FULL PAPER AVAILABLE: Identification of African Elephant Polyomavirus in wild elephants and the creation of a vector expressing its viral tumor antigens to transform elephant primary cells

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Identification of African Elephant Polyomavirus in wild elephants and the
creation of a vector expressing its viral tumor antigens to transform
elephant primary cellsVirginia R. Pearson, Jens B. Bosse, Orkide O.
Koyuncu, Julian Scherer, Cristhian Toruno, Rosann Robinson, Lisa M.
Abegglen, Joshua D. Schiffman, Lynn W. Enquist & Glenn F. RallPLOS
ONEFebruary 5, 2021 Abstract

Wild elephant populations are declining rapidly due to rampant killing for
ivory and body parts, range fragmentation, and human-elephant conflict.
Wild and captive elephants are further impacted by viruses, including
highly pathogenic elephant endotheliotropic herpesviruses. Moreover, while
the rich genetic diversity of the ancient elephant lineage is disappearing,
elephants, with their low incidence of cancer, have emerged as a surprising
resource in human cancer research for understanding the intrinsic cellular
response to DNA damage. However, studies on cellular resistance to
transformation and herpesvirus reproduction have been severely limited, in
part due to the lack of established elephant cell lines to enable in vitro
experiments. This report describes creation of a recombinant plasmid,
pAelPyV-1-Tag, derived from a wild isolate of African Elephant Polyomavirus
(AelPyV-1), that can be used to create immortalized lines of elephant
cells. This isolate was extracted from a trunk nodule biopsy isolated from
a wild African elephant, Loxodonta africana, in Botswana. The AelPyV-1
genome contains open-reading frames encoding the canonical large (LTag) and
small (STag) tumor antigens. We cloned the entire early region spanning the
LTag and overlapping STag genes from this isolate into a high-copy vector
to construct a recombinant plasmid, pAelPyV-1-Tag, which effectively
transformed primary elephant endothelial cells. We expect that the
potential of this reagent to transform elephant primary cells will, at a
minimum, facilitate study of elephant-specific herpesviruses.

FULL PAPER PDF
LINKhttps://drive.google.com/file/d/13bf0jGsGCjY1LPfeO0lG8j7fpSFOv9gl/view?usp=sharing
https://drive.google.com/file/d/13bf0jGsGCjY1LPfeO0lG8j7fpSFOv9gl/view?usp=sharing
FULL
PAPER WEB
LINKhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0244334
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0244334

*Identification of African Elephant Polyomavirus in wild elephants and the creation of a vector expressing its viral tumor antigens to transform elephant primary cellsVirginia R. Pearson, Jens B. Bosse, Orkide O. Koyuncu, Julian Scherer, Cristhian Toruno, Rosann Robinson, Lisa M. Abegglen, Joshua D. Schiffman, Lynn W. Enquist & Glenn F. RallPLOS ONEFebruary 5, 2021 Abstract* Wild elephant populations are declining rapidly due to rampant killing for ivory and body parts, range fragmentation, and human-elephant conflict. Wild and captive elephants are further impacted by viruses, including highly pathogenic elephant endotheliotropic herpesviruses. Moreover, while the rich genetic diversity of the ancient elephant lineage is disappearing, elephants, with their low incidence of cancer, have emerged as a surprising resource in human cancer research for understanding the intrinsic cellular response to DNA damage. However, studies on cellular resistance to transformation and herpesvirus reproduction have been severely limited, in part due to the lack of established elephant cell lines to enable in vitro experiments. This report describes creation of a recombinant plasmid, pAelPyV-1-Tag, derived from a wild isolate of African Elephant Polyomavirus (AelPyV-1), that can be used to create immortalized lines of elephant cells. This isolate was extracted from a trunk nodule biopsy isolated from a wild African elephant, Loxodonta africana, in Botswana. The AelPyV-1 genome contains open-reading frames encoding the canonical large (LTag) and small (STag) tumor antigens. We cloned the entire early region spanning the LTag and overlapping STag genes from this isolate into a high-copy vector to construct a recombinant plasmid, pAelPyV-1-Tag, which effectively transformed primary elephant endothelial cells. We expect that the potential of this reagent to transform elephant primary cells will, at a minimum, facilitate study of elephant-specific herpesviruses. *FULL PAPER PDF LINKhttps://drive.google.com/file/d/13bf0jGsGCjY1LPfeO0lG8j7fpSFOv9gl/view?usp=sharing <https://drive.google.com/file/d/13bf0jGsGCjY1LPfeO0lG8j7fpSFOv9gl/view?usp=sharing> FULL PAPER WEB LINKhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0244334 <https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0244334>*