Altan Akineden, Cemal ÇiÇek, SelÇuk TÜrkel, Izhar U H Khan, Amir Abdulmawjood
{"title":"图尔基耶中部地区重症监护室患者耐万古霉素肠球菌分离物的表型和基因型流行病学特征。","authors":"Altan Akineden, Cemal ÇiÇek, SelÇuk TÜrkel, Izhar U H Khan, Amir Abdulmawjood","doi":"10.33073/pjm-2024-030","DOIUrl":null,"url":null,"abstract":"<p><p>Vancomycin-resistant <i>Enterococcus faecium</i> (VRE) has been detected in Türkiye. Only limited information is available on its dissemination in the central regions of the country. This study describes the first epidemiological characterization of VRE clinical isolates detected in patients in a hospital in the province of Aksaray. In this one-year study conducted between 2021 and 2022, stool samples from intensive care unit patients were screened for VRE using the phenotypic E-test method, and the antibiotic sensitivity test was analyzed by using the VITEK<sup>®</sup> 2 system. A molecular assay for confirmation of species level was carried out by 16S rRNA gene-based sequencing and testing for antibiotic resistance (<i>van</i>A or <i>van</i>B) and virulence factor-encoding genes (<i>esp, asa1</i>, and <i>hyl</i>). Further, genotypic characterization was determined by macro-restriction fragment pattern analysis (MRFPA) of genomic DNA digested with <i>Sma</i>I restriction enzyme. Of the total 350 <i>Enterococcus</i> positive patients from different hospital intensive care units, 22 (6.3%) were positive for VRE using the phenotypic E-test method. All isolates showed resistance to ampicillin, ciprofloxacin, vancomycin, and teicoplanin and positive amplification for the <i>van</i>A gene. However, none of the isolates was positive for the <i>van</i>B gene. The most prevalent virulence gene was <i>esp</i>. The results indicate that the isolates are persistent in the hospital environment and subsequently transmitted to hospitalized patients, thus representing challenges to an outbreak and infection control. These study results would also help formulate more effective strategies to reduce the transmission and propagation of VRE contamination in various hospital settings.</p>","PeriodicalId":94173,"journal":{"name":"Polish journal of microbiology","volume":"73 3","pages":"403-410"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11395416/pdf/","citationCount":"0","resultStr":"{\"title\":\"Pheno- and Genotypic Epidemiological Characterization of Vancomycin-Resistant <i>Enterococcus faecium</i> Isolates from Intensive Care Unit Patients in Central Türkiye.\",\"authors\":\"Altan Akineden, Cemal ÇiÇek, SelÇuk TÜrkel, Izhar U H Khan, Amir Abdulmawjood\",\"doi\":\"10.33073/pjm-2024-030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Vancomycin-resistant <i>Enterococcus faecium</i> (VRE) has been detected in Türkiye. 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引用次数: 0
摘要
在土耳其发现了耐万古霉素肠球菌(VRE)。有关该菌在该国中部地区传播的信息十分有限。本研究首次描述了在阿克萨赖省一家医院的患者中检测到的 VRE 临床分离株的流行病学特征。在这项于 2021 年至 2022 年进行的为期一年的研究中,使用表型 E 测试法对重症监护病房患者的粪便样本进行了弧菌病毒筛查,并使用 VITEK® 2 系统进行了抗生素敏感性测试分析。通过基于 16S rRNA 基因的测序和抗生素耐药性(vanA 或 vanB)及毒力因子编码基因(esp、asa1 和 hyl)检测,进行分子检测以确认物种水平。此外,还通过对用 SmaI 限制性酶消化的基因组 DNA 进行宏限制性片段模式分析(MRFPA)来确定基因型特征。在来自不同医院重症监护室的 350 名肠球菌阳性患者中,有 22 人(6.3%)通过表型 E 测试法检测出疱疹病毒阳性。所有分离株都显示出对氨苄西林、环丙沙星、万古霉素和替考拉宁的耐药性,并显示出 vanA 基因的阳性扩增。然而,没有一个分离物的 vanB 基因呈阳性。结果表明,这些分离物在医院环境中具有持久性,随后会传播给住院患者,因此对疫情爆发和感染控制构成了挑战。这些研究结果还有助于制定更有效的策略,减少疱疹病毒污染在各种医院环境中的传播和扩散。
Pheno- and Genotypic Epidemiological Characterization of Vancomycin-Resistant Enterococcus faecium Isolates from Intensive Care Unit Patients in Central Türkiye.
Vancomycin-resistant Enterococcus faecium (VRE) has been detected in Türkiye. Only limited information is available on its dissemination in the central regions of the country. This study describes the first epidemiological characterization of VRE clinical isolates detected in patients in a hospital in the province of Aksaray. In this one-year study conducted between 2021 and 2022, stool samples from intensive care unit patients were screened for VRE using the phenotypic E-test method, and the antibiotic sensitivity test was analyzed by using the VITEK® 2 system. A molecular assay for confirmation of species level was carried out by 16S rRNA gene-based sequencing and testing for antibiotic resistance (vanA or vanB) and virulence factor-encoding genes (esp, asa1, and hyl). Further, genotypic characterization was determined by macro-restriction fragment pattern analysis (MRFPA) of genomic DNA digested with SmaI restriction enzyme. Of the total 350 Enterococcus positive patients from different hospital intensive care units, 22 (6.3%) were positive for VRE using the phenotypic E-test method. All isolates showed resistance to ampicillin, ciprofloxacin, vancomycin, and teicoplanin and positive amplification for the vanA gene. However, none of the isolates was positive for the vanB gene. The most prevalent virulence gene was esp. The results indicate that the isolates are persistent in the hospital environment and subsequently transmitted to hospitalized patients, thus representing challenges to an outbreak and infection control. These study results would also help formulate more effective strategies to reduce the transmission and propagation of VRE contamination in various hospital settings.