Abstract
Infection Human skin hosts an ecosystem of microorganisms. Infections can therefore involve more than one organism, but antibiotic therapy options rarely consider the possibility of interference by a nontarget species. Staphylococcus aureus is a member of the normal skin microbiota that can show a spectrum of virulence and cause persistent and intractable infections. Radlinski et al. show that co-infections of S. aureus and Pseudomonas aeruginosa can synergize in multiple ways to antagonize or potentiate antibiotic susceptibility in S. aureus. P. aeruginosa secretes a series of secondary products in a strain-specific manner. Some, such as rhamnolipids or LasA endopeptidase, increase S. aureus susceptibility to antibiotics. Others, such as HQNO, induce multidrug tolerance and potentiate antibiotic resistance in S. aureus . Some of these interactions could theoretically be exploited to assist treatment, but the reciprocal effects of S. aureus on P. aeruginosa , coupled with strain variation, mean each case is different. PLOS Biol. 10.1371/journal.pbio.2003981 (2017).
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