다양한 지역에서 유래한 흰다리 새우 (Litopenaus vannamei)에서의 간췌장 바이러스의 검출과 염기서열 비교
- Alternative Title
- Detection and sequence comparison of Hepatopancreatic parvovirus (HPV) among farmed whiteleg shrimps (Litopenaus vannamei) from different geographical orgins
- Abstract
- The Hepatopancreatic parvovirus (HPV) causing Hepatopancreatic parvovirus disease is one of the viruses that has been affecting the shrimp industry for the past 50 years. Hepatopancreatic parvovirus (HPV) diseases in recent years have been found in wild and farmed penaeid shrimps around the different geographical locations of the World. This is an indication that there may be changes that may lead into differences in sequences among shrimps. Currently, there are four complete genome sequences/isolates of HPV that have been reported with a large number of other partial sequences. In this experiment, I collected five different shrimp samples of whiteleg shrimp (Litopenaus vannamei) from five different geographical origins, four locations in South Korea, and one sample from Malaysia. In order to detect the presence of viruses and compare sequences of five groups of whiteleg shrimp with different geographical origins. The collected shrimp samples were subjected to DNA extraction, Polymerase Chain Reaction (PCR), Cloning, Transformation, Quantitative Realtime PCR and Sequencing. The five samples showed to be similar in their sequences to the Korean isolate of HPV strain (FcDNV)
- Author(s)
- Mashiranga Oscar Musa
- Issued Date
- 2023
- Awarded Date
- 2023-02
- Type
- Dissertation
- Keyword
- Chinese White Shrimp (F. chinensis), Hepatopancreatic parvovirus (HPV), Polymerase Chain Reaction (PCR), Sequencing, Quantitative Real Time Polymerase Chain Reaction (qPCR), Korean isolate of HPV strain (FcDNV)
- Publisher
- 부경대학교
- URI
- https://repository.pknu.ac.kr:8443/handle/2021.oak/33040
http://pknu.dcollection.net/common/orgView/200000668656
- Affiliation
- 부경대학교 글로벌수산대학원
- Department
- 글로벌수산대학원 국제수산과학협동과정
- Advisor
- 최태진
- Table Of Contents
- 1. Introduction 1
2. Materials and Methods 5
1) Collection of samples 5
2) DNA Extraction 8
3) Confirmation of HPV 9
4) DNA Cloning 0 Gel preparation 9
5) Ligation and transformation 11
6) Sequencing 12
7) Sequence analysis 13
8) Quantitative Real-time PCR 13
9) Primer designing 14
3. Results and Discussion 16
1) Confirmation of HPV infection by PCR 18
2) Sequence and analysis of the viral genome 24
3) Quantification of viral loads 29
4) Multiple sequencing and phylogenetic tree 31
4. Acknowledgment 37
5. References 38
- Degree
- Master
-
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- 글로벌수산대학원 > 국제수산과학협동과정
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