Instituto de Microbiología y Parasitología Médica, Universidad de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Tecnológicas (IMPAM, UBA-CONICET), Facultad de Medicina, Argentina.
Infect Genet Evol. 2013 Mar;14:294-301. doi: 10.1016/j.meegid.2012.12.020. Epub 2013 Jan 8.
As a way to contribute to the assessment of Acinetobacter baumannii clinical population structure, multi-locus sequence typing (MLST) was performed in a collection of 93 isolates from Buenos Aires (1983-2012) and Rosario (2006-2009) hospitals. Sequence types (STs) were achieved by Bartual (B) and Institut Pasteur (P) schemes. PFGE typing, antimicrobial susceptibility assays, and the amplification of the OXA carbapenemase genes most prevalent in our region, were also performed. e-Burst clustered the 25 STs(B) (15 novels) into 5 clonal complexes (CC) and 5 singletons, and grouped the 18 STs(P) (12 novels) into 3 CC and 4 singletons. Bartual scheme divided the CC79(P) into two groups. CC113(B)/CC79(P) prevailed in Buenos Aires at least in 1992-2009, being responsible for epidemic and for endemic infections and acquiring the XDR (extensively drug-resistant) pattern throughout the years. While, CC119(B)/CC79(P) was apparently present before the CC113(B)/CC79(P)domain. CC103(B)/CC15(P) was the second most prevalent CC. Interestingly, CC110(B)/ST25(P) apparently increased over the last years. Conversely, CC109(B)/CC1(P) (international clone I) predominated in Rosario, although the presence of CC113(B)/CC79(P), CC103(B)/CC15(P) and CC110(B)/ST25(P) was observed. Nineteen novel STs clustered in CC79(P), CC15(P), CC113(B), CC109(B) and CC103(B), suggesting their clonal expansion during persistence. PFGE typing proved transmission of strains intra- and inter-hospitals in each city. Except for one, all the recent isolates (2007-2012) harboured the blaOXA-23-like. All isolates were susceptible to colistin. Tigecycline MIC(90) was 1mg/L and the rifampicin MIC>512mg/l was found among isolates in three hospitals. In conclusion, the international clone II (CC92(B)/CC2(P)) was not found among our isolates. CC113(B)/CC79(P), CC103(B)/CC15(P), and ST25(P), suggested also as major components in the A. baumannii population together with the international clone I, were present in Buenos Aires and Rosario with different prevalence rate. Their recent isolates showed high distribution of the blaOXA-23-like as well as the XDR pattern.
为了评估鲍曼不动杆菌临床群体结构,对来自布宜诺斯艾利斯(1983-2012 年)和罗萨里奥(2006-2009 年)医院的 93 株分离株进行了多位点序列分型(MLST)。序列类型(STs)通过 Bartual(B)和巴斯德研究所(P)方案获得。还进行了 PFGE 分型、抗菌药物敏感性试验以及我们地区最常见的 OXA 碳青霉烯酶基因的扩增。e-Burst 将 25 个 STs(B)(15 个新序列)聚类为 5 个克隆复合体(CC)和 5 个单倍型,18 个 STs(P)(12 个新序列)聚类为 3 个 CC 和 4 个单倍型。Bartual 方案将 CC79(P)分为两组。CC113(B)/CC79(P)至少在 1992-2009 年在布宜诺斯艾利斯流行,负责流行感染和地方性感染,并在多年来获得了 XDR(广泛耐药)模式。而 CC119(B)/CC79(P)则显然在 CC113(B)/CC79(P)之前存在。CC103(B)/CC15(P)是第二大流行 CC。有趣的是,CC110(B)/ST25(P)在过去几年中明显增加。相反,CC109(B)/CC1(P)(国际克隆 I)在罗萨里奥占主导地位,尽管观察到 CC113(B)/CC79(P)、CC103(B)/CC15(P)和 CC110(B)/ST25(P)的存在。19 个新 ST 聚类在 CC79(P)、CC15(P)、CC113(B)、CC109(B)和 CC103(B)中,表明它们在持续存在期间的克隆扩张。PFGE 分型证明了每座城市医院内和医院间菌株的传播。除了一个之外,所有最近的分离株(2007-2012 年)都携带 blaOXA-23 样基因。所有分离株对黏菌素均敏感。替加环素 MIC(90)为 1mg/L,三个医院的分离株中发现 rifampicin MIC>512mg/L。总之,我们的分离株中未发现国际克隆 II(CC92(B)/CC2(P))。CC113(B)/CC79(P)、CC103(B)/CC15(P)和 ST25(P),以及国际克隆 I,也被认为是鲍曼不动杆菌群体的主要组成部分,在布宜诺斯艾利斯和罗萨里奥以不同的流行率存在。它们最近的分离株显示出 blaOXA-23 样基因和 XDR 模式的高分布。