柴油微生态系统中微生物种群 ATP 与定量 PCR 生物因子之间的关系。

Access microbiology Pub Date : 2024-07-04 eCollection Date: 2024-01-01 DOI:10.1099/acmi.0.000695.v4
Frederick J Passman, Jordan Schmidt, Danika Nicoletti
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引用次数: 0

摘要

一直以来,燃料微生物学研究都依赖于培养数据。潜在相关但无法培养的细菌未被检测到。虽然 ATP 可以量化燃料中的微生物生物菌总量,但它无法区分存在的类群。定量 PCR(qPCR)测试有望通过量化目标扩增片段序列来填补这一空白,从而检测可培养和不可培养的类群,并量化特定的目标类群。在本研究中,对从燃料、界面和水相的燃料过水微生态系统中提取的流体样本进行了细胞 ATP 浓度([cATP])和 qPCR 生物因子检测。此外,还收集了暴露于这三个阶段的钢腐蚀试样表面的表面拭子样本,并对总 ATP 浓度([tATP])和 qPCR 生物因子进行了检测。研究了 ATP 和 qPCR 生物因子之间的统计关系。两个变量之间的相关系数取决于矩阵,范围从可忽略(|r|=0.2)到强(|r|=0.7)不等。当结果分为可忽略、中等和重度生物负载时,参数的一致性同样取决于矩阵。ATP] 和 qPCR 基因拷贝之间的一致百分比从 11% 到 89% 不等,qPCR-生物负载等级通常高于 ATP-生物负载等级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relationship between microbial population ATP and quantitative PCR bioburdens in diesel fuel microcosms.

Historically, fuel microbiology studies have relied on culture data. Potentially relevant but unculturable bacteria were not detected. Although ATP can quantify total microbial bioburdens in fuels, it cannot differentiate among the taxa present. Quantitative PCR (qPCR) testing promises to fill this gap by quantifying targeted amplicon sequences thereby detecting both culturable and non-culturable taxa and quantifying specifically targeted taxa. In this study, fluid samples drawn from the fuel, interface and water phases of fuel over water microcosms were tested for cellular ATP concentration ([cATP]) and qPCR bioburdens. Additionally, surface swab samples from steel corrosion coupon surfaces exposed to each of these three phases were collected and tested for total ATP concentration ([tATP]) and qPCR bioburdens. Statistical relationships between ATP and qPCR bioburdens were examined. Correlation coefficients between the two variables were matrix dependent and ranged from negligible (|r|=0.2) to strong (|r|=0.7). When results were categorized into negligible, moderate and heavy bioburdens, parameter agreement was again matrix dependent. Percentage agreement between [ATP] and qPCR gene copies ranged from 11 % to 89 % - with qPCR-bioburden ratings typically being greater than ATP-bioburden ratings.

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