RESUMEN
Espírito Santo state is located on the eastern margin of Brazil, in a transitional tropical-subtropical area (18°S-21°S) dominated by oligotrophic waters. With the exception of humpback whales (Megaptera novaeangliae), the cetacean community of Espírito Santo has been understudied. In addition to the chronic impacts from fisheries, marine pollution, urban development, and coastal habitat degradation, in November 2015 the cetacean communities of Espírito Santo were challenged by the greatest environmental disaster in Brazil's history. The Mariana dam disaster caused 60 million cubic meters of mining waste to be washed into the Doce River, which ultimately flowed to the coastal waters of Espírito Santo, with a high concentration of heavy metals. This study reviews and updates information on cetacean strandings in the state of Espírito Santo (excluding humpback whales) prior to this disaster. From 1975 to September 2015, there were 461 recorded cetacean strandings, representing 20 species. An average 1.18 strandings per 100 km per month were recorded since a state-wide daily beach survey program was implemented in October 2010, contrasting with the 0.14 strandings per 100 km per month in previous years. Six species comprised the majority (94.7%) of stranding events: Guiana dolphin (Sotalia guianensis), Franciscana (Pontoporia blainvillei), rough-toothed dolphin (Steno bredanensis), bottlenose dolphin (Tursiops truncatus), sperm whale (Physeter macrocephalus), and melon-headed whale (Peponocephala electra). Oceanic cetaceans stranded most frequently on the southern portion of Espírito Santo, where the continental platform is narrower, whereas the strandings of coastal cetaceans such as Guiana dolphins and Franciscanas were concentrated near estuaries, especially the Doce River. This is particularly concerning in face of the Mariana dam disaster, which drastically altered the estuarine and coastal environment associated with the Doce River.
RESUMEN
Avian malaria is a mosquito-borne disease caused by Plasmodium spp. protozoa, and penguins are considered particularly susceptible to this disease, developing rapid outbreaks with potentially high mortality. We report on an outbreak of avian malaria in Magellanic penguins (Spheniscus magellanicus) at a rehabilitation center in Espírito Santo, southeast Brazil. In August and September 2015, a total of 89 Magellanic penguins (87 juveniles and 2 adults) received care at Institute of Research and Rehabilitation of Marine Animals. Over a period of 2 weeks, Plasmodium infections were identified in eight individuals (9.0%), four of which died (mortality = 4.5%, lethality = 50%). Blood smears and sequencing of the mitochondrial cytochrome b gene revealed the presence of Plasmodium lutzi SPMAG06, Plasmodium elongatum GRW06, Plasmodium sp. PHPAT01, Plasmodium sp. SPMAG10, and Plasmodium cathemerium (sequencing not successful). Two unusual morphological features were observed in individuals infected with lineage SPMAG06: (a) lack of clumping of pigment granules and (b) presence of circulating exoerythrocytic meronts. Hematological results (packed cell volume, plasma total solids, complete blood cell counts) of positive individuals showed differences from those of negative individuals depending on the lineages, but there was no overarching pattern consistently observed for all Plasmodium spp. The epidemiology of the outbreak and the phylogeography of the parasite lineages detected in this study support the notion that malarial infections in penguins undergoing rehabilitation in Brazil are the result of the spillover inoculation by plasmodia that circulate in the local avifauna, especially Passeriformes.
Asunto(s)
Enfermedades de las Aves/parasitología , Malaria Aviar/parasitología , Plasmodium/crecimiento & desarrollo , Spheniscidae/parasitología , Animales , Enfermedades de las Aves/sangre , Enfermedades de las Aves/epidemiología , Brasil/epidemiología , Brotes de Enfermedades , Femenino , Hematología , Malaria Aviar/sangre , Malaria Aviar/epidemiología , Masculino , Filogenia , Plasmodium/clasificación , Plasmodium/genética , Plasmodium/aislamiento & purificaciónRESUMEN
Este trabalho apresenta valores hematológicos e bioquímicos de pinguins-de-Magalhães (Spheniscus magellanicus) juvenis que arribaram no Espírito Santo e Rio de Janeiro, litoral sudeste do Brasil, e foram encaminhados a reabilitação. Os valores médios obtidos foram: eritrócitos 2.55±0.54 milhões/µL; hemoglobina 13,37±3,91g/dL; hematócrito 41,5±0,04%; proteína plasmática 6,34±0,81g/dL; leucócitos 16.301±6.402/µL; trombócitos 20.516±4.591 células/µL; volume corpuscular médio (VCM) 172,0±53,0 fL; concentração de hemoglobina corpuscular média (CHCM) 26,41±0,02%; alanina transaminase (ALT) 50,0±17,89 U/L; ácido úrico 8,93±3,0mg/dL; albumina 1,68±0,53g/dL; cálcio 9,7±0,57mg/dL; fósforo 10,39±8,5mg/dL e glicose 211,6±30,3mg/dL. Valores de eritrócitos, VCM e CHCM foram discrepantes em relação aos valores de referência atuais. Valores de leucócitos e trombócitos tem significado inconclusivo. Hematócrito, hemoglobina, proteína plasmática e valores bioquímicos forneceram importante contribuição para o estabelecimento de parâmetros de referência.(AU)
This paper reports hematological and biochemical values of juveniles Magellanic penguins (Spheniscus magellanicus) stranded in Espírito Santo and Rio de Janeiro, Southeastern Brazil, that were sent for rehabilitation. The average values were: erythrocytes 2.55±0,54 milhões/µL, hemoglobin 13.37±3,91g/dL, hematocrit 41.5±0.04%, plasma protein 6.34±0.81g/dL, leukocytes 16,301±6,402/µL, thrombocytes 20,516±4,591 células/µL3, mean cell volume (MCV) 172.0±53.0 fL, mean cell hemoglobin concentration (MCHC) 26.41±0.02%, alanine transaminase (ALT) 50.0±17.89 U/L, uric acid 8.93±3.0mg/dL, albumin 1.68±0.53mg/dL, calcium 9.7±0.57mg/dL, phosphorus 10.39±8.5mg/dL and glucose 211.6±30.3mg/dL. Values of erythrocytes, MCV and MCH were discrepant in relation to the current reference values. Leukocytes and thrombocytes values has meant inconclusive. Hematocrit, hemoglobin, plasma protein and biochemical values provided important contribution for the establishment of reference parameters.(AU)
Asunto(s)
Animales , Fenómenos Bioquímicos , Análisis Químico de la Sangre/veterinaria , Rehabilitación , Spheniscidae/sangre , Pruebas Hematológicas/veterinariaRESUMEN
A novel avipoxvirus caused diphtheritic lesions in the oesophagus of five and in the bronchioli of four Magellanic penguins (Spheniscus magellanicus) and also cutaneous lesions in eight Magellanic penguins housed in outdoor enclosures in a Rehabilitation Centre at Florianópolis, Santa Catarina State, Brazil. At the same time, another avipoxvirus strain caused cutaneous lesions in three Magellanic penguins at a geographically distinct Rehabilitation Centre localized at Vila Velha, Espírito Santo State, Brazil. Diagnosis was based on clinical signs, histopathology and use of the polymerase chain reaction (PCR). Clinical signs in the penguins included cutaneous papules and nodules around eyelids and beaks, depression and restriction in weight gain. The most common gross lesions were severely congested and haemorrhagic lungs, splenomegaly and cardiomegaly. Histological examination revealed Bollinger inclusion bodies in cutaneous lesions, mild to severe bronchopneumonia, moderate periportal lymphocytic hepatitis, splenic lymphopenia and lymphocytolysis. Other frequent findings included necrotizing splenitis, enteritis, oesophagitis, dermatitis and airsacculitis. Cytoplasmic inclusion bodies were seen within oesophageal epithelial cells in five birds and in epithelial cells of the bronchioli in four penguins. DNA from all samples was amplified from skin tissue by PCR using P4b-targeting primers already described in the literature for avipoxvirus. The sequences showed two different virus strains belonging to the genus Avipoxvirus of the Chordopoxvirinae subfamily, one being divergent from the penguinpox and avipoxviruses already described in Magellanic penguins in Patagonia, but segregating within a clade of canarypox-like viruses implicated in diphtheritic and respiratory disease.