Laboratory of Systems Biology and Bioinformatics (LBB), Department of Bioinformatics, Kish International Campus, University of Tehran, Kish Island, Iran.
Molecular Biology Research Center, Systems Biology and Poisonings Institute, Tehran, Iran.
BMC Pulm Med. 2024 Jan 2;24(1):2. doi: 10.1186/s12890-023-02789-7.
BACKGROUND: Chronic respiratory diseases, such as chronic obstructive pulmonary disease (COPD) and bronchiectasis, present significant threats to global health. Recent studies have revealed the crucial role of the lung microbiome in the development of these diseases. Pathogens have evolved complex strategies to evade the immune response, with the manipulation of host cellular epigenetic mechanisms playing a pivotal role. There is existing evidence regarding the effects of Pseudomonas on epigenetic modifications and their association with pulmonary diseases. Therefore, this study aims to directly assess the connection between Pseudomonas abundance and chronic respiratory diseases. We hope that our findings will shed light on the molecular mechanisms behind lung pathogen infections. METHODS: We analyzed data from 366 participants, including individuals with COPD, acute exacerbations of COPD (AECOPD), bronchiectasis, and healthy individuals. Previous studies have given limited attention to the impact of Pseudomonas on these groups and their comparison with healthy individuals. Two independent datasets from different ethnic backgrounds were used for external validation. Each dataset separately analyzed bacteria at the genus level. RESULTS: The study reveals that Pseudomonas, a bacterium, was consistently found in high concentrations in all chronic lung disease datasets but it was present in very low abundance in the healthy datasets. This suggests that Pseudomonas may influence cellular mechanisms through epigenetics, contributing to the development and progression of chronic respiratory diseases. CONCLUSIONS: This study emphasizes the importance of understanding the relationship between the lung microbiome, epigenetics, and the onset of chronic pulmonary disease. Enhanced recognition of molecular mechanisms and the impact of the microbiome on cellular functions, along with a better understanding of these concepts, can lead to improved diagnosis and treatment.
背景:慢性呼吸系统疾病,如慢性阻塞性肺疾病(COPD)和支气管扩张症,对全球健康构成重大威胁。最近的研究揭示了肺部微生物组在这些疾病发展中的关键作用。病原体已经进化出复杂的策略来逃避免疫反应,其中操纵宿主细胞表观遗传机制起着关键作用。已有证据表明铜绿假单胞菌对表观遗传修饰及其与肺部疾病的关联的影响。因此,本研究旨在直接评估铜绿假单胞菌丰度与慢性呼吸道疾病之间的联系。我们希望我们的发现能揭示肺部病原体感染背后的分子机制。
方法:我们分析了 366 名参与者的数据,包括 COPD 患者、COPD 急性加重(AECOPD)患者、支气管扩张症患者和健康个体。以前的研究对铜绿假单胞菌对这些组的影响以及与健康个体的比较关注有限。我们使用了来自不同种族背景的两个独立数据集进行外部验证。每个数据集分别在属水平上分析细菌。
结果:该研究表明,一种名为铜绿假单胞菌的细菌在所有慢性肺部疾病数据集中都以高浓度持续存在,但在健康数据集中却以极低的丰度存在。这表明铜绿假单胞菌可能通过表观遗传学影响细胞机制,导致慢性呼吸系统疾病的发展和进展。
结论:本研究强调了理解肺部微生物组、表观遗传学和慢性肺部疾病发病之间关系的重要性。增强对分子机制和微生物组对细胞功能的影响的认识,以及更好地理解这些概念,可以导致改进的诊断和治疗。
Expert Rev Respir Med. 2024
Kaohsiung J Med Sci. 2020-2
Lancet Respir Med. 2019-4-8
Crit Rev Microbiol. 2021-2
Clin Respir J. 2021-2
Respir Res. 2019-6-6
Chin Med J (Engl). 2017-9-5
Int J Mol Sci. 2023-8-1
Int J Mol Sci. 2023-1-21
Nat Rev Microbiol. 2023-4