Laboratory of Human Bacterial Pathogenesis, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, MT 59840, USA.
Microbes Infect. 2010 Jun;12(6):446-56. doi: 10.1016/j.micinf.2010.02.005. Epub 2010 Feb 19.
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 (Deltapvl) 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 Deltapvl 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.
Panton-Valentine 白细胞毒素 (PVL) 是一种细胞溶解毒素,与严重的社区获得性耐甲氧西林金黄色葡萄球菌 (CA-MRSA) 感染有关。然而,PVL 对 CA-MRSA 感染过程中宿主细胞溶解的相对贡献尚不清楚。在这里,我们通过使用野生型和同源性 lukS/F-PV 阴性 (Deltapvl) USA300 和 USA400 菌株的培养上清液,在体外研究了 PVL 对人多形核白细胞 (PMN) 质膜通透性和溶解的相对贡献。在有利于选择性高产生 PVL 的金黄色葡萄球菌培养条件下(CCY 培养基),与 Deltapvl 菌株相比,来自野生型菌株的上清液平均导致更多的 PMN 质膜通透性和细胞溶解。出乎意料的是,质膜通透性不一定与最终的细胞溶解相关。此外,培养上清液引起的孔形成水平差异很大(例如,在 30 分钟时,野生型 USA300 上清液的范围为 0.32-99.09%),并且不能归因于人类献血者对 PVL 的敏感性差异。我们得出结论,利用金黄色葡萄球菌培养上清液进行 PMN 孔形成测定,对于估计 PVL 对发病机制(或体外或体内细胞溶解)的相对贡献的能力有限,尤其是在使用促进选择性高产生 PVL 的培养基进行测定时。