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Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater.
Schurig, Sarah; Kobialka, Rea; Wende, Andy; Ashfaq Khan, Md Anik; Lübcke, Phillip; Eger, Elias; Schaufler, Katharina; Daugschies, Arwid; Truyen, Uwe; Abd El Wahed, Ahmed.
Afiliação
  • Schurig S; Institute of Animal Hygiene and Veterinary Public Health, Leipzig University, 04103 Leipzig, Germany.
  • Kobialka R; Xpedite Diagnostics GmbH, 80687 Munich, Germany.
  • Wende A; Institute of Animal Hygiene and Veterinary Public Health, Leipzig University, 04103 Leipzig, Germany.
  • Ashfaq Khan MA; Xpedite Diagnostics GmbH, 80687 Munich, Germany.
  • Lübcke P; Institute of Animal Hygiene and Veterinary Public Health, Leipzig University, 04103 Leipzig, Germany.
  • Eger E; Institute of Pharmacy, University of Greifswald, 17489 Greifswald, Germany.
  • Schaufler K; Institute of Infection Medicine, Christian-Albrecht University Kiel, 24105 Kiel, Germany.
  • Daugschies A; University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
  • Truyen U; Institute of Pharmacy, University of Greifswald, 17489 Greifswald, Germany.
  • Abd El Wahed A; Institute of Infection Medicine, Christian-Albrecht University Kiel, 24105 Kiel, Germany.
Microorganisms ; 11(3)2023 Mar 22.
Article em En | MEDLINE | ID: mdl-36985386
ABSTRACT
Wastewater monitoring became a promising solution in the early detection of outbreaks. Despite the achievements in the identification of pathogens in wastewater using real-time PCR, there is still a lack of reliable rapid nucleic acid extraction protocols. Therefore, in this study, samples were subjected to alkali, proteinase K and/or bead-beating followed by reverse purification magnetic beads-based separation. Wastewater samples spiked with S. aureus, E. coli and C. parvum were used as examples for Gram-positive and -negative bacteria and protozoa, respectively. All results were compared with a spin column technology as a reference method. Proteinase K with bead beating (vortexing with 0.1 mm glass beads for three minutes) was particularly successful for bacterial DNA extraction (three- to five-fold increase). The most useful extraction protocol for protozoa was pre-treatment with proteinase K (eight-fold increase). The selected methods were sensitive as far as detecting one bacterial cell per reaction for S. aureus, ten bacterial cells for E. coli and two oocysts for C. parvum. The extraction reagents are cold chain independent and no centrifuge or other large laboratory equipment is required to perform DNA extraction. A controlled validation trial is needed to test the effectiveness at field levels.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Screening_studies Idioma: En Revista: Microorganisms Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Screening_studies Idioma: En Revista: Microorganisms Ano de publicação: 2023 Tipo de documento: Article