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2020
DOI: 10.1111/cla.12422
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Genomics‐based re‐examination of the taxonomy and phylogeny of human and simian Mastadenoviruses: an evolving whole genomes approach, revealing putative zoonosis, anthroponosis, and amphizoonosis

Abstract: Genomics-based re-examination of the taxonomy and phylogeny Genomics-based re-examination of the taxonomy and phylogeny of human and simian Mastadenoviruses: an evolving whole of human and simian Mastadenoviruses: an evolving whole genomes approach, revealing putative zoonosis, anthroponosis, genomes approach, revealing putative zoonosis, anthroponosis, and amphizoonosis Genomics-based re-examination of the taxonomy and phylogeny of human and simian Mastadenoviruses: an evolving whole genomes approach, reveali… Show more

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Cited by 14 publications
(15 citation statements)
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References 79 publications
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“…These analyses, combined with their distinct genome sizes, and the differences in nucleotide composition warrant the human AdVs, the gorilla AdVs, and the combined group of bonobo and chimpanzee AdVs to be considered as clades of different taxa. These data confirm and extend the results of Kang and collaborators who used full genome sequence analyses of a large set of human and simian adenoviruses to provide a proposal for a more consistent and revised taxonomy for the primate adenoviruses [ 32 ]. Based on the observation that many of the clades encompass AdV isolates from humans as well as from non-human primates, they propose the designation of all AdVs isolated from humans and from non-human primates as ‘primate adenoviruses’ (PrAdV).…”
Section: Discussionsupporting
confidence: 85%
See 1 more Smart Citation
“…These analyses, combined with their distinct genome sizes, and the differences in nucleotide composition warrant the human AdVs, the gorilla AdVs, and the combined group of bonobo and chimpanzee AdVs to be considered as clades of different taxa. These data confirm and extend the results of Kang and collaborators who used full genome sequence analyses of a large set of human and simian adenoviruses to provide a proposal for a more consistent and revised taxonomy for the primate adenoviruses [ 32 ]. Based on the observation that many of the clades encompass AdV isolates from humans as well as from non-human primates, they propose the designation of all AdVs isolated from humans and from non-human primates as ‘primate adenoviruses’ (PrAdV).…”
Section: Discussionsupporting
confidence: 85%
“…This clade includes all AdVs isolated from humans and from simians. The human-, gorilla-, chimpanzee-, and bonobo-derived AdVs that are conventionally grouped in the HAdV-C species are proposed to be reclassified as three distinct species: PrAdV-C (the human-derived HAdV-C types such as C1, C2, C5, C6, and C57), PrAdV-K (gorilla-derived isolates as SAdV-43 and SAdV45), and PrAdV-S (bonobo- and chimpanzee-derived isolates such as SAdV-34 and SAdV-44) [ 32 ]. This PrAdV classification is fully supported by the analyses of the HAdV-C isolates presented in our study.…”
Section: Discussionmentioning
confidence: 99%
“…Ads are non-enveloped doublestranded DNA viruses most commonly responsible for mild selflimiting respiratory and ocular infections in humans 27 . Over 150 primate Ads have been characterized, with many Ads in development for vaccine purposes 28,29 . Like mRNA vaccines, Ad vaccines are a relatively new technology, although Ads have been used as gene delivery vehicles since the earliest days of gene therapy.…”
Section: Adenoviral Vector Vaccinesmentioning
confidence: 99%
“…We reported SAdV-F-like AdVs for the first time in freeroaming NHPs and after ~six decades from captive NHPs. The detection of SAdV-Flike AdVs and SAdV-F/SAdV-17/18 in related host species (AGMs and grivet monkeys, respectively, genus Chlorocebus) mirrored the hypothesis that AdVs have a narrow host range [1][2][3][4]14,15,17]. SAdV-F/SADV-17 and -18 were detected in the intestinal contents of grivet monkeys [47], whilst the SAdV-F-like AdVs from AGMs were identified in both fecal/rectal and nasal samples.…”
Section: Discussionmentioning
confidence: 93%
“…On the other ha the origin of KNA-S6 appear to be complex, with a SAdV-F/SAdV-18-like Pol, and a he and a penton base that was more closely related to HAdV-F/HAdV-40(HAdV-F/HA 40-like) and SAdV-F/SAdV-17, respectively. The AdV hexon has been proposed to b active site for recombination events [3,[14][15][16][17][18]. Although recombination analysis should performed on complete genomes of AdVs [17], we a empted to evaluate the comp hexon coding sequence of KNA-S6 (and KNA-08975) for possible recombination eve However, inconclusive results were obtained with the RDP4 program.…”
Section: Putativementioning
confidence: 99%