Identification of antimicrobial peptides from the human gut microbiome using deep learning

被引:275
作者
Ma, Yue [1 ,2 ]
Guo, Zhengyan [3 ,4 ]
Xia, Binbin [1 ,2 ]
Zhang, Yuwei [2 ,3 ]
Liu, Xiaolin [1 ,2 ]
Yu, Ying [1 ,2 ]
Tang, Na [2 ,3 ]
Tong, Xiaomei [1 ]
Wang, Min [2 ,3 ]
Ye, Xin [1 ,2 ]
Feng, Jie [2 ,3 ]
Chen, Yihua [2 ,3 ]
Wang, Jun [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Chinese Acad Sci, Inst Microbiol, State Key Lab Microbial Resources, Beijing, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biotechnol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
5;
D O I
10.1038/s41587-022-01226-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The human gut microbiome encodes a large variety of antimicrobial peptides (AMPs), but the short lengths of AMPs pose a challenge for computational prediction. Here we combined multiple natural language processing neural network models, including LSTM, Attention and BERT, to form a unified pipeline for candidate AMP identification from human gut microbiome data. Of 2,349 sequences identified as candidate AMPs, 216 were chemically synthesized, with 181 showing antimicrobial activity (a positive rate of >83%). Most of these peptides have less than 40% sequence homology to AMPs in the training set. Further characterization of the 11 most potent AMPs showed high efficacy against antibiotic-resistant, Gram-negative pathogens and demonstrated significant efficacy in lowering bacterial load by more than tenfold against a mouse model of bacterial lung infection. Our study showcases the potential of machine learning approaches for mining functional peptides from metagenome data and accelerating the discovery of promising AMP candidate molecules for in-depth investigations. © 2022, The Author(s), under exclusive licence to Springer Nature America, Inc.
引用
收藏
页码:921 / 931
页数:11
相关论文
共 5 条
[1]   An Autoimmunogenic and Proinflammatory Profile Defined by the Gut Microbiota of Patients With Untreated Systemic Lupus Erythematosus [J].
Zhang, Xuan .
ARTHRITIS & RHEUMATOLOGY, 2021, 73 (02) :A20-A20
[2]   Antimicrobial Resistance in ESKAPE Pathogens [J].
De Oliveira, David M. P. ;
Forde, Brian M. ;
Kidd, Timothy J. ;
Harris, Patrick N. A. ;
Schembri, Mark A. ;
Beatson, Scott A. ;
Paterson, David L. ;
Walker, Mark J. .
CLINICAL MICROBIOLOGY REVIEWS, 2020, 33 (03)
[3]   Antimicrobial peptides: Application informed by evolution [J].
Lazzaro, Brian P. ;
Zasloff, Michael ;
Rolff, Jens .
SCIENCE, 2020, 368 (6490) :487-+
[4]  
Li J., 2019, MINING HUMAN TONSILL, DOI 10.1101/719807
[5]   Large-Scale Analyses of Human Microbiomes Reveal Thousands of Small, Novel Genes [J].
Sberro, Hila ;
Fremin, Brayon J. ;
Zlitni, Soumaya ;
Edfors, Fredrik ;
Greenfield, Nicholas ;
Snyder, Michael P. ;
Pavlopoulos, Georgios A. ;
Kyrpides, Nikos C. ;
Bhatt, Ami S. .
CELL, 2019, 178 (05) :1245-+