Real-time PCR TaqMan assay for rapid screening of bloodstream infection

被引:6
作者
Wang, Hye-young [1 ]
Kim, Sunghyun [2 ,3 ]
Kim, Hyunjung [2 ]
Kim, Jungho [2 ]
Kim, Yeun [2 ]
Park, Soon-Deok [2 ,4 ]
Jin, Hyunwoo [5 ]
Choi, Yeonim [6 ]
Uh, Young [4 ]
Lee, Hyeyoung [2 ]
机构
[1] M&D Inc, Wonju Eco Environm Technol Ctr, Wonju 220722, Gangwon, South Korea
[2] Yonsei Univ, Coll Hlth Sci, Dept Biomed Lab Sci, Wonju 220710, Gangwon, South Korea
[3] Yonsei Univ, Inst Life Sci & Biotechnol, Seoul 120749, South Korea
[4] Yonsei Univ, Wonju Coll Med, Dept Lab Med, Wonju 220701, Gangwon, South Korea
[5] Catholic Univ Pusan, Coll Hlth Sci, Dept Clin Lab Med, Pusan 609757, South Korea
[6] Songho Coll, Dept Biomed Lab Sci, Hoengseong 225704, South Korea
来源
ANNALS OF CLINICAL MICROBIOLOGY AND ANTIMICROBIALS | 2014年 / 13卷
关键词
Real-time polymerase chain reaction; Blood culture; Gram-positive bacteria; Gram-negative bacteria; Candida; RIBOSOMAL-RNA GENE; GRAM-NEGATIVE BACTERIA; CLINICAL MICROBIOLOGY; PATHOGENIC BACTERIA; CEREBROSPINAL-FLUID; IDENTIFICATION; DNA; DIAGNOSIS; SEPSIS; EPIDEMIOLOGY;
D O I
10.1186/1476-0711-13-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Sepsis is one of the main causes of mortality and morbidity. The rapid detection of pathogens in blood of septic patients is essential for adequate antimicrobial therapy and better prognosis. This study aimed to accelerate the detection and discrimination of Gram-positive (GP) and Gram-negative (GN) bacteria and Candida species in blood culture samples by molecular methods. Methods: The Real-GP (R), -GN (R), and -CAN (R) real-time PCR kit (M&D, Wonju, Republic of Korea) assays use the TaqMan probes for detecting pan-GP, pan-GN, and pan-Candida species, respectively. The diagnostic performances of the real-time PCR kits were evaluated with 115 clinical isolates, 256 positive and 200 negative blood culture bottle samples, and the data were compared to results obtained from conventional blood culture. Results: Eighty-seven reference strains and 115 clinical isolates were correctly identified with specific probes corresponding to GP-bacteria, GN-bacteria and Candida, respectively. The overall sensitivity and specificity of the real-time PCR kit with blood culture samples were 99.6% and 89.5%, respectively. Conclusions: The Real-GP (R), -GN (R), and -CAN (R) real-time PCR kits could be useful tools for the rapid and accurate screening of bloodstream infections (BSIs).
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页数:10
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