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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Detection of chimpanzee polyomavirus-specific antibodies in captive and wild-caught chimpanzees using yeast-expressed virus-like particles.
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Detection of chimpanzee polyomavirus-specific antibodies in captive and wild-caught chimpanzees using yeast-expressed virus-like particles.

机译:使用酵母表达的病毒样颗粒检测圈养和野生黑猩猩中的黑猩猩多瘤病毒特异性抗体。

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摘要

Chimpanzee polyomavirus (ChPyV) was originally detected in the faeces of a captive chimpanzee by random screening using broad-spectrum PCR. Its pathogenicity and the distribution among chimpanzees are unknown so far. Here, the major capsid protein VP1 of ChPyV was expressed in yeast cells. Virus-like particles (VLPs) with a diameter of approximately 45nm were demonstrated although the efficiency of VLP formation was low as compared to monkey polyomavirus SV40-VLPs. The ChPyV-VLP preparation did not agglutinate human erythrocytes. Low cross-reactions between ChPyV- and SV40-VLP-specific sera were detected by immunoblotting, but not by ELISA. Testing of 163 sera derived from captive and wild-caught healthy chimpanzees using an ELISA based on the ChPyV-VLPs resulted in 11.7% positive results, ranging from 0% to 56% in different groups. The VLPs may be used in future to assess the distribution of ChPyV infections among other animal species and humans.
机译:黑猩猩多瘤病毒(ChPyV)最初是通过使用广谱PCR随机筛选在圈养黑猩猩的粪便中检测到的。迄今为止,其致病性和在黑猩猩中的分布尚不清楚。在此,ChPyV的主要衣壳蛋白VP1在酵母细胞中表达。尽管与猴多瘤病毒SV40-VLP相比,VLP形成的效率低,但是已证明具有约45nm直径的病毒样颗粒(VLP)。 ChPyV-VLP制剂不会凝集人的红细胞。 ChPyV和SV40-VLP特异性血清之间的低交叉反应通过免疫印迹法检测到,但未通过ELISA检测。使用基于ChPyV-VLP的ELISA对源自圈养和野生健康黑猩猩的163种血清进行测试,得出阳性结果为11.7%,不同组的结果为0%至56%。 VLP可能会在将来用于评估ChPyV感染在其他动物物种和人类中的分布。

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