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Volume 50, Number 6, December 2017

Epidemiology of human coronavirus NL63 infection among hospitalized patients with pneumonia in Taiwan 


Su-Hua Huang, Mei-Chi Su, Ni Tien, Chien-Jhen Huang, Yu-Ching Lan, Chen-Sheng Lin, Chao-Hsien Chen, Cheng-Wen Lin


 

Corresponding author:

Cheng-Wen Lin, Corresponding author. Department of Medical Laboratory Science and Biotechnology, China Medical University, Number 91, Hsueh-Shih Road, Taichung 40402, Taiwan. 



 

Background and purpose: 

Human coronavirus (HCoV) NL63 is recognized in association with upper or lower respiratory tract illnesses in children. This study surveyed the prevalence of HCoV-NL63 and influenza viruses in patients with influenza-like illness in Taiwan during 2010–2011. 



 

Methods:

Throat samples from 107 hospitalized patients with pneumonia and 175 outpatients with influenza-like illness were examined using real-time polymerase chain reaction assays with virus-specific primers, and then virus-positive specimens were confirmed by sequencing the polymerase chain reaction products. 



 

Results:

HCoV-NL63 infection was identified in 8.4% (9/107) of hospitalized patients with pneumonia, but not found in outpatients with influenza-like illness. Age distribution of HCoV-NL63 infection in hospitalized patients with pneumonia indicated that the group aged 16–25 years (20%) had the highest positive rate compared with the other groups, and exhibited a similar age-specific pattern to influenza A/H1N1 infection, but not influenza A/H3N2 and B infections in hospitalized patients. Seasonal prevalence of HCoV-NL63 infection was late winter, overlapping the highest peak of the influenza A/H1N1 epidemic during December 2010 to March 2011 in Taiwan. Co-infection of HCoV-NL63 and influenza A/H1N1 was detected in three hospitalized patients. Clinical manifestation analysis indicated that the main symptoms for HCoV-NL63 infection included fever (88.9%), cough (77.8%), and pneumonia (100%). Co-infection caused significantly higher rates of breathing difficulties, cough, and sore throat than those of single infection with HCoV-NL63 and influenza A/H1N1. Phylogenetic analysis indicated a low level of heterogeneity between Taiwan and global HCoV-NL63 strains. 



 

Conclusion:

Understanding epidemiology of HCoV-NL63 in Taiwan provides an insight for worldwide surveillance of HCoV-NL63 infection. 



 

Key words:

age distribution, human coronavirus NL63, phylogenetic analysis, pneumonia, seasonality