Proteomics

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SARS-CoV-2 Spike Protein and Murine Hepatitis Virus Inhib-its S. pneumoniae and S. aureus Biofilms


ABSTRACT: The recovery of other pathogens in COVID-19 patients has been reported. The presence of either co-infection or superinfection with bacterial pathogens was associated with poor outcomes, including increased mortality. The recognition of possibility of SARS-CoV-2 co-infection is important as it enables the implementation of appropriate infection control measures and therapy. This is a proof-of-concept study uses in vitro approaches (including crystal violet assay, microrheology, and LC-MS-based prote-omics) to investigate the interaction between SARS-CoV-2 and biofilms of bacteria (S. pneumoniae and S. aureus). SARS-CoV-2 spike protein S1 subunit was found to suppress biofilm formation of both bacteria. The effect of coronavirus and spike protein on bac-terial biofilm was supported by proteomics data that shows variations in proteins in-volved in quorum sensing and biofilm formation/maturation. Preliminary in vitro data suggest that dispersion of opportunistic pathogens from biofilm may be associated with poor prognosis in co-infections. However, further investigations are needed to establish bacterial biofilm as a risk factor for secondary pneumonia in COVID-19 patients.

INSTRUMENT(S): TripleTOF 5600

ORGANISM(S): Staphylococcus Aureus Streptococcus Pneumoniae

SUBMITTER: Mun Fai Loke  

LAB HEAD: Vincent Chow

PROVIDER: PXD029967 | Pride | 2022-04-04

REPOSITORIES: Pride

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Publications

SARS-CoV-2 Spike Protein and Mouse Coronavirus Inhibit Biofilm Formation by <i>Streptococcus pneumoniae</i> and <i>Staphylococcus aureus</i>.

Loke Mun Fai MF   Yadav Indresh I   Lim Teck Kwang TK   van der Maarel Johan R C JRC   Sham Lok-To LT   Chow Vincent T VT  

International journal of molecular sciences 20220318 6


The presence of co-infections or superinfections with bacterial pathogens in COVID-19 patients is associated with poor outcomes, including increased morbidity and mortality. We hypothesized that SARS-CoV-2 and its components interact with the biofilms generated by commensal bacteria, which may contribute to co-infections. This study employed crystal violet staining and particle-tracking microrheology to characterize the formation of biofilms by <i>Streptococcus pneumoniae</i> and <i>Staphylococc  ...[more]

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