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Viral load and genotype analysis of Hepatitis E virus among HEV infected women in Bangladesh

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dc.contributor.advisor Choudhury, Dr. Naiyyum
dc.contributor.author Rakhshanda, Shagoofa
dc.date.accessioned 2018-01-09T06:07:18Z
dc.date.available 2018-01-09T06:07:18Z
dc.date.copyright 2016
dc.date.issued 2016-07
dc.identifier.other ID 16176007
dc.identifier.uri http://hdl.handle.net/10361/8985
dc.description This dissertation is submitted in partial fulfilment of the requirements for the degree of Bachelor of Science in Biotechnology, 2016. en_US
dc.description Cataloged from PDF version of thesis report.
dc.description Includes bibliographical references (page 55- 60).
dc.description.abstract With an increase in the number of hepatitits E viral infected patients since the identification of the virus in 1983, there is a rising concern in Bangladesh. A better understanding of the virus at the genetic level can help further in the treatment of the patients. Acute and chronic HEV infections can be much severe in pregnant women, people with an underlying liver disease and immunocompromised and/or immunosuppressed patients. The present study aimed at determining the viral load in HEV positive patients at Dhaka, analyzing bioinformatically the genetic composition of HEV to find any new substitution mutation and, with the aid of the level of liver damage biomarkers found in the samples, predicting the effect and functional change due to nucleic acid sequence variation on binding affinity of peptides to HLAs. Although there was no significant differences in viral copy number among pregnant, post-natal and non-pregnant women, the average copy numbers for the pregnant and post-natal women were higher than that of the non-pregnant women (3360.84 copies/mL). At the 1592nd position in the nucleic acid sequence of three of the HEV RNA positive patients, A and T substituted each other resulting in an amino acid change at the 531st position, which was unlike those observed in other countries. The substitution corresponded with the liver damage biomarkers and binding properties of antigenic epitopes to the host cell receptor. These results may mend ways for further analysis of such substitutions and can eventually help in understanding the virus, and developing an appropriate treatment therapy. en_US
dc.description.statementofresponsibility Shagoofa Rakhshanda
dc.format.extent 69 pages
dc.language.iso en en_US
dc.publisher BRAC Univeristy en_US
dc.rights BRAC University dissertations are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subject Hepatitis E en_US
dc.subject Women health en_US
dc.title Viral load and genotype analysis of Hepatitis E virus among HEV infected women in Bangladesh en_US
dc.type Dissertation en_US
dc.contributor.department Department of Mathematics and Natural Sciences, BRAC University
dc.description.degree B. Biotechnology


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