4.4 Article

Description of Loxtox protein family and identification of a new group of Phospholipases D from Loxosceles similis venom gland

期刊

TOXICON
卷 120, 期 -, 页码 97-106

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.toxicon.2016.08.002

关键词

Venom; Loxosceles; Loxosceles similis; NGS; RNA-seq; Phospholipase D; Loxtox

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  2. Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [Edital Toxinologia 63/2010, PNPD AUXPE 2262/2011]

向作者/读者索取更多资源

Envenoming resulting from Loxosceles spider bites (loxoscelism) is a recognized public health problem in Brazil. However, the pathophysiology of loxoscelism caused by L similis bites, which is widespread in Brazil, remains poorly understood. In the present work, the RNA sequencing (RNA-Seq - Next Generation sequencing - NGS) of the L. similis venom gland was performed to identify and analyze the sequences of the key component phospholipase D. The sequences were aligned based on their classical domains, and a phylogenetic tree was constructed. In the bioinformatics analysis, 23 complete sequences of phospholipase D proteins were found and classified as Loxtox proteins, as they contained the characteristic domains of phospholipase D: the active site, the Mg2+-binding domain, and the catalytic loop. Three phospholipase D sequences with non-canonical domains were also found in this work. They were analyzed separately and named PLDs from L similis (PLD-Ls). This study is the first to characterize phospholipase D sequences from Loxosceles spiders by RNA-Seq. These results contribute new knowledge about the composition of L. similis venom, revealing novel tools that could be used for pharmacological, immunological, and biotechnological applications. (C) 2016 Elsevier Ltd. All rights reserved.

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