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Emerging morbillivirus infections of marine mammals: development of two diagnostic approaches
Jeremiah T Saliki1, Emily J Cooper, Jonathan P Gustavson
1Oklahoma Animal Disease Diagnostic Laboratory, College of Veterinary Medicine, Oklahoma State University, Stillwater, Oklahoma 74078, USA. jsaliki@okstate.edu
Abstract:
In the last 13 years, four viruses belonging in the Morbillivirus genus of the Paramyxoviridae family have emerged as significant causes of disease and mortality in marine mammals. The viruses involved are canine distemper virus (CDV) in seals and polar bears, dolphin morbillivirus (DMV) and porpoise morbillivirus (PMV) in cetaceans, and phocine distemper virus (PDV) in pinnipeds. The two cetacean morbilliviruses (DMV and PMV) are now considered to be the same viral species, named cetacean morbillivirus (CMV). All three morbillivirus species (CDV, CMV, and PDV) are genetically and antigenically related and cross-react in various serological tests. The diagnosis of morbilliviral infections in marine mammal specimens poses two challenges. First, various marine mammal species can be infected by more than one closely related but distinct morbilliviruses, making definitive virus identification unattainable by classical virology methods. Second, standard immunological reagents such as anti-species conjugates are unavailable for most marine mammal species, rendering definitive serological diagnosis difficult by classical serological techniques. The objectives of this study were to develop two diagnostic approaches that alleviate these difficulties, providing simple, rapid, and cost-effective diagnostic methods. For nucleic acid detection, reverse transcription-polymerase chain reaction (RT-PCR) and restriction endonuclease digestions were used to differentiate the three viruses. For antibody detection, a monoclonal antibody-based competitive enzyme-linked immunosorbent assay (c-ELISA) was used on sera from several species, thus avoiding the need for multiple anti-species enzyme conjugates.
Insights
New diagnostic methods were developed to accurately identify morbilliviruses in marine mammals. These approaches overcome challenges in distinguishing related viruses and the lack of species-specific reagents for reliable diagnosis.
Area of Science:
- Veterinary Virology
- Marine Mammal Health
- Wildlife Disease Diagnostics
Background:
- Morbilliviruses (canine distemper virus, cetacean morbillivirus, phocine distemper virus) have caused significant marine mammal mortality.
- Distinguishing between these genetically related viruses is challenging using classical methods.
- Lack of species-specific reagents hinders accurate serological diagnosis in diverse marine mammal populations.
Purpose of the Study:
- To develop novel diagnostic tools for morbilliviral infections in marine mammals.
- To enable rapid, cost-effective differentiation of closely related morbilliviruses.
- To overcome limitations of classical diagnostic techniques in marine mammal virology.
Main Methods:
- Nucleic acid detection utilized reverse transcription-polymerase chain reaction (RT-PCR) combined with restriction endonuclease digestion.
- Antibody detection employed a monoclonal antibody-based competitive enzyme-linked immunosorbent assay (c-ELISA).
- These methods were designed to avoid the need for specific anti-species conjugates.
Main Results:
- RT-PCR and restriction digestion successfully differentiated the three main morbillivirus species (CDV, CMV, PDV).
- The c-ELISA provided a reliable method for detecting antibodies across multiple marine mammal species.
- The developed assays offer improved accuracy and efficiency for morbillivirus diagnostics.
Conclusions:
- The developed RT-PCR and c-ELISA assays provide effective solutions for diagnosing morbilliviral infections in marine mammals.
- These methods address key challenges, enabling better identification and surveillance of morbillivirus outbreaks.
- The study contributes significantly to the understanding and management of marine mammal diseases.
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