Abstract

As a result of the continuous evolution of microbial pathogens towards antibiotic-resistance, there have been demands for the development of new and effective antimicrobial compounds. Since the 1960s, the scientific literature has accumulated many publications about novel pharmaceutical compounds produced by a diverse range of marine bacteria. Indeed, marine micro-organisms continue to be a productive and successful focus for natural products research, with many newly isolated compounds possessing potentially valuable pharmacological activities. In this regard, the marine environment will undoubtedly prove to be an increasingly important source of novel antimicrobial metabolites, and selective or targeted approaches are already enabling the recovery of a significant number of antibiotic-producing micro-organisms. The aim of this review is to consider advances made in the discovery of new secondary metabolites derived from marine bacteria, and in particular those effective against the so called “superbugs”, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin resistant enterococci (VRE), which are largely responsible for the increase in numbers of hospital acquired, i.e., nosocomial, infections.

Highlights

  • The search for new antibiotics is an important element in the fight against the threat posed by the increase in the number of infections caused by antibiotic-resistant pathogens

  • This review has focused on compounds derived from marine bacteria that exhibit anti-methicillin-resistant Staphylococcus aureus (MRSA) and anti-vancomycin resistant enterococci (VRE) activity

  • Only approximately 3000 compounds have been characterised from marine bacteria, there are already a number of promising compounds demonstrating high levels of activity against MRSA

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Summary

Marine Drugs

Hafizur Rahman 1, Brian Austin 1,2,*, Wilfrid J. Adams 3, Andrew Mearns Spragg 4 and Michael Schweizer 1. Aquapharm Biodiscovery Limited, European Centre for Marine Biotechnology, Dunstaffnage. Received: 3 February 2010; in revised form: 1 March 2010 / Accepted: 2 March 2010 /

Introduction
OH OH pseudomonic acid C thiomarinol G
Conclusions
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