Application of targeted metagenomic next-generation sequencing in pneumonia patients

被引:0
作者
Ren, Guanjun [1 ]
Ma, Liyun [1 ]
Yan, Chunliang [1 ]
Xue, Qishan [1 ]
Zhang, Huijuan [1 ]
Wang, Wei [1 ]
Ren, Xiyan [1 ]
Lei, Yun [1 ]
Li, Shaofei [1 ]
Liu, Yafeng [1 ]
Zheng, Qingyue [1 ]
Wei, Shigang [1 ]
Zhang, Yue [1 ]
Wang, Xiao [1 ]
机构
[1] Beijing Aerosp Gen Hosp, Pulm & Crit Care Med, Beijing, Peoples R China
关键词
targeted metagenomic next-generation sequencing; capture hybridization; multiplex PCR; pneumonia; mixed infections; COMMUNITY-ACQUIRED PNEUMONIA; DISEASE;
D O I
10.1128/spectrum.01713-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
After the coronavirus disease 2019 (COVID-19) pandemic, the incidence rate of mixed infections, especially in critically ill patients with severe pneumonia, increases due to the immunity gap and has also been proven to be associated with mortality, increasing the difficulty in accurate and rapid diagnoses. Here, we evaluated the performance of targeted metagenomic next-generation sequencing (mNGS), including capture hybridization-based mNGS (chNGS) and multiplex PCR-based targeted mNGS (tNGS), in diagnosing pneumonia. Patients admitted to the Pulmonary and Critical Care Medicine, Beijing Aerospace General Hospital, and diagnosed as suspected pulmonary infections from April 2022 to March 2024 were retrospectively evaluated, and 110 patients were finally enrolled. According to the final comprehensive clinical diagnoses, there were 99 patients diagnosed with definite infectious diseases. Single infections accounted for 58.6% of these patients (58/99), while mixed infections occurred in about half of these patients (41.4%, 41/99) and were found in most of the death cases. Pseudomonas aeruginosa (n = 22), Pneumocystis jirovecii (n = 15), and severe acute respiratory syndrome coronavirus 2 (n = 13) were found to be the most common bacterial, fungal, and viral pathogens, respectively. Taking final comprehensive clinical diagnoses as the reference standard, the total coincidence rate (TCR) of chNGS can reach up to 64.1% (95% confidence interval [CI], 54.8%-73.3%), while the TCR of conventional methods was only 39.8% (95% CI, 30.4%-49.3%). The performance of tNGS was slightly superior to that of chNGS, while chNGS yielded more false-negative results, especially for viral detection. Additionally, chNGS combined with tNGS can improve the TCR to 81.3% (95% CI, 62.1%-100.0%).IMPORTANCEThis is the first report on evaluating the performance of capture hybridization-based metagenomicnext-generation sequencing (chNGS), multiplex PCR-based targeted mNGS (tNGS), and conventional methods in diagnosing pneumonia. Our findings emphasized the importance of chNGS and tNGS in diagnosing, managing, and ruling out infections, and an era of widespread application of regional tNGS in monitoring and diagnosing infections with high sensitivity and low economic burden on patients can be expected.
引用
收藏
页数:14
相关论文
共 56 条
[1]   Acute respiratory failure in immunocompromised adults [J].
Azoulay, Elie ;
Mokart, Djamel ;
Kouatchet, Achille ;
Demoule, Alexandre ;
Lemiale, Virginie .
LANCET RESPIRATORY MEDICINE, 2019, 7 (02) :173-186
[2]   Co-infection associated with SARS-CoV-2 and their management [J].
Chavda, Vivek P. ;
Patel, Aayushi B. ;
Pandya, Anjali ;
Vora, Lalitkumar K. ;
Patravale, Vandana ;
Tambuwala, Zara M. ;
Aljabali, Alaa A. A. ;
Serrano-Aroca, Angel ;
Mishra, Vijay ;
Tambuwala, Murtaza M. .
FUTURE SCIENCE OA, 2022, 8 (09)
[3]   Evaluation of metagenomic and pathogen-targeted next-generation sequencing for diagnosis of meningitis and encephalitis in adults: A multicenter prospective observational cohort study in China [J].
Chen, Weibi ;
Liu, Gang ;
Cui, Lili ;
Tian, Fei ;
Zhang, Jiatang ;
Zhao, Jiahua ;
Lv, Ying ;
Du, Jianxin ;
Huan, Xinyu ;
Wu, Yingfeng ;
Zhang, Yan .
JOURNAL OF INFECTION, 2024, 88 (05)
[4]   Application of Metagenomic Next-Generation Sequencing in the Diagnosis of Pulmonary Infectious Pathogens From Bronchoalveolar Lavage Samples [J].
Chen, Yuqian ;
Feng, Wei ;
Ye, Kai ;
Guo, Li ;
Xia, Han ;
Guan, Yuanlin ;
Chai, Limin ;
Shi, Wenhua ;
Zhai, Cui ;
Wang, Jian ;
Yan, Xin ;
Wang, Qingting ;
Zhang, Qianqian ;
Li, Cong ;
Liu, Pengtao ;
Li, Manxiang .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2021, 11
[5]   Promoting the use of social networks in pneumonia [J].
Cilloniz, Catia ;
Greenslade, Leith ;
Dominedo, Cristina ;
Garcia-Vidal, Carolina .
PNEUMONIA, 2020, 12 (01)
[6]   Pediatric Infectious Disease Group (GPIP) position paper on the immune debt of the COVID-19 pandemic in childhood, how can we fill the immunity gap? [J].
Cohen, Robert ;
Ashman, Marion ;
Taha, Muhamed-Kheir ;
Varon, Emmanuelle ;
Angoulvant, Francois ;
Levy, Corinne ;
Rybak, Alexis ;
Ouldali, Naim ;
Guiso, Nicole ;
Grimprel, Emmanuel .
INFECTIOUS DISEASES NOW, 2021, 51 (05) :418-423
[7]   Bacterial and viral infections and related inflammatory responses in chronic obstructive pulmonary disease [J].
D'Anna, Silvestro Ennio ;
Maniscalco, Mauro ;
Cappello, Francesco ;
Carone, Mauro ;
Motta, Andrea ;
Balbi, Bruno ;
Ricciardolo, Fabio L. M. ;
Caramori, Gaetano ;
Di Stefano, Antonino .
ANNALS OF MEDICINE, 2021, 53 (01) :135-150
[8]   A theoretical and generalized approach for the assessment of the sample-specific limit of detection for clinical metagenomics [J].
Ebinger, Arnt ;
Fischer, Susanne ;
Hoeper, Dirk .
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2021, 19 (19) :732-742
[9]   Invasive Saprochaete Infections: An Emerging Threat to Immunocompromised Patients [J].
El Zein, Said ;
Hindy, Joya-Rita ;
Kanj, Souha S. .
PATHOGENS, 2020, 9 (11) :1-14
[10]   A Method for Selectively Enriching Microbial DNA from Contaminating Vertebrate Host DNA [J].
Feehery, George R. ;
Yigit, Erbay ;
Oyola, Samuel O. ;
Langhorst, Bradley W. ;
Schmidt, Victor T. ;
Stewart, Fiona J. ;
Dimalanta, Eileen T. ;
Amaral-Zettler, Linda A. ;
Davis, Theodore ;
Quail, Michael A. ;
Pradhan, Sriharsa .
PLOS ONE, 2013, 8 (10)