Authors
Mayu Hachiya, Kenji Kondo, Hikaru Takahashi, Yukiko Higashide, Jun Kunizaki, Emiko Hoshino, Nodoka Sakurai, Toshihiko Mori
Published in
The Pediatric infectious disease journal. Jul 14, 2026. Epub Jul 14, 2026.
Abstract
Seasonal human coronaviruses (HCoVs) can cause acute respiratory infections in children; however, their epidemiology and clinical features in the post-coronavirus disease 2019 era remain incompletely characterized.
We retrospectively analyzed children under 16 years old with respiratory symptoms who underwent multiplex polymerase chain reaction testing at a hospital in Hokkaido, Japan, between April 2021 and September 2025. Demographic and clinical data were extracted from medical records.
Among 15,197 specimens, 1212 (8.0%) tested positive for HCoVs, including 361 (29.8%) single infections. OC43 was the most frequently detected species (530/1212; 43.7%), followed by NL63 (382/1212; 31.5%), HKU1 (277/1212; 22.9%) and 229E (56/1212; 4.6%). HCoVs circulated year-round, with seasonal peaks shifting from autumn to winter in 2021 and summer in 2022 to winter-spring from 2023 onward. Among single HCoV infections, the median age was 2.0 (interquartile range, 1.0-4.0) years, and 64.8% were male children. Upper respiratory infection was the most common diagnosis, and 14.7% of patients required hospitalization. Species-specific differences were observed: OC43 was associated with younger age, NL63 with croup and HKU1 with headache. Compared with severe acute respiratory syndrome coronavirus 2, seasonal HCoV infections occurred at younger ages and were more frequently associated with lower respiratory tract involvement, despite similar hospitalization rates.
Seasonal patterns of HCoVs were temporarily altered during the coronavirus disease 2019 pandemic but returned to their pre-pandemic winter-spring predominance from 2023. Species-specific clinical differences were observed; compared with severe acute respiratory syndrome coronavirus 2, HCoV infections occurred at younger ages and were more often associated with lower respiratory tract involvement.
PMID:
42444019
Bibliographic data and abstract were imported from PubMed on 14 Jul 2026.
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