TY - JOUR
T1 - Identification of a Novel Myxoma Virus C7-Like Host Range Factor That Enabled a Species Leap from Rabbits to Hares
AU - Águeda-Pinto, Ana
AU - Kraberger, Simona
AU - Everts, Anne
AU - Gutierrez-Jensen, Ami
AU - Glenn, Honor L.
AU - Dalton, Kevin P.
AU - Podadera, Ana
AU - Parra, Francisco
AU - Martinez-Haro, Monica
AU - Viñuelas, José Alberto
AU - Varsani, Arvind
AU - McFadden, Grant
AU - Rahman, Masmudur M.
AU - Esteves, Pedro J.
N1 - Funding Information:
Confocal data were collected at the Arizona State University Biodesign Imaging Facility microscopy core. The FCT (Foundation for Science and Technology) supported the doctoral fellowship of A.A.-P. (reference no. SFRH/BD/128752/2017) and the investigator grant of P.J.E. (IF/00376/2015). This research is a result of the project NORTE-01-0145-FEDER-000007, supported by the Norte Portugal Regional Operational Programme (NORTE2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). F.P. received funding from the Spanish Ministry for Science Innovation and Universities (grant no. AGL2017-83395-R) and INTERCUN. K.P.D. acknowledges funding from the Spanish Ministry for Science Innovation and Universities (reference no. PID2020-120349RB-100) cofinanced by FEDER. M.M.H. was supported by a research project (I-FEDEXCAZA202013) funded by the Extremadura Hunting Federation. This work was also supported by National Institutes of Health (NIH) grants R01 AI080607 and R21 AI163910. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Publisher Copyright:
© 2022 Águeda-Pinto et al.
PY - 2022/4
Y1 - 2022/4
N2 - Myxoma virus (MYXV) is naturally found in rabbit Sylvilagus species and is known to cause lethal myxomatosis in European rabbits (Oryctolagus cuniculus). In 2019, an MYXV strain (MYXV strain Toledo [MYXV-Tol]) causing myxomatosis-like disease in Iberian hares (Lepus granatensis) was identified. MYXV-Tol acquired a recombinant region of ;2.8 kb harboring several new genes, including a novel host range gene (M159) that we show to be an orthologous member of the vaccinia virus C7 host range family. Here, to test whether M159 alone has enabled MYXV to alter its host range to Iberian hares, several recombinant viruses were generated, including an MYXV-Tol DM159 (knockout) strain. While MYXV-Tol underwent fully productive infection in hare HN-R cells, neither the wild-type MYXV-Lau strain (lacking M159) nor vMyxTol-DM159 (deleted for M159) was able to infect and replicate, showing that the ability of MYXV-Tol to infect these cells and replicate depends on the presence of M159. Similar to other C7L family members, M159 was shown to be expressed as an early/late gene but was translocated into the nucleus at later time points, indicating that further studies are needed to elucidate its role in the nucleus. Finally, in rabbit cells, the M159 protein did not contribute to increased replication but was able to upregulate the replication levels of MYXV in nonpermissive and semipermissive human cancer cells, suggesting that the M159-targeted pathway is conserved across mammalian species. Altogether, these observations demonstrate that the M159 protein plays a critical role in determining the host specificity of MYXV-Tol in hare and human cells by imparting new host range functions.
AB - Myxoma virus (MYXV) is naturally found in rabbit Sylvilagus species and is known to cause lethal myxomatosis in European rabbits (Oryctolagus cuniculus). In 2019, an MYXV strain (MYXV strain Toledo [MYXV-Tol]) causing myxomatosis-like disease in Iberian hares (Lepus granatensis) was identified. MYXV-Tol acquired a recombinant region of ;2.8 kb harboring several new genes, including a novel host range gene (M159) that we show to be an orthologous member of the vaccinia virus C7 host range family. Here, to test whether M159 alone has enabled MYXV to alter its host range to Iberian hares, several recombinant viruses were generated, including an MYXV-Tol DM159 (knockout) strain. While MYXV-Tol underwent fully productive infection in hare HN-R cells, neither the wild-type MYXV-Lau strain (lacking M159) nor vMyxTol-DM159 (deleted for M159) was able to infect and replicate, showing that the ability of MYXV-Tol to infect these cells and replicate depends on the presence of M159. Similar to other C7L family members, M159 was shown to be expressed as an early/late gene but was translocated into the nucleus at later time points, indicating that further studies are needed to elucidate its role in the nucleus. Finally, in rabbit cells, the M159 protein did not contribute to increased replication but was able to upregulate the replication levels of MYXV in nonpermissive and semipermissive human cancer cells, suggesting that the M159-targeted pathway is conserved across mammalian species. Altogether, these observations demonstrate that the M159 protein plays a critical role in determining the host specificity of MYXV-Tol in hare and human cells by imparting new host range functions.
KW - C7 family
KW - M159 protein
KW - Poxviridae
KW - host range
KW - leporids
KW - myxoma virus
KW - species leap
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UR - http://www.scopus.com/inward/citedby.url?scp=85129099821&partnerID=8YFLogxK
U2 - 10.1128/mbio.03461-21
DO - 10.1128/mbio.03461-21
M3 - Article
C2 - 35352978
AN - SCOPUS:85129099821
SN - 2161-2129
VL - 13
JO - mBio
JF - mBio
IS - 2
ER -