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mNGS on BALF samples shows higher pathogen detection in pulmonary infections vs. conventional testingmNGS detects more lung infection pathogens than standard tests

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Key Takeaway
Consider mNGS as a complementary diagnostic tool for pulmonary infections, noting its higher detection rates in this observational cohort.

This was an observational cohort study conducted in the Department of Respiratory Medicine at Shandong Provincial Hospital. The population included 136 patients with suspected pulmonary infections. The intervention was metagenomic next-generation sequencing (mNGS) on bronchoalveolar lavage fluid (BALF) samples, compared to conventional microbiological testing (CMT) on BALF samples.

The main results showed that mNGS had a higher overall pathogen detection rate than CMT (77.2% [105/136] vs. 50.0% [68/136], P < 0.001). The sensitivity for pathogen detection was also higher with mNGS (74.6% vs. 46.7%, P < 0.001). mNGS detected mixed infections more frequently (19.1% vs. 8.8%, P < 0.05). In immunocompromised patients, the incidence of mixed infections was higher (35.1% vs. 13.1% in immunocompetent, P < 0.05), and antimicrobial therapy adjustments guided by mNGS were more common in immunocompromised patients (56.8% vs. 35.4%, χ² = 5.094, P < 0.05).

Safety and tolerability were not reported. Key limitations include the retrospective, single-center design and that it was not reported if patients were consecutive or randomly selected. The practice relevance suggests mNGS offers superior sensitivity and broader pathogen coverage for pulmonary infections, especially in immunocompromised patients, and can guide antimicrobial therapy adjustments. This is an observational study comparing diagnostic methods; it does not establish causation for treatment outcomes.

Researchers in a Shandong hospital compared a genetic test called metagenomic next-generation sequencing (mNGS) with conventional microbiological testing on bronchoalveolar lavage fluid from 136 patients with suspected pulmonary infections. The goal was to see which method more often identified germs and how results affected treatment decisions.

Overall, mNGS identified pathogens in 77.2% of patients, compared with 50.0% by conventional methods. It also showed higher sensitivity (74.6% vs. 46.7%) and detected mixed infections more often (19.1% vs. 8.8%). Mixed infections were more common in immunocompromised patients (35.1% vs. 13.1% in immunocompetent), and mNGS results led to more frequent adjustments to antimicrobial therapy in immunocompromised patients (56.8% vs. 35.4%).

Safety events were not reported. The study has important limits: it was retrospective, done at a single center, and it’s unclear if patients were selected consecutively or randomly. Because it compares diagnostic methods, it cannot show that treatment changes improve outcomes.

What to take away: mNGS can complement standard tests by finding more pathogens and mixed infections, especially in immunocompromised patients, but its impact on patient outcomes needs further study.

What this means for you:
mNGS may find more lung pathogens than standard tests, but its effect on outcomes is uncertain.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundPulmonary infections represent a significant global health concern, contributing substantially to morbidity and mortality worldwide. Metagenomic next-generation sequencing (mNGS) represents an advanced, comprehensive, and unbiased diagnostic approach for pathogen identification, effectively overcoming many limitations inherent in conventional diagnostic methods. This study aimed to systematically evaluate the clinical performance of mNGS in the etiological diagnosis of pulmonary infections, with a particular emphasis on its utility across diverse immune statuses.MethodsThis retrospective study included 136 patients with suspected pulmonary infections admitted to the Department of Respiratory Medicine at Shandong Provincial Hospital from June 2023 to April 2025. Bronchoalveolar lavage fluid (BALF) samples were collected from all patients and concurrently subjected to mNGS and conventional microbiological testing (CMT). The pathogen detection spectrum and diagnostic performance of mNGS were systematically compared against those of CMT.ResultsmNGS exhibited a significantly higher overall pathogen detection rate compared to CMT (77.2% vs. 50.0%, P < 0.001). Regarding the pathogen spectrum, mNGS identified a broader array of microorganisms, encompassing 19 bacterial, 9 fungal, and 2 mycobacterial species, in contrast to the 11 bacterial, 5 fungal, and 1 mycobacterial species detected by CMT. Diagnostic performance analysis further revealed that mNGS sensitivity was significantly superior to that of CMT (74.6% vs. 46.7%, P < 0.001). Furthermore, mNGS demonstrated a distinct advantage in detecting mixed infections, with a detection rate of 19.1%, significantly exceeding that of CMT (8.8%, P < 0.05). Subgroup analysis indicated a significantly higher incidence of mixed infections in immunocompromised patients compared to immunocompetent patients (35.1% vs. 13.1%, P < 0.05). Additionally, immunocompromised patients were more frequently subjected to adjustments in antimicrobial therapy guided by mNGS results (56.8% vs. 35.4%, χ² = 5.094, P < 0.05).ConclusionsIn conclusion, mNGS offers superior sensitivity and broader pathogen coverage for the etiological diagnosis of pulmonary infections compared to conventional microbiological testing. Its enhanced capability to detect mixed infections significantly improves diagnostic accuracy in immunocompromised patients and effectively facilitates the dynamic optimization of antimicrobial therapy. Serving as a powerful complement to traditional diagnostic methods, mNGS holds particular value for the rapid diagnosis of complex and immunosuppression-associated pulmonary infections.
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