4.7 Article

Bovine-associated non-aureus staphylococci suppress Staphylococcus aureus biofilm dispersal in vitro yet not through agr regulation

Journal

VETERINARY RESEARCH
Volume 52, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13567-021-00985-z

Keywords

Non-aureus staphylococci; Staphylococcus aureus; biofilm; agr; quorum sensing; bovine mastitis

Funding

  1. Brazilian research funding agency CAPES
  2. Research Foundation Flanders (FWO-Vlaanderen) [G0H2516N (AUGE/15/05)]

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The formation of biofilms in Staphylococcus aureus strains causing subclinical mastitis in dairy cows is influenced by environmental signals and communication systems, with different staphylococci species impacting S. aureus biofilm formation and dispersion. Specifically, S. chromogenes enhances biofilm formation of an agr-positive S. aureus strain, while NAS isolates suppress biofilm dispersion of S. aureus. Additionally, the effects on biofilm formation and dispersion do not depend on the capacity of NAS to repress the agr system.
Biofilm formation is a significant virulence factor in Staphylococcus (S.) aureus strains causing subclinical mastitis in dairy cows. A role of environmental signals and communication systems in biofilm development, such as the agr system in S. aureus, is suggested. In the context of multispecies biofilm communities, the presence of non-aureus staphylococci (NAS) might influence S. aureus colonization of the bovine mammary gland, yet, such interspecies interactions have been poorly studied. We determined whether 34 S. chromogenes, 11 S. epidermidis, and 14 S. simulans isolates originating from bovine milk samples and teat apices (TA) were able to affect biofilm formation and dispersion of S. aureus, and if so, how isolate traits such as the capacity to regulate the S. aureus agr quorum sensing system are determinants in this process. The capacity of an agr-positive S. aureus strain to form biofilm was increased more in the presence of S. chromogenes than in the presence of S. simulans and S. epidermidis isolates and in the presence of NAS isolates that do not harbor biofilm related genes. On the other hand, biofilm dispersion of this particular S. aureus strain was suppressed by NAS as a group, an effect that was more pronounced by isolates from TA. Furthermore, the observed effects on biofilm formation and dispersion of the agr-positive S. aureus strain as well as of an agr-negative S. aureus strain did not depend on the capacity of NAS to repress the agr system.

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