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鱼类诺达病毒生命周期与鱼类逆转录病毒的相互干扰。

Interference of the life cycle of fish nodavirus with fish retrovirus.

作者信息

Lee K W, Chi S C, Cheng T M

机构信息

Department of Zoology, National Taiwan University, Taipei, Taiwan, Republic of China1.

出版信息

J Gen Virol. 2002 Oct;83(Pt 10):2469-2474. doi: 10.1099/0022-1317-83-10-2469.

Abstract

Interference of the life cycle of grouper nervous necrosis virus (GNNV), a member of the Nodaviridae, genus Betanodavirus, by snakehead retrovirus (SnRV) has been studied in vitro. SGF-1, a new fish cell line that is persistently infected with SnRV, was induced by inoculating SnRV into the grouper fin cell line GF-1. Culture supernatants and cell pellets from both GNNV-infected SGF-1 and GF-1 cells were collected and employed for virus productivity analysis. The yields of GNNV RNA and capsid protein in GNNV-infected SGF-1 cells were similar to those in GNNV-infected GF-1 cells. However, when GF-1 cells were used for titration, the titre of the culture supernatant from GNNV-infected SGF-1 cells was much higher than that from GNNV-infected GF-1 cells. The titration result suggested that SnRV enhanced the infection or cytopathic effect (CPE) of GNNV during GNNV and SnRV coinfection of the GF-1 cell titration system, although SnRV cannot induce any CPE in GF-1 cells alone, nor can it increase the yield of GNNV after GNNV superinfection of SGF-1 cells. Moreover, GNNV cDNA was detected in both the pellet and the supernatant from GNNV-infected SGF-1 cells. This result indicated that SnRV reverse-transcribed the GNNV single-stranded genomic RNA into cDNA during GNNV superinfection of SGF-1 cells and created a new cDNA stage in the life cycle of the fish nodavirus.

摘要

已在体外研究了蛇头逆转录病毒(SnRV)对诺达病毒科β诺达病毒属成员石斑鱼神经坏死病毒(GNNV)生命周期的干扰。通过将SnRV接种到石斑鱼鳍细胞系GF-1中,诱导出持续感染SnRV的新鱼细胞系SGF-1。收集GNNV感染的SGF-1细胞和GF-1细胞的培养上清液和细胞沉淀,用于病毒生产力分析。GNNV感染的SGF-1细胞中GNNV RNA和衣壳蛋白的产量与GNNV感染的GF-1细胞中的产量相似。然而,当使用GF-1细胞进行滴定时,GNNV感染的SGF-1细胞培养上清液的滴度远高于GNNV感染的GF-1细胞培养上清液的滴度。滴定结果表明,在GF-1细胞滴定系统中GNNV和SnRV共感染期间,SnRV增强了GNNV的感染或细胞病变效应(CPE),尽管SnRV单独不能在GF-1细胞中诱导任何CPE,在SGF-1细胞被GNNV超感染后也不能增加GNNV的产量。此外,在GNNV感染的SGF-1细胞的沉淀和上清液中均检测到GNNV cDNA。这一结果表明,在SGF-1细胞被GNNV超感染期间,SnRV将GNNV单链基因组RNA逆转录为cDNA,并在鱼类诺达病毒的生命周期中创造了一个新的cDNA阶段。

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