Suppr超能文献

铜绿假单胞菌与正常菌落金黄色葡萄球菌的慢性合并感染导致囊性纤维化大鼠的肺结构损伤。

Chronic Coinfection with Pseudomonas aeruginosa and Normal Colony Staphylococcus aureus Causes Lung Structural Damage in the Cystic Fibrosis Rat.

作者信息

Bollar Gretchen E, Keith Johnathan D, Stanford Denise D, Oden Ashley M, Raju S Vamsee, Poore T Spencer, Birket Susan E

机构信息

Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama; Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, Alabama.

Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, Alabama.

出版信息

Am J Pathol. 2025 Feb;195(2):174-187. doi: 10.1016/j.ajpath.2024.09.008. Epub 2024 Oct 28.

Abstract

Cystic fibrosis (CF) respiratory outcomes are heavily influenced by complications of infection. Pseudomonas aeruginosa and Staphylococcus aureus are the most common colonizers of the cystic fibrosis lung, and frequently overlap to cause chronic and persistent coinfections associated with severe disease. However, the dynamics of P. aeruginosa and S. aureus coinfection and its impacts on the development of CF lung structural damage are poorly understood. Additionally, small colony variants (SCVs) of S. aureus have been associated with P. aeruginosa infections in people with CF, but their role in disease progression is largely unknown. In this work, the CF rat was used to model chronic lung coinfection with P. aeruginosa and S. aureus, using clinically and laboratory-derived normal colony and SCV strains of S. aureus to evaluate the impact of phenotype on clinical outcomes. Rats coinfected with clinically derived S. aureus of both phenotypes experienced increased inflammation in the lung. However, only the combination of P. aeruginosa and clinically normal colony S. aureus led to lung structural decline, including mucus obstruction and bronchiectasis. Regression analyses showed that the damage was associated with a higher burden of P. aeruginosa. These data indicate that chronic coinfection with normal colony S. aureus and P. aeruginosa may support the progression CF lung decline driven by P. aeruginosa, which might be avoided when coinfecting S. aureus exhibits the SCV phenotype.

摘要

囊性纤维化(CF)的呼吸道预后受到感染并发症的严重影响。铜绿假单胞菌和金黄色葡萄球菌是囊性纤维化肺部最常见的定植菌,且常同时存在,导致与严重疾病相关的慢性持续性混合感染。然而,铜绿假单胞菌和金黄色葡萄球菌混合感染的动态变化及其对CF肺部结构损伤发展的影响尚不清楚。此外,金黄色葡萄球菌的小菌落变体(SCV)与CF患者的铜绿假单胞菌感染有关,但其在疾病进展中的作用 largely unknown。在这项研究中,使用CF大鼠对铜绿假单胞菌和金黄色葡萄球菌的慢性肺部混合感染进行建模,使用临床和实验室来源的金黄色葡萄球菌正常菌落和SCV菌株来评估表型对临床结果的影响。两种表型的临床来源金黄色葡萄球菌混合感染的大鼠肺部炎症增加。然而,只有铜绿假单胞菌与临床正常菌落金黄色葡萄球菌的组合导致肺部结构衰退,包括黏液阻塞和支气管扩张。回归分析表明,这种损伤与铜绿假单胞菌的较高负荷有关。这些数据表明,正常菌落金黄色葡萄球菌和铜绿假单胞菌的慢性混合感染可能会促进由铜绿假单胞菌驱动的CF肺部衰退进展,而当混合感染的金黄色葡萄球菌表现出SCV表型时,这种情况可能会避免。

相似文献

2
Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis.
Cochrane Database Syst Rev. 2017 Apr 25;4(4):CD004197. doi: 10.1002/14651858.CD004197.pub5.
5
Prophylactic anti-staphylococcal antibiotics for cystic fibrosis.
Cochrane Database Syst Rev. 2017 Apr 18;4(4):CD001912. doi: 10.1002/14651858.CD001912.pub4.
6
Interventions for the eradication of meticillin-resistant Staphylococcus aureus (MRSA) in people with cystic fibrosis.
Cochrane Database Syst Rev. 2018 Jul 21;7(7):CD009650. doi: 10.1002/14651858.CD009650.pub4.
7
Bronchoscopy-guided antimicrobial therapy for cystic fibrosis.
Cochrane Database Syst Rev. 2016 Jan 21(1):CD009530. doi: 10.1002/14651858.CD009530.pub3.
8
Prophylactic anti-staphylococcal antibiotics for cystic fibrosis.
Cochrane Database Syst Rev. 2012 Dec 12;12:CD001912. doi: 10.1002/14651858.CD001912.pub2.
9
Prophylactic antibiotics for cystic fibrosis.
Cochrane Database Syst Rev. 2003(3):CD001912. doi: 10.1002/14651858.CD001912.
10
Interventions for the eradication of meticillin-resistant Staphylococcus aureus (MRSA) in people with cystic fibrosis.
Cochrane Database Syst Rev. 2022 Dec 13;12(12):CD009650. doi: 10.1002/14651858.CD009650.pub5.

引用本文的文献

1
Targeting the MEK1/2 pathway to combat infection and inflammation in cystic fibrosis.
mBio. 2025 Jul 9;16(7):e0077525. doi: 10.1128/mbio.00775-25. Epub 2025 May 27.

本文引用的文献

1
Revisiting Host-Pathogen Interactions in Cystic Fibrosis Lungs in the Era of CFTR Modulators.
Int J Mol Sci. 2023 Mar 5;24(5):5010. doi: 10.3390/ijms24055010.
3
Effects of Mucin and DNA Concentrations in Airway Mucus on Pseudomonas aeruginosa Biofilm Recalcitrance.
mSphere. 2022 Aug 31;7(4):e0029122. doi: 10.1128/msphere.00291-22. Epub 2022 Aug 15.
4
A Commensal Streptococcus Dysregulates the Nitrosative Stress Response.
Front Cell Infect Microbiol. 2022 May 10;12:817336. doi: 10.3389/fcimb.2022.817336. eCollection 2022.
5
Muc5b Contributes to Mucus Abnormality in Rat Models of Cystic Fibrosis.
Front Physiol. 2022 Apr 28;13:884166. doi: 10.3389/fphys.2022.884166. eCollection 2022.
6
Neutrophil dysfunction in the pathogenesis of cystic fibrosis.
Blood. 2022 Apr 28;139(17):2622-2631. doi: 10.1182/blood.2021014699.
7
Static mucus impairs bacterial clearance and allows chronic infection with in the cystic fibrosis rat.
Eur Respir J. 2022 Sep 7;60(3). doi: 10.1183/13993003.01032-2021. Print 2022 Sep.
9
Induction of ciliary orientation by matrix patterning and characterization of mucociliary transport.
Biophys J. 2021 Apr 20;120(8):1387-1395. doi: 10.1016/j.bpj.2021.01.041. Epub 2021 Mar 9.
10
Sustained Coinfections with and in Cystic Fibrosis.
Am J Respir Crit Care Med. 2021 Feb 1;203(3):328-338. doi: 10.1164/rccm.202004-1322OC.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验