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  • 1
    Publication Date: 2002-04-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Worobey, Michael -- Rambaut, Andrew -- Pybus, Oliver G -- Robertson, David L -- New York, N.Y. -- Science. 2002 Apr 12;296(5566):211 discussion 211.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology, University of Oxford, South Parks Road, Oxford, OX1 3PS, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11951002" target="_blank"〉PubMed〈/a〉
    Keywords: Disease Outbreaks ; Evolution, Molecular ; Hemagglutinin Glycoproteins, Influenza Virus/*genetics ; Humans ; Influenza A virus/*genetics/pathogenicity ; Influenza, Human/*epidemiology/*virology ; Likelihood Functions ; Phylogeny ; *Recombination, Genetic ; Virulence
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2008-10-04
    Description: Human immunodeficiency virus type 1 (HIV-1) sequences that pre-date the recognition of AIDS are critical to defining the time of origin and the timescale of virus evolution. A viral sequence from 1959 (ZR59) is the oldest known HIV-1 infection. Other historically documented sequences, important calibration points to convert evolutionary distance into time, are lacking, however; ZR59 is the only one sampled before 1976. Here we report the amplification and characterization of viral sequences from a Bouin's-fixed paraffin-embedded lymph node biopsy specimen obtained in 1960 from an adult female in Leopoldville, Belgian Congo (now Kinshasa, Democratic Republic of the Congo (DRC)), and we use them to conduct the first comparative evolutionary genetic study of early pre-AIDS epidemic HIV-1 group M viruses. Phylogenetic analyses position this viral sequence (DRC60) closest to the ancestral node of subtype A (excluding A2). Relaxed molecular clock analyses incorporating DRC60 and ZR59 date the most recent common ancestor of the M group to near the beginning of the twentieth century. The sizeable genetic distance between DRC60 and ZR59 directly demonstrates that diversification of HIV-1 in west-central Africa occurred long before the recognized AIDS pandemic. The recovery of viral gene sequences from decades-old paraffin-embedded tissues opens the door to a detailed palaeovirological investigation of the evolutionary history of HIV-1 that is not accessible by other methods.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682493/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682493/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Worobey, Michael -- Gemmel, Marlea -- Teuwen, Dirk E -- Haselkorn, Tamara -- Kunstman, Kevin -- Bunce, Michael -- Muyembe, Jean-Jacques -- Kabongo, Jean-Marie M -- Kalengayi, Raphael M -- Van Marck, Eric -- Gilbert, M Thomas P -- Wolinsky, Steven M -- R21 AI065371/AI/NIAID NIH HHS/ -- England -- Nature. 2008 Oct 2;455(7213):661-4. doi: 10.1038/nature07390.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ecology and Evolutionary Biology, University of Arizona, Tucson, Arizona 85721, USA. worobey@email.arizona.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18833279" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Canada ; Democratic Republic of the Congo/epidemiology ; *Evolution, Molecular ; Female ; Genetic Variation/*genetics ; HIV Infections/*epidemiology/pathology/*virology ; HIV-1/classification/*genetics/*isolation & purification ; History, 20th Century ; Humans ; Male ; Microtomy ; Molecular Sequence Data ; Paraffin Embedding ; Phylogeny ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Analysis, DNA
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2009-06-12
    Description: In March and early April 2009, a new swine-origin influenza A (H1N1) virus (S-OIV) emerged in Mexico and the United States. During the first few weeks of surveillance, the virus spread worldwide to 30 countries (as of May 11) by human-to-human transmission, causing the World Health Organization to raise its pandemic alert to level 5 of 6. This virus has the potential to develop into the first influenza pandemic of the twenty-first century. Here we use evolutionary analysis to estimate the timescale of the origins and the early development of the S-OIV epidemic. We show that it was derived from several viruses circulating in swine, and that the initial transmission to humans occurred several months before recognition of the outbreak. A phylogenetic estimate of the gaps in genetic surveillance indicates a long period of unsampled ancestry before the S-OIV outbreak, suggesting that the reassortment of swine lineages may have occurred years before emergence in humans, and that the multiple genetic ancestry of S-OIV is not indicative of an artificial origin. Furthermore, the unsampled history of the epidemic means that the nature and location of the genetically closest swine viruses reveal little about the immediate origin of the epidemic, despite the fact that we included a panel of closely related and previously unpublished swine influenza isolates. Our results highlight the need for systematic surveillance of influenza in swine, and provide evidence that the mixing of new genetic elements in swine can result in the emergence of viruses with pandemic potential in humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, Gavin J D -- Vijaykrishna, Dhanasekaran -- Bahl, Justin -- Lycett, Samantha J -- Worobey, Michael -- Pybus, Oliver G -- Ma, Siu Kit -- Cheung, Chung Lam -- Raghwani, Jayna -- Bhatt, Samir -- Peiris, J S Malik -- Guan, Yi -- Rambaut, Andrew -- BB/E009670/1/Biotechnology and Biological Sciences Research Council/United Kingdom -- HHSN266200700005C/PHS HHS/ -- Biotechnology and Biological Sciences Research Council/United Kingdom -- England -- Nature. 2009 Jun 25;459(7250):1122-5. doi: 10.1038/nature08182.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉State Key Laboratory of Emerging Infectious Diseases & Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong SAR, China.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19516283" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Disease Outbreaks ; *Evolution, Molecular ; Genome, Viral/*genetics ; Humans ; Influenza A Virus, H1N1 Subtype/classification/*genetics ; *Influenza, Human/epidemiology/virology ; Molecular Sequence Data ; Orthomyxoviridae Infections/epidemiology/veterinary/virology ; Phylogeny ; Reassortant Viruses/classification/*genetics ; Swine ; Swine Diseases/*virology ; Time Factors
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2014-02-18
    Description: Zoonotic infectious diseases such as influenza continue to pose a grave threat to human health. However, the factors that mediate the emergence of RNA viruses such as influenza A virus (IAV) are still incompletely understood. Phylogenetic inference is crucial to reconstructing the origins and tracing the flow of IAV within and between hosts. Here we show that explicitly allowing IAV host lineages to have independent rates of molecular evolution is necessary for reliable phylogenetic inference of IAV and that methods that do not do so, including 'relaxed' molecular clock models, can be positively misleading. A phylogenomic analysis using a host-specific local clock model recovers extremely consistent evolutionary histories across all genomic segments and demonstrates that the equine H7N7 lineage is a sister clade to strains from birds--as well as those from humans, swine and the equine H3N8 lineage--sharing an ancestor with them in the mid to late 1800s. Moreover, major western and eastern hemisphere avian influenza lineages inferred for each gene coalesce in the late 1800s. On the basis of these phylogenies and the synchrony of these key nodes, we infer that the internal genes of avian influenza virus (AIV) underwent a global selective sweep beginning in the late 1800s, a process that continued throughout the twentieth century and up to the present. The resulting western hemispheric AIV lineage subsequently contributed most of the genomic segments to the 1918 pandemic virus and, independently, the 1963 equine H3N8 panzootic lineage. This approach provides a clear resolution of evolutionary patterns and processes in IAV, including the flow of viral genes and genomes within and between host lineages.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098125/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098125/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Worobey, Michael -- Han, Guan-Zhu -- Rambaut, Andrew -- 092807/Wellcome Trust/United Kingdom -- 095831/Wellcome Trust/United Kingdom -- R01 AI084691/AI/NIAID NIH HHS/ -- R01AI084691/AI/NIAID NIH HHS/ -- England -- Nature. 2014 Apr 10;508(7495):254-7. doi: 10.1038/nature13016. Epub 2014 Feb 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, Arizona 85721, USA. ; 1] Institute of Evolutionary Biology, University of Edinburgh, Edinburgh EH9 3JT, UK [2] Fogarty International Center, National Institutes of Health, Bethesda, Maryland 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24531761" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Birds/virology ; Evolution, Molecular ; Genes, Viral/*genetics ; Genome, Viral/genetics ; Hemagglutinin Glycoproteins, Influenza Virus/classification/genetics ; Horses/virology ; Host Specificity ; Humans ; Influenza A Virus, H3N8 Subtype/classification/genetics ; Influenza A Virus, H7N7 Subtype/classification/genetics ; Influenza A virus/*classification/enzymology/*genetics ; Influenza in Birds/transmission/*virology ; Molecular Sequence Data ; Neuraminidase/classification/genetics ; Pandemics ; *Phylogeny ; Swine/virology ; Zoonoses/transmission/virology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2010-09-18
    Description: Simian immunodeficiency virus (SIV) lineages have been identified that are endemic to Bioko Island. The time the island formed offers a geological time scale calibration point for dating the most recent common ancestor of SIV. The Bioko viruses cover the whole range of SIV genetic diversity, and each Bioko SIV clade is most closely related to viruses circulating in hosts of the same genus on the African mainland rather than to SIVs of other Bioko species. Our phylogeographic approach establishes that SIV is ancient and at least 32,000 years old. Our conservative calibration point and analyses of gene sequence saturation and dating bias suggest it may be much older.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Worobey, Michael -- Telfer, Paul -- Souquiere, Sandrine -- Hunter, Meredith -- Coleman, Clint A -- Metzger, Michael J -- Reed, Patricia -- Makuwa, Maria -- Hearn, Gail -- Honarvar, Shaya -- Roques, Pierre -- Apetrei, Cristian -- Kazanji, Mirdad -- Marx, Preston A -- 1R01AI27698/AI/NIAID NIH HHS/ -- 1R01AI44596/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2010 Sep 17;329(5998):1487. doi: 10.1126/science.1193550.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Arizona, Tucson, AZ 85721, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20847261" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cercopithecidae/*virology ; Cercopithecus/virology ; Colobus/virology ; Equatorial Guinea ; Evolution, Molecular ; Genes, pol ; Genetic Variation ; Geography ; Mandrillus/virology ; Molecular Sequence Data ; Phylogeny ; Simian Acquired Immunodeficiency Syndrome/*virology ; Simian Immunodeficiency Virus/*classification/*genetics/isolation & purification ; Time Factors
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2008-03-12
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 7
    Publication Date: 2007-10-31
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 8
    Publication Date: 2014-04-28
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 9
    Publication Date: 1999-06-22
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 10
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