z-logo
open-access-imgOpen Access
Evaluation of DNA extraction methods for quantifying Helicobacter pylori in water with PCR inhibitors
Author(s) -
Eun-Sook Lee,
So-Yang Cha,
Jong-Soon Jung
Publication year - 2021
Publication title -
water supply
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.318
H-Index - 39
eISSN - 1607-0798
pISSN - 1606-9749
DOI - 10.2166/ws.2021.197
Subject(s) - dna extraction , extraction (chemistry) , dna , chromatography , real time polymerase chain reaction , immunomagnetic separation , nucleic acid , polymerase chain reaction , water extraction , chemistry , biology , biochemistry , gene
DNA extraction methods were evaluated to reduce PCR inhibitors and quantify Helicobacter pylori directly from water samples using real-time PCR. Three nucleic acid extraction methods were evaluated for different types of water samples. While the QIAamp DNA mini kit for tissue was suitable for DNA extraction from treated water, the QIAamp DNA stool mini kit was still efficient in analyzing samples from river water after heavy rain and with high concentration of PCR inhibitors. The FastDNA SPIN Kit for Soil could extract DNA effectively from microbes in river and stream waters without heavy rain. Immunomagnetic separation (IMS) was used prior to DNA extraction and was a useful tool for reducing PCR inhibitors in influent and stream samples. H. pylori in various waters could be quantified directly by real-time PCR while minimizing the effect of PCR inhibitors by an appropriate method through the evaluation of DNA extraction methods considering the characteristics of the matrix water. The findings of the present study suggest that the types or characteristics of water sample by source and precipitation are an important factor in detecting H. pylori and they can be applied when detecting and monitoring of other pathogens in water.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here