Developmental toxicants including polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and chlorophenols (e.g., pentachlorophenol - PCP) are persistent organic contaminants found at many hazardous waste sites throughout the United States. These contaminants are of great concern because they present high toxicological risk in terms of their potential for bioaccumulation in the food chain as well as adverse health effects. Hydrophobic organic contaminants (HOCs) such as PAHs, PCBs and PCP are particularly challenging to bioremediate because their chemical characteristics diminish their bioavailability to microorganisms thereby limiting their potential for efficient biodegradation. As a result of this constraint, HOC remediation strategies tend to focus on physical-chemical approaches consisting of either complete excavation of contaminated media or contaminant in situ immobilization via amendment mediated sequestration which can have significant negative long term impacts on local ecosystems. In this project, we propose an alternative treatment approach which consists of stimulating cooperative bacterial-fungal biofilms for HOC biodegradation. Using this approach, indigenous fungi will first be stimulated to degrade toxicants using nonspecific extracellular enzymes and generate by-products more bioavailable to bacteria for subsequent biodegradation. While using remediation treatment approaches based on the production of fungal extracellular enzymes is not entirely new, the novelty of this project resides in the fact that our focus will be directed towards the promotion of indigenous Ascomycetes associated with sediment microbial biofilms, a phylum which has not received much attention for bioremediation. The overall objective of this project is to maximize HOC biodegradation in sediment settings by stimulating the growth of synergistic fungal-bacterial biofilms using engineered composite organic amendments. The general hypothesis for Project 5 is that the physico-chemical environment can be altered using composite organic amendments to stimulate the formation of a cooperative bacterial-fungal biofilms in which indigenous fungi produce extracellular enzymes breaking down hydrophobic contaminants into by-products which are more readily transported into bacterial cells and broken down by indigenous bacteria.
The specific aims for this project are to: 1) Perform microbial and geochemical characterizations of contaminated sediments for the construction of a microbial association network model; 2) Identify organic amendments which support the growth of cooperative fungal-bacterial biofilm and maximize HOC degradation in microcosms; 3) Engineer and test composite amendments for delivery in sediment treatment scenarios and; 4) Implement the composite amendment strategy in large-scale mesocosms as well as validate its efficiency for HOC degradation by stimulated mixed fungal-bacterial biofilms. Ultimately, this project will create a framework to better understand cooperative fungal-bacterial biofilms in the context of sediment bioremediation and yield field translatable approaches for the bioremediation of HOCs.

Public Health Relevance

Developmental toxicants including polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and chlorophenols such as pentachlorophenol (PCP) are contaminants of great concern because they present high toxicological risk in terms of their potential for bioaccumulation in the food chain as well as adverse health effects. In this project, we will develop innovative bioremediation approaches which harness a critical, yet previously largely unexplored group of microorganisms, namely non-basidiomycete fungi. In particular, we will engineer composite organic amendment materials which enhance the degradation of these highly recalcitrant contaminants by cooperative fungal-bacterial biofilms in sediments, ultimately reducing the potential for human and environmental exposure.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES010356-18
Application #
9942442
Study Section
Special Emphasis Panel (ZES1)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
18
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Meyer, Joel N; Hartman, Jessica H; Mello, Danielle F (2018) Mitochondrial Toxicity. Toxicol Sci 162:15-23
Oliveri, Anthony N; Ortiz, Erica; Levin, Edward D (2018) Developmental exposure to an organophosphate flame retardant alters later behavioral responses to dopamine antagonism in zebrafish larvae. Neurotoxicol Teratol 67:25-30
Slotkin, Theodore A; Skavicus, Samantha; Seidler, Frederic J (2018) Developmental neurotoxicity resulting from pharmacotherapy of preterm labor, modeled in vitro: Terbutaline and dexamethasone, separately and together. Toxicology 400-401:57-64
Lefèvre, Emilie; Bossa, Nathan; Gardner, Courtney M et al. (2018) Biochar and activated carbon act as promising amendments for promoting the microbial debromination of tetrabromobisphenol A. Water Res 128:102-110
Kollitz, Erin M; Kassotis, Christopher D; Hoffman, Kate et al. (2018) Chemical Mixtures Isolated from House Dust Disrupt Thyroid Receptor ? Signaling. Environ Sci Technol :
Hartman, Jessica H; Smith, Latasha L; Gordon, Kacy L et al. (2018) Swimming Exercise and Transient Food Deprivation in Caenorhabditis elegans Promote Mitochondrial Maintenance and Protect Against Chemical-Induced Mitotoxicity. Sci Rep 8:8359
Luz, Anthony L; Kassotis, Christopher D; Stapleton, Heather M et al. (2018) The high-production volume fungicide pyraclostrobin induces triglyceride accumulation associated with mitochondrial dysfunction, and promotes adipocyte differentiation independent of PPAR? activation, in 3T3-L1 cells. Toxicology 393:150-159
Day, D B; Xiang, J; Mo, J et al. (2018) Combined use of an electrostatic precipitator and a high-efficiency particulate air filter in building ventilation systems: Effects on cardiorespiratory health indicators in healthy adults. Indoor Air 28:360-372
Slotkin, Theodore A; Ko, Ashley; Seidler, Frederic J (2018) Does growth impairment underlie the adverse effects of dexamethasone on development of noradrenergic systems? Toxicology 408:11-21
Rock, Kylie D; Horman, Brian; Phillips, Allison L et al. (2018) EDC IMPACT: Molecular effects of developmental FM 550 exposure in Wistar rat placenta and fetal forebrain. Endocr Connect 7:305-324

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