Direct identification of Staphylococcus aureus from positive blood culture bottles

被引:55
作者
Oliveira, K
Brecher, SM
Durbin, A
Shapiro, DS
Schwartz, DR
De Girolami, PC
Dakos, J
Procop, GW
Wilson, D
Hanna, CS
Haase, G
Peltroche-Llacsahuanga, H
Chapin, KC
Musgnug, MC
Levi, MH
Shoemaker, C
Stender, H
机构
[1] AdvanDx, Concord, MA 01742 USA
[2] Appl Biosyst Inc, Bedford, England
[3] Boston VA Healthcare Syst, W Roxbury, MA USA
[4] Lahey Clin Fdn, Burlington, MA USA
[5] Boston Med Ctr, Boston, MA USA
[6] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[7] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[8] NYU, Sch Med, Bellevue Hosp, New York, NY USA
[9] Montefiore Med Ctr, Bronx, NY 10467 USA
[10] Rhein Westfal TH Aachen, Univ Hosp, D-5100 Aachen, Germany
关键词
D O I
10.1128/JCM.41.2.889-891.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Fluorescence in situ hybridization (FISH) using peptide nucleic acid (PNA) probes targeting Staphylococcus aureus 16S rRNA is a novel method for direct identification of S. aureus from positive blood culture bottles. The test (S. aureus PNA FISH) is performed on smears made directly from positive blood culture bottles with gram-positive cocci in clusters (GPCC) and provides results within 2.5 h. A blinded comparison of S. aureus PNA FISH with standard identification methods was performed in collaboration with eight clinical microbiology laboratories. A total of 564 routine blood culture bottles positive for GPCC recovered from both aerobic and anaerobic media from three different manufacturers (ESP, BACTEC, and BacT/Alert) were included in the study. The sensitivity and specificity of S. aureus PNA FISH were 100% (57 of 57) and 99.2% (116 of 117), respectively, with 174 GPCC-positive ESP blood culture bottles, 98.5% (67 of 68) and 98.5% (129 of 131), respectively, with 200 GPCC-positive BACTEC blood culture bottles, and 100% (74 of 74) and 99.1% (115 of 116), respectively, with 190 GPCC-positive BacT/Alert blood culture bottles. It is concluded that S. aureus PNA FISH performs well with commonly used continuously monitoring blood culture systems.
引用
收藏
页码:889 / 891
页数:3
相关论文
共 10 条
[1]  
BARON EJ, 1998, ESSENTIAL PROCEDURES, P58
[2]   Rapid differentiation of Staphylococcus aureus from staphylococcal species by arbitrarily primed-polymerase chain reaction [J].
Benito, M.J. ;
Rodríguez, M.M. ;
Córdoba, M.G. ;
Aranda, E. ;
Córdoba, J.J. .
2000, Blackwell Publishing Ltd. (31)
[3]   DIRECT IDENTIFICATION OF BACTERIAL ISOLATES IN BLOOD CULTURES BY USING A DNA PROBE [J].
DAVIS, TE ;
FULLER, DD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (10) :2193-2196
[4]  
EGHOLM M, 1993, NATURE, V365, P556
[5]   Fluorescent in situ hybridization allows rapid identification of microorganisms in blood cultures [J].
Kempf, VAJ ;
Trebesius, K ;
Autenrieth, IB .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :830-838
[6]   RAPID IDENTIFICATION OF STAPHYLOCOCCUS-AUREUS FROM BLOOD CULTURE BOTTLES BY A CLASSIC 2-HOUR TUBE COAGULASE TEST [J].
MCDONALD, CL ;
CHAPIN, K .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (01) :50-52
[7]   Rapid identification of Staphylococcus aureus directly from blood cultures by fluorescence in situ hybridization with peptide nucleic acid probes [J].
Oliveira, K ;
Procop, GW ;
Wilson, D ;
Coull, J ;
Stender, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (01) :247-251
[8]  
PEZZLO M, 1998, ESSENTIAL PROCEDURES, P51
[9]   EVALUATION OF SEVERAL COMMERCIAL BIOCHEMICAL AND IMMUNOLOGICAL METHODS FOR RAPID IDENTIFICATION OF GRAM-POSITIVE COCCI DIRECTLY FROM BLOOD CULTURES [J].
RAPPAPORT, T ;
SAWYER, KP ;
NACHAMKIN, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (07) :1335-1338
[10]   Evaluation of four methods for rapid identification of Staphylococcus aureus from blood cultures [J].
Speers, DJ ;
Olma, TR ;
Gilbert, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (04) :1032-1034