Hayama M, Oana K, Kozakai T, Umeda S, Fujimoto J, Ota H, Kawakami Y
Department of Biomedical Laboratory Sciences, School of Health Sciences, Shinshu University School of Medicine, Matsumoto 390-8621, Japan.
Eur J Med Res. 2007 Aug 16;12(8):356-9.
As the bacterial spores are difficult to stain, a number of staining techniques including their modifications have been proposed to date. Most of the conventional staining procedures unexceptionally contain the step of staining with steamed dye reagent in order to increase the stainability of the spores. We made an attempt to improve the conventional Moeller's methods for staining bacterial spores.
Spores of Bacillus species were stained with our modified Moeller's spore stain and evaluated for its staining properties. We investigated the stainability of both of the conventional and the modified Moeller's methods and the evaluation was made whether or not the step of steaming of Kinyoun's carbol-fuchsine dye reagent could be omitted by adding to aliquots of Tergitol 7, in place of the conventional dye solution steamed for some interval over hot blue flame of a Bunsen burner.
We successfully omitted the heating step of steaming the Kinyoun's carbol fuchsine dye solution in the Moeller's method of bacterial spore stain, by the replacement of Kinyoun's carbol-fuchsine dye solution involving 2 drops of Tergitol 7, nonionic polyglycol ether surfactants type NP-7 (Sigma-Aldrich Japan, Tokyo, Japan) per 10 ml of Kinyoun's carbol-fuchsine dye solution. Bacillus spores stained pink to red and vegetative bacterial cells stained blue, although without applying any heating step during the whole course of staining processes including the fixation process. The novel staining method of our proposal resulted in far better satisfactory stainability in comparison with the conventional Moeller's method with the steaming dye solution.
The modified spore stain without applying any heating step using the Kinyoun's carbol-fuchsine dye solution with an addition of Tergitol 7 aliquots was demonstrated to be reproducible and yielded consistent and satisfactory stainability. This simplified staining procedure is rapid to perform and found to be applicable to detect the bacterial spores in routine clinical microbiology laboratories.
由于细菌芽孢难以染色,迄今为止已提出了许多染色技术及其改进方法。大多数传统染色程序无一例外地包含用蒸汽染料试剂染色的步骤,以提高芽孢的可染性。我们试图改进传统的莫勒氏细菌芽孢染色方法。
用我们改进的莫勒氏芽孢染色法对芽孢杆菌属的芽孢进行染色,并评估其染色特性。我们研究了传统莫勒氏法和改进莫勒氏法的可染性,并评估了是否可以通过添加特洁士7(Tergitol 7)来省略金扬氏石炭酸复红染料试剂的蒸汽处理步骤,而不是像传统方法那样在本生灯的热蓝色火焰上蒸一定时间的染料溶液。
我们成功地在莫勒氏细菌芽孢染色法中省略了金扬氏石炭酸复红染料溶液的加热步骤,方法是在每10毫升金扬氏石炭酸复红染料溶液中加入2滴特洁士7(一种非离子聚乙二醇醚表面活性剂,型号NP - 7,日本东京西格玛奥德里奇公司生产)。芽孢杆菌的芽孢染成粉红色至红色,营养细菌细胞染成蓝色,尽管在包括固定过程在内的整个染色过程中未进行任何加热步骤。与使用蒸汽染料溶液的传统莫勒氏法相比,我们提出的新染色方法具有更好的可染性。
使用添加了特洁士7的金扬氏石炭酸复红染料溶液且不进行任何加热步骤的改进芽孢染色法被证明具有可重复性,并且产生一致且令人满意的可染性。这种简化的染色程序操作快速,适用于常规临床微生物实验室检测细菌芽孢。