Beaty B J, Bishop D H
Dept. of Microbiology, Colorado State University, Fort Collins 80523.
Virus Res. 1988 Jun;10(4):289-301. doi: 10.1016/0168-1702(88)90071-8.
Recent advances in the genetics and molecular biology of bunyaviruses have been applied to understanding bunyavirus-vector interactions. Such approaches have revealed which virus gene and gene products are important in establishing infections in vectors and in transmission of viruses. However, much more information is required to understand the molecular mechanisms of persistent infections of vectors which are lifelong but apparently exert no untoward effect. In fact, it seems remarkable that LAC viral antigen can be detected in almost every cell in an ovarian follicle, yet no untoward effect on fecundity and no teratology is seen. Similarly the lifelong infection of the vector would seem to provide ample opportunity for bunyavirus evolution by genetic drift and, under the appropriate circumstances, by segment reassortment. The potential for bunyavirus evolution by segment reassortment in vectors certainly exists. For example the Group C viruses in a small forest in Brazil seem to constitute a gene pool, with the 6 viruses related alternately by HI/NT and CF reactions, which assay respectively M RNA and S RNA gene products (Casals and Whitman, 1960; Shope and Causey, 1962). Direct evidence for naturally occurring reassortant bunyaviruses has also been obtained. Oligonucleotide fingerprint analyses of field isolates of LAC virus and members of the Patois serogroup of bunyaviruses have demonstrated that reassortment does occur in nature (El Said et al., 1979; Klimas et al., 1981; Ushijima et al., 1981). Determination of the genotypic frequencies of viruses selected by the biological interactions of viruses and vectors after dual infection and segment reassortment is an important issue. Should a virus result that efficiently interacts with alternate vector species, the virus could be expressed in different circumstances with serious epidemiologic consequences. Dual infection of vectors with different viruses is not unlikely, because many bunyaviruses are sympatric in nature. For example, the Ae. trivittatus-cottontail rabbit and the Ae. triseriatus-squirrel arbovirus cycles are sympatric in the ecotone between their respective grassland and forest ecosystems (LeDuc, 1979). Should a LaCrosse virus variant or reassortant evolve that was efficiently vectored by Ae. trivittatus mosquitoes, significantly more human infections with La Crosse virus would likely occur. Unlike Ae. triseriatus, Ae. trivittatus mosquitoes are not restricted to forested areas and consequently are more likely to encounter and to feed upon humans.(ABSTRACT TRUNCATED AT 400 WORDS)
布尼亚病毒的遗传学和分子生物学方面的最新进展已被应用于理解布尼亚病毒与媒介的相互作用。这些方法揭示了哪些病毒基因和基因产物在媒介中建立感染以及病毒传播过程中很重要。然而,要了解媒介持续感染的分子机制还需要更多信息,这种持续感染是终身的,但显然没有不良影响。事实上,在卵巢卵泡的几乎每个细胞中都能检测到拉科病毒抗原,却未见对繁殖力有不良影响,也没有致畸现象,这似乎很不寻常。同样,媒介的终身感染似乎为布尼亚病毒通过基因漂移以及在适当情况下通过节段重配进行进化提供了充足机会。布尼亚病毒在媒介中通过节段重配进化的可能性肯定存在。例如,巴西一小片森林中的C组病毒似乎构成了一个基因库,这6种病毒通过血凝抑制/中和试验(HI/NT)和补体结合试验(CF)反应交替相关,这两种试验分别检测M RNA和S RNA基因产物(卡萨尔斯和惠特曼,1960年;肖普和考西,1962年)。也已获得自然发生的重配布尼亚病毒的直接证据。对拉科病毒的野外分离株和布尼亚病毒帕图伊斯血清群成员进行的寡核苷酸指纹分析表明,重配确实在自然界中发生(埃尔·赛义德等人,1979年;克利马斯等人,1981年;潮岛等人,1981年)。确定双重感染和节段重配后通过病毒与媒介的生物学相互作用选择的病毒的基因型频率是一个重要问题。如果产生一种能与其他媒介物种有效相互作用的病毒,那么这种病毒在不同情况下可能会传播,从而产生严重的流行病学后果。不同病毒双重感染媒介并非不可能,因为许多布尼亚病毒在自然界中是同域分布的。例如,三带喙库蚊 - 棉尾兔和三带库蚊 - 松鼠虫媒病毒循环在它们各自的草原和森林生态系统之间的交错带是同域分布的(勒杜克,1979年)。如果进化出一种能被三带喙库蚊有效传播的拉科病毒变体或重配病毒,那么很可能会有更多人感染拉科病毒。与三带库蚊不同,三带喙库蚊不限于森林地区,因此更有可能接触并叮咬人类。(摘要截选至400字)