Development of real-time PCR for detection and quantitation of Streptococcus parauberis

© 2014 John Wiley & Sons Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Journal of fish diseases. - 1998. - 39(2016), 1 vom: 08. Jan., Seite 31-9
1. Verfasser: Nguyen, T L (VerfasserIn)
Weitere Verfasser: Lim, Y J, Kim, D-H, Austin, B
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2016
Zugriff auf das übergeordnete Werk:Journal of fish diseases
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Real-time PCR Streptococcus parauberis TaqMan probe gyrB qPCR DNA Primers DNA, Bacterial Fluorescent Dyes mehr... DNA Gyrase EC 5.99.1.3
Beschreibung
Zusammenfassung:© 2014 John Wiley & Sons Ltd.
Streptococcus parauberis is an increasing threat to aquaculture of olive flounder, Paralichthys olivaceus Temminck & Schlegel, in South Korea. We developed a real-time polymerase chain reaction (PCR) method using the TaqMan probe assay to detect and quantify S. parauberis by targeting the gyrB gene sequences, which are effective for molecular analysis of the genus Streptococcus. Our real-time PCR assay is capable of detecting 10 fg of genomic DNA per reaction. The intra- and interassay coefficient of variation (CV) values ranged from 0.42-1.95%, demonstrating that the assay has good reproducibility. There was not any cross-reactivity to Streptococcus iniae or to other streptococcal/lactococcal fish pathogens, such as S. agalactiae and Lactococcus garvieae, indicating that the assay is highly specific to S. parauberis. The results of the real-time PCR assay corresponded well to those of conventional culture assays for S. parauberis from inoculated tissue homogenates (r = 0.957; P < 0.05). Hence, this sensitive and specific real-time PCR is a valuable tool for diagnostic quantitation of S. parauberis in clinical samples
Beschreibung:Date Completed 13.12.2016
Date Revised 30.09.2020
published: Print-Electronic
GENBANK: GU324260.1, NC_015558
Citation Status MEDLINE
ISSN:1365-2761
DOI:10.1111/jfd.12322