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 40 条
[1]   Legionella-like amebal pathogens - Phylogenetic status and possible role in respiratory disease [J].
Adeleke, A ;
Pruckler, J ;
Benson, R ;
Rowbotham, T ;
Halablab, M ;
Fields, B .
EMERGING INFECTIOUS DISEASES, 1996, 2 (03) :225-230
[2]   Use of Flow Cytometry To Monitor Legionella Viability [J].
Allegra, Severine ;
Berger, Francoise ;
Berthelot, Philippe ;
Grattard, Florence ;
Pozzetto, Bruno ;
Riffard, Serge .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (24) :7813-7816
[3]   Rapid detection and enumeration of Legionella pneumophila in hot water systems by solid-phase cytometry [J].
Aurell, H ;
Catala, P ;
Farge, P ;
Wallet, F ;
Le Brun, M ;
Helbig, JH ;
Jarraud, S ;
Lebaron, P .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (03) :1651-1657
[4]   Effects of humic substances on fluorometric DNA quantification and DNA hybridization [J].
Bachoon, DS ;
Otero, E ;
Hodson, RE .
JOURNAL OF MICROBIOLOGICAL METHODS, 2001, 47 (01) :73-82
[5]   GENOME ANALYSIS OF LEGIONELLA SSP BY ORTHOGONAL FIELD ALTERNATION GEL-ELECTROPHORESIS (OFAGE) [J].
BENDER, L ;
OTT, M ;
MARRE, R ;
HACKER, J .
FEMS MICROBIOLOGY LETTERS, 1990, 72 (03) :253-257
[6]   Preparation of DNA extracted from environmental water samples for PCR amplification [J].
Boccuzzi, VM ;
Straube, WL ;
Ravel, J ;
Colwell, RR ;
Hill, RT .
JOURNAL OF MICROBIOLOGICAL METHODS, 1998, 31 (03) :193-199
[7]   Evaluation of Legionella pneumophila contamination in Italian hotel water systems by quantitative real-time PCR and culture methods [J].
Bonetta, Sa. ;
Bonetta, Si. ;
Ferretti, E. ;
Balocco, F. ;
Carraro, E. .
JOURNAL OF APPLIED MICROBIOLOGY, 2010, 108 (05) :1576-1583
[8]   Removal of PCR inhibitors from soil DNA by chemical flocculation [J].
Braid, MD ;
Daniels, LM ;
Kitts, CL .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 52 (03) :389-393
[9]   Molecular characterization of Legionella populations present within slow sand filters used for fungal plant pathogen suppression in horticultural crops [J].
Calvo-Bado, LA ;
Morgan, JAW ;
Sergeant, M ;
Pettitt, TR ;
Whipps, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (01) :533-541
[10]   Commercial potting soils as an alternative infection source of Legionella pneumophila and other Legionella species in Switzerland [J].
Casati, S. ;
Gioria-Martinoni, A. ;
Gaia, V. .
CLINICAL MICROBIOLOGY AND INFECTION, 2009, 15 (06) :571-575