Unexpected Inheritance: Multiple Integrations of Ancient Bornavirus and Ebolavirus/Marburgvirus Sequences in Vertebrate Genomes

被引:210
作者
Belyi, Vladimir A. [1 ]
Levine, Arnold J. [1 ]
Skalka, Anna Marie [2 ]
机构
[1] Inst Adv Study, Simons Ctr Syst Biol, Princeton, NJ 08540 USA
[2] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
基金
美国国家卫生研究院;
关键词
EBOLA-VIRUS; DISEASE-VIRUS; MOLECULAR PHYLOGENY; RNA VIRUSES; IDENTIFICATION; NUCLEOPROTEIN; GLYCOPROTEIN; RESISTANCE; RATES; BATS;
D O I
10.1371/journal.ppat.1001030
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vertebrate genomes contain numerous copies of retroviral sequences, acquired over the course of evolution. Until recently they were thought to be the only type of RNA viruses to be so represented, because integration of a DNA copy of their genome is required for their replication. In this study, an extensive sequence comparison was conducted in which 5,666 viral genes from all known non-retroviral families with single-stranded RNA genomes were matched against the germline genomes of 48 vertebrate species, to determine if such viruses could also contribute to the vertebrate genetic heritage. In 19 of the tested vertebrate species, we discovered as many as 80 high-confidence examples of genomic DNA sequences that appear to be derived, as long ago as 40 million years, from ancestral members of 4 currently circulating virus families with single strand RNA genomes. Surprisingly, almost all of the sequences are related to only two families in the Order Mononegavirales: the Bornaviruses and the Filoviruses, which cause lethal neurological disease and hemorrhagic fevers, respectively. Based on signature landmarks some, and perhaps all, of the endogenous virus-like DNA sequences appear to be LINE element-facilitated integrations derived from viral mRNAs. The integrations represent genes that encode viral nucleocapsid, RNA-dependent-RNA-polymerase, matrix and, possibly, glycoproteins. Integrations are generally limited to one or very few copies of a related viral gene per species, suggesting that once the initial germline integration was obtained (or selected), later integrations failed or provided little advantage to the host. The conservation of relatively long open reading frames for several of the endogenous sequences, the virus-like protein regions represented, and a potential correlation between their presence and a species' resistance to the diseases caused by these pathogens, are consistent with the notion that their products provide some important biological advantage to the species. In addition, the viruses could also benefit, as some resistant species (e. g. bats) may serve as natural reservoirs for their persistence and transmission. Given the stringent limitations imposed in this informatics search, the examples described here should be considered a low estimate of the number of such integration events that have persisted over evolutionary time scales. Clearly, the sources of genetic information in vertebrate genomes are much more diverse than previously suspected.
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页码:1 / 13
页数:13
相关论文
共 47 条
[31]   Conservation of coding potential and terminal sequences in four different isolates of Borna disease virus [J].
Pleschka, S ;
Staeheli, P ;
Kolodziejek, J ;
Richt, JA ;
Nowotny, N ;
Schwemmle, M .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :2681-2690
[32]   The natural history of Ebola virus in Africa [J].
Pourrut, X ;
Kumulungui, B ;
Wittmann, T ;
Moussavou, G ;
Délicat, A ;
Yaba, P ;
Nkoghe, D ;
Gonzalez, JP ;
Leroy, EM .
MICROBES AND INFECTION, 2005, 7 (7-8) :1005-1014
[33]   Large serological survey showing cocirculation of Ebola and Marburg viruses in Gabonese bat populations, and a high seroprevalence of both viruses in Rousettus aegyptiacus [J].
Pourrut, Xavier ;
Souris, Marc ;
Towner, Jonathan S. ;
Rollin, Pierre E. ;
Nichol, Stuart T. ;
Gonzalez, Jean-Paul ;
Leroy, Eric .
BMC INFECTIOUS DISEASES, 2009, 9 :159
[34]  
PRINS KC, 2010, J VIROL
[35]   Crystal structure of the Borna disease virus nucleoprotein [J].
Rudolph, MG ;
Kraus, I ;
Dickmanns, A ;
Eickmann, M ;
Garten, W ;
Ficner, R .
STRUCTURE, 2003, 11 (10) :1219-1226
[36]  
Sanchez A., 2007, FIELDS VIROLOGY, V5th
[37]   A filovirus-unique region of Ebola virus nucleoprotein confers aberrant migration and mediates its incorporation into virions [J].
Shi, Wei ;
Huang, Yue ;
Sutton-Smith, Mark ;
Tissot, Berangere ;
Panico, Maria ;
Morris, Howard R. ;
Dell, Anne ;
Haslam, Stuart M. ;
Boyington, Jeffrey ;
Graham, Barney S. ;
Yang, Zhi-Yong ;
Nabell, Gary J. .
JOURNAL OF VIROLOGY, 2008, 82 (13) :6190-6199
[38]   Epidemiology of Borna disease virus [J].
Staeheli, P ;
Sauder, C ;
Hausmann, J ;
Ehrensperger, F ;
Schwemmle, M .
JOURNAL OF GENERAL VIROLOGY, 2000, 81 :2123-2135
[39]   A gene atlas of the mouse and human protein-encoding transcriptomes [J].
Su, AI ;
Wiltshire, T ;
Batalov, S ;
Lapp, H ;
Ching, KA ;
Block, D ;
Zhang, J ;
Soden, R ;
Hayakawa, M ;
Kreiman, G ;
Cooke, MP ;
Walker, JR ;
Hogenesch, JB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (16) :6062-6067
[40]   Experimental inoculation of plants and animals with Ebola virus [J].
Swanepoel, R ;
Leman, PA ;
Burt, FJ ;
Zachariades, NA ;
Braack, LEO ;
Ksiazek, TG ;
Rollin, PE ;
Zaki, SR ;
Peters, CJ .
EMERGING INFECTIOUS DISEASES, 1996, 2 (04) :321-325