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本文引用的文献

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Vaccines for bovine neosporosis: current status and key aspects for development.牛新孢子虫病疫苗:现状与研发关键要点
Parasite Immunol. 2016 Dec;38(12):709-723. doi: 10.1111/pim.12342. Epub 2016 Jul 7.
2
Development of an Orally Available and Central Nervous System (CNS) Penetrant Toxoplasma gondii Calcium-Dependent Protein Kinase 1 (TgCDPK1) Inhibitor with Minimal Human Ether-a-go-go-Related Gene (hERG) Activity for the Treatment of Toxoplasmosis.开发一种口服可用且能穿透中枢神经系统(CNS)的弓形虫钙依赖性蛋白激酶1(TgCDPK1)抑制剂,其对人醚孔相关基因(hERG)的活性最小,用于治疗弓形虫病。
J Med Chem. 2016 Jul 14;59(13):6531-46. doi: 10.1021/acs.jmedchem.6b00760. Epub 2016 Jul 1.
3
SAR Studies of 5-Aminopyrazole-4-carboxamide Analogues as Potent and Selective Inhibitors of CDPK1.5-氨基吡唑-4-甲酰胺类似物作为CDPK1强效和选择性抑制剂的构效关系研究
ACS Med Chem Lett. 2015 Oct 22;6(12):1184-1189. doi: 10.1021/acsmedchemlett.5b00319. eCollection 2015 Dec 10.
4
Approaches for the vaccination and treatment of Neospora caninum infections in mice and ruminant models.在小鼠和反刍动物模型中针对犬新孢子虫感染的疫苗接种和治疗方法。
Parasitology. 2016 Mar;143(3):245-59. doi: 10.1017/S0031182015001596. Epub 2015 Dec 2.
5
In Vitro and In Vivo Effects of the Bumped Kinase Inhibitor 1294 in the Related Cyst-Forming Apicomplexans Toxoplasma gondii and Neospora caninum.碰撞激酶抑制剂1294对相关形成囊肿的顶复门原虫刚地弓形虫和犬新孢子虫的体外及体内作用
Antimicrob Agents Chemother. 2015 Oct;59(10):6361-74. doi: 10.1128/AAC.01236-15. Epub 2015 Jul 27.
6
Dose-dependent effects of experimental infection with the virulent Neospora caninum Nc-Spain7 isolate in a pregnant mouse model.在怀孕小鼠模型中,用强毒力的犬新孢子虫Nc-Spain7分离株进行实验性感染的剂量依赖性效应。
Vet Parasitol. 2015 Jul 30;211(3-4):133-40. doi: 10.1016/j.vetpar.2015.05.021. Epub 2015 Jun 5.
7
Buparvaquone is active against Neospora caninum in vitro and in experimentally infected mice.丁喹酯在体外以及在实验感染的小鼠体内对犬新孢子虫均具有活性。
Int J Parasitol Drugs Drug Resist. 2015 Feb 13;5(1):16-25. doi: 10.1016/j.ijpddr.2015.02.001. eCollection 2015 Apr.
8
In vitro effects of new artemisinin derivatives in Neospora caninum-infected human fibroblasts.新青蒿素衍生物在感染弓形虫的人成纤维细胞中的体外作用。
Int J Antimicrob Agents. 2015 Jul;46(1):88-93. doi: 10.1016/j.ijantimicag.2015.02.020. Epub 2015 Apr 14.
9
The effect of a live Neospora caninum tachyzoite vaccine in naturally infected pregnant dairy cows.活的犬新孢子虫速殖子疫苗对自然感染的怀孕奶牛的影响。
Prev Vet Med. 2015 Jun 15;120(2):232-235. doi: 10.1016/j.prevetmed.2015.03.020. Epub 2015 Apr 8.
10
Influence of the gestational stage on the clinical course, lesional development and parasite distribution in experimental ovine neosporosis.妊娠期对实验性绵羊新孢子虫病临床病程、病变发展及寄生虫分布的影响
Vet Res. 2015 Mar 3;46:19. doi: 10.1186/s13567-014-0139-y.

两种新型钙依赖性蛋白激酶1抑制剂干扰感染犬新孢子虫速殖子的小鼠的垂直传播。

Two Novel Calcium-Dependent Protein Kinase 1 Inhibitors Interfere with Vertical Transmission in Mice Infected with Neospora caninum Tachyzoites.

作者信息

Müller Joachim, Aguado-Martínez Adriana, Balmer Vreni, Maly Dustin J, Fan Erkang, Ortega-Mora Luis-Miguel, Ojo Kayode K, Van Voorhis Wesley C, Hemphill Andrew

机构信息

Institute of Parasitology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Department of Chemistry, University of Washington, Seattle, Washington, USA.

出版信息

Antimicrob Agents Chemother. 2017 Mar 24;61(4). doi: 10.1128/AAC.02324-16. Print 2017 Apr.

DOI:10.1128/AAC.02324-16
PMID:28137808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5365725/
Abstract

We present the effects of two novel bumped kinase inhibitors, BKI-1517 and BKI-1553, against tachyzoites and in experimentally infected pregnant mice. These compounds inhibited tachyzoite proliferation of a transgenic beta-galactosidase reporter strain cultured in human foreskin fibroblasts with 50% inhibitory concentrations (ICs) of 0.05 ± 0.03 and 0.18 ± 0.03 μM, respectively. As assessed by an alamarBlue assay, fibroblast ICs were above 20 μM; however, morphological changes occurred in cultures treated with >5 μM BKI-1517 after prolonged exposure (>6 days). Treatment of intracellular tachyzoites with 5 μM BKI-1553 for 6 days inhibited endodyogeny by interfering with the separation of newly formed zoites from a larger multinucleated parasite mass. In contrast, parasites treated with 5 μM BKI-1517 did not form large complexes and showed much more evidence of cell death. However, after a treatment duration of 10 days , both compounds failed to completely prevent the regrowth of parasites from culture. BALB/c mice experimentally infected with Spain7 (Nc-Spain7) and then treated during 6 days with BKI-1517 or BKI-1553 at different dosages showed a significant reduction of the cerebral parasite load. However, fertility was impaired by BKI-1517 when applied at 50 mg/kg of body weight/day. At 20 mg/kg/day, BKI-1517 significantly inhibited the vertical transmission of to pups and increased the rate of survival of offspring. BKI-1553 was less detrimental to fertility and also provided significant but clearly less pronounced protection of dams and offspring. These results demonstrate that, when judiciously applied, this compound class protects offspring from vertical transmission and disease.

摘要

我们展示了两种新型的碰撞激酶抑制剂BKI-1517和BKI-1553对速殖子以及对实验性感染的怀孕小鼠的影响。这些化合物抑制了在人包皮成纤维细胞中培养的转基因β-半乳糖苷酶报告菌株的速殖子增殖,其50%抑制浓度(IC)分别为0.05±0.03和0.18±0.03μM。通过alamarBlue检测评估,成纤维细胞的IC高于20μM;然而,长时间暴露(>6天)后,用>5μM BKI-1517处理的培养物中出现了形态变化。用5μM BKI-1553处理细胞内速殖子6天,通过干扰新形成的子体从较大的多核寄生虫团块中的分离来抑制内二分裂生殖。相比之下,用5μM BKI-1517处理的寄生虫没有形成大的复合体,并且显示出更多细胞死亡的迹象。然而,处理10天后,两种化合物都未能完全阻止培养物中寄生虫的再生长。用Spain7(Nc-Spain7)实验感染的BALB/c小鼠,然后用不同剂量的BKI-1517或BKI-1553处理6天,脑内寄生虫负荷显著降低。然而,当以50mg/kg体重/天的剂量应用时,BKI-1517损害了生育能力。以20mg/kg/天的剂量,BKI-1517显著抑制了向幼崽的垂直传播并提高了后代的存活率。BKI-1553对生育能力的损害较小,并且也为母鼠和后代提供了显著但明显较弱的保护。这些结果表明,如果谨慎应用,这类化合物可保护后代免受垂直传播和疾病的影响。