Methods used for the isolation, enumeration, characterisation and identification of Enterococcus spp.: 2.: Pheno- and genotypic criteria

被引:71
作者
Domig, KJ [1 ]
Mayer, HK [1 ]
Kneifel, W [1 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Dept Dairy Res & Bacteriol, A-1180 Vienna, Austria
关键词
Enterococcus; fundamental characteristics; phenotyping; genotyping; biochemical typing-biotyping; ribotyping; polyphasic approach; polymerase chain reaction (PCR); random amplified polymorphic DNA (RAPD); pulsed field gel electrophoresis (PFGE); PCR-based typing methods; SDS-PAGE of whole cell proteins;
D O I
10.1016/S0168-1605(03)00178-8
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
This paper reviews the methodology applied for the identification and characterisation of enterococci and covers phenotypic, genotypic and phylogenctic techniques. Although conventional phenotypic typing schemes are useful for rapid and simple identification of enterococcal species for routine applications, other methods like standardised sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE), multilocus enzyme electrophoresis (MLEE), antimicrobial susceptibility testing, serotyping, pyrolysis mass spectrometry (pyMS) and vibrational spectroscopic methods allow a more in-depth characterisation of enterococci. Many of the recently described enterococcal species exhibit deviations from hitherto so-called classical enterococci with regard to their phenotypical properties. Therefore, genotypic methods have to be used to clarify their possible assignment to the genus Enterococcus. In this review, special emphasis is given on recently developed polymerase chain reaction (PCR)-based typing methods such as random amplified polymorphic DNA (RAPD), amplified fragment length polymorphism (AFLP), specific and random amplification (SARA) and modifications of PCR-ribotyping as well as pulsed-field gel electrophoresis (PFGE) and partial sequence analysis. The use of PCR and probes for genus and species identification of enterococci is also considered like the application of sequence data of conserved DNA regions (e.g., ribosomal ribonucleic acid (rRNA) genes) in the case of species identification. (C) 2003 Elsevier B.V All rights reserved.
引用
收藏
页码:165 / 188
页数:24
相关论文
共 251 条
[1]   Characterization of glycopeptide-resistant Enterococcus faecium (GRE) from broilers and pigs in Denmark:: Genetic evidence that persistence of GRE in pig herds is associated with coselection by resistance to macrolides [J].
Aarestrup, FM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2774-2777
[2]   Phenotypic and genetic diversity of enterococci isolated from Italian cheeses [J].
Andrighetto, C ;
Knijff, E ;
Lombardi, A ;
Torriani, S ;
Vancanneyt, M ;
Kersters, K ;
Swings, J ;
Dellaglio, F .
JOURNAL OF DAIRY RESEARCH, 2001, 68 (02) :303-316
[3]   Routine molecular identification of enterococci by gene-specific PCR and 16S ribosomal DNA sequencing [J].
Angeletti, S ;
Lorino, G ;
Gherardi, G ;
Battistoni, F ;
De Cesaris, M ;
DiCuonzo, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (02) :794-797
[4]  
[Anonymous], 1994, ELECTROPHORESIS ENZY
[5]  
[Anonymous], 2006, HDB MICROBIOLOGICAL
[6]   Evaluation of fluorescence-based amplified fragment length polymorphism analysis for molecular typing in hospital epidemiology:: Comparison with pulsed-field gel electrophoresis for typing strains of vancomycin-resistant Enterococcus faecium [J].
Antonishyn, NA ;
McDonald, RR ;
Chan, EL ;
Horsman, G ;
Woodmansee, CE ;
Falk, PS ;
Mayhall, CG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (11) :4058-4065
[7]   Application of tRNA intergenic spacer PCR for identification of Enterococcus species [J].
Baele, M ;
Baele, P ;
Vaneechoutte, M ;
Storms, V ;
Butaye, P ;
Devriese, LA ;
Verschraegen, G ;
Gillis, M ;
Haesebrouck, F .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (11) :4201-4207
[8]   Random amplified polymorphic DNA typing versus pulsed-field gel electrophoresis for epidemiological typing of vancomycin-resistant enterococci [J].
Barbier, N ;
Saulnier, P ;
Chachaty, E ;
Dumontier, S ;
Andremont, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (05) :1096-1099
[9]  
BATES J, 1994, J ANTIMICROB CHEMOTH, V34, P505
[10]  
Batish V. K., 1984, Food Microbiology, V1, P269, DOI 10.1016/0740-0020(84)90061-3