Relative contribution of Panton-Valentine leukocidin to PMN plasma membrane permeability and lysis caused by USA300 and USA400 culture supernatants

被引:33
作者
Graves, Shawna F. [1 ,2 ]
Kobayashi, Scott D. [1 ]
Braughton, Kevin R. [1 ]
Diep, Binh An [3 ]
Chambers, Henry F. [3 ]
Otto, Michael [4 ]
DeLeo, Frank R. [1 ]
机构
[1] NIAID, Lab Human Bacterial Pathogenesis, Rocky Mt Labs, NIH, Hamilton, MT 59840 USA
[2] Univ Montana, Div Biol Sci, Dept Biochem & Biophys, Missoula, MT 59812 USA
[3] Univ Calif San Francisco, Dept Med, Div Infect Dis, San Francisco, CA USA
[4] NIAID, Lab Human Bacterial Pathogenesis, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Staphylococcus aureus; Virulence; Leukocidins; RESISTANT STAPHYLOCOCCUS-AUREUS; HUMAN POLYMORPHONUCLEAR LEUKOCYTES; HUMAN NEUTROPHILS; VIRULENCE; LEUCOCIDIN; PNEUMONIA; TOXIN; IDENTIFICATION; PURIFICATION; INFECTIONS;
D O I
10.1016/j.micinf.2010.02.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Panton-Valentine leukocidin (PVL) is a cytolytic toxin associated with severe community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) infections. However, the relative contribution of PVL to host cell lysis during CA-MRSA infection remains unknown. Here we investigated the relative contribution of PVL to human polymorphonuclear leukocyte (PMN) plasma membrane permeability and lysis in vitro by using culture supernatants from wild-type and isogenic lukS/F-PV negative (Delta pvl) USA300 and USA400 strains. Using S. aureus culture conditions that favor selective high production of PVL (CCY medium), there was on average more PMN plasma membrane permeability and cell lysis caused by supernatants derived from wild-type strains compared with those from Delta pvl strains. Unexpectedly, plasma membrane permeability did not necessarily correlate with ultimate cell lysis. Moreover, the level of pore formation caused by culture supernatants varied dramatically (e.g., range was 0.32-99.09% for wild-type USA300 supernatants at 30 min) and was not attributable to differences in PMN susceptibility to PVL among human blood donors. We conclude that PMN pore formation assays utilizing S. aureus culture supernatants have limited ability to estimate the relative contribution of PVL to pathogenesis (or cytolysis in vitro or in vivo), especially when assayed using culture media that promote selective high production of PVL. Published by Elsevier Masson SAS.
引用
收藏
页码:446 / 456
页数:11
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