Fatal systemic morbillivirus infection in bottlenose dolphin, Canary Islands, Spain.
We report a unique morbillivirus that caused documented systemic infection in a bottlenose dolphin from the eastern North Atlantic Ocean. Although this case occurred nearly 9 years ago, the nucleotide sequence of a fragment of the morbillivirus phosphoprotein (P) gene shows high homology with sequences recently reported for morbilliviruses from striped dolphins (Stenella coeruleoalba) in the Mediterranean Sea. This information is of value because no other sequences of morbillivirus from bottlenose dolphins are available in GenBank, despite the seriousness of this fatal disease, which causes mass deaths of marine mammals worldwide.
On July 18, 2005, a juvenile female bottlenose dolphin was stranded alive in Arrieta, Lanzarote (Canary Islands, Spain). The animal was 250 cm long and in moderate body condition, according to anatomic parameters. The animal died shortly after stranding, and a complete standardized necropsy was performed within 6 hours after death. Required permission for the management of stranded cetaceans in the Canarian archipelago is issued by the environmental department of the Canary Islands' government.
Tissues of all the major organs and lesions were collected and stored in neutral buffered 10% formalin fixative solution for histologic and immunohistochemical analyses. Fixed tissue samples were trimmed and then routinely processed, embedded in paraffin, sectioned at 5 [micro]m, and stained with hematoxylin and eosin for examination by light microscopy. A monoclonal antibody against the nucleoprotein of CDV (MoAb CDV-NP, VMRD, Inc., Pullman, WA, USA) known to react with DMV was used as primary antiserum. Immunohistochemical analysis was performed on selected samples of brain, intestinal, lymphatic, pancreatic, pulmonary, renal, and splenic tissues, as described (4). Samples of lung, spleen, and brain were collected and held frozen at -80[degrees]C until processed for molecular virology.
On gross examination, the most remarkable findings were moderate to severe multiorgan parasitic infection, mainly cirripedes (Xenobalanus sp.) in the caudal fin; larval cestodes (Phyllobothrium sp. and Monorygma grimaldi) within the subcutaneous and peritoneum tissues; nematodes (Anisakis spp.), trematodes (Pholeter sp.), and taeniform cestodes in the stomachs and intestine, and trematodes (Nasitrema sp.) and nematodes (Crassicauda sp.) within both pterygoid sinuses; bilateral serous-suppurative and proliferative arthritis at the scapula-humeral junction; and generalized lymphadenomegalia. Within the brain; the leptomeninges were enlarged and fibrotic at the cortex area.
Histologically, the lesions were consistent with findings from the gross examination. Other histopathologic findings were multifocal nonsuppurative hepatitis, adrenalitis, and bronchointerstitial pneumonia. In lung, a multifocal suppurative bronchitis associated with larval and adult nematode parasites (morphologically identified as Halocercus spp. and Stenurus spp.) were observed. Alveolar septa were expanded by macrophages and lymphocytes admixed with scattered karyorrhectic debris. Alveoli were often lined by hyperplastic type II pneumocytes and filled with large numbers of multinucleated syncytial cells.
The immunohistochemical study demonstrated morbilliviral antigen in bronchiolar epithelium, type 2 pneumocytes, and multinucleate (syncytial) cells from lung (Figure 1).
The syncytia also were found within the lymph nodes, pancreas, spleen, kidney, and intestine, and they were characterized by a moderate amount of eosinophilic cytoplasm and 2 to > 20 nuclei, often containing weak stained eosinophilic inclusion bodies. Lymphocytolysis was remarkable within the spleen and multiple lymph nodes and were characterized by loss of cellular detail and accumulation of karyorrhectic and eosinophilic cellular debris. Syncytia from lymph nodes, spleen, pancreas, and kidney also were immunostained against CDV antibody. Severe nonsuppurative meningitis (with > 20 layers of lymphohistiocytic cells), perineuritis, and encephalomyelitis were found within the nervous system. Multiple microhemorrhages were a common associated lesion. The brain showed severe inflammatory changes, but only a few neurons were immunopositive, and they were limited to some lymphohistiocytic cells surrounding vessels, glial, and endothelial cells. The epithelial tropism of the virus was demonstrated immunohistochemically within the lung, intestine, kidney, and pancreatic duct epithelium.
Molecular detection of cetacean morbillivirus was performed by a 1-step reverse transcription PCR of a 426-bp conserved region of the P gene, as described (10). All the samples tested from this dolphin were reverse transcription PCR positive for morbillivirus. Sequences were the same in all positive samples from the animal. We conducted a BLAST (www.ncbi.nlm.nih.gov/blast/ Blast.cgi) search to compare sequenced products with sequences described in GenBank for morbillivirus. The common sequence of 411-nt fragment of the P gene showed a 99% homology with those sequences obtained in 2007 and 2011 from striped dolphins stranded along the coastline of the Mediterranean Sea.
We used MEGA 5.0 software (www.megasoftware. net) to construct maximum-likelihood phylogenetic trees. A bootstrap resampling (1,000 replicates) was used to assess the reliability of the trees (Figure 2).
We describe a systemic morbillivirus infection in a bottlenose dolphin in the Canary Islands. A previous morbillivirus infection had been described in a bottlenose dolphin found dead along the Atlantic coast of Mauritania in 1998; the virus was exclusively detected by hybridization in the stomach tissue sample (11).
Other cases that illustrate the systemic and neurologic features of the disease have been described in bottlenose dolphins in the Mediterranean Sea (12-14), and the first reported case of a fatal morbillivirus infection in cetaceans within the Southern Hemisphere (southwestern Pacific Ocean) has been described (15). No sequences from these studies were provided to GenBank, although the phylogenetic analyses showed high homology with other DMV. The P gene fragment of the virus obtained from the current study is molecularly almost identical to that reported in striped dolphins in the Mediterranean Sea during the last 5 years. This fact supports the hypothesis that transmission occurs between species, as it was reported in the 2006-2007 Mediterranean epizootic between pilot whales (Globicephala melas and G. macrorhynchus) and striped dolphins (3), and demonstrates that dolphin populations of the Mediterranean Sea and the Atlantic Ocean are in contact through the Gibraltar Straits. This particular point is critical to better understand the epidemiology and transmission of morbilliviruses between cetaceans and could be essential to clarifying the infection source of the die-off of bottlenose dolphins alson the East Coast of the United States (9).
We thank the other members of the Canary Islands Cetacean Stranding Network, SECAC (Society for the Study of the Cetaceans in the Canarian Archipelago), and Canarias Conservacion.
This study was possible thanks to the partial funding by National Project CGL2012-39681 (Subprograma BOS); Regional
Project SolSub C200801000288, and ProID 20100091; and Technical Assistant Contract by Canary Islands Government delegation (TEC0002955).
Dr Sierra is a researcher at the Institute for Animal Health at the University of Las Palmas de Gran Canaria. Her areas of expertise include veterinary pathology (including whale and dolphin pathology) and pathogenesis of animal infectious diseases, and her research interests include muscular pathologies on whales and dolphins.
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Address for correspondence: Eva Sierra, Institute for Animal Health, Veterinary School, University of Las Palmas de Gran Canaria, Canary Islands, Spain; email: firstname.lastname@example.org
Author affiliation: University of Las Palmas de Gran Canaria, Arucas, Canary Islands, Spain
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|Author:||Sierra, Eva; Zucca, Daniele; Arbelo, Manuel; Garcia-Alvarez, Natalia; Andrada, Marisa; Deniz, Soraya|
|Publication:||Emerging Infectious Diseases|
|Article Type:||Author abstract|
|Date:||Feb 1, 2014|
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