Combinations of PBPs and MurM protein variants in early and contemporary high-level penicillin-resistant Streptococcus pneumoniae isolates in Spain

被引:13
作者
del Campo, R [1 ]
Cafini, F
Morosini, MI
Fenoll, A
Liñares, J
Alou, L
Sevillano, D
Cantón, R
Prieto, J
Baquero, F
机构
[1] Hosp Univ Ramon & Cajal, Microbiol Serv, Ctra Colmenar Km 9-1, Madrid 28034, Spain
[2] Univ Complutense, Fac Med, Dept Microbiol, E-28040 Madrid, Spain
[3] Inst Nacl Salud Carlos 3, Dept Microbiol, Majadahonda 28220, Spain
[4] Hosp Univ Bellvitge, Microbiol Serv, Barcelona 08097, Spain
关键词
resistance; clones; mutations; penicillin-binding proteins;
D O I
10.1093/jac/dkl083
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: High-level penicillin resistance in Streptococcus pneumoniae requires extensive re-modulation of the penicillin-binding proteins (PBPs), and murM gene function is also required for the expression of resistance. In this work, we determined whether specific changes in PBPs were associated with specific MurM variants. Methods: Two collections of highly penicillin-resistant (MIC 2-8 mg/L) isolates, including 10 early (1997-1998) and 23 contemporary (2002-2004) isolates, were studied. Results: Most of the isolates belonged to clones Spain(6B)-2 (13 strains), Spain(23F)-1 (10 isolates) and Spain(14)-5 (20 isolates). Different protein variants of MurM (MA, MB5, MB6, MB9 and MB10), PBP1A (A-C), PBP2B (A-D) and PBP2X (A-C) were recognized, including two murM alleles not previously described. Particular [MurM-PBP1A-2B-2X] allelic combinations were predominant among the different clones, including [MA-B-B-B] for old (MIC 2 mg/L) and [MB10-C-A-B] for recent (MIC 4-8 mg/L) Spain(6B)-2 isolates, [MA-A-C-A] for Spain(23F)-1 and [MB5-A-A-A] in Spain(14)-5 isolates. Conclusions: Although S. pneumoniae has a basic recombinational population structure, our results indicate remarkable conservation of PBPs and MurM protein types within each clone. This suggests that particular PBPs-MurM combinations tend to be preserved and may have an independent evolutionary history in particular clones.
引用
收藏
页码:983 / 986
页数:4
相关论文
共 11 条
[1]   Alterations of the penicillin-binding proteins and murM alleles of clinical Streptococcus pneumoniae isolates with high-level resistance to amoxicillin in Spain [J].
Cafini, F ;
del Campo, R ;
Alou, L ;
Sevillano, D ;
Morosini, MI ;
Baquero, F ;
Prieto, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (02) :224-229
[2]   Identical penicillin-binding domains in penicillin-binding proteins of Streptococcus pneumoniae clinical isolates with different levels of β-lactam resistance [J].
Chesnel, L ;
Carapito, R ;
Croizé, J ;
Dideberg, O ;
Vernet, T ;
Zapun, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (07) :2895-2902
[3]   EXTENSIVE REMODELING OF THE TRANSPEPTIDASE DOMAIN OF PENICILLIN-BINDING PROTEIN-2B OF A PENICILLIN-RESISTANT SOUTH-AFRICAN ISOLATE OF STREPTOCOCCUS-PNEUMONIAE [J].
DOWSON, CG ;
HUTCHISON, A ;
SPRATT, BG .
MOLECULAR MICROBIOLOGY, 1989, 3 (01) :95-102
[4]   Analysis of penicillin-binding protein genes of clinical isolates of Streptococcus pneumoniae with reduced susceptibility to amoxicillin [J].
du Plessis, M ;
Bingen, E ;
Klugman, KP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (08) :2349-2357
[5]   Evolution of Streptococcus pneumoniae serotypes and antibiotic resistance in Spain:: Update (1990 to 1996) [J].
Fenoll, A ;
Jado, I ;
Vicioso, D ;
Pérez, A ;
Casal, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (12) :3447-3454
[6]   The murMN operon:: A functional link between antibiotic resistance and antibiotic tolerance in Streptococcus pneumoniae [J].
Filipe, SR ;
Severina, E ;
Tomasz, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1550-1555
[7]   Distribution of the mosaic structured murM genes among natural populations of Streptococcus pneumoniae [J].
Filipe, SR ;
Severina, E ;
Tomasz, A .
JOURNAL OF BACTERIOLOGY, 2000, 182 (23) :6798-6805
[8]   INTERCONTINENTAL SPREAD OF A MULTIRESISTANT CLONE OF SEROTYPE-23F STREPTOCOCCUS-PNEUMONIAE [J].
MUNOZ, R ;
COFFEY, TJ ;
DANIELS, M ;
DOWSON, CG ;
LAIBLE, G ;
CASAL, J ;
HAKENBECK, R ;
JACOBS, M ;
MUSSER, JM ;
SPRATT, BG ;
TOMASZ, A .
JOURNAL OF INFECTIOUS DISEASES, 1991, 164 (02) :302-306
[9]   Altered PBP 2A and its role in the development of penicillin, cefotaxime, and ceftriaxone resistance in a clinical isolate of Streptococcus pneumoniae [J].
Smith, AM ;
Feldman, C ;
Massidda, O ;
McCarthy, K ;
Ndiweni, D ;
Klugman, KP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (05) :2002-2007
[10]   Emergence of a pneumococcal clone with cephalosporin resistance and penicillin susceptibility [J].
Smith, AM ;
Botha, RF ;
Koornhof, HJ ;
Klugman, KP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (09) :2648-2650