Giannecchini Simone, Pistello Mauro, Isola Patrizia, Matteucci Donatella, Mazzetti Paola, Freer Giulia, Bendinelli Mauro
Retrovirus Center and Virology Section, Department of Experimental Pathology, University of Pisa, Via San Zeno, 37 I-56127 Pisa, Italy.
J Virol. 2007 Oct;81(19):10474-85. doi: 10.1128/JVI.01064-07. Epub 2007 Jul 18.
A more or less pronounced resistance to superinfection by a second strain of the infecting virus has been observed in many lentivirus-infected hosts. We used a chimeric feline immunodeficiency virus (FIV), designated FIVchi, containing a large part of the env gene of a clade B virus (strain M2) and all the rest of the genome of a clade A virus (a p34TF10 molecular clone of the Petaluma strain modified to grow in lymphoid cells), to gain insights into such resistance. FIVchi was infectious and moderately pathogenic for cats and in vitro exhibited the neutralization specificity of the env donor. The experiments performed were bidirectional, in that cats preinfected with either parental virus were challenged with FIVchi and vice versa. The preinfected animals were partially or completely protected relative to what was observed in naïve control animals, most likely due, at least in part, to the circumstance that in all the preinfecting/challenge virus combinations examined, the first and the second virus shared significant viral components. Based on the proportions of complete protection observed, the role of a strongly matched viral envelope appeared to be modest and possibly dependent on the time interval between the first and the second infection. Furthermore, complete protection and the presence of measurable neutralizing antibodies capable of blocking the second virus in vitro were not associated.
在许多感染慢病毒的宿主中,已观察到对感染病毒的第二种毒株的超感染或多或少存在明显抗性。我们使用了一种嵌合猫免疫缺陷病毒(FIV),命名为FIVchi,它包含B亚型病毒(M2毒株)env基因的大部分以及A亚型病毒(经修饰可在淋巴细胞中生长的Petaluma毒株的p34TF10分子克隆)基因组的其余部分,以深入了解这种抗性。FIVchi对猫具有传染性且致病性中等,并且在体外表现出env供体的中和特异性。所进行的实验是双向的,即先用亲本病毒之一感染猫,然后用FIVchi进行攻击,反之亦然。相对于未感染的对照动物所观察到的情况,预先感染的动物受到了部分或完全保护,这很可能至少部分是由于在所检查的所有预先感染/攻击病毒组合中,第一种和第二种病毒共享了重要的病毒成分。根据所观察到的完全保护的比例,高度匹配的病毒包膜的作用似乎不大,并且可能取决于第一次和第二次感染之间的时间间隔。此外,完全保护与体外能够阻断第二种病毒的可测量中和抗体的存在无关。