Laboratory of Infectious Diseases, RNA Viruses Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS One. 2013;8(3):e59462. doi: 10.1371/journal.pone.0059462. Epub 2013 Mar 19.
The cellular ESCRT (endosomal sorting complex required for transport) system functions in cargo-sorting, in the formation of intraluminal vesicles that comprise multivesicular bodies (MVB), and in cytokinesis, and this system can be hijacked by a number of enveloped viruses to promote budding. The respiratory pathogen human parainfluenza virus type I (HPIV1) encodes a nested set of accessory C proteins that play important roles in down-regulating viral transcription and replication, in suppressing the type I interferon (IFN) response, and in suppressing apoptosis. Deletion or mutation of the C proteins attenuates HPIV1 in vivo, and such mutants are being evaluated preclinically and clinically as vaccines. We show here that the C proteins interact and co-localize with the cellular protein Alix, which is a member of the class E vacuolar protein sorting (Vps) proteins that assemble at endosomal membranes into ESCRT complexes. The HPIV1 C proteins interact with the Bro1 domain of Alix at a site that is also required for the interaction between Alix and Chmp4b, a subunit of ESCRT-III. The C proteins are ubiquitinated and subjected to proteasome-mediated degradation, but the interaction with AlixBro1 protects the C proteins from degradation. Neither over-expression nor knock-down of Alix expression had an effect on HPIV1 replication, although this might be due to the large redundancy of Alix-like proteins. In contrast, knocking down the expression of Chmp4 led to an approximately 100-fold reduction in viral titer during infection with wild-type (WT) HPIV1. This level of reduction was similar to that observed for the viral mutant, P(C-) HPIV1, in which expression of the C proteins were knocked out. Chmp4 is capable of out-competing the HPIV1 C proteins for binding Alix. Together, this suggests a possible model in which Chmp4, through Alix, recruits the C proteins to a common site on intracellular membranes and facilitates budding.
细胞的 ESCRT(必需的内体分选复合物用于运输)系统在货物分拣、形成包含多泡体(MVB)的腔内小泡以及细胞分裂中起作用,该系统可被多种包膜病毒劫持以促进出芽。呼吸道病原体人副流感病毒 1 型(HPIV1)编码一组嵌套的辅助 C 蛋白,这些蛋白在下调病毒转录和复制、抑制 I 型干扰素(IFN)反应和抑制细胞凋亡方面发挥重要作用。C 蛋白的缺失或突变会使 HPIV1 在体内减毒,并且这些突变体正在进行临床前和临床评估作为疫苗。我们在这里表明,C 蛋白与细胞蛋白 Alix 相互作用并共定位,Alix 是 E 类液泡蛋白分选(Vps)蛋白的成员,该蛋白在内体膜上组装成 ESCRT 复合物。HPIV1 C 蛋白与 Alix 的 Bro1 结构域相互作用,该位点也是 Alix 与 ESCRT-III 的 Chmp4b 亚基相互作用所必需的。C 蛋白被泛素化并被蛋白酶体介导的降解,但与 AlixBro1 的相互作用保护 C 蛋白免受降解。Alix 表达的过表达或敲低均未对 HPIV1 复制产生影响,尽管这可能是由于 Alix 样蛋白的大量冗余所致。相比之下,敲低 Chmp4 的表达会导致野生型(WT)HPIV1 感染时病毒滴度降低约 100 倍。这种降低水平与 C 蛋白表达被敲除的病毒突变体 P(C-) HPIV1 观察到的水平相似。Chmp4 能够与 HPIV1 C 蛋白竞争结合 Alix。综上所述,这表明了一种可能的模型,即 Chmp4 通过 Alix 将 C 蛋白募集到细胞内膜上的共同部位,并促进出芽。