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  1. NTU Theses and Dissertations Repository
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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/15758
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor闕玲玲(Ling-Ling Chueh)
dc.contributor.authorWan-Ting Tsaien
dc.contributor.author蔡婉婷zh_TW
dc.date.accessioned2021-06-07T17:51:30Z-
dc.date.copyright2012-10-12
dc.date.issued2012
dc.date.submitted2012-09-17
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/15758-
dc.description.abstract貓傳染性腹膜炎 (Feline infectious peritonitis, FIP) 為貓冠狀病毒 (Feline coronavirus, FCoV) 所引起之一免疫媒介高度致死性疾病,目前尚無有效之疫苗及治療方法。本研究利用以severe acute respiratory syndrome coronavirus (SARS-CoV) 及FCoV之棘蛋白(spike protein, S) heptad repeat 2 (HR2) 序列為基礎所合成之胜肽,藉由抑制FCoV感染之融合效應,測試其抑制病毒複製之效力。結果顯示在20 μM濃度下,SARS-CoV HR胜肽具33% 至55% 之抑制病毒效力,而FCoV-HR 胜肽之抑制病毒效力則可達到72% 至97%。此結果表示相較於SARS-CoV HR 胜肽,FCoV HR 胜肽對於FCoV之抑制更具特異性。進一步探討HR 胜肽與其他已知具抗FCoV複製藥物之加乘作用 (Synergistic antiviral effect),將SARS-CoV HR胜肽與nelfinavir、Galanthus nivalis agglutinin (GNA) 合併未出現加乘作用,而與人源Interferon-α (IFN-α) 合併,則發現以20 μM FCoV HR胜肽與不同濃度之IFN-α合併後皆出現加乘抗病毒效應。探討此FCoV HR胜肽之抑制機制發現其主要是藉由干擾病毒與標的細胞之融合,進而抑制病毒之複製。總結本實驗之結果,FCoV HR 胜肽為一具有潛力可應用於FIP臨床預防及治療之藥物。zh_TW
dc.description.abstractFeline infectious peritonitis (FIP) is an immune-mediated disease with high mortality rate in felids caused by feline coronavirus (FCoV). At present, no effective vaccine or treatments are available for FIP. We carried out fusion inhibition assay to analyze the designed peptides based on spike protein (S) heptad repeat 2 (HR2) sequences of severe acute respiratory syndrome coronavirus (SARS-CoV) and FCoV. The results showed the inhibition percentages of FCoV replication for 20 μM of SARS-CoV and FCoV peptides were 31% to 55% and 72% to 97%, respectively. This indicates that the peptides derived from FCoV are more specific than from SARS-CoV. The effective FCoV-derived peptides were further tested for their synergistic antiviral effect with other known anti-FCoV agents, i.e. Galanthus nivalis agglutinin 會, nelfinavir and human interferon-α (IFN-α). When 20 μM of FCoV HR peptide was combined with different concentrations of IFN-α, a significant synergistic anti-FCoV effect can be observed, however not with GNA and nelfinavir. Investigation of the inhibition mechanism for FCoV-derived HR peptide revealed that the peptide interferes with virus-cell fusion thus leading to a reduction in viral replication. Taken together, the peptides derived from FCoV have the potential to be used as a therapeutic agent in the prevention and treatment of FIP.en
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dc.description.tableofcontents口試委員會審定書 i
中文摘要 ii
ABSTRACT iii
目錄 iv
表次 vii
圖次 viii
第一章、 文獻探討 1
第一節、歷史背景 1
第二節、 病毒分類 1
第三節、 基因體特性 2
第四節、 貓冠狀病毒之分型 5
第五節、 貓冠狀病毒之感染與疾病 5
一、 宿主與流行病 5
二、 傳染途徑及排毒模式 6
三、 致病機制 6
四、 臨床症狀 7
五、 診斷 8
六、 治療 9
七、 預防與控制 11
第六節、 抗病毒胜肽 12
第二章、 序言 13
第三章、 材料與方法 15
第一節、 病毒與細胞 15
第二節、 抗病毒胜肽 15
一、 SARS-CoV S protein HR2抗病毒胜肽 15
二、 FCoV S protein HR2抗病毒胜肽 15
第三節、 細胞活性試驗 15
第四節、 抗病毒胜肽效力之體外評估 16
一、 篩選具抗病毒效應之胜肽 16
二、 藥物合併效力試驗 17
三、 FCoV S protein HR胜肽抑制FCoV複製機制之探討 18
四、 統計分析 18
第四章、 結果 19
第五章、 討論 23
附表 29
附圖 31
參考文獻 39
dc.language.isozh-TW
dc.title抗病毒胜肽抑制貓冠狀病毒複製之評估zh_TW
dc.titleEvaluation of the Inhibitory Effect of Anti-Viral Peptides against Feline Coronavirusen
dc.typeThesis
dc.date.schoolyear101-1
dc.description.degree碩士
dc.contributor.coadvisor劉薏蓉(I-Jung Liu)
dc.contributor.oralexamcommittee項千芸(Chien-Yun Hsiang),張淑媛(Shu-Yuan Chang),林昭男(Chao-Nan Lin)
dc.subject.keyword貓冠狀病毒,貓傳染性腹膜炎,抗病毒藥物,胜&#32957,zh_TW
dc.subject.keywordFCoV,FIP,antiviral agent,peptide,en
dc.relation.page52
dc.rights.note未授權
dc.date.accepted2012-09-18
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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