Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12985-016-0488-4
Title: Molecular epidemiology and evolutionary histories of human coronavirus OC43 and HKU1 among patients with upper respiratory tract infections in Kuala Lumpur, Malaysia
Authors: Al-Khannaq, M.N
Ng, K.T 
Oong, X.Y
Pang, Y.K
Takebe, Y
Chook, J.B
Hanafi, N.S
Kamarulzaman, A
Tee, K.K
Keywords: virus glycoprotein
virus RNA
adult
Article
Betacoronavirus
China
cohort analysis
controlled study
Coronavirus infection
disease severity
female
gene mapping
genetic recombination
genetic variability
genotype phenotype correlation
human
Human coronavirus HKU1
Human coronavirus OC43
Japan
major clinical study
Malaysia
male
molecular dynamics
molecular epidemiology
molecular evolution
multiplex polymerase chain reaction
nonhuman
phylogeny
sequence analysis
symptom
Thailand
upper respiratory tract infection
virus 1a gene
virus detection
virus gene
virus isolation
virus nucleocapsid
virus strain
virus transmission
aged
classification
Coronavirus Infections
genetic variation
genetics
genotype
health survey
Human coronavirus OC43
isolation and purification
middle aged
nasopharynx
Respiratory Tract Infections
virology
young adult
Adult
Aged
Coronavirus Infections
Coronavirus OC43, Human
Evolution, Molecular
Female
Genes, Viral
Genetic Variation
Genotype
Humans
Malaysia
Male
Middle Aged
Nasopharynx
Phylogeny
Population Surveillance
Respiratory Tract Infections
RNA, Viral
Young Adult
Issue Date: 2016
Citation: Al-Khannaq, M.N, Ng, K.T, Oong, X.Y, Pang, Y.K, Takebe, Y, Chook, J.B, Hanafi, N.S, Kamarulzaman, A, Tee, K.K (2016). Molecular epidemiology and evolutionary histories of human coronavirus OC43 and HKU1 among patients with upper respiratory tract infections in Kuala Lumpur, Malaysia. Virology Journal 13 (1) : 33. ScholarBank@NUS Repository. https://doi.org/10.1186/s12985-016-0488-4
Rights: Attribution 4.0 International
Abstract: Background: Despite the worldwide circulation of human coronavirus OC43 (HCoV-OC43) and HKU1 (HCoV-HKU1), data on their molecular epidemiology and evolutionary dynamics in the tropical Southeast Asia region is lacking. Methods: The study aimed to investigate the genetic diversity, temporal distribution, population history and clinical symptoms of betacoronavirus infections in Kuala Lumpur, Malaysia between 2012 and 2013. A total of 2,060 adults presented with acute respiratory symptoms were screened for the presence of betacoronaviruses using multiplex PCR. The spike glycoprotein, nucleocapsid and 1a genes were sequenced for phylogenetic reconstruction and Bayesian coalescent inference. Results: A total of 48/2060 (2.4 %) specimens were tested positive for HCoV-OC43 (1.3 %) and HCoV-HKU1 (1.1 %). Both HCoV-OC43 and HCoV-HKU1 were co-circulating throughout the year, with the lowest detection rates reported in the October-January period. Phylogenetic analysis of the spike gene showed that the majority of HCoV-OC43 isolates were grouped into two previously undefined genotypes, provisionally assigned as novel lineage 1 and novel lineage 2. Sign of natural recombination was observed in these potentially novel lineages. Location mapping showed that the novel lineage 1 is currently circulating in Malaysia, Thailand, Japan and China, while novel lineage 2 can be found in Malaysia and China. Molecular dating showed the origin of HCoV-OC43 around late 1950s, before it diverged into genotypes A (1960s), B (1990s), and other genotypes (2000s). Phylogenetic analysis revealed that 27.3 % of the HCoV-HKU1 strains belong to genotype A while 72.7 % belongs to genotype B. The tree root of HCoV-HKU1 was similar to that of HCoV-OC43, with the tMRCA of genotypes A and B estimated around the 1990s and 2000s, respectively. Correlation of HCoV-OC43 and HCoV-HKU1 with the severity of respiratory symptoms was not observed. Conclusions: The present study reported the molecular complexity and evolutionary dynamics of human betacoronaviruses among adults with acute respiratory symptoms in a tropical country. Two novel HCoV-OC43 genetic lineages were identified, warranting further investigation on their genotypic and phenotypic characteristics. © 2016 Al-Khannaq et al.
Source Title: Virology Journal
URI: https://scholarbank.nus.edu.sg/handle/10635/179940
ISSN: 1743422X
DOI: 10.1186/s12985-016-0488-4
Rights: Attribution 4.0 International
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