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dc.contributor.advisorNguyen, Thi Thu Hoai
dc.contributor.authorLy, Nguyen Hoang Trinh
dc.date.accessioned2025-02-17T05:10:30Z
dc.date.available2025-02-17T05:10:30Z
dc.date.issued2024-07-12
dc.identifier.urihttp://keep.hcmiu.edu.vn:8080/handle/123456789/6688
dc.description.abstractHepatitis E virus (HEV) is a non-enveloped single stranded RNA virus that cause acute viral infection in most Asian and African nations. HEV mostly transmits through fecal-oral pathway, occurred in both human and animal feces; furthermore, the presence of this virus also contained in contaminated water that potentially affect another surrounding stream by sewage elimination from piggery. Shellfish, especially crustacean works as vectors to carry the viral transmission to human through contaminated water supplement. With the herpesvirus such as HEV, the transmission usually occurs in the hatchery-larvae and juvenile stages of some bivalve shellfish. In some local piggery, the farming areas meet some hygienic obstacles that potentially serve as vector for viral transmission. By applying Nested PCR, 120 shellfish samples were collected in various local markets for detecting ORF1’s genes of HEV and they included: 20 tiger prawns (Macrobrachium rosenbergii), 50 giant river prawns (Penaeus monodon), and 50 mussels (Mytilus edulis). Nested PCR provided the specificity and efficiency in amplifying the target sequence whose low abundance; due to the higher sensitivity than conventional PCR, Nested PCR usually used to detect various viral and bacterial pathogens that low abundance. After screening total 120 samples, all the samples showed negative results in gel electrophoresis when comparing with the positive control. In the other hand, the result might not prove strongly that there was no HEV presence in all samples, the obstacles could come from the applied conditions might not be optimal enough for shellfish samples or sample size need to be expanded as well as the source of sample selection.en_US
dc.subjectHepatitis E virusen_US
dc.subjectShellfishen_US
dc.subjectGenotype 3en_US
dc.subjectNested PCRen_US
dc.subjectHEVen_US
dc.titleASSESSMENT OF THE INCIDIENCE OF THE HEPATITIS E VIRUS IN SHELLFISHen_US
dc.typeThesisen_US


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