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2009 - 2012年德国侵袭性流感嗜血杆菌分离株的氨苄西林耐药性

Ampicillin resistance of invasive Haemophilus influenzae isolates in Germany 2009-2012.

作者信息

Lâm Thiên-Trí, Claus Heike, Elias Johannes, Frosch Matthias, Vogel Ulrich

机构信息

Institute for Hygiene and Microbiology, National Reference Centre for Meningococci and Haemophilus influenzae, University of Würzburg, Josef-Schneider-Str. 2 (E1), 97080 Würzburg, Germany.

Institute for Hygiene and Microbiology, National Reference Centre for Meningococci and Haemophilus influenzae, University of Würzburg, Josef-Schneider-Str. 2 (E1), 97080 Würzburg, Germany.

出版信息

Int J Med Microbiol. 2015 Oct;305(7):748-55. doi: 10.1016/j.ijmm.2015.08.028. Epub 2015 Aug 21.

Abstract

In this retrospective study covering a four-year observation period (2009-2012) the prevalence of aminopenicillin resistance of invasive Haemophilus influenzae (Hi) in Germany was analyzed. The main resistance mechanism against aminopenicillins is conferred by β-lactamase production, which can be inhibited by clavulanate or sulbactam. Apart from that, β-lactamase negative ampicillin resistance (BLNAR) has been reported due to mutations in the penicillin-binding protein PBP3. The prevalence of BLNAR varies considerably in different countries. Representative data from Germany have not been reported. We analyzed 704 culture positive cases with bacteraemia or detection of Hi in cerebrospinal fluid; 82 isolates (11.6%) were phenotypically resistant to ampicillin. Among these isolates, 65 (79.3%) showed β-lactamase production, and 17 isolates (20.7%) were phenotypic BLNAR Hi. The proportion of ampicillin resistant isolates remained stable over the observation period. Analysis of the PBP3 sequences of 133 isolates with different susceptibility phenotypes including susceptible, BLNAR, and β-lactamase positive isolates, revealed a high genetic diversity. Previously described PBP3 mutations were associated to elevated MIC values, albeit not exclusively, since few highly susceptible strains were found to be positive for the mutations. Furthermore, since ampicillin susceptible strains with elevated MIC values frequently harboured these mutations, prediction of the resistance phenotype using ftsI sequencing appears to be impossible.

摘要

在这项涵盖四年观察期(2009 - 2012年)的回顾性研究中,分析了德国侵袭性流感嗜血杆菌(Hi)对氨基青霉素的耐药率。针对氨基青霉素的主要耐药机制是由β-内酰胺酶产生介导的,克拉维酸或舒巴坦可抑制该酶。除此之外,由于青霉素结合蛋白PBP3发生突变,已报道了β-内酰胺酶阴性氨苄西林耐药(BLNAR)情况。BLNAR的发生率在不同国家差异很大。德国的代表性数据尚未见报道。我们分析了704例血培养阳性或脑脊液中检测到Hi的病例;82株分离株(11.6%)对氨苄西林表型耐药。在这些分离株中,65株(79.3%)产生β-内酰胺酶,17株(20.7%)为表型BLNAR Hi。在观察期内,氨苄西林耐药分离株的比例保持稳定。对133株具有不同药敏表型(包括敏感、BLNAR和β-内酰胺酶阳性分离株)的分离株的PBP3序列分析显示,其具有高度的遗传多样性。先前描述的PBP3突变与MIC值升高有关,尽管并非唯一相关,因为发现很少有高度敏感菌株的突变呈阳性。此外,由于MIC值升高的氨苄西林敏感菌株经常携带这些突变,因此使用ftsI测序预测耐药表型似乎是不可能的。

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