Mazzariol Annarita, Koncan Raffaella, Vitali Luca Agostino, Cornaglia Giuseppe
Dipartimento di Patologia, Sezione di Microbiologia, Università degli Studi di Verona, Strada Le Grazie 8, Verona, Italy.
J Antimicrob Chemother. 2007 Jun;59(6):1171-6. doi: 10.1093/jac/dkm089. Epub 2007 Apr 3.
To test four 16-membered macrolides (josamycin, spiramycin, midecamycin and rokitamycin) along with other compounds in the same class (erythromycin, clarithromycin, roxithromycin and azithromycin) plus clindamycin and telithromycin, against Streptococcus pyogenes and Streptococcus pneumoniae isolates with well-characterized resistance genotypes.
Four hundred and eighty-six isolates of S. pyogenes and 375 isolates of S. pneumoniae were assayed for their macrolide susceptibilities and investigated by PCR to detect their different erythromycin resistance genes. All strains had been isolated over the period 2002-2003 from specimens of different human origin obtained in 14 different Italian centres.
All 16-membered macrolides showed very low MICs (MIC(50)s and MIC(90)s, < or =0.06-0.5 mg/L) for the erythromycin-susceptible isolates and for those with the M phenotype, but the telithromycin MICs for the M-type isolates were at least four times higher (MIC(90)s, 0.5 mg/L). In S. pyogenes, the MIC(50)s of 16-membered macrolides for the cMLS(B) isolates were > or = 256 mg/L, whereas that for telithromycin was 4 mg/L; the MIC(50)s of 16-membered macrolides and telithromycin ranged from < or = 0.06 to 0.5 mg/L for the iMLS(B) isolates with erm(A) and from 0.12 to > or = 256 mg/L for those with erm(B). In S. pneumoniae, the MIC(50)s of the 16-membered macrolides for the cMLS(B) isolates ranged from 0.5 to 128 mg/L, whereas for the iMLS(B) isolates their values ranged from < or = 0.06 to 4 mg/L; the MIC(50)s and MIC(90)s of telithromycin for both the cMLS(B) and the iMLS(B) isolates ranged from < or = 0.06 to 0.12 mg/L.
MICs ranged for all the drugs, except telithromycin, from < or = 0.06 to > or = 256 mg/L, with 15% to 30% resistant S. pyogenes for all drugs tested except clindamycin (8%) and telithromycin (5.4%) and 10% to 40% resistant S. pneumoniae for all drugs tested except telithromycin (0.3%). In both S. pyogenes and S. pneumoniae, erythromycin resistance related to a mef gene meant that telithromycin MICs were definitely higher than in erythromycin-susceptible isolates, although telithromycin susceptibility was preserved in all cases. In S. pyogenes, the activity of both 16-membered macrolides and telithromycin against the iMLS(B) strains proved to be dependent on the erm gene involved, being greater against isolates with erm(A).
检测四种16元大环内酯类药物(交沙霉素、螺旋霉素、麦迪霉素和罗他霉素)以及同一类别的其他化合物(红霉素、克拉霉素、罗红霉素和阿奇霉素)加克林霉素和泰利霉素,对具有明确耐药基因型的化脓性链球菌和肺炎链球菌分离株的抗菌活性。
对486株化脓性链球菌和375株肺炎链球菌进行大环内酯类药物敏感性检测,并通过聚合酶链反应(PCR)检测其不同的红霉素耐药基因。所有菌株均于2002年至2003年期间从意大利14个不同中心采集的不同人类来源标本中分离得到。
所有16元大环内酯类药物对红霉素敏感分离株和具有M表型的分离株显示出非常低的最低抑菌浓度(MIC50和MIC90,≤0.06 - 0.5mg/L),但泰利霉素对M型分离株的MIC至少高四倍(MIC90,0.5mg/L)。在化脓性链球菌中,16元大环内酯类药物对cMLS(B)分离株的MIC50≥256mg/L,而泰利霉素为4mg/L;16元大环内酯类药物和泰利霉素对具有erm(A)的iMLS(B)分离株的MIC50范围为≤0.06至0.5mg/L,对具有erm(B)的分离株为0.12至≥256mg/L。在肺炎链球菌中,16元大环内酯类药物对cMLS(B)分离株的MIC50范围为0.5至128mg/L,而对iMLS(B)分离株的值范围为≤0.06至4mg/L;泰利霉素对cMLS(B)和iMLS(B)分离株的MIC50和MIC90范围为≤0.06至0.12mg/L。
除泰利霉素外,所有药物的MIC范围为≤0.06至≥256mg/L,化脓性链球菌对所有测试药物(除克林霉素(8%)和泰利霉素(5.4%)外)的耐药率为15%至30%,肺炎链球菌对所有测试药物(除泰利霉素(0.3%)外)的耐药率为10%至40%。在化脓性链球菌和肺炎链球菌中,与mef基因相关的红霉素耐药意味着泰利霉素的MIC肯定高于红霉素敏感分离株,尽管在所有情况下泰利霉素仍保持敏感性。在化脓性链球菌中,16元大环内酯类药物和泰利霉素对iMLS(B)菌株的活性证明取决于所涉及的erm基因,对具有erm(A)的分离株活性更强。