dc.contributor.author |
Azakir, Amanda Mahmoud |
dc.date.accessioned |
2022-09-29T13:26:49Z |
dc.date.available |
2022-09-29T13:26:49Z |
dc.date.issued |
2018 |
dc.date.submitted |
2018 |
dc.identifier.other |
b22094799 |
dc.identifier.uri |
http://hdl.handle.net/10938/23668 |
dc.description |
Thesis. M.Sc. American University of Beirut. Department of Experimental Pathology, Immunology and Microbiology. Faculty of Medicine 2018. W 4 A991w 2018; Advisor: Hassan Zaraket, Assistant Professor, Department of Experimental Pathology, Immunology, and Microbiology ; Committee members: Dr. Ghassan Dbaibo, M.D., Professor, Department of Pediatrics and Adolescent Medicine and Biochemistry and Department of Biochemistry and Molecular Genetics ; Dr. Ghassan M. Matar, Ph.D ; Professor and Vice Chair, Department of Experimental Pathology, Immunology, and Microbiology ; Nada M. Melhem, Ph.D., Associate Professor, Department of Infectious Diseases and Microbiology, Medical Laboratory Sciences Program, Faculty of Health Sciences. |
dc.description |
Includes bibliographical references (leaves 66-92) |
dc.description.abstract |
Rotavirus is considered globally the leading cause of severe diarrheal infections among children under the age of 5 years and is responsible for about 215 000 deaths annually. Rotaviruses are classified based on their outermost shell proteins, VP7 (G-genotype) and VP4 (P-genotype) with at least 36 G genotypes and 51 P genotypes identified up-to-date. Although there are common globally circulating genotypes (G1P[8],G3P[8], G9P[8],G2P[4]), the segmented genome of the virus and possible vaccine pressure might explain the emergence of unique genotypes such as G9P[4]. In Lebanon, a hospital-based study conducted between 2011-2013 revealed that 30.3percent of gastroenteritis-hospitalizations were attributed to rotavirus A (RVA), with major genotypes being G1P[8] (36percent) and G9P[8] (26.4percent). Newly emerging, unique genotypes such as G9P[4] constituted 1percent. In this study we performed full genome characterization these unique G9P[4] strains and one G9P[8] strain in Lebanon by using virome capture technology and phylogenetic analysis. Our goal was to elucidate their origin and genetic relatedness compared to globally circulating G9P[4] and G9P[8] specimens as well as their genetic vaccine matching. One G9P[4] specimen was of pure DS-1 like origin and the remaining two were of mixed and diverse Wa-like-DS-1-like genotypes: RVA-Human-LEB-A095-2011-G9P[4] (G9-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2), RVA-Human-LEB-H017-2011-G9P[4] (G9-P[4]-I2-R2-C2-M2-A2-N1-T2-E2-H2), RVA-Human-LEB-H199-2011-G9P[4] (G9-P[4]-I1-R1-C1-M1-A2-N1-T1-E1-H1). The RVA-Human-LEB-NG184-2011-G9P[8] was of pure Wa-like origin (G9-P[8]-I1-R1-C1-M1-A1-N1-T1-E1-H1). Phylogenetic analysis revealed that the G9P[4] strains with mixed genomic constellation emerged from a reassortment events between G2P[4] and G9P[8] stains. Overall, unlike the G9P[8] strains’ pure genomic backbone, multiple lineages of G9P[4] seemed to have emerged globally. The analysis indicated that Lebanese G9P[4] strains seemed to have emerged through multiple introductions or reassortment event |
dc.format.extent |
xi, 92 leaves : illustrations ; 30 cm + 1 CD-ROM (4 3-4 in.)||1 online resource (92 leaves) |
dc.language.iso |
eng |
dc.subject.classification |
A991w 2018 |
dc.subject.lcsh |
Dissertations, Academic.||Rotaviruses. |
dc.subject.lcsh |
Lebanon. |
dc.title |
Whole Genome characterization of G9P[4] and G9P[8] Rotaviruses strains identified in Lebanon |
dc.type |
Thesis |
dc.contributor.department |
Department of Experimental Pathology, Immunology and Microbiology |
dc.contributor.institution |
American University of Beirut |
dc.contributor.authorFaculty |
Faculty of Medicine |