Using core genome and machine learning for serovar prediction in Salmonella enterica subspecies I strains.

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Xiang Li, Adelumola Oladeinde, Michael Rothrock, Tae Jung Chung, Walid Ghazi Al Hakeem
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引用次数: 0

Abstract

This study presents a dual investigation of Salmonella enterica subspecies I, focusing on serovar prediction and core genome characteristics. We utilized two large genomic datasets (panX and NCBI Pathogen Detection) to test machine learning methods for predicting Salmonella serovars based on genomic differences. Among the four tested algorithms, the Random Forest model demonstrated higher performance, achieving 90.3% accuracy with the panX dataset and 95.3% with the NCBI dataset, particularly effective when trained on >50% of available data. When combined with hierarchical clustering validation, our approach achieved 100% prediction accuracy on the simulated data. Parallel analysis of panX core genome characteristics revealed that pathogenicity-related genes (including sseA, invA, mgtC, phoP, phoQ, and sitA) exhibited similar phylogenetic topologies distinct from the core genome phylogenetic tree, suggesting shared evolutionary histories. Notably, all identified core antibiotic resistance genes and virulence factors showed evidence of negative selection, indicating their essential role in bacterial survival. This study not only presents a promising machine learning-based alternative for Salmonella serovar classification, particularly valuable when analyzing newly identified serovars alongside known reference strains but also provides insights into the evolutionary dynamics of core virulence-associated genes, contributing to our understanding of Salmonella genomic architecture and pathogenicity.

利用核心基因组和机器学习预测肠沙门氏菌I亚种菌株的血清型。
本研究提出了肠道沙门氏菌I亚种的双重调查,重点是血清型预测和核心基因组特征。我们利用两个大型基因组数据集(panX和NCBI病原体检测)来测试基于基因组差异预测沙门氏菌血清型的机器学习方法。在四种测试算法中,随机森林模型表现出更高的性能,在panX数据集上达到90.3%的准确率,在NCBI数据集上达到95.3%的准确率,当在50%的可用数据上训练时尤其有效。结合分层聚类验证,该方法对模拟数据的预测准确率达到100%。对panX核心基因组特征的平行分析显示,致病性相关基因(包括sseA、invA、mgtC、phoP、phoQ和sitA)具有与核心基因组系统发育树不同的相似系统发育拓扑结构,表明具有共同的进化历史。值得注意的是,所有鉴定出的核心抗生素耐药基因和毒力因子都显示出负选择的证据,表明它们在细菌生存中起着重要作用。这项研究不仅为沙门氏菌血清型分类提供了一种有前途的基于机器学习的替代方法,在分析新发现的血清型和已知参考菌株时尤其有价值,而且还提供了对核心毒力相关基因进化动力学的见解,有助于我们对沙门氏菌基因组结构和致病性的理解。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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