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Targeting the host-pathogen interface for treatment of Staphylococcus aureus infection

Journal

SEMINARS IN IMMUNOPATHOLOGY
Volume 34, Issue 2, Pages 299-315

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00281-011-0297-1

Keywords

S. aureus; MRSA; Virulence; Antibiotic resistance; Probiotics; Inflammation

Funding

  1. Burroughs-Wellcome Career Award
  2. National Institutes of Health [AI074832]

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Recent emergence of methicillin-resistant Staphylococcus aureus both within and outside healthcare settings has accelerated the use of once reserved last line antibiotics such as vancomycin. With increased use of antibiotics, there has been a rapid rise in the rate of resistance development to the anti-MRSA drugs. As the antibiotic pipeline becomes strained, alternative strategies are being sought for future treatment of S. aureus. Here, we review several novel antistaphylococcal strategies that, unlike conventional antibiotics, do not target essential gene products elaborated by the pathogen. The approaches seek instead to weaken the S. aureus defense by neutralizing its virulence factors or boosting host immunity. Other strategies target commensal bacteria that naturally colonize the human host to inhibit S. aureus colonization. Ultimately, the aim is to shift the balance between host defense and pathogen virulence in favor of inhibition of S. aureus pathogenic activities.

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