Diversity of domain V of 23S rRNA gene sequence in different Enterococcus species

被引:12
作者
Tsiodras, S
Gold, HS
Coakley, EPG
Wennersten, C
Moellering, RC
Eliopoulos, GM
机构
[1] Beth Israel Deaconess Med Ctr, Div Infect Dis, Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
关键词
D O I
10.1128/JCM.38.11.3991-3993.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The highly conserved central loop of domain V of 23S RNA (nucleotides 2042 to 2628; Escherichia coli numbering) is implicated in peptidyltransferase activity and represents one of the target sites for macrolide, lincosamide, and streptogramin B antibiotics. DNA encoding domain V (590 bp) of several species of Enterococcus was amplified by PCR Twenty enterococcal isolates were tested, including Enterococcus faecium (six isolates), Enterococcus faecalis, Enterococcus avium, Enterococcus durans, Enterococcus gallinarum, Enterococcus casseliflavus (two isolates of each), and Enterococcus raffinosus, Enterococcus mundtii, Enterococcus malodoratus, and Enterococcus hirae tone isolate of each). For all isolates, species identification by biochemical testing was corroborated by 16S rRNA gene sequencing, The sequence of domain V of the 23S rRNA gene from E, faecium and E, faecalis differed from those of all other enterococci, The domain V sequences of E, durans and E, hirae were identical. This was also true for E, gallinarum and E, casseliflavus, E, avium differed from E, casseliflavus by 23 bases, from E, durans by 16 bases, and from E, malodoratus by 2 bases. E, avium differed from E, raffinosus by one base. Despite the fact that domain V is considered to be highly conserved, substantial differences were identified between several enterococcal species.
引用
收藏
页码:3991 / 3993
页数:3
相关论文
共 16 条
[1]   IDENTIFICATION OF ENTEROCOCCUS-FAECALIS STRAINS BY DNA HYBRIDIZATION AND PULSED-FIELD GEL-ELECTROPHORESIS [J].
COQUE, TM ;
MURRAY, BE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (12) :3368-3369
[2]   CHARACTERIZATION OF THE CHROMOSOMAL AAC(6')-II GENE-SPECIFIC FOR ENTEROCOCCUS-FAECIUM [J].
COSTA, Y ;
GALIMAND, M ;
LECLERCQ, R ;
DUVAL, J ;
COURVALIN, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (09) :1896-1903
[3]  
Frahm E, 1998, SYST APPL MICROBIOL, V21, P450, DOI 10.1078/072320202320771525
[4]  
HIGGINS DG, 1989, COMPUT APPL BIOSCI, V5, P151
[5]  
Ludwig W, 1999, ASM NEWS, V65, P752
[6]   Ribosomal RNA is the target for oxazolidinones, a novel class of translational inhibitors [J].
Matassova, NB ;
Rodnina, MV ;
Endermann, R ;
Kroll, HP ;
Pleiss, U ;
Wild, H ;
Wintermeyer, W .
RNA, 1999, 5 (07) :939-946
[7]   CHLORAMPHENICOL, ERYTHROMYCIN, CARBOMYCIN AND VERNAMYCIN-B PROTECT OVERLAPPING SITES IN THE PEPTIDYL TRANSFERASE REGION OF 23S-RIBOSOMAL RNA [J].
MOAZED, D ;
NOLLER, HF .
BIOCHIMIE, 1987, 69 (08) :879-884
[8]   Determination of the nucleotide sequence of the 23S ribosomal RNA and flanking spacers of an Enterococcus faecium strain, reveals insertion-deletion events in the ribosomal spacer 1 of enterococci [J].
Naimi, A ;
Beck, G ;
Monique, M ;
Lefèbvre, G ;
Branlanti, C .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1999, 22 (01) :9-21
[9]   GENETIC-BASIS OF MACROLIDE RESISTANCE IN MYCOBACTERIUM-AVIUM ISOLATED FROM PATIENTS WITH DISSEMINATED DISEASE [J].
NASH, KA ;
INDERLIED, CB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (12) :2625-2630
[10]   Determination of 16S rRNA sequences of enterococci and application to species identification of nonmotile Enterococcus gallinarum isolates [J].
Patel, R ;
Piper, KE ;
Rouse, MS ;
Steckelberg, JM ;
Uhl, JR ;
Kohner, P ;
Hopkins, MK ;
Cockerill, FR ;
Kline, BC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (11) :3399-3407