Frequent high-level rifaximin resistance in Escherichia coli associated with long-term treatment of patients with liver cirrhosis: a prospective, controlled study.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
L Boll, W V Kern, S Schuster, M Schultheiß, C Schneider, M Vavra, R Thimme, S Rieg, J Camp
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Abstract

We conducted a prospective, controlled study to assess the prevalence of high-level rifaximin resistance in intestinal Escherichia coli (E. coli) among patients with liver cirrhosis (LC). Rectal swabs were collected from consenting adult LC patients at Freiburg University Medical Center. Swabs were cultured on MacConkey agar plates supplemented with rifaximin at two concentrations (32 µg/mL and 256 µg/mL), and pink/red colonies were identified as E. coli using standard methods. Minimum inhibitory concentrations (MICs) of rifaximin and a panel of additional agents were determined using microdilution assays. Of the 100 patients enrolled, 49 received rifaximin (median duration 22 weeks), and 51 served as controls. Patients receiving rifaximin had more advanced LC (Child B/C, 75% vs. 50%) and more frequent concurrent antibiotic use (22% vs. 12%). High-level rifaximin-resistant E. coli strains were recovered from 67% (33/49) of rifaximin-treated patients, compared to 12% (6/51) of controls (P < 0.001). Cross-resistance to rifampicin was complete, with no clear associations with other resistance phenotypes. A subset of five high-level resistance swabs was assessed for homogeneity of colonization by randomly picking E. coli strains from a non-supplemented MacConkey agar plate. Homogeneous colonization with high-level rifaximin-resistant E. coli was found in 80% of cases. The prevalence of high-level rifaximin-resistant intestinal E. coli in LC patients on long-term rifaximin treatment is extremely high (67% vs. 12%). While rifaximin may remain effective in preventing hepatic encephalopathy (HE), its potential use in preventing spontaneous bacterial peritonitis might be severely limited by the emergence of resistance.IMPORTANCEThis study highlights the emergence of antibiotic-resistant E. coli as an important consequence of long-term rifaximin use in patients with liver cirrhosis: the development of antibiotic resistance in gut bacteria. Rifaximin is commonly used to prevent complications like hepatic encephalopathy (HE) by targeting gut bacteria. However, this research shows that prolonged use can lead to the emergence of highly resistant E. coli strains, potentially compromising the drug's effectiveness and limiting its utility in preventing HE and infections, such as spontaneous bacterial peritonitis. By identifying specific resistance patterns and genetic mutations, this study highlights the need for cautious use of rifaximin and further research into balancing its benefits with the risks of resistance. These findings contribute to a broader understanding of how antibiotics affect gut bacteria over time and offer a basis for exploring strategies to preserve the effectiveness of this important medication for patients with advanced liver disease.

与肝硬化患者长期治疗相关的大肠杆菌频繁的高水平利福昔明耐药:一项前瞻性对照研究
我们进行了一项前瞻性对照研究,以评估肝硬化(LC)患者肠道大肠杆菌(E. coli)对利福昔明的高水平耐药性。直肠拭子采集自弗莱堡大学医学中心同意的成年LC患者。拭子在添加利福昔明(32µg/mL和256µg/mL)两种浓度的MacConkey琼脂板上培养,采用标准方法鉴定粉红色/红色菌落为大肠杆菌。最低抑制浓度(mic)利福昔明和一组额外的药物确定使用微量稀释试验。在入组的100例患者中,49例接受利福昔明治疗(中位持续时间22周),51例作为对照。接受利福昔明治疗的患者有更多的晚期LC(儿童B/C, 75%对50%)和更频繁的同时使用抗生素(22%对12%)。在接受利福昔明治疗的患者中,检出了67%(33/49)的高水平利福昔明耐药大肠杆菌菌株,而在对照组中,这一比例为12% (6/51)(P < 0.001)。对利福平的交叉耐药是完全的,与其他耐药表型没有明确的关联。通过从未添加的麦康基琼脂平板上随机挑选大肠杆菌菌株,评估5个高水平耐药拭子的定殖均匀性。在80%的病例中发现了高水平利福昔明耐药大肠杆菌的均匀定植。在长期接受利福昔明治疗的LC患者中,高水平利福昔明耐药肠道大肠杆菌的患病率极高(67%对12%)。虽然利福昔明在预防肝性脑病(HE)方面可能仍然有效,但由于耐药性的出现,其在预防自发性细菌性腹膜炎方面的潜在应用可能受到严重限制。这项研究强调了耐抗生素大肠杆菌的出现是肝硬化患者长期使用利福昔明的一个重要后果:肠道细菌中抗生素耐药性的发展。利福昔明通常用于通过靶向肠道细菌来预防肝性脑病(HE)等并发症。然而,这项研究表明,长期使用可能导致高耐药性大肠杆菌菌株的出现,这可能会损害药物的有效性,并限制其在预防HE和感染(如自发性细菌性腹膜炎)方面的应用。通过确定特定的耐药模式和基因突变,本研究强调需要谨慎使用利福昔明,并进一步研究平衡其益处与耐药风险。这些发现有助于更广泛地了解抗生素如何随着时间的推移影响肠道细菌,并为探索策略提供基础,以保持这种重要药物对晚期肝病患者的有效性。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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