Identification of Robust Antibiotic Subgroups by Integrating Multi-Species Drug-Drug Interactions

被引:3
作者
Lv, Ji [1 ,2 ]
Liu, Guixia [1 ,2 ]
Ju, Yuan [3 ]
Huang, Houhou [4 ]
Li, Dalin [5 ]
Sun, Ying [6 ]
机构
[1] Jilin Univ, Coll Comp Sci & Technol, Changchun 130000, Peoples R China
[2] Jilin Univ, Key Lab Symbol Computat & Knowledge Engn, Minist Educ, Changchun 130000, Peoples R China
[3] Sichuan Univ, Sichuan Univ Lib, Chengdu 610000, Peoples R China
[4] Jilin Univ, Coll Chem, Changchun 130000, Peoples R China
[5] Zhuhai Coll Sci & Technol, Sch Comp Sci, Zhuhai 519041, Peoples R China
[6] Jilin Univ, Dept Resp Med, Hosp 1, Changchun 130000, Peoples R China
基金
中国国家自然科学基金;
关键词
PREDICTION; INFORMATION; MECHANISM; EVOLUTION;
D O I
10.1021/acs.jcim.3c00937
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Previous studies have shown that antibiotics can be dividedintogroups, and drug-drug interactions (DDI) depend on their groups.However, these studies focused on a specific bacteria strain (i.e., Escherichia coli BW25113). Existing datasets oftencontain noise. Noisy labeled data may have a bad effect on the clusteringresults. To address this problem, we developed a multi-source informationfusion method for integrating DDI information from multiple bacterialstrains. Specifically, we calculated drug similarities based on theDDI network of each bacterial strain and then fused these drug similaritymatrices to obtain a new fused similarity matrix. The fused similaritymatrix was combined with the T-distributed stochastic neighbor embeddingalgorithm, and hierarchical clustering algorithm can effectively identifyantibiotic subgroups. These antibiotic subgroups are strongly correlatedwith known antibiotic classifications, and group-group interactionsare almost monochromatic. In summary, our method provides a promisingframework for understanding the mechanism of action of antibioticsand exploring multi-species group-group interactions.
引用
收藏
页码:4970 / 4978
页数:9
相关论文
共 47 条
[1]   The toxicity of poisons applied jointly [J].
Bliss, CI .
ANNALS OF APPLIED BIOLOGY, 1939, 26 (03) :585-615
[2]   Species-specific activity of antibacterial drug combinations [J].
Brochado, Ana Rita ;
Telzerow, Anja ;
Bobonis, Jacob ;
Banzhaf, Manuel ;
Mateus, Andre ;
Selkrig, Joel ;
Huth, Emily ;
Bassler, Stefan ;
Beas, Jordi Zamarreno ;
Zietek, Matylda ;
Ng, Natalie ;
Foerster, Sunniva ;
Ezraty, Benjamin ;
Py, Beatrice ;
Barras, Frederic ;
Savitski, Mikhail M. ;
Bork, Peer ;
Goettig, Stephan ;
Typas, Athanasios .
NATURE, 2018, 559 (7713) :259-+
[3]   Antibiotic interactions that select against resistance [J].
Chait, Remy ;
Craney, Allison ;
Kishony, Roy .
NATURE, 2007, 446 (7136) :668-671
[4]   Chemogenomics and orthology-based design of antibiotic combination therapies [J].
Chandrasekaran, Sriram ;
Cokol-Cakmak, Melike ;
Sahin, Nil ;
Yilancioglu, Kaan ;
Kazan, Hilal ;
Collins, James J. ;
Cokol, Murat .
MOLECULAR SYSTEMS BIOLOGY, 2016, 12 (05)
[5]   Bioactive triterpenoids from Sambucus java']javanica Blume [J].
Chen, Feilong ;
Liu, Dong-Li ;
Wang, Wei ;
Lv, Xiao-Man ;
Li, Weixi ;
Shao, Li-Dong ;
Wang, Wen-Jing .
NATURAL PRODUCT RESEARCH, 2020, 34 (19) :2816-2821
[6]   Chemogenomic model identifies synergistic drug combinations robust to the pathogen microenvironment [J].
Cokol, Murat ;
Li, Chen ;
Chandrasekaran, Sriram .
PLOS COMPUTATIONAL BIOLOGY, 2018, 14 (12)
[7]   Systematic exploration of synergistic drug pairs [J].
Cokol, Murat ;
Chua, Hon Nian ;
Tasan, Murat ;
Mutlu, Beste ;
Weinstein, Zohar B. ;
Suzuki, Yo ;
Nergiz, Mehmet E. ;
Costanzo, Michael ;
Baryshnikova, Anastasia ;
Giaever, Guri ;
Nislow, Corey ;
Myers, Chad L. ;
Andrews, Brenda J. ;
Boone, Charles ;
Roth, Frederick P. .
MOLECULAR SYSTEMS BIOLOGY, 2011, 7
[8]   CHARACTERIZATION AND DETECTION OF NOISE IN CLUSTERING [J].
DAVE, RN .
PATTERN RECOGNITION LETTERS, 1991, 12 (11) :657-664
[9]   A multimodal deep learning framework for predicting drug-drug interaction events [J].
Deng, Yifan ;
Xu, Xinran ;
Qiu, Yang ;
Xia, Jingbo ;
Zhang, Wen ;
Liu, Shichao .
BIOINFORMATICS, 2020, 36 (15) :4316-4322
[10]  
Duran-Frigola M, 2020, NAT BIOTECHNOL, V38, P1087, DOI 10.1038/s41587-020-0502-7