A real-time reverse transcriptase polymerase chain reaction for detection and quantification of Vesiculovirus

被引:6
|
作者
Tolardo, Aline Lavado [1 ]
de Souza, William Marciel [1 ]
Romeiro, Marilia Farignoli [1 ]
Vieira, Luiz Carlos [1 ]
de Souza Luna, Luciano Kleber [1 ]
Henriques, Dyana Alves [2 ]
de Araujo, Jansen [2 ]
Hassegawa Siqueira, Carlos Eduardo [3 ]
Colombo, Tatiana Elias [4 ]
Aquino, Victor Hugo [5 ]
Lopes da Fonseca, Benedito Antonio [1 ]
de Morais Bronzoni, Roberta Vieira [3 ]
Nogueira, Mauricio Lacerda [4 ]
Durigon, Edison Luiz [2 ]
Moraes Figueiredo, Luiz Tadeu [1 ]
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Ctr Pesquisa Virol, Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Inst Ciencias Biomed, Lab Virol Clin & Mol, Sao Paulo, SP, Brazil
[3] Univ Fed Mato Grosso, Inst Ciencias Saude, Ctr Univ Sinop, Sinop, MT, Brazil
[4] Fac Med Sao Jose Rio Preto, Lab Pesquisa Virol, Sao Jose Do Rio Preto, SP, Brazil
[5] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, Dept Anal Clin Toxicol & Bromatol, Lab Virol, Ribeirao Preto, SP, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2016年 / 111卷 / 06期
基金
巴西圣保罗研究基金会;
关键词
Vesiculovirus; quantitative real-time RT-PCR; diagnosis of vesicular stomatitis; zoonotic virus; VESICULAR-STOMATITIS-VIRUS; CHANDIPURA VIRUS; REACTION ASSAY; PCR ASSAY; BRAZIL; ANTIBODIES; MULTIPLEX; TRANSMISSION; DIAGNOSIS; SEROTYPE;
D O I
10.1590/0074-02760150456
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Vesiculoviruses (VSV) are zoonotic viruses that cause vesicular stomatitis disease in cattle, horses and pigs, as well as sporadic human cases of acute febrile illness. Therefore, diagnosis of VSV infections by reliable laboratory techniques is important to allow a proper case management and implementation of strategies for the containment of virus spread. We show here a sensitive and reproducible real-time reverse transcriptase polymerase chain reaction (RT-PCR) for detection and quantification of VSV. The assay was evaluated with arthropods and serum samples obtained from horses, cattle and patients with acute febrile disease. The real-time RT-PCR amplified the Piry, Carajas, Alagoas and Indiana Vesiculovirus at a melting temperature 81.02 +/- 0.8 degrees C, and the sensitivity of assay was estimated in 10 RNA copies/mL to the Piry Vesiculovirus. The viral genome has been detected in samples of horses and cattle, but not detected in human sera or arthropods. Thus, this assay allows a preliminary differential diagnosis of VSV infections.
引用
收藏
页码:385 / 390
页数:6
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