Abstract
Staphylococcus aureus is a bacterium causing a broad variety of infections, ranging from minor skin infections to severe pneumonia and sepsis. The genetic adaptation occurred after the introduction of meticillin into clinical practice in the 1960s [1] has led to a multidrug-resistant pathogen, meticillin-resistant S. aureus (MRSA). MRSA is characterized by the mecA gene that encodes the penicillin binding protein 2a (PBP2a) that permits growth in the presence of meticillin and tends to have multidrug resistance. MRSA is resistant to b-lactam antibiotics, including penicillin and cephalosporins but not ceftaroline that is able to bind PBP2a.
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Scaglione, F. (2014). Rationale of Antibiotics Anti-MRSA in Pneumonia. In: Gullo, A. (eds) Anaesthesia, Pharmacology, Intensive Care and Emergency A.P.I.C.E.. Springer, Milano. https://doi.org/10.1007/978-88-470-5516-2_12
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DOI: https://doi.org/10.1007/978-88-470-5516-2_12
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