Instituto de Agrobiotecnología, CSIC-Gobierno de Navarra, 31192 Mutilva Baja, Navarra, Spain.
Appl Environ Microbiol. 2010 Feb;76(3):803-9. doi: 10.1128/AEM.01894-09. Epub 2009 Dec 11.
The stabilities of the Spodoptera frugiperda multiple nucleopolyhedrovirus (SfMNPV) complete genome bacmid (Sfbac) and a deletion recombinant (Sf29null) in which the Sf29 gene was replaced by a kanamycin resistance cassette were determined during sequential rounds of per os infection in insect larvae. The Sf29 gene is a viral factor that determines the number of virions in occlusion bodies (OBs). The Sf29null bacmid virus was able to recover the Sf29 gene during passage. After the third passage (P3) of Sf29null bacmid OBs, the population was observed to reach an equilibrium involving a mixture of those with a kanamycin resistance cassette and those with the Sf29 gene. The biological activity of Sf29null bacmid OBs at P3 was similar to that of Sfbac OBs. The recovered gene in the Sf29null virus was 98 to 100% homologous to the Sf29 genes of different SfMNPV genotypes. Reverse transcription-PCR analysis of uninoculated S. frugiperda larvae confirmed the expression of the SfMNPV ie-0 and Sf29 genes, indicating that the insect colony harbors a covert SfMNPV infection. Additionally, the nonessential bacterial artificial chromosome vector was spontaneously deleted from both viral genomes upon passage in insects.
在昆虫幼虫的连续口服感染过程中,测定了夜蛾多粒核型多角体病毒(SfMNPV)完整基因组 bacmid(Sfbac)和缺失重组体(Sf29null)的稳定性,后者的 Sf29 基因被卡那霉素抗性盒取代。Sf29 基因是决定多角体中病毒粒子数量的病毒因子。Sf29null bacmid 病毒在传代过程中能够恢复 Sf29 基因。在 Sf29null bacmid OB 的第三次传代(P3)后,观察到种群达到了一种平衡,其中包含带有卡那霉素抗性盒和带有 Sf29 基因的混合物。P3 时 Sf29null bacmid OB 的生物活性与 Sfbac OB 的相似。在 Sf29null 病毒中恢复的基因与不同 SfMNPV 基因型的 Sf29 基因同源性为 98%至 100%。对未接种的 S. frugiperda 幼虫进行反转录-PCR 分析证实了 SfMNPV ie-0 和 Sf29 基因的表达,表明昆虫群体中存在隐性 SfMNPV 感染。此外,在昆虫传代过程中,非必需的细菌人工染色体载体自发从两种病毒基因组中缺失。