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Escherichia coli and Enterococcus spp. in Rainwater Tank Samples: . Comparison of Culture-Based Methods and 23S rRNA Gene Quantitative PCR Assays

机译:大肠杆菌和肠球菌属。在雨水箱样本中:基于文化的方法和23S rRNA基因定量PCR检测方法的比较

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摘要

In this study, culture-based methods and quantitative PCR (qPCR) assays were compared with each other for the measurement of Escherichia coli and Enterococcus spp. in water samples collected from rainwater tanks in Southeast Queensland, Australia. Among the 50 rainwater tank samples tested, 26 (52%) and 46 (92%) samples yielded E. coli numbers as measured by EPA Method 1603 and E coli 23S rRNA gene qPCR assay, respectively. Similarly, 49 (98%) and 47 (94%) samples yielded Enterococcus spp. numbers as measured by EPA Method 1600 and Enterococcus spp. 23S rRNA gene qPCR assay, respectively. The mean E. coli (2.49 ± 0.85) log_(10) and Enterococcus spp. (2.72 ± 0.32) log_(10) numbers as measured by qPCR assays were significantly (P < 0001) different than E. coli (0.91 ± 0.80) Iog_(10) and Enterococcus spp. (1.86 ± 0.60) log_(10) numbers as measured by culture-based method. Weak but significant correlations were observed between both EPA Method 1603 and the E. coli qPCR assay (r = 0.47, P = 0.0009), and EPA Method 1600 and the Enterococcus spp. qPCR assay (r = 0.42, P = 0.002). Good qualitative agreement was found between the culture-based method and the Enterococcus spp. qPCR assay in terms of detecting fecal pollution in water samples from the studied rainwater tanks. More research studies, however, are needed to shed some light on the discrepancies associated with the culture-based methods and qPCR assays for measuring fecal indicator bacteria.
机译:在这项研究中,比较了基于培养的方法和定量PCR(qPCR)分析方法对大肠杆菌和肠球菌的测量。从澳大利亚昆士兰州东南部雨水箱收集的水样中。在测试的50个雨水箱样品中,分别有26个(52%)和46个(92%)样品产生的大肠杆菌数分别通过EPA方法1603和大肠杆菌23S rRNA基因qPCR测定法测得。同样,有49个(98%)和47个(94%)样品产生了肠球菌。通过EPA方法1600和肠球菌spp。 23S rRNA基因qPCR分析。平均大肠杆菌(2.49±0.85)log_(10)和肠球菌属。通过qPCR分析测得的(2.72±0.32)log_(10)值与大肠杆菌(0.91±0.80)Iog_(10)和肠球菌(pp.Enterococcus spp)有显着(P <0001)差异。通过基于文化的方法测得的(1.86±0.60)log_(10)数。在EPA方法1603和E.coli qPCR分析之间(r = 0.47,P = 0.0009)和EPA方法1600与肠球菌之间均观察到微弱但显着的相关性。 qPCR分析(r = 0.42,P = 0.002)。在基于培养的方法和肠球菌之间发现了良好的定性一致性。从检测雨水水箱中水样中粪便污染的角度进行qPCR分析。然而,需要进行更多的研究来阐明与基于培养物的方法和用于测量粪便指示菌的qPCR测定法相关的差异。

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  • 来源
    《Environmental Science & Technology》 |2012年第20期|p.11370-11376|共7页
  • 作者单位

    CSIRO Land and Water, Ecosriences Precinct, 41 Boggo Road, Brisbane 4102, Australia,Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore, DC, Q1d 4558, Australia;

    CSIRO Land and Water, Ecosriences Precinct, 41 Boggo Road, Brisbane 4102, Australia,SchooI of Population Health, University of Queensland, Herston Road, Brisbane 4006, Australia;

    CSIRO Land and Water, Ecosriences Precinct, 41 Boggo Road, Brisbane 4102, Australia,Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore, DC, Q1d 4558, Australia;

    CSIRO Land and Water, Ecosriences Precinct, 41 Boggo Road, Brisbane 4102, Australia,SchooI of Population Health, University of Queensland, Herston Road, Brisbane 4006, Australia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-17 14:03:02

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