| Literature DB >> 27496061 |
Arthur Estanislau Dantas1, A O Carmo2, Carolina Campolina Rebello Horta3, Hortênsia Gomes Leal4, Bárbara Bruna Ribeiro Oliveira-Mendes5, Ana Paula Vimieiro Martins6, Carlos Chávez-Olórtegui7, Evanguedes Kalapothakis8.
Abstract
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 Mg(2+)-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.Entities:
Keywords: Loxosceles; Loxosceles similis; Loxtox; NGS; Phospholipase D; RNA-seq; Venom
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Year: 2016 PMID: 27496061 DOI: 10.1016/j.toxicon.2016.08.002
Source DB: PubMed Journal: Toxicon ISSN: 0041-0101 Impact factor: 3.033