Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish

Isopropylated phenyl phosphates (IPP) are an additive organophosphate flame retardant (OPFR) that has been extensively used in furniture, electronics, automobiles, plastics, and children’s products to slow down the spread of fire but its continued leaching leads to toxicity concerns. Toxicological i...

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Main Authors: Sunil Sharma, Alfredo Rojas, Abhishek Gour, Rosemaria Serradimigni, Connor Leong, Abhisheak Sharma, Subham Dasgupta
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Ecotoxicology and Environmental Safety
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Online Access:http://www.sciencedirect.com/science/article/pii/S0147651324016956
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author Sunil Sharma
Alfredo Rojas
Abhishek Gour
Rosemaria Serradimigni
Connor Leong
Abhisheak Sharma
Subham Dasgupta
author_facet Sunil Sharma
Alfredo Rojas
Abhishek Gour
Rosemaria Serradimigni
Connor Leong
Abhisheak Sharma
Subham Dasgupta
author_sort Sunil Sharma
collection DOAJ
description Isopropylated phenyl phosphates (IPP) are an additive organophosphate flame retardant (OPFR) that has been extensively used in furniture, electronics, automobiles, plastics, and children’s products to slow down the spread of fire but its continued leaching leads to toxicity concerns. Toxicological information on this important legacy contaminant is limiting. Using zebrafish, our prior whole embryonic RNA-seq data revealed disruption of gene sets enriched for DNA methylation, neurotransmitter synthesis, retinoic acid signaling and eye development. Within this study, we used zebrafish embryos to systemically study these biological targets. Our initial range-finding experiments revealed significant morphological impacts like pericardial edema, yolk sac edema and spinal curvature, coupled with a significant increase in the levels of dopamine and 3-methoxytyramine. We then conducted an in vitro retinoic acid receptor (RAR) assay and showed that IPP inhibits RARα, but not RARβ and RARγ. Following this, our larval behavioral (photomotor and acoustic response assays) at environmentally relevant, sub-μM concentrations showed significant hypoactivity, indicating sensorimotor deficits within exposed embryo. We then assessed global DNA methylation using a combination of whole-mount immunohistochemistry and ELISA for 5-methylcytosine (5-mC) and showed significant IPP-induced hypermethylation within whole embryo in situ. Finally, we focused on eye and brains as targets. We dissected eyes and brains from IPP-exposed larvae and conducted 5-mC assessments and mRNA-sequencing. Interestingly, neither of the organs showed differences in 5-mC levels and the brains also did not show substantial transcriptomic effects. However, for eyes, mRNA sequencing showed 135 differentially expressed genes and these were enriched for several nervous system-associated pathways, including voltage gated ion channel activity, synaptic transmission and neurotransmitter signaling. Collectively, our data shows that IPP exposures can disrupt a battery of biological pathways spanning neurometabolomic, genetic, epigenetic as well as organ-level targets. Notably, these impacts occur at concentrations within environmental relevance where overt toxic morphological phenotypes are not recorded. Future work will focus on understanding the contribution of these molecular targets to behavioral phenotypes.
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spelling doaj-art-618b03121b5343bfbf506628ec6b15742025-02-12T05:30:00ZengElsevierEcotoxicology and Environmental Safety0147-65132025-01-01290117619Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafishSunil Sharma0Alfredo Rojas1Abhishek Gour2Rosemaria Serradimigni3Connor Leong4Abhisheak Sharma5Subham Dasgupta6Department of Biological Sciences, Clemson University, Clemson, SC, USADepartment of Biological Sciences, Clemson University, Clemson, SC, USACollege of Pharmacy, University of Florida, Gainesville, FL, USADepartment of Biological Sciences, Clemson University, Clemson, SC, USADepartment of Microbiology, Oregon State University, Corvallis, OR, USACollege of Pharmacy, University of Florida, Gainesville, FL, USADepartment of Biological Sciences, Clemson University, Clemson, SC, USA; Corresponding author.Isopropylated phenyl phosphates (IPP) are an additive organophosphate flame retardant (OPFR) that has been extensively used in furniture, electronics, automobiles, plastics, and children’s products to slow down the spread of fire but its continued leaching leads to toxicity concerns. Toxicological information on this important legacy contaminant is limiting. Using zebrafish, our prior whole embryonic RNA-seq data revealed disruption of gene sets enriched for DNA methylation, neurotransmitter synthesis, retinoic acid signaling and eye development. Within this study, we used zebrafish embryos to systemically study these biological targets. Our initial range-finding experiments revealed significant morphological impacts like pericardial edema, yolk sac edema and spinal curvature, coupled with a significant increase in the levels of dopamine and 3-methoxytyramine. We then conducted an in vitro retinoic acid receptor (RAR) assay and showed that IPP inhibits RARα, but not RARβ and RARγ. Following this, our larval behavioral (photomotor and acoustic response assays) at environmentally relevant, sub-μM concentrations showed significant hypoactivity, indicating sensorimotor deficits within exposed embryo. We then assessed global DNA methylation using a combination of whole-mount immunohistochemistry and ELISA for 5-methylcytosine (5-mC) and showed significant IPP-induced hypermethylation within whole embryo in situ. Finally, we focused on eye and brains as targets. We dissected eyes and brains from IPP-exposed larvae and conducted 5-mC assessments and mRNA-sequencing. Interestingly, neither of the organs showed differences in 5-mC levels and the brains also did not show substantial transcriptomic effects. However, for eyes, mRNA sequencing showed 135 differentially expressed genes and these were enriched for several nervous system-associated pathways, including voltage gated ion channel activity, synaptic transmission and neurotransmitter signaling. Collectively, our data shows that IPP exposures can disrupt a battery of biological pathways spanning neurometabolomic, genetic, epigenetic as well as organ-level targets. Notably, these impacts occur at concentrations within environmental relevance where overt toxic morphological phenotypes are not recorded. Future work will focus on understanding the contribution of these molecular targets to behavioral phenotypes.http://www.sciencedirect.com/science/article/pii/S0147651324016956Flame retardantsZebrafishRNA-sequencingDNA methylationBehaviorNeurotoxicity
spellingShingle Sunil Sharma
Alfredo Rojas
Abhishek Gour
Rosemaria Serradimigni
Connor Leong
Abhisheak Sharma
Subham Dasgupta
Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish
Ecotoxicology and Environmental Safety
Flame retardants
Zebrafish
RNA-sequencing
DNA methylation
Behavior
Neurotoxicity
title Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish
title_full Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish
title_fullStr Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish
title_full_unstemmed Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish
title_short Assessing molecular changes underlying isopropylated phenyl phosphate (IPP)-induced larval sensorimotor response deficits in zebrafish
title_sort assessing molecular changes underlying isopropylated phenyl phosphate ipp induced larval sensorimotor response deficits in zebrafish
topic Flame retardants
Zebrafish
RNA-sequencing
DNA methylation
Behavior
Neurotoxicity
url http://www.sciencedirect.com/science/article/pii/S0147651324016956
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