Molecular methods for diagnosis of infective endocarditis

被引:39
作者
Lisby, G
Gutschik, E
Durack, DT
机构
[1] Univ Copenhagen, Panum Inst, DK-2200 Copenhagen N, Denmark
[2] Univ Copenhagen, Hvidovre Hosp, Dept Clin Microbiol, DK-2650 Hvidovre, Denmark
[3] Becton Dickinson, Dept Med, Sparks, MD 21152 USA
关键词
D O I
10.1016/S0891-5520(01)00002-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The culture of viable microorganisms from the blood or from cardiac tissue is currently the most important test for diagnosis of IE. This is followed by phenotypic identification methods used for taxonomic positioning of isolates. However, in those cases where the invading microorganism is difficult or impossible to culture (including instances of prior antimicrobial treatment), molecular methods provide the best means for detection. Molecular identification methods, either nucleic acid target or signal amplification alone or in combination with sequence analysis can offer a more specific and in some cases a more rapid alternative to the phenotypic methods. We propose revised Duke criteria of IE, including positive identification of an organism by molecular biology methods.
引用
收藏
页码:393 / +
页数:21
相关论文
共 101 条
[91]  
WATABE Y, 1993, INT S VIR HEP LIV DI
[92]  
WEINSTEIN L, 1996, INFECT ENDOCARDITIS
[93]  
Weinstein MP, 1997, CLIN INFECT DIS, V24, P584, DOI 10.1093/clind/24.4.584
[94]   FINGERPRINTING GENOMES USING PCR WITH ARBITRARY PRIMERS [J].
WELSH, J ;
MCCLELLAND, M .
NUCLEIC ACIDS RESEARCH, 1990, 18 (24) :7213-7218
[95]  
WILLIAMS JGK, 1993, METHOD ENZYMOL, V218, P704
[96]   DNA POLYMORPHISMS AMPLIFIED BY ARBITRARY PRIMERS ARE USEFUL AS GENETIC-MARKERS [J].
WILLIAMS, JGK ;
KUBELIK, AR ;
LIVAK, KJ ;
RAFALSKI, JA ;
TINGEY, SV .
NUCLEIC ACIDS RESEARCH, 1990, 18 (22) :6531-6535
[97]   BACTERIAL EVOLUTION [J].
WOESE, CR .
MICROBIOLOGICAL REVIEWS, 1987, 51 (02) :221-271
[98]  
YAMADA G, 1995, HEPATOLOGY, V22, P1351, DOI 10.1016/0270-9139(95)90135-3
[99]   Quantification of human immunodeficiency virus type 1 RNA levels in plasma by using small-volume-format branched-DNA assays [J].
Yeghiazarian, T ;
Zhao, WQ ;
Read, SE ;
Kabat, W ;
Li, XY ;
Hamren, SJ ;
Sheridan, PJ ;
Wilber, JC ;
Chernoff, DN ;
Yogev, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (07) :2096-2098
[100]   DETECTION OF HIV-1 RNA IN PLASMA BY ISOTHERMAL AMPLIFICATION (NASBA) IRRESPECTIVE OF THE STAGE OF HIV-1 INFECTION [J].
ZAAIJER, HL ;
KOK, W ;
TENVEEN, JH ;
REESINK, HW ;
FOOLEN, H ;
WINKEL, IN ;
HUISMAN, JG ;
CUYPERS, HTM ;
KIEVITS, T ;
LELIE, PN .
JOURNAL OF VIROLOGICAL METHODS, 1995, 52 (1-2) :175-181