下呼吸道感染患者肺泡灌洗液金黄色葡萄球菌丰度和分布特征

Abundance and distribution of Staphylococcus aureus isolated from bronchoalveolar lavage fluid of patients with lower respiratory tract infections

  • 摘要:
    目的 本研究旨在利用高通量测序技术,分析下呼吸道肺泡灌洗液(BALF)中的微生物群落结构,特别关注金黄色葡萄球菌的丰度和分布情况。
    方法 收集云南省第一人民医院2022-2023年间的1 650例BALF样本,通过BALF培养和恒温扩增与微流控技术进行金黄色葡萄球菌基因检测,并将代表性21例金黄色葡萄球菌阳性样本进行分组:金黄色葡萄球菌肺炎组、新冠病毒共感染组、慢性阻塞性肺病组,并进行16S rDNA扩增子高通量测序。
    结果 三个组别的微生物群落组成存在显著差异,种水平的样本层级聚类分析图显示金黄色葡萄球菌肺炎组金黄色葡萄球菌检出多且占比高,慢性阻塞性肺病组以无色杆菌居多,而新冠病毒共感染组则以水甲基杆菌和无色杆菌为主要的构成对象,三组中只有在金黄色葡萄球菌肺炎组金黄色葡萄球菌居优势菌。
    结论 BALF微生物群落的组成与不同疾病状态密切相关,为深入了解肺部感染性疾病的微生物学基础提供参考依据。

     

    Abstract:
    OBJECTIVE To analyze the microbial community structure in Bronchoalveolar Lavage Fluid (BALF) using high-throughput sequencing technology, with a particular focus on the abundance and distribution of Staphylococcus aureus.
    METHODS A total of 1, 650 bronchoalveolar lavage fluid (BALF) samples were collected from the First People′s Hospital of Yunnan Province between 2022 and 2023. S. aureus gene detection was performed using BALF culture, isothermal amplification and microfluidic technology. Representative 21 S. aureus-positive samples were grouped into S. aureus pneumonia group, SARS-CoV-2 co-infection group and chronic obstructive pulmonary disease (COPD) group, followed by 16S rDNA amplicon high-throughput sequencing.
    RESULTS The microbial community compositions among the three groups exhibited significant differences. Species-level hierarchical clustering analysis revealed that S. aureus was more frequently detected and accounted for a higher proportion in the S. aureus pneumonia group, while the COPD group was dominated by Achromobacter. In contrast, the SARS-CoV-2 co-infection group was mainly composed of Methylobacterium aquatique and Achromobacter. Only in the S. aureus pneumonia group was S. aureus the dominant bacterium.
    CONCLUSION The composition of the BALF microbiota is closely related to different disease states, providing an important reference for a deeper understanding of the microbiological basis of pulmonary infectious diseases.

     

/

返回文章
返回