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胰蛋白酶增强新生牛腹泻冠状病毒在牛胚胎肺细胞中的复制。

Trypsin-enhanced replication of neonatal calf diarrhea coronavirus in bovine embryonic lung cells.

作者信息

Toth T E

出版信息

Am J Vet Res. 1982 Jun;43(6):967-72.

PMID:7103187
Abstract

Bovine embryonic lung (BEL) cells, grown in 8-chamber cell-culture slides, were inoculated with 2.5, 25, and 250 TCID50 of neonatal calf diarrhea coronavirus (NCDCV)/chamber. The NCDCV inocula were prepared in serum-free, trypsin-free regular medium (RM), and in serum-free medium containing 1 microgram (TM1), 5 microgram (TM5), and 10 microgram (TM10) of trypsin/ml; the the cells were maintained under identical media. Cytopathic effect (CPE), hemadsorption of rat RBC, formation of syncytia, appearance of immunofluorescing cells, and release of infectious virus was followed from postinoculation hours 4 to 100. Maintaining the BEL cells in medium containing trypsin up to 10 microgram/ml did not affect them adversely. The BEL cells appeared resistant to infection with NCDCV in RM by CPE, syncytia, immunofluorescing cells, or infectious virus-release parameters. In TM1, TM5, and TM10, all parameters were positive for NCDCV replication. They manifested and developed in positive correlation with increasing trypsin concentration from 1 microgram to 10 microgram/ml. Release of infectious virions preceded all other parameters of virus replication. Replication of NCDCV was demonstrated earlier by hemadsorption and immunofluorescing cells than by syncytia or CPE. The TM5 and TM10 increased the susceptibility of BEL cells to NCDCV by more than a millionfold, as measured by the titer of released virus in these media (greater than 1-(6) TCID50/ml) as compared with those in RM (infectious virus not demonstrated).

摘要

将生长在8孔细胞培养载玻片上的牛胚胎肺(BEL)细胞,每孔接种2.5、25和250半数组织培养感染剂量(TCID50)的新生牛腹泻冠状病毒(NCDCV)。NCDCV接种物在无血清、无胰蛋白酶的常规培养基(RM)以及含有1微克(TM1)、5微克(TM5)和10微克(TM10)胰蛋白酶/毫升的无血清培养基中制备;细胞在相同培养基中培养。接种后4至100小时观察细胞病变效应(CPE)、大鼠红细胞的血细胞吸附、多核巨细胞的形成、免疫荧光细胞的出现以及传染性病毒的释放。将BEL细胞维持在含有高达10微克/毫升胰蛋白酶的培养基中对其没有不利影响。通过CPE、多核巨细胞、免疫荧光细胞或传染性病毒释放参数,BEL细胞在RM中似乎对NCDCV感染具有抗性。在TM1、TM5和TM10中,所有参数对于NCDCV复制均呈阳性。它们随着胰蛋白酶浓度从1微克/毫升增加到10微克/毫升而呈正相关表现和发展。传染性病毒粒子的释放在病毒复制的所有其他参数之前出现。通过血细胞吸附和免疫荧光细胞比通过多核巨细胞或CPE更早地证明NCDCV的复制。与RM中(未证明有传染性病毒)相比,TM5和TM10使BEL细胞对NCDCV的敏感性增加了超过一百万倍,这通过这些培养基中释放病毒的滴度(大于10⁶TCID50/毫升)来衡量。

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