Development of a highly sensitive nucleic acid amplification-based detection for human leptospirosis infection

Highly sensitive diagnostic tools are crucial for individual screening during an epidemic of leptospirosis. To aid in developing a diagnostic tool for the sensitive detection of pathogenic strains, a new approach targeting nucleic acid amplification that combines quantitative PCR (qPCR) and strand d...

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Veröffentlicht in:BioTechniques. - 1991. - 73(2022), 1 vom: 01. Juni, Seite 18-24
1. Verfasser: Jiradechbadee, Thanyatorn (VerfasserIn)
Weitere Verfasser: Sawangjaroen, Nongyao, Ranong, Gorrawee Na, Sila, Thanit, Buncherd, Hansuk, Tun, Aung Win, Thanapongpichat, Supinya
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Journal Article Research Support, Non-U.S. Gov't LipL32 gene PCDR SD polymerase leptospirosis polymerase chain displacement reaction qPCDR quantitative polymerase chain displacement reaction strand displacement amplification Nucleic Acids
Beschreibung
Zusammenfassung:Highly sensitive diagnostic tools are crucial for individual screening during an epidemic of leptospirosis. To aid in developing a diagnostic tool for the sensitive detection of pathogenic strains, a new approach targeting nucleic acid amplification that combines quantitative PCR (qPCR) and strand displacement isothermal amplification was evaluated. The effectiveness of the combined approach, a quantitative polymerase chain displacement reaction (qPCDR), was compared with a qPCR technique. The results showed that qPCDR presented higher sensitivity (at least tenfold) and shorter reaction time than the qPCR approach for pathogenic Leptospira spp. detection. Thus, the qPCDR-based technique developed in this study is a promising approach for pathogenic Leptospira spp. detection and the further development of a diagnostic kit
Beschreibung:Date Completed 14.07.2022
Date Revised 31.07.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1940-9818
DOI:10.2144/btn-2021-0124