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从兔鱼(Siganus oramin)血清中分离得到的一种新型蛋白可杀死刺激隐核虫。

A novel protein isolated from the serum of rabbitfish (Siganus oramin) is lethal to Cryptocaryon irritans.

机构信息

State Key Laboratory of Biocontrol, Key Laboratory for Aquatic Products Safety of Ministry of Education, Sun Yat-sen University, 135 Xingang West Street, Haizhu District, Guangzhou 510275, Guangdong Province, The People's Republic of China.

出版信息

Fish Shellfish Immunol. 2010 Jul;29(1):32-41. doi: 10.1016/j.fsi.2010.01.006. Epub 2010 Feb 1.

Abstract

The susceptibility of eight marine fish species cultured in South China were tested for infection by the parasitic ciliate, Cryptocaryon irritans, via a challenge examination and an immobilization assay. All species of fish (representing six different families) that we investigated were infected by C. irritans except the rabbitfish (Siganus oramin), which displayed resistance to C. irritans infection. The infection intensity of rabbitfish (0.92+/-0.97, p<0.05) was significantly lower while the immobilization titres of rabbitfish serum were significantly higher (44.51+/-22.98, p<0.05) than the other seven species of fish. Additionally, the serum of the rabbitfish presented a strong killing effect to C. irritans in vitro. Light microscopy, scanning electron microscopy and fluorescence microscopy confirmed that rabbitfish serum could induce the theront cilia fall off, rupture of the cell membrane because of the swell and rupture of the macronucleus. Rabbitfish serum could also induce the rupture of the trophont membrane and content efflux. Herein a novel antiparasitic protein (APP) was isolated and purified from the serum of rabbitfish (S. oramin) by using a series of salting-out, cation exchange chromatography and two step of reversed phase high performance liquid chromatography (RP-HPLC). Analysis of sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) showed that APP was a homogenous polymeric protein with an N-terminal amino acid sequence of SSVEKNLAACLRDND. Its monomeric molecular mass, determined by matrix-assisted laser desorption ionization tandem time-of-flight mass spectrometer (MALDI-TOF-TOF-MS), was found to be 61,739.87 Da. Results of homology analyses indicated that this protein was a newly discovered functional protein in the rabbitfish serum. Laser confocal fluorescence microscopy conformed that the action site of the APP was mainly on the cell membrane and nucleus of theront, which agreed with the results of light microscopy, fluorescence microscopy and scanning electron microscopy. These findings suggest that this protein may contribute considerably to the innate host defence mechanism to combat microbes of the rabbitfish.

摘要

在中国南方养殖的 8 种海水鱼对寄生虫纤毛虫 Cryptocaryon irritans 的易感性进行了测试,方法是通过挑战试验和固定化试验。除了兔鱼(Siganus oramin)外,我们研究的所有鱼类(代表六个不同的科)都被 C. irritans 感染,而兔鱼对 C. irritans 感染具有抗性。兔鱼的感染强度(0.92+/-0.97,p<0.05)明显较低,而兔鱼血清的固定化效价(44.51+/-22.98,p<0.05)明显较高。此外,兔鱼血清对体外 C. irritans 具有很强的杀伤作用。光镜、扫描电镜和荧光显微镜证实,兔鱼血清可诱导游仆虫纤毛脱落,细胞膜破裂,原因是大核肿胀破裂。兔鱼血清还可以诱导滋养体膜破裂和内容物流出。本文从兔鱼(S. oramin)血清中分离纯化出一种新型抗寄生虫蛋白(APP),方法是采用一系列盐析、阳离子交换层析和两步反相高效液相色谱(RP-HPLC)。十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)分析表明,APP 是一种均一的聚合蛋白,N 端氨基酸序列为 SSVEKNLAACLRDND。基质辅助激光解吸电离串联飞行时间质谱(MALDI-TOF-TOF-MS)测定其单体分子量为 61739.87 Da。同源性分析结果表明,该蛋白是兔鱼血清中一种新发现的功能蛋白。激光共聚焦荧光显微镜证实,该蛋白的作用部位主要在游仆虫的细胞膜和细胞核上,这与光镜、荧光显微镜和扫描电镜的结果一致。这些发现表明,该蛋白可能对兔鱼的先天宿主防御机制抵抗微生物有重要作用。

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