A Real Time PCR strategy for the detection and quantification of Candida albicans in human blood.

Abstract:

:Candidemia is a significant cause of bloodstream infections (BSI) in nosocomial settings. The identification of species can potentially improve the quality of care and decrease human mortality. Quantitative PCR (qPCR) was evaluated for Candida albicans detection using culture suspensions containing C. albicans , spiked human blood, the cloned qPCR target fragment (ITS2 region) and the results of these assays were compared. The assays showed a good detection limit: C. albicans DNA extracted from yeast (sensitivity 0.2 CFU/µL), spiked human blood (sensitivity 10 CFU/mL), and cloned fragment of ITS2 region (sensitivity 20 target copies/μL). The efficiency of ITS2 fragment-qPCR ranged from 89.67 to 97.07, and the linearity (R2) of the standard curve ranged from 0.992 to 0.999. The results showed that this ITS2-qPCR has a great potential as a molecular prototype model for the development of a test to be applied in clinical practice, greatly reducing the time of candidemia diagnosis, which is extremely important in this clinical setting.

authors

Busser FD,Coelho VC,Fonseca CA,Del Negro GMB,Shikanai-Yasuda MA,Lopes MH,Magri MMC,Freitas VLT

doi

10.1590/S1678-9946202062009

subject

Has Abstract

pub_date

2020-02-07 00:00:00

pages

e9

eissn

0036-4665

issn

1678-9946

pii

S0036-46652020000100600

journal_volume

62

pub_type

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