AI Article Synopsis

  • Loxoscelism, the envenoming from Loxosceles spider bites, is a significant health issue in Brazil, particularly concerning the L. similis species, but the mechanisms behind its effects are not well understood.
  • The researchers performed RNA sequencing on the venom glands of L. similis to identify key components, focusing on phospholipase D proteins, which are crucial for understanding the venom's composition.
  • This study identified 23 phospholipase D sequences classified as Loxtox proteins and discovered three non-canonical variants, providing vital insights that could have applications in medicine and biotechnology.

Article 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.

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http://dx.doi.org/10.1016/j.toxicon.2016.08.002DOI Listing

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