Billie Velapatiño , Kerstin Locher , Corrie R Belanger , Marthe K Charles
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引用次数: 0
Abstract
This proof-of-concept study aimed to assess whether digital PCR (dPCR) technology could improve the detection of M. tuberculosis complex (MTB) from formalin-fixed paraffin-embedded (FFPE) tissue when compared to real-time PCR. A laboratory developed test using real-time PCR assay targeting the MTB-IS6110 was transitioned to dPCR technology. The analytical sensitivity of dPCR using strain H37Rv genomic DNA was 2.5 fg/reaction, which was lower than the 5 fg/reaction detected by real-time PCR. Archived DNA from 72 samples were evaluated retrospectively and compared to real-time PCR. The dPCR demonstrated 100 % (33/33) PPA and 94.7 % (38/39) NPA with real-time PCR. Thirteen samples with results near the limit of detection by real-time PCR were also at the limit of detection by dPCR. This study demonstrated that, while dPCR provided high analytical sensitivity, its performance for the MTB detection in FFPE tissues was comparable to that of real-time PCR. Both dPCR and real-time PCR are valuable tools for MTB detection especially in the absence of mycobacterial culture.
期刊介绍:
Diagnostic Microbiology and Infectious Disease keeps you informed of the latest developments in clinical microbiology and the diagnosis and treatment of infectious diseases. Packed with rigorously peer-reviewed articles and studies in bacteriology, immunology, immunoserology, infectious diseases, mycology, parasitology, and virology, the journal examines new procedures, unusual cases, controversial issues, and important new literature. Diagnostic Microbiology and Infectious Disease distinguished independent editorial board, consisting of experts from many medical specialties, ensures you extensive and authoritative coverage.