PESQUISA VETERINÁRIA BRASILEIRA

Abstract in English:

ABSTRACT.- Aversi-Ferreira R.A.G.M.F., Marin K.A., Carneiro e Silva F.O. & Aversi-Ferreira T.A.A. 2011. Comparative anatomy of the thigh nerves of Cebus libidinosus (Rylands et al., 2000). [Anatomia comparativa dos nervos da coxa de Cebus libidinosus (Rylands et al., 2000).] Pesquisa Veterinária Brasileira 31(3):261-266. Departamento de Enfermagem, Universidade Federal de Goiás, Av. Dr. Lamartine Pinto de Avelar 1120, Catalão, GO 75704-020, Brazil. E-mail: aversiferreira@gmail.com Non-human primates have constituted an important group among animals subjected to various studies. Ethological, evolutionary and paleontological studies have revealed changes in anatomical structures linked to the evolution of primates, considered in studies on the comparative anatomy between Cebus libidinosus and other neotropical monkeys or those from the Old World, and the detailed knowledge on their anatomy may represent an important factor for their preservation and protection when the animals are brought to veterinary clinics after accidents or illnesses. In terms of veterinary importance, sometimes these animals arrive in the veterinary medical clinics after accidents, needing surgery or clinical treatment, but the little data available on anatomy has impaired the correct proceedings. The main justification for studies on C. libidinosus, is due to little information about the anatomy related to C. libidinosus in Brazilian and worldwide scientific literature. In this study, the distribution, enervation and path of the femoral and sciatic nerves of the pelvic limb (thigh) of C. libidinosus were studied and these results were compared with literature on the anatomy of humans, chimpanzees and baboons. In general, the enervation model of the four primates is identical, but in specific terms, the differences in enervations indicate evolution convergence closer to the branch of baboons in the evolutionary tree, and these data corroborate other comparative studies in relation to the same primates to vessels, muscles and nerves. In conclusion, the nerve organization in the thigh of C. libidinosus is identical to baboon, chimpanzee and homo, but more similar to baboon. The specific differences found indicate an ancient phylogenic origin to C. libidinosus and baboons (data corroborated by other studies).

• Cebus libidinosus capuchin monkey thigh nerves macaco-prego nervos pélvicos

Abstract in Portuguese:

RESUMO.- Aversi-Ferreira R.A.G.M.F., Marin K.A., Carneiro e Silva F.O. & Aversi-Ferreira T.A.A. 2011. Comparative anatomy of the thigh nerves of Cebus libidinosus (Rylands et al., 2000). [Anatomia comparativa dos nervos da coxa de Cebus libidinosus (Rylands et al., 2000).] Pesquisa Veterinária Brasileira 31(3):261-266. Departamento de Enfermagem, Universidade Federal de Goiás, Av. Dr. Lamartine Pinto de Avelar 1120, Catalão, GO 75704-020, Brazil. E-mail: aversiferreira@gmail.com Primatas não-humanos têm constituído um importante grupo entre os animais submetidos a vários estudos. Estudos etológicos, evolutivos e paleontológicos revelaram alterações das estruturas anatômicas ligada à evolução dos primatas, considerado em estudos sobre a anatomia comparativa entre Cebus libidinosus e outros primatas neotropicais ou provenientes do Velho Mundo, e as modalidades de conhecimento sobre sua anatomia pode representar um fator importante para a sua preservação e proteção quando os animais são levados às clínicas veterinárias após acidentes ou doenças. Em termos de importância veterinária, ás vezes esses animais chegam na clínica médica veterinária após acidentes, necessitando de cirurgia ou tratamento clínico, mas os poucos dados disponíveis sobre a anatomia tem dificultado o procedimento correto. A principal justificativa para os estudos sobre C. libidinosus é devido a pouca informação sobre sua anatomia na literatura científica no Brasil e no mundo. Neste trabalho, a distribuição, inervação e os trajetos dos nervos femoral e isquiático do membro pélvico (coxa) de C. libidinosus foram estudados e os resultados foram comparados com a literatura sobre a anatomia dos seres humanos, chimpanzés e babuínos. Em geral (Anatomia Macroscópica), o modelo de inervação dos quatro primatas é idêntico, mas em termos específicos, as diferenças nas inervações indicam uma convergência evolucionária em direção à árvore genealógica dos babuínos, dados corroborados por outros estudos comparativos em relação aos mesmos primatas para vasos, músculos e nervos. Em conclusão, a organização dos nervos na coxa de C. libidinosus é idêntico ao do babuíno, chimpanzé e homo, mas mais semelhante ao babuíno. As diferenças específicas encontradas indicam uma origem filogenética antiga para C. libidinosus e babuínos (dados corroborados por outros estudos).

Abstract in English:

ABSTRACT.- Barbosa J.D., Oliveira C.M.C., Pinheiro C., Lopes C.T.A., Marquiore D., Brito M.F., Yamasaki E.M. & Tokarnia C.H. 2010. [Poisoning by Cestrum laevigatum (Solanaceae) in buffaloes.] Intoxicação por Cestrum laevigatum (Solanaceae) em bubalinos. Pesquisa Veterinária Brasileira 30(12):1049-1052. Central de Diagnóstico Veterinário, Universidade Federal do Pará, Rua Maximino Porpino da Silva 1000, Pirapora, Castanhal, PA 68743-080, Brazil. E-mail: diomedes@ufpa.br Based on the history and clinical and pathological data, as well as on inspection of the pastures, a mortality of buffaloes in the county of Itaguaí/RJ, Brazil, was diagnosed as poisoning by Cestrum laevigatum Schlecht., a plant of the Solanaceae family. The poisoning was reproduced in two buffaloes. Dried leaves of the shrub were administered by hand, in single doses corresponding to 20g/kg and 40g/kg of the fresh leaves, to four buffaloes of the Murrah breed. The dose corresponding to 40g/kg of the fresh leaves caused signs of poisoning, as apathy, anorexia, absence of rumen movements, dysmetria, excitement and aggressiveness, followed by death of the two buffaloes within 65 hours after administration. From the two buffaloes that received the corresponding dose of 20g/kg of the fresh plant, one presented clinical signs characterized mainly by decrease of the rumen movements, but recovered 97h22min after the administration; the other buffalo did not show symptoms of poisoning. Laboratory analyses for biochemical evaluation accused hepatic alterations. In one buffalo that died, the main macroscopic finding was an orange liver with a clear nutmeg appearance; in the second buffalo, the orange liver had no nutmeg appearance. Other alterations found in these two buffaloes were slight edema of the gall bladder wall, a slightly reddish mucous membrane of the abomasum, extensive echymoses in the endocard of the left ventricle and few petechiae in the endocard of the right ventricle; the abomasum content was slightly dry, and the large intestine had little and slightly dry contents wrapped by mucus. Histopatological examination revealed severe coagulative necrosis of the liver parenchyma in the centrolobular and intermediate lobular areas, with a halo of vacuolated hepatocytes at the periphery of the necrotic areas.

• Poisonous plants Cestrum laevigatum Solanaceae plant poisoning plantas tóxicas intoxicação por planta

Abstract in Portuguese:

RESUMO.- Barbosa J.D., Oliveira C.M.C., Pinheiro C., Lopes C.T.A., Marquiore D., Brito M.F., Yamasaki E.M. & Tokarnia C.H. 2010. [Poisoning by Cestrum laevigatum (Solanaceae) in buffaloes.] Intoxicação por Cestrum laevigatum (Solanaceae) em bubalinos. Pesquisa Veterinária Brasileira 30(12):1049-1052. Central de Diagnóstico Veterinário, Universidade Federal do Pará, Rua Maximino Porpino da Silva 1000, Pirapora, Castanhal, PA 68743-080, Brazil. E-mail: diomedes@ufpa.br Com base no histórico e em dados clínico-patológicos, bem como a inspeção das pastagens, foi estabelecido o diagnóstico de intoxicação por Cestrum laevigatum Schlecht. em uma mortandade de búfalos no município de Itaguaí, RJ. A intoxicação foi reproduzida em dois búfalos. Amostras de folhas dessecadas de C. laevigatum foram administradas manualmente por via oral a quatro bubalinos da raça Murrah, em doses únicas correspondentes a 20g/kg e 40g/kg da planta fresca. A dose correspondente a 40g/kg provocou o aparecimento dos sinais clínicos que consistiram principalmente em apatia, anorexia, ausência dos movimentos ruminais, dismetria, excitação e agressividade, e levaram à morte os dois animais em até 65 horas após a administração da planta. Dos outros dois bufalos que receberam a dose correspondente a de 20g/kg da planta fresca, um apresentou sinais clínicos, caracterizados principalmente por diminuição dos movimentos ruminais, e recuperou-se em 97h22min após a administração da planta; o outro não apresentou sinais clínicos. Os exames laboratoriais para avaliação bioquímica indicaram lesão hepática. Em um búfalo que morreu, as principais alterações macroscópicas foram fígado de cor alaranjada, com superfície externa e de corte com nítido aspecto de noz moscada; no outro, o fígado tinha a superfície externa e de corte de cor alaranjada, sem aspecto de noz moscada. Outras alterações encontradas nos dois búfalos foram leve edema da parede da vesícula biliar, endocárdio do ventrículo esquerdo com equimoses extensas e endocárdio do ventrículo direito com algumas petéquias; mucosa do abomaso levemente avermelhada e conteúdo levemente ressecado; intestino grosso com pouco conteúdo, levemente ressecado e envolto por muco. Os exames histopatológicos revelaram no fígado, acentuada necrose de coagulação dos hepatócitos nas zonas centrais e intermediárias dos lóbulos. Na periferia dessas regiões necrosadas observou-se um halo de hepatócitos com vacuolização.

Abstract in English:

ABSTRACT.- Teixeira L.V., Lopes S.T.A., Martins D.B., França R.T. & Fighera R.A. 2010. [Fine-needle aspiration cytology as a sampling method for histopathology in canine osteosarcoma.] Punção aspirativa por agulha fina como método de coleta de material para a histopatologia no osteossarcoma canino. Pesquisa Veterinária Brasileira 30(2):145-148. Laboratório de Análises Clínicas Veterinárias, Departamento de Clínica de Pequenos Animais, Hospital Veterinário Universitário, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil. E-mail: luciele.sm@gmail.com Cytopathologic and histopathologic tests are important to obtain a definitive diagnosis of osteosarcoma. The sample for cytopathological exam is collected through fine-needle aspiration cytology (FNA). On the other hand, histopathological exams need a larger sample that is usually obtained by incisional biopsy. The objective of this article is to develop a FNA technique to biopsy and evaluate histopatologically samples of dogs with suspected osteosarcoma. Two FNS samples were collected from 12 such dogs. Samples obtained in the first procedure were examined cytologically. The material sampled at the second biopsy was fixed in 10% formalin and submitted to histopathological analysis. Four out of the 12 samples (33.3%) examined by the herein proposed method were diagnosed as osteosarcoma. These results indicate a possible adaptation of FNA for histopathological examination.

• Osteossarcoma citopatologia

Abstract in Portuguese:

RESUMO.- Teixeira L.V., Lopes S.T.A., Martins D.B., França R.T. & Fighera R.A. 2010. [Fine-needle aspiration cytology as a sampling method for histopathology in canine osteosarcoma.] Punção aspirativa por agulha fina como método de coleta de material para a histopatologia no osteossarcoma canino. Pesquisa Veterinária Brasileira 30(2):145-148. Laboratório de Análises Clínicas Veterinárias, Departamento de Clínica de Pequenos Animais, Hospital Veterinário Universitário, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil. E-mail: luciele.sm@gmail.com Para a obtenção do diagnóstico definitivo do osteossarcoma realizam-se exames citopatológico e histopatológico. O material para exame citopatológico é coletado através de punção aspirativa por agulha fina (PAAF), já para a realização do exame histopatológico é necessário uma amostra de tamanho maior, geralmente conseguida através de biópsia incisional. Este trabalho tem como objetivo desenvolver uma técnica de coleta de material em cães com suspeita de osteossarcoma através de PAAF para a realização de exame histopatológico. Foram coletadas duas amostras de 12 cães suspeitos de osteossarcoma por PAAF. O material obtido pela primeira coleta foi utilizado para confirmar o diagnóstico através do exame citopatológico, enquanto que o material oriundo da segunda coleta foi fixado em formol a 10% para a análise histopatológica. Quatro das 12 amostras (33,3%) avaliadas histopatologicamente pela metodologia proposta obtiveram também o diagnóstico de osteossarcoma. Esses resultados apontam para uma possível adequação da técnica de coleta de material por PAAF para exame histopatológico.

Abstract in English:

ABSTRACT.- Ramos C.A.N., Araújo F.R., Souza I.I.F., Guedes Jr D.S., Oliveira R.H.M., Farias T.A., Oliveira J.B., Alves L.C. & Faustino M.A.G. 2010. [Comparison between several antigens for diagnosis of Anaplasma marginale by ELISA.] Comparação entre diversos antígenos para o diagnóstico de Anaplasma marginale por ELISA. Pesquisa Veterinária Brasileira 30(1):37-41. Laboratório de Doenças Parasitárias, Departamento de Medicina Veterinária, Universidade Federal Rural de Pernambuco, Recife, PE 52171-900, Brazil. E-mail: carlosanramos@yahoo.com.br Bovine anaplasmosis is a major disease in tropical and subtropical regions of the world by determine economical loss due mortality and productive reduction. The disease is caused by Anaplasma marginale, an intraerythrocytic rickettsia whose control requires, besides an efficient vaccine, the accurate identification of chronically infected cattle. Although the existence of diverse methods of diagnosis of this rickettsia, the serological methods, in particular the enzyme immunosorbent assays (ELISAs), are the most used due to its versatility and practice. However, due to the high number of antigens currently available, an evaluation becomes necessary to define which antigens present the better performance in the diagnosis of anaplasmosis. Sera from cattle positive or negative to A. marginale by PCR, and sera from cattle proceeding from Brazil and Costa Rica, were tested by ELISAs based in recombinant MSP1a, MSP2, and MSP5, a pool of the three recombinant proteins, and initial body lisate antigen (CI). Using sera from A. marginale positive cattle by PCR, the highest sensitivity was shown by CI ELISA. Nevertheless, the highest specificity, with sera from negative cattle by PCR, was shown by recombinants ELISAs. The percentiles of positive cattle from Brazil and Costa Rica were higher with CI ELISA. Reasons for such differences were discussed.

• Anaplasma marginale

Abstract in Portuguese:

RESUMO.- Ramos C.A.N., Araújo F.R., Souza I.I.F., Guedes Jr D.S., Oliveira R.H.M., Farias T.A., Oliveira J.B., Alves L.C. & Faustino M.A.G. 2010. [Comparison between several antigens for diagnosis of Anaplasma marginale by ELISA.] Comparação entre diversos antígenos para o diagnóstico de Anaplasma marginale por ELISA. Pesquisa Veterinária Brasileira 30(1):37-41. Laboratório de Doenças Parasitárias, Departamento de Medicina Veterinária, Universidade Federal Rural de Pernambuco, Recife, PE 52171-900, Brazil. E-mail: carlosanramos@yahoo.com.br Anaplasmose bovina é uma doença com grande importância nas regiões tropicais e subtropicais do mundo por determinar perdas econômicas devido à mortalidade e redução da produtividade. É causada por Anaplasma marginale, uma riquétsia intraeritrocítica obrigatória cujo controle requer, além de uma vacina eficiente, uma acurada identificação de bovinos cronicamente infectados. Apesar de existirem atualmente diversos métodos de diagnóstico dessa riquétsia, os métodos sorológicos, em particular o ensaio de imunoadsorção enzimática–ELISAs, são os mais utilizados devido à sua versatilidade e praticidade. No entanto, devido ao grande número de antígenos disponíveis, atualmente torna-se necessária uma avaliação para definir quais antígenos apresentam um melhor desempenho no diagnóstico da anaplasmose. Soros de bovinos positivos e negativos para A. marginale por PCR, e soros de animais provenientes do Brasil e Costa Rica, foram testados em ELISAs baseados em MSP1a, MSP2 e MSP5 recombinantes, um pool das três proteínas recombinantes, e antígeno de lisado de corpúsculos iniciais da riquétsia (CI). Utilizando soro de bovinos positivos para A. marginale por PCR, uma maior sensibilidade foi observada no ELISA CI. No entanto, uma maior especificidade, com soro de bovinos negativos a PCR, foi observada com os ELISAs recombinantes. O porcentual de bovinos positivos do Brasil e Costa Rica foi maior com ELISA CI. Razões para essas diferenças são discutidas.

Abstract in English:

ABSTRACT.- Fonteque J.H., Kohayagawa A., Mattoso C.R.S., Lopes S.T.A., Paes P.R.O., Cassetari M.L. & Langoni H. 2010. [Electrophoretic profile and concentration of immunoglobulins G (IgG) in blood serum of Saanen goats with experimental mastitis induced by Staphylococcus aureus suplemented with vitamin E.] Perfil eletroforético e concentração de imunoglobulinas G (IgG) do soro sanguíneo de cabras Saanen com mastite experimental induzida por Staphylococcus aureus suplementadas com vitamina E. Pesquisa Veterinária Brasileira 30(1):79-86. Departamento de Medicina Veterinária, Hospital de Clínica Veterinária, Centro de Ciências Agroveterinárias, Universidade do Es-tado de Santa Catarina, Lages, SC 88520-000, Brazil. E-mail: fonteque@cav.udesc.br The objective was to evaluate the electrophoretic profile of proteins and serum concentration of immunoglobulin G (IgG) in Saanen goats with mastitis experimentally induced by Staphylococcus aureus (dl-a-tocopherol acetated). 14 adult goats, (supplemented with vitamin E DL-a-tocopherol) primiparous pregnant, seronegative for caprine arthritis encephalitis (CAEV), clinically healthy, were divided into two groups of seven animals: Not supplemented group (G1) and group supplemented with 2.000 UI of DL-a-tocopherol (G2 Vit E), by intramuscular injection on the day of the parturition and seven days later. At the 9th day after delivery 300 UFCs of the S. aureus ATCC 225923 strain were inoculated into the left half of the mammary gland of each animal. The mastitis was determined through collection of milk samples for evidence of infection by means of bacteriological examination, somatic cell count (SCC) and California Mastitis Test (CMT). Then samples were collected after 12, 24, 48 and 72 hours, antimicrobial intra-mammary gland treatment was initiated, with new evaluation 48 hours after treatment. The electrophoretic profile of serum protein of the goats, showed five fractions, as follows: albumin and globulin (a, b1, b2 e g-globulin). There was an increase in the production of g-globulin and lower production of b2-globulin fraction 12 hours after infection, and faster decrease in the supplemented group, showing the influence of vitamin E in the production of acute phase proteins. There was no influence of vitamin E in the serum concentration of immunoglobulin G (IgG) in supplemented animals. The supplementation with vitamin E increased the concentration of immunoglobulin and decreased the production of acute phase proteins, probably the antioxidant effect minimizing the tissue injury during the inflammatory process in the mammary gland.

• Staphylococcus aureus mastitis vitamin E

Abstract in Portuguese:

RESUMO.- Fonteque J.H., Kohayagawa A., Mattoso C.R.S., Lopes S.T.A., Paes P.R.O., Cassetari M.L. & Langoni H. 2010. [Electrophoretic profile and concentration of immunoglobulins G (IgG) in blood serum of Saanen goats with experimental mastitis induced by Staphylococcus aureus suplemented with vitamin E.] Perfil eletroforético e concentração de imunoglobulinas G (IgG) do soro sanguíneo de cabras Saanen com mastite experimental induzida por Staphylococcus aureus suplementadas com vitamina E. Pesquisa Veterinária Brasileira 30(1):79-86. Departamento de Medicina Veterinária, Hospital de Clínica Veterinária, Centro de Ciências Agroveterinárias, Universidade do Es-tado de Santa Catarina, Lages, SC 88520-000, Brazil. E-mail: fonteque@cav.udesc.br O objetivo do trabalho foi avaliar o perfil eletroforético das proteínas e a concentração sérica de imunoglobulina G (IgG) em cabras da raça Saanen com mastite induzida experimentalmente por Staphylococcus aureus e suplementadas com vitamina E (acetato de dl-a-tocoferol). Utilizaram-se 14 cabras adultas, gestantes, primíparas, com sorologia negativa para Artrite Encefalite Caprina (CAEV), clinicamente sadias, divididas em dois grupos experimentais de sete animais. Grupo não suplementado (G1) e grupo suplementado com 2.000 U.I. de acetato de dl-a-tocoferol (G2 Vit E) via intramuscular no dia do parto e sete dias após o parto. Ao nono dia do pós-parto foram inoculados 300 UFCs da cepa de S. aureus ATCC 225923, na metade esquerda da glândula mamária de cada animal. A mastite foi determinada pela colheita das amostras de leite para a comprovação da infecção, por meio de exames bacteriológicos, contagem de células somáticas (CCS) e California Mastitis Test (CMT), a partir deste momento foram efetuadas colheitas às 12, 24, 48 e 72 horas, sendo posteriormente instituído o tratamento intramamário com antimicrobiano e nova avaliação 48 horas após o tratamento. O perfil eletroforético em gel de agarose das proteínas séricas das cabras, apresentaram cinco frações, sendo: albumina e globulinas (a, b1, b2 e g). Houve aumento na produção de g-globulina e menor produção da fração b2-globulina 12 horas após a infecção, com os valores reduzindo mais rapidamente no grupo suplementado, evidenciando a influência da vitamina E na diminuição da produção das proteínas de fase aguda. Não houve influência da vitamina E na concentração sérica de imunoglobulina G (IgG) nos animais suplementados. A suplementação com vitamina E aumentou a concentração de imunoglobulinas e diminuiu a produção de proteínas de fase aguda, provavelmente pelo efeito antioxidante minimizando a lesão tecidual durante o processo inflamatório localizado na glândula mamária.

Abstract in English:

ABSTRACT.- Nakazato G., Campos T.A., Stehling E.G., Brocchi M. & Silveira W.D. 2009. Virulence factors of avian pathogenic Escherichia coli (APEC). Pesquisa Veterinária Brasileira 29(7):479-486. Departamento de Microbiologia e Imunologia, Instituto de Biologia, Universidade Estadual de Campinas (Unicamp), Cidade Universitária Zeferino Vaz s/n, Cx. Postal 6109, Barão Geraldo, Campinas, SP 13081-862, Brazil. E-mail: wds@unicamp.br Avian pathogenic Escherichia coli (APEC) strains cause a great diversity of diseases in birds and are responsible for great economic losses in the avian industry. To date, several studies have been carried out to better understand the APEC pathogenesis for a possible development of tools which could prevent the economics losses caused by these strains. This review discusses the virulence factors described do date to be expressed by these strains and the advances made to understand and identify virulence determinants present in APEC.

• APEC avian Escherichia coli virulence factors

Abstract in Portuguese:

RESUMO.- Nakazato G., Campos T.A., Stehling E.G., Brocchi M. & Silveira W.D. 2009. Virulence factors of avian pathogenic Escherichia coli (APEC). [Fatores de virulência de Escherichia coli aviária patogênica (APEC).] Pesquisa Veterinária Brasileira 29(7):479-486. Departamento de Microbiologia e Imunologia, Instituto de Biologia, Universidade Estadual de Campinas (Unicamp), Cidade Universitária Zeferino Vaz s/n, Cx. Postal 6109, Barão Geraldo, Campinas, SP 13081-862, Brazil. E-mail: wds@unicamp.br Linhagens de Escherichia coli patogênicas para aves (APEC) causam uma grande diversidade de doenças em aves e são responsáveis por grandes prejuízos na indústria aviária. Nos últimos anos, vários estudos foram realizados para melhor entender a patogênese de linhagens APEC e para desenvolver ferramentas que podem prevenir as perdas econômicas causadas por estas linhagens. Esta revisão discute os fatores de virulência descritos nestas linhagens e os avanços realizados para entender e identificar os determinantes de virulência presentes em APEC.

Abstract in English:

ABSTRACT.- Campos T.A., Nakazato G., Stehling E.G., Brocchi M. & Silveira W.D. 2008. Clonal study of avian Escherichia coli strains by fliC conserved-DNA-sequence regions analysis. Pesquisa Veterinária Brasileira 28(10):508-514. Departamento de Microbiologia e Imunologia, Instituto de Biologia, Cx. Postal 6109, Universidade Estadual de Campinas, Cidade Universitária Zeferino Vaz s/n, Barão Geraldo, Campinas, SP 3081-862, Brazil. *Corresponding author: wds@unicamp.br The clonal relationship among avian Escherichia coli strains and their genetic proximity with human pathogenic E. coli, Salmonela enterica, Yersinia enterocolitica and Proteus mirabilis, was determined by the DNA sequencing of the conserved 5’ and 3’regions fliC gene (flagellin encoded gene). Among 30 commensal avian E. coli strains and 49 pathogenic avian E. coli strains (APEC), 24 commensal and 39 APEC strains harbored fliC gene with fragments size varying from 670bp to 1,900bp. The comparative analysis of these regions allowed the construction of a dendrogram of similarity possessing two main clusters: one compounded mainly by APEC strains and by H-antigens from human E. coli, and another one compounded by commensal avian E. coli strains, S. enterica, and by other H-antigens from human E. coli. Overall, this work demonstrated that fliC conserved regions may be associated with pathogenic clones of APEC strains, and also shows a great similarity among APEC and H-antigens of E. coli strains isolated from humans. These data, can add evidence that APEC strains can exhibit a zoonotic risk.

• APEC clonal analysis fliC gene

Abstract in Portuguese:

ABSTRACT.- Campos T.A., Nakazato G., Stehling E.G., Brocchi M. & Silveira W.D. 2008. Clonal study of avian Escherichia coli strains by fliC conserved-DNA-sequence regions analysis. Pesquisa Veterinária Brasileira 28(10):508-514. Departamento de Microbiologia e Imunologia, Instituto de Biologia, Cx. Postal 6109, Universidade Estadual de Campinas, Cidade Universitária Zeferino Vaz s/n, Barão Geraldo, Campinas, SP 3081-862, Brazil. *Corresponding author: wds@unicamp.br The clonal relationship among avian Escherichia coli strains and their genetic proximity with human pathogenic E. coli, Salmonela enterica, Yersinia enterocolitica and Proteus mirabilis, was determined by the DNA sequencing of the conserved 5’ and 3’regions fliC gene (flagellin encoded gene). Among 30 commensal avian E. coli strains and 49 pathogenic avian E. coli strains (APEC), 24 commensal and 39 APEC strains harbored fliC gene with fragments size varying from 670bp to 1,900bp. The comparative analysis of these regions allowed the construction of a dendrogram of similarity possessing two main clusters: one compounded mainly by APEC strains and by H-antigens from human E. coli, and another one compounded by commensal avian E. coli strains, S. enterica, and by other H-antigens from human E. coli. Overall, this work demonstrated that fliC conserved regions may be associated with pathogenic clones of APEC strains, and also shows a great similarity among APEC and H-antigens of E. coli strains isolated from humans. These data, can add evidence that APEC strains can exhibit a zoonotic risk.

Abstract in English:

ABSTRACT.- Campos T.A., Lago J.C., Nakazato G., Stehling E.G., Brocchi M., Castro A.F.P. & Silveira W.D. 2008. Occurrence of virulence-related sequences and phylogenetic analysis of commensal and pathogenic avian Escherichia coli strains (APEC). Pesquisa Veterinária Brasileira 28(10):533-540. Departamento de Microbiologia e Immunologia, Instituto de Biologia, Unicamp, Cidade Universitrária Zeferino Vaz s/n, Campinas, SP 13081-862, Brazil. E-mail: wds@unicamp.br The presence of iron uptake (irp-2, fyuA, sitA, fepC, iucA), adhesion (iha, lpfAO157/O141, lpfAO157/O154, efa, toxB) and invasion (inv, ial-related DNA sequences and assignment to the four main Escherichia coli phylogenetic groups (A, B1, B2 e D) were determined in 30 commensal E. coli strains isolated from healthy chickens and in 49 APEC strains isolated from chickens presenting clinical signs of septicemia (n=24) swollen head syndrome (n=14) and omphalitis (n=11) by PCR. None of the strains presented DNA sequences related to the inv, ial, efa, and toxB genes. DNA sequences related to lpfAO157/O154, iucA, fepC, and irp-2 genes were significantly found among pathogenic strains, where iucA gene was associated with septicemia and swollen head syndrome and fepC and irp-2 genes were associated with swollen head syndrome strains. Phylogenetic typing showed that commensal and omphalitis strains belonged mainly to phylogenetic Group A and swollen head syndrome to phylogenetic Group D. Septicemic strains were assigned in phylogenetic Groups A and D. These data could suggest that clonal lineage of septicemic APEC strains have a multiple ancestor origin; one from a pathogenic bacteria ancestor and other from a non-pathogenic ancestor that evolved by the acquisition of virulence related sequences through horizontal gene transfer. Swollen head syndrome may constitute a pathogenic clonal group. By the other side, omphalitis strains probably constitute a non-pathogenic clonal group, and could cause omphalitis as an opportunistic infection. The sharing of virulence related sequences by human pathogenic E. coli and APEC strains could indicate that APEC strains could be a source of virulence genes to human strains and could represent a zoonotic risk.

• Avian colibacillosis Escherichia coli APEC virulence related-genes pathogenic clones

Abstract in Portuguese:

ABSTRACT.- Campos T.A., Lago J.C., Nakazato G., Stehling E.G., Brocchi M., Castro A.F.P. & Silveira W.D. 2008. Occurrence of virulence-related sequences and phylogenetic analysis of commensal and pathogenic avian Escherichia coli strains (APEC). Pesquisa Veterinária Brasileira 28(10):533-540. Departamento de Microbiologia e Immunologia, Instituto de Biologia, Unicamp, Cidade Universitrária Zeferino Vaz s/n, Campinas, SP 13081-862, Brazil. E-mail: wds@unicamp.br The presence of iron uptake (irp-2, fyuA, sitA, fepC, iucA), adhesion (iha, lpfAO157/O141, lpfAO157/O154, efa, toxB) and invasion (inv, ial-related DNA sequences and assignment to the four main Escherichia coli phylogenetic groups (A, B1, B2 e D) were determined in 30 commensal E. coli strains isolated from healthy chickens and in 49 APEC strains isolated from chickens presenting clinical signs of septicemia (n=24) swollen head syndrome (n=14) and omphalitis (n=11) by PCR. None of the strains presented DNA sequences related to the inv, ial, efa, and toxB genes. DNA sequences related to lpfAO157/O154, iucA, fepC, and irp-2 genes were significantly found among pathogenic strains, where iucA gene was associated with septicemia and swollen head syndrome and fepC and irp-2 genes were associated with swollen head syndrome strains. Phylogenetic typing showed that commensal and omphalitis strains belonged mainly to phylogenetic Group A and swollen head syndrome to phylogenetic Group D. Septicemic strains were assigned in phylogenetic Groups A and D. These data could suggest that clonal lineage of septicemic APEC strains have a multiple ancestor origin; one from a pathogenic bacteria ancestor and other from a non-pathogenic ancestor that evolved by the acquisition of virulence related sequences through horizontal gene transfer. Swollen head syndrome may constitute a pathogenic clonal group. By the other side, omphalitis strains probably constitute a non-pathogenic clonal group, and could cause omphalitis as an opportunistic infection. The sharing of virulence related sequences by human pathogenic E. coli and APEC strains could indicate that APEC strains could be a source of virulence genes to human strains and could represent a zoonotic risk.

Abstract in English:

ABSTRACT.- Pissinatti T.A., Pissinatti A. & Burity C.H.F. 2007. Myocardial stereology in captive Callithrix kuhlii (Callitrichidae, Primates): healthy animals versus animals affected by wasting marmoset syndrome (WMS). Pesquisa Veterinária Brasileira 27(2):75-79. Setor de Morfologia, IBC, Universidade do Grande Rio (Unigranrio), Rua Prof. José de Souza Herdy 1160, uque de Caxias, RJ 25071-202, Brazil. E-mail: cburity@unigranrio.com.br This study comprised 12 hearts of Wied´s black-tufted-ear marmoset, Callithrix kuhlii (Coimbra-Filho 1985), 6 with Wasting Marmoset Syndrome (WMS) and 6 non-affected. Biometry was performed after death. After necropsy, the hearts were weighed, dissected, fixed in 10% formalin solution (pH 7.2), and processed for optical microscopy at 5µm sections stained with Haematoxylin-Eosin. Quantitative analysis was performed by stereological techniques. The statistical differences between the biometrical and stereological parameters were assessed by the Mann-Whitney test. The morphometric results showed that WMS causes a significant reduction in body and cardiac weights, and also in the volume density of vessels in those animals. Further studies are necessary to understand some of the results shown here.

• Wasting marmoset syndrome myocardium stereology Callithrix Callitrichidae

Abstract in Portuguese:

ABSTRACT.- Pissinatti T.A., Pissinatti A. & Burity C.H.F. 2007. Myocardial stereology in captive Callithrix kuhlii (Callitrichidae, Primates): healthy animals versus animals affected by wasting marmoset syndrome (WMS). Pesquisa Veterinária Brasileira 27(2):75-79. Setor de Morfologia, IBC, Universidade do Grande Rio (Unigranrio), Rua Prof. José de Souza Herdy 1160, uque de Caxias, RJ 25071-202, Brazil. E-mail: cburity@unigranrio.com.br This study comprised 12 hearts of Wied´s black-tufted-ear marmoset, Callithrix kuhlii (Coimbra-Filho 1985), 6 with Wasting Marmoset Syndrome (WMS) and 6 non-affected. Biometry was performed after death. After necropsy, the hearts were weighed, dissected, fixed in 10% formalin solution (pH 7.2), and processed for optical microscopy at 5µm sections stained with Haematoxylin-Eosin. Quantitative analysis was performed by stereological techniques. The statistical differences between the biometrical and stereological parameters were assessed by the Mann-Whitney test. The morphometric results showed that WMS causes a significant reduction in body and cardiac weights, and also in the volume density of vessels in those animals. Further studies are necessary to understand some of the results shown here.

Abstract in English:

Abstract.- Brocchi M., Ferreira A., Lancellotti M., Stehling E.G., Campos T.A., Nakazato G., Pestana de Castro A.F. & Silveira W.D. 2006. Typing of avian pathogenic Escherichia coli strains by REP-PCR. Pesquisa Veterinária Brasileira 26(2):69-73. Departamento de Microbiologia e Imunologia, Instituto de Biologia, Universidade de Campinas, Cx. Postal 6109, Campinas, SP 13081-862, Brazil. E-mail: wds@unicamp.br In the present study the repetitive extragenic palindromic (REP) polymerase chain reaction (PCR) technique was used to establish the clonal variability of 49 avian Escherichia coli (APEC) strains isolated from different outbreak cases of septicemia (n=24), swollen head syndrome (n=14) and omphalitis (n=11). Thirty commensal strains isolated from poultry with no signs of these illnesses were used as control strains. The purified DNA of these strains produced electrophoretic profiles ranging from 0 to 15 bands with molecular sizes varying from 100 bp to 6.1 kb, allowing the grouping of the 79 strains into a dendrogram containing 49 REP-types. Although REP-PCR showed good discriminating power it was not able to group the strains either into specific pathogenic classes or to differentiate between pathogenic and non-pathogenic strains. On the contrary, we recently demonstrated that other techniques such as ERIC-PCR and isoenzyme profiles are appropriate to discriminate between commensal and APEC strains and also to group these strains into specific pathogenic classes. In conclusion, REP-PCR seems to be a technique neither efficient nor universal for APEC strains discrimination. However, the population clonal structure obtained with the use of REP-PCR must not be ignored particularly if one takes into account that the APEC pathogenic mechanisms are not completely understood yet.

• Avian Escherichia coli typing REP-PCR.

Abstract in Portuguese:

Abstract.- Brocchi M., Ferreira A., Lancellotti M., Stehling E.G., Campos T.A., Nakazato G., Pestana de Castro A.F. & Silveira W.D. 2006. Typing of avian pathogenic Escherichia coli strains by REP-PCR. Pesquisa Veterinária Brasileira 26(2):69-73. Departamento de Microbiologia e Imunologia, Instituto de Biologia, Universidade de Campinas, Cx. Postal 6109, Campinas, SP 13081-862, Brazil. E-mail: wds@unicamp.br In the present study the repetitive extragenic palindromic (REP) polymerase chain reaction (PCR) technique was used to establish the clonal variability of 49 avian Escherichia coli (APEC) strains isolated from different outbreak cases of septicemia (n=24), swollen head syndrome (n=14) and omphalitis (n=11). Thirty commensal strains isolated from poultry with no signs of these illnesses were used as control strains. The purified DNA of these strains produced electrophoretic profiles ranging from 0 to 15 bands with molecular sizes varying from 100 bp to 6.1 kb, allowing the grouping of the 79 strains into a dendrogram containing 49 REP-types. Although REP-PCR showed good discriminating power it was not able to group the strains either into specific pathogenic classes or to differentiate between pathogenic and non-pathogenic strains. On the contrary, we recently demonstrated that other techniques such as ERIC-PCR and isoenzyme profiles are appropriate to discriminate between commensal and APEC strains and also to group these strains into specific pathogenic classes. In conclusion, REP-PCR seems to be a technique neither efficient nor universal for APEC strains discrimination. However, the population clonal structure obtained with the use of REP-PCR must not be ignored particularly if one takes into account that the APEC pathogenic mechanisms are not completely understood yet.