Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Sep;8(9):1095-116.
doi: 10.1517/17460441.2013.807246. Epub 2013 Jul 6.

Advances in MRSA drug discovery: where are we and where do we need to be?

Affiliations
Review

Advances in MRSA drug discovery: where are we and where do we need to be?

Michio Kurosu et al. Expert Opin Drug Discov. 2013 Sep.

Abstract

Introduction: Methicillin-resistant Staphylococcus aureus (MRSA) have been on the increase during the past decade, due to the steady growth of the elderly and immunocompromised patients, and the emergence of multidrug-resistant (MDR) bacterial strains. Although there are a limited number of anti-MRSA drugs available, a number of different combination antimicrobial drug regimens have been used to treat serious MRSA infections. Thus, the addition of several new antistaphylococcal drugs into clinical practice should broaden clinician's therapeutic options. As MRSA is one of the most common and problematic bacteria associated with increasing antimicrobial resistance, continuous efforts for the discovery of lead compounds as well as development of alternative therapies and faster diagnostics are required.

Areas covered: This article summarizes the FDA-approved drugs to treat MRSA infections, the drugs in clinical trials, and the drug leads for MRSA and related Gram-positive bacterial infections. In addition, the article discusses the mode of action of antistaphylococcal molecules and the resistant mechanisms of some molecules.

Expert opinion: The number of pipeline drugs presently undergoing clinical trials is not particularly encouraging. There are limited and rather expensive therapeutic options for MRSA infections in the critically ill. Further research efforts are required for effective phage therapy on MRSA infections in clinical use, which seem to be attractive therapeutic options for the future.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Antibacterial agents used to treat MRSA infections.
Figure 2
Figure 2
Clinical trial drugs for MRSA and other related bacterial infections.
Figure 3
Figure 3
Drug leads for MRSA and other related bacterial infections
Figure 3
Figure 3
Drug leads for MRSA and other related bacterial infections

References

    1. Grenet K, Guillemot D, Jarlier V, et al. Antibacterial resistance, Wayampis Amerindians, French Guyana. Emerg Infect Dis. 2004;10:1150–4. - PMC - PubMed
    1. Cosgrove SE, Fowler VG. Management of methicillin-resistant Staphylococcus aureus bacteremia. Clin Infect Dis. 2008;46:S386–93. Overview of the management of MRSA. - PubMed
    1. Cunha BA. Vancomycin revisited: a reappraisal of clinical use. Critical Care Clinics. 2008;24:393–420. - PubMed
    1. Loffler CA, Macdougall C. Update on prevalence and treatment of methicillin-resistant Staphylococcus aureus infections. Expert Rev Anti-Infect Ther. 2007;5:961–81. Review of MRSA infections. - PubMed
    1. Tacconelli E, Cataldo MA. Antimicrobial therapy of Staphylococcus aureus bloodstream infection. Exp Opin Pharmacother. 2007;8:2505–18. - PubMed

Publication types

MeSH terms

Substances