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一种用于定量检测刚地弓形虫感染性的新型体外替代方法。

A new alternative in vitro method for quantification of Toxoplasma gondii infectivity.

作者信息

Useo Romain, Husson Florence, De Coninck Joelle, Khaldi Samira, Gervais Patrick

机构信息

UMR PAM, AgroSup Dijon, Université de Bourgogne, 1 Esplanade Erasme, 21000 Dijon, France.

出版信息

J Parasitol. 2012 Apr;98(2):299-303. doi: 10.1645/GE-2873.1. Epub 2011 Oct 19.

Abstract

An in vitro method to determine the infectious potency of an unknown suspension of the protozoan parasite Toxoplasma gondii based on kinetics of host cells lysis was developed. Mic1-3KO a mutant strain of T. gondii RH tachyzoites was inoculated in 25-cm² flasks containing a 90% confluent monolayer of human foreskin fibroblasts. Lysis kinetics was monitored for infection ratios ranging from 1∶10⁶ to 1∶10; we defined 10⁶ tachyzoites/ml⁻¹ as the threshold value for parasite egress. Results allowed us to build a calibration curve relating the initial infection ratios to the time needed to reach 10⁶ tachyzoites/ml⁻¹. Finally, we validated the method using a known mixture of dead and live parasites. This method was found to estimate with accuracy the initial ratio of infection of the unknown parasite suspension. This easy-to-use method is reproducible and can be applied to any T. gondii tachyzoite RH strain, genetically modified or not. This method is also suitable for testing promising candidates for an effective live vaccine.

摘要

基于宿主细胞裂解动力学,开发了一种体外方法来测定未知的原生动物寄生虫刚地弓形虫悬浮液的感染效力。将刚地弓形虫RH速殖子的突变株Mic1-3KO接种到含有90%汇合单层人包皮成纤维细胞的25 cm²培养瓶中。监测感染率从1∶10⁶到1∶10时的裂解动力学;我们将10⁶个速殖子/ml⁻¹定义为寄生虫逸出的阈值。结果使我们能够建立一条校准曲线,将初始感染率与达到10⁶个速殖子/ml⁻¹所需的时间联系起来。最后,我们使用已知的死寄生虫和活寄生虫混合物验证了该方法。发现该方法能够准确估计未知寄生虫悬浮液的初始感染率。这种易于使用的方法具有可重复性,可应用于任何刚地弓形虫RH速殖子株,无论是否经过基因改造。该方法也适用于测试有效的活疫苗的有前景的候选物。

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