Suppr超能文献

从伊朗粗尾蝎中开发重组磷脂酶D1(rPLD1)类毒素及其在BALB/c小鼠中的保护作用。

Developing recombinant phospholipase D1 (rPLD1) toxoid from Iranian Hemiscorpius lepturus scorpion and its protective effects in BALB/c mice.

作者信息

Safari Foroushani Narges, Modarressi Mohammad Hossein, Behdani Mahdi, Torabi Elham, Pooshang Bagheri Kamran, Shahbazzadeh Delavar

机构信息

Islamic Azad University, Science and Research Branch, Tehran, Iran.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Toxicon. 2018 Sep 15;152:30-36. doi: 10.1016/j.toxicon.2018.07.003. Epub 2018 Jul 6.

Abstract

Hemiscorpius lepturus (H. lepturus) is one of the most dangerous scorpions and the most medically important scorpion in Iran. The clinical signs of H. lepturus envenomation, including dermonecrosis, hematuria, renal failure and early death, are attributed to phospholipase D activity. This study was conducted to develop a novel recombinant phospholipase D1 (rPLD1) toxoid and investigate its immunogenicity and protective effects against the lethality of H. lepturus venom. The lethal protein recombinant phospholipase D1 was expressed from PLD H. lepturus venom gland. The rPLD1 toxin was converted into toxoid (the first toxoid of H. lepturus PLD) with a 0.25% concentration of formalin and stored for ten days at room temperature. In the toxicity test, the lethal activity of recombinant phospholipase D1 was fully inhibited. When it reached up to 3 times higher than the maximal effective concentration of the purified toxin (11.1 μg), rPLD1 toxoid was used. The sphingomyelinase activity was inhibited when up to 5.4 times of the LD100 of the purified toxin (20 μg), toxoid was used. It was then used to produce an antibody in BALB/c as an antigen and the mice were then challenged with rPLD1 toxin and the whole venom. The immunogenicity of rPLD1 toxoid was evaluated and the maximum titer of the raised antibodies was determined by ELISA assay. The optimum titer for anti-rPLD1 toxoid sera was obtained at the third intraperitoneal injection of rPLD1 toxoid, and a high titer was reached at the fourth injection in the mice. This toxoid increased the amount of antibodies and produced a protective antiserum against the whole venom of H. lepturus and rPLD1 toxin. The in-vivo test results showed that the mice were completely resistant against 200 times the LD100 of recombinant phospholipase D1 and the whole venom of H. lepturus. To conclude, rPLD1 can be used in toxoid form as an immunogen in the production of a new generation of neutralizing antibodies against the lethality and toxicity of H. lepturus whole venom.

摘要

细尾半蝎(H. lepturus)是伊朗最危险且在医学上最重要的蝎子之一。细尾半蝎蜇伤的临床症状,包括皮肤坏死、血尿、肾衰竭和早期死亡,都归因于磷脂酶D的活性。本研究旨在开发一种新型重组磷脂酶D1(rPLD1)类毒素,并研究其免疫原性以及对细尾半蝎毒液致死性的保护作用。致死性蛋白重组磷脂酶D1是从细尾半蝎毒腺中表达出来的。rPLD1毒素用0.25%浓度的福尔马林转化为类毒素(细尾半蝎PLD的首个类毒素),并在室温下保存十天。在毒性试验中,重组磷脂酶D1的致死活性被完全抑制。当rPLD1类毒素的浓度达到纯化毒素最大有效浓度(11.1μg)的3倍以上时使用。当使用的类毒素浓度达到纯化毒素LD100(20μg)的5.4倍时,鞘磷脂酶活性受到抑制。然后将其作为抗原在BALB/c小鼠中产生抗体,随后用rPLD1毒素和全毒液对小鼠进行攻毒。评估rPLD1类毒素的免疫原性,并通过ELISA测定法确定产生的抗体的最大效价。抗rPLD1类毒素血清的最佳效价在第三次腹腔注射rPLD1类毒素时获得,在小鼠第四次注射时达到高效价。这种类毒素增加了抗体量,并产生了针对细尾半蝎全毒液和rPLD1毒素的保护性抗血清。体内试验结果表明,小鼠对200倍LD100剂量的重组磷脂酶D1和细尾半蝎全毒液具有完全抗性。总之,rPLD1可以以类毒素形式用作免疫原,用于生产新一代针对细尾半蝎全毒液致死性和毒性的中和抗体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验