Evaluation of buffy coat 16S rRNA PCR, buffy coat culture and whole blood PCR for detection of bacteraemia

被引:9
作者
Valle, Demetrio L., Jr. [1 ,2 ,3 ]
Andrade, Jeannie I. [3 ]
Cabrera, Esperanza C. [4 ]
Rivera, Windell L. [1 ]
机构
[1] Univ Philippines, Coll Sci, Inst Biol, Quezon City 1101, Philippines
[2] Ospital Ng Makati, Dept Labs, Makati, Philippines
[3] Makati Med Ctr, Dept Pathol, Makati, Philippines
[4] De La Salle Univ, Dept Biol, Manila, Philippines
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2010年 / 105卷 / 02期
关键词
bacteraemia; buffy coat culture; leukocyte count; PCR; blood culture; PSEUDOMONAS-CEPACIA; DNA AMPLIFICATION; COLONIZATION; INFECTION; DIAGNOSIS; OUTBREAK; ASSAY; GENE;
D O I
10.1590/S0074-02762010000200001
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The use of Gram type-specific PCR on buffy coat from clinical specimens for the detection of bacteraemia was evaluated for the first time using whole blood culture as the gold standard. In addition, the established buffy coat culture and whole blood PCR were also compared. Gram-positive bacteria belonging to six species and Gram-negative bacteria from 10 species were isolated and identified by culture and detected using broad-range 16S rDNA primers and Gram-specific primers. Data from the three methods all conferred very high sensitivity, specificity, positive and negative predictive values when compared to whole blood culture. The Kappa coefficients of agreement were 0.9819 (buffy coat PCR), 0.9458 (whole blood PCR) and 1.0 (buffy coat culture), which establishes their validity as alternative methods to routine blood culture in detecting bacteraemia. In addition, results showed that there was a direct correlation of WBC counts greater than 12,000 cells per mm(3) to the occurrence of bacteraemia as detected by the four methods (p < 0.05).
引用
收藏
页码:117 / 122
页数:6
相关论文
共 31 条
[1]  
Abu Al-Soud W, 2000, J CLIN MICROBIOL, V38, P345
[2]   PROLONGED SURVIVAL OF PSEUDOMONAS-CEPACIA IN COMMERCIALLY MANUFACTURED POVIDONE-IODINE [J].
ANDERSON, RL ;
VESS, RW ;
PANLILIO, AL ;
FAVERO, MS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (11) :3598-3600
[3]   Bacteremias: A leading cause of death [J].
Bearman, GML ;
Wenzel, RP .
ARCHIVES OF MEDICAL RESEARCH, 2005, 36 (06) :646-659
[4]   DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ .
CHEST, 1992, 101 (06) :1644-1655
[5]  
BURKHOLDER WH, 1950, PHYTOPATHOLOGY, V40, P115
[6]   Distinguishing cytomegalovirus (CMV) infection and disease with CMV nucleic acid assays [J].
Caliendo, AM ;
St George, K ;
Allega, J ;
Bullotta, AC ;
Gilbane, L ;
Rinaldo, CR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (05) :1581-1586
[7]  
Centers for Disease Control and Prevention (CDC), 1998, MMWR Morb Mortal Wkly Rep, V47, P926
[8]  
de Vries JE, 2001, CLIN CHEM, V47, P1701
[9]   Outbreak of Burkholderia cepacia bacteremia in a pediatric hospital due to contamination of lipid emulsion stoppers [J].
Doit, C ;
Loukil, C ;
Simon, AM ;
Ferroni, A ;
Fontan, JE ;
Bonacorsi, S ;
Bidet, P ;
Jarlier, V ;
Aujard, Y ;
Beaufils, F ;
Bingen, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (05) :2227-2230
[10]   PCR PRIMERS AND PROBES FOR THE 16S RIBOSOMAL-RNA GENE OF MOST SPECIES OF PATHOGENIC BACTERIA, INCLUDING BACTERIA FOUND IN CEREBROSPINAL-FLUID [J].
GREISEN, K ;
LOEFFELHOLZ, M ;
PUROHIT, A ;
LEONG, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (02) :335-351