Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12985-016-0488-4
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dc.titleMolecular epidemiology and evolutionary histories of human coronavirus OC43 and HKU1 among patients with upper respiratory tract infections in Kuala Lumpur, Malaysia
dc.contributor.authorAl-Khannaq, M.N
dc.contributor.authorNg, K.T
dc.contributor.authorOong, X.Y
dc.contributor.authorPang, Y.K
dc.contributor.authorTakebe, Y
dc.contributor.authorChook, J.B
dc.contributor.authorHanafi, N.S
dc.contributor.authorKamarulzaman, A
dc.contributor.authorTee, K.K
dc.date.accessioned2020-10-26T05:11:54Z
dc.date.available2020-10-26T05:11:54Z
dc.date.issued2016
dc.identifier.citationAl-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
dc.identifier.issn1743422X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179940
dc.description.abstractBackground: 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectvirus glycoprotein
dc.subjectvirus RNA
dc.subjectadult
dc.subjectArticle
dc.subjectBetacoronavirus
dc.subjectChina
dc.subjectcohort analysis
dc.subjectcontrolled study
dc.subjectCoronavirus infection
dc.subjectdisease severity
dc.subjectfemale
dc.subjectgene mapping
dc.subjectgenetic recombination
dc.subjectgenetic variability
dc.subjectgenotype phenotype correlation
dc.subjecthuman
dc.subjectHuman coronavirus HKU1
dc.subjectHuman coronavirus OC43
dc.subjectJapan
dc.subjectmajor clinical study
dc.subjectMalaysia
dc.subjectmale
dc.subjectmolecular dynamics
dc.subjectmolecular epidemiology
dc.subjectmolecular evolution
dc.subjectmultiplex polymerase chain reaction
dc.subjectnonhuman
dc.subjectphylogeny
dc.subjectsequence analysis
dc.subjectsymptom
dc.subjectThailand
dc.subjectupper respiratory tract infection
dc.subjectvirus 1a gene
dc.subjectvirus detection
dc.subjectvirus gene
dc.subjectvirus isolation
dc.subjectvirus nucleocapsid
dc.subjectvirus strain
dc.subjectvirus transmission
dc.subjectaged
dc.subjectclassification
dc.subjectCoronavirus Infections
dc.subjectgenetic variation
dc.subjectgenetics
dc.subjectgenotype
dc.subjecthealth survey
dc.subjectHuman coronavirus OC43
dc.subjectisolation and purification
dc.subjectmiddle aged
dc.subjectnasopharynx
dc.subjectRespiratory Tract Infections
dc.subjectvirology
dc.subjectyoung adult
dc.subjectAdult
dc.subjectAged
dc.subjectCoronavirus Infections
dc.subjectCoronavirus OC43, Human
dc.subjectEvolution, Molecular
dc.subjectFemale
dc.subjectGenes, Viral
dc.subjectGenetic Variation
dc.subjectGenotype
dc.subjectHumans
dc.subjectMalaysia
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNasopharynx
dc.subjectPhylogeny
dc.subjectPopulation Surveillance
dc.subjectRespiratory Tract Infections
dc.subjectRNA, Viral
dc.subjectYoung Adult
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/s12985-016-0488-4
dc.description.sourcetitleVirology Journal
dc.description.volume13
dc.description.issue1
dc.description.page33
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