tetano
Editor, Senior Moderator
Small GTPases. 2016 Jun 23:0. [Epub ahead of print]
[h=1]Clustering of Rab11 vesicles in influenza A virus infected cells creates hotspots containing the eight viral ribonucleoproteins.[/h] Vale-Costa S[SUP]1[/SUP], Amorim MJ[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus is an important human pathogen causative of yearly epidemics and occasional pandemics. The ability to replicate within the host cell is a determinant of virulence, amplifying viral numbers for host-to-host transmission. This process requires multiple rounds of entering permissive cells, replication, and virion assembly at the plasma membrane, the site of viral budding and release. The assembly of influenza A virus involves packaging of several viral (and host) proteins and of a segmented genome, composed of eight distinct RNAs in the form of viral ribonucleoproteins (vRNPs). The selective assembly of the eight-segment core remains one of the most interesting unresolved problems in virology. The recycling endosome regulatory GTPase Rab11 was shown to contribute to the process, by transporting vRNPs to the periphery, giving rise to enlarged cytosolic puncta rich in Rab11 and the eight vRNPs. We recently reported that vRNP hotspots were formed of clustered vesicles harbouring protruding electron-dense structures that resembled vRNPs. Mechanistically, vRNP hotspots were formed as vRNPs outcompeted the cognate effectors of Rab11, the Rab11-Family-Interacting-Proteins (FIPs) for binding, and as a consequence impair recycling sorting at an unknown step. Here, we speculate on the impact that such impairment might have in host immunity, membrane architecture and viral assembly.
[h=4]KEYWORDS:[/h] Rab11 Family interacting proteins (FIPs); Rab11 GTPase; Recycling endosome; correlative light and electron microscopy; influenza A virus assembly; segmented genome; viral ribonucleoproteins (vRNPs)
PMID: 27337591 [PubMed - as supplied by publisher]
[h=1]Clustering of Rab11 vesicles in influenza A virus infected cells creates hotspots containing the eight viral ribonucleoproteins.[/h] Vale-Costa S[SUP]1[/SUP], Amorim MJ[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus is an important human pathogen causative of yearly epidemics and occasional pandemics. The ability to replicate within the host cell is a determinant of virulence, amplifying viral numbers for host-to-host transmission. This process requires multiple rounds of entering permissive cells, replication, and virion assembly at the plasma membrane, the site of viral budding and release. The assembly of influenza A virus involves packaging of several viral (and host) proteins and of a segmented genome, composed of eight distinct RNAs in the form of viral ribonucleoproteins (vRNPs). The selective assembly of the eight-segment core remains one of the most interesting unresolved problems in virology. The recycling endosome regulatory GTPase Rab11 was shown to contribute to the process, by transporting vRNPs to the periphery, giving rise to enlarged cytosolic puncta rich in Rab11 and the eight vRNPs. We recently reported that vRNP hotspots were formed of clustered vesicles harbouring protruding electron-dense structures that resembled vRNPs. Mechanistically, vRNP hotspots were formed as vRNPs outcompeted the cognate effectors of Rab11, the Rab11-Family-Interacting-Proteins (FIPs) for binding, and as a consequence impair recycling sorting at an unknown step. Here, we speculate on the impact that such impairment might have in host immunity, membrane architecture and viral assembly.
[h=4]KEYWORDS:[/h] Rab11 Family interacting proteins (FIPs); Rab11 GTPase; Recycling endosome; correlative light and electron microscopy; influenza A virus assembly; segmented genome; viral ribonucleoproteins (vRNPs)
PMID: 27337591 [PubMed - as supplied by publisher]