Abstract
Objective: Clinical diagnostics often requires the detection of multiple bacterial species in limited clinical samples with a single DNA extraction method. This study aimed to compare the bacterial DNA extraction efficiency of two lysis methods automated with the MagNA-Pure LC instrument. The samples included five oral bacterial species (three Gram-positive and two Gram-negative) with or without human saliva background. Methods: Genomic DNA (gDNA) was extracted from bacterial cultures by bead-beating lysis (BMP) or chemical lysis (MP), followed by automated purification and measurement by quantitative PCR. Results: For pure bacterial cultures, the MP method yielded higher quantities of extracted DNA and a lower detection limit than the BMP method, except where the samples contained high numbers of Gram-positive bacteria. For bacterial cultures with a saliva background, no difference in gDNA extraction efficacy was observed between the two methods. Conclusions: The efficiency of a bacterial DNA extraction method is not only affected by the bacterial cell wall structure but also by the sample milieu. The MP method provided superior gDNA extraction efficiency when the samples contained a single bacterial species, whereas either of the BMP and MP methods could be applied with similar efficiencies to samples containing multiple species of bacteria.
Original language | English |
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Pages (from-to) | 1-12 |
Number of pages | 12 |
Journal | Journal of International Medical Research |
Volume | 48 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2020 |
Funding
This work was supported by the National Natural Science Foundation of China [grant number 81400505]; the Medical Scientific Research Foundation of Guangdong Province of China [grant number A2015198]; and the State Scholarship Fund of China Scholarship Council [grant number 201706385079].
Funders | Funder number |
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National Natural Science Foundation of China | 81400505 |
Guangdong Medical Research Foundation | A2015198 |
China Scholarship Council | 201706385079 |