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A 组链球菌在食源性流行期间产生的毒力因子的时间进程。

Time course of virulence factors produced by group A streptococcus during a food-borne epidemic.

机构信息

Laboratory of Pathologic Biochemistry, School of Environmental Health Sciences, Azabu University, 1-17-71 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa, 252-5201, Japan.

出版信息

J Infect Chemother. 2012 Feb;18(1):35-40. doi: 10.1007/s10156-011-0280-8. Epub 2011 Jul 13.

Abstract

We studied the protein amount and activity of the major virulence factors hemolysin, cysteine protease streptococcal pyrogenic exotoxin B (SpeB), and NAD glycohydrolase (NADase), which are produced by Streptococcus pyogenes type T-25, with a food poisoning outbreak. The three virulence factors were analyzed by activity and amount of protein using supernatants at 2-30 h of culture. All these virulence factors were confirmed by their activity. Streptolysin O (SLO), SpeB, and NADase were immunochemically confirmed at protein level by Western blot analysis. Two hemolytic forms (70 and 60 kDa) of SLO were identified. SpeB was detected as a 44-kDa precursor form and a 30-kDa mature form. NADase was 50 kDa. SLO protein peaked at 8 h of culture, which corresponded with the hemolytic activity peak. Conversion from precursor to SpeB protein peaked at 14 h of culture. The conversion peak corresponded to the activity expression time. Also, mature SpeB protein peaked at 24 h of culture and corresponded to SpeB activity peak. Electrophoretic analysis clarified the relationship between SLO protein and SpeB protein, although amounts of SLO and SpeB have been reported to be inversely proportional to activity. NADase protein peaked at 12 h of culture, but protein level did not correspond to the peak. Because the NADase protein peak was closer to SpeB activity than SLO protein, our results suggested NADase protein was degraded at 12 h of culture. The time course production of these virulence factors is discussed.

摘要

我们研究了产毒因子溶血素、半胱氨酸蛋白酶化脓性链球菌外毒素 B(SpeB)和烟酰胺核苷水解酶(NADase)的蛋白含量和活性,这些因子由 T-25 型酿脓链球菌引起食物中毒爆发。通过 2-30 小时培养的上清液分析了这三种毒力因子的蛋白含量和活性。所有这些毒力因子均通过活性得到证实。通过 Western blot 分析在蛋白水平上免疫化学证实了链球菌溶血素 O(SLO)、SpeB 和 NADase。鉴定出 SLO 的两种溶血形式(70 和 60 kDa)。SpeB 被检测为 44 kDa 的前体形式和 30 kDa 的成熟形式。NADase 为 50 kDa。SLO 蛋白在培养 8 小时时达到高峰,与溶血活性高峰相对应。SpeB 蛋白从前体到成熟的转化在培养 14 小时时达到高峰,与活性表达时间相对应。此外,成熟 SpeB 蛋白在培养 24 小时时达到高峰,与 SpeB 活性高峰相对应。电泳分析阐明了 SLO 蛋白和 SpeB 蛋白之间的关系,尽管 SLO 和 SpeB 的量据报道与活性成反比。NADase 蛋白在培养 12 小时时达到高峰,但蛋白水平与高峰不对应。由于 NADase 蛋白峰比 SLO 蛋白更接近 SpeB 活性,我们的结果表明 NADase 蛋白在培养 12 小时时被降解。讨论了这些毒力因子的时程产生。

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