Cargando…

Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater

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 subj...

Descripción completa

Detalles Bibliográficos
Autores principales: Schurig, Sarah, Kobialka, Rea, Wende, Andy, Ashfaq Khan, Md Anik, Lübcke, Phillip, Eger, Elias, Schaufler, Katharina, Daugschies, Arwid, Truyen, Uwe, Abd El Wahed, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056086/
https://www.ncbi.nlm.nih.gov/pubmed/36985386
http://dx.doi.org/10.3390/microorganisms11030813
_version_ 1785016039706198016
author Schurig, Sarah
Kobialka, Rea
Wende, Andy
Ashfaq Khan, Md Anik
Lübcke, Phillip
Eger, Elias
Schaufler, Katharina
Daugschies, Arwid
Truyen, Uwe
Abd El Wahed, Ahmed
author_facet Schurig, Sarah
Kobialka, Rea
Wende, Andy
Ashfaq Khan, Md Anik
Lübcke, Phillip
Eger, Elias
Schaufler, Katharina
Daugschies, Arwid
Truyen, Uwe
Abd El Wahed, Ahmed
author_sort Schurig, Sarah
collection PubMed
description 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.
format Online
Article
Text
id pubmed-10056086
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-100560862023-03-30 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 Microorganisms Article 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. MDPI 2023-03-22 /pmc/articles/PMC10056086/ /pubmed/36985386 http://dx.doi.org/10.3390/microorganisms11030813 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schurig, Sarah
Kobialka, Rea
Wende, Andy
Ashfaq Khan, Md Anik
Lübcke, Phillip
Eger, Elias
Schaufler, Katharina
Daugschies, Arwid
Truyen, Uwe
Abd El Wahed, Ahmed
Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater
title Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater
title_full Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater
title_fullStr Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater
title_full_unstemmed Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater
title_short Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater
title_sort rapid reverse purification dna extraction approaches to identify microbial pathogens in wastewater
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056086/
https://www.ncbi.nlm.nih.gov/pubmed/36985386
http://dx.doi.org/10.3390/microorganisms11030813
work_keys_str_mv AT schurigsarah rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT kobialkarea rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT wendeandy rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT ashfaqkhanmdanik rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT lubckephillip rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT egerelias rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT schauflerkatharina rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT daugschiesarwid rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT truyenuwe rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater
AT abdelwahedahmed rapidreversepurificationdnaextractionapproachestoidentifymicrobialpathogensinwastewater