rt-pcr法定量测定生物膜中霍乱弧菌细胞

S. V. Titova, E. Menshikova, Sergei Olegovich Vodop'yanov, I. P. Oleynikov, T. N. Borodina
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引用次数: 0

摘要

霍乱弧菌可以浮游和生物膜形式存在。没有统一的方法记录生物膜的形成和微生物的定量测定;已知的方法[3-6]是费力的,不能客观评估霍乱弧菌在生物膜中的浓度。目的:探讨实时荧光定量PCR法测定生物膜和浮游形态霍乱弧菌的方法。材料与方法采用细菌学方法测定浮游生物中孔弧菌的浓度,以每1 ml菌落形成单位数为标准;在生物膜中,采用琼脂板刻印耗尽法。使用文献中描述的引物和探针进行Real-time PCR检测hlyA和ctx基因。使用内置软件和已知细菌细胞浓度的标准制剂对霍乱弧菌进行定量。结果在Microsoft Office Excel 2016电子表格中使用十进制对数进行处理;使用STATISTICA 13.3程序进行统计分析。结果观察期内,几丁质和塑料生物膜中的霍乱弧菌浓度随潜伏期的延长而增加。甲壳素上生物膜和浮游生物组成中霍乱弧菌的数量超过了作为塑料基质时的数量。在第30天,差异是两个或更多的数量级。两种方法的结果具有重复性和可比性;在同一阶段,霍乱弧菌的浓度在同一数量级内变化,表明PCRRT结果的可靠性。结论细菌学方法可用于生物膜的定性评价和霍乱弧菌的生存能力测定。然而,由于其复杂性,不可能快速测定甲壳素上生物膜中霍乱弧菌的浓度,因此更可取的方法是使用实时PCR,它可以准确快速地评估浮游生物和生物膜中霍乱弧菌的浓度。
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QUANTITATIVE DETERMINATION OF VIBRIO CHOLERAE CELLS IN BIOFILMS BY RT-PCR
Introduction Vibrio cholerae can exist in planktonic and biofilm forms. There are no unified methods for recording the formation of a biofilm and the quantitative determination of microorganisms; the known methods [3-6] are laborious and do not allow an objective assessment of the concentration of V. cholerae in biofilms.Aims - to evaluate the method for the quantitative determination of Vibrio cholerae in biofilm and planktonic forms based on real-time PCR.Materials and methods The concentration of Vibrio сholerae in plankton was determined by the bacteriological method by the number of colony-forming units per 1 ml; in biofilms, the method of imprint depletion on agar plates was used. Real-time PCR was performed using the primers and probes described in the literature for the detection of the hlyA and ctx genes. Vibrio cholerae were quantified using built-in software and standard preparations with a known concentration of bacterial cells. The results were processed in Microsoft Office Excel 2016 spreadsheets using the decimal logarithm; statistical analysis was performed using the STATISTICA 13.3 program.Results During the observation period, the concentration of V. cholerae in biofilms on chitin and plastic increases as the incubation period increases. The amount of V. cholerae in the composition of biofilms and plankton on/above chitin exceeded those when used as a plastic substrate. On the 30th day, the difference was two or more orders of magnitude. The results of the two methods were reproducible and comparable; at the same stages, the concentration of V. cholerae varied within the same order of magnitude, which indicated the reliability of the PCRRT results.Conclusion The bacteriological method is informative in the qualitative assessment of biofilms, in determining the viability of cholera vibrios. However, due to its complexity, the impossibility of quickly determining the concentration of V. cholerae in a biofilm on chitin, it is preferable to use real-time PCR, which allows you to assess the concentration of V. cholerae in plankton and biofilm accurately and quickly.
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