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本文引用的文献

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Development of a bacteriophage cocktail with high specificity against high-risk avian pathogenic Escherichia coli.一种对高危禽致病性大肠杆菌具有高特异性的噬菌体鸡尾酒的研发。
Poult Sci. 2025 Jun;104(6):105038. doi: 10.1016/j.psj.2025.105038. Epub 2025 Mar 18.
2
Inferring strain-level mutational drivers of phage-bacteria interaction phenotypes arising during coevolutionary dynamics.推断在共同进化动力学过程中出现的噬菌体-细菌相互作用表型的菌株水平突变驱动因素。
Virus Evol. 2024 Nov 29;10(1):veae104. doi: 10.1093/ve/veae104. eCollection 2024.
3
Prediction of strain level phage-host interactions across the Escherichia genus using only genomic information.仅使用基因组信息预测整个大肠埃希氏菌属中噬菌体-宿主相互作用的应变水平。
Nat Microbiol. 2024 Nov;9(11):2847-2861. doi: 10.1038/s41564-024-01832-5. Epub 2024 Oct 31.
4
Phage therapy: an alternative treatment modality for MDR bacterial infections.噬菌体疗法:治疗多重耐药菌感染的一种替代疗法。
Infect Dis (Lond). 2024 Oct;56(10):785-817. doi: 10.1080/23744235.2024.2379492. Epub 2024 Jul 17.
5
Prediction of Klebsiella phage-host specificity at the strain level.预测克雷伯氏菌噬菌体在菌株水平上的宿主特异性。
Nat Commun. 2024 May 22;15(1):4355. doi: 10.1038/s41467-024-48675-6.
6
Inferring strain-level mutational drivers of phage-bacteria interaction phenotypes arising during coevolutionary dynamics.推断在共同进化动力学过程中出现的噬菌体-细菌相互作用表型的菌株水平突变驱动因素。
bioRxiv. 2024 Nov 21:2024.01.08.574707. doi: 10.1101/2024.01.08.574707.
7
Phages overcome bacterial immunity via diverse anti-defence proteins.噬菌体通过多种抗防御蛋白克服细菌免疫。
Nature. 2024 Jan;625(7994):352-359. doi: 10.1038/s41586-023-06869-w. Epub 2023 Nov 22.
8
Rapid bacteria-phage coevolution drives the emergence of multiscale networks.快速的细菌-噬菌体共同进化驱动多尺度网络的出现。
Science. 2023 Nov 10;382(6671):674-678. doi: 10.1126/science.adi5536. Epub 2023 Nov 9.
9
Development and characterization of a bacteriophage cocktail with high lytic efficacy against field-isolated Salmonella enterica.开发并鉴定了一种具有高效裂解活性的噬菌体鸡尾酒,可有效对抗分离自现场的沙门氏菌。
Poult Sci. 2023 Dec;102(12):103125. doi: 10.1016/j.psj.2023.103125. Epub 2023 Sep 18.
10
GSPHI: A novel deep learning model for predicting phage-host interactions via multiple biological information.GSPHI:一种通过多种生物信息预测噬菌体-宿主相互作用的新型深度学习模型。
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一种预测菌株特异性噬菌体-宿主相互作用的机器学习方法。

A machine learning approach to predict strain-specific phage-host interactions.

作者信息

Camejo Pamela Yael, Rojas Felipe, Ossa Antonio, Hurtado Rodrigo, Tichy Daniel, Pieringer Christian, Pino Michael, Mora-Uribe Paola, Ulloa Soledad, Norambuena Rodrigo, Tobar-Calfucoy Eduardo, Aguilera Matías, Rojas-Martínez Victoria, Cifuentes Onix, Sabag Andrea, Cifuentes Nicolas, San Martín Daniel, Infante Claudia, Cifuentes Pablo, Pieringer Hans, León Luis E

机构信息

PhageLab Chile SpA, Santiago, Chile.

出版信息

Sci Rep. 2025 Oct 31;15(1):38249. doi: 10.1038/s41598-025-22075-2.

DOI:10.1038/s41598-025-22075-2
PMID:41174147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12579225/
Abstract

The use of bacteriophages for biological control of bacterial infections is a promising approach to combat antimicrobial resistant bacteria. Prediction of phage-bacteria interactions is key to identify sensitive bacterial strains to phage therapy. Since these interactions are governed by multiple biological mechanisms, it is not a simple task to predict the outcome of a phage infection, which varies even among strains from the same species. In this study, machine learning-based models capable of predicting the host range of phages from sequencing data were developed. Models were trained using phage-bacteria protein-protein interactions (PPI), predicted from PPI databases, and a host-range dataset obtained from experimental assays with 10 Salmonella enterica and 3 Escherichia coli bacteriophages. The performance of prediction models differed among bacteriophages, ranging from 78 to 92% of accuracy in the case of Salmonella and 84-94% in Escherichia phages, with the highest accuracy (94%) achieved for E. coli phage CBDS-07. Results demonstrated the effectiveness of using PPI as a feature to design ML models for phage-bacteria phenotype prediction.

摘要

利用噬菌体对细菌感染进行生物控制是对抗抗菌耐药菌的一种有前景的方法。预测噬菌体与细菌的相互作用是确定对噬菌体疗法敏感的细菌菌株的关键。由于这些相互作用受多种生物学机制支配,预测噬菌体感染的结果并非易事,即使在同一物种的菌株之间结果也会有所不同。在本研究中,开发了基于机器学习的模型,能够从测序数据预测噬菌体的宿主范围。使用从PPI数据库预测的噬菌体-细菌蛋白质-蛋白质相互作用(PPI)以及通过对10种肠炎沙门氏菌和3种大肠杆菌噬菌体进行实验分析获得的宿主范围数据集对模型进行训练。预测模型的性能在不同噬菌体之间存在差异,沙门氏菌噬菌体的准确率在78%至92%之间,大肠杆菌噬菌体的准确率在84%至94%之间,其中大肠杆菌噬菌体CBDS-07的准确率最高(94%)。结果证明了使用PPI作为特征来设计用于噬菌体-细菌表型预测的机器学习模型的有效性。