Yang Fengzhen, Jiang Lihua, Cao Qingmei, Yi Maoli, Zhao Qi
Department of Laboratory Medicine, Qingdao University Affiliated Yantai Yuhuangding Hospital, Yantai, China.
Front Microbiol. 2025 Aug 18;16:1615965. doi: 10.3389/fmicb.2025.1615965. eCollection 2025.
To evaluate the performance of targeted next-generation sequencing (tNGS) in pathogen detection in acute lower respiratory infection.
The retrospective study was conducted between July 2023 and May 2024 at the Yantai Yuhuangding Hospital. Patients with acute lower respiratory infections were included. Qualified sputum or bronchoalveolar lavage fluid samples were collected for tNGS and conventional microbiological tests(CMTs), including culture, staining, polymerase chain reaction (PCR), and reverse transcription-PCR (RT-PCR). The time required and cost were counted.
A total of 968 patients were enrolled. Study analysis discovered 1,019 strains of bacteria, 259 strains of fungi, 302 strains of viruses, 76 strains of , and two strains of using tNGS. In addition, tNGS also identified 39 , four , 19 , and two genes. The positive rates for bacteria, fungi, viruses, mycoplasma, and chlamydia obtained using tNGS were significantly higher than those determined using traditional methods. Among them, tNGS showed high consistence with mycobacterium DNA test, nucleic acid test and nucleic acid test. Poor consistency between drug resistance genes and bacterial resistance phenotypes was found. In addition, tNGS also had advantages over traditional methods in terms of detection time and cost.
Compared to traditional methods, tNGS had higher sensitivity in detecting bacteria, fungi, viruses, and other pathogens in acute lower respiratory infection, and also had the advantages of timeliness and cost-effectiveness, making it a promising method for guiding clinical diagnosis.
评估靶向新一代测序(tNGS)在急性下呼吸道感染病原体检测中的性能。
回顾性研究于2023年7月至2024年5月在烟台毓璜顶医院进行。纳入急性下呼吸道感染患者。收集合格的痰液或支气管肺泡灌洗液样本进行tNGS和传统微生物学检测(CMT),包括培养、染色、聚合酶链反应(PCR)和逆转录PCR(RT-PCR)。计算所需时间和成本。
共纳入968例患者。研究分析发现,使用tNGS检测出1019株细菌、259株真菌、302株病毒、76株支原体和2株衣原体。此外,tNGS还鉴定出39个耐药基因、4个毒力基因、19个管家基因和2个新型冠状病毒基因。使用tNGS获得的细菌、真菌、病毒、支原体和衣原体的阳性率显著高于传统方法测定的阳性率。其中,tNGS与结核分枝杆菌DNA检测、肺炎支原体核酸检测和肺炎衣原体核酸检测具有较高的一致性。发现耐药基因与细菌耐药表型之间的一致性较差。此外,tNGS在检测时间和成本方面也优于传统方法。
与传统方法相比,tNGS在检测急性下呼吸道感染中的细菌、真菌、病毒等病原体方面具有更高的灵敏度,并且具有及时性和成本效益优势,使其成为指导临床诊断的一种有前景的方法。