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dc.contributor.authorSantos, Priscilla Nunes dos-
dc.date.accessioned2025-01-30T20:54:37Z-
dc.date.available2025-01-30T20:54:37Z-
dc.date.issued2020-06-23-
dc.identifier.citationSANTOS, Priscilla Nunes dos. Diversidade do Gene Msp1α de Anaplasma Marginale e Isolamento e Propagação de um Novo Genótipo de Anaplasma Sp. em Células Ide8. 2020. 127 f. Tese (Doutorado em Ciências Veterinárias) - Instituto de Veterinária, Universidade Federal Rural do Rio de Janeiro, Seropédica, 2020.pt_BR
dc.identifier.urihttps://rima.ufrrj.br/jspui/handle/20.500.14407/19943-
dc.description.abstract-pt_BR
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESpt_BR
dc.languageporpt_BR
dc.publisherUniversidade Federal Rural do Rio de Janeiropt_BR
dc.subjectDiversitypt_BR
dc.subjectRhipicephalus micropluspt_BR
dc.subjectIDE8pt_BR
dc.subjectmsp1αpt_BR
dc.titleDiversidade do Gene Msp1α de Anaplasma Marginale e Isolamento e Propagação de um Novo Genótipo de Anaplasma Sp. em Células Ide8pt_BR
dc.title.alternativeDiversity of the Anaplasma marginale msp1α gene and isolation and propagation of a novel genotype of Anaplasma sp. in IDE8 cellsen
dc.typeTesept_BR
dc.description.abstractOtherThis thesis consists of two chapters: The purpose of the first chapter was to evaluate the tandem repeat diversity in the major surface protein MSP1a of Anaplasma marginale in experimentally infected cattle and in Rhipicephalus microplus over the span of 1 year, and the re-isolation of AmRio1 strain of A. marginale, using the buffy coat separation protocol, was performed. The second chapter was aimed at isolating, propagating, and characterizing a novel Anaplasma sp. genotype from Portugal in IDE8 cells. To evaluate A. marginale genetic diversity, cattle were infested with R. microplus larvae and subsequently infected by A. marginale from tick cell cultures. The strains AmRio1 and AmRio2 were inoculated in bovine 1 and bovine 2, respectively. Subsequently, blood samples were collected over 1 year for blood smears, hematocrit, plasma proteins, and semi-nested polymerase chain reaction (PCR) for the msp5 and msp1α genes. The buffy coat separation protocol was used to isolate Anaplasma sp. Ticks were collected and their salivary glands and guts DNA were tested using semi-nested PCR for the msp5 and msp1α genes. Both animals showed stability in the evaluated parameters and absence of clinical signs, showing that they had persistent infection. A blood smear from Animal 1 showed inclusions inside the leukocytes, and four attempts were made to isolate Anaplasma sp. using the buffy-coat as inoculum. Animal 1 became positive for the msp5 gene on day 12 after infection, while positivity was detected in Animal 2 only 105 days after first exposure to the agent. The tandem repeats were stable when the blood and tick samples of both animals were evaluated, demonstrating the presence of the strains AmRio1 in Animal 1 and AmRio2 in Animal 2. In the second chapter, erythrocytes from a naturally infected bovine from Portugal were used for isolating Anaplasma sp. in IDE8 cells. Suggestive inclusions of infection were observed in the IDE8 cells 35 days after inoculation. The Anaplasmataceae family 16S rRNA gene from the cultures was sequenced and showed that the isolated rickettsia was close to the A. platys species in the phylogenetic tree.en
dc.contributor.advisor1Fonseca, Adivaldo Henrique da-
dc.contributor.advisor1IDhttps://orcid.org/0000-0002-5834-141Xpt_BR
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/4411441162862608pt_BR
dc.contributor.advisor-co1Silva, Claudia Bezerra da-
dc.contributor.advisor-co1IDhttps://orcid.org/0000-0003-1761-2110pt_BR
dc.contributor.advisor-co1Latteshttp://lattes.cnpq.br/1386096108167039pt_BR
dc.contributor.advisor-co2Silva, Jenevaldo Barbosa da-
dc.contributor.advisor-co2Latteshttp://lattes.cnpq.br/3251119021411047pt_BR
dc.contributor.referee1Fonseca, Adivaldo Henrique da-
dc.contributor.referee1IDhttps://orcid.org/0000-0002-5834-141Xpt_BR
dc.contributor.referee1Latteshttp://lattes.cnpq.br/4411441162862608pt_BR
dc.contributor.referee2Santos, Huarrisson Azevedo-
dc.contributor.referee2IDhttps://orcid.org/0000-0002-8218-3626pt_BR
dc.contributor.referee2Latteshttp://lattes.cnpq.br/3751609492049306pt_BR
dc.contributor.referee3Peixoto, Maristela Peckle-
dc.contributor.referee3IDhttps://orcid.org/0000-0002-4208-1430pt_BR
dc.contributor.referee3Latteshttp://lattes.cnpq.br/8817867478588076pt_BR
dc.contributor.referee4Baêta, Bruna de Azevedo-
dc.contributor.referee4IDhttps://orcid.org/0000-0002-0172-556Xpt_BR
dc.contributor.referee4Latteshttp://lattes.cnpq.br/8016012971743463pt_BR
dc.contributor.referee5Zweygarth, Erich Peter-
dc.contributor.referee5Lattes-pt_BR
dc.creator.IDhttps://orcid.org/0000-0001-8985-283Xpt_BR
dc.creator.Latteshttp://lattes.cnpq.br/9669827127440973pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentInstituto de Veterináriapt_BR
dc.publisher.initialsUFRRJpt_BR
dc.publisher.programPrograma de Pós-Graduação em Ciências Veterináriaspt_BR
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dc.subject.cnpqMedicina Veterináriapt_BR
dc.subject.cnpqMedicina Veterináriapt_BR
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