Effects of Heme Modulation on Ovophis and Trimeresurus Venom Activity in Human Plasma
Affiliation
Univ Arizona, Coll Med, Dept AnesthesiolIssue Date
2018-08
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MDPICitation
Nielsen VG, Frank N, Matika RW. Effects of Heme Modulation on Ovophis and Trimeresurus Venom Activity in Human Plasma. Toxins. 2018; 10(8):322.Journal
TOXINSRights
© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Geographic isolation and other factors result in evolution-driven diversity of the enzymatic composition of venom of pit vipers in the same genus. The present investigation sought to characterize venoms obtained from such genetically diverse Ovophis and Trimeresurus pit vipers utilizing thrombelastographic coagulation kinetic analyses. The coagulation kinetics of human plasma were assessed after exposure to venom obtained from two Ovophis and three Trimeresurus species. The potency of each venom was defined (mu g/mL required to equivalently change coagulation); additionally, venoms were exposed to carbon monoxide (CO) or a metheme-inducing agent to modulate any enzyme-associated heme. All venoms had fibrinogenolytic activity, with four being CO-inhibitable. While Ovophis venoms had similar potency, one demonstrated the presence of a thrombin-like activity, whereas the other demonstrated a thrombin-generating activity. There was a 10-fold difference in potency and 10-fold different vulnerability to CO inhibition between the Trimeresurus species. Metheme formation enhanced fibrinogenolytic-like activity in both Ovophis species venoms, whereas the three Trimeresurus species venoms had fibrinogenolytic-like activity enhanced, inhibited, or not changed. This novel venom kinetomic approach has potential to identify clinically relevant enzymatic activity and assess efficacy of antivenoms between genetically and geographically diverse species.Note
Open access journal.ISSN
2072-6651PubMed ID
30096756Version
Final published versionSponsors
Department of Anesthesiology, the University of Arizona, College of Medicine, Tucson, Arizona, USAAdditional Links
http://www.mdpi.com/2072-6651/10/8/322ae974a485f413a2113503eed53cd6c53
10.3390/toxins10080322
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Except where otherwise noted, this item's license is described as © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.

