Ahmed R, Graham A F
J Virol. 1977 Aug;23(2):250-62. doi: 10.1128/JVI.23.2.250-262.1977.
Serial passage of reovirus temperature-sensitive (ts) mutant C(447) produced by passage 9 (P9) a heavily defective population of virus from which the double-stranded RNA genomic segments L(1), L(3), and M(1) were largely missing. Viral cores obtained from this P9 population were heterogeneous with respect to buoyant density in CsCl gradients, suggesting that particles were present with different combinations of deleted segments. Similar observations were made with the E(320) ts mutant of reovirus. By serial passage P15, 90% of the E(320) viral population was defective and the major missing genomic segments were L(1) and L(3). Persistent infections were readily established in monolayer cultures of L cells with P9 of C(447) virus and P15 of E(320) virus and in Vero cells with P9 of C(447) virus. Under similar conditions persistent infections could not be initiated with defective-free populations of C(447) or E(320) viruses. The greater the capacity of defective virus in the population to interfere with viral growth, the more readily persistent infection was initiated. During their maintenance persistently infected cells were subcultured approximately twice a week. More than 80% of the cells continuously produced virus. By subculture 6 the original ts infectious viral component had been replaced by a small-plaque mutant with a ts(+) phenotype. Defective virus was always present in the carrier cells. In addition to the more commonly observed defectives whose cores banded at approximately rho = 1.40 to 1.415 g/ml in CsCl gradients, a new class of defective core was seen banding in the region of 1.34 to 1.36 g/ml. This latter particle, which has not been thoroughly characterized as yet, is termed "light defective." Persistently infected cells underwent periodic crises during their maintenance, during which the cultures partially lysed and then rapidly grew to confluence. Crises corresponded to a burst of infectious virus from the cells and a relatively low concentration of light defectives. During quiescent periods the concentration of light defectives amounted to as much as 98% of the total viral population. The function of light defectives is not yet clear, but it seems essential to assign major importance to defective virus in maintaining persistent infections in this system.
呼肠孤病毒温度敏感(ts)突变体C(447)经9代传代(P9)后产生的连续传代病毒群体严重缺陷,双链RNA基因组片段L(1)、L(3)和M(1)在很大程度上缺失。从该P9群体获得的病毒核心在CsCl梯度中的浮力密度方面具有异质性,这表明存在具有不同缺失片段组合的颗粒。对呼肠孤病毒的E(320) ts突变体也进行了类似观察。经15代连续传代后,90%的E(320)病毒群体存在缺陷,主要缺失的基因组片段为L(1)和L(3)。用C(447)病毒的P9代和E(320)病毒的P15代在L细胞单层培养物中以及用C(447)病毒的P9代在Vero细胞中很容易建立持续感染。在类似条件下,用无缺陷的C(447)或E(320)病毒群体无法引发持续感染。群体中缺陷病毒干扰病毒生长的能力越强,就越容易引发持续感染。在维持培养期间,持续感染的细胞大约每周传代两次。超过80%的细胞持续产生病毒。到第6次传代时,原来的ts感染性病毒成分已被具有ts(+)表型的小噬斑突变体所取代。缺陷病毒始终存在于载体细胞中。除了在CsCl梯度中核心带密度约为rho = 1.40至1.415 g/ml的更常见的缺陷病毒外,还观察到一类新的缺陷核心在1.34至1.36 g/ml区域内出现条带。后一种颗粒尚未得到充分表征,被称为“轻度缺陷病毒”。持续感染的细胞在维持培养期间会经历周期性危机,在此期间培养物部分裂解,然后迅速生长至汇合。危机对应于细胞中传染性病毒的爆发以及相对较低浓度的轻度缺陷病毒。在静止期,轻度缺陷病毒的浓度高达病毒总群体的98%。轻度缺陷病毒的功能尚不清楚,但在该系统中维持持续感染时,似乎必须高度重视缺陷病毒。