Hematological parameters and total plasma protein values of captive strigiformes occurring in Brazil / Parâmetros hematológicos e valores de proteínas plasmáticas totais de Strigiformes cativos de ocorrência no Brasil

Brazil has the highest number of birds of prey in the world, which are important environmental quality indicators. Nevertheless, few studies of the clinical pathology of raptors have been developed in this country. The objectives of this study were to create a database of owl hematology in Brazil and to compare the values between sex in Asio clamator, Megascops spp. and Tyto furcata. Blood samples were collected from 81 captive owls of 10 species located in Rio Grande do Sul, Santa Catarina, Paraná and São Paulo states, Brazil. Hemogram and Total Plasma Protein (TPP) values were determined. Reference intervals (RIs) and descriptive statistic values were established using an Excel program with Reference Value Advisor. The reference intervals were the following: A. clamator: RBC (×106/μL) 1.0-2.5; PCV (%) 30.2-50.1; Hb (g dL-¹) 6.7-15.3; MCV (fL) 123.8-355.2; MCHC (%) 17.1-38.6; WBC (× 10³/μL) 1.2-23.6; Heterophils (× 10³/μL) 0.6-16.6; Lymphocytes (× 10³/μL) 0.6-10.2; Eosinophils (× 10³/μL) 0.0-1.9; Basophils (× 10³/μL) 0.0-1.0; Thrombocytes (× 10³/μL) 10.8-56.6; H/L 0.0-10.8. Megascops spp.: RBC (× 106/μL) 0.8-2.3; PCV (%) 29.7-44.6; Hb (g dL-¹) 6.4-12.4; MCV (fL) 131.6-374.4; MCHC (%) 12.1-34; WBC (× 10³/μL) 0.7-23.1; Heterophils (× 10³/μL) 1.1-10.3; Lymphocytes (× 10³/μL) 0.0-11.5; Eosinophils (× 10³/μL) 0.0-2.2; Basophils (× 10³/μL) 0.0-0.7; Thrombocytes (× 10³/μL) 10.3-43.6; H/L 0.5-7.3; TPP (g dL-¹) 2.9-5.1. The parameters for Tyto furcata were presented with descriptive statistics values. Individual data were provided for the others Strigiformes species sampled. This study provides a wide database of hematological and TPP references for Megascops spp., A. clamator and T. furcata and hematological values for Athene cunicularia, Bubo virginianus, Pulsatrix perspicillata, Asio stygius, Pulsatrix koeniswaldiana, Strix virgata and Asio flammeus in Brazil.

O Brasil tem o maior número de aves de rapina do mundo, e estas aves são, como topo de cadeia alimentar, importantes indicadores de qualidade ambiental. No entanto, poucos estudos sobre a patologia clínica de rapinantes foram desenvolvidos no Brasil. Os objetivos deste estudo foram criar uma base de dados para hematologia de corujas no país e comparar os valores entre sexos em Asio clamator, Megascops spp. e Tyto furcata. Amostras de sangue foram coletadas de 81 corujas em cativeiro, de 10 espécies diferentes, localizadas nos estados do Rio Grande do Sul, Santa Catarina, Paraná e São Paulo, Brasil. Foi determinado o hemograma e as proteínas plasmáticas totais (PPT). Os intervalos de referência (IR) e os valores de estatística descritiva foram estabelecidos através da utilização do Excel com o suplemento do Reference Value Advisor. Os IR foram os seguintes: A. clamator: Eritócitos (x106 76 /μL) 1.0-2.5;Ht (%) 30.2-50.1; Hb (g/dL) 6.7-15.3; VCM (fL) 123.8-355.2; CHCM (%) 17.1-38.6; Leucócitos (x10³/μL) 1.2-23.6; Heterófilos (x10³/μL) 0.6-16.6; Linfócitos (x10³/μL) 0.6-10.2; Eosinófilos (x10³/μL) 0.0-1.9; Basófilos (x10³/μL) 0.0-1.0; Trombócitos (x10³/μL) 0.0-81.65; H:L 0.0-10.8. Megascops spp.: Eritócitos (x106/μL) 0.8-2.3; Ht (%) 29.7-44.6; Hb (g/dL) 6.4-12.4; VCM (fL) 131.6-374.4; CHCM (%)12.1-34; Leucócitos (x10³/μL) 0.7-23.1; Heterófilos (x10³/μL) 1.1-10.3; Linfócitos (x10³/μL) 0.0-11.5; Eosinófilos (x10³/μL) 0.0-2.2; Basófilos (x10³/μL) 0.0-0.7; Trombócitos (x10³/μL) 10.3-43.6; H:L 0.5-7.3; PPT (g/dL) 2.9-5.1. Os parâmetros para Tyto furcata foram apresentados com valores de estatística descritiva. Para as outras espécies de Strigiformes amostradas, os valores individuais foram incluidos. Este estudo forneceu uma ampla base de dados de valores hematológicos e de proteínas plasmáticas totais para Megascops spp., A. clamator [...].

Hematological parameters and total plasma protein values of captive strigiformes occurring in Brazil / Parâmetros hematológicos e valores de proteínas plasmáticas totais de Strigiformes cativos de ocorrência no Brasil

Brazil has the highest number of birds of prey in the world, which are important environmental quality indicators. Nevertheless, few studies of the clinical pathology of raptors have been developed in this country. The objectives of this study were to create a database of owl hematology in Brazil and to compare the values between sex in Asio clamator, Megascops spp. and Tyto furcata. Blood samples were collected from 81 captive owls of 10 species located in Rio Grande do Sul, Santa Catarina, Paraná and São Paulo states, Brazil. Hemogram and Total Plasma Protein (TPP) values were determined. Reference intervals (RIs) and descriptive statistic values were established using an Excel program with Reference Value Advisor. The reference intervals were the following: A. clamator: RBC (×106/μL) 1.0-2.5; PCV (%) 30.2-50.1; Hb (g dL-¹) 6.7-15.3; MCV (fL) 123.8-355.2; MCHC (%) 17.1-38.6; WBC (× 10³/μL) 1.2-23.6; Heterophils (× 10³/μL) 0.6-16.6; Lymphocytes (× 10³/μL) 0.6-10.2; Eosinophils (× 10³/μL) 0.0-1.9; Basophils (× 10³/μL) 0.0-1.0; Thrombocytes (× 10³/μL) 10.8-56.6; H/L 0.0-10.8. Megascops spp.: RBC (× 106/μL) 0.8-2.3; PCV (%) 29.7-44.6; Hb (g dL-¹) 6.4-12.4; MCV (fL) 131.6-374.4; MCHC (%) 12.1-34; WBC (× 10³/μL) 0.7-23.1; Heterophils (× 10³/μL) 1.1-10.3; Lymphocytes (× 10³/μL) 0.0-11.5; Eosinophils (× 10³/μL) 0.0-2.2; Basophils (× 10³/μL) 0.0-0.7; Thrombocytes (× 10³/μL) 10.3-43.6; H/L 0.5-7.3; TPP (g dL-¹) 2.9-5.1. The parameters for Tyto furcata were presented with descriptive statistics values. Individual data were provided for the others Strigiformes species sampled. This study provides a wide database of hematological and TPP references for Megascops spp., A. clamator and T. furcata and hematological values for Athene cunicularia, Bubo virginianus, Pulsatrix perspicillata, Asio stygius, Pulsatrix koeniswaldiana, Strix virgata and Asio flammeus in Brazil.(AU)

O Brasil tem o maior número de aves de rapina do mundo, e estas aves são, como topo de cadeia alimentar, importantes indicadores de qualidade ambiental. No entanto, poucos estudos sobre a patologia clínica de rapinantes foram desenvolvidos no Brasil. Os objetivos deste estudo foram criar uma base de dados para hematologia de corujas no país e comparar os valores entre sexos em Asio clamator, Megascops spp. e Tyto furcata. Amostras de sangue foram coletadas de 81 corujas em cativeiro, de 10 espécies diferentes, localizadas nos estados do Rio Grande do Sul, Santa Catarina, Paraná e São Paulo, Brasil. Foi determinado o hemograma e as proteínas plasmáticas totais (PPT). Os intervalos de referência (IR) e os valores de estatística descritiva foram estabelecidos através da utilização do Excel com o suplemento do Reference Value Advisor. Os IR foram os seguintes: A. clamator: Eritócitos (x106 76 /μL) 1.0-2.5;Ht (%) 30.2-50.1; Hb (g/dL) 6.7-15.3; VCM (fL) 123.8-355.2; CHCM (%) 17.1-38.6; Leucócitos (x10³/μL) 1.2-23.6; Heterófilos (x10³/μL) 0.6-16.6; Linfócitos (x10³/μL) 0.6-10.2; Eosinófilos (x10³/μL) 0.0-1.9; Basófilos (x10³/μL) 0.0-1.0; Trombócitos (x10³/μL) 0.0-81.65; H:L 0.0-10.8. Megascops spp.: Eritócitos (x106/μL) 0.8-2.3; Ht (%) 29.7-44.6; Hb (g/dL) 6.4-12.4; VCM (fL) 131.6-374.4; CHCM (%)12.1-34; Leucócitos (x10³/μL) 0.7-23.1; Heterófilos (x10³/μL) 1.1-10.3; Linfócitos (x10³/μL) 0.0-11.5; Eosinófilos (x10³/μL) 0.0-2.2; Basófilos (x10³/μL) 0.0-0.7; Trombócitos (x10³/μL) 10.3-43.6; H:L 0.5-7.3; PPT (g/dL) 2.9-5.1. Os parâmetros para Tyto furcata foram apresentados com valores de estatística descritiva. Para as outras espécies de Strigiformes amostradas, os valores individuais foram incluidos. Este estudo forneceu uma ampla base de dados de valores hematológicos e de proteínas plasmáticas totais para Megascops spp., A. clamator [...].(AU)

Survey of Toxoplasma gondii, Neospora caninum and Sarcocystis neurona antibodies in wild red-tailed Amazon parrots (Amazona brasiliensis) / Pesquisa de anticorpos anti-Toxoplasma gondii, anti-Neospora caninum e anti-Sarcocystis neurona em papagaios-de-cara-roxa (Amazona brasiliensis) de vida livre

Toxoplasma gondii, Neospora caninum and Sarcocystis neurona are obligate intracellular parasites within the phylum Apicomplexa. The red-tailed Amazon parrot (Amazona brasiliensis) is a near-threatened species of psittacine that is endemic to the Atlantic Forest of Brazil and has been designated as a bioindicator because of its sensitivity to environmental qualitative status and changes. The aim of this study was to evaluate the presence of antibodies against T. gondii, N. caninum and S. neurona in wild red-tailed Amazon parrot nestlings on Rasa Island, Brazil. Blood samples were collected from 51 parrots and plasma samples were stored at 20 °C until immunofluorescence antibody tests (IFAT) were performed. Antigen slides were prepared using tachyzoites of T. gondii (RH strain) and, N. caninum (NC-1 strain) and using merozoites of S. neurona (SNR37 strain). Plasma samples were tested at initial dilutions of 1:16 for T. gondii, 1:50 for N. caninum and 1:5 for S. neurona. An anti-chicken antibody conjugated with FITC was used as a secondary antibody at 1:50 dilution. No antibodies for any of these three protozoa were found, thus suggesting that these wild red-tailed Amazon parrot nestlings had not been exposed to these parasites.(AU)

Toxoplasma gondii, Neospora caninum e Sarcocystis neurona são protozoários intracelulares do filo Apicomplexa. O papagaio-de-cara-roxa (Amazona brasiliensis) é um psitacídeo endêmico da floresta atlântica, considerado uma espécie quase ameaçada de extinção e bioindicadora por sua sensibilidade às mudanças no ambiente. O objetivo do presente estudo foi detectar a presença de anticorpos contra T. gondii, N. caninum e S. neurona em filhotes de papagaios-de-cara-roxa (Amazona brasiliensis) de vida livre na Ilha Rasa, Brasil. Amostras de sangue foram coletadas de 51 papagaios e armazenadas a - 20ºC até a realização da Reação de Imunofluorescência Indireta (RIFI). As lâminas de RIFI com os antígenos, foram preparadas com taquizoítos de T. gondii (cepa RH) e N. caninum (cepa NC-1) e com merozoítos de S. neurona (cepa SNR37). Os plasmas foram diluídos em PBS (Ph 7,2) nas diluições 1:16 para T. gondii, 1:50 para N. caninum e 1:5 para S. neurona. O conjugado anti-IgG de galinhas marcado com fluoresceína (FITC) foi utilizado na diluição de 1:50. Não foram detectados anticorpos para os três protozoários nas amostras sugerindo que os filhotes de papagaios-de-cara-roxa não foram expostos aos protozoários.(AU)

Detection of Neospora caninum and Toxoplasma gondii in semen of naturally infected rams

Background: Neospora caninum and Toxoplasma gondii are closely related cyst-forming apicomplexan parasites identified as important causes of reproductive failure in cattle. Moreover, abortion cases attributed to N. caninum and T. gondiiinfection have been occasionally reported in sheep. Due to the relatively scarce information on the molecular detection ofN. caninum in the semen of naturally infected rams, this study aimed to detect parasitic DNA in fresh semen samples andin frozen extended semen straws from male sheep from artificial inseminations centers in Southern Brazil.Materials, Methods & Results: Semen samples of 38 rams from artificial insemination centers were evaluated. Eleven ramswere naturally infected (seropositive for anti-N. caninum and/or anti-T. gondii IgG) and were selected for fresh semen collection.We tested all the samples for the closely related protozoan T. gondii to detect a possible cross-reaction and co-infection, due tothe close similarity with N. caninum. The indirect fluorescent antibody test was used to detect IgG antibodies in the 11 serumsamples from rams. Fresh semen samples were collected from 11 rams on days 1, 50, 55, and 58 using an artificial vaginaand ewe in estrus. Other 27 rams had their frozen extended semen straws analyzed. A total of 20 fresh semen samples and27 frozen extended semen straws samples were used to detect the presence of N. caninum and T. gondii DNA by polymerasechain reaction (PCR). Nc-5 and B1 genes were used as target regions to detect N. caninum and T. gondii DNA, respectively.The presence of N. caninum DNA was confirmed in the third collection of a fresh semen sample of one seropositive ram. T.gondii DNA was detected in a fresh semen sample of one seropositive ram. The DNA sequences of 186 bp from N. caninum(GenBank accession: MH806393) and 492 bp from T. gondii (GenBank accession: MH793503)...

Detection of Neospora caninum and Toxoplasma gondii in semen of naturally infected rams

Background: Neospora caninum and Toxoplasma gondii are closely related cyst-forming apicomplexan parasites identified as important causes of reproductive failure in cattle. Moreover, abortion cases attributed to N. caninum and T. gondiiinfection have been occasionally reported in sheep. Due to the relatively scarce information on the molecular detection ofN. caninum in the semen of naturally infected rams, this study aimed to detect parasitic DNA in fresh semen samples andin frozen extended semen straws from male sheep from artificial inseminations centers in Southern Brazil.Materials, Methods & Results: Semen samples of 38 rams from artificial insemination centers were evaluated. Eleven ramswere naturally infected (seropositive for anti-N. caninum and/or anti-T. gondii IgG) and were selected for fresh semen collection.We tested all the samples for the closely related protozoan T. gondii to detect a possible cross-reaction and co-infection, due tothe close similarity with N. caninum. The indirect fluorescent antibody test was used to detect IgG antibodies in the 11 serumsamples from rams. Fresh semen samples were collected from 11 rams on days 1, 50, 55, and 58 using an artificial vaginaand ewe in estrus. Other 27 rams had their frozen extended semen straws analyzed. A total of 20 fresh semen samples and27 frozen extended semen straws samples were used to detect the presence of N. caninum and T. gondii DNA by polymerasechain reaction (PCR). Nc-5 and B1 genes were used as target regions to detect N. caninum and T. gondii DNA, respectively.The presence of N. caninum DNA was confirmed in the third collection of a fresh semen sample of one seropositive ram. T.gondii DNA was detected in a fresh semen sample of one seropositive ram. The DNA sequences of 186 bp from N. caninum(GenBank accession: MH806393) and 492 bp from T. gondii (GenBank accession: MH793503)...(AU)

Detection of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii in horses, dogs and cat / Detecção de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos do estado do Paraná, Brasil

The occurrence and distribution of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii was investigated in horses, dogs and cats from Curitiba, Paraná state, Brazil. Serum samples were selected from 100 horses, 100 dogs and 100 cats from the routine of the Veterinary Clinical Pathology Laboratory in the Veterinary Hospital of the University of Paraná (UFPR). The 100 dog samples were divided into two groups: 35 samples from dogs with neurological sign (convulsion) and 65 samples from dogs without neurological signs. The animals were adults of different breeds, males and females. Samples were analyzed by indirect fluorescent antibody test (IFAT) for protozoa S. neurona, N. caninum andT. gondii at the following cut-off dilutions: horses: 1:50, 1:50 and 1:16; dogs: 1:50, 1:50 and 1:16; cats: 1:50, 1:50 and 1:50, respectively. The obtained results were 42% of horses, 7% of dogs and 5% of cats seropositive for S. neurona; 58% of horses, 68% of dogs and 42% of cats seropositive to N. caninum, and 36% of horses, 20% of dogs and 21% of cats seropositive for T. gondii. Among the dogs with neurological signs, 8.6%, 68.6% and 25.7% were seropositive for S. neurona, N. caninum and T. gondii, respectively. Among the dogs without neurological signs, 6.2% 67.7% and 16.9% were seropositiv

O presente trabalho investigou a ocorrência e distribuição de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos de Curitiba, estado do Paraná, Brasil. Amostras de soro de 100 cavalos, 100 cães e 100 gatos da rotina do Laboratório de Patologia Clínica Veterinária do Hospital Veterinário da Universidade Federal do Paraná (UFPR) foram selecionadas. As 100 amostras de cães foram divididas em dois grupos: 35 amostras de animais com sinal neurológico (convulsão) e 65 sem sinais neurológicos. Os animais eram adultos de diferentes raças, machos e fêmeas. As amostras foram analisadas pelo teste de reação de imunofluorescência indireta (RIFI) para os protozoários S. neurona, N. caninum e T. gondii nas seguintes diluições de corte: cavalos: 1:50, 1:50 e 1:16; cães: 1:50, 1:50 e 1:16; gatos: 1:50, 1:50 e 1:50, respectivamente. Os resultados obtidos foram 42% dos cavalos, 7% dos cães e 5% dosgatos soropositivos para S. neurona; 58% dos cavalos, 68% dos cães e 42% dos gatos soropositivos para N. caninum; e 36% dos cavalos, 20% dos cães e 21% dos gatos soropositivos para T. gondii. Entre os cães com sinal neurológico, 8.6%, 68.6% e 25.7% deles foram soropositivos para S. neurona, N. caninum e T. gondii, respectivamente. Entre os cães sem sinais neurológi

Detecção de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos do estado do Paraná, Brasil / Detection of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii in horses, dogs and cats from Paraná state, Brazil

The occurrence and distribution of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii was investigated in horses, dogs and cats from Curitiba, Paraná state, Brazil. Serum samples were selected from 100 horses, 100 dogs and 100 cats from the routine of the Veterinary Clinical Pathology Laboratory in the Veterinary Hospital of the University of Paraná (UFPR). The 100 dog samples were divided into two groups: 35 samples from dogs with neurological sign (convulsion) and 65 samples from dogs without neurological signs. The animals were adults of different breeds, males and females. Samples were analyzed by indirect fluorescent antibody test (IFAT) for protozoa S. neurona, N. caninum andT. gondii at the following cut-off dilutions: horses: 1:50, 1:50 and 1:16; dogs: 1:50, 1:50 and 1:16; cats: 1:50, 1:50 and 1:50, respectively. The obtained results were 42% of horses, 7% of dogs and 5% of cats seropositive for S. neurona; 58% of horses, 68% of dogs and 42% of cats seropositive to N. caninum, and 36% of horses, 20% of dogs and 21% of cats seropositive for T. gondii. Among the dogs with neurological signs, 8.6%, 68.6% and 25.7% were seropositive for S. neurona, N. caninum and T. gondii, respectively. Among the dogs without neurological signs, 6.2% 67.7% and 16.9% were seropositiv

O presente trabalho investigou a ocorrência e distribuição de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos de Curitiba, estado do Paraná, Brasil. Amostras de soro de 100 cavalos, 100 cães e 100 gatos da rotina do Laboratório de Patologia Clínica Veterinária do Hospital Veterinário da Universidade Federal do Paraná (UFPR) foram selecionadas. As 100 amostras de cães foram divididas em dois grupos: 35 amostras de animais com sinal neurológico (convulsão) e 65 sem sinais neurológicos. Os animais eram adultos de diferentes raças, machos e fêmeas. As amostras foram analisadas pelo teste de reação de imunofluorescência indireta (RIFI) para os protozoários S. neurona, N. caninum e T. gondii nas seguintes diluições de corte: cavalos: 1:50, 1:50 e 1:16; cães: 1:50, 1:50 e 1:16; gatos: 1:50, 1:50 e 1:50, respectivamente. Os resultados obtidos foram 42% dos cavalos, 7% dos cães e 5% dosgatos soropositivos para S. neurona; 58% dos cavalos, 68% dos cães e 42% dos gatos soropositivos para N. caninum; e 36% dos cavalos, 20% dos cães e 21% dos gatos soropositivos para T. gondii. Entre os cães com sinal neurológico, 8.6%, 68.6% e 25.7% deles foram soropositivos para S. neurona, N. caninum e T. gondii, respectivamente. Entre os cães sem sinais neurológi

Detection molecular of Rangelia vitalii in dogs from Parana State, Southern Brazil / Detecção molecular de Rangelia vitalii em cães do Estado do Paraná, Sul do Brasil

Rangelia vitalii infects erythrocytes, leukocytes and endothelial cells of dogs. The present study aimed to report the molecular detection confirmed by sequencing of R. vitalii in the state of Paraná, as well as describe the clinical, hematological and biochemical alterations of the infected dogs. Three sick dogs from the metropolitan area of Curitiba, PR, Brazil, underwent a physical exam, and laboratory tests included hematology, biochemistry, polymerase chain reaction (PCR), and gene sequencing. Clinical signs included apathy, anorexia, and hemorrhage. Intra-erythrocytic and extracellular piroplasms were found on peripheral blood smears from all three dogs. Blood samples from these animals were positive for Babesia sp. by PCR targeting 18S rRNA. PCR products from all three dogs were sequenced, and BLAST analysis showed that the PCR-generated sequences were highly homologous with those of R. vitalii previously reported. Hematologic findings included severe anemia, shift of neutrophils to the regenerative left, and thrombocytopenia. Serum urea levels were increased in all three dogs, and direct bilirubin levels were elevated in one dog.(AU)

Rangelia vitalii infecta eritrócitos, leucócitos e células endoteliais de cães. O presente estudo objetivou relatar a detecção molecular confirmada por sequenciamento de R. vitalii no estado do Paraná e descrever as alterações clínicas, hematológicas e bioquímicas dos cães infectados. Três cães doentes da região metropolitana de Curitiba, PR, Brasil, foram submetidos a exame físico e exames laboratoriais que incluíram hematologia, bioquímica, reação em cadeia da polimerase (PCR) e sequenciamento genético. Os sinais clínicos incluíram apatia, anorexia e hemorragia. Piroplasmas intra-eritrocíticos e extracelulares foram encontrados em esfregaços de sangue periférico dos três cães. As amostras de sangue destes animais foram positivas para Babesia sp. pela PCR baseada no gene 18S rRNA. Os produtos de PCR dos três cães foram sequenciados e a análise de BLAST mostrou que as seqüências geradas por PCR eram altamente homólogas com as de R. vitalii previamente relatadas. Os achados hematológicos incluíram anemia grave, desvio de neutrófilos à esquerda regenerativo e trombocitopenia. Os níveis de uréia no soro aumentaram nos três cães, e os níveis de bilirrubina direta foram elevados em um cão.(AU)

Detection molecular of Rangelia vitalii in dogs from Parana State, Southern Brazil / Detecção molecular de Rangelia vitalii em cães do Estado do Paraná, Sul do Brasil

Rangelia vitalii infects erythrocytes, leukocytes and endothelial cells of dogs. The present study aimed to report the molecular detection confirmed by sequencing of R. vitalii in the state of Paraná, as well as describe the clinical, hematological and biochemical alterations of the infected dogs. Three sick dogs from the metropolitan area of Curitiba, PR, Brazil, underwent a physical exam, and laboratory tests included hematology, biochemistry, polymerase chain reaction (PCR), and gene sequencing. Clinical signs included apathy, anorexia, and hemorrhage. Intra-erythrocytic and extracellular piroplasms were found on peripheral blood smears from all three dogs. Blood samples from these animals were positive for Babesia sp. by PCR targeting 18S rRNA. PCR products from all three dogs were sequenced, and BLAST analysis showed that the PCR-generated sequences were highly homologous with those of R. vitalii previously reported. Hematologic findings included severe anemia, shift of neutrophils to the regenerative left, and thrombocytopenia. Serum urea levels were increased in all three dogs, and direct bilirubin levels were elevated in one dog.(AU)

Rangelia vitalii infecta eritrócitos, leucócitos e células endoteliais de cães. O presente estudo objetivou relatar a detecção molecular confirmada por sequenciamento de R. vitalii no estado do Paraná e descrever as alterações clínicas, hematológicas e bioquímicas dos cães infectados. Três cães doentes da região metropolitana de Curitiba, PR, Brasil, foram submetidos a exame físico e exames laboratoriais que incluíram hematologia, bioquímica, reação em cadeia da polimerase (PCR) e sequenciamento genético. Os sinais clínicos incluíram apatia, anorexia e hemorragia. Piroplasmas intra-eritrocíticos e extracelulares foram encontrados em esfregaços de sangue periférico dos três cães. As amostras de sangue destes animais foram positivas para Babesia sp. pela PCR baseada no gene 18S rRNA. Os produtos de PCR dos três cães foram sequenciados e a análise de BLAST mostrou que as seqüências geradas por PCR eram altamente homólogas com as de R. vitalii previamente relatadas. Os achados hematológicos incluíram anemia grave, desvio de neutrófilos à esquerda regenerativo e trombocitopenia. Os níveis de uréia no soro aumentaram nos três cães, e os níveis de bilirrubina direta foram elevados em um cão.(AU)

Dynamics of hematological parameters in female lambs during the first four months of life / Dinâmica dos parâmetros hematológicos em cordeiras durante os primeiros quatro meses de vida

Important physiological changes affect the blood profile of ruminants during the growth phase, but few studies approach the factors involved in these dynamics in lambs. The aim of this study was to characterize the dynamics of hematological parameters, of total plasma protein (TPP), and of fibrinogen in healthy female lambs during the first four months of life. Blood samples of 35 female lambs were collected at 30, 60, 90, and 120 days old to perform the complete blood count (CBC). The erythrocyte and leukocyte parameters, TPP, and fibrinogen were determined. The means for total red blood cell (RBC) counts at 60 and 120 days differed (P < 0.05) from the initial mean, showing a peak of 13.6 x 106 cells μL-1 at 60 days old. The mean values for packed cell volume (PCV) and hemoglobin (Hgb) concentration increased (P < 0.05) until 90 days and decreased at 120 days (36.6% to 33.7% and 11.4 g dL-1 to 10.6 g dL-1 between 90 and 120 days, respectively). The means for mean corpuscular volume (MCV) and for mean corpuscular hemoglobin concentration (MCHC) increased (P < 0.05) between 30 and 120 days (27.5 μm3 to 29.7 μm3 and 26.6% to 31.4%, respectively). The total white blood cell (WBC) count increased (P < 0.05) and reached a peak at 90 days (9,314 cells μL-1). The peaks for segmented neutrophils (5,141 cells μL-1) and lymphocyte counts (4,236 cells μL-1) occurred at 60 and 90 days, respectively. The means for neutrophil/lymphocyte ratio were similar (P > 0.05) between the ages (mean of 1.8) but higher than the reference value for adult sheep (0.5). The initial mean for eosinophil counts (2 cells μL-1) was lower (P < 0.05) than all subsequent ones, and the monocyte count showed the lowest level (P < 0.05) at 120 days (232 cells μL-1). The mean for TPP at 60 days (6.4 g dL-1) was higher (P < 0.05) than the other ages.(AU)

Important physiological changes affect the blood profile of ruminants during the growth phase, but few studies approach the factors involved in these dynamics in lambs. The aim of this study was to characterize the dynamics of hematological parameters, of total plasma protein (TPP), and of fibrinogen in healthy female lambs during the first four months of life. Blood samples of 35 female lambs were collected at 30, 60, 90, and 120 days old to perform the complete blood count (CBC). The erythrocyte and leukocyte parameters, TPP, and fibrinogen were determined. The means for total red blood cell (RBC) counts at 60 and 120 days differed (P < 0.05) from the initial mean, showing a peak of 13.6 x 106 cells μL-1 at 60 days old. The mean values for packed cell volume (PCV) and hemoglobin (Hgb) concentration increased (P < 0.05) until 90 days and decreased at 120 days (36.6% to 33.7% and 11.4 g dL-1 to 10.6 g dL-1 between 90 and 120 days, respectively). The means for mean corpuscular volume (MCV) and for mean corpuscular hemoglobin concentration (MCHC) increased (P < 0.05) between 30 and 120 days (27.5 μm3 to 29.7 μm3 and 26.6% to 31.4%, respectively). The total white blood cell (WBC) count increased (P < 0.05) and reached a peak at 90 days (9,314 cells μL-1). The peaks for segmented neutrophils (5,141 cells μL-1) and lymphocyte counts (4,236 cells μL-1) occurred at 60 and 90 days, respectively. The means for neutrophil/lymphocyte ratio were similar (P > 0.05) between the ages (mean of 1.8) but higher than the reference value for adult sheep (0.5). The initial mean for eosinophil counts (2 cells μL-1) was lower (P < 0.05) than all subsequent ones, and the monocyte count showed the lowest level (P < 0.05) at 120 days (232 cells μL-1). The mean for TPP at 60 days (6.4 g dL-1) was higher (P < 0.05) than the other ages.(AU)

Detection molecular of Rangelia vitalii in dogs from Parana State, Southern Brazil

Abstract Rangelia vitalii infects erythrocytes, leukocytes and endothelial cells of dogs. The present study aimed to report the molecular detection confirmed by sequencing of R. vitalii in the state of Paraná, as well as describe the clinical, hematological and biochemical alterations of the infected dogs. Three sick dogs from the metropolitan area of Curitiba, PR, Brazil, underwent a physical exam, and laboratory tests included hematology, biochemistry, polymerase chain reaction (PCR), and gene sequencing. Clinical signs included apathy, anorexia, and hemorrhage. Intra-erythrocytic and extracellular piroplasms were found on peripheral blood smears from all three dogs. Blood samples from these animals were positive for Babesia sp. by PCR targeting 18S rRNA. PCR products from all three dogs were sequenced, and BLAST analysis showed that the PCR-generated sequences were highly homologous with those of R. vitalii previously reported. Hematologic findings included severe anemia, shift of neutrophils to the regenerative left, and thrombocytopenia. Serum urea levels were increased in all three dogs, and direct bilirubin levels were elevated in one dog.

Resumo Rangelia vitalii infecta eritrócitos, leucócitos e células endoteliais de cães. O presente estudo objetivou relatar a detecção molecular confirmada por sequenciamento de R. vitalii no estado do Paraná e descrever as alterações clínicas, hematológicas e bioquímicas dos cães infectados. Três cães doentes da região metropolitana de Curitiba, PR, Brasil, foram submetidos a exame físico e exames laboratoriais que incluíram hematologia, bioquímica, reação em cadeia da polimerase (PCR) e sequenciamento genético. Os sinais clínicos incluíram apatia, anorexia e hemorragia. Piroplasmas intra-eritrocíticos e extracelulares foram encontrados em esfregaços de sangue periférico dos três cães. As amostras de sangue destes animais foram positivas para Babesia sp. pela PCR baseada no gene 18S rRNA. Os produtos de PCR dos três cães foram sequenciados e a análise de BLAST mostrou que as seqüências geradas por PCR eram altamente homólogas com as de R. vitalii previamente relatadas. Os achados hematológicos incluíram anemia grave, desvio de neutrófilos à esquerda regenerativo e trombocitopenia. Os níveis de uréia no soro aumentaram nos três cães, e os níveis de bilirrubina direta foram elevados em um cão.

Detection molecular of Rangelia vitalii in dogs from Parana State, Southern Brazil

Abstract Rangelia vitalii infects erythrocytes, leukocytes and endothelial cells of dogs. The present study aimed to report the molecular detection confirmed by sequencing of R. vitalii in the state of Paraná, as well as describe the clinical, hematological and biochemical alterations of the infected dogs. Three sick dogs from the metropolitan area of Curitiba, PR, Brazil, underwent a physical exam, and laboratory tests included hematology, biochemistry, polymerase chain reaction (PCR), and gene sequencing. Clinical signs included apathy, anorexia, and hemorrhage. Intra-erythrocytic and extracellular piroplasms were found on peripheral blood smears from all three dogs. Blood samples from these animals were positive for Babesia sp. by PCR targeting 18S rRNA. PCR products from all three dogs were sequenced, and BLAST analysis showed that the PCR-generated sequences were highly homologous with those of R. vitalii previously reported. Hematologic findings included severe anemia, shift of neutrophils to the regenerative left, and thrombocytopenia. Serum urea levels were increased in all three dogs, and direct bilirubin levels were elevated in one dog.

Resumo Rangelia vitalii infecta eritrócitos, leucócitos e células endoteliais de cães. O presente estudo objetivou relatar a detecção molecular confirmada por sequenciamento de R. vitalii no estado do Paraná e descrever as alterações clínicas, hematológicas e bioquímicas dos cães infectados. Três cães doentes da região metropolitana de Curitiba, PR, Brasil, foram submetidos a exame físico e exames laboratoriais que incluíram hematologia, bioquímica, reação em cadeia da polimerase (PCR) e sequenciamento genético. Os sinais clínicos incluíram apatia, anorexia e hemorragia. Piroplasmas intra-eritrocíticos e extracelulares foram encontrados em esfregaços de sangue periférico dos três cães. As amostras de sangue destes animais foram positivas para Babesia sp. pela PCR baseada no gene 18S rRNA. Os produtos de PCR dos três cães foram sequenciados e a análise de BLAST mostrou que as seqüências geradas por PCR eram altamente homólogas com as de R. vitalii previamente relatadas. Os achados hematológicos incluíram anemia grave, desvio de neutrófilos à esquerda regenerativo e trombocitopenia. Os níveis de uréia no soro aumentaram nos três cães, e os níveis de bilirrubina direta foram elevados em um cão.

Dynamics of hematological parameters in female lambs during the first four months of life / Dinâmica dos parâmetros hematológicos em cordeiras durante os primeiros quatro meses de vida

Important physiological changes affect the blood profile of ruminants during the growth phase, but few studies approach the factors involved in these dynamics in lambs. The aim of this study was to characterize the dynamics of hematological parameters, of total plasma protein (TPP), and of fibrinogen in healthy female lambs during the first four months of life. Blood samples of 35 female lambs were collected at 30, 60, 90, and 120 days old to perform the complete blood count (CBC). The erythrocyte and leukocyte parameters, TPP, and fibrinogen were determined. The means for total red blood cell (RBC) counts at 60 and 120 days differed (P 0.05) between the ages (mean of 1.8) but higher than the reference value for adult sheep (0.5). The initial mean for eosinophil counts (2 cells μL-1) was lower (P < 0.05) than all subsequent ones, and the monocyte count showed the lowest level (P < 0.05) at 120 days (232 cells μL-1). The mean for TPP at 60 days (6.4 g dL-1) was higher (P < 0.05) than the other ages.

Important physiological changes affect the blood profile of ruminants during the growth phase, but few studies approach the factors involved in these dynamics in lambs. The aim of this study was to characterize the dynamics of hematological parameters, of total plasma protein (TPP), and of fibrinogen in healthy female lambs during the first four months of life. Blood samples of 35 female lambs were collected at 30, 60, 90, and 120 days old to perform the complete blood count (CBC). The erythrocyte and leukocyte parameters, TPP, and fibrinogen were determined. The means for total red blood cell (RBC) counts at 60 and 120 days differed (P 0.05) between the ages (mean of 1.8) but higher than the reference value for adult sheep (0.5). The initial mean for eosinophil counts (2 cells μL-1) was lower (P < 0.05) than all subsequent ones, and the monocyte count showed the lowest level (P < 0.05) at 120 days (232 cells μL-1). The mean for TPP at 60 days (6.4 g dL-1) was higher (P < 0.05) than the other ages.

Detection of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii in horses, dogs and cat / Detecção de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos do estado do Paraná, Brasil

The occurrence and distribution of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii was investigated in horses, dogs and cats from Curitiba, Paraná state, Brazil. Serum samples were selected from 100 horses, 100 dogs and 100 cats from the routine of the Veterinary Clinical Pathology Laboratory in the Veterinary Hospital of the University of Paraná (UFPR). The 100 dog samples were divided into two groups: 35 samples from dogs with neurological sign (convulsion) and 65 samples from dogs without neurological signs. The animals were adults of different breeds, males and females. Samples were analyzed by indirect fluorescent antibody test (IFAT) for protozoa S. neurona, N. caninum andT. gondii at the following cut-off dilutions: horses: 1:50, 1:50 and 1:16; dogs: 1:50, 1:50 and 1:16; cats: 1:50, 1:50 and 1:50, respectively. The obtained results were 42% of horses, 7% of dogs and 5% of cats seropositive for S. neurona; 58% of horses, 68% of dogs and 42% of cats seropositive to N. caninum, and 36% of horses, 20% of dogs and 21% of cats seropositive for T. gondii. Among the dogs with neurological signs, 8.6%, 68.6% and 25.7% were seropositive for S. neurona, N. caninum and T. gondii, respectively. Among the dogs without neurological signs, 6.2% 67.7% and 16.9% were seropositiv

O presente trabalho investigou a ocorrência e distribuição de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos de Curitiba, estado do Paraná, Brasil. Amostras de soro de 100 cavalos, 100 cães e 100 gatos da rotina do Laboratório de Patologia Clínica Veterinária do Hospital Veterinário da Universidade Federal do Paraná (UFPR) foram selecionadas. As 100 amostras de cães foram divididas em dois grupos: 35 amostras de animais com sinal neurológico (convulsão) e 65 sem sinais neurológicos. Os animais eram adultos de diferentes raças, machos e fêmeas. As amostras foram analisadas pelo teste de reação de imunofluorescência indireta (RIFI) para os protozoários S. neurona, N. caninum e T. gondii nas seguintes diluições de corte: cavalos: 1:50, 1:50 e 1:16; cães: 1:50, 1:50 e 1:16; gatos: 1:50, 1:50 e 1:50, respectivamente. Os resultados obtidos foram 42% dos cavalos, 7% dos cães e 5% dosgatos soropositivos para S. neurona; 58% dos cavalos, 68% dos cães e 42% dos gatos soropositivos para N. caninum; e 36% dos cavalos, 20% dos cães e 21% dos gatos soropositivos para T. gondii. Entre os cães com sinal neurológico, 8.6%, 68.6% e 25.7% deles foram soropositivos para S. neurona, N. caninum e T. gondii, respectivamente. Entre os cães sem sinais neurológi

Detecção de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos do estado do Paraná, Brasil / Detection of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii in horses, dogs and cats from Paraná state, Brazil

The occurrence and distribution of antibodies against Sarcocystis neurona, Neospora caninum and Toxoplasma gondii was investigated in horses, dogs and cats from Curitiba, Paraná state, Brazil. Serum samples were selected from 100 horses, 100 dogs and 100 cats from the routine of the Veterinary Clinical Pathology Laboratory in the Veterinary Hospital of the University of Paraná (UFPR). The 100 dog samples were divided into two groups: 35 samples from dogs with neurological sign (convulsion) and 65 samples from dogs without neurological signs. The animals were adults of different breeds, males and females. Samples were analyzed by indirect fluorescent antibody test (IFAT) for protozoa S. neurona, N. caninum andT. gondii at the following cut-off dilutions: horses: 1:50, 1:50 and 1:16; dogs: 1:50, 1:50 and 1:16; cats: 1:50, 1:50 and 1:50, respectively. The obtained results were 42% of horses, 7% of dogs and 5% of cats seropositive for S. neurona; 58% of horses, 68% of dogs and 42% of cats seropositive to N. caninum, and 36% of horses, 20% of dogs and 21% of cats seropositive for T. gondii. Among the dogs with neurological signs, 8.6%, 68.6% and 25.7% were seropositive for S. neurona, N. caninum and T. gondii, respectively. Among the dogs without neurological signs, 6.2% 67.7% and 16.9% were seropositiv

O presente trabalho investigou a ocorrência e distribuição de anticorpos contra Sarcocystis neurona, Neospora caninum e Toxoplasma gondii em cavalos, cães e gatos de Curitiba, estado do Paraná, Brasil. Amostras de soro de 100 cavalos, 100 cães e 100 gatos da rotina do Laboratório de Patologia Clínica Veterinária do Hospital Veterinário da Universidade Federal do Paraná (UFPR) foram selecionadas. As 100 amostras de cães foram divididas em dois grupos: 35 amostras de animais com sinal neurológico (convulsão) e 65 sem sinais neurológicos. Os animais eram adultos de diferentes raças, machos e fêmeas. As amostras foram analisadas pelo teste de reação de imunofluorescência indireta (RIFI) para os protozoários S. neurona, N. caninum e T. gondii nas seguintes diluições de corte: cavalos: 1:50, 1:50 e 1:16; cães: 1:50, 1:50 e 1:16; gatos: 1:50, 1:50 e 1:50, respectivamente. Os resultados obtidos foram 42% dos cavalos, 7% dos cães e 5% dosgatos soropositivos para S. neurona; 58% dos cavalos, 68% dos cães e 42% dos gatos soropositivos para N. caninum; e 36% dos cavalos, 20% dos cães e 21% dos gatos soropositivos para T. gondii. Entre os cães com sinal neurológico, 8.6%, 68.6% e 25.7% deles foram soropositivos para S. neurona, N. caninum e T. gondii, respectivamente. Entre os cães sem sinais neurológi