Marquart Mary E, Monds Kathryn S, McCormick Clare C, Dixon Sherrina N, Sanders Melissa E, Reed Julian M, McDaniel Larry S, Caballero Armando R, O'Callaghan Richard J
Department of Microbiology, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2661-6. doi: 10.1167/iovs.07-0017.
The purpose of this study was to determine whether cholesterol, the host cell receptor for pneumolysin of Streptococcus pneumoniae, could effectively treat pneumococcal keratitis.
New Zealand White rabbits were intrastromally injected with 10(5) colony-forming units (CFUs) of S. pneumoniae D39. Corneas were treated with topical drops of 1% cholesterol every 2 hours beginning 25 hours after infection and were examined by slit lamp microscopy 24, 36, and 48 hours after infection. Rabbits were killed, and CFUs were recovered from the corneas after the final slit lamp examination (SLE). Minimal inhibitory concentration (MIC) assays of cholesterol against bacteria were performed. Specific inhibition of pneumolysin by cholesterol in the rabbit cornea was tested by intrastromal injection of pneumolysin with or without cholesterol and was compared with cholesterol inhibition of pneumolysin in vitro using hemolysis assays with rabbit erythrocytes.
Corneas treated with cholesterol had significantly lower SLE scores 48 hours after infection than corneas treated with vehicle (P = 0.0015). Treated corneas also had significantly less log(10) CFUs than vehicle-treated corneas (P = 0.0006). Cholesterol at a 1% concentration was bactericidal to bacteria in vitro, and lower concentrations of cholesterol were partially inhibitory in a concentration-dependent manner. Cholesterol also specifically inhibited 1 mug pneumolysin in vivo and up to 50 ng pneumolysin in vitro.
Topical cholesterol is an effective treatment for S. pneumoniae keratitis. Cholesterol not only inhibits pneumolysin, it is also bactericidal.
本研究旨在确定肺炎链球菌溶血素的宿主细胞受体胆固醇是否能有效治疗肺炎球菌性角膜炎。
给新西兰白兔角膜基质内注射10⁵个肺炎链球菌D39菌落形成单位(CFU)。感染后25小时开始,每2小时用1%胆固醇滴眼液局部滴眼处理角膜,并在感染后24、36和48小时用裂隙灯显微镜检查。在最后一次裂隙灯检查(SLE)后处死兔子,从角膜中回收CFU。进行胆固醇对细菌的最低抑菌浓度(MIC)测定。通过在有或无胆固醇的情况下向角膜基质内注射溶血素,测试胆固醇对兔角膜中溶血素的特异性抑制作用,并与使用兔红细胞溶血试验在体外进行的胆固醇对溶血素的抑制作用进行比较。
感染后48小时,用胆固醇处理的角膜的SLE评分显著低于用赋形剂处理的角膜(P = 0.0015)。处理后的角膜中的log₁₀CFU也显著少于用赋形剂处理过的角膜(P = 0.0006)。1%浓度的胆固醇在体外对细菌具有杀菌作用,较低浓度的胆固醇以浓度依赖的方式具有部分抑制作用。胆固醇在体内还能特异性抑制1μg溶血素,在体外能抑制高达50ng的溶血素。
局部应用胆固醇是治疗肺炎球菌性角膜炎的有效方法。胆固醇不仅能抑制溶血素,还具有杀菌作用。