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Cellular Proteins in Influenza Virus Particles

mixin

Well-known member
Cellular Proteins in Influenza Virus Particles
Megan L. Shaw1*, Kathryn L. Stone2, Christopher M. Colangelo2, Erol E. Gulcicek2, Peter Palese1,3

1 Department of Microbiology, Mount Sinai School of Medicine, New York, New York, United States of America2 Northeast Biodefense Center Proteomics Core, W.M. Keck Foundation Biotechnology Laboratory, Yale University, New Haven, Connecticut, United States of America3 Department of Medicine, Mount Sinai School of Medicine, New York, New York, United States of America

Abstract
Virions are thought to contain all the essential proteins that govern virus egress from the host cell and initiation of replication in the target cell. It has been known for some time that influenza virions contain nine viral proteins; however, analyses of other enveloped viruses have revealed that proteins from the host cell can also be detected in virions. To address whether the same is true for influenza virus, we used two complementary mass spectrometry approaches to perform a comprehensive proteomic analysis of purified influenza virus particles. In addition to the aforementioned nine virus-encoded proteins, we detected the presence of 36 host-encoded proteins. These include both cytoplasmic and membrane-bound proteins that can be grouped into several functional categories, such as cytoskeletal proteins, annexins, glycolytic enzymes, and tetraspanins. Interestingly, a significant number of these have also been reported to be present in virions of other virus families. Protease treatment of virions combined with immunoblot analysis was used to verify the presence of the cellular protein and also to determine whether it is located in the core of the influenza virus particle. Immunogold labeling confirmed the presence of membrane-bound host proteins on the influenza virus envelope. The identification of cellular constituents of influenza virions has important implications for understanding the interactions of influenza virus with its host and brings us a step closer to defining the cellular requirements for influenza virus replication. While not all of the host proteins are necessarily incorporated specifically, those that are and are found to have an essential role represent novel targets for antiviral drugs and for attenuation of viruses for vaccine purposes.

Author Summary
Viruses are released from infected cells in the form of virions, which contain all the essential factors necessary for initiating infection in a new target cell. For influenza virus, it is known that virions contain the viral genome, a lipid envelope, and at least nine viral proteins. We performed a detailed proteomic analysis of purified influenza virus particles using mass spectrometry and database searching for protein identification, and in addition to the nine viral proteins, we identified 36 host proteins. These host proteins are present both inside the influenza virus particle and on the viral envelope. All viruses require host cell factors to complete their replication cycles, and they also have to contend with the antiviral defense mechanisms of the host. Virus?host interactions may therefore provide the key to understanding viral pathogenesis and may also present us with new targets for the design of antiviral drugs. For influenza virus, information on the requirement of cellular factors is limited, but the description of these 36 host proteins that are packaged into the virion provides a foundation for further analysis into the involvement of these cellular pathways in the influenza virus life cycle.

Full article here:
http://www.plospathogens.org/articl...5;jsessionid=ED680FAE739536100E46D00AFC3A07C7
 
Re: Cellular Proteins in Influenza Virus Particles

Thank you mixin, it's very incredible...32 human proteins !

this small piece for gsgs ::)
" Therefore, as discussed above for CD59, virion-associated host proteins can be one of the determinants of virus host range due to their species-specific activity. It will also be interesting to compare the identity and abundance of host proteins in influenza viruses that produce virions with a filamentous morphology. One would assume that the increased volume and surface area of these particles would allow for greater levels of host protein incorporation but whether or not there is increased diversity may depend on specific versus non-specific incorporation."
 
Re: Cellular Proteins in Influenza Virus Particles

aren't there 11 influenza "proteins" , not nine ?
ahh, well. Two of the 11 (which) are maybe not present as proteins
in the virus, only encoded as RNA, but at some process in the virus
living cycle (during infection ?) become decoded and active

> we detected the presence of 36 host-encoded proteins

human host ?

> These include both cytoplasmic and membrane-bound proteins that can be grouped into
> several functional categories, such as cytoskeletal proteins, annexins, glycolytic enzymes,
> and tetraspanins

> ...presence of membrane-bound host proteins on the influenza virus envelope

as I understand it, they steal their envelope from the host-cell membrane when "budding"
off from the host cell.

> These host proteins are present both inside the influenza virus particle and on the viral envelope.
 
Re: Cellular Proteins in Influenza Virus Particles

I suppose it depends on whether you are counting coded proteins or biologically active proteins i.e. HA0 or HA1 & HA2. The coat would mainly be a phospholipid bi layer.
The question is not so much what can you sometimes find but what do you always find? Which, if any, are there by design (and have a biological significance) rather than just being in close proximity to the vRNA during encapsulation or budding.
 
Re: Cellular Proteins in Influenza Virus Particles

I was very surprised by the fact that some of theses proteins are included in NP

http://www.ncbi.nlm.nih.gov/sites/e...ternalization into polarized epithelial cells.


Role of the actin cytoskeleton during influenza virus internalization into polarized epithelial cells.

Sun X, Whittaker GR.

Department of Microbiology & Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.

The in vivo site of influenza virus infection is a polarized epithelium, and it is well established that the virus preferentially enters from the apical surface of polarized epithelial cells; however, many of the molecular events involved during the endocytosis of the virus into polarized epithelia remain unclear. Here we examined the role of actin microfilaments and the myosin VI motor protein during influenza entry into a panel of polarized and non-polarized cells. By treatment of cells with cytochalasin D and jasplakinolide, we show that influenza virus entry into all the polarized epithelial cells tested requires actin dynamics, with a specific role for the actin cytoskeleton in the process of virus internalization from the plasma membrane. In contrast, influenza could still could efficiently enter and infect all non-polarized cells tested after disruption or stabilization of the actin cytoskeleton. To examine the role of the actin motor protein, myosin VI, we expressed a dominant-negative construct in both polarized and non-polarized cells. Influenza virus infectivity in myosin VI tail mutant-transfected cells was significantly decreased in polarized epithelial cells, but not in non-polarized cells. As a whole, our data suggest indispensable roles of a dynamic actin cytoskeleton for influenza virus entry into polarized epithelial cells, a feature not shared with non-polarized cells.
 
Re: Cellular Proteins in Influenza Virus Particles

Mamabird
Am I right in thinking that the Matrix protein is translated as a single protein and then cleaved into M1 & M2 which are the biologically active structural proteins? or do they have their own start and stop codons?
 
Re: Cellular Proteins in Influenza Virus Particles

Mamabird
Am I right in thinking that the Matrix protein is translated as a single protein and then cleaved into M1 & M2 which are the biologically active structural proteins? or do they have their own start and stop codons?

M2 can be found at the end of the MP segment. It can be isolated for comparative purposes with other viruses by retaining the first 27 nucleotids of MP, and then discarding everything up to position 716 (CCTACCAG).
 
Re: Cellular Proteins in Influenza Virus Particles

I assume they can't be "cleaved" because they overlap.
Just both are created from one segment.
Other than in HA they have end-codons
 
Re: Cellular Proteins in Influenza Virus Particles

I assume they can't be "cleaved" because they overlap.
Just both are created from one segment.
Other than in HA they have end-codons

Yes, I have not heard of the matrix protein itself "cleaving". M2 is important because it forms the hydrogen ion channel with the host cytoplasm that lowers the pH of the virus. After this occurs, it supports the HA cleavage which splits the entire endoplasm and spills the viral nuclear proteins into the host cell for replication.
 
Re: Cellular Proteins in Influenza Virus Particles

My - admittedly limited - understanding was the the M1 proteins form a lattice in which are some M2 trimers. The M1s act as an exoskeleton of kinds which gets a coating of phospholipids as it buds. Is this basically correct and if host proteins are being incorporated is there any evidence that any of the actually do anything or are or are they just along for the ride?
Thanks
 
Re: Cellular Proteins in Influenza Virus Particles

I don't know. (even more limited ;-) )

checking
http://www.topleyandwilson.com/pdf/Virology sample chapter.pdf

the M1-protein possibly serves as a molecular glue interacting with RNP
on the one hand and with HA,NA, or M2 on the other.


hmm, the vRNPs are already formed in the nucleus, not as I wrote : maybe when packing
occurs near the cell-membrane.
 
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