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Development of a standardized Gram stain procedure for bacteria and inflammatory cells using an automated staining instrument

机译:使用自动染色仪器开发用于细菌和炎症细胞的标准化革兰染液

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摘要

Gram stain is a subjective and poorly controlled test, and the resultant errors often perplex laboratory scientists. To reduce errors and make Gram stain a precisely controllable and meritorious test, a standardized Gram stain procedure for bacteria and inflammatory cells was developed using an automated staining instrument in this study. Freshly expectorated sputum specimens, used as the optimized targets, were smeared on slides by laboratory technicians, defining each slide loaded with uniform matrix and monolayer cell. And then, the staining and decolorizing time, as well as the stain and decolorant volume, were optimized as 15, 105, 1, and 25 s and 1.1, 1.4, 0.3, and 0.7 ml, respectively. Culture‐positive blood specimens and original purulent fluids were used for confirming the developed standardized Gram stain procedure. Distinct tinctures of bacteria and inflammatory cells adhered to slide uniformly in a monolayer were observed, and the obtained staining results of these samples were highly consistent with their cultured results. Furthermore, according to the staining results under different staining conditions, an updated molecular mechanism of Gram stain for bacteria and the probable staining mechanism for inflammatory cells were also proposed in this study.
机译:克染色是一个主观且受控的测试,所得误差通常是困扰实验室科学家。为了减少误差并使克染色精确可控和令人牢固的试验,使用本研究中的自动染色仪器开发了一种标准化的革兰染粒程和炎症细胞。使用作为优化目标的新咳痰痰样品在实验室技术人员的幻灯片上被涂抹,限定了装配均匀基质和单层细胞的每个滑块。然后,染色和脱色时间以及染色和脱滤剂体积分别优化为15,105,1和25 s和1.1,1.4,0.3和0.7mL。培养阳性血液标本和原始化脓性流体用于确认发育的标准化革兰污染过程。观察到粘附在单层中均匀地滑动以均匀地滑动的细菌和炎性细胞的不同酊剂,并将这些样品的得到的染色结果与其培养的结果高度一致。此外,根据不同染色条件下的染色结果,还提出了本研究中的革兰氏染色的更新分子机制和炎症细胞的可能染色机制。

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