Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica

Introduction: Perfluoroalkyl and poly-fluoroalkyl substances (PFASs) are widely used in industrial and consumer products. Due to their environmental persistence and bioaccumulation, PFASs can be found in the blood of humans and wild animals all over the world. Various fluorinated alternatives such a...

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Main Authors: Wenqi Cao, Katharine Horzmann, Bettina Schemera, Myra Petrofski, Trisha Kendall, Jennifer Spooner, Patricia E. Rynders, John L. VandeBerg, Xu Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-02-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2023.1073461/full
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author Wenqi Cao
Wenqi Cao
Katharine Horzmann
Bettina Schemera
Myra Petrofski
Trisha Kendall
Jennifer Spooner
Patricia E. Rynders
John L. VandeBerg
Xu Wang
Xu Wang
Xu Wang
author_facet Wenqi Cao
Wenqi Cao
Katharine Horzmann
Bettina Schemera
Myra Petrofski
Trisha Kendall
Jennifer Spooner
Patricia E. Rynders
John L. VandeBerg
Xu Wang
Xu Wang
Xu Wang
author_sort Wenqi Cao
collection DOAJ
description Introduction: Perfluoroalkyl and poly-fluoroalkyl substances (PFASs) are widely used in industrial and consumer products. Due to their environmental persistence and bioaccumulation, PFASs can be found in the blood of humans and wild animals all over the world. Various fluorinated alternatives such as GenX have been developed to replace the long-chain PFASs, but there is limited information about their potential toxicity.Methods:The current study developed blood culture protocols to assess the response to toxic compounds in the marsupial, Monodelphis domestica. After whole-blood culture conditions were tested and optimized, changes in gene expression in response to PFOA and GenX treatment were assessed.Results: More than 10,000 genes were expressed in the blood transcriptomes with and without treatment. Both PFOA and GenX treatment led to significant changes in the whole blood culture transcriptomes. A total of 578 and 148 differentially expressed genes (DEGs) were detected in the PFOA and GenX treatment groups, 32 of which overlapped. Pathway enrichment analysis revealed that DEGs involved in developmental processes were upregulated after PFOA exposure, while those enriched for metabolic and immune system processes were downregulated. GenX exposure upregulated genes associated with fatty acid transport pathways and inflammatory processes, which is consistent with previous studies using rodent models.Discussion: To our knowledge, this study is the first to investigate the effect of PFASs in a marsupial model. The findings provide supportive evidence for significant transcriptomic alterations, suggesting that this mammalian model may provide a mechanism for exploring the potential toxicity of PFOA and GenX.
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spelling doaj.art-d8f45ccfa2694853a446fde3a6c37bff2023-02-15T05:33:32ZengFrontiers Media S.A.Frontiers in Genetics1664-80212023-02-011410.3389/fgene.2023.10734611073461Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domesticaWenqi Cao0Wenqi Cao1Katharine Horzmann2Bettina Schemera3Myra Petrofski4Trisha Kendall5Jennifer Spooner6Patricia E. Rynders7John L. VandeBerg8Xu Wang9Xu Wang10Xu Wang11Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesAlabama Agricultural Experiment Station, Auburn University Center for Advanced Science, Innovation, and Commerce, Auburn, AL, United StatesDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesDivision of Laboratory Animal Health, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesDivision of Laboratory Animal Health, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesDivision of Laboratory Animal Health, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesDivision of Laboratory Animal Health, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesDivision of Laboratory Animal Health, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesDepartment of Human Genetics, School of Medicine, South Texas Diabetes and Obesity Institute, The University of Texas Rio Grande Valley, Brownsville, TX, United StatesDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL, United StatesAlabama Agricultural Experiment Station, Auburn University Center for Advanced Science, Innovation, and Commerce, Auburn, AL, United StatesHudsonAlpha Institute for Biotechnology, Huntsville, AL, United StatesIntroduction: Perfluoroalkyl and poly-fluoroalkyl substances (PFASs) are widely used in industrial and consumer products. Due to their environmental persistence and bioaccumulation, PFASs can be found in the blood of humans and wild animals all over the world. Various fluorinated alternatives such as GenX have been developed to replace the long-chain PFASs, but there is limited information about their potential toxicity.Methods:The current study developed blood culture protocols to assess the response to toxic compounds in the marsupial, Monodelphis domestica. After whole-blood culture conditions were tested and optimized, changes in gene expression in response to PFOA and GenX treatment were assessed.Results: More than 10,000 genes were expressed in the blood transcriptomes with and without treatment. Both PFOA and GenX treatment led to significant changes in the whole blood culture transcriptomes. A total of 578 and 148 differentially expressed genes (DEGs) were detected in the PFOA and GenX treatment groups, 32 of which overlapped. Pathway enrichment analysis revealed that DEGs involved in developmental processes were upregulated after PFOA exposure, while those enriched for metabolic and immune system processes were downregulated. GenX exposure upregulated genes associated with fatty acid transport pathways and inflammatory processes, which is consistent with previous studies using rodent models.Discussion: To our knowledge, this study is the first to investigate the effect of PFASs in a marsupial model. The findings provide supportive evidence for significant transcriptomic alterations, suggesting that this mammalian model may provide a mechanism for exploring the potential toxicity of PFOA and GenX.https://www.frontiersin.org/articles/10.3389/fgene.2023.1073461/fullper-and polyfluoroalkyl substances (PFAS)laboratory opossumlong-chain fatty acid transportinflammatory responsedevelopmental processestoxicology
spellingShingle Wenqi Cao
Wenqi Cao
Katharine Horzmann
Bettina Schemera
Myra Petrofski
Trisha Kendall
Jennifer Spooner
Patricia E. Rynders
John L. VandeBerg
Xu Wang
Xu Wang
Xu Wang
Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica
Frontiers in Genetics
per-and polyfluoroalkyl substances (PFAS)
laboratory opossum
long-chain fatty acid transport
inflammatory response
developmental processes
toxicology
title Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica
title_full Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica
title_fullStr Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica
title_full_unstemmed Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica
title_short Blood transcriptome responses to PFOA and GenX treatment in the marsupial biomedical model Monodelphis domestica
title_sort blood transcriptome responses to pfoa and genx treatment in the marsupial biomedical model monodelphis domestica
topic per-and polyfluoroalkyl substances (PFAS)
laboratory opossum
long-chain fatty acid transport
inflammatory response
developmental processes
toxicology
url https://www.frontiersin.org/articles/10.3389/fgene.2023.1073461/full
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