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一种分析持续性病毒感染建立效率的定量方法。

A quantitative method for analyzing establishing-efficiency of persistent viral infection.

作者信息

Ito Morihiro, Yamakawa Izumi, Nishio Machiko, Tsurudome Masato, Kawano Mitsuo, Komada Hiroshi, Ito Yasuhiko

机构信息

Department of Biomedical Sciences, College of Life and Health Sciences, Chubu University, Kasugai-City, Aichi-Prefecture 487-8501, Japan.

出版信息

Microbiol Immunol. 2009 May;53(5):259-65. doi: 10.1111/j.1348-0421.2009.00122.x. Epub 2009 Feb 9.

Abstract

A quantitative method for analyzing establishing-efficiency of persistent infection was devised. The efficiency of hPIV2 CA and SV5 T1 strains was found to be high, that is, 0.1 approximately 0.3 (an efficiency of 1.0 indicates that 100% of the virus-infected cells became persistently infected). The efficiency of the SV5 WR strain was also high, approximately 0.1, though the virus had no ability to immediately establish a steady state of persistent infection in whole cell-culture systems. At about 0.0007, the efficiency of SV41 was almost the same as that of the hPIV2 Toshiba strain. The establishing efficiencies of various rSeV were further analyzed in detail. The efficiencies of the rSeV(PA), rSeV(Ppi) and rSeV(HNpi) were below the limit of detection, while that of rSeV(Lpi) was nearly 1. Although the efficiency was around 0.001, the rSeV(Mpi) and the rSeV(Fpi) were unexpectedly found to be capable of forming persistently-infected cells, indicating that both the Fpi and Mpi proteins contribute to the establishing efficiency of persistent infection of SeVpi.

摘要

设计了一种分析持续性感染建立效率的定量方法。发现hPIV2 CA和SV5 T1毒株的效率较高,即0.1至0.3左右(效率为1.0表示100%的病毒感染细胞变成持续性感染)。SV5 WR毒株的效率也较高,约为0.1,尽管该病毒在全细胞培养系统中没有立即建立持续性感染稳定状态的能力。SV41的效率约为0.0007,与hPIV2东芝毒株的效率几乎相同。对各种重组Sendai病毒(rSeV)的建立效率进行了进一步详细分析。rSeV(PA)、rSeV(Ppi)和rSeV(HNpi)的效率低于检测限,而rSeV(Lpi)的效率接近1。尽管rSeV(Mpi)和rSeV(Fpi)的效率约为0.001,但意外发现它们能够形成持续性感染细胞,这表明Fpi和Mpi蛋白均有助于SeVpi持续性感染的建立效率。

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