PESQUISA VETERINÁRIA BRASILEIRA

Abstract in English:

Penatti M.P.A., Silva A.S., Valadares G.F. & Leite D.S. 2005. Occurrence of F42 colonization factor in Escherichia coli strains isolated from piglets with diarrhea. Pesquisa Veterinária Brasileira 25(1):31-33. Depto Microbiologia e Imunologia, Instituto de Biologia, Unicamp, Campinas, SP 13081-970, Brazil. E-mail: domingos@unicamp.br The objective of this study was to determine the presence of the colonization factor F42 in 168 strains of Escherichia coli isolated from diarrheic stools of newborn piglets. The presence of F42 in 12 (7.1%) strains was detected with the agglutination test. Through the Polymerase Chain Reaction (PCR) of F42 positive strains, gene encoding enterotoxins (ST-I, ST-II, LT-I and LT-II) were detected. The finding of ST-I/ST-II genes in 50% of the strains, ST-I (16%) and ST-II (25%) indicates a strong association of FC F42 with heat-stable enterotoxins (91%). In contrast, the thermolabile enterotoxin (LT-I and LT-II) genes were not detected. Serogroups of F42 positive strains were determined, serogroup O8 being the most prevalent (41,7%). Other serogroups, as there are O9, O11, O18, O32, O35, O98 and O101, were also identified. Thus, FC F42 was confirmed as an additional factor of virulence in the pathogenesis of porcine colibacillosis.

• Escherichia coli F42 piglets fimbriae diarrhea PCR.

Abstract in Portuguese:

Penatti M.P.A., Silva A.S., Valadares G.F. & Leite D.S. 2005. Occurrence of F42 colonization factor in Escherichia coli strains isolated from piglets with diarrhea. Pesquisa Veterinária Brasileira 25(1):31-33. Depto Microbiologia e Imunologia, Instituto de Biologia, Unicamp, Campinas, SP 13081-970, Brazil. E-mail: domingos@unicamp.br The objective of this study was to determine the presence of the colonization factor F42 in 168 strains of Escherichia coli isolated from diarrheic stools of newborn piglets. The presence of F42 in 12 (7.1%) strains was detected with the agglutination test. Through the Polymerase Chain Reaction (PCR) of F42 positive strains, gene encoding enterotoxins (ST-I, ST-II, LT-I and LT-II) were detected. The finding of ST-I/ST-II genes in 50% of the strains, ST-I (16%) and ST-II (25%) indicates a strong association of FC F42 with heat-stable enterotoxins (91%). In contrast, the thermolabile enterotoxin (LT-I and LT-II) genes were not detected. Serogroups of F42 positive strains were determined, serogroup O8 being the most prevalent (41,7%). Other serogroups, as there are O9, O11, O18, O32, O35, O98 and O101, were also identified. Thus, FC F42 was confirmed as an additional factor of virulence in the pathogenesis of porcine colibacillosis.

Abstract in English:

França T.N., Peixoto P.V., Brito M.F., Driemeier D., Mores N. & Zanella J. 2005. [Outbreak of Circovirosis (Porcine Postweaning Multisystemic Wasting Syndrome) in the state of Rio de Janeiro, Brazil.] Surto de Circovirose (Síndrome Definhante Multissistêmica de Suínos Desmamados) no estado do Rio de Janeiro. Pesquisa Veterinária Brasileira 25(1):39-53. Universidade Estácio de Sá, Curso de Medicina Veterinária, Disciplina de Anatomia Patológica, Estrada Boca do Mato 850, Vargem Pequena, RJ 22783-320, Brazil. E-mail: ticianaf@uol.com.br The first outbreak of Postweaning Multisystemic Wasting Syndrome (PMWS) in swine, which occurred in southeastern Brazil, in the state of Rio de Janeiro, is described. The disease, which affects mainly weaned about 4 month-old pigs, caused the death of at least 14 animals. The property, where the outbreak occurred, had inadequate sanitary and management conditions. Clinically the disease was characterized by wasting, poor development, cough, tachypnoea, dispnoea, diarrhoea, ataxia, tremors after stimulation, decubitus and convulsions. The course of the disease was acute or subacute. The most important post-mortem findings were enlarged lymphnodes, non-collapsed lungs, with consolidated areas mainly in the cranial lobes. Histological lesions consisted mainly of lymphohistiocytic infiltration with multinucleate giant cells in lymph nodes, spleen, Peyer’s patches, kidney, lung and liver, depletion or lymphoid hyperplasia, as well as lymphohistiocytic interstitial pneumonia and areas of secondary bronchopneumonia. The diagnosis was established through observations of the symptoms and typical lesions, and was confirmed by immunohistochemical examination and PCR. The objective of this study was to characterize the epidemiological, clinical and pathological aspects of the outbreak of PMWS, because of the severe direct or indirect economical losses caused by the disease to the world pig industry.

• Postweaning multisystemic wasting syndrome porcine circovirus type 2 pathology immunohistochemistry PCR.

Abstract in Portuguese:

França T.N., Peixoto P.V., Brito M.F., Driemeier D., Mores N. & Zanella J. 2005. [Outbreak of Circovirosis (Porcine Postweaning Multisystemic Wasting Syndrome) in the state of Rio de Janeiro, Brazil.] Surto de Circovirose (Síndrome Definhante Multissistêmica de Suínos Desmamados) no estado do Rio de Janeiro. Pesquisa Veterinária Brasileira 25(1):39-53. Universidade Estácio de Sá, Curso de Medicina Veterinária, Disciplina de Anatomia Patológica, Estrada Boca do Mato 850, Vargem Pequena, RJ 22783-320, Brazil. E-mail: ticianaf@uol.com.br The first outbreak of Postweaning Multisystemic Wasting Syndrome (PMWS) in swine, which occurred in southeastern Brazil, in the state of Rio de Janeiro, is described. The disease, which affects mainly weaned about 4 month-old pigs, caused the death of at least 14 animals. The property, where the outbreak occurred, had inadequate sanitary and management conditions. Clinically the disease was characterized by wasting, poor development, cough, tachypnoea, dispnoea, diarrhoea, ataxia, tremors after stimulation, decubitus and convulsions. The course of the disease was acute or subacute. The most important post-mortem findings were enlarged lymphnodes, non-collapsed lungs, with consolidated areas mainly in the cranial lobes. Histological lesions consisted mainly of lymphohistiocytic infiltration with multinucleate giant cells in lymph nodes, spleen, Peyer’s patches, kidney, lung and liver, depletion or lymphoid hyperplasia, as well as lymphohistiocytic interstitial pneumonia and areas of secondary bronchopneumonia. The diagnosis was established through observations of the symptoms and typical lesions, and was confirmed by immunohistochemical examination and PCR. The objective of this study was to characterize the epidemiological, clinical and pathological aspects of the outbreak of PMWS, because of the severe direct or indirect economical losses caused by the disease to the world pig industry.

Abstract in English:

Beltrão N., Furian T.Q., Leão J.A., Pereira R.A., Moraes L.B. & Canal C.W. 2004. [Detection of infectious laryngotracheitis virus in chickens in Brazil.] Detecção do vírus da laringotraqueíte das galinhas no Brasil. Pesquisa Veterinária Brasileira 24(2):85-88. Centro de Diagnóstico e Pesquisa em Patologia Aviária (CDPA), Faculdade de Veterinária, UFRGS, Porto Alegre, RS 91540-000, Brazil. E-mail: nilzaneb@hotmail.com A study was carried out in search for evidences of infectious laryngotracheitis virus (ILTV) infections in some Brazilian chicken flocks. Tracheal tissues and swabs were collected from 10 different flocks of layers and broilers displaying respiratory signs of disease. Samples were processes for virus isolation in embryonated eggs and the membranes examined by histopathology. In addition, specimens were examined by polymerase chain reaction (PCR). Three flocks had ILTV positive chickens by virus isolation and PCR. These results confirm the occurrence of ILTV in chickens in Brazil.

• Infectious laryngotracheitis virus PCR virus isolation avian pathology.

Abstract in Portuguese:

Beltrão N., Furian T.Q., Leão J.A., Pereira R.A., Moraes L.B. & Canal C.W. 2004. [Detection of infectious laryngotracheitis virus in chickens in Brazil.] Detecção do vírus da laringotraqueíte das galinhas no Brasil. Pesquisa Veterinária Brasileira 24(2):85-88. Centro de Diagnóstico e Pesquisa em Patologia Aviária (CDPA), Faculdade de Veterinária, UFRGS, Porto Alegre, RS 91540-000, Brazil. E-mail: nilzaneb@hotmail.com A study was carried out in search for evidences of infectious laryngotracheitis virus (ILTV) infections in some Brazilian chicken flocks. Tracheal tissues and swabs were collected from 10 different flocks of layers and broilers displaying respiratory signs of disease. Samples were processes for virus isolation in embryonated eggs and the membranes examined by histopathology. In addition, specimens were examined by polymerase chain reaction (PCR). Three flocks had ILTV positive chickens by virus isolation and PCR. These results confirm the occurrence of ILTV in chickens in Brazil.

Abstract in English:

ABSTRACT.- Caldas A.P.F., Leal E.S., Silva E.F.A. & Ravazzolo A.P. [Detection of feline immunodeficiency provirus in domestic cats by polymerase chain reaction.] Detecção do provírus da Imunodeficiência Felina em gatos domésticos pela técnica de Reação em Cadeia da Polimerase. Pesquisa Veterinária Brasileira 20(1):20-25. Centro de Biotecnologia/Faculdade de Veterinária, UFRGS, Av. Bento Gonçalves 9500, Porto Alegre, RS 91501-970, Brazil. Feline immunodeficiencyvirus (FIV) infection of domestic cats is one of the most promising animal models for the infection by the human immunodeficiency virus (HIV) which causes acquired immunodeficiency syndrome (AIDS). lnfected cats may develop a disease similar to that observed in AIDS patients, with increased susceptibility to opportunistic infections. Ln this study we used the polymerase chain reaction (PCR) to detect proviral DNA of feline immunodeficiency virus on the blood and tissue samples from cats with a clinical diagnosis of immunodeficiency. The PCR primers were used to amplify the gag gene, which is conserved among different isolates. From 40 samples analyzed, 15 were positive and 4 of them were submitted to hybridization to confirm the specificity of the amplified fragments. These results confirm the presence of FIV in domestic cats in Rio Grande do Sul, Brazil.

• Feline immunodeficiency virus FIV polymerase chain reaction PCR Vírus da Imunodeficiência Felina Reação em Cadeia da Polimerase.

Abstract in Portuguese:

SINOPSE.- Caldas A.P.F., Leal E.S., Silva E.F.A. & Ravazzolo A.P. [Detection of feline immunodeficiency provirus in domestic cats by polymerase chain reaction.] Detecção do provírus da Imunodeficiência Felina em gatos domésticos pela técnica de Reação em Cadeia da Polimerase. Pesquisa Veterinária Brasileira 20(1):20-25. Centro de Biotecnologia/Faculdade de Veterinária, UFRGS, Av. Bento Gonçalves 9500, Porto Alegre, RS 91501-970, Brazil. A infecção de gatos domésticos pelo Vírus da Imunodeficiência Felina (FIV) é um dos modelos mais promissores para o estudo da infecção pelo vírus da imunodeficiência humana (HIV) que causa a Síndrome de Imunodeficiência Adquirida (AIDS). O FIV causa, em gatos, uma enfermidade similar àquela observada em pacientes com AIDS, sobretudo no que diz respeito ao aumento da susceptibilidade a infecções oportunistas. No presente estudo, utilizou-se a Reação em Cadeia da Polimerase (PCR), com o objetivo de detectar o provírus do FIV em gatos com sinais clínicos de imunodeficiência. O fragmento de DNA escolhido como alvo para amplificação situa-se no gene gag do lentivírus felino, o qual é conservado entre as diferentes amostras do vírus. O DNA utilizado foi extraído a partir de amostras de sangue e de tecidos de animais com suspeita clínica de imunodeficiência. Das 40 amostras analisadas, 15 foram positivas, das quais 4 foram submetidas à hibridização, confirmando a especificidade dos fragmentos amplificados. Esses resultados demonstram a presença do FIV na população de gatos domésticos do Rio Grande do Sul, Brasil.

Abstract in English:

ABSTRACT.- González E.T., Norimine J., Valera A.R., Travería G., Oliva G.A. & Etcheverrigaray M.E. 1999. A rapid and sensitive diagnosis of bovine leukaemia virus infection using the nested shuttle polyrnerase chain reaction. [Diagnóstico rápido e sensível da infecção com o vírus da Leucemia Bovina através de Shuttle Nested Polyrnerase Chain Reaction.] Pesquisa Veterinária Brasileira 19(2):63-67. Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, 60 y 118, 1900 La Plata, Argentina. Bovine leukaemia virus (BLV) is the causative agent of enzootic bovine leukosis (EBL). In Argentina, where a program to eradicate EBL has been introduced, sensitive and reliable diagnosis has attained high priority. Although the importance of the agar gel immunodiffusiontest remains unchanged for routine work, an additional diagnostic technique is necessary to confirm cases of sera with equivocal results or of calves carrying maternal antibodies. Utilizing a nested shuttle polymerase chain reaction, the provira) DNA was detected from cows experimentally infected with as little as 5 ml of whole blood from BLV seropositive cows that were nonetheless normal in haematological terms. It proved to be a very sensitive technique, since it rapidly revealed the presence of the proviras, frequently at 2 weeks postinoculation and using a two-round procedure of nested PCR taking only 3 hours. Additionally, the primers used flanked a portion of the viral genome often employed to differentiate BLV type applying BamHI digestion. It is concluded that this method might offer a highly promising diagnostic tool for BLV infection.

• Bovine Ieukaemia virus diagnosis Nested-PCR Leucose bovina diagnóstico.

Abstract in Portuguese:

RESUMO.- González E.T., Norimine J., Valera A.R., Travería G., Oliva G.A. & Etcheverrigaray M.E. 1999. A rapid and sensitive diagnosis of bovine leukaemia virus infection using the nested shuttle polyrnerase chain reaction. [Diagnóstico rápido e sensível da infecção com o vírus da Leucemia Bovina através de Shuttle Nested Polyrnerase Chain Reaction.] Pesquisa Veterinária Brasileira 19(2):63-67. Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, 60 y 118, 1900 La Plata, Argentina. Bovine leukaemia virus (BLV) is the causative agent of enzootic bovine leukosis (EBL). O Vírus da leucemia bovina (BLV) é o agente causal da Leucose Enzoótica Bovina (EBL). Na Argentina, iniciou-se um programa de erradicação da EBL. Neste estágio, é prioritário possuir uma ferramenta de diagnóstico confiável. Embora seja indiscutível a importância do teste de agar gel imunodifusão, empregado rotineiramente no diagnóstico serológico da EBL, faz-se necessária uma técnica de diagnóstico adicional capaz de confirmar os resultados duvidosos. Foi possivel detectar ADN provira) aplicando Nested-PCR em novilhos experimentalmente infectados com pequenas doses de sangue total (5ml) obtidas de um bovino BLV soropositivo. Esta técnica, cujo procedimento leva 3 horas, demonstrou ser muito sensível, uma vez que foi capaz de detectar a presença do proviras duas semanas após a inoculação. Os primers utilizados são os que detectam uma porção do genoma virai que geralmente é usado para diferenciar os tipos de BLV, utilizando a digestão com BamHI. Sugerimos que este método possa ser um instrumento válido para o diagnóstico precoce da infeção pelo BLv.

Abstract in English:

ABSTRACT.- Marchesin D.M., Moojen V. & Ravazzolo A.P. 1998. [Molecular characterization of part of the gag gene of caprine arthritis-encephalitis virus isolated from naturally infected goats from Rio Grande do Sul, Brazil.] Caracterização molecular parcial do gene gag de amostras do vírus da artrite-encefalite caprina (CAEV) isoladas de animais naturalmente infectados no Rio Grande do Sul, Brasil. Pesquisa Veterinária Brasileira 18(3/4):119-126. Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9500, Cx. Postal 15005, Porto Alegre, RS 91501-970, Brazil. The gag gene of 5 CAEV samples, isolated from naturally infected goats from Rio Grande do Sul, Brazil, were analised by PCR and restriction endonuclease (Ddel, Haelll e Ndel) digestion. Fragments of about 600 bp were amplified by PCR and submitted to enzymatic digestion. The patterns observed were compared with the correspondinggag sequences from 6 small ruminant lentiviruses. The results obtained allowed the separation of 3 distinct groups. The restriction fragment profiles observed were different from those previously described.

• Caprine arthritis-encephalitis virus Ientivirus PCR RFLP Virus da artrite-encefalite caprina Lentivírus.

Abstract in Portuguese:

RESUMO.- Marchesin D.M., Moojen V. & Ravazzolo A.P. 1998. [Molecular characterization of part of the gag gene of caprine arthritis-encephalitis virus isolated from naturally infected goats from Rio Grande do Sul, Brazil.] Caracterização molecular parcial do gene gag de amostras do vírus da artrite-encefalite caprina (CAEV) isoladas de animais naturalmente infectados no Rio Grande do Sul, Brasil. Pesquisa Veterinária Brasileira 18(3/4):119-126. Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9500, Cx. Postal 15005, Porto Alegre, RS 91501-970, Brazil. Realizou-se a análise de parte do gene gag, que codifica para as proteínas do capsídeo viral, de 5 amostras de CAEV isolados de animais naturalmente infectados do Rio Grande do Sul, Brasil. As amostras foram analisadas por PCR e clivagem com enzimas de restrição (Ddel, Haelll e Ndel). Fragmentos de aproximadamente 600 pb foram amplificados na PCR e submetidos à digestão enzimática. Os perfis obtidos foram comparados com as seqüências gag de 6 lentivírus de pequenos ruminantes. Os resultados obtidos permitiram separar as amostras em 3 grupos distintos. Os fragmentos observados foram diferentes dos descritos previamente.