Evidence map›Paper›PMID 42773108›Full record

ArticleNature communications2026

Eradication of MRSA biofilm-associated implant infections by low-immunogenic sustained-release lysostaphin fused to thermosensitive polypeptides.

Guoqing Fan, Hao Wang, Yuxin Gong, Si Liu, Yuanzi Sun, Jie Tian, Hongbin Wang, Litao Zhang, Fan Zhang, Like Gong and 7 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Guoqing Fan *Beijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.
Hao Wang *Department of Orthopedics, Peking University First Hospital, Beijing, China.
Yuxin Gong *Beijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.
Si Liu *Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, State Key Laboratory of Digestive Health, National Clinical Research Center for Digestive Disease, Beijing, China.
Yuanzi SunBeijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.
Jie TianDepartment of Dermatology and Venereology, Peking University First Hospital, Beijing, China.
Hongbin WangDepartment of Orthopedics, Peking University First Hospital, Beijing, China.
Litao ZhangBeijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.
Fan ZhangBeijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.
Like GongBeijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.
Lin WangDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University, Beijing, China.ORCID 0000-0003-1555-9985
Fengmin LuDepartment of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University, Beijing, China.
Yongping CaoDepartment of Orthopedics, Peking University First Hospital, Beijing, China.
Wanliang LuState Key Laboratory of Natural and Biomimetic Drugs, Beijing Key Laboratory of Advanced Pharmaceutical Preparation, School of Pharmaceutical Sciences, Peking University, Beijing, China. luwl@bjmu.edu.cn.ORCID 0000-0002-5651-4890
Mingming XuDepartment of Geriatric Dentistry, Peking University School and Hospital of Stomatology, & National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, Beijing, China. xumingming@pkuss.bjmu.edu.cn.
Shengtao ZhuDepartment of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, State Key Laboratory of Digestive Health, National Clinical Research Center for Digestive Disease, Beijing, China. zhushengtao@ccmu.edu.cn.ORCID 0000-0002-2795-8943
Weiping GaoBeijing Advanced Center of Cellular Homeostasis and Aging-Related Diseases, Department of Biomedical Engineering, Institute of Advanced Clinical Medicine, Peking University, Beijing, China. gaoweiping@hsc.pku.edu.cn.ORCID 0000-0002-2916-3044

Funding

National Natural Science Foundation of China (National Science Foundation of China) 52473119National Natural Science Foundation of China (National Science Foundation of China) 82070550National Natural Science Foundation of China (National Science Foundation of China) 82470567Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) L2612014
6 · The paper itself

Abstract

Staphylococcal bacteria, particularly methicillin-resistant Staphylococcus aureus (MRSA), are responsible for intractable infections-especially those associated with implants-through biofilm formation, presenting a worldwide menace. Antibacterial enzymes like lysostaphin (Lst) are promising for combating staphylococcal infections but limited by poor stability, high immunogenicity, and suboptimal pharmacokinetics, which hamper their clinical translation as antibiotic alternatives. Herein, we report a strategy of fusing thermosensitive elastin-like polypeptides (ELPs) to Lst to overcome these inherent drawbacks and eradicate MRSA biofilm-induced implant infections. Guided by AlphaFold2, we rationally engineered a chimeric Lst-ELP fusion protein that preserves potent lytic activity, demonstrates markedly enhanced stability, and exhibits substantially reduced immunogenicity relative to free Lst. The thermosensitivity of Lst-ELP enables in situ formation of a sustained-release depot upon subcutaneous injection, translating to an increased maximum tolerated dose, improved pharmacokinetics, and optimized biodistribution. Consequently, a single injection of Lst-ELP not only fully eradicated MRSA biofilms on implants and MRSA from the bloodstream and wound tissues, but also eliminated local and systemic inflammatory responses. This approach achieved complete clearance of MRSA biofilm-associated implant infections without adverse effects, highlighting its potential for clinical translation.

Indexed as

Anti-Bacterial AgentsBiofilmsLysostaphinMethicillin-Resistant Staphylococcus aureusPeptidesProsthesis-Related InfectionsStaphylococcal InfectionsAnimalsDelayed-Action PreparationsElastinElastin-Like PolypeptidesFemaleHumansMiceMicrobial Sensitivity TestsRecombinant Fusion ProteinsAnti-Bacterial AgentsDelayed-Action PreparationsElastinElastin-Like PolypeptidesLysostaphinPeptidesRecombinant Fusion Proteins

Identifiers

PMID42773108
PMCPMC13598132

What OpenQuestion holds

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Registered trials

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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.