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抗珊瑚蛇毒血清的转录组学基础。

Transcriptomic basis for an antiserum against Micrurus corallinus (coral snake) venom.

作者信息

Leão Luciana I, Ho Paulo L, Junqueira-de-Azevedo Inacio de L M

机构信息

Centro de Biotecnologia, Instituto Butantan, São Paulo, SP, Brazil.

出版信息

BMC Genomics. 2009 Mar 16;10:112. doi: 10.1186/1471-2164-10-112.

Abstract

BACKGROUND

Micrurus corallinus (coral snake) is a tropical forest snake belonging to the family Elapidae. Its venom shows a high neurotoxicity associated with pre- and post-synaptic toxins, causing diaphragm paralysis, which may result in death. In spite of a relatively small incidence of accidents, serum therapy is crucial for those bitten. However, the adequate production of antiserum is hampered by the difficulty in obtaining sufficient amounts of venom from a small snake with demanding breeding conditions. In order to elucidate the molecular basis of this venom and to uncover possible immunogens for an antiserum, we generated expressed sequences tags (ESTs) from its venom glands and analyzed the transcriptomic profile. In addition, their immunogenicity was tested using DNA immunization.

RESULTS

A total of 1438 ESTs were generated and grouped into 611 clusters. Toxin transcripts represented 46% of the total ESTs. The two main toxin classes consisted of three-finger toxins (3FTx) (24%) and phospholipases A(2) (PLA(2)s) (15%). However, 8 other classes of toxins were present, including C-type lectins, natriuretic peptide precursors and even high-molecular mass components such as metalloproteases and L-amino acid oxidases. Each class included an assortment of isoforms, some showing evidence of alternative splicing and domain deletions. Five antigenic candidates were selected (four 3FTx and one PLA(2)) and used for a preliminary study of DNA immunization. The immunological response showed that the sera from the immunized animals were able to recognize the recombinant antigens.

CONCLUSION

Besides an improvement in our knowledge of the composition of coral snake venoms, which are very poorly known when compared to Old World elapids, the expression profile suggests abundant and diversified components that may be used in future antiserum formulation. As recombinant production of venom antigens frequently fails due to complex disulfide arrangements, DNA immunization may be a viable alternative. In fact, the selected candidates provided an initial evidence of the feasibility of this approach, which is less costly and not dependent on the availability of the venom.

摘要

背景

珊瑚蛇(Micrurus corallinus)是一种属于眼镜蛇科的热带森林蛇。其毒液具有与突触前和突触后毒素相关的高神经毒性,可导致膈肌麻痹,进而可能导致死亡。尽管咬伤事故的发生率相对较低,但血清疗法对被咬者至关重要。然而,由于难以从繁殖条件苛刻的小蛇身上获取足够量的毒液,抗血清的充足生产受到阻碍。为了阐明这种毒液的分子基础并发现抗血清可能的免疫原,我们从其毒腺中生成了表达序列标签(EST)并分析了转录组图谱。此外,还使用DNA免疫测试了它们的免疫原性。

结果

共生成了1438个EST,并将其分组为611个簇。毒素转录本占总EST的46%。两种主要毒素类别包括三指毒素(3FTx)(24%)和磷脂酶A2(PLA2)(15%)。然而,还存在其他8类毒素,包括C型凝集素、利钠肽前体,甚至还有诸如金属蛋白酶和L-氨基酸氧化酶等高分子量成分。每一类都包含多种同工型,有些显示出可变剪接和结构域缺失的证据。选择了5种抗原候选物(4种3FTx和1种PLA2)并用于DNA免疫的初步研究。免疫反应表明,免疫动物的血清能够识别重组抗原。

结论

除了增进我们对珊瑚蛇毒液成分的了解(与旧大陆眼镜蛇相比,人们对其了解甚少)之外,表达谱表明可能有丰富多样的成分可用于未来抗血清的配制。由于毒液抗原的重组生产常常因复杂的二硫键排列而失败,DNA免疫可能是一种可行的替代方法。事实上,所选候选物为这种成本较低且不依赖毒液可用性的方法的可行性提供了初步证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1856/2662881/0c9998589328/1471-2164-10-112-1.jpg

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