The respiratory microbiome in patients with post-COVID-19 residual lung abnormalities resembles that of healthy individuals and is distinct from idiopathic pulmonary fibrosis.

IF 4.3 3区 医学 Q1 RESPIRATORY SYSTEM
ERJ Open Research Pub Date : 2025-05-27 eCollection Date: 2025-05-01 DOI:10.1183/23120541.00826-2024
David J F Smith, Nancy M Y Teng, Emma K Denneny, Puja Mehta, Stefan C Stanel, John F Blaikley, Rachel C Chambers, Nazia Chaudhuri, Ben Garfield, Justin L Garner, Peter M George, Poonam Ghai, Onn Min Kon, Yonghua Li, William D-C Man, Joanna C Porter, Valerie Quinn, Pilar Rivera-Ortega, Clare Ross, Leopoldo N Segal, Simone A Walker, Benjamin G Wu, Clare M Lloyd, Iain Stewart, R Gisli Jenkins, Philip L Molyneaux
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引用次数: 0

Abstract

Introduction: Up to 11% of patients are left with residual lung abnormalities following COVID-19 infection. It is unclear whether these changes resolve over time or progress to fibrosis. The airway microbiome is altered in interstitial lung disease, potentially contributing to pathogenesis and disease progression. We hypothesised that the airway microbiome in patients with post-COVID-19 residual lung abnormalities may be altered.

Methods: The POST COVID-19 interstitial lung DiseasE (POSTCODE) study recruited subjects with post-COVID-19 residual lung abnormalities for bronchoscopy. 16S ribosomal RNA gene amplicon sequencing was performed on DNA extracted from bronchoalveolar lavage fluid and compared with that from patients with idiopathic pulmonary fibrosis, fibrotic hypersensitivity pneumonitis and control subjects.

Results: 28 subjects with post-COVID-19 residual lung abnormalities were recruited an average of 11 months after infection. No significant associations were found between the lower airway microbiome or bacterial burden and disease severity or trajectory. There was no difference in bacterial burden between post-COVID-19 patients and interstitial lung disease or control subjects. Furthermore, no differences in microbial composition were observed between these patients and those with fibrotic hypersensitivity pneumonitis or controls. However, compared with idiopathic pulmonary fibrosis, there was an increased abundance of Streptococcus and higher α-diversity in subjects with post-COVID-19 residual lung abnormalities.

Conclusions: The microbiome and bacterial burden in the lower airways of subjects with post-COVID-19 residual lung abnormalities do not differ from those of controls. The microbiome differs from idiopathic pulmonary fibrosis. This, and the absence of associations between microbial features and disease severity or clinical outcomes, suggests that the microbiome is unlikely to contribute to residual lung abnormalities in patients recovering from COVID-19 infection.

covid -19后残留肺异常患者的呼吸微生物组与健康个体相似,与特发性肺纤维化不同。
导语:高达11%的患者在COVID-19感染后留下残留的肺部异常。目前尚不清楚这些变化是随时间消退还是进展为纤维化。在间质性肺病中,气道微生物组发生改变,可能有助于发病和疾病进展。我们假设covid -19后残留肺异常患者的气道微生物组可能会改变。方法:新冠肺炎后肺间质性疾病(POSTCODE)研究招募了新冠肺炎后残留肺异常的受试者进行支气管镜检查。对支气管肺泡灌洗液中提取的DNA进行16S核糖体RNA基因扩增子测序,并与特发性肺纤维化、纤维化超敏性肺炎患者及对照组进行比较。结果:在感染后平均11个月招募28例新冠肺炎后残留肺异常受试者。下气道微生物组或细菌负荷与疾病严重程度或发展轨迹之间未发现显著关联。covid -19后患者与间质性肺疾病或对照组之间的细菌负担无差异。此外,在这些患者与纤维化过敏性肺炎患者或对照组之间没有观察到微生物组成的差异。然而,与特发性肺纤维化相比,在covid -19后残留肺异常的受试者中,链球菌的丰度增加,α-多样性更高。结论:新冠肺炎后残留肺异常患者下气道微生物组和细菌负荷与对照组无明显差异。微生物组不同于特发性肺纤维化。这一点,以及微生物特征与疾病严重程度或临床结果之间缺乏相关性,表明微生物组不太可能导致COVID-19感染康复患者的残留肺异常。
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来源期刊
ERJ Open Research
ERJ Open Research Medicine-Pulmonary and Respiratory Medicine
CiteScore
6.20
自引率
4.30%
发文量
273
审稿时长
8 weeks
期刊介绍: ERJ Open Research is a fully open access original research journal, published online by the European Respiratory Society. The journal aims to publish high-quality work in all fields of respiratory science and medicine, covering basic science, clinical translational science and clinical medicine. The journal was created to help fulfil the ERS objective to disseminate scientific and educational material to its members and to the medical community, but also to provide researchers with an affordable open access specialty journal in which to publish their work.
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