| Literature DB >> 26160745 |
Hirono Yoshikai1, Hayato Kizaki1, Yuki Saito1, Yosuke Omae1, Kazuhisa Sekimizu1, Chikara Kaito1.
Abstract
Phenol-soluble modulins (PSMs) are Staphylococcus aureus cytolytic toxins that lyse erythrocytes and neutrophils and have important functions in the S. aureus infectious process. The molecular mechanisms of PSM secretion, however, are not well understood. Here we report that knockout of the multidrug-resistance ABC transporter AbcA, which contributes to S. aureus resistance against antibiotics and chemicals, diminished the secreted amount of PSM, leading to the accumulation of PSM in the intracellular fraction. The amount of PSM in the culture supernatants of the abcA knockout mutants was restored by introduction of the wild-type abcA gene, whereas it was not completely restored by introduction of mutant abcA genes encoding AbcA mutant proteins carrying amino acid substitutions in the adenosine triphosphate binding motifs. The abcA knockout mutant exhibited attenuated virulence in a mouse systemic infection model. These findings suggest that the multidrug resistance transporter AbcA secretes PSMs and contributes to S. aureus virulence.Entities:
Keywords: Staphylococcus aureus; cytolytic toxins; multidrug resistance transporter; phenol-soluble modulins
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Year: 2015 PMID: 26160745 DOI: 10.1093/infdis/jiv376
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226