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Etiology of Severe Community-Acquired Pneumonia in Adults Based on Metagenomic Next-Generation Sequencing: A
Xiaodong Wu1, Yuanyuan Li2, Ming Zhang3
1Department of Respiratory and Critical Care Medicine, Shanghai East Hospital, Tongji University, Shanghai, China.
Background:
Metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) has the potential to improve the pathogen identification in severe community-acquired pneumonia (SCAP).
Methods:
In this 1.5-year, multicenter, prospective study, we investigated the usefulness of mNGS of BALF for identifying pathogens of SCAP in hospitalized adults, comparing it with other laboratory methods.
Results:
Of 329 SCAP adults, a microbial etiology was established in 304 cases (92.4%). The overall microbial yield was 90.3% for mNGS versus 39.5% for other methods (P < 0.05). The most frequently detected pathogens in immunocompetent patients were Streptococcus pneumoniae (14.8%), rhinovirus (9.8%), Haemophilus influenzae (9.1%), Staphylococcus aureus (8.7%), and Chlamydia psittaci (8.0%), while in immunocompromised patients they were Pneumocystis jirovecii (44.6%), Klebsiella pneumoniae (18.5%), Streptococcus pneumoniae (15.4%), Haemophilus influenzae (13.8%), and Pseudomonas aeruginosa (13.8%). Notably, novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was identified from two patients solely by mNGS in January 2020; uncommon pathogens including Orientia tsutsugamushi and Nocardia otitidiscaviarum were identified from one patient, respectively. Furthermore, mixed infections were detected in 56.8% of the patients.
Conclusions:
A high microbial detection rate was achieved in SCAP adults using mNGS testing of BALF. The most frequently detected pathogens of SCAP differed between immunocompetent and immunocompromised patients. mNGS testing may be an powerful tool for early identification of potential pathogens for SCAP to initiate a precise antimicrobial therapy.
Insights
Metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) significantly improves pathogen identification in severe community-acquired pneumonia (SCAP). This method offers a higher microbial yield compared to traditional techniques, aiding in precise antimicrobial therapy.
Area of Science:
- Medical Microbiology
- Infectious Diseases
- Genomics
Background:
- Severe community-acquired pneumonia (SCAP) diagnosis relies on accurate pathogen identification.
- Traditional laboratory methods have limitations in detecting all causative agents of SCAP.
- Metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) presents a promising advancement.
Purpose of the Study:
- To evaluate the diagnostic utility of mNGS of BALF for SCAP in hospitalized adults.
- To compare the pathogen detection rate of mNGS with conventional laboratory methods.
- To identify common and uncommon pathogens in SCAP patients, differentiating between immunocompetent and immunocompromised individuals.
Main Methods:
- A 1.5-year, multicenter, prospective study involving hospitalized adults with SCAP.
- Collection and analysis of bronchoalveolar lavage fluid (BALF) using mNGS.
- Comparison of mNGS results with other standard laboratory diagnostic methods.
Main Results:
- A microbial etiology was established in 92.4% of SCAP cases.
- mNGS demonstrated a significantly higher overall microbial yield (90.3%) compared to other methods (39.5%).
- Distinct pathogen profiles were observed in immunocompetent versus immunocompromised patients, with mNGS identifying novel and uncommon pathogens, including SARS-CoV-2.
Conclusions:
- mNGS of BALF achieves a high microbial detection rate in SCAP.
- Pathogen prevalence in SCAP varies between immunocompetent and immunocompromised hosts.
- mNGS is a powerful tool for early and precise pathogen identification in SCAP, guiding antimicrobial therapy.
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