Analysis of NGS data from Peruvian Loxosceles laeta spider venom gland reveals toxin diversity.


Journal

Comparative biochemistry and physiology. Part D, Genomics & proteomics
ISSN: 1878-0407
Titre abrégé: Comp Biochem Physiol Part D Genomics Proteomics
Pays: Netherlands
ID NLM: 101270611

Informations de publication

Date de publication:
09 2022
Historique:
received: 14 03 2022
revised: 12 07 2022
accepted: 27 07 2022
pubmed: 7 8 2022
medline: 18 8 2022
entrez: 6 8 2022
Statut: ppublish

Résumé

Accidents involving spiders from the genus Loxosceles cause medical emergencies in several countries of South America. The species Loxosceles laeta is ubiquitously present in Peru and is responsible for severe accidents in this country. To further characterize L. laeta venom components and to unveil possible variations in the Peruvian population, we provide an overview of the toxins-related transcripts present in the venom gland of Peruvian L. laeta. A dataset from a cDNA library previously sequenced by MiSeq sequencer (Illumina) was re-analyzed and the obtained data was compared with available sequences from Loxosceles toxins. Phospholipase-D represent the majority (69,28 %) of the transcripts related to venom toxins, followed by metalloproteases (20,72 %), sicaritoxins (6,03 %), serine-proteases (2,28 %), hyaluronidases (1,80 %) and Translationally Controlled Tumor Protein (TCTP) (0,56 %). New sequences of phospholipases D,sicaritoxins, hyaluronidase, TCTP and serine proteinases were described. Differences between the here-described toxin sequences and others, previously identified in venom glands from other spiders, were visualized upon sequence alignments. In addition, an in vitro hyaluronidase activity assay was also performed to complement comparisons between Peruvian and Brazilian L. laeta venom enzymatic activities, revealing a superior activity in the venom from Brazilian specimens. These new data provide a molecular basis that can help to explain the difference in toxicity among L. laeta venoms from different countries in South America.

Identifiants

pubmed: 35932519
pii: S1744-117X(22)00059-4
doi: 10.1016/j.cbd.2022.101017
pii:
doi:

Substances chimiques

Spider Venoms 0
Hyaluronoglucosaminidase EC 3.2.1.35

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101017

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Raíssa Medina-Santos (R)

Biochemistry and Immunology Department, Federal University of Minas Gerais, Brazil; Genetic, Ecology and Evolution Department, Federal University of Minas Gerais, Brazil.

Tamara G Fernandes Costa (TG)

Biochemistry and Immunology Department, Federal University of Minas Gerais, Brazil.

Thamyres C Silva de Assis (TC)

Biochemistry and Immunology Department, Federal University of Minas Gerais, Brazil.

Yan Kalapothakis (Y)

Genetic, Ecology and Evolution Department, Federal University of Minas Gerais, Brazil.

Sabrina de Almeida Lima (S)

Biochemistry and Immunology Department, Federal University of Minas Gerais, Brazil.

Anderson Oliveira do Carmo (AO)

Genetic, Ecology and Evolution Department, Federal University of Minas Gerais, Brazil.

Edgar E Gonzalez-Kozlova (EE)

Department of Genetics and Genomic Sciences, Icahn School for Data Science and Genomic Technology, New York, United States of America.

Evanguedes Kalapothakis (E)

Genetic, Ecology and Evolution Department, Federal University of Minas Gerais, Brazil.

Carlos Chávez-Olórtegui (C)

Biochemistry and Immunology Department, Federal University of Minas Gerais, Brazil.

Clara Guerra-Duarte (C)

Ezequiel Dias Foundation, Brazil. Electronic address: clara.duarte@funed.mg.gov.br.

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Classifications MeSH