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Polymerase chain reaction and nested-PCR approaches for detecting Cryptosporidium in water catchments of water treatment plants in Curitiba, State of Paraná, Brazil
Osaki, Silvia Cristina; Soccol, Vanete Thomaz; Costa, Adriana Oliveira; Oliveira-Silva, Marcia Benedita; Pereira, Juliana Tracz; Procopio, Antonio Eduardo.
  • Osaki, Silvia Cristina; Universidade Federal do Parana. Centro Politecnico. Programa de Pos-Graduacao em Processos Biotecnologicos e Biotecnologia. Curitiba. BR
  • Soccol, Vanete Thomaz; Universidade Federal do Parana. Centro Politecnico. Programa de Pos-Graduacao em Processos Biotecnologicos e Biotecnologia. Curitiba. BR
  • Costa, Adriana Oliveira; Universidade Federal do Parana. Centro Politecnico. Programa de Pos-Graduacao em Processos Biotecnologicos e Biotecnologia. Curitiba. BR
  • Oliveira-Silva, Marcia Benedita; Universidade Federal do Parana. Centro Politecnico. Programa de Pos-Graduacao em Processos Biotecnologicos e Biotecnologia. Curitiba. BR
  • Pereira, Juliana Tracz; Universidade Federal do Parana. Centro Politecnico. Programa de Pos-Graduacao em Processos Biotecnologicos e Biotecnologia. Curitiba. BR
  • Procopio, Antonio Eduardo; Universidade Federal do Parana. Centro Politecnico. Programa de Pos-Graduacao em Processos Biotecnologicos e Biotecnologia. Curitiba. BR
Rev. Soc. Bras. Med. Trop ; 46(3): 270-276, May-Jun/2013. tab, graf
Article in English | LILACS | ID: lil-679524
ABSTRACT
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, Paraná, 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. .
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Full text: Available Index: LILACS (Americas) Main subject: DNA, Ribosomal / Polymerase Chain Reaction / Water Purification / Cryptosporidium / Fresh Water Country/Region as subject: South America / Brazil Language: English Journal: Rev. Soc. Bras. Med. Trop Journal subject: Tropical Medicine Year: 2013 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Parana/BR

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Full text: Available Index: LILACS (Americas) Main subject: DNA, Ribosomal / Polymerase Chain Reaction / Water Purification / Cryptosporidium / Fresh Water Country/Region as subject: South America / Brazil Language: English Journal: Rev. Soc. Bras. Med. Trop Journal subject: Tropical Medicine Year: 2013 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Parana/BR