TY - JOUR
T1 - Comparative analysis of two broad-range PCR assays for pathogen detection in positive-blood-culture bottles
T2 - PCR-high-resolution melting analysis versus PCR-mass spectrometry
AU - Jeng, Kevin
AU - Gaydos, Charlotte A.
AU - Blyn, Lawrence B.
AU - Yang, Samuel
AU - Won, Helen
AU - Matthews, Heather
AU - Toleno, Donna
AU - Hsieh, Yu Hsiang
AU - Carroll, Karen C.
AU - Hardick, Justin
AU - Masek, Billy
AU - Kecojevic, Alexander
AU - Sampath, Rangarajan
AU - Peterson, Stephen
AU - Rothman, Richard E.
PY - 2012/10
Y1 - 2012/10
N2 - Detection of pathogens in bloodstream infections is important for directing antimicrobial treatment, but current culture-based approaches can be problematic. Broad-range PCR assays which target conserved genomic motifs for postamplification amplicon analysis permit detection of sepsis-causing pathogens. Comparison of different broad-range assays is important for informing future implementation strategies. In this study, we compared positive-blood-culture bottles processed by PCR coupled to high-resolution melting curve analysis (PCR/HRMA) and PCR coupled to electrospray ionization-mass spectrometry (PCR/ESI-MS) to microbiology culture results. Genus-level concordance was 90% (confidence interval [CI], 80 to 96%) for PCR/HRMA and 94% (CI, 85 to 98%) for PCR/ESI-MS. Species-level concordance was 90% (CI, 80 to 96%) for PCR/HRMA and 86% (CI, 75 to 93%) for PCR/ESI-MS. Unlike PCR/HRMA, PCR/ESI-MS was able to resolve polymicrobial samples. Our results demonstrated that the two assays have similar overall concordance rates but may have different roles as potential adjunctive tests with standard blood culture, since each method has different capabilities, advantages, and disadvantages.
AB - Detection of pathogens in bloodstream infections is important for directing antimicrobial treatment, but current culture-based approaches can be problematic. Broad-range PCR assays which target conserved genomic motifs for postamplification amplicon analysis permit detection of sepsis-causing pathogens. Comparison of different broad-range assays is important for informing future implementation strategies. In this study, we compared positive-blood-culture bottles processed by PCR coupled to high-resolution melting curve analysis (PCR/HRMA) and PCR coupled to electrospray ionization-mass spectrometry (PCR/ESI-MS) to microbiology culture results. Genus-level concordance was 90% (confidence interval [CI], 80 to 96%) for PCR/HRMA and 94% (CI, 85 to 98%) for PCR/ESI-MS. Species-level concordance was 90% (CI, 80 to 96%) for PCR/HRMA and 86% (CI, 75 to 93%) for PCR/ESI-MS. Unlike PCR/HRMA, PCR/ESI-MS was able to resolve polymicrobial samples. Our results demonstrated that the two assays have similar overall concordance rates but may have different roles as potential adjunctive tests with standard blood culture, since each method has different capabilities, advantages, and disadvantages.
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U2 - 10.1128/JCM.00677-12
DO - 10.1128/JCM.00677-12
M3 - Article
C2 - 22855511
AN - SCOPUS:84866450325
SN - 0095-1137
VL - 50
SP - 3287
EP - 3292
JO - Journal of Clinical Microbiology
JF - Journal of Clinical Microbiology
IS - 10
ER -