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Detection of Dengue Viral Migration to Sri Lanka

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dc.contributor.author Withanage, G.P. en
dc.contributor.author Hapuarachchi, H.C. en
dc.contributor.author Gunawardene, Y.I.N.S. en
dc.contributor.author Hapugoda, M.D. en_US
dc.date.accessioned 2018-12-31T10:23:09Z en
dc.date.available 2018-12-31T10:23:09Z en
dc.date.issued 2018 en
dc.identifier.citation Withanage,G.P., Hapuarachchi ,H.C.,Gunawardena ,Y. I. N.S. and Hapudoda,M.D.(2018). Detection of Dengue Viral Migration to Sri Lanka. 19th Conference on Postgraduate Research, International Postgraduate Research Conference 2018, Faculty of Graduate Studies,University of Kelaniya, Sri Lanka. p26 en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/19196 en_US
dc.description.abstract Dengue is one of the most important mosquito-borne viral infectionsin Sri Lanka.The causative agent is Dengue Viruses (DENV) and the primary vector of the virus is Aedesaegypti(Linnaeus) while Ae. albopictus (Skuse) is the subsidiary vector. The current research was focused on the detection of DENV serotypes and genotypes circulating in mosquitoes during the dengue epidemic in June and July, 2017 in the EriyawetiyaGramaNiladhari division, where one of the dengue high-risk area in Kelaniya Medical Officer of Health (MOH) area in the District of Gampaha, Sri Lanka. Aedesmosquitoes were collected following WHO guidelinesandthe field-caught mosquitoes were transported to the laboratory for species identification and subsequent analysis. Head and thorax of each mosquito was removed and mosquito samples were pooled separately. Total RNA was extracted from mosquito samples and semi-nested Polymerase Chain Reaction (PCR) was performed to identify DENV serotypes present in the mosquito samples. The results of the PCR indicated the presence of DENV2 in both Ae. aegypti (1/5) and Ae. albopictus (1/27) mosquitoes. Then complete Envelope (E) gene was amplified with DENV2 specific primers for genotyping of the virus which is required to identify the molecular evolution of the DENV2. Prior to sequencing the PCR products were purified and sequencing results were analyzed usingLaserGene software. The generated sequences were aligned with retrieved DENV2 sequences available at NCBI database and the phylogenetic trees were developed using MEGA7 software with General Time Reversible (GTR) substitution model with gamma distributed rates. The robustness of clades was determined by using bootstrap analysis of 500 replicates. The result of the phylogenetic analysis illustrates that the E gene sequences of DENV2 obtained from two DENVpositive mosquito poolsbelong to DENV2 Cosmopolitan Clade Ib, which has been the dominant strain in South-East Asia, specially Singapore, Indonesia, Malaysia, and China since August, 2015.The evidence suggests recent introduction of this DENV strain into Sri Lanka en_US
dc.language.iso en en_US
dc.publisher 19th Conference on Postgraduate Research, International Postgraduate Research Conference 2018, Faculty of Graduate Studies,University of Kelaniya, Sri Lanka en_US
dc.subject Dengue Virus en_US
dc.subject Serotyping en_US
dc.subject Genotyping en_US
dc.subject Dengue Viral Migration en_US
dc.title Detection of Dengue Viral Migration to Sri Lanka en_US
dc.type Conference Abstract en_US


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