Microbiology Department, IDIBELL, Hospital Universitari de Bellvitge, Universitat de Barcelona, Feixa Llarga s/n, 08907 L'Hospitalet de Llobregat, Barcelona, Spain.
J Antimicrob Chemother. 2011 Aug;66(8):1712-8. doi: 10.1093/jac/dkr193. Epub 2011 May 31.
To analyse the epidemiology of isolates of serotype 6C among invasive pneumococci isolated from children and adults in Spain between 1997 and 2009, and to characterize serotype 6C clones and macrolide and quinolone resistance mechanisms.
Antimicrobial susceptibility was determined following CLSI guidelines. Phenotypic characterization of macrolide-resistant isolates was performed by the double disc diffusion method. Genes associated with resistance to erythromycin and tetracycline were sought by PCR, while quinolone resistance was analysed by restriction fragment length polymorphism of the quinolone resistance-determining region. Isolates were typed by multilocus sequence typing.
Seven hundred and eighty-nine of 866 serotype 6A pneumococci collected from 1997 to 2009 were available. Of these, 213 (27.0%) were serotype 6C; 16/163 (9.8%) in the 1997-2001 (pre-PCV7) period, 37/322 (11.5%) in the 2002-05 (early-PCV7) period and 160/381 (42.0%) in the 2006-09 (late-PCV7) period. The overall proportions of serotype 6C increased from 0.1% (pre-PCV7) to 1% (late-PCV7) for paediatric isolates and from 0.3% to 1.7% among adult isolates. A major serotype 6C lineage (ST224/ST1150/ST4821), accounting for 66.7% of the isolates, was identified across the whole period. In the late-PCV7 period the antimicrobial non-susceptibility of serotype 6C increased in association with the emergence of the ST386/ST4310/ST4825 lineage, which carried a Tn6002 transposon [erm(B) and tet(M) genes].
Serotype 6C pneumococci were identified in Spain during the period 1997-2009. The increase in serotype 6C in the late-PCV7 period was associated with the spread of the ST224/ST1150/ST4821 lineage and the emergence of the ST386/ST4310/ST4825 lineage.
分析 1997 年至 2009 年间西班牙儿童和成人侵袭性肺炎球菌分离株中血清型 6C 分离株的流行病学,并对血清型 6C 克隆和大环内酯类和喹诺酮类耐药机制进行特征描述。
按照 CLSI 指南进行抗生素敏感性测定。采用双纸片扩散法对耐大环内酯类的分离株进行表型特征分析。通过 PCR 寻找与红霉素和四环素耐药相关的基因,而喹诺酮类耐药则通过喹诺酮类耐药决定区的限制性片段长度多态性进行分析。通过多位点序列分型对分离株进行分型。
1997 年至 2009 年间共收集了 866 株血清型 6A 肺炎球菌,其中 789 株可用于分析。其中,213 株(27.0%)为血清型 6C;16/163(9.8%)在 1997-2001 年(PCV7 前)期间,37/322(11.5%)在 2002-05 年(PCV7 早期)期间,160/381(42.0%)在 2006-09 年(PCV7 后期)期间。血清型 6C 的总体比例从 PCV7 前的 0.1%(0.1%)增加到 PCV7 后的 1%(1.7%),儿科分离株的比例从 0.3%增加到 1.7%,而成人分离株的比例从 0.3%增加到 1.7%。在整个研究期间,发现了一个主要的血清型 6C 谱系(ST224/ST1150/ST4821),占分离株的 66.7%。在 PCV7 后期,与 ST386/ST4310/ST4825 谱系的出现相关,该谱系携带 Tn6002 转座子[erm(B)和 tet(M)基因],血清型 6C 的抗菌非敏感性增加。
1997 年至 2009 年间在西班牙发现了血清型 6C 肺炎球菌。PCV7 后期血清型 6C 的增加与 ST224/ST1150/ST4821 谱系的传播以及 ST386/ST4310/ST4825 谱系的出现有关。