Project - Marine Debris Clearinghouse
Do Microplastics Increase Disease Susceptibility in a Commercially Important Salmonid Species?
Project Abstract
This project examined whether microplastic ingestion modulates disease expression in a Pacific Northwest (PNW) salmonid species (rainbow trout). The physical presence of microplastics in some marine organisms is known to elicit an immune response. In situations where an organism is exposed to and ingests microplastics, the immune system may be compromised and thus be less capable of dealing with additional stressors, namely a virus common to salmonid species particularly where they exist in close proximity in large numbers (i.e., aquaculture facility). The virus in question is Infectious Hematopoietic Necrosis Virus (IHNV), one of the primary causes of infectious disease loss of salmonids in the PNW. Rainbow trout were reared from eggs in a controlled system to the size of interest. Kidney immune cells from these fish were assayed with weathered and virgin microplastics to observe the humoral immune system response and potential phagocytosis using 3 size ranges of polystyrene and nylon because these are the likely polymers encountered in the aquaculture facility (from buoys and netting). A number of biomarkers were examined, the presence of which would indicate an immune response has been triggered (i.e., expansion of innate cells, developing B cells, and plasmoblasts). The project then measured fish mortality in response to various microplastics concentrations, microplastics coincident with IHNV, and a control exposed to natural fibers (Spartina alterniflora). Mortality was tracked to generate LD50. Fish were tested to confirm death was due to the virus and in vivo humoral immune response markers were examined. In addition, the pathways by which microplastics gain entry into the internal tissues were determined (= mechanism of toxicity) by examining the gills, the gastrointestinal tract and other blood filtering organs for microplastics accumulation and checking for concentration of relevant chemical additives. This interdisciplinary work will make significant contributions to our understanding of the nexus of microplastics, immunology and fish disease.
Project Results
Exposure of fish to microplastics alone did not result in mortality. Exposure of fish to the virus alone did induce some mortality. However, when fish were exposed to microplastics and the virus together, mortality increased significantly. In fact, the risk of mortality was 4 times greater in the presence of nylon microfibers over exposure to the virus alone. This represents a unique finding that microplastics may have a significant impact on population health when presented with another stressor. Further, mortality was correlated with host viral load, gill inflammation, immune responses, and transmission potential, leading the researchers to hypothesize that microplastics can compromise host tissues, allowing pathogens to bypass defenses.
It was also reported that that rainbow trout phagocytic B cells efficiently took up small
(0.83-3.1µm) PS microbeads within hours of exposure. In addition, our data revealed that PS microplastic exposure most significantly decreased the abundance of a population of nonphagocytic developing B cells, using both flow cytometry and RT-qPCR. PS microplastics induced loss of developing B cells further correlated with reduced gene expression of RAG1 and the membrane form of immunoglobulin heavy chains mu and tau. Based on the induced loss of developing B cells observed in the in vitro studies, the researchers speculate that in vivo, chronic PS microplastic-exposure may lead to suboptimal IgM/IgT levels in response to pathogens in other teleost species.
Metrics
There are no project metrics
Contact Information
Robert Hale
1208 Greate Road
Gloucester Point, VA 23062
804-684-7228
hale@vims.edu
Patty Zwollo
pxzwol@wm.edu
Andrew Wargo
arwargo@vims.edu
Wolfgang Vogelbein
wolf@vims.edu
Meredith Evans Seeley
meseeley@vims.edu
1208 Greate Road
Gloucester Point, VA 23062
804-684-7228
hale@vims.edu
Patty Zwollo
pxzwol@wm.edu
Andrew Wargo
arwargo@vims.edu
Wolfgang Vogelbein
wolf@vims.edu
Meredith Evans Seeley
meseeley@vims.edu
Project Details
Funding Year:
2019
State/Territory Coverage:
Virginia
Start Date:
08/01/2019
Stop Date:
07/31/2023
Status:
Closed
Project Category:
Research
Region:
Mid-Atlantic
Debris Type(s):
Microplastics
Activities:
Assessment
Research
Research
Budget
Federal Funding:
$280,839.00
Non-Federal Match:
$280,839.00
Total Cost:
$561,678.00
Funding Mechanism:
Marine Debris Research
Funding Provider:
NOAA Marine Debris Program
Grant ID:
NA19NOS9990085
Partner Organizations
- Gulf of Alaska Keeper
Downloads
Where available, project outputs are available here for download. This may include photos, outreach or communication materials, data products, final reports, and data management or data sharing documentation.
IMAGES
Exposure of fish to microplastics alone did not result in mortality. Exposure of fish to the virus alone did induce some mortality. However, when fish were exposed to microplastics and the virus together, mortality increased significantly. In fact, the risk of mortality was 4 times greater in the presence of nylon microfibers over exposure to the virus alone.
Rainbow trout in a tank undergoing a research experiment looking at the effects of microplastics and a virus on fish mortality.
DOCUMENTS + LINKS
Do microplastics increase disease susceptibility in a commercially important salmonid species?(pdf)
Executive Summary
Microplastics and Disease in Rainbow Trout
Blog
Microplastics exacerbate virus-mediated mortality in fish
Publication
Polystyrene microplastics reduce abundance of developing B cells in rainbow trout (Oncorhynchus mykiss) primary cultures
Publication
Uncovering the influence of microplastics on disease dynamics in a commercially valuable fish and virus system
Webinar recording