Abstract

The US Department of Defense (DOD) is developing insensitive munitions (IMs) that are resistant to unintended detonation to protect warfighters. To enable material life-cycle analysis for the IM, 1-methyl-3-nitro-1-nitroguanidine (MeNQ), ecotoxicological impacts assessment was required. A previous investigation of MeNQ exposures in Daphnia pulex revealed concentration-responsive decreases in reproduction relative to controls (0 mg/L) across a 174, 346, 709, 1385, and 2286 mg/L exposure range. The present study used those exposures to conduct global transcriptomic expression analyses to establish hypothetical mode(s) of action underlying inhibited reproduction. The number of significantly affected transcripts and the magnitude of fold-change differences relative to controls tended to increase with increasing MeNQ concentration where hierarchical clustering analysis identified separation among the “low” (174 and 346 mg/L) and “high” (709, 1385, and 2286 mg/L) exposures. Vitellogenin is critical to Daphnia reproductive processes and MeNQ exposures significantly decreased transcriptional expression for vitellogenin-1 precursor at the lowest exposure level (174 mg/L) with benchmark dose (BMD) levels closely tracking concentrations that caused inhibited reproduction. Additionally, juvenile hormone-inducible protein, chorion peroxidase, and high choriolytic enzyme transcriptional expression were impacted by MeNQ exposure having potential implications for egg production / maturation and overall fecundity. In concert with these effects on specific genes involved in Daphnia reproductive physiology, MeNQ exposures caused significant enrichment of several canonical-pathways responsible for metabolism of cellular energy substrates where BMD levels for transcriptional expression were observed at ≤100 mg/L. These observations imply possible effects on whole-organism energy budgets that may also incur indirect costs on reproduction.

Highlights

  • MethodsThe present study was initiated using D. pulex sampled at the termination of the three-brood chronic reproduction assay described in Lotufo et al (2021) to conduct microarray-based global transcriptomic investigations

  • The US Department of Defense (DOD) has been required by law to replace conventional munitions with insensitive

  • The present study provides evidence of MeNQ-induced changes in transcriptional expression for genes directly involved in D. pulex reproductive physiology as well as systems-level effects on energy metabolic processes that have logical connections to observed impacts on D. pulex reproduction

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Summary

Methods

The present study was initiated using D. pulex sampled at the termination of the three-brood chronic reproduction assay described in Lotufo et al (2021) to conduct microarray-based global transcriptomic investigations. In the Lotufo et al (2021) study, D. pulex were exposed to MeNQ at control (0 mg/L), 174, 346, 709, 1385, and 2286 mg/L (measured concentrations) as juveniles through three-broods of reproduction. This exposure caused reproductive inhibition, resulting in a 50% inhibitory concentration (IC50) of 424 mg/L with a 95% confidence interval (C.I) of (159–609 mg/L). The sample set was utilized to conduct global transcriptomic expression analysis to identify hypothetical modes of action related to the decreased reproductive rates observed by Lotufo et al (2021) in response to the MeNQ exposures

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