Identifying the causes of community-acquired pneumonia (CAP) is challenging due to the disease’s complex etiology and the limitations of traditional microbiological diagnostic methods. Recent advances in next generation sequencing (NGS)-based metagenomics allow pan-pathogen detection in a single assay, and may have significant advantages over culture-based techniques.
We conducted a cohort study of 159 CAP patients to assess the diagnostic performance of a clinical metagenomics assay and its impact on clinical management and patient outcomes. When compared to other techniques, clinical metagenomics detected more pathogens in more CAP cases, and identified a substantial number of polymicrobial infections. Moreover, metagenomics results led to changes in or confirmation of clinical management in 35 of 59 cases; these 35 cases also had significantly improved patient outcomes.
Clinical metagenomics could be a valuable tool for the diagnosis and treatment of CAP.
Trial registration number with the Chinese Clinical Trial Registry: ChiCTR2100043628.
Community-acquired pneumonia (CAP) is one of the most common and morbid conditions encountered in clinical practice [1,2,3,4,5]. Although some pathogens such as Streptococcus pneumoniae  are commonly detected in CAP patients, over 100 bacterial, viral, fungal, and parasitic causes of CAP have been reported . Due to the limitations of culture-based testing and a lack of diagnostic tests for rare pathogens, in up to 62% of cases, the infectious cause remains unidentified despite extensive microbiological evaluation [8,9,10]. Failure to obtain a timely diagnosis contributes to poor clinical outcomes, increased patient anxiety, and higher costs.
Since its first reported clinical application in 2014, metagenomic next-generation sequencing (mNGS) has shown promise for the diagnosis of infectious diseases due to its ability to identify multiple pathogens by a single assay [11,12,13]. Recent studies have reported the validation of mNGS for pathogen detection in various specimen types and infectious diseases [14,15,16,17]. Importantly, application of clinical mNGS also led to the rapid identification of SARS-CoV-2, the causative agent for the recent COVID-19 pandemic, further highlighting its value in the diagnosis of infections [18,19,20]. However, most previous studies focused on its usefulness for detecting uncommon CAP pathogens [21,22,23], or diagnosing certain patient subgroups such as immunocompromised hosts or culture-negative cases [24,25,26]. Moreover, these studies mainly evaluated its diagnostic performance, and were often conducted in a relatively small cohort . Prospective assessments of both the diagnostic and clinical impact of mNGS application in hospitalized CAP patients are still lacking.
In the present study, we evaluated the diagnostic performance and the impact on clinical outcome of our mNGS assay and compared the results with conventional microbiological testing in a cohort of 159 hospitalized CAP patients.
Cohort and study design
We recruited 159 patients admitted into the Respiratory ICU of the People’s Liberation Army General Hospital in Beijing, China from December 2018 to November 2019 with a diagnosis of CAP according to Chinese guidelines [2, 27, 28]. Patients who met the following criteria (1 + 2) and at least one of the criteria (3)–(7) were enrolled this prospective study and randomly assigned into either the control or mNGS groups with informed consents signed by patients or surrogates: (1) Admitted at our ICU and considered for pneumonia acquired outside of the hospital setting; (2) A new or progressive pulmonary infiltration with/without pleural effusion on a chest radiograph; (3) New or increased cough with or without sputum production; (4) Purulent sputum or a change in sputum characteristics; (5) Fever; (6) Signs of lung consolidation or moist rales; (7) Peripheral white blood cell (WBC) count ≥10 × 109/L or ≤ 4 × 109/L. Demographic characteristics of the cohort are provided in Table 1.
Sample collection was reviewed and approved by the Chinese People’s Liberation Army General Hospital Ethics Committee Review Board. Informed consents were signed by patients or surrogates. Patients were classified using APACHE II criteria on the first day of ICU admission . The cohort was random divided into two groups. In the control group (100 cases), only standard non-NGS methods (culture or smear, acid-fast staining, T-spot and X-pert MTB/RIF for M. tuberculosis) were employed for pathogen detection. In the mNGS group (59 cases), samples underwent traditional clinical microbiological assays and mNGS testing in parallel.
Results of mNGS were reviewed along with other clinical evidence by the physicians, and changes in the treatment plans were made when warranted. We evaluated the impact of mNGS-based testing on clinical management and outcomes by categorizing each patient’s clinical outcome into three groups as of his/her last day in the Intensive Care Unit (ICU): Improved, Resolved, or Mortality. In the improved group, patients had resolution of abnormal vital signs, including heart rate, respiratory rate, blood pressure, oxygen saturation, and temperature; ability to eat; and normal cognition . In the Resolved group, patients showed all the above signs of clinical stability and no lesions on chest CT. Patients who died during hospitalization comprised the Mortality category. In the mNGS group who had beneficial clinical outcomes, levels of alanine aminotransferase, aspartate aminotransferase, albumin, blood urea nitrogen, and creatinine were examined to evaluate the impact on patients’ liver and kidney function.
Sample processing and sequencing
Within 2 days of enrollment, samples of blood, sputum, or bronchoalveolar lavage (BALF) were collected and transported to the laboratory following standard procedures (https://emergency.cdc.gov). Cerebrospinal fluid (n = 3), pleural effusion (n = 2), tissue (n = 1), and urine were also collected in a small number of cases. About 3 mL of samples were collected from the patients and stored at room temperature (for blood) or at − 80 °C (for other specimen types) prior to testing. Blood were stored in EDTA tubes, from which plasma was seperated by centrifuging at 1600 g for 10 min at 4 °C. Trypsin-liquefied sputum and BALF were centrifuged at 8000 g for 5 min. Pellets were resuspended and vortexed at 3000 rpm for 30 min in lysis buffer with the aid of glass beads to break the cell walls. DNA extraction was performed with 300 ul of specimens as described above (plasma, liquefied sputum or BALF). One hundred ng of DNA, as measured by a Qubit Fluorometer (Invitrogen, Carlsbad, CA), were then subjected to library preparation with a transposase-based method. Pooled libraries were sequenced on an Nextseq 550 sequencing system (Illumina, San Diego, CA) using a 75 bp, single-end sequencing kit.
Raw sequencing data were first subjected to a quality control process including removal ow-quality, low-complexity, short reads (< 35 bp) and adapter trimming before further analyses. At least 10 M reads were generated for each sample. Prior to microbial classification, reads derived from the human genome were depleted by aligning to the human reference genome (hg38) using the Burrows-Wheeler Alignment (BWA) tool . Microbial classification were performed by mapping the remaining sequencing reads to a reference microbial database comprising genomes of archaea, bacteria, fungi, protozoa, viruses and parasites, which was curated from the NCBI genome databases.
Comparative analyses were conducted by Pearson’s χ2 test, Fisher’s exact test, or the McNemar test for discrete variables where appropriate. Multiple testing correction was performed using the false discovery rate (FDR) approach. Data analyses were performed using SPSS 22.0 software. Multivariate logistic regression analyses were conducted by R software, with factors of sex, age and concurrent conditions included in the model. P-values < 0.05 were considered significant, and all tests were 2-tailed (unless indicated otherwise).
Sample and patient characteristics
As shown in Fig. 1a, this prospective study enrolled patients who met our inclusion criteria and randomly assigned them into either the control or mNGS groups with informed consents. The average Acute Physiologic Assessment and Chronic Health Evaluation II (APACHE II) scores were 12.6 ± 7.9 and 11.1 ± 7.0 in the control and mNGS groups, respectively (Fig. 1b). The lack of significant differences (P = 0.24) in APACHE scores between the two groups suggests balanced enrollment with regard to disease severity.
In the control group, a total of 109 samples were collected from 100 patients, including BALF (53), sputum (46), tissue (2), blood (8). For the mNGS group, a total of 104 samples were collected from 59 patients, including bronchoalveolar lavage fluid (BALF) (47), blood (45), sputum (5), cerebrospinal fluid (3), pleural effusion (2), tissue (1) and urine (1) (Fig. 1c). Generally, BALF and blood samples were tested in pairs in the mNGS group.
Diagnostic performance of NGS-based Metagenomics for pathogen detection
In this study, an NGS test was only considered positive when potential pathogen(s) were identified in the specimens. Tests that detected no microbes or only bacteria that were clinically considered commensal (for instance, Propionibacteria spp., Veillonella spp., Rothia spp., and Neisseria flavescens) were defined as negative (Supplementary Table S1). A total of 284 pathogens were detected in the overall cohort. These included 105 pathogens (78 bacteria and 27 fungi) in the control group and 179 pathogens in the mNGS group (113 bacteria, 32 fungi and 34 viruses). In line with these findings, 79.7%(47/59) of those in the mNGS group were positive compared to 37.0% (37/100) in the controls (P < 0.001, Fig. 2a).
The mNGS result was considered to be in agreement with clinical diagnosis if the results confirmed either non-infection or infection with certain pathogens. For instance, two patients (a 52-year-old woman and a 51-year-old man) who had been taking immunosuppressive drugs were admitted to this study. Both had diffuse ground-glass opacity on chest CT images and but normal oxygenation index and normal levels of white blood cells, neutrophils, C-reactive protein, and interleukin-6. In both patients, Pneumocystis jiroveci was identified by mNGS. Based on their clinical presentations, the clinician prescribed caspofungin and compound sulfamethoxazole tablets to treat their pneumonia. Both patients recovered and were discharged. In these two cases, the results of mNGS agreed with the treatment outcome and were considered concordant with clinical diagnosis.
mNGS results agreed with clinical diagnosis in 40 (60.8%) infection cases and 6 (10.2%) non-infection cases (Fig. 2b). NGS-based assays identified significantly more pathogens (179 vs 39) in significantly more cases (29 out of 59, 49.2% vs 47 out of 59, 79.7%, P < 0.01) (Fig. 2c) compared to conventional techniques. A total of 34 bacterial and 5 fungal pathogens were reported by conventional testing, whereas 113 bacteria, 34 DNA viruses and 32 fungi were found by metagenomics (Fig. 2d). Discordant positive results included unculturable bacteria, viruses, and eukaryotic pathogens. The most common organisms detected by mNGS were A. baumannii (23.7%), P. jirovecii (23.7%), and cytomegalovirus (18.6%) (Fig. 2e). Our mNGS assay confirmed the diagnosis in all four cases of tuberculosis (Table 2). Multiple pathogens were identified in a substantial portion of the cases (30/59, 50.8%); in 3 cases, co-infections with bacteria, fungi, and viruses were detected (Fig. 2f, g).
In 37 of 59 mNGS patients, a pair of plasma and BALF samples were collected for testing. Among those, the same pathogens, including bacteria, viruses and fungi, were detected in both samples in 11 cases (29.7%). There were 3 additional cases (0.8%) in which both BALF and blood samples were negative for pathogen identification (Fig. 2h). In most of the remaining samples, BALF samples yielded better pathogen detection results than blood samples (Table 3). As indicated by the number of sequencing reads detected, the abundance of bacteria and fungi in cell-free DNA was generally lower than in the corresponding respiratory specimen (Table 3).
Impact of metagenomic NGS approach on clinical management and outcome
Compared to the control group, the mNGS group has a considerably lower mortality rate (13.6% vs 26.0%, or 8/59 vs 26/100; Fig. 3a) and a significantly higher rate of complete symptom resolution (55.9% vs 7.0%, or 33/59 vs 7/100, P < 0.001; Fig. 3b). The duration of mechanical ventilation was also significantly reduced in the mNGS group (average of 7.4 days versus 17.3 days in the control group) (P < 0.05, Fig. 3c). No significant differences were found in the length of stay or medical costs in the ICU (data not shown).
In the mNGS group, the results of metagenomics testing led to a) change in clinical management in 11 patients (18.6%) and b) confirmation of ongoing treatment in 24 patients (40.7%). In addition, one patient was transferred to a specialized hospital after confirmation of tuberculosis by mNGS. In the 11 cases with treatment changes in the control group, 8 showed complete resolution of symptoms (72.7% vs 7.0%, P < 0.001) and a decreased mortality rate (2 out of 11, 18.2% vs 26.0%, Fig. 3a, b, Supplementary Table S2). None of the 11 cases required mechanical ventilation.
To assess whether mNGS affected ongoing clinical management, we evaluated clinical outcomes in the 11 patients with changed treatment and the 24 patients with confirmed treatment. Consistently, compared with the control group, outcomes improved, manifested by a significantly higher rate of disease resolution (22/35, 62.9% vs 7/100, 7.0%, P < 0.001) and a reduced mortality rate during hospitalization (3/35 8.6%, vs 26/100, 26.0%, P = 0.055) (Fig. 3a, b). The duration of mechanical ventilation was also significantly shorter in 2 of the 36 cases, with an average of 8.5 days (Fig. 3c). Consistently, multivariate logistic regression analyses with factors of sex, age and concurrent conditions included also showed significant correlations between mNGS testing and improved sympton resolution (P<.001, control vs. mNGS groups; P<0.001, control cases vs. cases with treatment changed/confirmed based on mNGS results; Supplementary Table S3).
The levels of alanine aminotransferase, aspartate aminotransferase, albumin, blood urea nitrogen, and creatinine were examined in the 51 patients from the mNGS group who had beneficial clinical outcomes. As shown in Fig. 3d, fewer patients in the mNGS group had abnormal levels of these clinical indicators at discharge (compared to admission).
In our study, we systematically compared mNGS and standard methods in parallel for the diagnosis of CAP. mNGS analyses yielded greater pathogen detection and were associated with better clinical outcomes.
In the 14 samples that yielded a diagnosis by mNGS only (although tested by both mNGS metagenomics and culture), the causative pathogens were either not considered by treating clinicians or had tested negative by culture. These findings highlight a key advantage of the metagenomic NGS approach – it detects a broad array of potential infectious agents in a single assay. Moreover, among the 59 cases in the mNGS group, a significant portion of 31 cases were identified as polymicrobial infections by NGS, including three where co-infections of bacteria, fungi, and viruses were identified. With more clinical application of metagenomic testing, our understanding of the etiology of infectious diseases (in this case CAP) is very likely to include a more comprehensive spectrum of unculturable infectious agents and co-infections. The results of metagenomic NGS can be valuable even when they are concordant with results of conventional testing or confirm empirical treatment plans. In those cases, it provides reassurance of the diagnosis and potentially rules out non-infection cases.
Although previous studies mostly focused on the diagnostic usefulness of mNGS assays, the current study further assessed the impact of this approach on clinical management and outcomes. In our study, treatment plans were changed in 11 patients and confirmed in 24 based on the mNGS results. These patients showed significantly better outcomes than the control group. In our cohort, BALF samples were in general more likely to yield better pathogen detection compared to blood samples. This finding suggests that although testing blood samples can facilitate pathogen detection in CAP patients, they may not offer the best negative predictive value.
Currently, mNGS-based methods still have limitations. With the current technology workflow, most laboratories require a minimum of 24 h (and often 36–48 h) from sample receipt to report results , as the analyses consist of multiple complex steps of wet-lab processing and bioinformatics analysis. Further realization of its clinical value for infectious diseases, especially in the ICU setting, a shorter turn-around time and a less skill-demanding workflow will be very critical . Furthermore, the cost of clinical mNGS (for instance, $500 per test in China) prohibits its broader application [33, 34]. However, rapid development of technology and reductions in costs of sequencing will reduce its costs and likely drive its wider adaptation .
With mNGS technology, a meta-transcriptomic assay could expand its capability to include RNA viruses and thus provide more clinically relevant insights into infectious diseases . With the ability to analyze the transcriptomes of both the microbes and the host, distinguishing biomarkers may be identified to guide better clinical management [12, 13].
Our data show that a clinical mNGS approach represents a potential step forward in the diagnosis and management of community-acquired pneumonia. This diagnostic technology may advance the identification of infectious agents, improve diagnosis and treatment, and potentially lead to favorable clinical outcome. Further research is warranted to better define, validate, and improve its clinical applications and usefulness.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Next generation sequencing
Metagenomic next-generation sequencing
- APACHE II:
Acute physiologic assessment and chronic health evaluation II
Bronchoalveolar lavage fluid
Intensive care unit
Polverino, ETorres Marti, A. Community-acquired pneumonia. Minerva Anestesiol. 2011;77:196–211.
Mandell LA, Wunderink RG, Anzueto A, et al. Infectious diseases society of America/American thoracic society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007;44(Suppl 2):S27–72. https://doi.org/10.1086/511159.
Lim WS, Baudouin SV, George RC, et al. BTS guidelines for the management of community acquired pneumonia in adults: update 2009. Thorax. 2009;64(Suppl 3):iii1–55. https://doi.org/10.1136/thx.2009.121434.
Jain S, Self WH, Wunderink RG, Fakhran S, Balk R, Bramley AM, et al. Community-Acquired Pneumonia Requiring Hospitalization among U.S. Adults. N Engl J Med. 2015;373(5):415–27. https://doi.org/10.1056/NEJMoa1500245.
Torres A, Chalmers JD, Dela Cruz CS, et al. Challenges in severe community-acquired pneumonia: a point-of-view review. Intensive Care Med. 2019;45(2):159–71. https://doi.org/10.1007/s00134-019-05519-y.
Carbonara S, Monno L, Longo, BAngarano, G. Community-acquired pneumonia. Curr Opin Pulm Med. 2009;15(3):261–73. https://doi.org/10.1097/MCP.0b013e3283287c3f.
Tao LL, Hu BJ, He LX, Wei L, Xie HM, Wang BQ, et al. Etiology and antimicrobial resistance of community-acquired pneumonia in adult patients in China. Chin Med J. 2012;125(17):2967–72.
Schlaberg R, Chiu CY, Miller S, Procop GW, Weinstock G, the Professional Practice Committee and Committee on Laboratory Practices of the American Society for Microbiology, et al. Validation of metagenomic next-generation sequencing tests for universal pathogen detection. Arch Pathol Lab Med. 2017;141(6):776–86. https://doi.org/10.5858/arpa.2016-0539-RA.
Ewig S, Torres A, Angeles Marcos M, Angrill J, Rano A, de Roux A, et al. Factors associated with unknown aetiology in patients with community-acquired pneumonia. Eur Respir J. 2002;20(5):1254–62. https://doi.org/10.1183/09031936.02.01942001.
Louie JK, Hacker JK, Gonzales R, Mark J, Maselli JH, Yagi S, et al. Characterization of viral agents causing acute respiratory infection in a San Francisco University medical center clinic during the influenza season. Clin Infect Dis. 2005;41(6):822–8. https://doi.org/10.1086/432800.
Wilson MR, Naccache SN, Samayoa E, Biagtan M, Bashir H, Yu G, et al. Actionable diagnosis of neuroleptospirosis by next-generation sequencing. N Engl J Med. 2014;370(25):2408–17. https://doi.org/10.1056/NEJMoa1401268.
Chiu CY, Miller SA. Clinical metagenomics. Nat Rev Genet. 2019;20(6):341–55. https://doi.org/10.1038/s41576-019-0113-7.
Forbes JD, Knox NC, Ronholm J, Pagotto F, Reimer A. Metagenomics: The Next Culture-Independent Game Changer. Front Microbiol. 2017;8:1069. https://doi.org/10.3389/fmicb.2017.01069.
Blauwkamp TA, Thair S, Rosen MJ, Blair L, Lindner MS, Vilfan ID, et al. Analytical and clinical validation of a microbial cell-free DNA sequencing test for infectious disease. Nat Microbiol. 2019;4(4):663–74. https://doi.org/10.1038/s41564-018-0349-6.
Wilson MR, Sample HA, Zorn KC, Arevalo S, Yu G, Neuhaus J, et al. Clinical metagenomic sequencing for diagnosis of meningitis and encephalitis. N Engl J Med. 2019;380(24):2327–40. https://doi.org/10.1056/NEJMoa1803396.
Miller S, Naccache SN, Samayoa E, Messacar K, Arevalo S, Federman S, et al. Laboratory validation of a clinical metagenomic sequencing assay for pathogen detection in cerebrospinal fluid. Genome Res. 2019;29(5):831–42. https://doi.org/10.1101/gr.238170.118.
Gu W, Deng X, Lee M, et al. Rapid pathogen detection by metagenomic next-generation sequencing of infected body fluids. Nat Med. 2020. https://doi.org/10.1038/s41591-020-1105-z.
Zhu N, Zhang D, Wang W, et al. A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med. 2020;382(8):727–33.
Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395(10223):507–13. https://doi.org/10.1016/S0140-6736(20)30211-7.
Ren LL, Wang YM, Wu ZQ, Xiang ZC, Guo L, Xu T, et al. Identification of a novel coronavirus causing severe pneumonia in human: a descriptive study. Chin Med J. 2020;133(9):1015–24. https://doi.org/10.1097/cm9.0000000000000722.
Langelier C, Kalantar KL, Moazed F, Wilson MR, Crawford ED, Deiss T, et al. Integrating host response and unbiased microbe detection for lower respiratory tract infection diagnosis in critically ill adults. Proc Natl Acad Sci. 2018;115(52):E12353–62. https://doi.org/10.1073/pnas.1809700115.
Ai JW, Zhang Y, Zhang HC, Xu T, Zhang WH. Era of molecular diagnosis for pathogen identification of unexplained pneumonia, lessons to be learned. Emerg Microbes Infect. 2020;9(1):597–600. https://doi.org/10.1080/22221751.2020.1738905.
Chen X, Cao K, Wei Y, Qian Y, Liang J, Dong D, et al. Metagenomic next-generation sequencing in the diagnosis of severe pneumonias caused by chlamydia psittaci. Infection. 2020;48(4):535–42. https://doi.org/10.1007/s15010-020-01429-0.
Di Pasquale MF, Sotgiu G, Gramegna A, et al. Prevalence and etiology of community-acquired pneumonia in Immunocompromised patients. Clin Infect Dis. 2019;68(9):1482–93. https://doi.org/10.1093/cid/ciy723.
Zinter MS, Dvorak CC, Mayday MY, Iwanaga K, Ly NP, McGarry ME, et al. Pulmonary metagenomic sequencing suggests missed infections in Immunocompromised children. Clin Infect Dis. 2019;68(11):1847–55. https://doi.org/10.1093/cid/ciy802.
Wang K, Li P, Lin Y, et al. Metagenomic diagnosis for a culture-negative sample from a patient with severe pneumonia by nanopore and next-generation sequencing. Front Cell Infect Microbiol. 2020;10. https://doi.org/10.3389/fcimb.2020.00182.
Cao B, Huang Y, She DY, Cheng QJ, Fan H, Tian XL, et al. Diagnosis and treatment of community-acquired pneumonia in adults: 2016 clinical practice guidelines by the Chinese thoracic society, Chinese Medical Association. Clin Respir J. 2018;12(4):1320–60. https://doi.org/10.1111/crj.12674.
Metlay JP, Waterer GW, Long AC, et al. Diagnosis and treatment of adults with community-acquired pneumonia an official clinical practice guideline of the American thoracic society and infectious diseases society of America. Am J Respir Crit Care Med. 2019;200(7):e45–67. https://doi.org/10.1164/rccm.201908-1581ST.
Niewiński G, Starczewska, MKański, A. Prognostic scoring systems for mortality in intensive care units--the APACHE model. Anaesthesiol Intensive Ther. 2014;46(1):46–9. https://doi.org/10.5603/ait.2014.0010.
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009;25:1754–60. https://doi.org/10.1093/bioinformatics/btp324.
Simner PJ, Miller S, Carroll KC. Understanding the promises and hurdles of metagenomic next-generation sequencing as a diagnostic tool for infectious diseases. Clin Infect Dis. 2018;66(5):778–88. https://doi.org/10.1093/cid/cix881.
Greninger AL. The challenge of diagnostic metagenomics. Expert Rev Mol Diagn. 2018;18(7):605–15. https://doi.org/10.1080/14737159.2018.1487292.
Miao Q, Ma Y, Wang Q, Pan J, Zhang Y, Jin W, et al. Microbiological diagnostic performance of metagenomic next-generation sequencing when applied to clinical practice. Clincal Infect Dis. 2018;67(suppl_2):S231–s240. https://doi.org/10.1093/cid/ciy693.
Ramachandran PS, Wilson MR. Metagenomics for neurological infections - expanding our imagination. Nat Rev Neurol. 2020;16(10):547–56. https://doi.org/10.1038/s41582-020-0374-y.
Han D, Li Z, Li R, Tan P, Zhang R, Li J. mNGS in clinical microbiology laboratories: on the road to maturity. Crit Rev Microbiol. 2019;45(5-6):668–85. https://doi.org/10.1080/1040841x.2019.1681933.
Zhang YZ, Shi M, Holmes EC. Using metagenomics to characterize an expanding virosphere. Cell. 2018;172(6):1168–72. https://doi.org/10.1016/j.cell.2018.02.043.
This work was supported by the National Natural Science Foundation of China (No. 61976223), Military Medical Innovation Research Project of PLA General Hospital (CX19030) and the Key Program of Translational Medicine of PLA General Hospital (No. 2018TM-03). The funding bodies had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
Sample collection was reviewed and approved by the Chinese People’s Liberation Army General Hospital Ethics Committee Review Board. Informed consents were signed by patients or surrogates. No minors were enrolled in this study. In the cases of adults with cognitive decline, consents to participate were obtained from their legal guardians or representatives.
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Xie, F., Duan, Z., Zeng, W. et al. Clinical metagenomics assessments improve diagnosis and outcomes in community-acquired pneumonia. BMC Infect Dis 21, 352 (2021). https://doi.org/10.1186/s12879-021-06039-1
- Next-generation sequencing
- Clinical metagenomics
- Community-acquired pneumonia
- Polymicrobial infections
- Clinical study