Quantification of Legionella pneumophila by real-time quantitative PCR from samples with humic acid and ferric ion

被引:5
|
作者
Chen, Nai-Tzu [1 ]
Chang, Ching-Wen [1 ,2 ,3 ]
机构
[1] Natl Taiwan Univ, Coll Publ Hlth, Inst Environm Hlth, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Ctr Res Environm & Occupat Hlth, Taipei 100, Taiwan
[3] Natl Taiwan Univ, Res Ctr Genes Environm & Human Hlth, Taipei 100, Taiwan
关键词
Legionellae; Humic acid; Ferric ion; PCR inhibition; Real-time quantitative PCR; POLYMERASE-CHAIN-REACTION; ENVIRONMENTAL WATER SAMPLES; RAPID DETECTION; DNA EXTRACTION; PONTIAC FEVER; SOIL DNA; AMPLIFICATION; INHIBITION; SEDIMENTS; SYSTEMS;
D O I
10.1016/j.scitotenv.2011.10.005
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study determined and overcame the influences of humic acid (HA) and/or ferric ion (Fe) on quantification of Legionella pneumophila by real-time quantitative PCR (qPCR). Four commonly used DNA isolation methods, QiAamp DNA Mini Kit (Q), Q with Sepharose 4B gel column (Q/G), freeze-thaw/phenol-chloroform lysis (FT-PC), and FT-PC/G, were adopted to isolate L pneumophila DNA from samples containing Fe alone (0-30 mg l(-1)) or Fe/HA (0/0-3/100 mg l(-1)). Among the four DNA isolation methods, Q removed HA effectively and obtained the greatest DNA yield regardless of Fe and HA concentration (P<0.05). For samples containing Fe (0.3-3 mg l(-1)) or Fe/HA (0.3/10-3/100 mg l(-1)), qPCR inhibition was found in all isolated DNA, especially in those obtained by Q/G and FT-PC/G. DNA dilution at either 10 or 100 folds reduced qPCR inhibition and increased cell recovery (P<0.05). Under 10-fold dilution, Q acquired the highest concentrations of L. pneumophila determined by qPCR. Consequently, Q with post 10-fold dilution is suggested prior to qPCR for quantifying L. pneumophila from water containing Fe (<= 3 mg l(-1)) or Fe/HA (<= 3/100 mg l(-1)). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:608 / 613
页数:6
相关论文
共 50 条
  • [41] Quantification of enterococci and human adenoviruses in environmental samples by real-time PCR
    He, JW
    Jiang, S
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (05) : 2250 - 2255
  • [42] Detection and quantification of Mycobacterium leprae in tissue samples by real-time PCR
    Stefanie Kramme
    Gisela Bretzel
    Marcus Panning
    Joseph Kawuma
    Christian Drosten
    Medical Microbiology and Immunology, 2004, 193 : 189 - 193
  • [43] Detection and quantification of Mycobacterium leprae in tissue samples by real-time PCR
    Kramme, S
    Bretzel, G
    Panning, M
    Kawuma, J
    Drosten, C
    MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 2004, 193 (04) : 189 - 193
  • [44] Quantification of Clostridium difficile by real-time PCR in hospital environmental samples
    Nonnenmacher, C.
    Kropatsch, R.
    Schumacher, S.
    Mutters, R.
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2007, 29 : S190 - S191
  • [45] Real-time quantitative PCR
    Schmittgen, TD
    METHODS, 2001, 25 (04) : 383 - 385
  • [46] Identification and quantification of lactic acid bacteria by real-time PCR
    Phandanouvong L, Vienvilay
    Betancourt L, Liliana
    Rodriguez, Fernando, V
    REVISTA MVZ CORDOBA, 2010, 15 (01) : 1897 - 1906
  • [47] Quantification of V(D)J recombination by real-time quantitative PCR
    Braikia, Fatima-Zohra
    Chemin, Guillaume
    Moutahir, Mohammed
    Khamlichi, Ahmed Amine
    IMMUNOLOGY LETTERS, 2014, 162 (01) : 119 - 123
  • [48] Validation of quantitative real-time polymerase chain reaction for detection of Legionella pneumophila in hospital water networks
    Sauget, M.
    Richard, M.
    Chassagne, S.
    Hocquet, D.
    Bertrand, X.
    Jeanvoine, A.
    JOURNAL OF HOSPITAL INFECTION, 2023, 138 : 74 - 80
  • [49] Comparison between quantitative nucleic acid sequence-based amplification, real-time reverse transcriptase PCR, and real-time PCR for quantification of Leishmania parasites
    van der Meide, Wendy
    Guerra, Jorge
    Schoone, Gerard
    Farenhorst, Marit
    Coelho, Leila
    Faber, William
    Peekel, Inge
    Schallig, Henk
    JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (01) : 73 - 78
  • [50] Legionellosis and Lung Abscesses: Contribution of Legionella Quantitative Real-Time PCR to an Adapted Followup
    Descours, G.
    Tellini, C.
    Flamens, C.
    Philit, F.
    Celard, M.
    Etienne, J.
    Lina, G.
    Jarraud, S.
    CASE REPORTS IN INFECTIOUS DISEASES, 2013, 2013