# Clinical Outcomes and Molecular Epidemiology of Human Metapneumovirus in Romanian Hospitalized Patients

**Authors:** Ovidiu Vlaicu, Oana Săndulescu, Anca Streinu-Cercel, Anca Cristina Drăgănescu, Victor Daniel Miron

PMC · DOI: 10.3390/microorganisms14020403 · Microorganisms · 2026-02-08

## TL;DR

This study examines hMPV infections in hospitalized Romanian patients, revealing nonspecific symptoms and distinct age-related severity patterns, along with evolving virus subclades over time.

## Contribution

The study provides new insights into the clinical and molecular epidemiology of hMPV in hospitalized patients in Romania, including age-specific disease patterns and subclade dynamics.

## Key findings

- Children made up 62% of hMPV cases, with nonspecific symptoms like cough and fever.
- Adults were more likely to experience dyspnea and respiratory failure requiring oxygen.
- Molecular analysis showed subclade A2b1 in 2023–2024 and A2b2 in 2024–2025.

## Abstract

Human metapneumovirus (hMPV) is an important cause of acute respiratory tract infections. This study aimed to describe the clinical characteristics, outcomes, and molecular features of hMPV infection among hospitalized patients in Romania. We performed an analysis of prospectively collected surveillance data from patients hospitalized with influenza-like illness or severe acute respiratory infection and tested by RT-PCR for the presence of respiratory viruses between November 2023 and May 2025. Only cases of hMPV monoinfection were analyzed. Clinical, laboratory, and outcome data were analyzed, and a subset of samples with high viral load underwent genetic sequencing of the hMPV fusion (F) gene. A total of 71 patients met the criteria. Children accounted for 62.0% of cases. The clinical features were nonspecific, dominated by cough (87.3%), fever (80.3%), and nasal congestion (47.9%). Adults were significantly more likely to develop dyspnea and respiratory failure requiring oxygen supplementation (51.9% vs. 6.8%, p < 0.001). The median length of hospital stay was 5 days (interquartile range: 2, 7 days), and dyspnea at admission was the strongest factor associated with prolongation of hospitalization. The rate of intensive care unit admission was 4.2%, and overall outcomes were favorable, with no deaths recorded. Molecular analysis revealed the circulation of different hMPV subclades across consecutive seasons, with A2b1 predominating in 2023–2024 and A2b2 in 2024–2025. hMPV infection in hospitalized patients presents with nonspecific clinical features and shows distinct age-related patterns of severity and complications. Early identification of respiratory involvement, particularly dyspnea at presentation, may support risk stratification and optimized clinical management. Preliminary molecular data indicate dynamic circulation of hMPV subclades, underscoring the value of integrated clinical and molecular surveillance. These findings support the inclusion of hMPV in the differential diagnosis of severe acute respiratory infections and highlight the importance of continued monitoring in the post-pandemic period.

## Linked entities

- **Diseases:** respiratory failure (MONDO:0021113)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** rhinorrhea (MESH:D012818), bacterial co-infections (MESH:D060085), viral (MESH:D014777), immunodeficiency (MESH:D007153), sore throat (MESH:D010612), malnutrition (MESH:D044342), deaths (MESH:D003643), COVID-19 (MESH:D000086382), end-stage renal disease (MESH:D007676), nasal congestion (MESH:D009668), hMPV infection (MESH:D007239), dehydration (MESH:D003681), cough (MESH:D003371), wheezing (MESH:D012135), congestive heart failure (MESH:D006333), Myalgia (MESH:D063806), coronary artery disease (MESH:D003324), cardiac complications (MESH:D006331), interstitial pneumonia (MESH:D017563), neuromuscular disorders (MESH:D009468), bronchiolitis (MESH:D001988), SARI (MESH:D045169), Infectious Diseases (MESH:D003141), injury to (MESH:D014947), respiratory co-infections (MESH:D012141), inflammatory (MESH:D007249), enterovirus (MESH:D004769), otitis (MESH:D010031), headache (MESH:D006261), ILI (MESH:D007251), respiratory tract disease (MESH:D012140), pulmonary consolidation (MESH:D008171), lymphopenia (MESH:D008231), diabetes mellitus (MESH:D003920), malignancies (MESH:D009369), Dyspnea (MESH:D004417), inflammatory syndrome (MESH:D018746), bacterial superinfection (MESH:D015163), respiratory failure (MESH:D012131), pneumonia (MESH:D011014), COPD (MESH:D029424), hMPV (MESH:D001734), fever (MESH:D005334), acute (MESH:D000208), Frailty (MESH:D000073496), hypoxemia (MESH:D000860), Otitis media (MESH:D010033)
- **Chemicals:** SYBR Safe (-), agarose (MESH:D012685), oxygen (MESH:D010100), ribavirin (MESH:D012254)
- **Species:** Respiratory syncytial virus (no rank) [taxon 12814], Adenoviridae (family) [taxon 10508], Homo sapiens (human, species) [taxon 9606], Mycoplasmoides pneumoniae (Filterable agent of primary atypical pneumonia, species) [taxon 2104], Human rhinovirus sp. (species) [taxon 169066], Chlamydia pneumoniae (species) [taxon 83558], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Bordetella pertussis (species) [taxon 520], human metapneumovirus (no rank) [taxon 162145]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943196/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943196/full.md

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Source: https://tomesphere.com/paper/PMC12943196