The in vitro host cell immune response to bovine-adapted Staphylococcus aureus varies according to bacterial lineage

Mastitis is the most economically important disease affecting dairy cattle worldwide. Staphylococcus aureus is a highly prevalent cause of mastitis, causing infections ranging from sub-clinical to gangrenous. However, the interaction between the genotype of the infecting strain of S . aureus and the...

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Veröffentlicht in:Scientific reports 2019-04, Vol.9 (1), p.6134-6134, Article 6134
Hauptverfasser: Murphy, Mark P., Niedziela, Dagmara A., Leonard, Finola C., Keane, Orla M.
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Sprache:eng
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Zusammenfassung:Mastitis is the most economically important disease affecting dairy cattle worldwide. Staphylococcus aureus is a highly prevalent cause of mastitis, causing infections ranging from sub-clinical to gangrenous. However, the interaction between the genotype of the infecting strain of S . aureus and the host response remains largely uncharacterised. To better understand the variation in presentation and outcomes of S . aureus -mediated bovine mastitis, we studied the interaction of a panel of mastitis isolates from several prominent bovine-associated lineages with bovine mammary epithelial cells (bMEC) and neutrophils. Significant differences in immune gene expression by infected primary or immortalised bMEC, or their elaboration of neutrophil chemoattractants, were observed and were dependent on the lineage of the infecting strain. Differences were also apparent in the invasiveness of S . aureus strains and their ability to survive killing by neutrophils. Our results demonstrate that a range of immune responses occur, suggesting the importance of S . aureus strain in dictating mastitis disease course. S . aureus lineages may therefore have adopted differing strategies for exploitation of the intramammary niche. Consequently, improved diagnosis of infecting lineage may enable better prognosis for S . aureus mastitis and reduce morbidity and economic loss.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-019-42424-2