High rates of macrolide resistance among clinical isolates of Streptococcus agalactiae in Tunisia.

M Rachdi, I Boutiba-ben Boubaker, M Hraoui, S Ben Redjeb
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Abstract

One hundred sixty non duplicate erythromycin resistant Streptococcus agalactiae isolates were collected in Tunisia from January 2005 to December 2007 They were investigated to determine their resistance level to different macrolides and the mechanisms involved. Most erythromycin resistant S. agalactiae isolates were isolated from urinary specimens (38.75%, 62/160). The constitutive MLSB phenotype (cMLS) showed in 84.3% (135/160) with high MICs of macrolides and lincosamides (MIC90>256 microg/mL) and 8.2% (13/160) inducible MLSB phenotype (iMLS) with high MICs of macrolides (MIC90>256 microg/mL) and moderately increased MICs of lincosamides (MIC90=8 microg/mL). The M phenotype showed in 7.5% (12/160) with moderately increased MICs of macrolides (MIC90=32 microg/mL) and low MICs of lincosamides (MIC90=0.75 microg/mL). All strains were susceptible to quinupristun-dalfopristin association and linezolid (MIC90: 05 and 0.38 microg/mL respectively). Strains with MLSB phenotype harboured erm(B) gene with 825% (n=132), erm(TR) gene with 8.12% (n=13) and erm(B) plus mef (A) with 1.88% (n=3). All strains categorized as M phenotype carried the mef(A) gene (75%, n=12). cMLSB phenotype conferring cross resistance to macrolides, lincosamides and streptogramins B with high level of resistance was the most prevalent.

突尼斯无乳链球菌临床分离株大环内酯类药物耐药率高。
对2005年1月至2007年12月在突尼斯采集的非重复耐红霉素无乳链球菌分离株160株进行了对不同大环内酯类药物的耐药水平及耐药机制的研究。大多数耐药无乳链球菌从尿标本中分离得到(38.75%,62/160)。组成型MLSB表型(cMLS)占84.3%(135/160),大环内酯类药物和lincosamides的mic值较高(MIC90>256 μ g/mL);诱导型MLSB表型(iMLS)占8.2%(13/160),大环内酯类药物mic值较高(MIC90>256 μ g/mL), lincosamides的mic值中等升高(MIC90=8 μ g/mL)。其中,大环内酯类药物mic中等升高(MIC90=32 μ g/mL),林科胺类药物mic较低(MIC90=0.75 μ g/mL)。所有菌株对奎奴普司汀-达福普司汀联合和利奈唑胺敏感(MIC90分别为0.05和0.38 μ g/mL)。MLSB表型菌株中erm(B)基因占825% (n=132), erm(TR)基因占8.12% (n=13), erm(B) + mef (A)基因占1.88% (n=3)。所有M型菌株均携带mef(A)基因(75%,n=12)。cMLSB表型对大环内酯类、林肯胺类和链状葡聚糖B交叉耐药,且高水平耐药最为普遍。
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