Department of Ophthalmology and Regenerative Medicine, Ehime University Graduate School of Medicine, Shitsukawa, Toon, Ehime, Japan.
J Clin Microbiol. 2012 May;50(5):1606-12. doi: 10.1128/JCM.06461-11. Epub 2012 Feb 15.
The usefulness of 5-cyano-2,3-ditolyl-tetrazolium chloride (CTC) staining to determine the respiratory activity of Acanthamoeba was evaluated in this study. Acanthamoeba trophozoites and cysts have a red fluorescence after staining with CTC. To determine the effectiveness of CTC staining as a CTC biocidal assay for Acanthamoeba, the trophozoites and cysts of Acanthamoeba castellanii (ATCC 5037) were treated with serial concentrations of disinfectant solutions, namely, polyhexamethylene biguanide (PHMB) and commercial soft contact lens (SCL) disinfectant solutions. The treated Acanthamoeba organisms were stained with CTC, and their respiratory activity was determined by the intensity of fluorescence in a fluorescence microplate reader. The survival rates of the same samples were determined by a culture-dependent biocidal assay using the Spearman-Karber method. Our results showed that the respiratory activities determined by the CTC biocidal assay and the survival rates determined by the culture-dependent biocidal assay for Acanthamoeba trophozoites and cysts decreased in a dose-dependent way after PHMB treatments, and the results were significantly correlated (r = 0.83 and P < 0.01 for trophozoites; r = 0.60 and P < 0.01 for cysts; Spearman rank correlation test). The respiratory activities in the trophozoites and cysts treated with SCL disinfectant solutions were significantly correlated with the survival rate (r = 0.70 and P < 0.01 for trophozoites; r = 0.64 and P < 0.01 for cysts; Spearman rank correlation test). The significant correlation of the results indicated that the CTC biocidal assay can be used as an alternative method to a culture-dependent biocidal assay. The CTC biocidal assay is a rapid and simple method to test the effectiveness of disinfectant solutions against Acanthamoeba trophozoites and cysts.
本研究评估了 5-氰基-2,3-二苯四唑氯(CTC)染色在确定棘阿米巴呼吸活性中的用途。棘阿米巴滋养体和包囊在用 CTC 染色后呈现红色荧光。为了确定 CTC 染色作为棘阿米巴 CTC 杀菌测定的有效性,用一系列消毒剂处理棘阿米巴 castellanii(ATCC 5037)的滋养体和包囊,即聚六亚甲基双胍(PHMB)和商业软性隐形眼镜(SCL)消毒剂。用 CTC 对处理过的棘阿米巴生物进行染色,并通过荧光微孔板读数器测定其荧光强度来确定其呼吸活性。通过使用 Spearman-Karber 方法的基于培养的杀菌测定法确定相同样品的存活率。我们的结果表明,在用 PHMB 处理后,棘阿米巴滋养体和包囊的 CTC 杀菌测定法确定的呼吸活性和基于培养的杀菌测定法确定的存活率呈剂量依赖性下降,并且结果呈显著相关性(r = 0.83 和 P < 0.01 用于滋养体;r = 0.60 和 P < 0.01 用于包囊;Spearman 等级相关检验)。用 SCL 消毒剂处理的滋养体和包囊中的呼吸活性与存活率显著相关(r = 0.70 和 P < 0.01 用于滋养体;r = 0.64 和 P < 0.01 用于包囊;Spearman 等级相关检验)。结果的显著相关性表明,CTC 杀菌测定法可作为基于培养的杀菌测定法的替代方法。CTC 杀菌测定法是一种快速简便的方法,可用于测试消毒剂对棘阿米巴滋养体和包囊的有效性。