Development and evaluation of a real-time PCR assay for quantification of Giardia and Cryptosporidium in sewage samples

被引:23
作者
Alonso, Jose L. [1 ]
Amoros, Inmaculada [1 ]
Canigral, Irene [2 ]
机构
[1] Univ Politecn Valencia, Inst Ingn Agua & Medio Ambiente, Valencia 46022, Spain
[2] Univ Politecn Valencia, Ctr Avanzado Microbiol Alimentos, Valencia 46022, Spain
关键词
Cryptosporidium; Giardia; LightCycler; LNA probe; qPCR; Sewage; TaqMan; LOCKED NUCLEIC-ACIDS; FECAL SAMPLES; WASTE-WATER; LNA; PARVUM; LAMBLIA; RNA; DNA; DIFFERENTIATION; EFFICIENCY;
D O I
10.1007/s00253-010-2984-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cryptosporidium and Giardia are major causes of diarrheal disease in humans worldwide and are major causes of protozoan waterborne diseases. Two DNA TaqMan PCR-based Giardia and Cryptosporidium methods targeting a 74-bp sequence of the beta-giardin Giardia gene and a 151-bp sequence of the COWP Cryptosporidium gene, respectively, were used as models to compare two different LNA/DNA TaqMan probes to improve the detection limit in a real-time PCR assay. The LNA probes were the most sensitive resulting in 0.96 to 1.57 lower C (t) values than a DNA Giardia TaqMan probe and 0.56 to 2.21 lower than a DNA Cryptosporidium TaqMan probe. Evaluation of TaqMan Giardia and Cryptosporidium probes with LNA substitutions resulted in real-time PCR curves with an earlier C (t) values than conventional DNA TaqMan probes. In conclusion, the LNA probes could be useful for more sensitive detection limits.
引用
收藏
页码:1203 / 1211
页数:9
相关论文
共 37 条
[1]   LNA probes in a real-time TaqMan PCR assay for genotyping of Giardia duodenalis in wastewaters [J].
Alonso, J. L. ;
Amoros, I. ;
Cuesta, G. .
JOURNAL OF APPLIED MICROBIOLOGY, 2010, 108 (05) :1594-1601
[2]   Improved specificity for Giardia lamblia cyst quantification in wastewater by development of a real-time PCR method [J].
Bertrand, I ;
Gantzer, C ;
Chesnot, T ;
Schwartzbrod, J .
JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 57 (01) :41-53
[3]   Giardia cysts in wastewater treatment plants in Italy [J].
Cacciò, SM ;
De Giacomo, M ;
Aulicino, FA ;
Pozio, E .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (06) :3393-3398
[4]   THE INFECTIVITY OF CRYPTOSPORIDIUM-PARVUM IN HEALTHY-VOLUNTEERS [J].
DUPONT, HL ;
CHAPPELL, CL ;
STERLING, CR ;
OKHUYSEN, PC ;
ROSE, JB ;
JAKUBOWSKI, W .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (13) :855-859
[5]   Development of a TaqMan quantitative PCR assay specific for Cryptosporidium parvum [J].
Fontaine, M ;
Guillot, E .
FEMS MICROBIOLOGY LETTERS, 2002, 214 (01) :13-17
[6]   Study of 18S rRNA and rDNA stability by real-time RT-PCR in heat-inactivated Cryptosporidium parvum oocysts [J].
Fontaine, M ;
Guillot, E .
FEMS MICROBIOLOGY LETTERS, 2003, 226 (02) :237-243
[7]  
GIOVANNI GD, 2005, APPL ENVIRON MICROB, V71, P1495
[8]   Real-time PCR assay for detection and genotype differentiation of Giardia lamblia in stool specimens [J].
Guy, RA ;
Xiao, CX ;
Horgen, PA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (07) :3317-3320
[9]   Real-time PCR for quantification of Giardia and Cryptosporidium in environmental water samples and sewage [J].
Guy, RA ;
Payment, P ;
Krull, UJ ;
Horgen, PA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (09) :5178-5185
[10]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994