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从血液培养物和相应的粪便标本中分离到的大肠杆菌中发现的广谱β-内酰胺酶。

Extended-spectrum beta-lactamases found in Escherichia coli isolates obtained from blood cultures and corresponding stool specimen.

机构信息

Institute Medical Microbiology and Virology, Microbiology Department, Leipzig University, Johannisallee 30, 04103, Leipzig, Germany.

出版信息

Sci Rep. 2023 Jun 2;13(1):8940. doi: 10.1038/s41598-023-36240-y.

Abstract

With extended-spectrum β-lactamases (ESBLs) and CTX-M enzymes being on the rise, antimicrobial treatment of enterobacterial infections is becoming more and more challenging. Our study aimed at a molecular characterization of phenotypically ESBL-positive E. coli strains obtained from blood cultures of patients of the University Hospital of Leipzig (UKL), Germany. The presence of CMY-2, CTX-M-14 and CTX-M-15 was investigated using Streck ARM-D Kit (Streck, USA). Real-time amplifications were performed by QIAGEN Rotor-Gene Q MDx Thermocycler (QIAGEN, Thermo Fisher Scientific, USA). Antibiograms as well as epidemiological data were evaluated. Among 117 cases, 74.4% of the isolates showed a resistance to ciprofloxacin, piperacillin and ceftazidime or cefotaxime while being susceptible to imipenem/meropenem. The proportion of ciprofloxacin resistance was significantly higher than the proportion of ciprofloxacin susceptibility. At least one of the investigated genes was detected in 93.1% of the blood culture E. coli isolates: CTX-M-15 (66.7%), CTX-M-14 (25.6%) or the plasmid-mediated ampC gene CMY-2 (3.4%). 2.6% were tested positive for two resistance genes. 94 of the corresponding stool specimens tested positive for ESBL producing E. coli (94/112, 83.9%). 79 (79/94, 84%) E. coli strains found in the stool samples matched with the respective patient's blood culture isolate phenotypically (MALDI-TOF, antibiogram). The distribution of resistance genes was in accordance with recent studies in Germany as well as worldwide. This study provides indications of an endogenous focus of infection and emphasize the importance of screening programs for high-risk patients.

摘要

随着广谱β-内酰胺酶(ESBLs)和 CTX-M 酶的出现,肠杆菌感染的抗菌治疗变得越来越具有挑战性。我们的研究旨在对德国莱比锡大学医院(UKL)血培养中分离出的表型 ESBL 阳性大肠杆菌菌株进行分子特征分析。使用 Streck ARM-D 试剂盒(Streck,美国)检测 CMY-2、CTX-M-14 和 CTX-M-15 的存在。通过 QIAGEN Rotor-Gene Q MDx 热循环仪(QIAGEN,Thermo Fisher Scientific,美国)进行实时扩增。评估抗生素谱和流行病学数据。在 117 例病例中,74.4%的分离株对环丙沙星、哌拉西林和头孢他啶或头孢噻肟表现出耐药性,而对亚胺培南/美罗培南敏感。耐环丙沙星的比例明显高于耐环丙沙星的比例。在血液培养的大肠杆菌分离株中,至少检测到一种被研究基因的比例为 93.1%:CTX-M-15(66.7%)、CTX-M-14(25.6%)或质粒介导的 ampC 基因 CMY-2(3.4%)。有 2.6%的分离株检测到两种耐药基因呈阳性。在 112 个对应的粪便标本中,有 94 个(94/112,83.9%)检测出产 ESBL 的大肠杆菌呈阳性。在粪便样本中发现的 79 株(79/94,84%)大肠杆菌与相应患者的血培养分离株表型一致(MALDI-TOF,抗生素谱)。耐药基因的分布与德国以及全球最近的研究一致。这项研究提供了感染内源性焦点的迹象,并强调了对高危患者进行筛查计划的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6913/10238490/0b2a8e4626df/41598_2023_36240_Fig1_HTML.jpg

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