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1.
Zookeys ; 1083: 109-128, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35115874

RESUMO

A main priority in conservation is the protection of species in their natural habitat. However, ex situ management of threatened species is a recognised strategy of conservation. Harpy Eagles (Harpiaharpyja) are removed from the wild due to illegal capture, nest tree destruction, or other conflict sources. This study presents a review of the current ex situ Harpy Eagle populations in Brazil and worldwide, including information on the origin, sex, and year of entrance or year of birth under human care. Worldwide, until 2020 there were 205 Harpy Eagles in 77 different facilities in 16 countries, with 40 institutions in Brazil and 37 in other countries. The largest ex situ Harpy Eagle population is maintained in Brazil, with 139 individuals (75 females and 64 males) in 40 institutions. Of these institutions, there were 24 zoos, seven conservation breeding centres, six commercial breeders, two wildlife shelters, and one wildlife sorting centre. In Brazil, 62% (n = 86) of the individuals were hatched in the wild and 38% (n = 53) were bred in captivity under human care; for the wild individuals, only 73% (n = 64) have a known state of origin, with the majority from Pará state. This investigation provided relevant information to establish an ex situ demographic database. These individuals may potentially constitute a genetically and demographically viable safety population for future conservation strategies, as well as a source for research and education applied to Harpy Eagle integrated conservation.

2.
Theriogenology ; 181: 190-201, 2022 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-35121563

RESUMO

Currently, 52% of all raptor species demonstrate a decreasing population tendency, and the American harpy eagle (Harpia harpyja) has been categorized as "near threatened" by the IUCN. Habitat loss, persecution, and subsequent reduction of genetic diversity are regarded as major threats to the world's strongest eagle. Captive breeding and reintroduction into protected habitats are approaches of species conservation projects, but captive propagation is difficult due to low ex-situ numbers and scarce successful breeding pairs. The aim of the present study was to collect, analyze, and store semen from harpy eagles and to use aliquots for artificial insemination to increase the number of offspring and to include more individuals into the ex-situ gene pool. First, semen collection and semen availability were assessed in four males during the course of 1 year in European zoos. Second, these experiences were transferred to ex-situ breeding programs in Brazilian zoos to attempt semen collection in 13 male eagles. Semen collection was successful in 51.7% of the attempts and in 8/13 males (individual success rates 20-100%) using electro-stimulation. Most commonly, whey-like to milky, whitish semen samples were collected, regularly containing urate impurities (67.7%). The median semen volume was 106 µl and the median sperm concentration 5,000 sperm/µl (750-22,500 sperm/µl). Mean values for pH were 6.7, for sperm motility 27.7 ± 22.6%, for progressive motility 2.9 ± 5.6%, and for sperm viability 46.6 ± 16.3%. Using semen extenders, a sperm motility of 8% was maintained for 27 h in the refrigerator. Artificial insemination was performed in one female, but the success of fertilization could not be assessed due to egg destruction. In this study, methods for assisted reproduction were refined for use in harpy eagles, and the first semen samples were evaluated as a start to establish species-specific orientation values.


Assuntos
Águias , Animais , Feminino , Inseminação Artificial/veterinária , Masculino , Projetos Piloto , Sêmen , Análise do Sêmen/veterinária , Motilidade dos Espermatozoides , Espermatozoides
3.
Vet Microbiol ; 227: 143-147, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30473345

RESUMO

Bela Vista Biological Sanctuary (RBV) is a protected area of Itaipu Binacional, a hydroelectric power company located on the border of Brazil and Paraguay. A captive population of Brazilian dwarf brocket deer (Mazama nana, Cervidae, Artiodactyla) is maintained for conservation purposes. Despite the reproductive success of the animals, outbreaks of a fatal hemorrhagic disease have been registered over the years, compromising conservation efforts. In order to identify the etiological agents of these hemorrhagic diseases, 32 captive Brazilian dwarf brockets were sampled to investigate bluetongue virus (BTV), epizootic hemorrhagic disease (EHD), and adenovirus hemorrhagic disease (AHD), in 2015. Only one deer (1/32; 3.12%) was seropositive for BTV. After this survey, five animals died in the early autumn of 2015 and 2016, again presenting clinical signs of hemorrhagic disease. Using RT-qPCR, RT-PCR and DNA sequencing, five BTV serotypes (3, 14, 18, 19, and 22) were identified in blood and tissues collected during necropsies. These BTV serotypes had not been previously described or isolated in Brazil, either in wild or domestic ruminants. Additionally, differential diagnosis was performed for EHD and AHD, but all samples were negative for both diseases. The multiple distinct BTV serotypes identified in these outbreaks resulted in a high lethality (100%) of Brazilian dwarf brockets and indicated that various BTV serotypes are circulating in the area.


Assuntos
Vírus Bluetongue/imunologia , Vírus Bluetongue/patogenicidade , Bluetongue/epidemiologia , Cervos/virologia , Sorogrupo , Animais , Animais Domésticos/virologia , Bluetongue/sangue , Bluetongue/mortalidade , Bluetongue/virologia , Vírus Bluetongue/genética , Vírus Bluetongue/isolamento & purificação , Brasil/epidemiologia , Surtos de Doenças , Vírus da Doença Hemorrágica Epizoótica/genética , Vírus da Doença Hemorrágica Epizoótica/isolamento & purificação , RNA Viral/genética , Reação em Cadeia da Polimerase em Tempo Real
4.
BMC Res Notes ; 11(1): 536, 2018 Jul 31.
Artigo em Inglês | MEDLINE | ID: mdl-30064496

RESUMO

OBJECTIVE: Despite malaria epidemiology has been extensively studied in primates, few studies were conducted in ungulates. After half a century without descriptions of Plasmodium spp. in deer since its first identification, recent research has rediscovered Plasmodium on ungulates in Africa, Asia, North America and South America, including Central Brazil. Here, a captive herd was evaluated in southern Brazil using light microscopy and PCR. DNA samples were tested for fragment amplification of two Plasmodium spp. genes: mitochondrial cytochrome b and small subunit ribosomal RNA. RESULTS: All analyses were negative. However, the tests were performed on samples that were collected at a single time point, and parasitemia may fluctuate over the parasite's life cycle. Thus, the possibility of occult infection cannot be ruled out. Despite the negative results of all of the methods applied, it cannot be categorically stated that these animals are free from Plasmodium sp. infection. Further monitoring and/or multiple sequential sampling may improve the success rate of detecting parasites. Moreover, although this survey of Plasmodium represents the first molecular study on ungulate malaria parasites from Southern Brazil, further analysis of samples from different ungulate species is important for characterizing the epidemiology of Plasmodium of these mammals in this region.


Assuntos
Cervos/parasitologia , Plasmodium/isolamento & purificação , Animais , Brasil , DNA de Protozoário , Malária
5.
Rev Bras Parasitol Vet ; 24(4): 482-7, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26689185

RESUMO

A large number of Brazilian zoos keep many endangered species of deer, however, very few disease surveillance studies have been conducted among captive cervids. Blood samples from 32 Brazilian deer (Blastocerus dichotomus, Mazama nana and Mazama americana) kept in captivity at Bela Vista Biological Sanctuary (Foz do Iguaçu, Brazil) were investigated for 10 ruminant pathogens, with the aims of monitoring deer health status and evaluating any potential zoonotic risk. Deer serum samples were tested for Brucella abortus, Leptospira (23 serovars), Toxoplasma gondii, Neospora caninum, bovine viral diarrhea virus, infectious bovine rhinotracheitis virus, foot-and-mouth disease virus, western equine encephalitis virus, eastern equine encephalitis virus and Venezuelan equine encephalitis virus. Antibodies against T. gondii (15.6%), N. caninum (6.2%) and L. interrogans serogroup Serjoe (3.1%) were detected. The serological results for all other infectious agents were negative. The deer were considered to be clinically healthy and asymptomatic regarding any disease. Compared with studies on free-ranging deer, the prevalences of the same agents tested among the captive deer kept at the Sanctuary were lower, thus indicating good sanitary conditions and high-quality management practices at the zoo.


Assuntos
Animais de Zoológico/imunologia , Anticorpos Antiprotozoários/sangue , Cervos/imunologia , Leptospira interrogans/imunologia , Neospora/imunologia , Toxoplasma/imunologia , Animais , Brasil/epidemiologia , Brucella abortus/imunologia , Coccidiose/epidemiologia , Vírus da Diarreia Viral Bovina/imunologia , Vírus da Encefalite/imunologia , Vírus da Febre Aftosa/imunologia , Herpesvirus Bovino 1/imunologia , Estudos Soroepidemiológicos , Toxoplasmose Animal/epidemiologia
6.
Vet Microbiol ; 152(3-4): 415-9, 2011 Sep 28.
Artigo em Inglês | MEDLINE | ID: mdl-21640523

RESUMO

Hemotrophic mycoplasmas (hemoplasmas) are bacteria that attach to red blood cells of mammals, leading to acute and/or subclinical disease in infected animals. It has been suggested that Mycoplasma ovis, a hemoplasma that infects sheep and goats worldwide, may also infect deer. The aim of this study was to evaluate whether South American deer are infected with M. ovis. EDTA-anticoagulated blood samples from a herd of 32 captive South American deer were collected. DNA extraction of blood samples was performed followed by PCR amplification of the 16S and 23S rRNA genes, and sequencing of products. Using M. ovis PCR, 27/31 (87%) were positive, including 21/22 Mazama nana; 2/3 Mazama americana and 4/6 Blastocerus dichotomus. Sequencing of the nearly entire 16S rRNA gene of 26/27 positive samples showed 98.2-98.8% identity to M. ovis of sheep (GenBank, AF338268) and 98.6-99.4% identity to M. ovis-like of a fawn (FJ824847); the 23S rRNA gene from one of these isolates and the fawn's had 97.6% identity. The remaining isolate had just 94.9% identity to the 16S rRNA gene of M. ovis and only 89.4% identity to the 23S rRNA gene of the fawn's M. ovis. This is the first report of M. ovis in captive South American deer, revealing a high prevalence of hemoplasma infection in these animals.


Assuntos
Infecções por Mycoplasma/veterinária , Mycoplasma/isolamento & purificação , Animais , Brasil/epidemiologia , Cervos , Mycoplasma/classificação , Mycoplasma/genética , Infecções por Mycoplasma/epidemiologia , Infecções por Mycoplasma/genética , Infecções por Mycoplasma/microbiologia , Filogenia , Reação em Cadeia da Polimerase , Prevalência , Ribotipagem
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