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Investigation of dengue virus serotypes and genetic variability in relation to disease severity and transmission

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dc.contributor.author Jayasooriya, D.H.S.W.
dc.date.accessioned 2016-06-07T03:56:52Z
dc.date.available 2016-06-07T03:56:52Z
dc.date.issued 2012
dc.identifier.citation Jayasooriya, D.H.S.W. , Investigation of dengue virus serotypes and genetic variability in relation to disease severity and transmission[M.Phil thesis]. Kelaniya: University of Kelaniya; 2012: 271 p en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/13466
dc.description Dissertation: M.Phil., University of Kelaniya, 2012 en_US
dc.description.abstract Sri Lanka has been experiencing more or less periodic dengue outbreaks. METHODOLOGY: Acute phase blood samples were collected from patients clinically suspected of having dengue as determined by the WHO criteria (WHO 1997) within 4 days of onset of fever, from the hospitals in the Sri Lankan districts of Colombo, Gampaha, Kandy, Kurunegala throughout the year. Dengue vector Aedes mosquitoes were colleted from the above geographical areas where positive cases were reported, Pooled mosquitoes and sera were subjected to analysis. RT-PCR and RT-PCR-LH established methods were used to detect dengue virus. Envelope glycoprotein gene (E gene) of DENY serotypes were sequenced and were compared with available sequences representative of the Americas, Oceania, Africa, South Asia, East Asia, and the Middle East. Deduced amino acid sequences of the Present Study Sri Lankan isolates (PSSL-iso) were compared with the past Sri Lankan isolates and South Asian isolates. Sequences of DF an DHF patients were compared as well. Clinical symptoms among serotypes in relation to severity were investigated. RESULTS AND DISCUSSION: In each district a minimum of 3 serotypes were in circulation. DEN-2 and DEN-3 were the most abundant .There was greater degree of conservation among the geographical isolates of DEN-2 compared to that of DEN-3. Evolutionary pressures act on the two serotypes differently despite both being co-transmitted within close proximities. Specific substitutions or substitution patters which could differentiate between DF and DHF/DSS were not found. However phylogentic analysis in DEN-3 revealed clustering of five isolates which showed an increased tendency to be associated with DHF or severe form of disease than the rest which harboured amino acid substitution Asn383^Lys383 on the lateral ridge of ED-III domain within the "informative sites" or sites known as unique conserved site for G-III. DEN-2 isolates belonged to the Cosmopolitan genotype were shown to have more of an Indian ancestry than a Sri Lankan one as they were closer in terms of phylogeny to the Indian origin isolates than to the previously existed Sri Lankan isolates. DEN-2 harboured unique Ile226 lying within the Previously Determined Antigenic Regions (PDAR) a substitution which was not present in any of the South Asian isolates analysed. Simultaneous co-infections by DEN-2& DEN-3 and DEN-4 &DEN-3 surprisingly lead to a reduction in disease severity. The results indicated that it is not in fact the number of amino acid substitutions which could determine the severity of disease but the type of substitution and the position within the domains which they occur. Most abundant vector species found in all districts was Aedes dlbopictus and all pools positive for DENY were Aedes albopictus pools. Moreover positive DENY transmission was observed in localities where Breteau index (BI) was as less as 5.55 suggesting the importance of the role of A .albopictus an "underrated vector". The findings in total suggest that all districts studied are hyperendemic to dengue and Sri Lanka is highly susceptible to successive outbreaks in the future while the difference of evolutionary pressures acting on the predominant serotypes and the reasons said above are likely to shape the nature of future outbreaks en_US
dc.language.iso en_US en_US
dc.publisher University of Kelaniya en_US
dc.subject dengue en_US
dc.title Investigation of dengue virus serotypes and genetic variability in relation to disease severity and transmission en_US
dc.type Thesis en_US


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