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A novel mouse model of chronic Pseudomonas aeruginosa infection inducing bronchiectasis-like phenotype
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Heng Yang1, 2, Yang Liu1, 2, Yuqing Wang1, 2, Yuhua Wen2, Yan Chen2, Rui Fan2, Jiayan Xu2, Shunlian Hu1, Hao Qian1, Rui Jiang1, Weijun Cao2, Jinfu Xu1, 2
Animal Models and Experimental Medicine | 2026, 9(7) : 1409 - 1419
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Animal Models and Experimental Medicine | 2026, 9(7): 1409-1419
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A novel mouse model of chronic Pseudomonas aeruginosa infection inducing bronchiectasis-like phenotype
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Heng Yang1, 2, Yang Liu1, 2, Yuqing Wang1, 2, Yuhua Wen2, Yan Chen2, Rui Fan2, Jiayan Xu2, Shunlian Hu1, Hao Qian1, Rui Jiang1, Weijun Cao2, Jinfu Xu1, 2
Affiliations
  • 1Department of Respiratory and Critical Care Medicine, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China
  • 2Institute of Respiratory Medicine, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China
Published: 2026-07-28 doi: 10.1002/ame2.70245
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Background:

Given the need to translate basic research into human therapies, the development and refinement of clinically relevant animal models for bronchiectasis are critically important. To date, there are no well-established animal models for bronchiectasis. Thus, our aim was to develop a novel animal model that accurately recapitulates bronchiectasis-like pathologies.

Methods:

To address this question, clinical strains of chronic Pseudomonas aeruginosa (CPA) were embedded in agar beads in vitro; then CPA-loaded agar beads and papain were repeatedly instilled intratracheally in female C57BL/6 J mice. Experimental assessments included micro-computed tomography (micro-CT) imaging, histological analysis, immune cell infiltration, cytokines, and lung function parameter measurements to evaluate structural damage, immune responses, and lung function impairments in the mouse model.

Results:

In this mouse model, we observed that lung micro-CT imaging revealed significant bronchiectasis, with visible airways in the periphery, cylindrical airway expansion, and an airway-to-artery ratio > 1. Histopathology highlighted immune cell infiltration around the trachea, including lymphocytes, neutrophils, and monocytes, along with Periodic acid-Schiff staining-positive hypermucinous secretion. Compared to controls, the bronchiectasis group exhibited elevated pro-inflammatory cytokines in bronchoalveolar lavage fluid and worse lung function.

Conclusion:

Our study presented a novel mouse model that better replicated the bronchiectasis-like phenotype than the CPA airway infection model, showing the advantages of the "CPA-loaded agar beads and papain"-driven approach in optimizing the disease models. The model mimicked the progression of bronchiectasis closely and could be used for studies on disease pathogenesis as well as the evaluation of novel therapies in the near future.

bronchiectasis  /  micro-computed tomography (micro-CT)  /  mouse model  /  Pseudomonas aeruginosa
Heng Yang, Yang Liu, Yuqing Wang, Yuhua Wen, Yan Chen, Rui Fan, Jiayan Xu, Shunlian Hu, Hao Qian, Rui Jiang, Weijun Cao, Jinfu Xu. A novel mouse model of chronic Pseudomonas aeruginosa infection inducing bronchiectasis-like phenotype[J]. Animal Models and Experimental Medicine, 2026 , 9 (7) : 1409 -1419 . DOI: 10.1002/ame2.70245
  • The Noncommunicable Chronic DiseasesNational Science and Technology Major Project(2024ZD0522400)
  • Natural Science Foundation of China(81925001; 82330070)
  • Innovation Program of Shanghai Municipal Education Commission(202101070007-E00097)
  • Program of the Shanghai Municipal Science and Technology Commission(21DZ2201800)
  • Program of the Shanghai Shenkang Development Center(SHDC12023110)
  • Major Project of Guangzhou National Laboratory(GZNL2024A02003)
Year 2026 volume 9 Issue 7
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Article Info
doi: 10.1002/ame2.70245
  • Receive Date:2025-12-03
  • Online Date:2026-08-06
  • Published:2026-07-28
Article Data
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History
  • Received:2025-12-03
  • Revised:2026-05-03
  • Accepted:2026-05-20
Funding
The Noncommunicable Chronic DiseasesNational Science and Technology Major Project(2024ZD0522400)
Natural Science Foundation of China(81925001; 82330070)
Innovation Program of Shanghai Municipal Education Commission(202101070007-E00097)
Program of the Shanghai Municipal Science and Technology Commission(21DZ2201800)
Program of the Shanghai Shenkang Development Center(SHDC12023110)
Major Project of Guangzhou National Laboratory(GZNL2024A02003)
Affiliations
    1Department of Respiratory and Critical Care Medicine, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China
    2Institute of Respiratory Medicine, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China

Corresponding:

Jinfu Xu, Department of Respiratory and Critical Care Medicine, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai 200065, China. Email:
Weijun Cao, Institute of Respiratory Medicine, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, No. 507 Zhengmin Road, Shanghai 200433, China. Email:
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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