Molecular characterization of Cryptosporidium in ruminants and observation of natural infection by Cryptosporidium andersoni in sheep from Paraná, Brazil.

The aim of this study was to identify Cryptosporidium species found in cattle and sheep in Paraná, southern region of Brazil. Individual fecal samples from 458 bovines and 101 sheep were submitted for molecular analysis by PCR and nested PCR using specific primers for sequences of the 18S ribosomal unit (rRNA). Positive samples were analyzed using restriction fragment length polymorphism (RFLP), followed by genetic sequencing for species confirmation. The occurrence of Cryptosporidium was 11.27% (63/559). The highest occurrence was detected in lambs (12/59, 20.33%). From the 63 positive samples, it was possible to identify the species in 58 of them by RFLP and genetic sequencing. Five species of Cryptosporidium were identified: Cryptosporidium andersoni, Cryptosporidium bovis, Cryptosporidium ryanae, Cryptosporidium xiaoi, and Cryptosporidium parvum. The most prevalent species was C. andersoni (41.38%) and the least predominant was C. parvum (10.34%). The most abundant species of Cryptosporidium in dairy calves were C. andersoni (11/25) and C. ryanae (6/25). Of the 17 positive sheep, nine (52.94%) were infected with C. andersoni. This finding is the first report on the occurrence of C. andersoni in naturally infected sheep in Brazil and the first observation of a high absolute occurrence of this Cryptosporidium species in sheep.

Prevalence and risk factors of Eimeria spp. natural infection in sheep from northern Paraná, Brazil.

The present study aimed to perform an epidemiological and morphological identification of Eimeria infection in sheep in Brazil. Fecal samples from sheep were collected from 20 farms in northern Paraná, Brazil. An epidemiological questionnaire was used to evaluate the risk factors. Fecal samples containing oocysts per gram of feces (OoPG) ≥1000 were subjected to the modified Willis-Mollay method to perform oocyst identification. Sporulated oocysts were observed microscopically for morphological identification. A total of 807 fecal samples were collected. Based on the morphological characteristics of the sporulated oocysts, 10 species of Eimeria were identified, with main species observed: Eimeira ovinoidalis (98.1%), Eimeria crandallis (87.6%), Eimeria parva (79.1%), and Eimeria bakuensis (60.8%). Only 2.6% (7/268) of the sheep were infected with a single species, 4.8% (13/268) contained two different species, and 92.5% (248/268) were infected with three or more species. The analysis of risk factors showed that an intensive rearing, no rotation of pasture, dirt, and slatted floors, and age up to 12 months were associated with infection. This study showed a high prevalence of Eimeria natural infection in sheep from northern Paraná, Brazil. Furthermore, based on the risk factors, good management and hygiene practices must be employed to avoid infection.

Prevalence and risk factors of Eimeria spp. natural infection in sheep from northern Paraná, Brazil / Prevalência e fatores de risco da infecção natural por Eimeira spp. em ovinos na região norte do Paraná, Brasil

Abstract The present study aimed to perform an epidemiological and morphological identification of Eimeria infection in sheep in Brazil. Fecal samples from sheep were collected from 20 farms in northern Paraná, Brazil. An epidemiological questionnaire was used to evaluate the risk factors. Fecal samples containing oocysts per gram of feces (OoPG) ≥1000 were subjected to the modified Willis-Mollay method to perform oocyst identification. Sporulated oocysts were observed microscopically for morphological identification. A total of 807 fecal samples were collected. Based on the morphological characteristics of the sporulated oocysts, 10 species of Eimeria were identified, with main species observed: Eimeira ovinoidalis (98.1%), Eimeria crandallis (87.6%), Eimeria parva (79.1%), and Eimeria bakuensis (60.8%). Only 2.6% (7/268) of the sheep were infected with a single species, 4.8% (13/268) contained two different species, and 92.5% (248/268) were infected with three or more species. The analysis of risk factors showed that an intensive rearing, no rotation of pasture, dirt, and slatted floors, and age up to 12 months were associated with infection. This study showed a high prevalence of Eimeria natural infection in sheep from northern Paraná, Brazil. Furthermore, based on the risk factors, good management and hygiene practices must be employed to avoid infection.

Resumo O presente estudo teve como objetivo realizar uma avaliação epidemiológica e morfométrica da infecção por Eimeria em ovinos no Brasil. Amostras fecais de ovinos foram coletadas em 20 fazendas no sul do Brasil. Um questionário epidemiológico foi utilizado para avaliar os fatores de risco. Amostras fecais, contendo oocistos por grama de fezes (OoPG) ≥1000, foram submetidas ao método de Willis-Mollay modificado para realizar a identificação de oocistos. Oocistos esporulados foram observados microscopicamente para identificação morfológica. Foram coletadas 807 amostras fecais. Com base nas características morfológicas e morfométricas dos oocistos esporulados, foram identificadas 10 espécies de Eimeria, com as principais espécies observadas: Eimeria ovinoidalis (98,1%), Eimeria crandallis (87,6%), Eimeria parva (79,1%) e Eimeria bakuensis (60,8%). Apenas 2,6% (7/268) dos ovinos estavam infectados com uma única espécie, 4,8% (13/268) continham duas espécies diferentes e 92,5% (248/268) estavam infectados com três ou mais espécies. A análise dos fatores de risco mostrou que uma criação intensiva, sem rotação de pasto, terra, piso de ripa e idade até 12 meses foram associadas à infecção. Este estudo mostrou uma alta prevalência de infecção natural por Eimeria em ovinos do norte do Paraná, Brasil. Além disso, com base nos fatores de risco, boas práticas de manejo e higiene devem ser empregadas para evitar infecções.

Comparison of serological and molecular techniques to detect Toxoplasma gondii in free-range chickens (Gallus gallus domesticus).

The present study aimed to compare different indirect and direct diagnostic techniques to diagnose Toxoplasma gondii in free-range chickens. Samples of 386 chickens obtained from 24 Paraná properties were used for serological analysis by indirect fluorescent antibody test (IFAT), modified agglutination test (MAT), and enzyme-linked immunosorbent assay (ELISA). Animals positive by IFAT and/or MAT had their tissues submitted to the mouse bioassay, and those who were positive in this technique had their blood, tissues, and acidic pepsin tissue digestion submitted to PCR (conventional, nested, and quantitative-PCR (qPCR)). One hundred and nineteen chickens (30.8 %) were positive in at least one of the serological tests, being 102 (26.4 %) in the IFAT, 64 (16.6 %) in the MAT, and 62 (16.0 %) in the ELISA. The IFAT was used as a gold standard, and the MAT showed higher sensitivity (46.0 %) and specificity (94.0) compared to ELISA (43.5 % and 93.6 %, respectively). Ninety samples of eighteen chickens positive in the mouse bioassay were subjected to PCR, and according to molecular tests, the conventional PCR detected the T. gondii DNA in 30 % (27/90) of the samples, in 38.8 % (35/90) with nested-PCR and 40.0 % (36/90) with real-time. According to molecular analyzes, the sensitivity was higher in ITS1 nested-PCR (69.4 %) and specificity in conventional PCR-529bp (90.7 %), using the qPCR as the gold standard. MAT and ELISA had similarities in concordance analyzes. The IFAT was the serological technique with the highest agreement with the mouse bioassay, and serological tests in parallel showed to be a good screening option for the isolation of T. gondii in chick tissues. The PCR markers effectively detected the parasite DNA, and the heart was the tissue with the highest number of positives samples. The conventional PCR had sensitivity similar to nested-PCR and qPCR and could be a cheaper alternative to diagnose T. gondii infection in chicken tissues.

Development of a qPCR to diagnose the genus Eimeria in bovines / Desenvolvimento de uma qPCR para o diagnóstico do gênero Eimeria em bovinos

Bovine coccidiosis is caused by protozoa of the genus Eimeria. These protozoa mainly affect young animals, causing a decrease in production and consequent economic losses. The routine diagnosis is made through morphological observation of the oocysts, which has several limitations. The objective of the present study was to develop a qPCR technique for the diagnose of Eimeria spp. in cattle. For this purpose, the 18S rRNA region of the DNA of these parasites was selected, since it is a region with low variability among the species. The qPCR was developed using the SYBR Green, resulting in a PCR with a high sensitivity, able to amplify samples containing only one oocyst of Eimeria spp. of bovines. The feasibility of using qPCR in the diagnosis of the Eimeria Genus is demonstrated in this study, once this technique shows to be less laborious and needs less skills for diagnostic training when compared to the technique conventionally used in theroutine (micromorphometry).(AU)

A coccidiose em bovinos é causada por protozoários do gênero Eimeria. Estes protozoários acometem principalmente animais jovens, causando diminuição de produção e consequente perdas econômicas. O diagnóstico de rotina é realizado através de observação morfológica dos oocistos, que possui várias limitações. O objetivo do presente trabalho foi desenvolver uma técnica de qPCR para diagnóstico de Eimeria spp. em bovinos. Para isto foi selecionada a região 18S rRNA do DNA destes parasitas, pois a mesma é uma região com pouca variabilidade entre as espécies. A qPCR foi desenvolvida com a utilização de SYBR Green, tendo como resultado uma PCR com uma alta sensibilidade, capaz de amplificar amostras contendo apenas um oocisto de Eimeria spp de bovinos. Demonstra-se nesse estudo a viabilidade na utilização da qPCR no diagnóstico do gênero Eimeria, sendo esta técnica menos laboriosa e com menos necessidade de treinamento para diagnóstico quando comparada com a técnica convencionalmente utilizada em rotina (micromorfometria).(AU)

First molecular detection of Haemoproteus spp. and Plasmodium spp. in eared doves (Zenaida auriculata) in Brazil.

The aim of this study was to verify the presence and identify the species of haemosporidian parasites in eared doves (Zenaida auriculata) in Brazil. Two hundred and eleven male and female eared doves were trap-captured in four different regions of Londrina city, in southern Brazil. Whole blood was collected in EDTA tubes through heart puncture after euthanasia in a CO2 chamber. A nested PCR targeting the mitochondrial cytochrome b gene (cyt b) of Haemoproteus spp./Plasmodium spp. was performed, followed by an enzymatic digestion to identify the genus. Phylogenetic trees were constructed to determine the closely related species. Out of 211 eared doves, 209 (99.05%) were positive for Haemoproteus spp. and/or Plasmodium spp. RFLP analysis showed that 72.72% (152/209) of eared doves were positive only for Haemoproteus spp., 6.22% (13/209) were positive only for Plasmodium spp., and 21.05% (44/209) of eared doves had mixed infections. Genetic analysis found four samples that were homologous with Haemoproteus multipigmentatus and one that was homologous with Plasmodium sp. This is the first molecular study of hemoparasites from eared doves in Brazil, and it is also the first description of H. multipigmentatus and Plasmodium spp. infection in eared doves in Brazil.

Occurrence of gastrointestinal protozoans in cats from Londrina, Paraná, Brazil / Ocorrência de protozoários gastrointestinais em gatos de Londrina, Paraná, Brasil

Protozoans are widely distributed, and several species may parasitize the digestive tracts of cats (Felis catus), and can be transmitted to humans. The present study aimed to evaluate the species and occurrence of gastrointestinal protozoans in cats in the city of Londrina, Paraná, Brazil. A total of 206 cat fecal samples were tested, of which 141 were from shelter animals, and 65 were from pets owned by local people. Samples were processed by parasitological techniques. Coproparasitological techniques (Willis, Faust and Ziehl-Neelsen) were performed for detection of protozoan parasites. Subsequently, all samples were processed by PCR protocols specific to Toxoplasma gondii, Giardia spp., and Cryptosporidium spp. PCR products from positive samples were selected for sequencing. No samples were found to be positive for Cryptosporidium spp. using the Ziehl-Neelsen technique. Using specific PCR protocols, 1/206 (0.48%) samples tested positive for Cryptosporidium spp. After purification, this one positive sample was sequenced, and it demonstrated a 100% identity match to Cryptosporidium muris. Using specific PCR protocols, 13/206 (9.22%) cat fecal samples tested, including 2/65 (3.08%) pet cat fecal samples, were positive for T. gondii. PCR analysis revealed that 37/206 (17.96%) of cat fecal samples were positive for Giardia spp., including 27/141 (19.15%) of shelter cat fecal samples, and 10/65 (15.38%) pet cat fecal samples (p = 0.5124). When sequenced, these positive samples showed a 100% identity match with Giardia duodenalis. This study demonstrated that infections with Cryptosporidium spp., Toxoplasma gondii, and Giardia duodenalis are present in the population of both pet cats and shelter cats in the city of Londrina. This poses a risk to public health, because these parasites have a high zoonotic potential.(AU)

Os protozoários são amplamente distribuídos, e várias espécies podem parasitar o trato digestivo de gatos (Felis catus) e podem ser transmitidas para humanos. O presente estudo teve como objetivo avaliar as espécies e a ocorrência de protozoários gastrintestinais em gatos na cidade de Londrina, Paraná, Brasil. Um total de 206 amostras de fezes de gato foram testadas, das quais 141 eram de animais de abrigo, e 65 eram de animais de propriedade da população local. As amostras foram processadas por técnicas parasitológicas. Willis e esfregaços fecais foram confeccionados e corados pela técnica de Ziehl-Neelsen modificada para detecção de oocistos de Cryptosporidium spp. Posteriormente, todas as amostras foram processadas por protocolos de PCR específicos para Toxoplasma gondii, Giardia spp. e Cryptosporidium spp. Os produtos de PCR de amostras positivas foram selecionados para sequenciamento. Nenhuma amostra foi considerada positiva para Cryptosporidium spp. usando a técnica de Ziehl-Neelsen. Utilizando protocolos específicos de PCR, 1/206 (0,48%) amostras apresentaram resultados positivos para Cryptosporidium spp. Após a purificação, essa amostra positiva foi sequenciada e demonstrou 100% de equivalência de identidade com Cryptosporidium muris. Utilizando protocolos específicos de PCR, 13/206 (9,22%) amostras fecais de gatos testadas, incluindo 2/65 (3,08%) amostras fecais de gatos de estimação, foram positivas para T. gondii. A análise de PCR revelou que 37/206 (17,96%) das amostras de fezes de gatos foram positivas para Giardia spp., Incluindo 27/141 (19,15%) de amostras fecais de gatos de abrigo, e 10/65 (15,38%) amostras fecais de gatos de estimação (p = 0,5124). Quando sequenciadas, essas amostras positivas apresentaram 100% de equivalência de identidade com Giardia duodenalis. Este estudo demonstrou que as infecções por Cryptosporidium spp., Toxoplasma gondii e Giardia duodenalis estão presentes na população de gatos de estimação e gatos de abrigo na...(AU)

Occurrence of gastrointestinal protozoans in cats from Londrina, Paraná, Brazil / Ocorrência de protozoários gastrointestinais em gatos de Londrina, Paraná, Brasil

Protozoans are widely distributed, and several species may parasitize the digestive tracts of cats (Felis catus), and can be transmitted to humans. The present study aimed to evaluate the species and occurrence of gastrointestinal protozoans in cats in the city of Londrina, Paraná, Brazil. A total of 206 cat fecal samples were tested, of which 141 were from shelter animals, and 65 were from pets owned by local people. Samples were processed by parasitological techniques. Coproparasitological techniques (Willis, Faust and Ziehl-Neelsen) were performed for detection of protozoan parasites. Subsequently, all samples were processed by PCR protocols specific to Toxoplasma gondii, Giardia spp., and Cryptosporidium spp. PCR products from positive samples were selected for sequencing. No samples were found to be positive for Cryptosporidium spp. using the Ziehl-Neelsen technique. Using specific PCR protocols, 1/206 (0.48%) samples tested positive for Cryptosporidium spp. After purification, this one positive sample was sequenced, and it demonstrated a 100% identity match to Cryptosporidium muris. Using specific PCR protocols, 13/206 (9.22%) cat fecal samples tested, including 2/65 (3.08%) pet cat fecal samples, were positive for T. gondii. PCR analysis revealed that 37/206 (17.96%) of cat fecal samples were positive for Giardia spp., including 27/141 (19.15%) of shelter cat fecal samples, and 10/65 (15.38%) pet cat fecal samples (p = 0.5124). When sequenced, these positive samples showed a 100% identity match with Giardia duodenalis. This study demonstrated that infections with Cryptosporidium spp., Toxoplasma gondii, and Giardia duodenalis are present in the population of both pet cats and shelter cats in the city of Londrina. This poses a risk to public health, because these parasites have a high zoonotic potential.

Os protozoários são amplamente distribuídos, e várias espécies podem parasitar o trato digestivo de gatos (Felis catus) e podem ser transmitidas para humanos. O presente estudo teve como objetivo avaliar as espécies e a ocorrência de protozoários gastrintestinais em gatos na cidade de Londrina, Paraná, Brasil. Um total de 206 amostras de fezes de gato foram testadas, das quais 141 eram de animais de abrigo, e 65 eram de animais de propriedade da população local. As amostras foram processadas por técnicas parasitológicas. Willis e esfregaços fecais foram confeccionados e corados pela técnica de Ziehl-Neelsen modificada para detecção de oocistos de Cryptosporidium spp. Posteriormente, todas as amostras foram processadas por protocolos de PCR específicos para Toxoplasma gondii, Giardia spp. e Cryptosporidium spp. Os produtos de PCR de amostras positivas foram selecionados para sequenciamento. Nenhuma amostra foi considerada positiva para Cryptosporidium spp. usando a técnica de Ziehl-Neelsen. Utilizando protocolos específicos de PCR, 1/206 (0,48%) amostras apresentaram resultados positivos para Cryptosporidium spp. Após a purificação, essa amostra positiva foi sequenciada e demonstrou 100% de equivalência de identidade com Cryptosporidium muris. Utilizando protocolos específicos de PCR, 13/206 (9,22%) amostras fecais de gatos testadas, incluindo 2/65 (3,08%) amostras fecais de gatos de estimação, foram positivas para T. gondii. A análise de PCR revelou que 37/206 (17,96%) das amostras de fezes de gatos foram positivas para Giardia spp., Incluindo 27/141 (19,15%) de amostras fecais de gatos de abrigo, e 10/65 (15,38%) amostras fecais de gatos de estimação (p = 0,5124). Quando sequenciadas, essas amostras positivas apresentaram 100% de equivalência de identidade com Giardia duodenalis. Este estudo demonstrou que as infecções por Cryptosporidium spp., Toxoplasma gondii e Giardia duodenalis estão presentes na população de gatos de estimação e gatos de abrigo na...

Development of a qPCR to diagnose the genus Eimeria in bovines / Desenvolvimento de uma qPCR para o diagnóstico do gênero Eimeria em bovinos

Bovine coccidiosis is caused by protozoa of the genus Eimeria. These protozoa mainly affect young animals, causing a decrease in production and consequent economic losses. The routine diagnosis is made through morphological observation of the oocysts, which has several limitations. The objective of the present study was to develop a qPCR technique for the diagnose of Eimeria spp. in cattle. For this purpose, the 18S rRNA region of the DNA of these parasites was selected, since it is a region with low variability among the species. The qPCR was developed using the SYBR Green, resulting in a PCR with a high sensitivity, able to amplify samples containing only one oocyst of Eimeria spp. of bovines. The feasibility of using qPCR in the diagnosis of the Eimeria Genus is demonstrated in this study, once this technique shows to be less laborious and needs less skills for diagnostic training when compared to the technique conventionally used in theroutine (micromorphometry).

A coccidiose em bovinos é causada por protozoários do gênero Eimeria. Estes protozoários acometem principalmente animais jovens, causando diminuição de produção e consequente perdas econômicas. O diagnóstico de rotina é realizado através de observação morfológica dos oocistos, que possui várias limitações. O objetivo do presente trabalho foi desenvolver uma técnica de qPCR para diagnóstico de Eimeria spp. em bovinos. Para isto foi selecionada a região 18S rRNA do DNA destes parasitas, pois a mesma é uma região com pouca variabilidade entre as espécies. A qPCR foi desenvolvida com a utilização de SYBR Green, tendo como resultado uma PCR com uma alta sensibilidade, capaz de amplificar amostras contendo apenas um oocisto de Eimeria spp de bovinos. Demonstra-se nesse estudo a viabilidade na utilização da qPCR no diagnóstico do gênero Eimeria, sendo esta técnica menos laboriosa e com menos necessidade de treinamento para diagnóstico quando comparada com a técnica convencionalmente utilizada em rotina (micromorfometria).

First molecular detection of Haemoproteus spp. and Plasmodium spp. in eared doves (Zenaida auriculata) in Brazil / Primeira detecção molecular de Haemoproteus spp. e Plasmodium spp. em pombos (Zenaida auriculata) no Brasil

The aim of this study was to verify the presence and identify the species of haemosporidian parasites in eared doves (Zenaida auriculata) in Brazil. Two hundred and eleven male and female eared doves were trap-captured in four different regions of Londrina city, in southern Brazil. Whole blood was collected in EDTA tubes through heart puncture after euthanasia in a CO2 chamber. A nested PCR targeting the mitochondrial cytochrome b gene (cyt b) of Haemoproteus spp./Plasmodium spp. was performed, followed by an enzymatic digestion to identify the genus. Phylogenetic trees were constructed to determine the closely related species. Out of 211 eared doves, 209 (99.05%) were positive for Haemoproteus spp. and/or Plasmodium spp. RFLP analysis showed that 72.72% (152/209) of eared doves were positive only for Haemoproteus spp., 6.22% (13/209) were positive only for Plasmodium spp., and 21.05% (44/209) of eared doves had mixed infections. Genetic analysis found four samples that were homologous with Haemoproteus multipigmentatus and one that was homologous with Plasmodium sp. This is the first molecular study of hemoparasites from eared doves in Brazil, and it is also the first description of H. multipigmentatus and Plasmodium spp. infection in eared doves in Brazil.(AU)

O objetivo deste estudo foi verificar a presença e a identificação espécies de parasitas hemosporídeos em pombos (Zenaida auriculata) no Brasil. Duzentos e onze pombos machos e fêmeas foram capturados em quatro regiões diferentes de Londrina, sul do Brasil. Amostra de sangue foi coletada em tubos contendo EDTA por meio de punção cardíaca, após eutanásia em câmara de CO2. Uma nested PCR com alvo no gene mitocondrial citocromo b (cyt b) de Haemoproteus spp./Plasmodium spp. foi realizada, seguida de digestão enzimática para identificar o gênero. A árvore filogenética foi construída para determinar a relação com outras espécies. Das 211 pombas, 209 (99,05%) foram positivas para Haemoproteus spp./Plasmodium spp. A análise RFLP demonstrou que 72,72% (152/209) das pombas foram positivas somente para Haemoproteus spp.; 6,22% (13/209) foram positivas somente para Plasmodium e 21,05% (44/209) das pombas tiveram infecções mistas. A análise genética mostrou quatro amostras homólogas com H. multipigmentatus e uma com Plasmodium spp. Este é o primeiro estudo molecular de hemoparasitas em pombos no Brasil. E é também a primeira descrição da infecção por H. multipigmentatus e Plasmodium spp. em pombos Z. auriculata no Brasil.(AU)

First molecular detection of Eimeria spp. in eared doves (Zenaida auriculata) from Brazil / Primeira detecção molecular de Eimeria spp. em pombos (Zenaida auriculata) do Brasil

The aim of the present study was to detect Eimeria spp. in eared doves (Zenaida auriculata) from Brazil. Two hundred and fourteen birds were trap-capture in different regions of Londrina city, Paraná state, Southern Brazil. Fecal samples were collected, and DNA extraction was performed. A nested PCR based on the subunit I of the cytochrome c oxidase gene of the Eimeria mitochondrial genome was used to detect the DNA presence of this coccidian in eared dove feces. From 214 birds, 171 (79.9%) were positive for Eimeria spp. There was significantly difference of positivity between the site of capture. When analyzing the genders, the numbers of positive males were 84/103 (81.5%) and females 87/111 (78.4%). To the best of the authors' knowledge, this is the first study with molecular prevalence of Eimeria sp. in Z. auriculata. Further studies should be done to identify the species of Eimeria that infect eared doves Z. auriculata.(AU)

O objetivo do presente estudo foi detectar Eimeria spp. em pombos (Zenaida auriculata) do Brasil. Duzentos e quatorze pombos foram capturados em diferentes regiões da cidade de Londrina, estado do Paraná, Sul do Brasil. Amostras fecais foram coletadas e realizada a extração de DNA. Uma nested-PCR baseada na subunidade I do gene oxidase do citocromo c oxidase do genoma mitocondrial de Eimeria spp. foi utilizada para detectar a presença de DNA deste coccídeo nas amostras fecais dos pombos. Das 214 aves, 171 (79,9%) foram positivas para Eimeria spp. Houve uma diferença significativa de positividade entre o local de captura. Quando analisado o gênero, o número de machos positivos foi 84/103 (81,5%) e fêmeas 87/111 (78,4%). Para o conhecimento, este é o primeiro estudo com prevalência molecular de Eimeria spp. em Z. auriculata. Novos estudos devem ser conduzidos para identificar as espécies de Eimeria que infectam pombos Z. auriculata.(AU)

First study of Cryptosporidium spp. occurrence in eared doves (Zenaida auriculata).

Cryptosporidium is a protozoan parasite with a wide range of hosts, including humans. However, only a few Cryptosporidium species have been described in birds (C. meleagridis, C. baileyi, C. galli and C. avium). The aim of this study was to investigate the occurrence of Cryptosporidium spp. in feces of eared doves (Zenaida auriculata), followed by molecular characterization of the parasite. A total of 196 animals of both sexes were trap-captured; the animals were culled and the intestinal contents were collected for DNA extraction. After extraction, a nested-PCR (nPCR), which amplifies a fragment of the 18S rRNA gene of Cryptosporidium spp., was performed. The amplicons obtained were purified and sequenced. PCR analysis revealed that 30 animals (15.3%) were positive for Cryptosporidium spp. There was no significant sex-dependent enrichment of Cryptosporidium occurrence (p > 0.05). Only 15 out of the 30 positive samples were successfully sequenced and their species determined, of which, 13 (86.7%) and 2 (13.3%) were C. meleagridis and C. galli, respectively. Herein, we present for the first time a molecular characterization of Cryptosporidium from feces of eared doves (Z. auriculata) and propose that these birds are a potential source of C. meleagridis infection in humans.

First study of Cryptosporidium spp. occurrence in eared doves (Zenaida auriculata) / Primeiro estudo de ocorrência de Cryptosporidium spp. em pomba-de-bando (Zenaida auriculata)

Abstract Cryptosporidium is a protozoan parasite with a wide range of hosts, including humans. However, only a few Cryptosporidium species have been described in birds (C. meleagridis, C. baileyi, C. galli and C. avium). The aim of this study was to investigate the occurrence of Cryptosporidium spp. in feces of eared doves (Zenaida auriculata), followed by molecular characterization of the parasite. A total of 196 animals of both sexes were trap-captured; the animals were culled and the intestinal contents were collected for DNA extraction. After extraction, a nested-PCR (nPCR), which amplifies a fragment of the 18S rRNA gene of Cryptosporidium spp., was performed. The amplicons obtained were purified and sequenced. PCR analysis revealed that 30 animals (15.3%) were positive for Cryptosporidium spp. There was no significant sex-dependent enrichment of Cryptosporidium occurrence (p > 0.05). Only 15 out of the 30 positive samples were successfully sequenced and their species determined, of which, 13 (86.7%) and 2 (13.3%) were C. meleagridis and C. galli, respectively. Herein, we present for the first time a molecular characterization of Cryptosporidium from feces of eared doves (Z. auriculata) and propose that these birds are a potential source of C. meleagridis infection in humans.

Resumo Cryptosporidium é um protozoário com uma grande variedade de hospedeiros, incluindo os seres humanos. No entanto, poucas espécies têm sido descritas em aves (Cryptosporidium meleagridis, C. baileyi, C. galli e C. avium). O objetivo do presente estudo foi investigar a ocorrência de Cryptosporidium spp. em fezes de pombas-de-bando (Zenaida auriculata), e realizar a caracterização molecular dos isolados. Um total de 196 animais de ambos os sexos foram capturados, eutanasiados e o conteúdo intestinal recolhido para extração de DNA. Após a extração, realizou-se uma nested-PCR (nPCR), que amplifica um fragmento do gene 18S rRNA do Cryptosporidium spp.. Os fragmentos obtidos foram purificados e encaminhados para sequenciamento. Os resultados da n-PCR revelaram 30 animais (15.3%) positivos para Cryptosporidium spp.. Quanto ao sexo dos animais não foram observadas diferenças estatísticas significativas (p > 0.05). Somente 15 de 30 amostras positivas foram sequenciadas com sucesso e as espécies determinadas, das quais, 13 (86.7%) e 2 (13.3%) foram C. meleagridis e C. galli, respectivamente. Esse é o primeiro estudo com caracterização molecular de Cryptosporidium de fezes de pombas-de-bando (Z. auriculata), e propõe serem esses animais potenciais fonte de infecção de C. meleagridis para humanos.

First study of Cryptosporidium spp. occurrence in eared doves (Zenaida auriculata) / Primeiro estudo de ocorrência de Cryptosporidium spp. em pomba-de-bando (Zenaida auriculata)

Cryptosporidium is a protozoan parasite with a wide range of hosts, including humans. However, only a few Cryptosporidium species have been described in birds (C. meleagridis, C. baileyi, C. galli and C. avium). The aim of this study was to investigate the occurrence of Cryptosporidium spp. in feces of eared doves (Zenaida auriculata), followed by molecular characterization of the parasite. A total of 196 animals of both sexes were trap-captured; the animals were culled and the intestinal contents were collected for DNA extraction. After extraction, a nested-PCR (nPCR), which amplifies a fragment of the 18S rRNA gene of Cryptosporidium spp., was performed. The amplicons obtained were purified and sequenced. PCR analysis revealed that 30 animals (15.3%) were positive for Cryptosporidium spp. There was no significant sex-dependent enrichment of Cryptosporidium occurrence (p > 0.05). Only 15 out of the 30 positive samples were successfully sequenced and their species determined, of which, 13 (86.7%) and 2 (13.3%) were C. meleagridis and C. galli, respectively. Herein, we present for the first time a molecular characterization of Cryptosporidium from feces of eared doves (Z. auriculata) and propose that these birds are a potential source of C. meleagridis infection in humans.(AU)

Cryptosporidium é um protozoário com uma grande variedade de hospedeiros, incluindo os seres humanos. No entanto, poucas espécies têm sido descritas em aves (Cryptosporidium meleagridis, C. baileyi, C. galli e C. avium). O objetivo do presente estudo foi investigar a ocorrência de Cryptosporidium spp. em fezes de pombas-de-bando (Zenaida auriculata), e realizar a caracterização molecular dos isolados. Um total de 196 animais de ambos os sexos foram capturados, eutanasiados e o conteúdo intestinal recolhido para extração de DNA. Após a extração, realizou-se uma nested-PCR (nPCR), que amplifica um fragmento do gene 18S rRNA do Cryptosporidium spp.. Os fragmentos obtidos foram purificados e encaminhados para sequenciamento. Os resultados da n-PCR revelaram 30 animais (15.3%) positivos para Cryptosporidium spp.. Quanto ao sexo dos animais não foram observadas diferenças estatísticas significativas (p > 0.05). Somente 15 de 30 amostras positivas foram sequenciadas com sucesso e as espécies determinadas, das quais, 13 (86.7%) e 2 (13.3%) foram C. meleagridis e C. galli, respectivamente. Esse é o primeiro estudo com caracterização molecular de Cryptosporidium de fezes de pombas-de-bando (Z. auriculata), e propõe serem esses animais potenciais fonte de infecção de C. meleagridis para humanos.(AU)

Occurrence of antibodies against Neospora caninum in cattle and dogs from dairy farms from the central northern region of Paraná State / Ocorrência de anticorpos contra Neospora caninum em bovinos e cães oriundo de propriedades produtoras de leite do Norte Central do Estado do Paraná

Neosporosis is one of the principal causes of reproductive problems in cattle worldwide. The aim of this study was to evaluate the occurrence of anti-Neospora caninum antibodies in cattle and dogs from dairy farms from the central northern region of Paraná state. Blood samples with and without EDTA were collected from 400 cattle and 46 dogs from 20 properties. Nested polymerase chain reaction (n-PCR) was performed on whole blood samples and indirect immunofluorescence reaction (IFR) on the serum samples (after clot retraction). Cattle and dogs with titers ? 100 and ? 50, respectively, were considered positive. Anti-N. caninum was detected in 20,1% (80/400) of cattle, with titers ranging from 100 to 1600. The n-PCR presented only two cattle positives (0.5%). Anti-N. caninum was detected in 19,6% (9/46) of the dogs, with titers ranging from 50 to 6400. The occurrence of antibodies against N. caninum obtained in the present study was similar to those in studies performed in other regions of Paraná and Brazil. The probability of detecting parasitemia in epidemiological studies is a rare event.(AU)

A neosporose é uma das principais causas de abortamentos em bovinos no mundo todo. O objetivo do presente estudo foi avaliar a ocorrência de anticorpos contra Neospora caninum em soros de bovinos de leite e cães provenientes de propriedades da região centro norte do estado do Paraná. Sangue com e sem EDTA foram colhidos de 400 bovinos e de 46 cães provenientes de 20 propriedades. Para detecção de anticorpos contra N. caninum a Reação de Imunofluorescência Indireta (RIFI) foi realizada, e bovinos e cães foram considerados positivos quando apresentaram títulos ? 100 e ? 50, respectivamente. Anticorpos contra-N. caninum foram detectados em 20,1% (80/400) dos bovinos, cujos títulos variaram de 100 a 1600. A n-PCR apresentou apenas dois animais positivos (0,5%) para os bovinos. Dos 46 cães estudados 19,6% (9/46) foram considerados positivos na RIFI, com títulos variando de 50 a 6400. Os resultados permitem concluir que a ocorrência de anticorpos contra N. caninum em bovinos e cães na mesorregião centro norte do Paraná foram semelhantes aos observados em outras mesorregiões do Paraná. A n-PCR de sangue total revelou uma baixa positividade em bovinos e cães, mostrando que a probabilidade de se detectar parasitemia em estudos epidemiológicos é baixa.(AU)

Cryptosporidium occurrence in ruminants from the North Pioneer mesoregion of Paraná, Brazil.

The aim of this study was to investigate the occurrence of Cryptosporidium in cattle and sheep from the North Pioneer mesoregion of the state of Paraná. For this, 317 stool samples were collected from cattle and sheep on 16 properties in six municipalities in the North Pioneer mesoregion of Paraná. For detection of Cryptosporidium species, molecular analysis was performed using nested-PCR techniques targeting the 18S rRNA gene. Of the 37 beef cows and 115 calves analyzed, four (10.8%) and 14 (12.2%), respectively, were positive for Cryptosporidium. Of the 12 cows and 52 calves, one (8.3%) and 14 (26.9%), respectively, were positive for Cryptosporidium; and of the 42 ewes and 59 lambs, six (14.3%) and 12 (20.3%), respectively were positive for Cryptosporidium. Cattle (15.3%) and sheep (17.8%) were both susceptible to infection. All the properties of the municipalities of Assaí, Ibaiti and, Leópolis presented infected animals. The study showed that Cryptosporidium occurs in most municipalities assessed, that dairy calves had a higher risk (Odds Ratio=2,66, p-value=0,018) for infection than beef calves, and that sheep are just as susceptible to infection as are cattle, and that further Cryptosporidium studies are developed.

Cryptosporidium occurrence in ruminants from the North Pioneer mesoregion of Paraná, Brazil / Ocorrência de Cryptosporidium em ruminantes da mesorregião norte pioneiro do Estado do Paraná, Brasil

Abstract The aim of this study was to investigate the occurrence of Cryptosporidium in cattle and sheep from the North Pioneer mesoregion of the state of Paraná. For this, 317 stool samples were collected from cattle and sheep on 16 properties in six municipalities in the North Pioneer mesoregion of Paraná. For detection of Cryptosporidium species, molecular analysis was performed using nested-PCR techniques targeting the 18S rRNA gene. Of the 37 beef cows and 115 calves analyzed, four (10.8%) and 14 (12.2%), respectively, were positive for Cryptosporidium. Of the 12 cows and 52 calves, one (8.3%) and 14 (26.9%), respectively, were positive for Cryptosporidium; and of the 42 ewes and 59 lambs, six (14.3%) and 12 (20.3%), respectively were positive for Cryptosporidium. Cattle (15.3%) and sheep (17.8%) were both susceptible to infection. All the properties of the municipalities of Assaí, Ibaiti and, Leópolis presented infected animals. The study showed that Cryptosporidium occurs in most municipalities assessed, that dairy calves had a higher risk (Odds Ratio=2,66, p-value=0,018) for infection than beef calves, and that sheep are just as susceptible to infection as are cattle, and that further Cryptosporidium studies are developed.

Resumo O objetivo deste estudo foi investigar a ocorrência de Cryptosporidium em bovinos e ovinos da mesorregião norte pioneiro do Estado do Paraná. Para tanto, 317 amostras de fezes destes ruminantes foram colhidas de 16 propriedades de seis municípios do Norte Pioneiro do Paraná. Para detecção de Cryptosporidium spp foi realizada análise molecular pela Técnica de nested-PCR direcionada ao gene 18S rRNA. Das 37 vacas de corte e 115 bezerros de corte analisados, quatro (10,8%) e 14 (12,2%) foram respectivamente positivos para Cryptosporidium . Das 12 vacas e 52 bezerros de leite, um (8,3%) e 14 (26,9%) foram positivos para Cryptosporidium e das 42 ovelhas e 59 cordeiros avaliados, seis (14,3%) e 12 (20,3%) amostras estavam positivas para Cryptosporidium, respectivamente. Bovinos (15,3%) e ovinos (17,8%) foram igualmente suscetíveis à infecção. Todas as propriedades dos municípios de Assaí, Ibaiti e Leópolis apresentaram animais infectados. Este estudo demonstrou que Cryptosporidium ocorre na maioria dos municípios avaliados, sendo que os bezerros de leite apresentam maior risco (Razão de chances=2,66, p-value=0,018) à infecção que os bezerros de corte e que os ovinos são tão suscetíveis à infecção quanto os bovinos e por isso, estudos nesta espécie animal devem ser mais desenvolvidos.

Cryptosporidium occurrence in ruminants from the North Pioneer mesoregion of Paraná, Brazil / Ocorrência de Cryptosporidium em ruminantes da mesorregião norte pioneiro do Estado do Paraná, Brasil

The aim of this study was to investigate the occurrence of Cryptosporidium in cattle and sheep from the North Pioneer mesoregion of the state of Paraná. For this, 317 stool samples were collected from cattle and sheep on 16 properties in six municipalities in the North Pioneer mesoregion of Paraná. For detection of Cryptosporidium species, molecular analysis was performed using nested-PCR techniques targeting the 18S rRNA gene. Of the 37 beef cows and 115 calves analyzed, four (10.8%) and 14 (12.2%), respectively, were positive for Cryptosporidium. Of the 12 cows and 52 calves, one (8.3%) and 14 (26.9%), respectively, were positive for Cryptosporidium; and of the 42 ewes and 59 lambs, six (14.3%) and 12 (20.3%), respectively were positive for Cryptosporidium. Cattle (15.3%) and sheep (17.8%) were both susceptible to infection. All the properties of the municipalities of Assaí, Ibaiti and, Leópolis presented infected animals. The study showed that Cryptosporidium occurs in most municipalities assessed, that dairy calves had a higher risk (Odds Ratio=2,66, p-value=0,018) for infection than beef calves, and that sheep are just as susceptible to infection as are cattle, and that further Cryptosporidium studies are developed.(AU)

O objetivo deste estudo foi investigar a ocorrência de Cryptosporidium em bovinos e ovinos da mesorregião norte pioneiro do Estado do Paraná. Para tanto, 317 amostras de fezes destes ruminantes foram colhidas de 16 propriedades de seis municípios do Norte Pioneiro do Paraná. Para detecção de Cryptosporidium spp foi realizada análise molecular pela Técnica de nested-PCR direcionada ao gene 18S rRNA. Das 37 vacas de corte e 115 bezerros de corte analisados, quatro (10,8%) e 14 (12,2%) foram respectivamente positivos para Cryptosporidium . Das 12 vacas e 52 bezerros de leite, um (8,3%) e 14 (26,9%) foram positivos para Cryptosporidium e das 42 ovelhas e 59 cordeiros avaliados, seis (14,3%) e 12 (20,3%) amostras estavam positivas para Cryptosporidium, respectivamente. Bovinos (15,3%) e ovinos (17,8%) foram igualmente suscetíveis à infecção. Todas as propriedades dos municípios de Assaí, Ibaiti e Leópolis apresentaram animais infectados. Este estudo demonstrou que Cryptosporidium ocorre na maioria dos municípios avaliados, sendo que os bezerros de leite apresentam maior risco (Razão de chances=2,66, p-value=0,018) à infecção que os bezerros de corte e que os ovinos são tão suscetíveis à infecção quanto os bovinos e por isso, estudos nesta espécie animal devem ser mais desenvolvidos.(AU)

Prevalence of Eimeria spp. in calves from dairy farms in northern Paraná state, Brazil.

Bovine coccidiosis is a disease of major importance in cattle herds across the world. The disorder mainly affects young calves, and E. bovis and E. zuernii are considered the most pathogenic species of the genus, however, E. alabamensis have been described in grazing calves. In this study, the prevalence of Eimeria spp. was evaluated in calves on dairy farms in the northern region of the state of Paraná, Brazil. Four hundred calves on 44 dairy farms were tested for the presence of coccidian oocysts. The positives were re-examined and the oocysts were morphometrically analyzed for species identification. All the farms were contaminated and 205 animals (51.25%) presented Eimeria spp. oocysts. Among these, 146 animals (71.22%) were co-infected by two or more species of coccidia. Ten species of Eimeria were identified: E. bovis (in 30.25% of the positive samples), E. alabamensis (26.75%), E. zuernii (22.00%), E. ellipsoidalis (18.50%), E. auburnensis (13.75%), E. canadensis (8.00%), E. cylindrica (7.25%), E. subspherica (5.00%), E. bukidnonensis (3.00%) and E. brasiliensis (0.75%). This study demonstrates the high prevalence of Eimeria spp. in the northern region of Paraná, Brazil, and detection for the first time in our region the pathogenic species E. alabamensis.

First identification of Cryptosporidium parvum subtype IIaA20G1R1 in water buffalos (Bubalus bubalis).

Cryptosporidium can infect a wide variety of vertebrate animals, including mammals, birds, amphibians, reptiles, and fish. There are few molecular characterizations of Cryptosporidium isolated from water buffalo. Thus, the present study investigated the occurrence and molecular characterization of Cryptosporidium spp. in water buffalos by nested-PCR. Non-diarrheic feces were obtained from 122 water buffalo calves. All samples were tested by nested-PCR based on the 18S rRNA gene, after which positive samples were analyzed by RFLP and genetic sequencing. Sixteen fecal (13.1%) samples were positive, and RFLP showed that fifteen presented patterns consistent with C. ryanae and one with C. parvum. Sequencing of the gp60 gene from the C. parvum positive sample indicated the subtype IIaA20G1R1. This is the first identification of the IIaA20G1R1 subtype in water buffalos.