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  • AlaskaDenise
    replied
    Re: New swine flu has avian flu genes

    <TABLE style="TABLE-LAYOUT: auto" cellSpacing=0 cellPadding=0 width="100%" summary="Main Page Table" border=0><TBODY><TR><TD vAlign=top><TABLE cellSpacing=10 cellPadding=0 summary="Main Content Table" border=0><TBODY><TR><TD vAlign=top align=left colSpan=2>CIDRAP article...

    New swine flu virus supports 'mixing vessel' theory

    Robert Roos News Editor


    Dec 20, 2007 (CIDRAP News) ? A new influenza virus discovered in Missouri pigs has a combination of genes from avian and swine flu viruses, supporting the theory that pigs can serve as a mixing vessel for flu viruses and a potential source for a human pandemic strain, according to a report published yesterday.

    Researchers found that the virus, an H2N3 subtype, caused illness in experimentally infected mice and was transmissible in swine and ferrets, suggesting it has adapted to mammals, according to the report, published in the Proceedings of the National Academy of Sciences (PNAS). In addition, genetic analysis showed the virus has a mutation linked with an increased ability to infect mammals.

    The discovery marks the first identification of an H2 virus in swine, according to the authors of the report. The flu pandemic of 1957-58 was caused by an H2 virus, namely H2N2. That virus was replaced by an H3N2 strain in the pandemic of 1968-69, and H2 viruses have not circulated in humans since then. Hence, people younger than 40 have little immunity to H2 viruses, scientists say.

    "Our results provide further evidence for the potential of swine to promote reassortment between different influenza viruses, and the genetic and biologic properties of the H2N3 viruses described suggest that it would be prudent to establish vigilant surveillance in pigs and in workers who have occupational exposure," states the PNAS report.

    It was written by scientists from Iowa State University and the US Department of Agriculture's (USDA's) Agricultural Research Service (ARS), both in Ames, Iowa; the University of Minnesota in St. Paul; and St. Jude Children's Research Hospital and the University of Tennessee, both in Memphis. The lead author is Wenjun Ma of Iowa State and the USDA.

    Two incidents 5 months apart

    The discovery of the new virus began with an illness outbreak in pigs at a Missouri swine nursery in September 2006, according to the report. The pigs' lungs showed obvious signs of pneumonia, and tests showed the presence of an influenza gene, but the subtype could not be determined. Samples were submitted to the ARS in Ames, where genetic sequencing and a search of a flu sequence database showed the virus subtype to be H2N3.

    After the virus was subtyped, a record search revealed that another unidentified virus had been submitted in April 2006, from a 12-week-old pig at another Missouri swine farm, according to the report. Analysis by the ARS showed that this isolate too was an H2N3, and the two viruses were nearly identical.

    The two outbreak sites are about 8 miles apart, according to Marie Gramer of the University of Minnesota College of Veterinary Medicine in St. Paul, a coauthor of the report. She said there was no connection between the two operations.

    Phylogenetic analysis showed that the virus's hemagglutinin (HA) gene most closely matched the genes of H2 viruses isolated from North American mallard ducks, while the neuraminidase (NA) gene was closely related to that of an H4N3 virus found in blue-winged teal. Five of the other six genes were derived from swine flu viruses currently circulating in the United States, the scientists determined.

    The source of the virus is unknown, but the likeliest possibility is pond water, which was used to clean barns and water the animals on both farms, according to the report. That transmission pathway has been described before.

    Looking for genetic evidence of the new viruses' adaptation to mammals, the authors compared their HA genes with the HA genes from avian H2N3 viruses. They found an amino-acid substitution at position 226 that, in other H2 and H3 viruses, has been associated with adaptation of avian viruses to humans, according to the report.

    To assess the new isolate's pathogenicity in swine, the scientists inoculated 20 4-week-old pigs with one of the viruses, and 3 days later housed 10 other pigs with the inoculated pigs. On necropsy, the inoculated pigs were found to have mild to moderate pneumonia, while the contact pigs had antibodies to the virus but slight or no signs of pneumonia.

    The researchers also exposed mice to one of the H2N3 viruses at three different doses. Mice that received the middle or highest doses showed signs of illness, and 75% of those with the highest dose died, but none exposed to the lower doses died.

    To test the virus's effect in ferrets, the scientists inoculated three 18-week-old, separately caged ferrets with it and then placed an uninfected ferret in each cage a day later. Subsequent tests showed the virus was present in all the animals, but none showed obvious signs of illness.

    Reason for public health concern

    The authors write that their findings are "of considerable concern to public health." In particular, the H2N3 viruses' mutation associated with an affinity for human-type cell-surface receptors and their ability to replicate and spread in swine and ferrets "suggests that the swine H2N3 viruses have undergone adaptation to the mammalian host and as such have the ability for sustained transmission."

    However, the report also says that "receptor-binding changes" are not sufficient by themselves to permit avian flu viruses to successfully adapt to humans. For example, swine H1N1 flu viruses prefer human-type receptors and have occasionally infected humans but have not become established in human populations.

    Gramer told CIDRAP News that no illnesses were reported among farm workers in connection with the swine cases, and no workers were tested at the time. However, serologic testing of the workers is currently being conducted under a grant from the Centers for Disease Control and Prevention, she reported.

    When asked whether the newfound virus currently represents a threat to humans, Gramer replied, "No more than any other influenza virus in the world. Transmission of flu from pigs to humans is likely rare. This flu itself is rare and we don't know if it is currently circulating in this farm or any other farm in the USA. We haven't found it again."

    Although pigs have long been regarded as a viral mixing vessel that could potentially produce human pandemic strains, whether this has ever happened is unclear, the PNAS report states. The 1957 and 1968 pandemic viruses both resulted from genetic reassortment of human and avian strains, but the mixing might have occurred in humans, pigs, quail, or some other host, it says.

    Gregory C. Gray, MD, MPH, an Iowa infectious disease expert who was not involved in the study, says the new findings should cause public health officials "much concern" and point up the need for careful and coordinated flu surveillance in swine, poulty, and humans who work with them.

    The report suggests that state and federal public health officials should work "aggressively" with the swine and poultry industries to study the prevalence of the new virus and find out whether it is infecting humans and to set up coordinated surveillance programs, said Gray, who is director of the Center for Emerging Infectious Diseases at the University of Iowa in Iowa City.

    Much effort is currently devoted to the hunt for highly pathogenic flu viruses in migratory and aquatic birds, Gray continued. "Influenza surveillance in agriculture is largely managed by the industries. Our agriculture industry and human influenza surveillance are not well coordinated. We might wake up one day to find a virus like the one in this report has become endemic in our agriculture industries and a major threat to the industries as well as to man."

    He added that numerous reports show that common swine flu viruses can cause severe disease in humans. "A novel virus like the one in the PNAS report, if highly transmissible between people, has potential to cause markedly more morbidity, even a pandemic," he said.

    Gray has previously written about the need to include agricultural workers in seasonal flu vaccination programs, flu surveillance, and pandemic planning. "The PNAS report greatly increases our concern," he commented.

    Another expert, Michael T. Osterholm, PhD, MPH, generally concurred with Gray. "I think it?s a potentially serious threat," said Osterholm, director of the University of Minnesota Center for Infectious Disease Research and Policy, publisher of CIDRAP News. "I think one of the problems we have is that we tend to think of influenza today, because of H5N1, as an Asian disease, with the roots of any future pandemic planted deep in Asia. But we have to be very careful because we don't know that."

    Gramer commented that flu is very common in pigs, particularly in the spring, fall, and early winter, and is typically mild and self-limiting. "Flu surveillance in pigs is entirely voluntary," she said. Some surveillance for flu in farm workers is carried on under research grants from the CDC and the National Institutes of Health, she added.

    Ma W, Vincent AL, Gramer MR, et al. Identification of H2N3 influenza A viruses from swine in the United States. Proc Natl Acad Sci 2007 Dec 26;104(52):20949-54 [Abstract]

    .

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  • AlaskaDenise
    replied
    Re: New swine flu has avian flu genes

    Originally posted by niman View Post
    Commentary

    Swine H2N3

    Recombinomics Commentary
    December 20, 2007

    Researchers have identified a new strain of swine influenza--H2N3--which belongs to the group of H2 influenza viruses that last infected humans during the 1957 pandemic. This new strain has a molecular twist: It is composed of avian and swine influenza genes.

    The research team studied an unknown pathogen that in 2006 infected two groups of pigs at separate production facilities. Both groups of pigs used water obtained from ponds frequented by migrating waterfowl.

    Molecular studies indicated the unknown pathogen was an H2N3 influenza virus that is closely related to an H2N3 strain found in mallard ducks

    The above comments describe a PNAS ahead of the press publication on H2N3 in two swine isolates from Missouri. The 1957 pandemic was caused by H2N2, which was replaced by H3N2 in the 1968 pandemic. Therefore, people born after 1968 have not been exposed to H2 and its re-emergence in the human population is cause for concern.

    Avian H2 has amino acids at position 226 and 228 which are distinct from the later human H2N2 isolates. Earlier human H2N2 only differed at position 226, but the swine isolates above have the sequence that matches the earlier human H2N2 at both positions (Q226L and S228G). Moreover, the swine H2N3 is pathogenic mice and can be efficiently transferred from ferret to ferret, although the infected ferrets were asymptomatic. However, the efficient transmission increases concerns for an emerging H2, which could continue to evolve.

    Recent swine isolates in the US also frequently have a human H1 and swine H1N1 has recently been isolated from humans in the US, so there is exchange of genetic information. Similarly, recent seasonal flu isolates in the US have acquired swine polymorphisms, providing more evidence for co-infections.


    .

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  • HenryN
    replied
    Re: New swine flu has avian flu genes

    Originally posted by niman View Post
    Data deposition: The sequences reported in this paper have been deposited in the GenBank

    database [accession nos. EU258935?EU258942 (A/Sw/2124514) and EU258943?EU258950
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    gi|163676522|gb|EU258941|[163676522]
    This record is not yet available.</TD></TR></TBODY></TABLE></TD></TR></TBODY></TABLE><SCRIPT language=JavaScript1.2><!-- var PopUpMenu2_LocalConfig_jsmenu3Config = [ ["ShowCloseIcon","yes"], ["Help","window.open('/entrez/query/static/popup.html','Links_Help','resizable=no, scrollbars=yes, toolbar=no, location=no, directories=no, status=no, menubar=no, copyhistory=no, alwaysRaised=no, depend=no, width=400, height=500');"], ["TitleText"," Links "] ] var jsmenu3Config = [ ["UseLocalConfig","jsmenu3Config","",""] ] function ShowLinks(url,linkscount) { var X,Y; var H = (linkscount + 5)*30, W = 300; if(parseFloat(navigator.appVersion)>= 4) { if(navigator.appName=="Netscape") { X=window.innerWidth;Y=window.innerHeight; if(H > window.innerHeight) { H=window.innerHeight-50;} }else{ X=document.body.offsetWidth;Y=document.body.offset Height; if(H > document.body.offsetHeight) { H=window.innerHeight-50;} } Y=(screen.height)/2-H/2; X=(screen.width)/2-W/2; } window.open(url, 'Links','alwaysRaised=yes,screenX='+String(X)+',sc reenY='+String(Y)+',resizable=no,scrollbars=yes,to olbar=no,location=no,directories=no,status=no,menu bar=no,title=no,copyhistory=yes,width='+String(W)+ ',height='+String(H)).focus(); } --></SCRIPT><!-- - - - - - - - - end Results - - - - - - --><!-- @Pager 2@ --><!-- @DisplayBar 2@ --><!-- end of right content column -->
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    gi|163676524|gb|EU258942|[163676524]
    This record is not yet available.</TD></TR></TBODY></TABLE></TD></TR></TBODY></TABLE><SCRIPT language=JavaScript1.2><!-- var PopUpMenu2_LocalConfig_jsmenu3Config = [ ["ShowCloseIcon","yes"], ["Help","window.open('/entrez/query/static/popup.html','Links_Help','resizable=no, scrollbars=yes, toolbar=no, location=no, directories=no, status=no, menubar=no, copyhistory=no, alwaysRaised=no, depend=no, width=400, height=500');"], ["TitleText"," Links "] ] var jsmenu3Config = [ ["UseLocalConfig","jsmenu3Config","",""] ] function ShowLinks(url,linkscount) { var X,Y; var H = (linkscount + 5)*30, W = 300; if(parseFloat(navigator.appVersion)>= 4) { if(navigator.appName=="Netscape") { X=window.innerWidth;Y=window.innerHeight; if(H > window.innerHeight) { H=window.innerHeight-50;} }else{ X=document.body.offsetWidth;Y=document.body.offset Height; if(H > document.body.offsetHeight) { H=window.innerHeight-50;} } Y=(screen.height)/2-H/2; X=(screen.width)/2-W/2; } window.open(url, 'Links','alwaysRaised=yes,screenX='+String(X)+',sc reenY='+String(Y)+',resizable=no,scrollbars=yes,to olbar=no,location=no,directories=no,status=no,menu bar=no,title=no,copyhistory=yes,width='+String(W)+ ',height='+String(H)).focus(); } --></SCRIPT><!-- - - - - - - - - end Results - - - - - - --><!-- @Pager 2@ --><!-- @DisplayBar 2@ --><!-- end of right content column -->

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    gi|163676526|gb|EU258943|[163676526]
    This record is not yet available.</TD></TR></TBODY></TABLE>
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    gi|163676528|gb|EU258944|[163676528]
    This record is not yet available.</TD></TR></TBODY></TABLE><TABLE cellPadding=0 width="100%"><TBODY><TR><TD style="WHITE-SPACE: nowrap" vAlign=top width="20%"><INPUT id=UidCheckBox type=checkbox value=163676531 name=EntrezSystem2.PEntrez.Nuccore.Sequence_Result sPanel.Sequence_RVDocSum.uid sid="1">1: EU258945</TD><TD vAlign=top align=left>
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    gi|163676531|gb|EU258945|[163676531]
    This record is not yet available.</TD></TR></TBODY></TABLE><TABLE cellPadding=0 width="100%"><TBODY><TR><TD style="WHITE-SPACE: nowrap" vAlign=top width="20%"><INPUT id=UidCheckBox type=checkbox value=163676533 name=EntrezSystem2.PEntrez.Nuccore.Sequence_Result sPanel.Sequence_RVDocSum.uid sid="1">1: EU258946</TD><TD vAlign=top align=left>
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    gi|163676533|gb|EU258946|[163676533]
    This record is not yet available.</TD></TR></TBODY></TABLE><TABLE cellPadding=0 width="100%"><TBODY><TR><TD style="WHITE-SPACE: nowrap" vAlign=top width="20%"><INPUT id=UidCheckBox type=checkbox value=163676535 name=EntrezSystem2.PEntrez.Nuccore.Sequence_Result sPanel.Sequence_RVDocSum.uid sid="1">1: EU258947</TD><TD vAlign=top align=left>
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    gi|163676535|gb|EU258947|[163676535]
    This record is not yet available.</TD></TR></TBODY></TABLE><TABLE cellPadding=0 width="100%"><TBODY><TR><TD style="WHITE-SPACE: nowrap" vAlign=top width="20%"><INPUT id=UidCheckBox type=checkbox value=163676538 name=EntrezSystem2.PEntrez.Nuccore.Sequence_Result sPanel.Sequence_RVDocSum.uid sid="1">1: EU258948</TD><TD vAlign=top align=left>
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    gi|163676538|gb|EU258948|[163676538]
    This record is not yet available.</TD></TR></TBODY></TABLE><TABLE cellPadding=0 width="100%"><TBODY><TR><TD style="WHITE-SPACE: nowrap" vAlign=top width="20%"><INPUT id=UidCheckBox type=checkbox value=163676540 name=EntrezSystem2.PEntrez.Nuccore.Sequence_Result sPanel.Sequence_RVDocSum.uid sid="1">1: EU258949</TD><TD vAlign=top align=left>
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    gi|163676540|gb|EU258949|[163676540]
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  • HenryN
    replied
    Re: New swine flu has avian flu genes

    Originally posted by Niko View Post
    Does anyone know if the flu was ever typed for these two cases from August:


    <TABLE cellSpacing=0 cellPadding=2 width="100%" border=0><TBODY><TR><TD style="FONT-WEIGHT: bold; FONT-SIZE: 12px; FONT-FAMILY: serif">08/18/2007</TD></TR><TR><TD style="FONT-WEIGHT: bold; FONT-SIZE: 19px; FONT-FAMILY: serif">Cases of flu hit Huron County Fair </TD></TR><TR><TD style="FONT-WEIGHT: bold; FONT-SIZE: 12px; FONT-FAMILY: serif">Morning Journal Staff </TD></TR></TBODY></TABLE>
    NORWALK -- There has been two confirmed cases of flu at the Huron County Fair that health officials are investigating to see if it was transmitted from pigs to humans.
    The influenza A cases were confirmed, through rapid screening, in a fair exhibitor and the exhibitor's father, according to the Huron County General Health District. There has also been reports of flu-like symptoms in pigs at the county fairgrounds.

    ''At this point, no connection has been medically established between the swine and human cases,'' said Tim Hollinger, administrator of the Huron County General Health District.

    No testing has been done yet to confirm what is causing the illness in the pigs, he said. Further testing will be done by the Ohio Department of Agriculture and the Ohio Department of Health to see if the two human cases can be matched to the illness in the pigs, according to the health department.

    Fair veterinarians believe the pigs are past the contagious period, but the Huron County Fair Board has decided to close the pig barns to the public. Today, is the last day of the fair.

    Type A influenza can be transmitted from pigs to humans, but it is rare. There had only been rare documented cases of human-to-human transmission of flu that originated from swine, according the health district.
    In mIchigan it was H1N2. For the two in Ohio, the CDC didn't say

    Three human cases of novel influenza A infection were reported from two states (Ohio (2) and Illinois (1)) in September. All three persons were infected with swine influenza A virus. Although human infection with swine influenza is uncommon, sporadic cases occur in many years, usually among persons in direct contact with ill pigs or who have been in places where pigs might have been present (e.g. agricultural fairs, farms, or petting zoos). The sporadic cases identified in recent years have not resulted in sustained human-to-human transmission or community outbreaks.

    Leave a comment:


  • JJackson
    replied
    Re: New swine flu has avian flu genes

    The articles do not make it clear if these were free-range with access to the pond (snout in the bird droppings - high viral load) or the water was being piped from the ponds to housed pigs. If anyone has seen this information please post. Thanks.

    Leave a comment:


  • Niko
    replied
    Re: New swine flu has avian flu genes

    Does anyone know if the flu was ever typed for these two cases from August:


    <table border="0" cellpadding="2" cellspacing="0" width="100%"><tbody><tr><td style="font-weight: bold; font-size: 12px; font-family: serif;">08/18/2007</td></tr><tr><td style="font-weight: bold; font-size: 19px; font-family: serif;"> Cases of flu hit Huron County Fair </td></tr><tr><td style="font-weight: bold; font-size: 12px; font-family: serif;"> Morning Journal Staff </td></tr></tbody></table>
    NORWALK -- There has been two confirmed cases of flu at the Huron County Fair that health officials are investigating to see if it was transmitted from pigs to humans.
    The influenza A cases were confirmed, through rapid screening, in a fair exhibitor and the exhibitor's father, according to the Huron County General Health District. There has also been reports of flu-like symptoms in pigs at the county fairgrounds.

    ''At this point, no connection has been medically established between the swine and human cases,'' said Tim Hollinger, administrator of the Huron County General Health District.

    No testing has been done yet to confirm what is causing the illness in the pigs, he said. Further testing will be done by the Ohio Department of Agriculture and the Ohio Department of Health to see if the two human cases can be matched to the illness in the pigs, according to the health department.

    Fair veterinarians believe the pigs are past the contagious period, but the Huron County Fair Board has decided to close the pig barns to the public. Today, is the last day of the fair.

    Type A influenza can be transmitted from pigs to humans, but it is rare. There had only been rare documented cases of human-to-human transmission of flu that originated from swine, according the health district.

    Leave a comment:


  • HenryN
    replied
    Re: New swine flu has avian flu genes

    Commentary at

    Leave a comment:


  • HenryN
    replied
    Re: New swine flu has avian flu genes

    INFLUENZA A (H2N3) VIRUS, SWINE - USA
    *************************************
    A ProMED-mail post
    <http://www.promedmail.org>
    ProMED-mail is a program of the
    International Society for Infectious Diseases
    <http://www.isid.org>

    Date: 17-18 Dec 2007
    Source: Proc Natl Acad Science USA Early Edition [edited]
    <http://www.pnas.org/cgi/content/abstract/0710286104v1?etoc>


    [Below is the abstract of a paper in the online edition of the Proceedings
    of the National Academy of Sciences of the USA (PNAS), which describes the
    characterization of an influenza virus with potential to become the
    precursor of a human pandemic virus.]

    Identification of H2N3 influenza A viruses from swine in the United States
    --------------------------------------------------------------------------
    By Wenjun Ma, Amy L Vincent, Marie R Gramer, Christy B Brockwell, Kelly M
    Lager, Bruce H Janke, et al. At the Department of Veterinary Diagnostic and
    Production Animal Medicine, College of Veterinary Medicine, Iowa State
    University, Ames, IA 50011; Virus and Prion Diseases of Livestock Research
    Unit, National Animal Disease Center, Agricultural Research Service, United
    States Department of Agriculture, Ames, IA 50010; Veterinary Diagnostic
    Laboratory, College of Veterinary Medicine, University of Minnesota, St.
    Paul, MN 55108; St. Jude Children's Research Hospital, Memphis, TN 38018;
    and Interdisciplinary Program, University of Tennessee Health Science
    Center, Memphis, TN 38163

    Abstract
    --------
    Although viruses of each of the 16 influenza A HA subtypes are potential
    human pathogens, only viruses of the H1, H2, and H3 subtype are known to
    have been successfully established in humans. H2 influenza viruses have
    been absent from human circulation since 1968, and as such they pose a
    substantial human pandemic risk. In this report, we isolate and
    characterize genetically similar avian/swine virus reassortant H2N3
    influenza A viruses isolated from diseased swine from 2 farms in the United
    States. These viruses contained leucine at position 226 of the H2 protein,
    which has been associated with increased binding affinity to the mammalian
    alpha-2,6Gal-linked sialic acid virus receptor. Correspondingly, the H2N3
    viruses were able to cause disease in experimentally infected swine and
    mice without prior adaptation. In addition, the swine H2N3 virus was
    infectious and highly transmissible in swine and ferrets. Taken together,
    these findings suggest that the H2N3 virus has undergone some adaptation to
    the mammalian host and that their spread should be very closely monitored.

    --
    communicated by:
    ProMED-mail <promed@promedmail.org>

    [The current concentration of attention on the potential of avian influenza
    A/H5N1 virus to evolve into a human pandemic pathogen should not divert
    attention from the presence in the environment of other potential
    precursors of influenza viruses with equal or perhaps greater potential to
    become human pandemic pathogens. - Mod.CP]

    [see also:
    Avian influenza, human (113): pandemic prediction 20070726.2410
    2005
    ---
    Influenza virus, 1918 pandemic strain: reconstruction (02) 20051006.2919
    Avian influenza, human - East Asia (111): pandemic preparedness 20050804.2264]

    .................cp/msp/sh

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  • wetDirt
    replied
    Re: New swine flu has avian flu genes

    Originally posted by niman View Post
    There is a lot of recombination between swine and avian sequences (especially H5N1 and H9N2).
    That's what I thought. Is there some consistent preference in mixing by strain? Does it depend more on random chance and abundance, or do certain strains combine "better" than others because of structural similarities? Does the extent depend on the initial degree of similiarity between strains?

    Leave a comment:


  • HenryN
    replied
    Re: New swine flu has avian flu genes

    ARS: New swine flu has avian flu genes
    Dec. 19, 2007

    Researchers have identified a new strain of swine influenza -- H2N3 -- which belongs to the group of H2 influenza viruses that last infected humans during the 1957 pandemic. This new strain has a molecular twist: It is composed of avian and swine influenza genes.

    Agricultural Research Service (ARS) veterinarians Juergen Richt, Amy Vincent, Kelly Lager and Phillip Gauger conducted this research with Iowa State University (ISU) visiting scientist Wenjun Ma, ISU veterinarian Bruce Janke and other colleagues at the University of Minnesota and St. Jude Children's Research Hospital. The ARS veterinarians work at the agency's National Animal Disease Center in Ames, Iowa.

    The research team studied an unknown pathogen that in 2006 infected two groups of pigs at separate production facilities. Both groups of pigs used water obtained from ponds frequented by migrating waterfowl.

    Molecular studies indicated the unknown pathogen was an H2N3 influenza virus that is closely related to an H2N3 strain found in mallard ducks. But this was the first time it had been observed in mammals.

    Influenza viruses have eight gene segments, all of which can be swapped between different virus strains. Two of these gene segments code for virus surface proteins that help determine whether an influenza virus is able to infect a specific host and start replicating -- the first step in the onset of influenza infection.

    In the newly isolated swine H2N3, the avian H2 and N3 gene segments mixed with gene segments from common swine influenza viruses. This exchange -- and additional mutations -- gave the H2N3 viruses the ability to infect swine. Lab tests confirmed that this strain of H2N3 could also infect mice and ferrets.

    These findings provide further evidence that swine have the potential to serve as a "mixing vessel" for influenza viruses carried by birds, pigs and humans. It also supports the need to continue monitoring swine -- and livestock workers -- for H2-subtype viruses and other influenza strains that might someday threaten swine and human health.

    Results of this study were published online this week in the Proceedings of the National Academy of Sciences of the United States of America.

    SOURCE: USDA news release.


    Leave a comment:


  • HenryN
    replied
    Re: New swine flu has avian flu genes

    Originally posted by wetDirt View Post
    This is interesting on several fronts. Interesting that in an industrialized country in 2006, swine at a production facility shared drinking water with wild ducks. Really? I thought that co-mingling of species, including humans, only happened in third-world countries.

    Nobody ever observed a jump from birds to swine? Then they could hardly have been looking, there are lots of H1N1 sequences with regions of identity between birds, humans, and swine.

    And finally, Iowa is on the Mississippi flyway. And there are speces that migrate between Asia and North America that don't stop in Alaska. This is not a reassuring article at all.
    There is a lot of recombination between swine and avian sequences (especially H5N1 and H9N2).

    Leave a comment:


  • wetDirt
    replied
    Re: New swine flu has avian flu genes

    The research team studied an unknown pathogen that in 2006 infected two groups of pigs at separate production facilities. Both groups of pigs used water obtained from ponds frequented by migrating waterfowl. Molecular studies indicated the unknown pathogen was an H2N3 influenza virus closely related to an H2N3 strain found in mallard ducks. However, this was the first time it had been observed in mammals.
    This is interesting on several fronts. Interesting that in an industrialized country in 2006, swine at a production facility shared drinking water with wild ducks. Really? I thought that co-mingling of species, including humans, only happened in third-world countries.

    Nobody ever observed a jump from birds to swine? Then they could hardly have been looking, there are lots of H1N1 sequences with regions of identity between birds, humans, and swine.

    And finally, Iowa is on the Mississippi flyway. And there are speces that migrate between Asia and North America that don't stop in Alaska. This is not a reassuring article at all.

    Leave a comment:


  • Shannon Bennett
    replied
    Re: New swine flu has avian flu genes



    <TABLE cellSpacing=0 cellPadding=0><TBODY><TR><TD>Animal: RNA Viruses

    </TD></TR></TBODY></TABLE>
    Transmission of Eurasian avian H2 influenza virus to shorebirds in North America

    <NOBR>N. V. Makarova<!-- null --><SUP>1</SUP><!-- null --><SUP>,2</SUP></NOBR>, <NOBR>N. V. Kaverin<!-- null --><SUP>1</SUP></NOBR>, <NOBR>S. Krauss<!-- null --><SUP>2</SUP></NOBR>, <NOBR>D. Senne<!-- null --><SUP>3</SUP></NOBR> and <NOBR>R. G. Webster<!-- null --><SUP>2</SUP></NOBR>


    The D. I. Ivanovsky Institute of Virology, Gamaleya Str. 16, Moscow 123098, Russia<SUP>1</SUP>
    St Jude Children?s Research Hospital, Department of Virology and Molecular Biology, 332 N. Lauderdale, Memphis, Tennessee 38105, USA<SUP>2</SUP>
    Avian Viruses Section, Diagnostic Virology Laboratory, National Veterinary Service Laboratories, APHIS, United States Department of Agriculture, PO Box 844, Ames, Iowa 50010, USA<SUP>3</SUP>

    Author for correspondence: Natalia Makarova (at The D. I. Ivanovsky Institute of Virology). Fax +7 095 5165314. e-mail finmed@glasnet.ru<SCRIPT type=text/javascript><!-- var u = "finmed", d = "glasnet.ru"; document.getElementById("em0").innerHTML = '<a href="mailto:' + u + '@' + d + '">' + u + '@' + d + '<\/a>'//--></SCRIPT>
    <!-- null -->
    <TABLE cellSpacing=0 cellPadding=0 width="100%" bgColor=#e1e1e1><TBODY><TR><TD vAlign=center align=left width="5%" bgColor=#ffffff></TD><TH vAlign=center align=left width="95%"> Abstract </TH></TR></TBODY></TABLE><TABLE cellPadding=5 align=right border=1><TBODY><TR><TH align=left>TOP
    Abstract
    Main text
    References
    </TH></TR></TBODY></TABLE>
    Influenza A virus of the H2 subtype caused a serious pandemic<SUP> </SUP>in 1957 and may cause similar outbreaks in the future. To assess<SUP> </SUP>the evolution and the antigenic relationships of avian influenza<SUP> </SUP>H2 viruses, we sequenced the haemagglutinin (HA) genes of H2<SUP> </SUP>isolates from shorebirds, ducks and poultry in North America<SUP> </SUP>and derived a phylogenetic tree to establish their interrelationships.<SUP> </SUP>This analysis confirmed the divergence of H2 HA into two geographical<SUP> </SUP>lineages, American and Eurasian. One group of viruses isolated<SUP> </SUP>from shorebirds in North America had HA belonging to the Eurasian<SUP> </SUP>lineage, indicating an interregional transmission of the H2<SUP> </SUP>gene. Characterization of HA with a monoclonal antibody panel<SUP> </SUP>revealed that the antigenicity of the Delaware strains differed<SUP> </SUP>from the other avian strains analysed. The data emphasizes the<SUP> </SUP>importance of avian influenza surveillance.<SUP> </SUP>
    <!-- null -->
    <TABLE cellSpacing=0 cellPadding=0 width="100%" bgColor=#e1e1e1><TBODY><TR><TD vAlign=center align=left width="5%" bgColor=#ffffff></TD><TH vAlign=center align=left width="95%"> Main text </TH></TR></TBODY></TABLE><TABLE cellPadding=5 align=right border=1><TBODY><TR><TH align=left>TOP
    Abstract
    Main text
    References
    </TH></TR></TBODY></TABLE>
    Influenza is a re-emerging epidemic disease, and during the<SUP> </SUP>last century there have been several human pandemics. Three<SUP> </SUP>influenza virus subtypes, H1N1, H2N2 and H3N2, were associated<SUP> </SUP>with these pandemics. Seroarcheological data suggest that H2<SUP> </SUP>influenza virus was responsible for the influenza pandemic of<SUP> </SUP>1889?1890 (Mulder & Masurel, 1958 ). There are no<SUP> </SUP>indications that influenza A viruses of the H2 subtype circulated<SUP> </SUP>in the human population during the 20th century until 1957,<SUP> </SUP>when there was a serious H2 influenza pandemic. The pandemic<SUP> </SUP>virus had haemagglutinin (HA), NA and PB1 genes derived from<SUP> </SUP>an H2N2 avian precursor; the remainder of its genes were derived<SUP> </SUP>from an H1N1 virus that circulated in the human population before<SUP> </SUP>1957 (Kawaoka et al., 1989 ; Scholtissek et al., 1978 ).<SUP> </SUP>
    Influenza viruses of the H2 subtype circulated in the human<SUP> </SUP>population until 1968, after which they continued to be detected<SUP> </SUP>in avian populations (Tumova et al., 1975 ; Shortridge, 1979<SUP> </SUP>; Sinnecker et al., 1983 ; Wright et al., 1992 ). Most H2N2<SUP> </SUP>viruses in wild and domestic birds are antigenically closely<SUP> </SUP>related to the viruses that circulated in the human population<SUP> </SUP>between 1957 and 1968, suggesting that viruses similar to the<SUP> </SUP>progenitor of the Asian/57 pandemic are still circulating in<SUP> </SUP>birds (Schafer et al., 1993 ). Serological data showed that<SUP> </SUP>the percentage of detection of anti-H2 antibodies in the sera<SUP> </SUP>of adults was low, and no anti-H2 antibodies were detected in<SUP> </SUP>the sera of children (Govorkova et al., 1993 ). These facts<SUP> </SUP>emphasize the importance of periodical surveillance of avian<SUP> </SUP>H2 influenza viruses and elucidation of the phylogenetic and<SUP> </SUP>evolutionary relationships among present and previously known<SUP> </SUP>avian H2 influenza viruses.<SUP> </SUP>
    The two distinct lineages of avian H2 influenza viruses, American<SUP> </SUP>and Eurasian, are distinguished by their geographical origins<SUP> </SUP>(Schafer et al., 1993 ). One virus isolated in the USA, A/Herring<SUP> </SUP>gull/Delaware/677/88, has been shown to belong to the Eurasian<SUP> </SUP>lineage, but that single observation could not be conclusively<SUP> </SUP>interpreted. To elucidate the evolutionary characteristics of<SUP> </SUP>recently isolated avian viruses of the H2 subtype, we investigated<SUP> </SUP>the antigenic and phylogenetic relationships among recent and<SUP> </SUP>previously described avian influenza H2 viruses.<SUP> </SUP>
    The viruses used in these studies (Table 1) were obtained as<SUP> </SUP>part of surveillance programs in the northeastern part of the<SUP> </SUP>USA and in Alberta, Canada, or from the virus repository at<SUP> </SUP>St Jude Children?s Research Hospital, Memphis, TN, USA.<SUP> </SUP>The shorebird and gull viruses were isolated from samples collected<SUP> </SUP>annually in mid-May from the Delmarva Peninsula region of the<SUP> </SUP>USA between 1985 and 1998 (Kawaoka et al., 1988 ). Influenza<SUP> </SUP>viruses from migratory ducks were isolated between 1977 and<SUP> </SUP>1997 from samples collected annually in late July to early September<SUP> </SUP>in Alberta, Canada (Sharp et al., 1993 ). Viruses were propagated<SUP> </SUP>at low m.o.i. in the allantoic cavity of 11-day-old embryonated<SUP> </SUP>chicken eggs.<SUP> </SUP>
    <!-- null -->
    <CENTER><TABLE cellSpacing=0 cellPadding=0 width="95%"><TBODY><TR bgColor=#e1e1e1><TD><TABLE cellSpacing=2 cellPadding=2><TBODY><TR bgColor=#e1e1e1><TD vAlign=top align=middle bgColor=#ffffff>View this table:
    <NOBR>[in this window]
    [in a new window]
    </NOBR> </TD><TD vAlign=top align=left>Table 1. Influenza A viruses used for phylogenetic analysis
    </TD></TR></TBODY></TABLE></TD></TR></TBODY></TABLE></CENTER>
    Phylogenetic analysis was based on the nucleotide sequences<SUP> </SUP>of 15 newly sequenced HA genes (HA1 subunit) and the previously<SUP> </SUP>sequenced HA genes of avian H2 viruses (Table 1). The sequences<SUP> </SUP>were determined by reverse transcription (Huddleston & Brownlee,<SUP> </SUP>1982 ), and PCR direct sequencing was performed by the Centre<SUP> </SUP>for Biotechnology at St Jude Children?s Research Hospital<SUP> </SUP>by using dye-terminator Cycle-Sequencing Ready-Reaction kits<SUP> </SUP>with AmpliTaq DNA polymerase FS (Perkin-Elmer, Applied Biosystems).<SUP> </SUP>Sequence data of each gene were analysed by the Wisconsin Package<SUP> </SUP>version 9.0, Genetics Computer Group, Madison, WI, USA. Phylogenetic<SUP> </SUP>analysis of new sequences, together with sequences from GenBank,<SUP> </SUP>was performed by a combination of the Neighbour-Joining method<SUP> </SUP>(Saitou & Nei, 1987 ) for detection of distances and the<SUP> </SUP>Maximum-Parsimony method (Fitch, 1970 ) for generation of a<SUP> </SUP>phylogenetic tree using PHYLIP (the PHYLogeny Inference Package)<SUP> </SUP>version 3.57c. The phylogenetic tree is rooted to the H5 HA1<SUP> </SUP>sequence from A/Chicken/Pennsylvania/1/83 (H5N1) (J04325) because<SUP> </SUP>of the high similarity (74%) between H2 and H5 serotypes (Air,<SUP> </SUP>1981 ; Nobusawa et al., 1991 ).<SUP> </SUP>

    The phylogenetic tree (Fig. 1) confirms the divergence of H2<SUP> </SUP>influenza A viruses into two distinct geographical lineages:<SUP> </SUP>American and Eurasian. All newly sequenced HA1 genes from domestic<SUP> </SUP>poultry were of the American lineage. However, a large group<SUP> </SUP>of recent American isolates from shorebirds in Delaware Bay<SUP> </SUP>belonged to the Eurasian lineage. As reported previously (Schafer<SUP> </SUP>et al., 1993 ), the A/Herring gull/Delaware/677/88 strain isolated<SUP> </SUP>in Delaware Bay also is of the Eurasian lineage. Together, the<SUP> </SUP>viruses isolated in Delaware Bay composed a divergent sublineage<SUP> </SUP>in the Eurasian section of the tree. All of these viruses were<SUP> </SUP>isolated from seabirds (gulls and shorebirds). Interestingly,<SUP> </SUP>two viruses previously isolated from gulls in North America<SUP> </SUP>(A/Gull/Maryland/19/77 and A/Laughing gull/New Jersey/75/85)<SUP> </SUP>were of the American lineage but diverged from other isolates<SUP> </SUP>of that lineage. A/Peking duck/Potsdam/1689-4/85 was the Eurasian<SUP> </SUP>virus most closely related to the group of American viruses<SUP> </SUP>with Eurasian HA. These data suggest that Eurasian H2 was transmitted<SUP> </SUP>from Eurasian to American avian hosts.<SUP> </SUP>
    <!-- null -->
    <CENTER><TABLE cellSpacing=0 cellPadding=0 width="95%"><TBODY><TR bgColor=#e1e1e1><TD><TABLE cellSpacing=2 cellPadding=2><TBODY><TR bgColor=#e1e1e1><TD vAlign=top align=middle bgColor=#ffffff>
    View larger version (20K):
    <NOBR>[in this window]
    [in a new window]
    </NOBR> </TD><TD vAlign=top align=left>Fig. 1. Phylogenetic tree of the HA1 genes of H2 influenza A viruses. The tree is rooted to the H5 HA sequence from A/Chicken/Pennsylvania/1/83 (accession no. J04325). Horizontal distances are proportional to the number of nucleotide changes in HA1. Strain abbreviations are listed in Table 1.
    </TD></TR></TBODY></TABLE></TD></TR></TBODY></TABLE></CENTER>
    The rates of evolution were determined from the nucleotide sequences<SUP> </SUP>of the HA1 of H2 influenza viruses using GeneDoc (Multiple sequence<SUP> </SUP>alignment editor and shading utility version 2.3000, 1997) for<SUP> </SUP>statistical analysis of the relationships between pairs of sequences.<SUP> </SUP>In the Delaware Bay group of viruses, the evolution rate was<SUP> </SUP>2?47?0?23 nucleotide substitutions per<SUP> </SUP>year, a rate significantly greater than that of the Eurasian<SUP> </SUP>viruses (1?57?0?23 substitutions per year)<SUP> </SUP>but less than that of the American viruses (3?8?0?5<SUP> </SUP>substitutions per year). The differences are statistically significant<SUP> </SUP>at P0?05. In the group of Delaware Bay viruses, 34?5%<SUP> </SUP>of all nucleotide substitutions led to amino acid replacements.<SUP> </SUP>In the American lineage, 25?6% of nucleotide substitutions<SUP> </SUP>resulted in amino acid replacements, and in the Eurasian lineage,<SUP> </SUP>20?4% of nucleotide substitutions resulted in amino acid<SUP> </SUP>replacements. Thus, although the Delaware Bay group falls between<SUP> </SUP>the Eurasian and the American viruses in the rate at which it<SUP> </SUP>acquires nucleotide substitutions, it has the highest percentage<SUP> </SUP>of nucleotide substitutions that result in amino acid changes.<SUP> </SUP>In the human H2 viruses having circulated in 1964?1968<SUP> </SUP>(A/Korea/426/68, A/Izumi/5/65, A/Berlin/3/64, A/Berkeley/1/68),<SUP> </SUP>a comparable percentage (35?7%) of nucleotide substitutions<SUP> </SUP>led to amino acid changes.<SUP> </SUP>

    As shown previously, human influenza viruses evolve rapidly<SUP> </SUP>because of the pressure of the neutralizing antibodies of the<SUP> </SUP>host (Both et al., 1983 ). Avian species produce humoral and<SUP> </SUP>cell-mediated responses to influenza virus infection, but their<SUP> </SUP>antibody responses are short-lived (Kida et al., 1980 ); moreover,<SUP> </SUP>a large number of young susceptible birds are produced every<SUP> </SUP>year, eliminating the immune pressure among avian viruses. The<SUP> </SUP>high rate of HA evolution in Eurasian-type American H2 viruses<SUP> </SUP>suggests the existence of an unknown positive selection mechanism<SUP> </SUP>that favours amino acid changes in the transferred virus, probably<SUP> </SUP>connected with the transfer to the new environment. This finding<SUP> </SUP>is also at variance with our earlier findings of evolutionary<SUP> </SUP>stasis among influenza viruses in their natural reservoirs (Webster<SUP> </SUP>et al., 1992 ) and indicates that this may not apply to all<SUP> </SUP>aquatic birds.<SUP> </SUP>
    The higher percentage of amino acid replacements in the HA of<SUP> </SUP>the Delaware group of viruses may lead to changes in their antigenic<SUP> </SUP>reactivity pattern. To investigate this possibility, haemagglutination<SUP> </SUP>titrations and haemagglutination inhibition (HI) assays were<SUP> </SUP>performed as previously described (Rogers et al., 1983 ). Ascitic<SUP> </SUP>fluids from mice containing monoclonal antibodies (MAbs) to<SUP> </SUP>the HA of the H2 influenza subtype (Yamada et al., 1984 ) were<SUP> </SUP>used in the HI tests. The HA of avian viruses isolated in North<SUP> </SUP>America demonstrated two patterns of reactivity with the panel<SUP> </SUP>of MAbs (Table 2). However, the antigenic and phylogenetic groups<SUP> </SUP>did not coincide. The American viruses react with most MAbs<SUP> </SUP>in the panel. In contrast, the Delaware Bay (shorebird and gull)<SUP> </SUP>viruses reacted with only two or three MAbs. This pattern of<SUP> </SUP>reactivity, which had been reported earlier for one Delaware<SUP> </SUP>Bay shorebird strain (A/Herring gull/Delaware/677/88), extended<SUP> </SUP>to all of the four shorebird viruses characterized. However,<SUP> </SUP>the Delaware Bay strains are not unique in this respect. One<SUP> </SUP>Eurasian strain, A/Duck/GDR/72, and one American strain, A/Chicken/New<SUP> </SUP>York/29878/91, had shown a similar pattern of reaction (Schafer<SUP> </SUP>et al., 1993 ).<SUP> </SUP>
    <!-- null -->
    <CENTER><TABLE cellSpacing=0 cellPadding=0 width="95%"><TBODY><TR bgColor=#e1e1e1><TD><TABLE cellSpacing=2 cellPadding=2><TBODY><TR bgColor=#e1e1e1><TD vAlign=top align=middle bgColor=#ffffff>View this table:
    <NOBR>[in this window]
    [in a new window]
    </NOBR> </TD><TD vAlign=top align=left>Table 2. Haemagglutination inhibition by monoclonal antibodies
    </TD></TR></TBODY></TABLE></TD></TR></TBODY></TABLE></CENTER>
    The disparity between the antigenic and phylogenetic groupings<SUP> </SUP>suggests that most of the amino acid replacements have not been<SUP> </SUP>affecting antigenic specificity. However, the changes at position<SUP> </SUP>137, 189 and 141?144 may be relevant to the antigenic<SUP> </SUP>variability of the H2 subtype. These substitutions are located<SUP> </SUP>in antigenic sites A and B as outlined for the 3D structure<SUP> </SUP>of H3 (Wiley et al., 1981 ).<SUP> </SUP>

    Several influenza A virus HA subtypes comprise geographically<SUP> </SUP>separate lineages (Garcia et al., 1997 ; Donis et al., 1989<SUP> </SUP>). These lineages may have emerged because of nonoverlapping<SUP> </SUP>migration routes. Most wild birds follow North?South migration<SUP> </SUP>routes that are separate for each hemisphere. Further, the birds<SUP> </SUP>that migrate across the Atlantic do so at times when North?South<SUP> </SUP>migrations are over. For example, the Canadian terns and gulls<SUP> </SUP>that cross the Atlantic (Curry-Lindahl, 1975 ) arrive in Europe<SUP> </SUP>after the European birds have migrated to Africa. On rare occasions,<SUP> </SUP>unusual weather conditions may bring the two populations into<SUP> </SUP>contact, allowing the interregional transmission of viruses.<SUP> </SUP>Turnstones, which are pelagic birds and whose migration is not<SUP> </SUP>fully resolved, may play a role in this transmission (Curry-Lindahl,<SUP> </SUP>1975 ). However, such occasional transmissions would be unlikely<SUP> </SUP>to lead in each case to circulation of the transferred virus;<SUP> </SUP>otherwise, the phylogenetically distinct lineages would not<SUP> </SUP>have arisen. The circulation of Eurasian H2 virus in the Delaware<SUP> </SUP>shorebirds for at least 10 years does not necessarily suggest<SUP> </SUP>the existence of some specific, as yet unknown, conditions in<SUP> </SUP>the area that favour the virus: new Eurasian-type H2 viruses<SUP> </SUP>may be circulating in other parts of America as well. All of<SUP> </SUP>the sequenced H2 viruses isolated from gulls in other parts<SUP> </SUP>of America were isolated earlier than 1988. The first Delaware<SUP> </SUP>Eurasian-type virus was isolated in 1988. If the transfer occurred<SUP> </SUP>not long before 1988, it is possible that the Eurasian-type<SUP> </SUP>viruses are in fact not restricted to Delaware Bay but are instead<SUP> </SUP>restricted to shorebirds and gulls (Kawaoka et al., 1988 ).<SUP> </SUP>
    H2 virus is the only pandemic influenza virus subtype that has<SUP> </SUP>not circulated in the human population for the last 30 years.<SUP> </SUP>Therefore, the probability that H2 viruses will reappear in<SUP> </SUP>humans may be high. It is generally accepted that the 1957 and<SUP> </SUP>1968 influenza pandemics were produced by reassortant human<SUP> </SUP>strains with HA genes that originated from avian influenza viruses.<SUP> </SUP>Although the details of the transfer of Eurasian H2 virus strains<SUP> </SUP>to North America are not yet clear, the existence of this transfer<SUP> </SUP>has important implications. The Eurasian avian influenza virus<SUP> </SUP>strains are those most closely related to human H2 viruses (Schafer<SUP> </SUP>et al., 1993 ) and are potential sources of genes for future<SUP> </SUP>pandemic influenza strains. These are compelling reasons for<SUP> </SUP>the further study and surveillance of avian H2 strains circulating<SUP> </SUP>in the Americas.<SUP> </SUP>
    <!-- null -->
    <TABLE cellSpacing=0 cellPadding=0 width="100%" bgColor=#e1e1e1><TBODY><TR><TD vAlign=center align=left width="5%" bgColor=#ffffff></TD><TH vAlign=center align=left width="95%"> Acknowledgments </TH></TR></TBODY></TABLE>
    The research described in this publication was made possible<SUP> </SUP>in part by award RN1-412 of the U. S. Civilian Research &<SUP> </SUP>Development Foundation for the Independent States of the Former<SUP> </SUP>Soviet Union (CRDF) and by Public Health Research Grant AI29680<SUP> </SUP>and Cancer Centre Support (CORE) grant CA-21765 from the National<SUP> </SUP>Institutes of Health, and by the American Lebanese Syrian Associated<SUP> </SUP>Charities. We thank Sharon Naron for editorial assistance.<SUP> </SUP>
    <!-- null -->
    <TABLE cellSpacing=0 cellPadding=0 width="100%" bgColor=#e1e1e1><TBODY><TR><TD vAlign=center align=left width="5%" bgColor=#ffffff></TD><TH vAlign=center align=left width="95%"> References </TH></TR></TBODY></TABLE><TABLE cellPadding=5 align=right border=1><TBODY><TR><TH align=left>TOP
    Abstract
    Main text
    References
    </TH></TR></TBODY></TABLE>
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    <!-- null -->Schafer, J. R., Kawaoka, Y., Bean, W. J., Suss, J., Senne, D. & Webster, R. G. (1993). Origin of the pandemic 1957 H2 influenza A virus and the persistence of its possible progenitors in the avian reservoir. Virology 194, 781-788.<!-- HIGHWIRE ID="80:12:3167:16" -->[Medline]<!-- /HIGHWIRE -->
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    <!-- null -->Yamada, A., Brown, L. E. & Webster, R. G. (1984). Characterization of H2 influenza virus hemagglutinin with monoclonal antibodies: influence of receptor specificity. Virology 138, 276-286.<!-- HIGHWIRE ID="80:12:3167:25" -->[Medline]<!-- /HIGHWIRE --> Received 13 May 1999; accepted 13 August 1999.

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  • Shannon Bennett
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    Re: New swine flu has avian flu genes

    PubMed® comprises more than 37 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full text content from PubMed Central and publisher web sites.


    <INPUT id=UidCheckBox type=checkbox value=7684877 name=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPa nel.Pubmed_RVAbstractPlus.uid sid="1">1: Virology. 1993 Jun;194(2):781-8. <SCRIPT language=JavaScript1.2><!-- var Menu7684877 = [ ["UseLocalConfig", "jsmenu3Config", "", ""], ["CoreNucleotide" , "window.top.location='/sites/entrez?Db=nuccore&DbFrom=pubmed&Cmd=Link&LinkName= pubmed_nuccore&LinkReadableName=CoreNucleotide&Ids FromResult=7684877&ordinalpos=1&itool=EntrezSystem 2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbst ractPlus' ", "", ""], ["Gene" , "window.top.location='/sites/entrez?Db=gene&DbFrom=pubmed&Cmd=Link&LinkName=pub med_gene&LinkReadableName=Gene&IdsFromResult=76848 77&ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed .Pubmed_ResultsPanel.Pubmed_RVAbstractPlus' ", "", ""], ["Protein (RefSeq)" , "window.top.location='/sites/entrez?Db=protein&DbFrom=pubmed&Cmd=Link&LinkName= pubmed_protein_refseq&LinkReadableName=Protein%20( RefSeq)&IdsFromResult=7684877&ordinalpos=1&itool=E ntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pu bmed_RVAbstractPlus' ", "", ""], ["Taxonomy via GenBank" , "window.top.location='/sites/entrez?Db=taxonomy&DbFrom=pubmed&Cmd=Link&LinkName =pubmed_taxonomy_entrez&LinkReadableName=Taxonomy% 20via%20GenBank&IdsFromResult=7684877&ordinalpos=1 &itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_Results Panel.Pubmed_RVAbstractPlus' ", "", ""], ["Nucleotide" , "window.top.location='/sites/entrez?Db=nucleotide&DbFrom=pubmed&Cmd=Link&LinkNa me=pubmed_nucleotide&LinkReadableName=Nucleotide&I dsFromResult=7684877&ordinalpos=1&itool=EntrezSyst em2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAb stractPlus' ", "", ""], ["Protein" , "window.top.location='/sites/entrez?Db=protein&DbFrom=pubmed&Cmd=Link&LinkName= pubmed_protein&LinkReadableName=Protein&IdsFromRes ult=7684877&ordinalpos=1&itool=EntrezSystem2.PEntr ez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstractPlu s' ", "", ""], ["Genome" , "window.top.location='/sites/entrez?Db=genome&DbFrom=pubmed&Cmd=Link&LinkName=p ubmed_genome&LinkReadableName=Genome&IdsFromResult =7684877&ordinalpos=1&itool=EntrezSystem2.PEntrez. Pubmed.Pubmed_ResultsPanel.Pubmed_RVAbstractPlus' ", "", ""], ["Cited in PMC" , "window.top.location='http://www.pubmedcentral.gov/tocrender.fcgi?action=cited&tool=pubmed&pubmedid=7 684877&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_R esultsPanel.Pubmed_RVAbstractPlus&ordinalpos=1' ", "", ""], ["LinkOut", "window.top.location='/sites/entrez?Cmd=ShowLinkOut&Db=pubmed&TermToSearch=7684 877&ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubme d.Pubmed_ResultsPanel.Pubmed_RVAbstractPlus' ", "", ""] ] --></SCRIPT>Links
    <DD class=abstract>Origin of the pandemic 1957 H2 influenza A virus and the persistence of its possible progenitors in the avian reservoir.

    <!--AuthorList-->Sch?fer JR, Kawaoka Y, Bean WJ, S?ss J, Senne D, Webster RG.
    St. Jude Children's Research Hospital, Department of Virology/Molecular Biology, Memphis, Tennessee 38105.
    H2N2 influenza A viruses caused the Asian pandemic of 1957 and then disappeared from the human population 10 years later. To assess the potential for similar outbreaks in the future, we determined the antigenicity of H2 hemagglutinins (HAs) from representative human and avian H2 viruses and then analyzed the nucleotide and amino acid sequences to determine their evolutionary characteristics in different hosts. The results of longitudinal virus surveillance studies were also examined to estimate the prevalence of avian H2 isolates among samples collected from wild ducks and domestic poultry. Reactivity patterns obtained with a large panel of monoclonal antibodies indicated antigenic drift in the HA of human H2 influenza viruses, beginning in 1962. Amino acid changes were clustered in two regions of HA1 that correspond to antigenic sites A and D of the H3 HA. By contrast, the antigenic profiles of the majority of avian H2 HAs were remarkably conserved through 1991, resembling the prototype Japan 57 (H2N2) strain. Amino acid changes were distributed throughout HA1, indicating that antibodies do not play a major role in the selection of avian H2 viruses. Phylogenetic analysis revealed two geographic site-specific lineages of avian H2 HAs: North American and Eurasian. Evidence is presented to support interregion transmission of gull H2 viruses. The human H2 HAs that circulated in 1957-1968 form a separate phylogenetic lineage, most closely related to the Eurasian avian H2 HAs. There was an increased prevalence of H2 influenza viruses among wild ducks in 1988 in North America, preceding the appearance of H2N2 viruses in domestic fowl. As the prevalence of avian H2N2 influenza viruses increased on turkey farms and in live bird markets in New York City and elsewhere, greater numbers of these viruses have come into direct contact with susceptible humans. We conclude that antigenically conserved counterparts of the human Asian pandemic strain of 1957 continue to circulate in the avian reservoir and are coming into closer proximity to susceptible human populations.
    PMID: 7684877 [PubMed - indexed for MEDLINE]
    </DD>

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  • HenryN
    replied
    Re: New swine flu has avian flu genes

    Data deposition: The sequences reported in this paper have been deposited in the GenBank
    database [accession nos. EU258935–EU258942 (A/Sw/2124514) and EU258943–EU258950
    (A/Sw/4296424)].

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