Polymerase chain reaction and nested-PCR approaches for detecting Cryptosporidium in water catchments of water treatment plants in Curitiba, State of Parana, Brazil

被引:15
作者
Osaki, Silvia Cristina [1 ,2 ]
Soccol, Vanete Thomaz [1 ,3 ]
Costa, Adriana Oliveira [4 ]
Oliveira-Silva, Marcia Benedita [5 ]
Pereira, Juliana Tracz [6 ]
Procopio, Antonio Eduardo [1 ]
机构
[1] Univ Fed Parana, Ctr Politecn, Programa Posgrad Proc Biotecnol & Biotecnol, BR-80060000 Curitiba, Parana, Brazil
[2] Univ Fed Parana, Curso Med Vet, Palotina, PR, Brazil
[3] Univ Positivo, Programa Pos Grad Gestao Ambiental, Curitiba, Parana, Brazil
[4] Univ Fed Minas Gerais, Fac Farm, Dept Anal Clin & Toxicol, Belo Horizonte, MG, Brazil
[5] Univ Fed Triangulo Mineiro, Dept Ciencias Biol, Disciplina Parasitol, Uberaba, MG, Brazil
[6] Univ Fed Parana, Ctr Politecn, Dept Patol Basica, BR-80060000 Curitiba, Parana, Brazil
关键词
Cryptosporidium; Polymerase chain reaction; Nested-PCR; DNA extraction technique; Water; PARVUM OOCYSTS; GIARDIA; SPP; INACTIVATION; SYSTEM; DNA;
D O I
10.1590/0037-8682-0053-2013
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Introduction: Cryptosporidium is an important protozoan cause of waterborne disease worldwide of concern to public health authorities. To prevent outbreaks of cryptosporidiosis, the monitoring of this parasite in drinking water is necessary. In the present work, the polymerase chain reaction (PCR) and nested-PCR techniques were used to detect Cryptosporidium in raw water from catchment points of four water treatment plants (WTP) in Curitiba, Parana, Brazil. Methods: First, DNA extraction techniques were tested in samples containing decreasing amount of oocysts in reagent water, and PCR and nested-PCR with specific primers for 18SSU rDNA of Cryptosporidium were conducted to determine their sensitivity. In reagent water, a commercial extraction kit provided the best analytical sensitivity, and PCR and nested-PCR allowed the detection of five and two oocysts, respectively, with the primers XIAOR/XIAOF and XIAO1F/XIAO2R. Results: In the spiking experiments, only the PCR with the primers AWA995F/AWA1206R was successful at detecting concentrations of 0.1 oocysts/mL. Two catchments samples of raw water and/or water sludge from four WTPs were contaminated with Cryptosporidium. Conclusions: The application of the techniques to monitor Cryptosporidium in water and detect contamination in water catchments of WTPs in Curitiba are discussed in the present work.
引用
收藏
页码:270 / 276
页数:7
相关论文
共 29 条
[1]   Presence of Cryptosporidium spp. and Giardia duodenalis in Drinking Water Samples in the North of Portugal [J].
Almeida, Andre ;
Moreira, Maria Joao ;
Soares, Sonia ;
Delgado, Maria de Lurdes ;
Figueiredo, Joao ;
Silva, Elisabete ;
Castro, Antonio ;
Correida Da Cosa, Jose Manuel .
KOREAN JOURNAL OF PARASITOLOGY, 2010, 48 (01) :43-48
[2]  
Almeida TTC, 2004, THESIS U SAO PAULO S
[3]  
[Anonymous], 1989, Molecular Cloning: A Laboratory
[4]   DETECTION AND SPECIES IDENTIFICATION OF CRYPTOSPORIDIUM OOCYSTS USING A SYSTEM BASED ON PCR AND ENDONUCLEASE RESTRICTION [J].
AWADELKARIEM, FM ;
WARHURST, DC ;
MCDONALD, V .
PARASITOLOGY, 1994, 109 :19-22
[5]   Cryptosporidium spp. and Giardia spp. in surface water supply of Campinas, Southeast Brazil [J].
Cantusio Neto, Romeu ;
dos Santos, Luciana Urbano ;
Zanoli Sato, Maria Ines ;
Bueno Franco, Regina Maura .
WATER SCIENCE AND TECHNOLOGY, 2010, 62 (01) :217-222
[6]   Cryptosporidium parvum:: Structural components of the oocyst wall [J].
Harris, JR ;
Petry, F .
JOURNAL OF PARASITOLOGY, 1999, 85 (05) :839-849
[7]   Rapid extraction of DNA from Escherichia coli and Cryptosporidium parvum for use in PCR [J].
Higgins, JA ;
Jenkins, MC ;
Shelton, DR ;
Fayer, R ;
Karns, JS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (11) :5321-5324
[8]   Evaluation of three flocculation methods for the purification of Cryptosporidium parvum oocysts from water samples [J].
Karanis, P ;
Kimura, A .
LETTERS IN APPLIED MICROBIOLOGY, 2002, 34 (06) :444-449
[9]  
Kuczynska E, 1999, APPL ENVIRON MICROB, V65, P2820
[10]  
Lemarchand K, 2003, FEMS MICROBIOL LETT, V218, P203, DOI 10.1111/j.1574-6968.2003.tb11519.x