首页> 外文期刊>Frontiers in Veterinary Science >The Impact of BKI-1294 Therapy in Mice Infected With the Apicomplexan Parasite Neospora caninum and Re-infected During Pregnancy
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The Impact of BKI-1294 Therapy in Mice Infected With the Apicomplexan Parasite Neospora caninum and Re-infected During Pregnancy

机译:BKI-1294治疗对小鼠的影响感染APICOMPLANAN寄生虫Neospora Caninum并在怀孕期间重新感染

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Exposure of Neospora caninum tachyzoites to BKI-1294 in vitro results in the formation of long-lived multinucleated complexes (MNCs). However, in vivo treatment of BALB/c mice with BKI-1294 shortly after N. caninum infection during pregnancy was safe and profoundly reduced pup mortality and vertical transmission. We hypothesized that the formation of MNCs could trigger immune responses that contribute to BKI efficacy in vivo. In this study, mice were first vaccinated with a sublethal dose of N. caninum tachyzoites and were treated with BKI-1294. We then investigated the effects of these treatments after mating and re-infection during pregnancy. Effects on fertility, pup survival, vertical transmission, and parasite load in dams were evaluated. Cytokines in sera or splenocyte culture supernatants were assessed by either ELISA or the Luminex? 200 system, and humoral immune responses against tachyzoite and MNC antigens were compared by ELISA, Western blotting and immunoproteomics. Our results showed that BKI-1294 treatment of live-vaccinated mice reduced the cerebral parasite load in the dams, but resulted in higher neonatal pup mortality and vertical transmission. In live-vaccinated mice, cytokine levels, most notably IFN-y, IL-10 and IL-12, were consistently lower in BKI-1294 treated animals compared to non-treated mice. In addition, comparative Western blotting identified two protein bands in MNC extracts that were only recognized by sera of live-vaccinated mice treated with BKI-1294, and were not found in tachyzoite extracts. We conclude that treatment of live-vaccinated mice with BKI-1294 influenced the cellular and humoral immune responses against infection, affected the safety of the live-vaccine, and decreased protection against re-infection and vertical transmission during pregnancy.
机译:Neospora caninum tachyzoites暴露于BKI-1294的体外导致长寿命的多核复合物(MNC)的形成。然而,在怀孕期间不久,在N aninum感染后不久,在BKI-1294的BKI-1294的体内治疗是安全且深刻地减少了幼崽死亡率和垂直传输。我们假设MNC的形成可以引发有助于体内BKI疗效的免疫应答。在该研究中,首先用亚甘氨烷Tachyzoites的亚硫醚剂量接种小鼠,并用BKI-1294治疗。然后我们调查了在怀孕期间交配和重新感染后这些治疗的影响。评估了对耐力,幼崽存活,垂直传动和盆地载荷的影响。通过ELISA或Luminex评估血清或脾细胞培养上清液中的细胞因子?通过ELISA,Western印迹和免疫蛋白组比较了200个系统和对Tachyzoite和MNC抗原的体液免疫应答。我们的研究结果表明,活疫苗的BKI-1294治疗疫苗的脑寄生虫载量降低了坝体中的脑寄生虫载荷,但导致新生儿幼一幼年幼年幼年幼年幼年死亡率和垂直传输。在活疫苗的小鼠中,细胞因子水平,最值得注意的是IFN-Y,IL-10和IL-12,与未处理的小鼠相比,BKI-1294处理的动物始终低。此外,对比例印迹鉴定了MNC提取物中的两种蛋白质带,其仅被用BKI-1294处理的活疫苗的小鼠血清识别,并且在Tachyzoite提取物中未发现。我们得出结论,用BKI-1294治疗活疫苗的小鼠影响了对感染的细胞和体液免疫反应,影响了活疫苗的安全性,并减少了对怀孕期间再感染和垂直传播的保护。

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