Lineage associated expression of virulence traits in bovine-adapted Staphylococcus aureus

- Bovine-adapted S. aureus isolates belonging to lineages CC71, CC97, CC151 and ST136, were tested for a number of virulence associated traits.
- Isolates differed significantly in their ability to adhere to and internalise within bovine mammary epithelial cells (bMEC) although there were no differences between lineages.
- Despite lacking the ability to bind bovine fibronectin in vitro, isolates from CC151 could adhere to and internalise within bMEC.
- There were significant differences between the lineages in ability to form a biofilm with ST136 forming the strongest biofilm and CC151 the weakest.
- There were significant differences between the lineages in ability to induce pro-inflammatory cytokines from bMEC with CC97 and CC71 eliciting the strongest immune response.

Bovine mastitis is the most costly disease to the dairy industry worldwide with Staphylococcus aureus commonly associated with intramammary infections that are persistent and refractory to treatment. The strains of S. aureus that cause mastitis predominantly belong to a number of well-described bovine-adapted lineages. The objective of this study was to determine if a variety of potential virulence traits were associated with lineage. Bovine-adapted S. aureus isolates (n = 120), belonging to lineages CC97, CC151 and ST136, were tested for their ability to adhere to and internalise within cultured bovine mammary epithelial cells (bMEC), to bind bovine fibronectin, to form a biofilm in TSB, TSB + 1% glucose and TSB + 4% NaCl, and to induce an immune response from bMEC. There were no significant differences between the lineages in ability to adhere to or internalise within bMEC although there were significant differences between individual isolates. For lineages CC97 and ST136, mammalian cell adherence was correlated with the ability to bind bovine fibronectin, however isolates from CC151 could not bind bovine fibronectin in vitro, but adhered to bMEC in a fibronectin-independent manner. There were significant differences between the lineages in ability to form a biofilm in all three growth media with ST136 forming the strongest biofilm while CC151 formed the weakest biofilm. Lineages also differed in their ability to elicit an immune response from bMEC with CC97 eliciting a stronger immune response than CC151 and ST136. These data indicate the potential for both lineage and strain-specific virulence and a strain-specific response to infection in vivo and caution against extrapolating an effect from a single strain of S. aureus to draw conclusions regarding virulence or the host response to infection in unrelated lineages.