Sabiia Seb
PortuguêsEspañolEnglish
Embrapa
        Busca avançada

Botão Atualizar


Botão Atualizar

Ordenar por: 

RelevânciaAutorTítuloAnoImprime registros no formato resumido
Registros recuperados: 230
Primeira ... 123456789 ... Última
Imagem não selecionada

Imprime registro no formato completo
Ovine leptospirosis in Brazil J. Venom. Anim. Toxins incl. Trop. Dis.
Lucheis,SB; Ferreira Jr.,RS.
Leptospirosis is a zoonosis distributed worldwide, endemic mainly in humid subtropical and tropical countries, with epidemic potential. It affects a range of both wild and domestic animals, including sheep, which transport leptospires in their urine and, therefore, can infect other animals and humans who deal with them. Therefore, leptospirosis is characterized as an occupational zoonosis. In individual herds leptospirosis can cause severe economic loss due to miscarriages and outbreaks of mastitis with a significant reduction of milk production. The disease is caused by Leptospira interrogans, which was reclassified into 13 pathogenic species, and distributed into more than 260 serovars classified into 23 serogroups. The clinical signs of infection may...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Sheep; Leptospira; Diagnosis; Animal diseases.
Ano: 2011 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992011000400006
Imagem não selecionada

Imprime registro no formato completo
American visceral Leishmaniasis: a case report J. Venom. Anim. Toxins incl. Trop. Dis.
Langoni,H.; Lucheis,S. B.; Da Silva,R. C.; Castro,A. P. B.; Paes,A. C..
Visceral leishmaniasis is a zoonotic disease caused by parasites of the Leishmania genus. Dog is the major source of infection to man, especially in urban areas. The authors report a case of visceral leishmaniasis in a pit bull female dog from Bocaina, São Paulo, Brazil. The animal presented clinical signs compatible with leishmaniasis, including skin lesions in the body and partial damage of the external ears. The indirect fluorescent antibody test (IFAT) demonstrated a titer of 1280, and promastigote forms of Leishmania sp were isolated by the culture of bone marrow puncture. Cytological analysis of the lymph node and smear of the bone marrow puncture revealed macrophages containing amastigote forms of Leishmania sp in their inner region. The test of...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Leishmania; Zoonosis; Dog; Diagnosis; Hemoculture; Serology; Polymerase chain reaction (PCR).
Ano: 2005 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992005000300012
Imagem não selecionada

Imprime registro no formato completo
Comparison of real-time PCR and conventional PCR for detection of Leishmania (Leishmania) infantum infection: a mini-review J. Venom. Anim. Toxins incl. Trop. Dis.
Paiva-Cavalcanti,M; Regis-da-Silva,CG; Gomes,YM.
In recent years, the polymerase chain reaction (PCR) technique has significantly advanced towards expanding its use and versatility by working with quantitative real-time PCR (qPCR). Data from the literature show that both methods present interesting characteristics for the diagnosis of visceral leishmaniasis. The benefits of qPCR in relation to conventional PCR include speed, reproducibility and quantitative ability. In addition to operational advantages, qPCR is more sensitive and reproducible and may replace conventional PCR in diagnostic routines. Regarding visceral leishmaniasis, the possibility of deployment of real-time PCR in highly complex diagnoses (reference services) in endemic areas will facilitate a swift and safe return for patients....
Tipo: Info:eu-repo/semantics/article Palavras-chave: Diagnosis; Molecular diagnosis; Visceral leishmaniasis.
Ano: 2010 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992010000400004
Imagem não selecionada

Imprime registro no formato completo
Morphology and DNA sequence data reveal the presence of Globodera ellingtonae in the Andean region Naturalis
Lax, P.; Rondan Dueñas, J.C.; Franco-Ponce, J.; Gardenal, C.N.; Doucet, M.E..
Potato cyst nematodes, G. rostochiensis and G. pallida, are the most economically important nematode pests of potatoes worldwide and are subject to strict quarantine regulations in many countries. Globodera ellingtonae was recently described from Oregon (USA), with its host-plant in the field being still unknown. Roots of Andean potatoes from the North of Argentina have been found attacked by this nematode, providing further evidence that this is a potato cyst nematode species, along with G. pallida and G. rostochiensis. New information about morphological, biological and molecular aspects of G. ellingtonae is provided for diagnostic purposes. The Argentine population showed morphological differences from specimens from Oregon; therefore, new diagnostic...
Tipo: Article / Letter to the editor Palavras-chave: Andean potato; Argentina; Diagnosis; Hsp90 gene; Morphology; Potato cyst nematode; 42.76; 42.64.
Ano: 2014 URL: http://www.repository.naturalis.nl/record/506790
Imagem não selecionada

Imprime registro no formato completo
Use of Contrast-Enhanced CT in the Diagnosis of Abscesses in Cattle OAK
LEE, Ki-Ja; KISHIMOTO, Miori; SHIMIZU, Junichiro; KOBAYASHI, Yoshiyasu; MATSUMOTO, Kotaro; SASAKI, Naoki; ISHII, Mitsuo; INOKUMA, Hisashi; IWASAKI, Toshiroh; MIYAKE, Yoh-Ichi; YAMADA, Kazutaka; 古林, 与志安; 松本, 高太郎; 佐々木, 直樹; 石井, 三都夫; 猪熊, 壽; 山田, 一孝.
We report here the non-contrast and contrast-enhanced computed tomography performed in two calves with brain abscess and multiple pulmonary abscesses with pharyngeal abscess, respectively. Contrast-enhanced computed tomography was useful in the diagnosis of these diseases in both calves. The diseases were confirmed by histopathological examination.
Palavras-chave: Abscess; Cattle; Contrast-enhanced CT; Diagnosis.
Ano: 2011 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/3891
Imagem não selecionada

Imprime registro no formato completo
Clinical usefulness of antibodies against Babesia gibsoni detected by ELISA with recombinant P50 OAK
Miyama, Takako; Inokuma, Hisashi; Itamoto, Kazuhito; Okuda, Masaru; Verdida, Rodolfo A.; Xuan, Xuenan; 猪熊, 壽; 玄, 学南.
The clinical usefulness of antibodies against Babesia gibsoni detected by ELISA with recombinant P50 was examined in dogs in an area where B. gibsoni infection was endemic. Only 8 among 14 dogs with acute type B. gibsoni infection without a previous history of infection were positive. This high percentage of false-negative results is thought to be a weak point of ELISA as a diagnostic tool. However, 14 other anemic dogs with a confirmed history of B. gibsoni infection were all positive, thus confirming the higher sensitivity of ELISA in detecting a history of infection.
Palavras-chave: Babesia gibsoni; Diagnosis; ELISA.
Ano: 2006 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/925
Imagem não selecionada

Imprime registro no formato completo
Expression of truncated Babesia gibsoni thrombospondin-related adhesive proteins in Escherichia coli and evaluation of their diagnostic potential by enzyme-linked immunosorbent assay OAK
Sandagdorj, Narantsatsral; Goo, Youn-Kyoung; Terkawi, Mohamad Alaa; Soma, Takehisa; Luo, Yuzi; Li, Yan; Cao, Shinuo; Aboge, Gabriel Oluga; Nishikawa, Yoshifumi; Badgar, Battsetseg; Xuan, Xuenan.
Among the previously established enzyme-linked immunosorbent assays (ELISAs), an ELISA using the full length of recombinant thrombospondin-related adhesive protein of Babesia gibsoni (rBgTRAPf) is considered as the most sensitive diagnostic method for the detection of antibody to B. gibsoni in dogs. However, the expression of rBgTRAPf in high concentration is poor and thus limits its usefulness as diagnostic antigen. To improve its expression level, we have truncated BgTRAPf into two fragments having either N- or C-terminus (BgTRAPn or BgTRAPc). The expression of BgTRAPc protein in Escherichia coli yielded adequate recombinant protein. The specificity and sensitivity of ELISAs with the truncated proteins were determined using B. gibsoni-experimentally...
Palavras-chave: Babesia gibsoni; Diagnosis; Enzyme-linked immunosorbent assay (ELISA); Thrombospondin-related adhesive protein (TRAP).
Ano: 2011 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/3115
Imagem não selecionada

Imprime registro no formato completo
Diagnosis Of Trypanosoma evansi Infection Among Sudanese Camels Imported To Egypt Using Card Agglutination Test (CATT) And Antigen Detection Latex Agglutination Test (Suratex) OAK
Elsaid, H. M.; Nantulya, V. M.; Hilali, M..
Palavras-chave: Trypanosoma evansi; Dromedary camel; Diagnosis; Card agglutination test; Suratex.
Ano: 1998 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/298
Imagem não selecionada

Imprime registro no formato completo
Comparison of PCR with Parasitology and Serology in the Diagnosis of a Low Virulent Strain of Trypanosoma brucei gambiense in mice OAK
Mbati, P. A.; Hirumi, K.; Inoue, Noboru; Situakibanza, N. H.; Hirumi, Hiroyuki; 井上, 昇.
Palavras-chave: Trypanosoma brucei gambiense; Mice; Mel-B; Diagnosis; PCR.
Ano: 1999 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/310
Imagem não selecionada

Imprime registro no formato completo
アフリカトリパノソーマ症に対する新規ワクチン法の開発および診断法の確立に関する研究 OAK
Kuboki, Noritaka.
平成18年度
Palavras-chave: African trypanosoma; Vaccine; Diagnosis.
Ano: 2006 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/970
Imagem não selecionada

Imprime registro no formato completo
Stability of Loop-Mediated Isothermal Amplification (LAMP) Reagents and its Amplification Efficiency on Crude Trypanosome DNA Templates OAK
THEKISOE, Oriel M. M; BAZIE, Raoul S. B; CORONEL-SERVIAN, Andrea M; SUGIMOTO, Chihiro; KAWAZU, Shin-ichiro; INOUE, Noboru; 井上, 昇.
This study evaluated the stability of LAMP reagents when stored at 25C and 37C, and also assessed its detection efficiency on different DNA template preparations. Accordingly, LAMP using reagents stored at 25C and 37C amplified DNA of in vitro cultured T. b. brucei (GUTat 3.1) from day 1 to day 15 of reagent storage. There were no significant differences (P>0.05) in detection sensitivity of LAMP among the reagents stored at 25C, 37C and –20C (recommended storage temperature). LAMP using the reagents stored at above-mentioned temperatures amplified serially diluted DNAs (genomic DNA extracted by phenol-chloroform method, FTA card and hemolysed blood) of T. b. gambiense (IL2343) with high sensitivity. Reactions were conducted on the reagents stored...
Palavras-chave: Diagnosis; DNA template; LAMP; Parasitic disease; Trypanosoma.
Ano: 2009 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/2691
Imagem não selecionada

Imprime registro no formato completo
Trypanosoma evansi Infections : Towards Penside Diagnosis OAK
Nantulya, V. M.; Diall, O..
Palavras-chave: Trypanosoma evansi; Diagnosis; Circulating antigens; Latex agglutination test (Suratex®).
Ano: 1998 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/296
Imagem não selecionada

Imprime registro no formato completo
Application of direct agglutination test and fast agglutination screening test for serodiagnosis of visceral leishmaniasis in endemic area of Minas Gerais, Brazil OAK
Silva, E. S.; Schalig, H. D. F. H.; Kroon, N. C. M.; Schoone, G. J.; Gontijo, C. M. F.; Pacheco, Raquel S.; Brazil, R. P..
We have tested an indirect fluorescence technique (IFAT), fast agglutination screening test (FAST) and direct agglutination test (DAT) for the detection of anti-Leishmania antibodies in serum and blood samples from patients with visceral and cutaneous leishmaniasis in Brazil. For visceral leishmaniasis the results obtained with DAT showed a sensitivity and specificity of 100% with a cut-off value of 1:800. The blood and serum samples could also be clearly read in FAST using a 1:100 dilution with the same high sensitivity. Both DAT and FAST were not able to detect significant amounts of antibodies in samples from cutaneous leishmaniasis patients.
Palavras-chave: Visceral leishmaniasis; Diagnosis; DAT; FAST.
Ano: 2001 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/140
Imagem não selecionada

Imprime registro no formato completo
CURRENT SERODIAGNOSTIC MEASURES FOR EQUINE BABESIOSIS OAK
Hirata, Haruyuki; Yokoyama, Naoaki; Xuan, Xuenan; Igarashi, Ikuo; 横山, 直明; 玄, 学南; 五十嵐, 郁男.
Palavras-chave: Babesia equi; Babesia caballi; Diagnosis; ELISA; ICT.
Ano: 2004 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/638
Imagem não selecionada

Imprime registro no formato completo
Identification and Characterization of a Trypanosoma congolense 46 kDa Protein as a Candidate Serodiagnostic Antigen OAK
ZHOU, Mo; SUGANUMA, Keisuke; RUTTAYAPORN, Ngasaman; NGUYEN, Thu-Thuy; YAMASAKI, Shino; IGARASHI, Ikuo; KAWAZU, Shin-ichiro; SUZUKI, Yasuhiko; INOUE, Noboru; 五十嵐, 郁男; 井上, 昇.
Trypanosoma congolense is a major livestock pathogen in Africa, causing large economic losses with serious effects on animal health. Reliable serodiagnostic tests are therefore urgently needed to control T. congolense infection. In this study, we have identified one T. congolense protein as a new candidate serodiagnostic antigen. The 46.4 kDa protein (TcP46, Gene ID: TcIL3000.0.25950) is expressed 5.36 times higher in metacyclic forms than epimastigote forms. The complete nucleotide sequences of TcP46 contained an open reading frame of 1,218 bp. Southern blot analysis indicated that at least two copies of the TcP46 gene were tandemly-arranged in the T. congolense genome. The recombinant TcP46 (rTcP46) was expressed in Escherichia coli as a glutathione...
Palavras-chave: Diagnosis; ELISA; Nagana; TcP46; Trypanosoma.
Ano: 2014 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/3983
Imagem não selecionada

Imprime registro no formato completo
Babesia gibsoni rhoptry-associated protein 1 and its potential use as a diagnostic antigen OAK
Zhou, Jinlin; Jia, Honglin; Nishikawa, Yoshifumi; Fujisaki, Kozo; Xuan, Xuenan.
A cDNA encoding the rhoptry-associated protein 1 (RAP-1) homologue was obtained by immunoscreening an expression library prepared from Babesia gibsoni merozoite mRNA. The complete nucleotide sequence of the gene was 1740bp. Computer analysis suggested that the sequence contains an open reading frame of 1425bp encoding an expected protein with a molecular weight of 52kDa. Based on the sequence similarity, this putative protein was designated as the B. gibsoni RAP-1 (BgRAP-1). The BgRAP-1 gene was expressed in the Escherichia coli BL21 strain, and the recombinant BgRAP-1 was used as the antigen in the enzyme-linked immunosorbent assay (ELISA). The results can differentiate between the B. gibsoni-infected dog sera and the Babesia canis infected dog sera or...
Palavras-chave: Babesia gibsoni; Rhoptry-associated protein; Enzyme-linked immunosorbent assay; Diagnosis.
Ano: 2007 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/811
Imagem não selecionada

Imprime registro no formato completo
Comparative Evaluation of Mehods for the Diagnosis of Bovine Tritrichomonas foetus Infection OAK
Felleisen, Richard S. J.; Schimid-Lambelet, Natacha; Walubengo, J..
Palavras-chave: Diagnosis; In vitro culture; Polymerase chain reaction (PCR).
Ano: 1997 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/266
Imagem não selecionada

Imprime registro no formato completo
Utility of Serum Thymidine Kinase Activity Measurements for Cases of Bovine Leukosis with Difficult Clinical Diagnoses OAK
TAWFEEQ, Mohammad Monir; MIURA, Saori; HORIUCHI, Noriyuki; KOBAYASHI, Yoshiyasu; FURUOKA, Hidefumi; INOKUMA, Hisashi; 堀内, 雅之; 古林, 与志安; 古岡, 秀文; 猪熊, 壽.
This study evaluated the clinical usefulness of serum thymidine kinase (TK) activity for diagnosing bovine leukosis cases for which clinical diagnosis was difficult (‘BL with difficult diagnosis’). Median TK activity values in 24 ‘BL with difficult diagnosis’ and 36 cattle for which BL was clinically confirmed by cytology findings of enlarged superficial lymph nodes (‘clinically confirmed BL’) were 36.8 and 39.4 U/l, respectively (no significant difference). The percentage with positive TK activity (>5.4 U/l) was also similar in both groups (83.3% for ‘BL with difficult diagnosis’ and 97.2% for ‘clinically confirmed BL’). TK activity was significantly higher in cows with ‘BL with difficult diagnosis’ compared to those with other tumors (N=13) and those...
Palavras-chave: Atypical bovine leukosis; Diagnosis; Thymidine kinase.
Ano: 2013 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/3869
Imagem não selecionada

Imprime registro no formato completo
Loop-mediated isothermal amplification (LAMP) assays for detection of Theileria parva infections targeting the PIM and p150 genes OAK
Thekisoe, Oriel M.M.; Rambritch, Natasha E.; Nakao, Ryo; Bazie, Raoul S.; Mbati, Peter; Namangala, Boniface; Malele, Imna; Skilton, Robert A.; Jongejan, Frans; Sugimoto, Chihiro; Kawazu, Shin-Ichiro; Inoue, Noboru.
We have developed two loop-mediated isothermal amplification (LAMP) assays for the detection of Theileria parva, the causative agent of East Coast fever (ECF), an economically important cattle disease in eastern, central and southern Africa. These assays target the polymorphic immunodominant molecule (PIM) and p150 LAMP genes. The primer set for each gene target consists of six primers, and each set recognises eight distinct regions on the target gene to give highly specific detection of T. parva. The detection limit of each primer set is 1 fg, which is equivalent to one copy of the PIM and p150 T. parva genes. These PIM and p150 LAMP primer sets amplify DNA of T. parva isolates from cattle and buffalo from different countries including Kenya, South...
Palavras-chave: Theileria parva; LAMP; Buffalo; Cattle; Diagnosis.
Ano: 2010 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/2672
Imagem não selecionada

Imprime registro no formato completo
Diagnostic Methods for the Detection of Cryptosporidium parvum Oocysts in Faeces OAK
Webster, K. A.; Green, J. A.; Dawson, C.; Giles, M.; Catchpole, J..
Palavras-chave: Cryptosporidium parvum; Diagnosis; Immunofluorescence; ELISA; Coproscopical.
Ano: 1996 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/253
Registros recuperados: 230
Primeira ... 123456789 ... Última
 

Empresa Brasileira de Pesquisa Agropecuária - Embrapa
Todos os direitos reservados, conforme Lei n° 9.610
Política de Privacidade
Área restrita

Embrapa
Parque Estação Biológica - PqEB s/n°
Brasília, DF - Brasil - CEP 70770-901
Fone: (61) 3448-4433 - Fax: (61) 3448-4890 / 3448-4891 SAC: https://www.embrapa.br/fale-conosco

Valid HTML 4.01 Transitional