AlaskaDenise
In Memoriam
Yes.
see (among many sources):
(this article discusses primarily WSN H1N1, but some comments are relevent)
http://jvi.asm.org/cgi/content/full/75/19/9297?pmid=11533192
.....Although the virulence of influenza A viruses is controlled polygenically, the HA plays a pivotal role in determining the<SUP> </SUP>severity of infection in avian strains (8, 11, 26). The<SUP> </SUP>HA cleavage site sequences in virulent and avirulent avian influenza<SUP> </SUP>viruses differ; the former possess a series of basic amino acids<SUP> </SUP>at this site, while the latter do not (10, 13). The ubiquitous<SUP> </SUP>host proteases furin and PC6, which specifically recognize these<SUP> </SUP>multiple basic residues, cleave the HAs of virulent viruses, leading<SUP> </SUP>to systemic infection (12, 27). By contrast, the HAs of avirulent<SUP> </SUP>viruses are not cleaved by these proteases because they lack the<SUP> </SUP>requisite series of basic residues at their cleavage sites. Instead,<SUP> </SUP>they are susceptible to proteases that are presumably localized<SUP> </SUP>in the respiratory and/or intestinal tract, thus leading to localized<SUP> </SUP>viral<SUP> </SUP>infection.
All mammalian influenza viruses, excluding equine H7N7 viruses, have a single Arg residue at the HA cleavage site. Thus, the<SUP> </SUP>HAs cannot be cleaved by ubiquitous furin or PC6 protease, resulting<SUP> </SUP>in a localized infection. However, a mouse-adapted human isolate,<SUP> </SUP>A/WSN/33 (WSN; H1N1), which is recognized as a neurovirulent strain,<SUP> </SUP>causes systemic infection when inoculated intranasally into mice<SUP> </SUP>(3). Studies with WSN-A/Hong Kong/68 (H3N2) reassortant viruses<SUP> </SUP>indicated that the NA gene determines WSN neurovirulence in mice<SUP> </SUP>by facilitating HA cleavage (24). Only a single Arg is present<SUP> </SUP>at the HA cleavage site of WSN virus, suggesting that the mechanism<SUP> </SUP>of HA cleavage mediated by the WSN NA differs from that in pathogenic<SUP> </SUP>avian<SUP> </SUP>viruses. ......
-------------------------------
The NA of the WSN33 H1N1 had systemic infection and neurovirulence due to the plasminogen-binding capabiltiy of a muation at postion 130. H5N! doesn't have this (to my knowledge).
However H5N1 DOES have the multi-basic amino acids, meaning that the above explanation about umbiqutous host proteases causing cleavage and systemic infections.
I've been reading like crazy trying to chase down all these items, and just read this article today. You can go back and find all the references to multi-basic amino acids and neurovirulence and you'll get the details on how and why H5N1 MAY produce systemic infections.
I hope some the the professionals here will correct any of my misunderstandings.
-----------------------------------------------
I found another one...
See also:
http://www.sciencemag.org/cgi/content/full/279/5349/393
...In addition to its role as a determinant of host range, the HA gene is important in determining the virulence of avian influenza<SUP> </SUP>A viruses for poultry (16). All human influenza virus HA genes<SUP> </SUP>characterized to date, including the 1918 viruses (17), have<SUP> </SUP>a single, basic Arg residue at the cleavage site between HA1 and<SUP> </SUP>HA2. An insertion similar to the basic amino acid insertion adjacent<SUP> </SUP>to the cleavage site in the HA gene of the A/Hong Kong/156/97<SUP> </SUP>virus has been found in several highly pathogenic avian H5 viruses.<SUP> </SUP>Basic amino acids adjacent to the cleavage site allow proteases<SUP> </SUP>other than trypsin-like proteases to cleave the HA into HA1 and<SUP> </SUP>HA2 domains. This event would enable the virus to spread systemically<SUP> </SUP>by altering the tissue range of these viruses from the respiratory<SUP> </SUP>and alimentary tract to other sites, such as the brain, heart,<SUP> </SUP>and blood vessels (18). It has been suggested that the acquisition<SUP> </SUP>of a ubiquitously cleavable avian HA by a human influenza A virus<SUP> </SUP>could make a virus lethal (16). It remains to be shown whether<SUP> </SUP>gene segments other than the HA may also have contributed to the<SUP> </SUP>ability of the virus to infect a human....
.<SUP> </SUP>
see (among many sources):
(this article discusses primarily WSN H1N1, but some comments are relevent)
http://jvi.asm.org/cgi/content/full/75/19/9297?pmid=11533192
.....Although the virulence of influenza A viruses is controlled polygenically, the HA plays a pivotal role in determining the<SUP> </SUP>severity of infection in avian strains (8, 11, 26). The<SUP> </SUP>HA cleavage site sequences in virulent and avirulent avian influenza<SUP> </SUP>viruses differ; the former possess a series of basic amino acids<SUP> </SUP>at this site, while the latter do not (10, 13). The ubiquitous<SUP> </SUP>host proteases furin and PC6, which specifically recognize these<SUP> </SUP>multiple basic residues, cleave the HAs of virulent viruses, leading<SUP> </SUP>to systemic infection (12, 27). By contrast, the HAs of avirulent<SUP> </SUP>viruses are not cleaved by these proteases because they lack the<SUP> </SUP>requisite series of basic residues at their cleavage sites. Instead,<SUP> </SUP>they are susceptible to proteases that are presumably localized<SUP> </SUP>in the respiratory and/or intestinal tract, thus leading to localized<SUP> </SUP>viral<SUP> </SUP>infection.
All mammalian influenza viruses, excluding equine H7N7 viruses, have a single Arg residue at the HA cleavage site. Thus, the<SUP> </SUP>HAs cannot be cleaved by ubiquitous furin or PC6 protease, resulting<SUP> </SUP>in a localized infection. However, a mouse-adapted human isolate,<SUP> </SUP>A/WSN/33 (WSN; H1N1), which is recognized as a neurovirulent strain,<SUP> </SUP>causes systemic infection when inoculated intranasally into mice<SUP> </SUP>(3). Studies with WSN-A/Hong Kong/68 (H3N2) reassortant viruses<SUP> </SUP>indicated that the NA gene determines WSN neurovirulence in mice<SUP> </SUP>by facilitating HA cleavage (24). Only a single Arg is present<SUP> </SUP>at the HA cleavage site of WSN virus, suggesting that the mechanism<SUP> </SUP>of HA cleavage mediated by the WSN NA differs from that in pathogenic<SUP> </SUP>avian<SUP> </SUP>viruses. ......
-------------------------------
The NA of the WSN33 H1N1 had systemic infection and neurovirulence due to the plasminogen-binding capabiltiy of a muation at postion 130. H5N! doesn't have this (to my knowledge).
However H5N1 DOES have the multi-basic amino acids, meaning that the above explanation about umbiqutous host proteases causing cleavage and systemic infections.
I've been reading like crazy trying to chase down all these items, and just read this article today. You can go back and find all the references to multi-basic amino acids and neurovirulence and you'll get the details on how and why H5N1 MAY produce systemic infections.
I hope some the the professionals here will correct any of my misunderstandings.
-----------------------------------------------
I found another one...
See also:
http://www.sciencemag.org/cgi/content/full/279/5349/393
...In addition to its role as a determinant of host range, the HA gene is important in determining the virulence of avian influenza<SUP> </SUP>A viruses for poultry (16). All human influenza virus HA genes<SUP> </SUP>characterized to date, including the 1918 viruses (17), have<SUP> </SUP>a single, basic Arg residue at the cleavage site between HA1 and<SUP> </SUP>HA2. An insertion similar to the basic amino acid insertion adjacent<SUP> </SUP>to the cleavage site in the HA gene of the A/Hong Kong/156/97<SUP> </SUP>virus has been found in several highly pathogenic avian H5 viruses.<SUP> </SUP>Basic amino acids adjacent to the cleavage site allow proteases<SUP> </SUP>other than trypsin-like proteases to cleave the HA into HA1 and<SUP> </SUP>HA2 domains. This event would enable the virus to spread systemically<SUP> </SUP>by altering the tissue range of these viruses from the respiratory<SUP> </SUP>and alimentary tract to other sites, such as the brain, heart,<SUP> </SUP>and blood vessels (18). It has been suggested that the acquisition<SUP> </SUP>of a ubiquitously cleavable avian HA by a human influenza A virus<SUP> </SUP>could make a virus lethal (16). It remains to be shown whether<SUP> </SUP>gene segments other than the HA may also have contributed to the<SUP> </SUP>ability of the virus to infect a human....
.<SUP> </SUP>