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Development and characterization of a synthetic DNA, NUversa, to be used as a standard in quantitative polymerase chain reactions for molecular pneumococcal serotyping.

FEMS Microbiology Letters. 2017-09; 
Fuminori Sakai, Griffin Sonaty, David Watson, Keith P. Klugman and Jorge E. Vidal
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PCR Cloning and Subcloning The final nucleotide sequence (∼8.2 kb) was synthesized and thensubclonedwithinpUC57-Amp-modified(GenScript,Piscataway, New Jersey, USA). Get A Quote

摘要

Identification of Streptococcus pneumoniae and its more than 90 serotypes is routinely conducted by culture and Quellung reactions. Quantitative polymerase chain reactions (qPCRs) have been developed for molecular detection, including a pan-pneumococcus lytA assay, and assays targeting 79 serotypes. Reactions require genomic DNA from every target to prepare standards, which can be time consuming. In this study, we have developed a synthetic DNA molecule as a surrogate for genomic DNA and present new single-plex qPCR reactions to increase molecular detection to 94 pneumococcal serotypes. Specificity of these new reactions was confirmed with a limit of detection between 2 and 20 genome equivalents/reaction. A syn... More

关键词

Streptococcus pneumoniae; serotype; qPCR; NUversa