Abstract

In the past decade, community-associated (CA-) infections with methicillin-resistant Staphylococcus aureus (MRSA) have emerged throughout the world. Different CA-MRSA strains dominate in different geographical locations. Many CA-MRSA lineages contain genes coding for the Pantón-Valentine leukocidin. However, the role of this leukotoxin in CA-MRSA pathogenesis is still controversial. The genome sequences of two key PVL-positive CA-MRSA strains (USA300, USA400) have been reported, but we lack information on the more recently found PVL-negative CA-MRSA strains. One such strain is the PVL-negative ST72, the main cause of CA-MRSA infections in Korea. Here, we report the entire genome sequence of CA-MRSA ST72 and analyze its gene content with a focus on virulence factors. Our results show that this strain does not have considerable differences in virulence factor content compared to other CA-MRSA strains (USA300, USA400), indicating that other toxins do not substitute for the lack of PVL in ST72. This finding is in accordance with the notion that differential expression of widespread virulence determinants, rather than the acquisition of additional virulence factors on mobile genetic elements, such as PVL, is responsible for the increased virulence of CA- compared to hospital-associated MRSA.

Highlights

  • Staphylococcus aureus is a dangerous human pathogen and S. aureus infections are among the most frequent causes of deaths in hospitals around the globe [1]

  • In the 1990s, methicillin-resistant S. aureus (MRSA) infections – previously limited to predisposed patients in hospitals – started occurring in otherwise healthy people in the community without connections to the hospital setting [4]. These community-associated (CA-) MRSA infections are on a worldwide surge, with the United States so far seeing the most pronounced CA-MRSA epidemic

  • The rise of CA-MRSA is due to the development of strains that combine methicillin resistance with a high level of aggressive virulence not commonly present in hospitalassociated (HA-) MRSA [5]

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Summary

Introduction

Staphylococcus aureus is a dangerous human pathogen and S. aureus infections are among the most frequent causes of deaths in hospitals around the globe [1]. In the 1990s, MRSA infections – previously limited to predisposed patients in hospitals – started occurring in otherwise healthy people in the community without connections to the hospital setting [4]. These community-associated (CA-) MRSA infections are on a worldwide surge, with the United States so far seeing the most pronounced CA-MRSA epidemic. The rise of CA-MRSA is due to the development of strains that combine methicillin resistance with a high level of aggressive virulence not commonly present in hospitalassociated (HA-) MRSA [5].

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