylococcus pseudintermedius biofilms secrete factors that induce inflammatory reactions in vitro
S Arima1, H Ochi2, M Mitsuhashi1
1Laboratory of Veterinary Microbiology, Nippon Veterinary and Life Science University, Musashino, Tokyo, Japan.
Abstract:
Biofilms, composed of bacterial cells embedded in a secreted polysaccharide and protein matrix, often cause problems such as chronic and refractory infections. Staphylococcus pseudintermedius, which is an important pathogen in veterinary medicine, has a high rate of biofilm production. Although it is considered that S. pseudintermedius biofilms are associated with prolonged inflammatory disorders, there are no reports that S. pseudintermedius biofilm directly regulates inflammatory reactions. In this study, we focused on the metabolites derived from biofilm cultures of S. pseudintermedius and evaluated their inflammatory effects in vitro. Expression levels of interleukin-1 beta and interleukin-6 mRNA significantly increased in RAW264.7 cells that were cultured with biofilm-conditioned medium (BCM). The secreted proteins in BCM were heat resistance and activated a Toll-like receptor (TLR) signalling pathway. Moreover, based on SDS-PAGE analysis, isolates with stronger biofilm-forming capabilities induced more inflammatory reactions and had specific banding patterns compared with those of weak biofilm producers. Collectively, our results suggest that the proteins derived from S. pseudintermedius biofilm induce a host inflammatory response via a TLR pathway. Furthermore, the severity of inflammation depends on the biofilm formation capacity of the S. pseudintermedius strain.
Significance And Impact Of The Study:
Staphylococcus pseudintermedius is a biofilm-forming bacterium. We identified some biofilm secreted heat-resistant proteins that induce inflammatory reactions through Toll-like receptor signalling. The expression of the secreted protein varied depending on the potency of biofilm production. Our data suggest that these proteins may be the factors causing biofilm-related inflammation during S. pseudintermedius infections. Identification of these proteins may lead to the development of novel medications to prevent the exacerbation of infections caused by S. pseudintermedius.
Insights
Proteins secreted by Staphylococcus pseudintermedius biofilms trigger inflammatory responses via Toll-like receptor signaling. The intensity of this inflammation correlates with the bacterium's biofilm-forming ability, suggesting therapeutic targets.
Area of Science:
- Veterinary microbiology
- Immunology
- Bacterial pathogenesis
Background:
- Bacterial biofilms, particularly from Staphylococcus pseudintermedius, are linked to chronic infections and inflammation.
- The direct role of S. pseudintermedius biofilms in regulating host inflammatory reactions remains unclear.
Purpose of the Study:
- To investigate the inflammatory effects of metabolites from S. pseudintermedius biofilms in vitro.
- To elucidate the mechanisms by which S. pseudintermedius biofilms modulate host immune responses.
Main Methods:
- Culturing S. pseudintermedius biofilms and collecting biofilm-conditioned medium (BCM).
- Assessing inflammatory marker expression (IL-1β, IL-6 mRNA) in RAW264.7 cells exposed to BCM.
- Analyzing heat resistance and Toll-like receptor (TLR) pathway activation of BCM components.
- Correlating biofilm formation capacity with inflammatory response intensity using SDS-PAGE.
Main Results:
- BCM significantly increased interleukin-1 beta and interleukin-6 mRNA expression in immune cells.
- Secreted proteins in BCM were heat-resistant and activated the TLR signaling pathway.
- Stronger biofilm producers induced greater inflammatory reactions and exhibited distinct protein profiles.
Conclusions:
- Proteins secreted by S. pseudintermedius biofilms induce host inflammatory responses through TLR signaling.
- The potency of biofilm production influences the severity of inflammation.
- Identified proteins may be key factors in biofilm-related inflammation, offering potential targets for novel therapeutics.
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