A Clinical Guide to the Necropsy of the Elasmobranch Cranium
IAAAM 2024
Ri K. Chang1*; Mark S. Okihiro2
1Monterey Bay Aquarium, Monterey, CA, USA; 2California Department of Fish and Wildlife, Vista, CA, USA

Abstract

Elasmobranchs are common, iconic species in aquaria, and their wild counterparts are often key members of their ecosystem.1 Both wild and managed elasmobranchs are particularly prone to infectious meningoencephalitis.2-6 Common pathogens in stranded elasmobranchs include Carnobacterium maltaromaticum and Miamiensis avidus, though other infectious agents have been reported in elasmobranchs under managed care.2-8 Potential routes of entry include the endolymphatic ducts, olfactory system, ampullary system, and hematogenous spread, but published literature commonly does not definitively identify a specific route of entry.2,5,6,8,9

Postmortem examination is a critical tool for disease monitoring of wild, stranded elasmobranchs and management of those under human care. Careful necropsy of the head with a focus on clinically relevant anatomy can ensure proper samples are collected, may increase the chance of presumptive diagnoses prior to histologic analysis, which can allow for faster management decisions, and can often identify the route of pathogenesis, which is a current shortcoming in the published literature.2,5,8-10

This protocol emphasizes careful dissection of the endolymphatic pores/ducts, inner ear, and olfactory system and provides methods for gross necropsy, sample collection for microbiology, cytology, and histopathology, and evaluation of wet-mount and stained cytology. The proposed protocol for the elasmobranch head necropsy and ancillary diagnostic sample collection and evaluation was developed through work with stranded, wild elasmobranchs and has been implemented in the necropsy of over 150 elasmobranchs across 16 species from 2011–2023, including both wild, stranded elasmobranchs and those under human care.

Acknowledgments

We gratefully acknowledge all the organizations and individuals who have helped with stranded elasmobranch response, including notification, collection, and providing necropsy space, particularly the University of California, Davis School of Veterinary Medicine, California Department of Fish and Wildlife, and Monterey Bay Aquarium.

*Presenting author

Literature Cited

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2.  Jalenques M, Lair S, Schmidt-Posthaus H, Jufer M, Lamglait B. Scuticociliate (Philasterides dicentrarchi) infection cluster in a multispecies marine aquarium system. Dis Aquat Org. 2021;144:107–115.

3.  Steele LM, Okihiro MS, Berlemont R, Dillon JG, Young KA, Hesami S, Sommeran SV, Lowe CG. Carnobacterium maltaromaticum associated with meningoencephalitis and otitis in stranded common thresher sharks (Alopias vulpinus). Vet Pathol. 2022;59(5):850–859.

4.  Retallack H, Okihiro MS, Britton E, Sommeran SV, DeRisi JL. Metagenomic next-generation sequencing reveals Miamiensis avidus (Ciliophora: Scuticociliatida) in the 2017 epizootic of leopard sharks (Triakis semifasciata) in San Francisco Bay, California, USA. J Wildl Dis. 2019;55(2):375–386.

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8.  Stidworthy MF, Garner MM, Bradway DS, Westfall BD, Joseph B, Repetto S, Guglielmi E, Schmidt-Posthaus H, Thornton SM. Systemic scuticociliatosis (Philasterides dicentrarchi) in sharks. Vet Pathol. 2014;51(3):628–632.

9.  Schaffer PA, Lifland B, Van Sommeran S, Casper DR, Davis CR. Meningoencephalitis associated with Carnobacterium maltaromaticum-like bacteria in stranded juvenile salmon sharks (Lamna ditropis). Vet Pathol. 2013;50(3):412–417.

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Speaker Information
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Ri K. Chang
Monterey Bay Aquarium
Monterey, CA, USA


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