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Liver Lesions in Estuarine Dolphins in the Indian River Lagoon, Florida: Does Microcystin Play a Role?
Ami Krasner1, Wendy Noke Durden2, Megan Stolen2,3
1Department of Ocean Engineering and Marine Sciences, Florida Institute of Technology, Melbourne, FL 32901, USA.
Abstract:
Microcystin (MC), a hepatotoxin produced by cyanobacteria, was introduced into the Indian River Lagoon (IRL), Florida, in 2005 through freshwater outflows. Since then, MC has been detected in humans, domestic animals, and wildlife in the lagoon. Potential public health effects associated with MC exposure along the IRL include an increased risk of non-alcoholic liver disease among area residents. Yet, there are limited studies characterizing liver disease, as well as the potential role of MC, in humans and animals in this region. Thus, histopathology reports (n = 133) were reviewed in the stranded common bottlenose dolphin (Tursiops truncatus truncatus) (n = 156, 2005-2024) to describe liver lesions in this important IRL sentinel. Liver and fecal samples (n = 161) from stranded individuals were screened for MC via an enzyme immunoassay (ELISA). These samples were then confirmed via the 2-methyl-3-methoxy-4-phenylbutyric acid technique (MMPB) to evaluate whether liver histopathologic lesions were linked to MC exposure. Minimally invasive MC screening methods were also assessed using respiratory swabs and vapor. Inflammation (24%, n = 32), fibrosis (23%, n = 31), lipidosis/vacuolation (11%, n = 15), and necrosis (11%, n = 14) were the most common liver anomalies observed. These non-specific lesions have been reported to be associated with MC exposure in numerous species in the peer-reviewed literature. Ten bottlenose dolphins tested positive for the toxin via ELISA, including two individuals with hepatic lipidosis, but none were confirmed by MMPB. Thus, this study did not provide evidence for MC-induced liver disease in IRL bottlenose dolphins. Other causes should be considered for the lesions observed (e.g., heavy metals, metabolic disease, and endoparasites). Respiratory swabs require further validation as a pre-mortem MC screening tool in free-ranging wildlife.
Insights
Microcystin (MC) toxin exposure was investigated in Indian River Lagoon bottlenose dolphins. No evidence linked MC to liver disease in these sentinel animals, suggesting other causes for observed lesions.
Area of Science:
- Environmental Toxicology
- Marine Mammal Health
- Cyanotoxin Research
Background:
- Microcystin (MC), a cyanobacterial hepatotoxin, entered the Indian River Lagoon (IRL) in 2005.
- MC exposure has been documented in IRL wildlife, humans, and domestic animals, with potential public health implications.
- Limited research exists on liver disease and MC's role in IRL wildlife.
Purpose of the Study:
- To investigate potential links between microcystin (MC) exposure and liver lesions in common bottlenose dolphins (Tursiops truncatus truncatus) from the IRL.
- To assess the prevalence of specific liver histopathologic findings in IRL dolphins.
- To evaluate the efficacy of ELISA and MMPB techniques for MC detection and explore minimally invasive screening methods.
Main Methods:
- Histopathological review of 133 liver samples from 156 stranded dolphins (2005-2024).
- Screening of 161 liver and fecal samples for MC using ELISA, with confirmation by the 2-methyl-3-methoxy-4-phenylbutyric acid (MMPB) technique.
- Assessment of respiratory swabs and vapor for MC screening.
Main Results:
- The most common liver anomalies were inflammation (24%), fibrosis (23%), lipidosis/vacuolation (11%), and necrosis (11%).
- Ten dolphins tested positive for MC via ELISA, but none were confirmed by MMPB.
- No definitive evidence of MC-induced liver disease was found in the studied dolphin population.
Conclusions:
- This study did not establish a causal link between microcystin (MC) exposure and liver disease in Indian River Lagoon bottlenose dolphins.
- Alternative etiologies, such as heavy metals, metabolic disease, or endoparasites, should be considered for the observed liver lesions.
- Further validation is needed for respiratory swabs as a pre-mortem MC screening tool in wildlife.
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