Investigation of metronidazole resistance-associated mutations and virulence genotypes in helicobacter pylori isolates from the Egyptian population: A cross-sectional study.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Infection and Chemotherapy Pub Date : 2024-10-02 DOI:10.1016/j.jiac.2024.10.001
Mohamed S Hemeda, Heba A Elsayed, ALMoatazbellah Mahmoud Elsayed Mohamad, Moustafa M Ibrahim, Alsayed Magdi Alsayed Farahat, Abdel Rahman Z Abdel Rahman, Bassam Mansour Salama, Ghada Mostafa Badawy, Ahmed I Amin, Mona Ibrahim Elyamany, Hatem Ali Ahmed Abdelmottaleb, Mohamed A Ibrahim, Aldosoky Abd Elaziz Alsaid, Ahmed A Elhagary, Mostafa I El-Amir
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Abstract

Introduction: This cross-sectional study assesses the prevalence of metronidazole resistance-associated mutations and virulence genotypes in Helicobacter pylori (H. pylori) strains isolated from the Egyptian population. H. pylori infection is a significant public health concern, with antibiotic resistance challenging its eradication.

Methods: Gastric biopsy samples were collected from symptomatic patients referred for upper gastrointestinal endoscopy at selected healthcare facilities. The study included 250 participants with symptoms suggestive of H. pylori infection and aged 18 years or older. Biopsy samples were obtained using standard endoscopic techniques, and H. pylori strains were isolated and identified in the laboratory. Antimicrobial susceptibility testing was conducted using standard methods. Molecular analysis, including polymerase chain reaction (PCR) and sequencing, was performed to identify metronidazole resistance-associated mutations (rdxA and frxA) and virulence genotypes (cagA and vacA).

Results: Antimicrobial susceptibility testing revealed that 43.6 % of the isolates were resistant to metronidazole, while 11.8 %, 4.5 %, and 55.4 % were resistant to clarithromycin, amoxicillin, and levofloxacin. Molecular analysis identified rdxA and frxA mutations in 36.3 % and 31.8 % of the isolates, respectively, indicating metronidazole resistance-associated mutations. Additionally, 60.0 % of the isolates were positive for the cagA gene, and 80.0 % had the vacA s1 type, both associated with increased virulence. A significant association was found between metronidazole resistance and the presence of cagA gene, vacA s1 type, rdxA mutation, and frxA mutation. Statistical analysis revealed associations between specific mutations and virulence genotypes with respective odds ratios, indicating higher likelihoods of metronidazole resistance in isolates exhibiting these genetic characteristics.

Conclusions: This study highlights the prevalence of metronidazole resistance and the association between specific mutations and virulence genotypes in H. pylori strains isolated from the Egyptian population. The findings underscore the importance of monitoring antibiotic resistance patterns and understanding the genetic determinants of virulence in H. pylori for effective management and treatment strategies.

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埃及人群幽门螺旋杆菌甲硝唑耐药性相关突变和病毒基因型调查:一项横断面研究。
导言:这项横断面研究评估了从埃及人群中分离出的幽门螺杆菌(H. pylori)菌株中甲硝唑耐药性相关突变和毒力基因型的流行情况。幽门螺杆菌感染是一个重大的公共卫生问题,抗生素耐药性给根除幽门螺杆菌带来了挑战:方法:在选定的医疗机构收集转诊至上消化道内窥镜检查的有症状患者的胃活检样本。研究对象包括 250 名有幽门螺杆菌感染症状且年龄在 18 岁或以上的患者。采用标准内窥镜技术获取活检样本,并在实验室中分离和鉴定幽门螺杆菌菌株。采用标准方法进行抗菌药物药敏试验。分子分析包括聚合酶链反应(PCR)和测序,以确定甲硝唑耐药性相关突变(rdxA 和 frxA)和毒力基因型(cagA 和 vacA):结果:抗菌药敏感性检测显示,43.6%的分离株对甲硝唑耐药,11.8%、4.5%和55.4%的分离株对克拉霉素、阿莫西林和左氧氟沙星耐药。分子分析分别在 36.3% 和 31.8% 的分离物中发现了 rdxA 和 frxA 突变,表明与甲硝唑耐药性相关的突变。此外,60.0%的分离株的 cagA 基因呈阳性,80.0%的分离株具有 vacA s1 型,这两种基因都与毒力增强有关。研究发现,甲硝唑耐药性与 cagA 基因、vacA s1 型、rdxA 突变和 frxA 突变之间存在明显关联。统计分析表明,特定突变和毒力基因型之间存在关联,并具有各自的几率比,这表明具有这些基因特征的分离物对甲硝唑耐药的可能性更高:本研究强调了从埃及人群中分离出的幽门螺杆菌菌株对甲硝唑耐药的普遍性以及特定突变和毒力基因型之间的关联。这些发现强调了监测抗生素耐药性模式和了解幽门螺杆菌毒力基因决定因素对有效管理和治疗策略的重要性。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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