TY - JOUR
T1 - Co-infections with Multiple Viruses
T2 - A Frequent cause of Community-Acquired Pneumonia in Sarawak Malaysia
AU - Toh, Teck Hock
AU - Lee, Jeffrey Soon Yit
AU - Yong, Sook Min
AU - Alfie, Nur Alfreena Binti
AU - Ting, Siew Ming
AU - Wong, Chew Ee
AU - Dahian, Kamilah
AU - Wong, See Chang
AU - Cheah, Cheng Foong
AU - Selvarajan, Anantha Raman
AU - Lee, Bee Shuang
AU - Oguzie, Judith U.
AU - Nguyen-Tien, Thang
AU - Trujillo-Vargas, Claudia M.
AU - Silva, Diego B.
AU - Robie, Emily R.
AU - Pulscher, Laura A.
AU - Suhaili, Mohd Raili
AU - Marushchak, Lyudmyla
AU - Gray, Gregory C.
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/12
Y1 - 2025/12
N2 - Objectives: Equatorial Sarawak, Malaysia, has been the site of important novel respiratory virus detections. During the COVID-19 pandemic, we sought to determine viral causes of pneumonia that were not SARS-CoV-2. Methods: Using an informed consent process, we enrolled patients from four hospitals in Sarawak for this cross-sectional study. Patients permitted a nasopharyngeal (NP) swab collection and completed a risk factor questionnaire. We studied NP swabs with molecular diagnostics for previously recognized respiratory viruses such as influenza A and D viruses, and pan-species assays for adenoviruses, coronaviruses, enteroviruses, pneumoviruses, and paramyxoviruses. Results: Among 441 patients, 78.2% had at least one virus detected, and 24.9% had multiple viruses detected. Among the viruses detected, a commercial multiplexing assay found the most prevalent detections were human rhinoviruses (43.1%), respiratory syncytial virus (18.6%), human metapneumovirus (8.6%), influenza A (7%), adenovirus (6.1%), and influenza B (5.6%). However, the pan-species assays detected evidence of 19 additional respiratory viruses that the commercial multiplexing assay missed. Conclusions: Patients with pneumonia in this hot and humid region often had evidence of multiple viral infections, especially children under 5 years old. Clinicians who rely on singleplex molecular assays for prevalent viruses such as influenza A, SARS-CoV-2, and respiratory syncytial virus may miss other important viral causes of illness in such patients.
AB - Objectives: Equatorial Sarawak, Malaysia, has been the site of important novel respiratory virus detections. During the COVID-19 pandemic, we sought to determine viral causes of pneumonia that were not SARS-CoV-2. Methods: Using an informed consent process, we enrolled patients from four hospitals in Sarawak for this cross-sectional study. Patients permitted a nasopharyngeal (NP) swab collection and completed a risk factor questionnaire. We studied NP swabs with molecular diagnostics for previously recognized respiratory viruses such as influenza A and D viruses, and pan-species assays for adenoviruses, coronaviruses, enteroviruses, pneumoviruses, and paramyxoviruses. Results: Among 441 patients, 78.2% had at least one virus detected, and 24.9% had multiple viruses detected. Among the viruses detected, a commercial multiplexing assay found the most prevalent detections were human rhinoviruses (43.1%), respiratory syncytial virus (18.6%), human metapneumovirus (8.6%), influenza A (7%), adenovirus (6.1%), and influenza B (5.6%). However, the pan-species assays detected evidence of 19 additional respiratory viruses that the commercial multiplexing assay missed. Conclusions: Patients with pneumonia in this hot and humid region often had evidence of multiple viral infections, especially children under 5 years old. Clinicians who rely on singleplex molecular assays for prevalent viruses such as influenza A, SARS-CoV-2, and respiratory syncytial virus may miss other important viral causes of illness in such patients.
KW - Community-acquired pneumonia
KW - Epidemiology
KW - Molecular diagnostics
KW - Respiratory viruses
KW - Sarawak
KW - Viral etiology
UR - https://www.scopus.com/pages/publications/105018013033
UR - https://www.scopus.com/pages/publications/105018013033#tab=citedBy
U2 - 10.1016/j.ijregi.2025.100748
DO - 10.1016/j.ijregi.2025.100748
M3 - Article
C2 - 41127489
AN - SCOPUS:105018013033
SN - 2772-7076
VL - 17
JO - IJID Regions
JF - IJID Regions
M1 - 100748
ER -