Genetic variations of penicillin-binding protein 1A: insights into the current status of amoxicillin-based regimens for Helicobacter pylori eradication in Malaysia.

Heng Kang Ng, Kek Heng Chua, Boon Pin Kee, Kee Huat Chuah, Lip Yee Por, Suat Moi Puah
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Abstract

Introduction. Resistance towards amoxicillin in Helicobacter pylori causes significant therapeutic impasse in healthcare settings worldwide. In Malaysia, the standard H. pylori treatment regimen includes a 14-day course of high-dose proton-pump inhibitor (rabeprazole, 20 mg) with amoxicillin (1000 mg) dual therapy.Hypothesis/Gap Statement. The high eradication rate with amoxicillin-based treatment could be attributed to the primary resistance rates of amoxicillin being relatively low at 0%, however, a low rate of secondary resistance has been documented in Malaysia recently.Aim. This study aims to investigate the amino acid mutations and related genetic variants in PBP1A of H. pylori, correlating with amoxicillin resistance in the Malaysian population.Methodology. The full-length pbp1A gene was amplified via PCR from 50 genomic DNA extracted from gastric biopsy samples of H. pylori-positive treatment-naïve Malaysian patients. The sequences were then compared with reference H. pylori strain ATCC 26695 for mutation and variant detection. A phylogenetic analysis of 50 sequences along with 43 additional sequences from the NCBI database was performed. These additional sequences included both amoxicillin-resistant strains (n=20) and amoxicillin-sensitive strains (n=23).Results. There was a total of 21 variants of amino acids, with three of them located in or near the PBP-motif (SKN402-404). The percentages of these three variants are as follows: K403X, 2%; S405I, 2% and E406K, 16%. Based on the genetic markers identified, the resistance rate for amoxicillin in our sample remained at 0%. The phylogenetic examination suggested that H. pylori might exhibit unique conserved pbp1A sequences within the Malaysian context.Conclusions. Overall, the molecular analysis of PBP1A supported the therapeutic superiority of amoxicillin-based regimens. Therefore, it is crucial to continue monitoring the amoxicillin resistance background of H. pylori with a larger sample size to ensure the sustained effectiveness of amoxicillin-based treatments in Malaysia.

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青霉素结合蛋白 1A 的基因变异:马来西亚以阿莫西林为基础的根除幽门螺旋杆菌疗法现状的启示。
导言。幽门螺旋杆菌对阿莫西林的耐药性导致全球医疗机构的治疗陷入僵局。在马来西亚,幽门螺杆菌的标准治疗方案包括为期14天的大剂量质子泵抑制剂(雷贝拉唑,20毫克)和阿莫西林(1000毫克)双重疗法。以阿莫西林为基础的治疗具有较高的根除率,这可能是由于阿莫西林的原发性耐药率相对较低,仅为0%,然而,最近在马来西亚也有低继发性耐药率的记录。本研究旨在调查马来西亚人群中幽门螺杆菌 PBP1A 的氨基酸突变和相关基因变异与阿莫西林耐药性的相关性。从马来西亚幽门螺杆菌阳性、未经治疗的患者的胃活检样本中提取 50 个基因组 DNA,通过 PCR 扩增出全长 pbp1A 基因。然后将序列与参考幽门螺杆菌菌株 ATCC 26695 进行比较,以检测突变和变异。对 50 个序列和来自 NCBI 数据库的 43 个附加序列进行了系统发生学分析。这些额外的序列包括耐阿莫西林菌株(n=20)和阿莫西林敏感菌株(n=23)。共有 21 个氨基酸变体,其中三个位于 PBP-motif(SKN402-404)或其附近。这三种变体的百分比如下:K403X,2%;S405I,2%;E406K,16%。根据已确定的遗传标记,样本中阿莫西林的耐药率仍为 0%。系统发生学研究表明,幽门螺杆菌在马来西亚可能表现出独特的pbp1A保守序列。总之,PBP1A 的分子分析支持了以阿莫西林为基础的治疗方案的优越性。因此,继续监测幽门螺杆菌的阿莫西林耐药性背景并扩大样本量以确保阿莫西林疗法在马来西亚的持续有效性至关重要。
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