Abstract
Phenol-soluble modulins (PSMs) are major determinants of Staphylococcus aureus virulence and their increased production in community-associated methicillin-resistant S. aureus (CA-MRSA) likely contributes to the enhanced virulence of MRSA strains. Here, we analyzed the differences in bacterial cell aggregation according to PSM presence in the specific human cerebrospinal fluid (CSF) environment. CSF samples from the intraventricular or lumbar intrathecal area of each patient and tryptic soy broth media were mixed at a 1:1 ratio, inoculated with WT and PSM-deleted mutants (Δpsm) of the CA-MRSA strain, USA300 LAC, and incubated overnight. Cell aggregation images were acquired after culture and image analysis was performed. The cell aggregation ratio in WT samples differed significantly between the two sampling sites (intraventricular: 0.2% vs. lumbar intrathecal: 6.7%, p < 0.001). The cell aggregation ratio in Δpsm samples also differed significantly between the two sampling sites (intraventricular: 0.0% vs. lumbar intrathecal: 1.2%, p < 0.001). Division of the study cases into two groups according to the aggregated area ratio (WT/Δpsm; group A: ratio of ≥ 2, group B: ratio of < 2) showed that the median aggregation ratio value differed significantly between groups A and B (5.5 and 0, respectively, p < 0.001). The differences in CSF distribution and PSM presence within the specific CSF environment are significant factors affecting bacterial cell aggregation.
Highlights
Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most infamous antibiotic-resistant pathogens [1]
This study aimed to report differences in bacterial cell aggregation according to cerebrospinal fluid (CSF) distribution and Phenol-soluble modulins (PSMs) presence in community-associated methicillin-resistant S. aureus (CA-MRSA) observed in the specific central nervous system (CNS) environment using wild type (WT) and PSM-deleted mutants (∆psm) of CA-MRSA
The results of the present study demonstrate that PSMs in the CNS environment may participate in cell aggregation and biofilm formation in CA-MRSA infection
Summary
Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most infamous antibiotic-resistant pathogens [1]. Rapidly emerging strains of CA-MRSA demonstrating unusually high virulence and ease of transmission are a significant cause of community-associated infections [4,5]. This is largely due to the fact that CA-MRSA strains carry genes that strongly impact virulence, such as short SCCmec types (IV or V), that play a crucial role in CA-MRSA evolution as well as accessory gene regulators that control the expression of most S. aureus toxins [2,6]. Given the alarming rise of CA-MRSA prevalence, it is highly likely that CA-MRSA infection with CNS involvement will be a major cause of CNS infection in the near future
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