Deciphering complex antibiotic resistance patterns in Helicobacter pylori through whole genome sequencing and machine learning

抗生素耐药性 背景(考古学) 生物 基因型 阿莫西林 克拉霉素 琼脂稀释 单核苷酸多态性 机器学习 计算生物学 抗药性 抗生素 人工智能 微生物学 遗传学 计算机科学 基因 最小抑制浓度 古生物学
作者
Jianwei Yu,Jia Yan,Qichao Yu,Lan Lin,Chao Li,Bowang Chen,Pingyu Zhong,Xueqing Lin,Huilan Li,Yinping Sun,Xuejing Zhong,Yuqi He,Xiaoyun Huang,Shuangming Lin,Yuanming Pan
出处
期刊:Frontiers in Cellular and Infection Microbiology [Frontiers Media SA]
卷期号:13: 1306368-1306368 被引量:10
标识
DOI:10.3389/fcimb.2023.1306368
摘要

Introduction Helicobacter pylori (H.pylori, Hp) affects billions of people worldwide. However, the emerging resistance of Hp to antibiotics challenges the effectiveness of current treatments. Investigating the genotype-phenotype connection for Hp using next-generation sequencing could enhance our understanding of this resistance. Methods In this study, we analyzed 52 Hp strains collected from various hospitals. The susceptibility of these strains to five antibiotics was assessed using the agar dilution assay. Whole-genome sequencing was then performed to screen the antimicrobial resistance (AMR) genotypes of these Hp strains. To model the relationship between drug resistance and genotype, we employed univariate statistical tests, unsupervised machine learning, and supervised machine learning techniques, including the development of support vector machine models. Results Our models for predicting Amoxicillin resistance demonstrated 66% sensitivity and 100% specificity, while those for Clarithromycin resistance showed 100% sensitivity and 100% specificity. These results outperformed the known resistance sites for Amoxicillin (A1834G) and Clarithromycin (A2147), which had sensitivities of 22.2% and 87%, and specificities of 100% and 96%, respectively. Discussion Our study demonstrates that predictive modeling using supervised learning algorithms with feature selection can yield diagnostic models with higher predictive power compared to models relying on single single-nucleotide polymorphism (SNP) sites. This approach significantly contributes to enhancing the precision and effectiveness of antibiotic treatment strategies for Hp infections. The application of whole-genome sequencing for Hp presents a promising pathway for advancing personalized medicine in this context.
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