An antimicrobial peptide as a potential therapy for bacterial pneumonia that alleviates antimicrobial resistance

Bacterial pneumonia remains a global health threat that is worsened by drug-resistant bacteria, underscoring the need for the development of new antimicrobial agents. Antimicrobial peptides are promising new candidates with broad-spectrum activity and low potential for resistance development. Here, we report a linear antimicrobial peptide (AMP) that consists of four repeating units of (D-tryptophan)-(D-arginine)-(D-lysine). This peptide exhibits high stability and robust antimicrobial activity against multidrug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus and Klebsiella pneumoniae, and improved biocompatibility. Furthermore, the AMP shows low potential for resistance development and the ability to alleviate resistance and restore antibiotic sensitivity due to multiple mechanisms, including membrane targeting and non-membrane lysis (DNA binding, reactive oxygen species accumulation, ATP depletion, metabolic interference). In vivo, the peptide showed promising therapeutic efficacy in a model of methicillin-resistant Staphylococcus aureus and K. pneumoniae pneumonia, as well as in a lipopolysaccharide-induced lung injury model.

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Publication Details

Journal
Nature Communications
Published
2025-11-25
DOI
https://doi.org/10.1038/s41467-025-65449-w
Citations
6
Primary Topic
Antimicrobial Peptides and Activities
Type
article
Field-Weighted Citation Impact
7.10

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article

An antimicrobial peptide as a potential therapy for bacterial pneumonia that alleviates antimicrobial resistance

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6 citations
Nature Communications
Antimicrobial Peptides and Activities
7.10
article

An antimicrobial peptide as a potential therapy for bacterial pneumonia that alleviates antimicrobial resistance

Wenjing Xue, Jingxin Wang, Sanhu Gou, Luyang Gao, Jingyi Zhu, Yun Zhang, Yongtao He, Jing Zou, Chao Zhong, Hui Liu, Jingman Ni
article en
6 citations

Abstract

Bacterial pneumonia remains a global health threat that is worsened by drug-resistant bacteria, underscoring the need for the development of new antimicrobial agents. Antimicrobial peptides are promising new candidates with broad-spectrum activity and low potential for resistance development. Here, we report a linear antimicrobial peptide (AMP) that consists of four repeating units of (D-tryptophan)-(D-arginine)-(D-lysine). This peptide exhibits high stability and robust antimicrobial activity against multidrug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus and Klebsiella pneumoniae, and improved biocompatibility. Furthermore, the AMP shows low potential for resistance development and the ability to alleviate resistance and restore antibiotic sensitivity due to multiple mechanisms, including membrane targeting and non-membrane lysis (DNA binding, reactive oxygen species accumulation, ATP depletion, metabolic interference). In vivo, the peptide showed promising therapeutic efficacy in a model of methicillin-resistant Staphylococcus aureus and K. pneumoniae pneumonia, as well as in a lipopolysaccharide-induced lung injury model.

Nature CommunicationsVol. 16(1)
Macau University of Science and Technology (MO), Jinan University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), University of Macau (MO), Lanzhou University (CN)
Lanzhou University, National Natural Science Foundation of China
Openalex Percentile: Top 2%
Antimicrobial Peptides and Activities
7.10
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