Accession Number:

ADA617744

Title:

Investigation of Evolved Paraoxonase-1 Variants for Prevention of Organophosphorous Pesticide Compound Intoxication

Descriptive Note:

Journal article

Corporate Author:

ARMY MEDICAL RESEARCH INST OF CHEMICAL DEFENSE ABERDEEN PROVING GROUND MD

Report Date:

2014-04-04

Pagination or Media Count:

40.0

Abstract:

We investigated the ability of the engineered paraoxonase-1 variants G3C9, VII-D11, I-F11 and VII-D2 to afford protection against paraoxon intoxication. Paraoxon is the toxic metabolite of parathion, a common pesticide still in use in many developing countries. An in vitro investigation showed that VII-D11 is the most efficient variant at hydrolyzing paraoxon for the enzyme expressed via adenovirus infection of 293A cells and mice, respectively. Compared to the G3C9 parent scaffold, VII-D11 is 15-20 fold more efficacious at hydrolyzing paraoxon. Coinciding with these results, mice expressing VII-D11 in their blood survived and showed no symptoms against a cumulative 6.3 LD50 dose of paraoxon while mice expressing G3C9 experienced tremors and only 50 survival. We then determined whether VII-D11 can offer protection against paraoxon when present at substoichiometric concentrations. Mice containing varying concentrations of VII-D11 in their blood 0.2 - 4.1 mgmL were challenged with doses of paraoxon at fixed stoichiometric ratios that constitute up to a ten-fold molar excess of paraoxon to enzyme 1.4 - 27 LDsub50 doses and were assessed for tremors and mortality. Mice were afforded complete asymptomatic protection below a paraoxon to enzyme ratio of 81, whereas higher ratios produced tremors andor mortality. VIID11 in mouse blood co-eluted with high density lipoprotein, suggesting an association between the two entities. Collectively, these results demonstrate that VII-D11 is a promising candidate for development as a prophylactic catalytic bioscavenger against organophosphorous pesticide toxicity.

Subject Categories:

  • Ecology
  • Toxicology

Distribution Statement:

APPROVED FOR PUBLIC RELEASE