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  • 學位論文

藉由共感染不同之桿狀病毒來探討桿狀病毒宿主域的研究

Investigating baculovirus’s host range through co-infect different baculoviruses

指導教授 : 吳宗遠

摘要


桿狀病毒依其分離自何宿主而命名,大多數桿狀病毒擁有專一宿主域,但有部分桿狀病毒具有廣泛的宿主域。例如加州苜蓿夜蛾核多角體病毒(Autographa californica multiple nucleopolyhedrovirus,AcMNPV),可感染33種鱗翅目昆蟲與多種昆蟲細胞株。與AcMNPV親源相似的有豆筴螟核多角體病毒(Marca vitrata multiple nucleopolyhedrovirus, MaviMNPV) 與家蠶核多角體病毒 (Bombyx mori multiple nucelopolyhedrovirus, BmNPV)。AcMNPV、BmNPV、MaviMNPV各自可感染Sf 21、BmN、NTU-MV532 細胞株。雖然三株病毒十分相似,卻不能感染另兩種非接受性細胞株。本研究使用帶有螢光基因的AcMNPV,BmNPV,MaviMNPV桿狀病毒分別對Sf21、BmN、NTU-MV532細胞株進行共感染,藉此探討病毒與病毒,病毒與宿主之間的交互作用。同時利用AcMNPV與MaviMNPV交叉感染Sf 21與NTU-MV532細胞株,期望能獲得單株具有感染Sf 21與NTU-MV532能力的跨宿主重組病毒。另一方面,我們於Sf 21細胞株先感染MaviMNPV 2,6,12,48小時後再感染AcMNPV,AcMNPV有協助MaviMNPV於Sf 21細胞中的複製,同時MaviMNPV亦有延遲AcMNPV的複製情形;當在NTU-MV532細胞株先感染AcMNPV 2,6,12,48小時再感染MaviMNPV,MaviMNPV反有拮抗作用,同時AcMNPV抑制MaviMNPV的複製。而在Sf 21細胞株中先感染BmNPV 2,6,12,48小時再感染AcMNPV,AcMNPV協助BmNPV 的複製,同時AcMNPV的複製受到BmNPV呈現延遲的結果。在BmN細胞中先感染AcMNPV 2,6,12,48小時再感染BmNPV有互相拮抗複製的結果。我們利用即時定量PCR來偵測各時期的表現。在Sf 21共感染MaviMNPV與AcMNPV,共感染下的AcMNPV的IE-1,IE-2,lef-2 36小時前都較單獨感染的高,而共感染下的MaviMNPV病毒基因表現則是高於單獨感染;在NTU-MV532中共感染AcMNPV與MaviMNPV,AcMNPV與MaviMNPV 的IE-1,IE-2,lef 2在共感染的情況下幾乎沒有表現。而為避免共感染克服宿主域是因為外泌性的因子影響,我們使用超高速離心機離心被AcMNPV之病毒上清液製作成控制培養液再共培養被MaviMNPV感染之Sf 21細胞株,MaviMNPV的感染情形並不如與AcMNPV共感染良好,從而屏除了外泌性因子的因素。

關鍵字

MaviMNPV AcMNPV 共感染 螢光報導基因 BmNPV

並列摘要


Baculovirus is named after the host that it infects. Most of baculoviruses have their own specific host range, but some have wide host range that can infect many different insectspecies, like Auotographa californica multiple nucleopolyhedrovirus (AcMNPV) can infect 33 kind of insects and different kind of insect cell lines. Moreover, Maruca vitrata multiple nucleopolyhedrovirus (MaviMNPV) and Bombyx mori multiple nucleopolyhedrovirus (BmNPV) are two baculovirus that are similar in genome and structure. Despite the similarity in genome and structure, they can only infect their host range for instance AcMNPV infects sf21 cell line, BmNPV infects BmN cell line, and MaviMNPV infects NTU-MV532 cell line. We tried to find out the relationship between viruses and host their interaction. Different baculoviruses was incorporated with a different fluorescent reporter gene to co-infect Sf21,BmN and NTU-MV532 cell lines. Recombinant virus of AcMNPV and MaviMNPV was produced by cross infecting in Sf21 and NTU-MV532 which could infect both Sf21 and NTU-MV532 cell lines. Late gene expression of respective gene driven by polyhedrin promoter was studied by observing their fluorescent expression after single or co-infection with AcMNPV and MaviMNPV in Sf21 and NTU-MV532 cells lines at different time intervals. Co-infection of AcMNPV and MaviMNPV in Sf21 cell suggests that AcMNPV and MaviMNPV help each other’s gene expression in late phase, but blocks gene expression in NTU-MV532 cell line. Similar, result was observed in BmN and Sf21 cells which was co-infected with AcMNPV and BmNPV. Additionally, to study the influence of secretion factor in host range ,condition medium was prepared byultracentrifugation of medium infected with AcMNPV which was used to culture theMaviMNPV infected Sf21 cells.The result suggests that the secretion factor didn't play any role in influencing host range.QRT-PCR was performed to identify the genes that are essential for specific host range and several early and core genes were targeted for the study and their gene expression was measured in different time intervals.The expression of IE-1, IE-2 and lef-2 geneswere higher in co-infectedSf21cells with AcMNPV and MaviMNPV at 24 and 36 hpi; than single infection of AcMNPV. However, the expression of IE-1, IE-2 and lef-2 geneswas higher in co-infected Sf21 cells with AcMNPV and MaviMNPV than single infection of MaviMNPV. No gene expression of IE-1, IE-2 and lef-2 genes observed inNTU-MV532 cells co-infected with AcMNPV and MaviMNPV or AcMNPV alone but high expression of genes observed in NTU-MV532 cells infected with MaviMNPV alone.

並列關鍵字

fluorescent expression Co-infect AcMNPV MaviMNPV BmNPV

參考文獻


Argaud, O., Croizier, L., López-Ferber, M., Croizier, G., 1998. Two key mutations in the host-range specificity domain of the p143 gene of Autographa californica nucleopolyhedrovirus are required to kill Bombyx mori larvae. J. Gen. Virol 79 ( Pt 4), 931-935.
Chen, Y.-R., Wu, C.-Y., Lee, S.-T., Wu, Y.-J., Lo, C.-F., Tsai, M.-F., Wang, C.-H., 2008. Genomic and host range studies of Maruca vitrata nucleopolyhedrovirus. J. Gen. Virol 89, 2315-2330.
Croizier, G., Croizier, L., Argaud, O., Poudevigne, D., 1994. Extension of Autographa californica nuclear polyhedrosis virus host range by interspecific replacement of a short DNA sequence in the p143 helicase gene. Proc. Natl. Acad. Sci. U.S.A 91, 48-52.
Gomi, S., Majima, K., Maeda, S., 1999. Sequence analysis of the genome of Bombyx mori nucleopolyhedrovirus. Journal of General Virology 80, 1323.
Guarino, L.A., Gonzalez, M.A., Summers, M.D., 1986. Complete Sequence and Enhancer Function of the Homologous DNA Regions of Autographa californica Nuclear Polyhedrosis Virus. J. Virol 60, 224-229.

被引用紀錄


王俊人(2010)。全球化與區域統合下之憲法新秩序:我國的挑戰與回應〔博士論文,國立臺灣師範大學〕。華藝線上圖書館。https://www.airitilibrary.com/Article/Detail?DocID=U0021-1610201315205074

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