Auxiliary factors: a chink in the armor of MRSA resistance to β-lactam antibiotics.

Terry Roemer, Tanja Schneider, Mariana G Pinho
Author Information
  1. Terry Roemer: Infectious Disease Research, Merck Research Laboratories, Kenilworth, NJ 07033, USA. Electronic address: terry_roemer@merck.com.

Abstract

Combination agents provide an important orthogonal approach to treat infectious diseases, particularly those caused by drug resistant pathogens. Indeed, applying a biologically 'rational' and systems-level paradigm to discover potent, selective, and synergistic agents would augment current (and arguably overly relied upon) empirical and serendipitous approaches to such discovery efforts. Here, we review the cellular mechanisms of β-lactam drug resistance and tolerance achieved amongst methicillin-resistant Staphylococcus aureus (MRSA) as well as their molecular targets and strategies to identify cognate inhibitors as potential combination agents to restore β-lactam efficacy against MRSA.

MeSH Term

Anti-Bacterial Agents
Bacterial Proteins
Drug Discovery
Methicillin-Resistant Staphylococcus aureus
Penicillin-Binding Proteins
beta-Lactam Resistance
beta-Lactams

Chemicals

Anti-Bacterial Agents
Bacterial Proteins
Penicillin-Binding Proteins
beta-Lactams

Word Cloud

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