Evidence map›Paper›PMID 39825096›Full record

ArticleNature microbiology2025

Explainable deep learning and virtual evolution identifies antimicrobial peptides with activity against multidrug-resistant human pathogens.

Beilun Wang, Peijun Lin, Yuwei Zhong, Xiao Tan, Yangyang Shen, Yi Huang, Kai Jin, Yan Zhang, Ying Zhan, Dian Shen and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed.

  1. Artificial intelligence catalyzes antimicrobial peptide design.Synthetic and systems biotechnology · 2027
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Beilun Wang *School of Computer Science and Engineering, Southeast University, Nanjing, China. beilun@seu.edu.cn.ORCID http://orcid.org/0000-0002-2646-1492
Peijun Lin *School of Computer Science and Engineering, Southeast University, Nanjing, China.
Yuwei Zhong *School of Environmental and Chemical Engineering, Shanghai University, Shanghai, China.
Xiao TanSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Yangyang ShenSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Yi HuangSchool of Environmental and Chemical Engineering, Shanghai University, Shanghai, China.
Kai JinSchool of Environmental and Chemical Engineering, Shanghai University, Shanghai, China.
Yan ZhangSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Ying ZhanSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Dian ShenSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Meng WangXAI Lab, College of Design and Innovation, Tongji University, Shanghai, China.
Zhou YuComputer Science Department, Columbia University, New York, NY, USA. zy2461@columbia.edu.ORCID http://orcid.org/0000-0002-1524-5890
Yihan WuSchool of Environmental and Chemical Engineering, Shanghai University, Shanghai, China. yihanw@shu.edu.cn.ORCID http://orcid.org/0000-0002-0776-8421

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32000036National Natural Science Foundation of China (National Science Foundation of China) 61972085
6 · The paper itself

Abstract

Artificial intelligence (AI) is a promising approach to identify new antimicrobial compounds in diverse microbial species. Here we developed an AI-based, explainable deep learning model, EvoGradient, that predicts the potency of antimicrobial peptides (AMPs) and virtually modifies peptide sequences to produce more potent AMPs, akin to in silico directed evolution. We applied this model to peptides encoded in low-abundance human oral bacteria, resulting in the virtual evolution of 32 peptides into potent AMPs. Of these, the 6 most effective were synthesized and tested against multidrug-resistant pathogens and demonstrated activity against carbapenem-resistant species Escherichia coli, Klebsiella pneumoniae and Acinetobacter baumannii, and vancomycin-resistant Enterococcus faecium. The most potent AMP, pep-19-mod, was validated in vivo, achieving over 95% reduction in bacterial loads in mouse models of thigh infection through both systemic and local administration. Our approach advances the automatic identification and optimization of AMPs.

Indexed as

Anti-Bacterial AgentsAntimicrobial PeptidesBacteriaDeep LearningDrug Resistance, Multiple, BacterialAcinetobacter baumanniiAnimalsEnterococcus faeciumEscherichia coliHumansKlebsiella pneumoniaeMiceMicrobial Sensitivity TestsAnti-Bacterial AgentsAntimicrobial Peptides

Identifiers

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.