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巨片形吸虫烯醇化酶是蠕虫体表部分中对绵羊片形吸虫病具有保护作用的主要成分。

Fasciola gigantica enolase is a major component of worm tegumental fraction protective against sheep fasciolosis.

作者信息

Mahana N, Abd-Allah H A-S, Salah M, Tallima H, El Ridi R

机构信息

Zoology Department, Faculty of Science, Cairo University, Cairo 12613, Egypt.

Schistosoma Biological Materials Supply Program, Theodore Bilharz Research Institute, Giza 12411, Egypt.

出版信息

Acta Trop. 2016 Jun;158:189-196. doi: 10.1016/j.actatropica.2016.03.009. Epub 2016 Mar 10.

Abstract

Infection of cattle and sheep with the parasite Fasciola gigantica is a cause of important economic losses throughout Asia and Africa. Many of the available anthelmintics have undesirable side effects, and the parasite may acquire drug resistance as a result of mass and repeated treatments of livestock. Accordingly, the need for developing a vaccine is evident. Triton-soluble surface membrane and tegumental proteins (TSMTP) of 60, 32, and 28 kDa previously shown to elicit protective immunity in mice against challenge F. gigantica infection were found to be strongly immunogenic in sheep eliciting vigorous specific antibody responses to a titer>1:16,000 as assessed by enzyme-linked immunosorbent assay. Furthermore, the 60 kDa fraction induced production of antibodies able to bind to the surface membrane of newly excysted juvenile flukes and mediate their attrition in antibody-dependent complement- and cell-mediated cytotoxicity assays, and significant (P<0.05) 40% protection of sheep against F. gigantica challenge infection. Amino acid micro sequencing of the 60 kDa-derived tryptic peptides revealed the fraction predominantly consists of F. gigantica enolase. The cDNA nucleotide and translated amino acid sequences of F. gigantica enolase showed homology of 92% and 95%, respectively to Fasciola hepatica enolase, suggesting that a fasciolosis vaccine might be effective against both tropical and temperate liver flukes.

摘要

牛羊感染寄生虫巨片形吸虫在亚洲和非洲造成了重大经济损失。许多现有的驱虫药都有不良副作用,而且由于对牲畜进行大规模反复治疗,寄生虫可能会产生抗药性。因此,开发疫苗的必要性显而易见。先前已证明能在小鼠中引发针对巨片形吸虫感染攻击的保护性免疫的60 kDa、32 kDa和28 kDa的 Triton 可溶性表面膜和皮层蛋白(TSMTP),在绵羊中具有很强的免疫原性,通过酶联免疫吸附测定评估,能引发强烈的特异性抗体反应,效价>1:16,000。此外,60 kDa 组分诱导产生的抗体能够结合新脱囊的幼虫的表面膜,并在抗体依赖性补体和细胞介导的细胞毒性试验中介导其损耗,且能使绵羊对巨片形吸虫攻击感染产生显著(P<0.05)40%的保护作用。对60 kDa衍生的胰蛋白酶肽进行氨基酸微量测序显示,该组分主要由巨片形吸虫烯醇酶组成。巨片形吸虫烯醇酶的cDNA核苷酸序列和翻译后的氨基酸序列与肝片形吸虫烯醇酶的同源性分别为92%和95%,这表明一种片形吸虫病疫苗可能对热带和温带肝吸虫都有效。

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