Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
Traffic. 2022 Aug;23(8):414-425. doi: 10.1111/tra.12860. Epub 2022 Jun 28.
Many intracellular pathogens, such as bacteria and large viruses, enter eukaryotic cells via phagocytosis, then replicate and proliferate inside the host. To avoid degradation in the phagosomes, they have developed strategies to modify vesicle trafficking. Although several strategies of bacteria have been characterized, it is not clear whether viruses also interfere with the vesicle trafficking of the host. Recently, we came across SNARE proteins encoded in the genomes of several bacteria of the order Legionellales. These pathogenic bacteria may use SNAREs to interfere with vesicle trafficking, since SNARE proteins are the core machinery for vesicle fusion during transport. They assemble into membrane-bridging SNARE complexes that bring membranes together. We now have also discovered SNARE proteins in the genomes of diverse giant viruses. Our biochemical experiments showed that these proteins are able to form SNARE complexes. We also found other key trafficking factors that work together with SNAREs such as NSF, SM, and Rab proteins encoded in the genomes of giant viruses, suggesting that viruses can make use of a large genetic repertoire of trafficking factors. Most giant viruses possess different collections, suggesting that these factors entered the viral genome multiple times. In the future, the molecular role of these factors during viral infection need to be studied.
许多细胞内病原体,如细菌和大型病毒,通过吞噬作用进入真核细胞,然后在宿主内部复制和增殖。为了避免在吞噬体中降解,它们已经开发出了改变囊泡运输的策略。尽管已经描述了几种细菌的策略,但尚不清楚病毒是否也会干扰宿主的囊泡运输。最近,我们在军团菌目(Legionellales)的几种细菌的基因组中发现了 SNARE 蛋白。这些致病性细菌可能利用 SNARE 来干扰囊泡运输,因为 SNARE 蛋白是运输过程中囊泡融合的核心机制。它们组装成膜桥接 SNARE 复合物,使膜融合。我们现在还在大型病毒的基因组中发现了 SNARE 蛋白。我们的生化实验表明,这些蛋白质能够形成 SNARE 复合物。我们还发现了其他与 SNARE 一起起作用的关键运输因子,如 NSF、SM 和 Rab 蛋白,这些蛋白编码在大型病毒的基因组中,这表明病毒可以利用大量的运输因子遗传库。大多数大型病毒具有不同的集合,这表明这些因子多次进入病毒基因组。将来,需要研究这些因子在病毒感染过程中的分子作用。