College of Pulmonary and Critical Care Medicine, Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Respiratory Intensive Care Unit, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
Front Cell Infect Microbiol. 2022 Jun 6;12:872899. doi: 10.3389/fcimb.2022.872899. eCollection 2022.
To evaluate the value of metagenomic next-generation sequencing (mNGS) for the early diagnosis of psittacosis, and to investigate its epidemiology by whole-genome capture.
Twenty-one bronchoalveolar lavage fluid (BALF) and blood samples of 16 psittacosis patients from multiple centers during August 2019 to September 2021 were analyzed retrospectively. mNGS with normal datasets (10 M 75-bp single-end reads after sequencing) and larger datasets (30 M 150-bp paired-end reads after sequencing) as well as quantitative real-time polymerase chain reaction (qPCR) were used to detect the pathogen. Also, whole-genome capture of was applied to draw the phylogenetic tree.
mNGS successfully detected the pathogen in all 16 cases (100%), while qPCR was positive only in 5 out of 10 cases (50%), indicating a significantly higher sensitivity of mNGS than qPCR ( < 0.01). BALF-mNGS performed better than blood-mNGS (16/16 versus 3/5, < 0.05). In addition, larger datasets (the read counts have tripled, and the base number was 12-fold larger compared to clinical mNGS with a normal dataset) of mNGS showed significantly increased contents of human DNA ( < 0.05) and decreased reads per million of the pathogen, suggesting no improvement. Whole-genome capture results of five samples (>60% coverage and >1 depth) were used to construct the phylogenetic tree.
Significant advantages of mNGS with normal datasets were demonstrated in early diagnosing psittacosis. It is the first study to use whole-genome capture to analyze epidemiological information.
评估宏基因组下一代测序(mNGS)在鹦鹉热早期诊断中的价值,并通过全基因组捕获来研究其流行病学。
回顾性分析 2019 年 8 月至 2021 年 9 月期间来自多个中心的 16 例鹦鹉热患者的 21 份支气管肺泡灌洗液(BALF)和血液样本。使用正常数据集(测序后 10M75-bp 单端读长)和更大数据集(测序后 30M150-bp 配对端读长)的 mNGS 以及定量实时聚合酶链反应(qPCR)来检测病原体。此外,还应用全基因组捕获来绘制系统发育树。
mNGS 成功检测到所有 16 例患者(100%)的病原体,而 qPCR 在 10 例中的 5 例(50%)为阳性,表明 mNGS 的灵敏度明显高于 qPCR( < 0.01)。BALF-mNGS 的性能优于血液-mNGS(16/16 与 3/5, < 0.05)。此外,更大数据集(读长数增加了三倍,碱基数量是正常数据集临床 mNGS 的 12 倍)的 mNGS 显示出人 DNA 的含量显著增加( < 0.05),而病原体的每百万读数减少,表明没有改善。5 个样本(覆盖率>60%且深度>1)的全基因组捕获结果用于构建系统发育树。
正常数据集的 mNGS 在早期诊断鹦鹉热方面具有明显优势。这是首次使用全基因组捕获来分析鹦鹉热的流行病学信息。