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首页> 外文期刊>Transboundary and emerging diseases >Prolonged Detection of PCV2 and Anti-PCV2 Antibody inOral Fluids Following Experimental Inoculation
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Prolonged Detection of PCV2 and Anti-PCV2 Antibody inOral Fluids Following Experimental Inoculation

机译:实验接种后延长检测口服液中PCV2和抗PCV2抗体的时间

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The onset, level and duration of PCV2 and anti-PCV2 antibody in oral fluidwere evaluated using samples collected from experimentally inoculated pigs for98 days post-inoculation (DPI). Pigs (n = 24) were obtained at 3 weeks of ageand randomly allocated to 4 treatment pens of 6 pigs each: (i) negative controlgroup; (ii) inoculated with PCV2a (strain ISU 40895) on DPI 0; (iii) inoculatedwith PCV2a (strain ISU-40895) on DPI 0 and re-challenged at DPIs 35 and 70;(iv) inoculated with PCV2a (ISU-40895), PCV2b (PVG4072) and PCV2a (ISU-4838) on DPIs 0, 35 and 70, respectively. Serum was collected from each animal,and one oral fluid sample was collected from each pen (group) everyother day from DPI 2 through DPI 14 and weekly through 98 DPI. Oral fluidsamples were assayed for the presence of PCV2 by quantitative polymerasechain reaction (qPCR) and anti-PCV2 IgG, IgA and IgM antibody isotypes byenzyme-linked immunosorbant assay (ELISA). Serum was assayed for anti-PCV2 IgG by ELISA. Anti-PCV2 antibodies (IgG, IgM and IgA) were detectedin oral fluid from experimentally inoculated pigs from DPI 14 with IgG andIgA clearly present at 98 DPI. PCV2 was detected in oral fluid samples from allpens of inoculated pigs at 2 DPI. Thereafter, PCV2 was detected in oral fluidthroughout 98 DPI. Overall, the data indicated that PCV2 infection in swine isprolonged, persists in the face of an active antibody response and can be efficientlymonitored using oral fluid specimens.
机译:使用接种后98天(DPI)的实验接种猪收集的样品评估口服液中PCV2和抗PCV2抗体的发作,水平和持续时间。在3周龄时获得猪(n = 24),并随机分配给4只处理猪,每只6只猪:(i)阴性对照组; (ii)在DPI 0上接种PCV2a(株ISU 40895); (iii)在DPI 0上接种PCV2a(菌株ISU-40895),并在DPI 35和70上再次攻击;(iv)在DPI 0上接种PCV2a(ISU-40895),PCV2b(PVG4072)和PCV2a(ISU-4838) ,分别为35和70。每隔一天从DPI 2到DPI 14,每周一次到98 DPI,从每只动物的血清中收集血清,并从每只笔(组)中收集一份口腔液样品。通过定量聚合酶链反应(qPCR)和抗PCV2 IgG,IgA和IgM抗体同种型,通过酶联免疫吸附法(ELISA)检测口腔液中PCV2的存在。通过ELISA测定血清的抗PCV2 IgG。在来自DPI 14的实验接种猪的口腔液中检测到抗PCV2抗体(IgG,IgM和IgA),其中IgG和IgA明显存在于98 DPI。在2 DPI时,从来自所有接种猪的猪的唾液中检测到PCV2。之后,在整个98 DPI的口腔液中都检测到PCV2。总体而言,数据表明猪中PCV2感染的时间延长了,面对活性抗体反应仍然持续存在,可以使用口腔液体标本进行有效监测。

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