Levy J A, Kazan P, Varnier O, Kleiman H
J Virol. 1975 Oct;16(4):844-53. doi: 10.1128/JVI.16.4.844-853.1975.
The xenotropic mouse type C virus, originally detected in cultured embryo cells from New Zealand Black (NZB) mice, has been recovered from over 50 adult NZB animals and 15 NZB embryos. Its presence is best detected by measuring its ability to rescue a murine sarcoma virus (MSV) genome from a non-virus-producing MSV-transformed rat cell. The virus can serve as a helper for replication of MSV. It has a distinct type-specific coat and is a prototype for a third serotype of mouse type C viruses, NZB. The xenotropic virus may have an evolutionary role since it has a wide host range, including the ability to infect avian cells. It is produced spontaneously by all cells cultivated from NZB tissues and accounts for the high concentration of viral antigens associated with NZB tissues. The extent of virus production is similar in both male and female mice. All cell clones established from embryos also produce the virus. A variability in the intracellular regulation of virus replication is suggested since tissue cells from the same animal differ quantitatively in their ability to produce xenotropic viruses. Since enhanced spontaneous virus production is associated with cells from NZB mice, the virus may play a role in the autoimmune disease of this mouse strain.
嗜异性小鼠C型病毒最初是在新西兰黑(NZB)小鼠的培养胚胎细胞中检测到的,现已从50多只成年NZB动物和15个NZB胚胎中分离出来。检测其存在的最佳方法是测量其从非病毒产生的MSV转化大鼠细胞中拯救鼠肉瘤病毒(MSV)基因组的能力。该病毒可作为MSV复制的辅助病毒。它具有独特的型特异性衣壳,是小鼠C型病毒第三血清型NZB的原型。嗜异性病毒可能具有进化作用,因为它具有广泛的宿主范围,包括感染禽类细胞的能力。它由NZB组织培养的所有细胞自发产生,并导致与NZB组织相关的高浓度病毒抗原。雌雄小鼠的病毒产生程度相似。从胚胎建立的所有细胞克隆也产生该病毒。由于同一动物的组织细胞产生嗜异性病毒的能力在数量上存在差异,提示病毒复制的细胞内调节存在变异性。由于自发病毒产生增强与NZB小鼠的细胞有关,该病毒可能在该小鼠品系的自身免疫性疾病中起作用。