Dataset Information

The world is your oyster: low-dose, long-term microplastic exposure of juvenile oysters.

ABSTRACT: Bivalve filter feeders, such as oysters, filter large volumes of water and are particularly exposed to microplastics (MP). Consequently, these animals digest and assimilate high levels of MP in their bodies that may likely impact their physiology, and potentially affect shellfish stocks, benthic habitats and, indirectly, the health status of the marine ecosystem and human consumers. In this study we exposed juvenile oysters, Crassostrea gigas, to 3 different MP concentrations (104, 105 and 106 particles L-1), represented by 6?m Polystyrene (PS) microbeads, compared to a control treatment receiving no MP. The study ran for a period of 80 days to test for the impacts of MP on growth, Condition Index and Lysosomal Stability. From histological analysis, microbeads were detected in the intestines of exposed oysters and in the digestive tubules, but no cellular inflammatory features were observed over time. Weight and shell length remained comparable between the different treatments and control. We found that Condition Index in the highest concentration increased initially but significantly reduced over time. The oysters in the highest MP exposure also showed the lowest mean Lysosomal Stability score throughout the experiment. Lysosomes play a vital role in the cells defense mechanisms and breakdown of constituents, crucial for the oysters' wellbeing. Most importantly, we detected an increased mortality in those oysters who were chronically exposed to the highest loads of MP.

SUBMITTER: Thomas M

PROVIDER: S-EPMC6938840 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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The world is your oyster: low-dose, long-term microplastic exposure of juvenile oysters.

Thomas Maes M Jon Barry B Craig Stenton S Edward Roberts R Ruth Hicks H John Bignell B Dick Vethaak A VA Heather Leslie A LA Matthew Sanders S

Heliyon 20191227 1

Bivalve filter feeders, such as oysters, filter large volumes of water and are particularly exposed to microplastics (MP). Consequently, these animals digest and assimilate high levels of MP in their bodies that may likely impact their physiology, and potentially affect shellfish stocks, benthic habitats and, indirectly, the health status of the marine ecosystem and human consumers. In this study we exposed juvenile oysters, <i>Crassostrea gigas,</i> to 3 different MP concentrations (10<sup>4</s ...[more]

PMID: 31909270

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Project description:Background. Radioiodide 131I is commonly used to treat thyroid cancer and hyperthyroidism, and 131I releases during nuclear accidents have resulted in increased incidence of thyroid cancer in children. To develop a better understanding of underlying cellular mechanisms behind 131I exposure and identify potential biomarkers, the aim of this work was to study the long-term dose-related effects of 131I exposure in thyroid tissue and plasma in young rats. Materials and methods. Male Sprague Dawley rats (5-week-old) were i.v. injected with 0.5, 5.0, 50 or 500 kBq 131I (Dthyroid ca 1–1000 mGy), and killed after nine months at which time the thyroid and blood samples were collected. Gene expression microarray analysis (thyroid samples) and LC-MS/MS analysis (thyroid and plasma samples) were performed to assess differential gene and protein expression patterns in treated and corresponding untreated control samples. Bioinformatics analyses were performed using the DAVID functional annotation tool and Ingenuity Pathway Analysis (IPA). Results. Nine 131I exposure-related biomarkers (Afp and RT1-Bb,ARF3, DLD, IKBKB, NONO, RAB6A, RPN2, and SLC25A5) were identified in thyroid tissue. Four dose-related biomarker candidates (APRT, LDHA) and (TGM3 and DSG4) were identified in thyroid and plasma, respectively. Candidate biomarkers for thyroid function were the upstream regulator PPARG and the proteins ACADL and SORBS2 (all activities), TPO and TG (low activities)). 131I exposure was shown to have a profound effect on metabolism, the immune system, apoptosis and cell death. Furthermore, several signalling pathways essential for normal cellular function (actin cytoskeleton signalling, HGF signalling, NRF2-mediated oxidative stress, integrin signalling, calcium signalling) were also significantly regulated. Conclusion. Exposure-related and dose-related effects on gene and protein expression were observed, thereby identifying several candidate genes that could be used as potential biomarkers for exposure, absorbed dose and thyroid function.

Project description:BackgroundRadioiodide (131I) is commonly used to treat thyroid cancer and hyperthyroidis.131I released during nuclear accidents, have resulted in increased incidence of thyroid cancer in children. Therefore, a better understanding of underlying cellular mechanisms behind 131I exposure is of great clinical and radiation protection interest. The aim of this work was to study the long-term dose-related effects of 131I exposure in thyroid tissue and plasma in young rats and identify potential biomarkers.Materials and methodsMale Sprague Dawley rats (5-week-old) were i.v. injected with 0.5, 5.0, 50 or 500 kBq 131I (Dthyroid ca 1-1000 mGy), and killed after nine months at which time the thyroid and blood samples were collected. Gene expression microarray analysis (thyroid samples) and LC-MS/MS analysis (thyroid and plasma samples) were performed to assess differential gene and protein expression profiles in treated and corresponding untreated control samples. Bioinformatics analyses were performed using the DAVID functional annotation tool and Ingenuity Pathway Analysis (IPA). The gene expression microarray data and LC-MS/MS data were validated using qRT-PCR and ELISA, respectively.ResultsNine 131I exposure-related candidate biomarkers (transcripts: Afp and RT1-Bb, and proteins: ARF3, DLD, IKBKB, NONO, RAB6A, RPN2, and SLC25A5) were identified in thyroid tissue. Two dose-related protein candidate biomarkers were identified in thyroid (APRT and LDHA) and two in plasma (DSG4 and TGM3). Candidate biomarkers for thyroid function included the ACADL and SORBS2 (all activities), TPO and TG proteins (low activities). 131I exposure was shown to have a profound effect on metabolism, immune system, apoptosis and cell death. Furthermore, several signalling pathways essential for normal cellular function (actin cytoskeleton signalling, HGF signalling, NRF2-mediated oxidative stress, integrin signalling, calcium signalling) were also significantly regulated.ConclusionExposure-related and dose-related effects on gene and protein expression generated few expression patterns useful as biomarkers for thyroid function and cancer.

Dataset Information

The world is your oyster: low-dose, long-term microplastic exposure of juvenile oysters.

Publications

The world is your oyster: low-dose, long-term microplastic exposure of juvenile oysters.

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