Author(s): Cursino, Andreia Elisa ; Vilela, Ana Paula Pessoa ; Franco-Luiz, Ana Paula Moreira ; de Oliveira, Jaquelline Germano ; Nogueira, Márcia Furlan ; Júnior, João Pessoa Araújo [UNESP] ; de Aguiar, Daniel Moura ; Kroon, Erna Geessien
Date: 2018
Persistent ID: http://hdl.handle.net/11449/176300
Origin: Oasisbr
Made available in DSpace on 2018-12-11T17:20:00Z (GMT). No. of bitstreams: 0 Previous issue date: 2018-09-01
Empresa Brasileira de Pesquisa Agropecuária
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Fundação de Amparo à Pesquisa do Estado de Mato Grosso
Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
Equine infectious anemia (EIA) has a worldwide distribution, and is widespread in Brazil. The Brazilian Pantanal presents with high prevalence comprising equine performance and indirectly the livestock industry, since the horses are used for cattle management. Although EIA is routinely diagnosed by the agar gel immunodiffusion test (AGID), this serological assay has some limitations, so PCR-based detection methods have the potential to overcome these limitations and act as complementary tests to those currently used. Considering the limited number of equine infectious anemia virus (EIAV) sequences which are available in public databases and the great genome variability, studies of EIAV detection and characterization molecular remain important. In this study we detected EIAV proviral DNA from 23 peripheral blood mononuclear cell (PBMCs) samples of naturally infected horses from Brazilian Pantanal using a semi-nested-PCR (sn-PCR). The serological profile of the animals was also evaluated by AGID and ELISA for gp90 and p26. Furthermore, the EIAV PCR amplified DNA was sequenced and phylogenetically analyzed. Here we describe the first EIAV sequences of the 5’ LTR of the tat gene in naturally infected horses from Brazil, which presented with 91% similarity to EIAV reference sequences. The Brazilian EIAV sequences also presented variable nucleotide similarities among themselves, ranging from 93,5% to 100%. Phylogenetic analysis showed that Brazilian EIAV sequences grouped in a separate clade relative to other reference sequences. Thus this molecular detection and characterization may provide information about EIAV circulation in Brazilian territories and improve phylogenetic inferences.
Laboratório de Vírus Departamento de Microbiologia Instituto de Ciências Biológicas Universidade Federal de Minas Gerais
Laboratório de Biologia Molecular Microbiologia e Sorologia Hospital Universitário Universidade Federal de Santa Catarina
Viriontech do Brasil Indústria de Insumos e Serviços em Biotecnologia
Instituto Rene Rachou Fiocruz-Minas
Embrapa Pantanal
Departamento de Microbiologia e Imunologia Instituto de Biociências e Instituto de Biotecnologia Universidade Estadual Paulista UNESP
Laboratório de Virologia e Rickettsioses Faculdade de Medicina Veterinária Universidade Federal de Mato Grosso
Departamento de Microbiologia e Imunologia Instituto de Biociências e Instituto de Biotecnologia Universidade Estadual Paulista UNESP
Empresa Brasileira de Pesquisa Agropecuária: 02.12.01.030.00.00
CNPq: 307423/2015-8
Fundação de Amparo à Pesquisa do Estado de Mato Grosso: 330980/2012
