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Global proteomic and functional analysis of Crotalus durissus collilineatus individual venom variation and its impact on envenoming.

Authors :
Oliveira IS
Cardoso IA
Bordon KCF
Carone SEI
Boldrini-França J
Pucca MB
Zoccal KF
Faccioli LH
Sampaio SV
Rosa JC
Arantes EC
Source :
Journal of proteomics [J Proteomics] 2019 Jan 16; Vol. 191, pp. 153-165. Date of Electronic Publication: 2018 Feb 17.
Publication Year :
2019

Abstract

Individual variations studies are important to understand the snakebite envenoming and to improve the antivenom production and its effectiveness. In this way, the objective of this study was a comparative analysis of intraspecific variation in the venom composition of 22 Crotalus durissus collilineatus specimens through proteomic techniques. Venoms were fractionated by RP-FPLC, and analyzed by SDS-PAGE and mass spectrometry. Although similar, chromatographic and electrophoretic profiles showed significant qualitative and quantitative differences. Some venom components were identified for the very first time in C. d. collilineatus, such as glutathione peroxidase, nerve growth factor, 5'-nucleotidase, angiotensin-converting enzyme, carboxypeptidase, phosphodiesterase, glutaminyl cyclase and phospholipase B. Regarding hyaluronidase activity, 2 venoms did not present detectable enzyme activity in the tested amounts. Additionally, in vivo crotalic envenoming in mice showed that venoms from different specimens resulted in diversified changes of biochemical and immunological parameters, such as creatine kinase and interleukin 6. This study demonstrated significant intraspecific variations in the venom of C. d. collilineatus, which may impact the production and effectiveness of the antivenom therapy. BIOLOGICAL SIGNIFICANCE: This study performed the proteomic and functional analyzes of 22 C. d. collilineatus individual venoms and verified the occurrence of quali and quantitative variations among them. The venoms evaluated caused envenomings with different changes in biochemical and immunological parameters. These results confirm the need to use a pool of venoms with the greatest possible variability in the preparation of antivenoms, in order to improve their effectiveness. In addition, this study was able to identify for the first time 8 different proteins in this subspecies venom, increasing knowledge about its composition and showing that it is a source of these proteins with possible biotechnological applications.<br /> (Copyright © 2018 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1876-7737
Volume :
191
Database :
MEDLINE
Journal :
Journal of proteomics
Publication Type :
Academic Journal
Accession number :
29462664
Full Text :
https://doi.org/10.1016/j.jprot.2018.02.020