# Declined Circulation and Seasonal Shifts of Human Coronavirus 229E in the Republic of Korea: Implications for Respiratory Virus Surveillance

**Authors:** Mi-Ru Oh, Jeong Su Han, Sung Hun Jang, Ga-Yeon Kim, Jae Kyung Kim

PMC · DOI: 10.3390/pathogens15020231 · 2026-02-19

## TL;DR

This study tracks the declining presence and seasonal patterns of HCoV-229E in South Korea from 2007 to 2024, highlighting the importance of ongoing virus surveillance.

## Contribution

The study provides the first long-term analysis of HCoV-229E circulation and seasonal trends in South Korea.

## Key findings

- HCoV-229E positivity declined significantly over time (OR per year, 0.916).
- Winter had the highest positivity (2.69%) and summer the lowest (0.29%).
- Children aged 1–5 years had the highest positivity rate (1.89%).

## Abstract

Human coronavirus 229E (HCoV-229E) is an alphacoronavirus that typically causes mild upper respiratory infections but remains understudied in terms of its long-term immuno-ecological behavior. Although the COVID-19 pandemic markedly altered human behavior and viral transmission, extended circulation patterns of HCoV-229E remain poorly defined. We analyzed annual, seasonal, and age-specific trends using real-time PCR–based respiratory virus surveillance data from Dankook University Hospital collected between 2007 and 2024. Among 23,284 nasopharyngeal swab specimens, 344 were positive for HCoV-229E (overall positivity, 1.43%). Positivity declined significantly over time (OR per year, 0.916; 95% CI, 0.894–0.939; p < 0.001). Compared with spring (1.04%), positivity was highest in winter (2.69%) and lowest in summer (0.29%) (both p < 0.001), whereas autumn (0.81%) showed no significant difference. Early childhood (1–5 years) demonstrated a higher likelihood of positivity than infants aged 0 years (aOR, 1.51; p = 0.007) and the highest crude positivity rate (1.89%). Although underlying mechanisms were not directly assessed, this long-term analysis documents a persistent decline and attenuation of seasonal dominance in HCoV-229E detection beyond the period of pandemic-related suppression. These findings underscore the value of sustained laboratory-based surveillance in identifying and tracking long-term changes in respiratory virus circulation patterns and in supporting public health monitoring aligned with Sustainable Development Goal 3 (SDG 3).

## Linked entities

- **Diseases:** upper respiratory infections (MONDO:0024355)

## Full-text entities

- **Genes:** ANPEP (alanyl aminopeptidase, membrane) [NCBI Gene 290] {aka AP-M, AP-N, APN, CD13, GP150, LAP1}
- **Diseases:** mumps (MESH:D009107), dyspnea (MESH:D004417), influenza (MESH:D007251), respiratory illness (MESH:D012140), injury to (MESH:D014947), respiratory infections (MESH:D012141), ARDS (MESH:D012128), pneumonia (MESH:D011014), cough (MESH:D003371), infection (MESH:D007239), COVID-19 (MESH:D000086382), co-infections (MESH:D060085), infectious-disease (MESH:D003141), parotitis (MESH:D010309)
- **Chemicals:** 229E (-)
- **Species:** Enterovirus (genus) [taxon 12059], H3N2 subtype (serotype) [taxon 119210], Human coronavirus OC43 (no rank) [taxon 31631], Orthocoronavirinae (subfamily) [taxon 2501931], Middle East respiratory syndrome-related coronavirus (no rank) [taxon 1335626], Human coronavirus HKU1 (no rank) [taxon 290028], Severe acute respiratory syndrome-related coronavirus (no rank) [taxon 694009], Human coronavirus 229E (no rank) [taxon 11137], Gammacoronavirus (genus) [taxon 694013], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Alphacoronavirus (genus) [taxon 693996], Betacoronavirus (genus) [taxon 694002], Human coronavirus NL63 (no rank) [taxon 277944]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943526/full.md

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Source: https://tomesphere.com/paper/PMC12943526