Haeberlé A M, Stussi-Garaud C
INRA, Station Grandes Cultures, Laboratoire de Pathologie Végétale, Colmar, France.
J Gen Virol. 1995 Mar;76 ( Pt 3):643-50. doi: 10.1099/0022-1317-76-3-643.
The in situ localization of the non-structural protein P25 encoded by beet necrotic yellow vein virus (BNYVV) RNA 3 and of the BNYVV coat protein (CP) was studied by immunoelectron microscopy in infected leaf and root cells of Chenopodium murale and C. quinoa. The CP was detected in the cytoplasm of all cell types except xylem, sieve elements, and companion cells. P25 was detected in the cytoplasm and nuclei of the same cell types. The intensity of CP labelling varied depending upon the stage of infection of the cell, whereas the P25 labelling intensity was similar in newly infected cells and in cels at later stages of infection. These results suggest that P25 may be synthesized at an earlier stage of infection than CP. Its presence in the nuclei of newly infected cells may be related to the reported effect of P25 on leaf symptom development.
通过免疫电子显微镜技术,研究了甜菜坏死黄脉病毒(BNYVV)RNA 3编码的非结构蛋白P25以及BNYVV外壳蛋白(CP)在感染的墙生藜和藜麦叶片及根细胞中的原位定位。除木质部、筛管分子和伴胞外,在所有细胞类型的细胞质中均检测到CP。在相同细胞类型的细胞质和细胞核中检测到P25。CP标记的强度因细胞感染阶段而异,而P25标记强度在新感染细胞和感染后期的细胞中相似。这些结果表明,P25可能比CP在感染的更早阶段合成。其在新感染细胞核中的存在可能与报道的P25对叶片症状发展的影响有关。