用于估计细菌种群间缺失比例的期望最大化算法,并将其应用于粪肠球菌抗生素耐药基因转移的研究。

IF 5.8 2区 生物学 Q1 MARINE & FRESHWATER BIOLOGY Marine Life Science & Technology Pub Date : 2023-01-01 Epub Date: 2023-01-31 DOI:10.1007/s42995-022-00144-z
Yu Zhang, Cong Zhang, Wenwen Huo, Xinlei Wang, Michael Zhang, Kelli Palmer, Min Chen
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引用次数: 0

摘要

细菌中抗生素耐药性的出现限制了用于治疗和感染控制的抗生素选择,从而对人类健康构成重大威胁。细菌基因组的新突变是细菌获得抗生素耐药性的重要机制。以前,细菌免疫系统中的缺失突变(长度从几十个碱基对到数千个碱基对不等)与抗生素耐药性的传播有关。目前大多数评估基因组结构变异(SV)的方法都集中在检测这些变异上,而不是估计携带不同 SV 的种群比例。我们需要更好地了解细菌种群中突变的分布和亚种群的动态,以了解抗生素耐药性的进化和耐药基因在种群中的移动。在此,我们提出了一种基于期望最大化(EM)算法和下一代测序(NGS)数据的统计模型,用于估计混合种群中基因组缺失的比例。该方法整合了插入片段大小和分裂读数映射信息,以迭代更新估计分布。对所提出的方法进行了三次模拟评估,结果表明该方法能做出准确的估计。然后将所提出的方法应用于研究抗生素抗性基因的水平转移与粪肠球菌 CRISPR-Cas 系统的变化:在线版本包含补充材料,可查阅 10.1007/s42995-022-00144-z。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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An expectation-maximization algorithm for estimating proportions of deletions among bacterial populations with application to study antibiotic resistance gene transfer in Enterococcus faecalis.

The emergence of antibiotic resistance in bacteria limits the availability of antibiotic choices for treatment and infection control, thereby representing a major threat to human health. The de novo mutation of bacterial genomes is an essential mechanism by which bacteria acquire antibiotic resistance. Previously, deletion mutations within bacterial immune systems, ranging from dozens to thousands of base pairs (bps) in length, have been associated with the spread of antibiotic resistance. Most current methods for evaluating genomic structural variations (SVs) have concentrated on detecting them, rather than estimating the proportions of populations that carry distinct SVs. A better understanding of the distribution of mutations and subpopulations dynamics in bacterial populations is needed to appreciate antibiotic resistance evolution and movement of resistance genes through populations. Here, we propose a statistical model to estimate the proportions of genomic deletions in a mixed population based on Expectation-Maximization (EM) algorithms and next-generation sequencing (NGS) data. The method integrates both insert size and split-read mapping information to iteratively update estimated distributions. The proposed method was evaluated with three simulations that demonstrated the production of accurate estimations. The proposed method was then applied to investigate the horizontal transfers of antibiotic resistance genes in concert with changes in the CRISPR-Cas system of E. faecalis.

Supplementary information: The online version contains supplementary material available at 10.1007/s42995-022-00144-z.

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来源期刊
Marine Life Science & Technology
Marine Life Science & Technology MARINE & FRESHWATER BIOLOGY-
CiteScore
9.60
自引率
10.50%
发文量
58
期刊介绍: Marine Life Science & Technology (MLST), established in 2019, is dedicated to publishing original research papers that unveil new discoveries and theories spanning a wide spectrum of life sciences and technologies. This includes fundamental biology, fisheries science and technology, medicinal bioresources, food science, biotechnology, ecology, and environmental biology, with a particular focus on marine habitats. The journal is committed to nurturing synergistic interactions among these diverse disciplines, striving to advance multidisciplinary approaches within the scientific field. It caters to a readership comprising biological scientists, aquaculture researchers, marine technologists, biological oceanographers, and ecologists.
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