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  1. NTU Theses and Dissertations Repository
  2. 生物資源暨農學院
  3. 獸醫專業學院
  4. 獸醫學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/43803
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dc.contributor.advisor萬灼華
dc.contributor.authorYi-Chun Liaoen
dc.contributor.author廖翊君zh_TW
dc.date.accessioned2021-06-15T02:29:07Z-
dc.date.available2012-08-20
dc.date.copyright2009-08-20
dc.date.issued2009
dc.date.submitted2009-08-17
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Ball-Goodrich, L.J., Leland, S.E., Johnson, E.A., Paturzo, F.X. and Jacoby, R.O., 1998. Rat parvovirus type 1: the prototype for a new rodent parvovirus serogroup. J Virol 72, 3289-99.
Besselsen, D.G., Pintel, D.J., Purdy, G.A., Besch-Williford, C.L., Franklin, C.L., Hook, R.R., Jr. and Riley, L.K., 1996. Molecular characterization of newly recognized rodent parvoviruses. J Gen Virol 77 ( Pt 5), 899-911.
Clemens, K.E. and Pintel, D., 1987. Minute virus of mice (MVM) mRNAs predominantly polyadenylate at a single site. Virology 160, 511-4.
Cotmore, S.F. and Tattersall, P., 1986. Organization of nonstructural genes of the autonomous parvovirus minute virus of mice. J Virol 58, 724-32.
Cotmore, S.F. and Tattersall, P., 1987. The autonomously replicating parvoviruses of vertebrates. Adv Virus Res 33, 91-174.
Crawford, L.V., 1966. A minute virus of mice. Virology 29, 605-12.
Iseki, H., Shimizukawa, R., Sugiyama, F., Kunita, S., Iwama, A., Onodera, M., Nakauchi, H. and Yagami, K., 2005. Parvovirus nonstructural proteins induce an epigenetic modification through histone acetylation in host genes and revert tumor malignancy to benignancy. J Virol 79, 8886-93.
Jongeneel, C.V., Sahli, R., McMaster, G.K. and Hirt, B., 1986. A precise map of splice junctions in the mRNAs of minute virus of mice, an autonomous parvovirus. J Virol 59, 564-73.
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McKisic, M.D., Lancki, D.W., Otto, G., Padrid, P., Snook, S., Cronin, D.C., 2nd, Lohmar, P.D., Wong, T. and Fitch, F.W., 1993. Identification and propagation of a putative immunosuppressive orphan parvovirus in cloned T cells. J Immunol 150, 419-28.
Moore, A.E. and Nicastri, A.D., 1965. Lethal infection and pathological findings in A x C rats inoculated with H virus and RV. J Natl Cancer Inst 35, 937-47.
Morgan, W.R. and Ward, D.C., 1986. Three splicing patterns are used to excise the small intron common to all minute virus of mice RNAs. J Virol 60, 1170-4.
Naeger, L.K., Cater, J. and Pintel, D.J., 1990. The small nonstructural protein (NS2) of the parvovirus minute virus of mice is required for efficient DNA replication and infectious virus production in a cell-type-specific manner. J Virol 64, 6166-75.
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Tamura, K., Dudley, J., Nei, M. and Kumar, S., 2007. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol. Biol. Evol 24 1596–1599.
Tattersall, P., Cawte, P.J., Shatkin, A.J. and Ward, D.C., 1976. Three structural polypeptides coded for by minute virus of mice, a parvovirus. J Virol 20, 273-89.
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/43803-
dc.description.abstract囓齒類動物小病毒 (Rodent parvoviruses)為囓齒類實驗動物中常見病原之一,已有相關研究指出此類病毒會影響in vivo和in vitro的實驗結果。本實驗室在2008年以PCR方式進行小規模實驗大鼠疾病調查,檢測結果發現台灣的實驗大鼠部分呈現囓齒類動物小病毒陽性反應。本研究將前次調查中檢出的陽性檢體,依據囓齒類動物小病毒的高保留區和高特異區之病毒基因序列所設計的引子,進行病毒基因複製與序列分析,將此台灣型的囓齒類動物小病毒之核苷酸序列及預期胺基酸序列與已知的囓齒類動物小病毒進行比較與分析。藉此基因複製及序列分析,完成總長約4759個核苷酸的基因序列,其中包含兩個大的轉譯讀窗(open reading frame, ORF)。序列分析後結果顯示,由台灣實驗大鼠所檢出的囓齒類動物小病毒與其他已知的囓齒類動物小病毒同樣具有rodent parvovirus的病毒調控轉錄及轉錄區域的特徵。在核苷酸與預期胺基酸序列分析方面,台灣型的囓齒類動物小病毒與目前已發現的Rat parvovirus, RPV-1a and RPV-1b 極為相似,但與RPV/UT及其他已知的囓齒類動物小病毒明顯不同。並經由演化樹之分析發現,台灣型的大鼠小病毒應歸屬於RPV-1族群,並命名為RPV-1c。本研究為首篇於美國以外地區發現的RPV-1的報告,並對病毒基因及蛋白質進行進一步的序列比較分析。zh_TW
dc.description.abstractRodent parvoviruses are one of the most prevalent infectious agents in the laboratory rodent and have been documented to interfere with in vivo and in vitro research. A newly recognized rat parvovirus (RPV) distinct from the prototypic RPV was recently identified in naturally infected laboratory rats in Taiwan. In present study, the viral DNA sequence and the predicted amino acid sequences of the new variant of RPV were determined and compared to RPV-1a, RPV-1b, RPV/UT and other rodent parvoviruses. DNA sequence fragment a total of 4759 nucleotides in length, encompassing two large and several small open reading frames (ORFs) were determined. Nucleotide and amino acid sequence comparisons showed that the variant of RPV is most closely related to RPV-1a and RPV-1b and distinctly different from RPV/UT and other rodent parvoviruses. The virus was designated rat parvovirus type 1c (RPV-1c). The phylogenetic analyses reveal that RPV-1c is a variant of RPV-1 group, including RPV-1a and RPV-1b. RPV-1c is the first molecularly characterized RPV variant identified outside of USA.en
dc.description.provenanceMade available in DSpace on 2021-06-15T02:29:07Z (GMT). No. of bitstreams: 1
ntu-98-R96629016-1.pdf: 705872 bytes, checksum: ae8eb4d41c6a6abde8f1796ef17c023b (MD5)
Previous issue date: 2009
en
dc.description.tableofcontentsTABLE OF CONTENTS
CERTIFICATE----------------------------------------------Ⅰ
ACKNOWLEDGMENTS------------------------------------------Ⅱ
ABSTRACT IN CHINESE--------------------------------------Ⅲ
ABSTRACT IN ENGLISH--------------------------------------Ⅳ
TABLE OF CONTENTS----------------------------------------Ⅴ
LIST OF FIGURES------------------------------------------Ⅶ
LIST OF TABLES-------------------------------------------Ⅷ
INTRODUCTION----------------------------------------------1
MATERIALS AND METHODS-------------------------------------6
Tissues and viral DNA-------------------------------------6
Oligonucleotide primers-----------------------------------7
PCR amplification-----------------------------------------7
DNA sequencing and analysis-------------------------------10
RESULTS---------------------------------------------------15
Identification of newly identified RPV in laboratory rats-15
DNA sequence analysis-------------------------------------16
Protein sequence analysis---------------------------------21
DISCUSSION------------------------------------------------38
REFERENCE-------------------------------------------------45
APPENDIX--------------------------------------------------51
 
LIST OF FIGURES
Figure
1.Strategy for sequencing RPV variant---------------------13
2.The PCR condition for each reaction---------------------14
3.Nucleotide sequence alignment of the RPV-1c and other rodent parvoviruses---------------------------------------29
4.Phylogeny of the RPV-1c and other parvoviruses----------44
5.Genetic organization of the MVM genome------------------51
LIST OF TABLES
Table 1.Sequences of oligonucleotide primers used in the PCR and sequencing reaction---------------------------------------12
2.The Sp1 binding site and the TAR element of the newly identified RPV-1c and other rodent parvoviruses-----------24
3.The intron donors and intron acceptors in the RPV-1c and other rodent parvoviruses---------------------------------25
4.Percentage nucleotide identity among the newly identifed RPV-1c and other rodent parvoviruses----------------------26
5.Percentage amino acid similarity among the RPV-1c and other rodent parvoviruse----------------------------------27
6.Carboxy termini of NS-2 protein in the the RPV-1c and other rodent parvoviruses---------------------------------28
dc.language.isoen
dc.subject台灣型大鼠小病毒基因序列zh_TW
dc.subject囓齒類實驗動物小病毒zh_TW
dc.subjectrodent parvovirusesen
dc.subjectrat parvovirus type 1cen
dc.title台灣新發現之大鼠小病毒的分子特徵zh_TW
dc.titleMolecular Characterization of a Newly Identified Rat Parvovirus in Taiwanen
dc.typeThesis
dc.date.schoolyear97-2
dc.description.degree碩士
dc.contributor.oralexamcommittee王明升,闕玲玲,廖欽?
dc.subject.keyword囓齒類實驗動物小病毒,台灣型大鼠小病毒基因序列,zh_TW
dc.subject.keywordrodent parvoviruses,rat parvovirus type 1c,en
dc.relation.page51
dc.rights.note有償授權
dc.date.accepted2009-08-17
dc.contributor.author-college獸醫專業學院zh_TW
dc.contributor.author-dept獸醫學研究所zh_TW
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