Beperet Inés, Simón Oihane, Williams Trevor, López-Ferber Miguel, Caballero Primitivo
Bioinsecticidas Microbianos, Instituto de Agrobiotecnología, CSIC-UPNA, Gobierno de Navarra, 31192 Mutilva Baja, Navarra, Spain.
Instituto de Ecología AC, Xalapa, Veracruz 91070, Mexico.
J Invertebr Pathol. 2015 May;127:101-9. doi: 10.1016/j.jip.2015.03.008. Epub 2015 Mar 20.
The "11K" gene family is notable for having homologs in both baculoviruses and entomopoxviruses and is classified as either type 145 or type 150, according to their similarity with the ac145 or ac150 genes of Autographa californica multiple nucleopolyhedrovirus (AcMNPV). One homolog of ac145 (sf138) and two homologs of ac150 (sf68 and sf95) are present in Spodoptera frugiperda multiple nucleopolyhedrovirus (SfMNPV). Recombinant bacmids lacking sf68, sf95 or sf138 (Sf68null, Sf95null and Sf138null, respectively) and the respective repair bacmids were generated from a bacmid comprising the complete virus genome. Occlusion bodies (OBs) of the Sf138null virus were ∼15-fold less orally infective to insects, which was attributed to a 100-fold reduction in ODV infectious titer. Inoculation of insects with Sf138null OBs in mixtures with an optical brightener failed to restore the pathogenicity of Sf138null OBs to that of the parental virus, indicating that the effects of sf138 deletion on OB pathogenicity were unlikely to involve an interaction with the gut peritrophic matrix. In contrast, deletion of sf68 and sf95 resulted in a slower speed-of-kill by 9h, and a concurrent increase in the yield of OBs. Phylogenetic analysis indicated that sf68 and sf95 were not generated after a duplication event of an ancestral gene homologous to the ac150 gene. We conclude that type 145 genes modulate the primary infection process of the virus, whereas type 150 genes appear to have a role in spreading systemic infection within the insect.
“11K”基因家族因在杆状病毒和昆虫痘病毒中均有同源物而备受关注,根据其与苜蓿银纹夜蛾多核型多角体病毒(AcMNPV)的ac145或ac150基因的相似性,可分为145型或150型。草地贪夜蛾多核型多角体病毒(SfMNPV)中存在ac145的一个同源物(sf138)和ac150的两个同源物(sf68和sf95)。分别缺失sf68、sf95或sf138的重组杆粒(分别为Sf68null、Sf95null和Sf138null)以及相应的修复杆粒,是从包含完整病毒基因组的杆粒中产生的。Sf138null病毒的包涵体(OBs)对昆虫的口服感染性降低了约15倍,这归因于ODV感染滴度降低了100倍。将Sf138null OBs与荧光增白剂混合接种昆虫,未能将Sf138null OBs的致病性恢复到亲本病毒的水平,这表明sf138缺失对OB致病性的影响不太可能涉及与肠道围食膜的相互作用。相比之下,sf68和sf95的缺失导致死亡速度减慢9小时,同时OBs产量增加。系统发育分析表明,sf68和sf95并非源自与ac150基因同源的祖先基因的复制事件。我们得出结论,145型基因调节病毒的初次感染过程,而150型基因似乎在昆虫体内传播全身感染中发挥作用。