Human Coronavirus Infections in Rural Thailand: A Comprehensive Study Using Real-Time Reverse-Transcription Polymerase Chain Reaction Assays

• Published in: The Journal of infectious diseases 2007-11, Vol.196 (9), p.1321-1328
• Main Authors: Dare, Ryan K., Fry, Alicia M., Chittaganpitch, Malinee, Sawanpanyalert, Pathom, Olsen, Sonja J., Erdman, Dean D.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Biological and medical sciences; Child; Child, Preschool; Coronavirus; Coronavirus infections; Coronavirus Infections - epidemiology; Coronavirus Infections - virology; Diseases; Epidemiology; Female; Fundamental and applied biological sciences. Psychology; Humans; Infant; Infections; Major; Male; Microbiology; Middle Aged; Miscellaneous; Pneumonia; Pneumonia, Viral - epidemiology; Pneumonia, Viral - virology; Respiratory diseases; Reverse Transcriptase Polymerase Chain Reaction; Rural Population; Sensitivity and Specificity; Thailand - epidemiology; Viral pneumonia; Virology; Viruses
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1086/521308

Background. We sought to determine whether infections with human coronaviruses (HCoVs) 229E, OC43, HKU1, and NL63 are associated with pneumonia and to define the epidemiology of HCoV infection in rural Thailand. Methods. We developed a real-time reverse-transcription polymerase chain reaction (RT-PCR) assay panel for the recognized HCoV types and compared HCoV infections in patients hospitalized with pneumonia, outpatients with influenza-like illness, and asymptomatic control patients between September 2003 and August 2005. Results. During study year 1, 43 (5.9%) of 734 patients with pneumonia had HCoV infections; 72.1% of the infections were with OC43. During study year 2, when control patients were available, 21 (1.8%) of 1156 patients with pneumonia, 12 (2.3%) of 513 outpatients, and 6 (2.1%) of 281 control patients had HCoV infections. Compared with infection in control patients, infection with any HCoV type or with all types combined was not associated with pneumonia (adjusted odds ratio for all HCoV types, 0.67 [95% confidence interval, 0.26–1.75]; P= .40 ). HCoV infections were detected throughout both study years; 93.6% of OC43 infections in the first year occurred from January through March. Conclusions. HCoV infections were infrequently detected in rural Thailand by use of sensitive real-time RTPCR assays. We found no association between HCoV infection and illness. However, we noted year-to-year variation in the prevalence of HCoV strains, which likely influenced our results.