Cafini Fabio, del Campo Rosa, Alou Luis, Sevillano David, Morosini María Isabel, Baquero Fernando, Prieto José
Departamento de Microbiología, Facultad de Medicina, Universidad Complutense de Madrid, Avda Complutense s/n, 28040 Madrid, Spain.
J Antimicrob Chemother. 2006 Feb;57(2):224-9. doi: 10.1093/jac/dki442. Epub 2005 Dec 20.
The aim of this study was to analyse the nucleotide sequences of regions encoding the penicillin-binding domains of pbp1A, pbp2B and pbp2X genes and murM alleles from 14 selected amoxicillin-resistant Streptococcus pneumoniae isolates (MICs 8-16 mg/L) obtained in Spain.
PFGE and dideoxynucleotide chain termination sequencing were used.
Analysis of PFGE profiles showed that the amoxicillin-resistant S. pneumoniae strains belonged to six different PFGE patterns including the Spain23F-1, Spain6B-2, Spain9V-3 and Spain(14)-5 international clones; however, 8 of the 14 strains belonged to the Spain9V-3 clone. These strains showed the typical changes in penicillin-binding proteins (PBPs) 1A and 2X and had 10 unique changes in the 590-641 region of PBP2B as described previously. Transformation experiments tried to incorporate the transpeptidase domain of PBP2B including the 590-641 region associated with amoxicillin-resistant pneumococci. Sequencing of the pbp2B genes revealed that part of the 3' region of the pbp2B sequence encoding a region of the domain (around amino acid 514-538 to the C terminus of PBP2B) did not recombine with the R6 pbp2B gene. The murM sequence analysis showed that 6, 6 and 2 amoxicillin-resistant S. pneumoniae strains had murMA, murMB5 and murMB6 alleles, respectively. However, strains with murMB5 or murMB6 alleles showed a single mutation (N537D) in the 537-581 region of PBP2B, while strains with the murMA allele had 12 unique changes.
Ten unique changes in the 590-641 region of PBP2B and no specific murM alleles were found in S. pneumoniae strains isolated in Spain with an amoxicillin MIC>or=8 mg/L (MICs from 6 to 12 mg/L by 1 mg/L step dilution). In addition, the presence of specific mutations in PBP2B seems to play a key role in the presence of different murM alleles in these amoxicillin-resistant pneumococcal strains.
本研究旨在分析来自西班牙的14株选定的阿莫西林耐药肺炎链球菌分离株(最低抑菌浓度为8 - 16mg/L)中pbp1A、pbp2B和pbp2X基因以及murM等位基因编码青霉素结合结构域区域的核苷酸序列。
采用脉冲场凝胶电泳(PFGE)和双脱氧核苷酸链终止测序法。
PFGE图谱分析表明,阿莫西林耐药肺炎链球菌菌株属于六种不同的PFGE模式,包括Spain23F - 1、Spain6B - 2、Spain9V - 3和Spain(14) - 5国际克隆株;然而,14株菌株中有8株属于Spain9V - 3克隆株。这些菌株在青霉素结合蛋白(PBPs)1A和2X中显示出典型变化,并且如先前所述,在PBP2B的590 - 641区域有10个独特变化。转化实验试图整合PBP2B的转肽酶结构域,包括与阿莫西林耐药肺炎球菌相关的590 - 641区域。pbp2B基因测序显示,pbp2B序列3'区域中编码该结构域一部分(围绕PBP2B C末端氨基酸514 - 538)的部分未与R6 pbp2B基因重组。murM序列分析表明,分别有6株、6株和2株阿莫西林耐药肺炎链球菌菌株具有murMA、murMB5和murMB6等位基因。然而,具有murMB5或murMB6等位基因的菌株在PBP2B的537 - 581区域显示单个突变(N537D),而具有murMA等位基因的菌株有12个独特变化。
在西班牙分离的阿莫西林最低抑菌浓度≥8mg/L(通过1mg/L梯度稀释法测定的最低抑菌浓度为6至12mg/L)的肺炎链球菌菌株中,在PBP2B的590 - 641区域发现了10个独特变化,且未发现特定的murM等位基因。此外,PBP2B中特定突变的存在似乎在这些阿莫西林耐药肺炎球菌菌株中不同murM等位基因的存在中起关键作用。