Combination of ARAD microfibre filtration and LAMP methodology for simple, rapid and cost-effective detection of human pathogenic Giardia duodenalis and Cryptosporidium spp. in drinking water

被引:48
作者
Plutzer, J. [1 ]
Toeroekne, A. [1 ]
Karanis, P. [2 ]
机构
[1] Natl Inst Environm Hlth, Dept Water Hyg, H-1096 Budapest, Hungary
[2] Univ Cologne, Ctr Anat, Inst 2, Cologne, Germany
关键词
detection; drinking water; environmental health; protozoa; rapid techniques; MEDIATED ISOTHERMAL AMPLIFICATION; POLYMERASE-CHAIN-REACTION; TOXOPLASMA-GONDII; NESTED PCR; OOCYSTS; PARVUM; RECOVERY; CYSTS; PURIFICATION; PREVALENCE;
D O I
10.1111/j.1472-765X.2009.02758.x
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
Aims: In this study, we report a new, simple methodology for the monitoring of Cryptosporidium oocysts and Giardia cysts in drinking water samples, ranging from 10- to 1000-l, which combines a new ARAD microfibre filtration of the (oo)cysts from drinking water and loop-mediated isothermal amplification (LAMP) of a human pathogenic Cryptosporidium parvum, Cryptosporidium hominis, Cryptosporidium meleagridis and Giardia duodenalis Assemblage A and B specific DNA sequence. Methods and Results: During the evaluation of the new concentration and detection technique, spiked reagent and matrix water samples plus blank samples were filtered and tested. In total, 27 samples have been investigated. The results clearly demonstrate that the methodology of using a new ARAD filter, which passed through 1000 l of drinking water with high turbidity (2 NTU), and followed by the LAMP assay was able to detect at least one (oo)cyst in 10 l of drinking water based on a 1000-l sample, taken over a 24-h period. Conclusions: The described protozoa detection methodology is sensitive, rapid and cost-effective. Significance and Impact of the Study: This effective procedure will be useful for small waterworks to achieve continuous monitoring and is also of value for screening catchments to identify those that require further treatment and more detailed microscopic counts.
引用
收藏
页码:82 / 88
页数:7
相关论文
共 32 条
[21]   Virulence of three distinct Cryptosporidium parvum isolates for healthy adults [J].
Okhuysen, PC ;
Chappell, CL ;
Crabb, JH ;
Sterling, CR ;
DuPont, HL .
JOURNAL OF INFECTIOUS DISEASES, 1999, 180 (04) :1275-1281
[22]   Pathogenesis of human and bovine Cryptosporidium parvum in gnotobiotic pigs [J].
Pereira, SJ ;
Ramirez, NE ;
Xiao, LH ;
Ward, LA .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (05) :715-718
[23]   Rapid identification of Giardia duodenalis by loop-mediated isothermal amplification (LAMP) from faecal and environmental samples and comparative findings by PCR and real-time PCR methods [J].
Plutzer, J. ;
Karanis, P. .
PARASITOLOGY RESEARCH, 2009, 104 (06) :1527-1533
[24]   Assessment of methods for detection of infectious Cryptosporidium oocysts and Giardia cysts in reclaimed effluents [J].
Quintero-Betancourt, W ;
Gennaccaro, AL ;
Scott, TM ;
Rose, JB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (09) :5380-5388
[25]   Modification to EPA Method 1623 to address a unique seasonal matrix effect encountered in some US source waters [J].
Shaw, Nancy J. ;
Villegas, Leah Fohl ;
Eldred, Bradley J. ;
Gaynor, Deborah H. ;
Warden, Paul S. ;
Pepich, Barry V. .
JOURNAL OF MICROBIOLOGICAL METHODS, 2008, 75 (03) :445-448
[26]   Evaluation of loop-mediated isothermal amplification for detection of Toxoplasma gondii in water samples and comparative findings by polymerase chain reaction and immunofluorescence test (IFT) [J].
Sotiriadou, Isaia ;
Karanis, Panagiotis .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2008, 62 (04) :357-365
[27]  
*USEPA, 2005, 815R05004 USEPA OFF
[28]  
*USEPA, 821R01025 USEPA OFF
[29]  
*USEPA, 1996, EPA600R95178 NAT EXP
[30]   Prevalence of Giardia cysts and Cryptosporidium oocysts and characterization of Giardia spp isolated from drinking water in Canada [J].
Wallis, PM ;
Erlandsen, SL ;
IsaacRenton, JL ;
Olson, ME ;
Robertson, WJ ;
VanKeulen, H .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (08) :2789-2797