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Title:Evaluation of DNA extraction methods for reliable quantification of Acinetobacter baumannii, Klebsiella pneumoniae, and Pseudomonas aeruginosa
Authors:ID Bogožalec Košir, Alexandra (Author)
ID Lužnik, Dane (Author)
ID Tomič, Viktorija (Author)
ID Milavec, Mojca (Author)
Files:URL URL - Source URL, visit https://doi.org/10.3390/bios13040463
 
.pdf PDF - Presentation file, download (1,59 MB)
MD5: C89877D282091DB80CD175C2BA236EE0
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Logo UKPBAG - University Clinic of Respiratory and Allergic Diseases Golnik
Abstract:Detection and quantification of DNA biomarkers relies heavily on the yield and quality of DNA obtained by extraction from different matrices. Although a large number of studies have compared the yields of different extraction methods, the repeatability and intermediate precision of these methods have been largely overlooked. In the present study, five extraction methods were evaluated, using digital PCR, to determine their efficiency in extracting DNA from three different Gram-negative bacteria in sputum samples. The performance of two automated methods (GXT NA and QuickPick genomic DNA extraction kit, using Arrow and KingFisher Duo automated systems, respectively), two manual kit-based methods (QIAamp DNA mini kit; DNeasy UltraClean microbial kit), and one manual non-kit method (CTAB), was assessed. While GXT NA extraction kit and the CTAB method have the highest DNA yield, they did not meet the strict criteria for repeatability, intermediate precision, and measurement uncertainty for all three studied bacteria. However, due to limited clinical samples, a compromise is necessary, and the GXT NA extraction kit was found to be the method of choice. The study also showed that dPCR allowed for accurate determination of extraction method repeatability, which can help standardize molecular diagnostic approaches. Additionally, the determination of absolute copy numbers facilitated the calculation of measurement uncertainty, which was found to be influenced by the DNA extraction method used.
Keywords:nucleic acid, dPCR, DNA extraction methods, Gram-negative bacteria
Publication status:Published
Publication version:Version of Record
Publication date:06.04.2023
Year of publishing:2023
Number of pages:str. 2458-2469
Numbering:iss. 9, Vol. 79
PID:20.500.12556/DiRROS-19255 New window
UDC:60
ISSN on article:2079-6374
DOI:10.3390/bios13040463 New window
COBISS.SI-ID:149291011 New window
Note:Soavtorji: Dane Lužnik, Viktorija Tomič and Mojca Milavec; Nasl. z nasl. zaslona; Opis vira z dne 17. 4. 2023;
Publication date in DiRROS:12.07.2024
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Downloads:278
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Record is a part of a journal

Title:Biosensors
Shortened title:Biosensors
Publisher:MDPI AG
ISSN:2079-6374
COBISS.SI-ID:523007769 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P4-0165-2022
Name:Biotehnologija in sistemska biologija rastlin

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:Z2-1860
Name:Meroslovje za sledenje bolnišničnih okužb respiratornega trakta, ki jih povzročajo Gram-negativne bakterije

Funder:EC - European Commission
Funding programme:European Union’s Horizon 2020 research and innovation program
Project number:18HLT03
Acronym:SEPTIMET

Funder:Other - Other funder or multiple funders
Funding programme:European Union, European Regional Development Fund

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:13.03.2024
Applies to:Version of Record valid from 2024-03-13

Secondary language

Language:Slovenian
Keywords:nukleinske kisline, dPCR, metode ekstrakcije DNK, gram-negativne bakterije


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