Helicobacter pylori infection and antibiotic resistance - from biology to clinical implications

被引:316
|
作者
Tshibangu-Kabamba, Evariste [1 ]
Yamaoka, Yoshio [1 ,2 ]
机构
[1] Oita Univ, Fac Med, Dept Environm & Prevent Med, Oita, Japan
[2] Baylor Coll Med, Gastroenterol & Hepatol Sect, Dept Med, Houston, TX 77030 USA
基金
日本学术振兴会;
关键词
23S RIBOSOMAL-RNA; MUTATIONS CONFERRING RESISTANCE; COMPETITIVE ACID BLOCKER; TIME PCR ASSAY; CLARITHROMYCIN RESISTANCE; METRONIDAZOLE RESISTANCE; POINT MUTATIONS; BIOFILM FORMATION; REAL-TIME; AMOXICILLIN RESISTANCE;
D O I
10.1038/s41575-021-00449-x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Helicobacter pylori is a major human pathogen for which increasing antibiotic resistance constitutes a serious threat to human health. Molecular mechanisms underlying this resistance have been intensively studied and are discussed in this Review. Three profiles of resistance- single drug resistance, multidrug resistance and heteroresistance -seem to occur, probably with overlapping fundamental mechanisms and clinical implications. The mechanisms that have been most studied are related to mutational changes encoded chromosomally and disrupt the cellular activity of antibiotics through target-mediated mechanisms. Other biological attributes driving drug resistance in H. pylon have been less explored and this could imply more complex physiological changes (such as impaired regulation of drug uptake and/or efflux, or biofilm and coccoid formation) that remain largely elusive. Resistance-related attributes deployed by the pathogen cause treatment failures, diagnostic difficulties and ambiguity in clinical interpretation of therapeutic outcomes. Subsequent to the increasing antibiotic resistance, a substantial drop in H. pylon treatment efficacy has been noted globally. In the absence of an efficient vaccine, enhanced efforts are needed for setting new treatment strategies and for a better understanding of the emergence and spread of drug-resistant bacteria, as well as for improving diagnostic tools that can help optimize current antimicrobial regimens.
引用
收藏
页码:613 / 629
页数:17
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