Expression Profile of Penaeus monodon Ubiquitin Conjugating Enzyme (PmUbc) at Protein Level in White spot syndrome virus Challenged Shrimp.

Indian Journal of Virology Pub Date : 2013-06-01 Epub Date: 2013-03-15 DOI:10.1007/s13337-013-0131-6
Jeena Keezhedath, Pani Prasad Kurcheti, Mujahid Khan Pathan, Gireesh P Babu, Gayatri Tripathi, Arun Sudhagar, Srinivas P Rao
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引用次数: 4

Abstract

White spot syndrome virus (WSSV) is one of the major pathogens in shrimp aquaculture. Four proteins of WSSV are predicted to encode a RING H2 domain, which in presence of ubiquitin conjugating enzyme (E2) in shrimps can function as viral E3 ligase and modulate the host ubiquitin proteasome pathway. Modulation of host ubiquitin proteasome pathway by viral proteins is implicated in viral pathogenesis. In the present study, expression profile of Penaeus monodon Ubiquitin conjugating enzyme (PmUbc) was studied at protein level in WSSV challenged shrimp. A time point analysis of the expression of PmUbc was carried out at 0, 3, 6, 12, 24, 48 and 72 h post WSSV challenge in P. monodon. Recombinant PmUbc (rPmUbc) was produced in prokaryotic expression vector, BL21 (DE3) pLys S. The PmUbc expression pattern was studied by ELISA with rPmUbc antibodies raised in rabbit. A significant increase in PmUbc expression at 24 h post infection (hpi) was observed followed by a decline till 72 hpi. Since the up-regulation and a tremendous decline of PmUbc protein expression was observed at 24 and in 72 hpi respectively in ELISA, it can be speculated that these proteins might interact with host ubiquitination pathway for viral pathogenesis. Many findings have shown that viral infection can up-regulate expression of ubiquitin and that the ubiquitin system plays a key role in the course of viral infection. The present study reveals the expression patterns of PmUbc at protein level in WSSV infected P. monodon. However, further studies are to be carried out to unfold the molecular mechanism of interaction between host and virus to devise efficient control strategies for this major culprit in shrimp culture industry.

单对虾泛素偶联酶(PmUbc)蛋白水平在白斑综合征病毒侵染对虾中的表达谱
白斑综合征病毒(WSSV)是对虾养殖的主要病原体之一。预测WSSV的4个蛋白编码一个RING H2结构域,该结构域在虾体内存在泛素偶联酶(E2)时可作为病毒E3连接酶,调节宿主泛素蛋白酶体途径。病毒蛋白对宿主泛素蛋白酶体途径的调节与病毒的发病机制有关。本研究在蛋白水平上研究了单对虾泛素偶联酶(PmUbc)在WSSV侵染对虾中的表达谱。分别在WSSV侵染后0、3、6、12、24、48和72 h对单胞假单胞菌PmUbc的表达进行时间点分析。在原核表达载体BL21 (DE3) pLys s中产生重组PmUbc (rPmUbc),用兔培养的rPmUbc抗体ELISA法研究了PmUbc的表达谱。PmUbc表达在感染后24小时(hpi)显著增加,随后下降至72 hpi。ELISA检测发现PmUbc蛋白表达在24 hpi和72 hpi时分别上调和大幅下降,推测这些蛋白可能与宿主泛素化途径相互作用,导致病毒发病。许多研究结果表明,病毒感染可上调泛素的表达,泛素系统在病毒感染过程中起关键作用。本研究揭示了PmUbc在WSSV感染单胞疟原虫蛋白水平上的表达模式。然而,寄主与病毒相互作用的分子机制有待进一步研究,以制定有效的防治策略。
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来源期刊
Indian Journal of Virology
Indian Journal of Virology 医学-病毒学
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6-12 weeks
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