Novel cytomegaloviruses in free-ranging and captive great apes: phylogenetic evidence for bidirectional horizontal transmission
dc.contributor.author | Leendertz, Fabian | |
dc.contributor.author | Deckers, Merlin | |
dc.contributor.author | Schempp, Werner | |
dc.contributor.author | Lankester, Felix | |
dc.contributor.author | Boesch, Christophe | |
dc.contributor.author | Mugisha, Lawrence | |
dc.contributor.author | Dolan, Aidan | |
dc.contributor.author | Gatherer, Derek | |
dc.contributor.author | McGeoch, Duncan J. | |
dc.contributor.author | Ehlers, Bernhard | |
dc.date.accessioned | 2018-05-07T14:18:09Z | |
dc.date.available | 2018-05-07T14:18:09Z | |
dc.date.created | 2010-12-17 | |
dc.date.issued | 2009-06-24 | none |
dc.identifier.other | http://edoc.rki.de/oa/articles/re6itqiuMIIGw/PDF/23fwJQP18yXU.pdf | |
dc.identifier.uri | http://edoc.rki.de/176904/776 | |
dc.description.abstract | Wild great apes often suffer from diseases of unknown aetiology. This is among the causes of population declines. Because human cytomegalovirus (HCMV) is an important pathogen, especially in immunocompromised individuals, a search for cytomegaloviruses (CMVs) in deceased wild and captive chimpanzees, gorillas and orang-utans was performed. By using a degenerate PCR targeting four conserved genes (UL54-UL57), several distinct, previously unrecognized CMVs were found for each species. Sequences of up to 9 kb were determined for ten novel CMVs, located in the UL54-UL57 block. A phylogenetic tree was inferred for the ten novel CMVs, the previously characterized chimpanzee CMV, HCMV strains and Old World and New World monkey CMVs. The primate CMVs fell into four clades, containing New World monkey, Old World monkey, orang-utan and human CMVs, respectively, plus two clades that each contained both chimpanzee and gorilla isolates (termed CG1 and CG2). The tree loci of the first four clades mirrored those for their respective hosts in the primate tree, suggesting that these CMV lineages arose through cospeciation with host lineages. The CG1 and CG2 loci corresponded to those of the gorilla and chimpanzee hosts, respectively. This was interpreted as indicating that CG1 and CG2 represented CMV lineages that had arisen cospeciationally with the gorilla and chimpanzee lineages, respectively, with subsequent transfer within each clade between the host genera. Divergence dates were estimated and found to be consistent with overall cospeciational development of major primate CMV lineages. However, CMV transmission between chimpanzees and gorillas in both directions has also occurred. | eng |
dc.language.iso | eng | |
dc.publisher | Robert Koch-Institut, Infektionskrankheiten / Erreger | |
dc.subject | Amino Acid Sequence | eng |
dc.subject | Humans | eng |
dc.subject | Gene Expression Regulation | eng |
dc.subject | Phylogeny | eng |
dc.subject | Animals | eng |
dc.subject | Base Sequence | eng |
dc.subject | Viral Proteins/genetics | eng |
dc.subject | Cytomegalovirus/genetics | eng |
dc.subject | Cytomegalovirus/isolation & purification | eng |
dc.subject | Cytomegalovirus Infections/virology | eng |
dc.subject | Ape Diseases/virology | eng |
dc.subject | Zoo | eng |
dc.subject | Cytomegalovirus/classification | eng |
dc.subject | Cytomegalovirus Infections/veterinary | eng |
dc.subject | Viral/physiology | eng |
dc.subject | Gorilla gorilla/virology | eng |
dc.subject | Pan troglodytes/virology | eng |
dc.subject | Pongo pygmaeus/virology | eng |
dc.subject | Viral Proteins/chemistry | eng |
dc.subject.ddc | 610 Medizin | |
dc.title | Novel cytomegaloviruses in free-ranging and captive great apes: phylogenetic evidence for bidirectional horizontal transmission | |
dc.type | periodicalPart | |
dc.identifier.urn | urn:nbn:de:0257-10011919 | |
dc.identifier.doi | 10.1099/vir.0.011866-0 | |
dc.identifier.doi | http://dx.doi.org/10.25646/701 | |
local.edoc.container-title | Journal of General Virology | |
local.edoc.container-text | This is an author manuscript that has been accepted for publication in Microbiology, copyright Society for General Microbiology, but has not been copy-edited, formatted or proofed. Cite this article as appearing in Microbiology. This version of the manuscript may not be duplicated or reproduced, other than for personal use or within the rule of ‘Fair Use of Copyrighted Materials’ (section 17, Title 17, US Code), without permission from the copyright owner, Society for General Microbiology. The Society for General Microbiology disclaims any responsibility or liability for errors or omissions in this version of the manuscript or in any version derived from it by any other parties. The final copy-edited, published article, which is the version of record, can be found at http://mic.sgmjournals.org, and is freely available without a subscription 12 months after publication. | |
local.edoc.fp-subtype | Artikel | |
local.edoc.type-name | Zeitschriftenartikel | |
local.edoc.container-type | periodical | |
local.edoc.container-type-name | Zeitschrift | |
local.edoc.container-url | http://vir.sgmjournals.org/cgi/content/abstract/90/10/2386 | |
local.edoc.container-publisher-name | Society for General Microbiology | |
local.edoc.container-volume | 90 | |
local.edoc.container-issue | 10 | |
local.edoc.container-year | 2009 |