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Recovery of infectious murine norovirus using pol II-driven expression of full-length cDNA

Recovery of infectious murine norovirus using pol II-driven expression of full-length cDNA
Recovery of infectious murine norovirus using pol II-driven expression of full-length cDNA
Noroviruses are the major cause of nonbacterial gastroenteritis in humans. These viruses have remained refractory to detailed molecular studies because of the lack of a reverse genetics system coupled to a permissive cell line for targeted genetic manipulation. There is no permissive cell line in which to grow infectious human noroviruses nor an authentic animal model that supports their replication. In contrast, murine norovirus (MNV) offers a tractable system for the study of noroviruses with the recent discovery of permissive cells and a mouse model. The lack of a reverse genetic system for MNV has been a significant block to understanding the biology of noroviruses. We report recovery of infectious MNV after baculovirus delivery of viral cDNA to human hepatoma cells under the control of an inducible DNA polymerase (pol) II promoter. Recovered virus replicated in murine macrophage (RAW264.7) cells, and the recovery of MNV from DNA was confirmed through recovery of virus containing a marker mutation. This pol II promoter driven expression of viral cDNA also generated infectious virus after transfection of HEK293T cells, thus providing both transduction and transfection systems for norovirus reverse genetics. We used norovirus reverse genetics to demonstrate by mutagenesis of the protease-polymerase (pro-pol) cleavage site that processing of pro-pol is essential for the recovery of infectious MNV. This represents the first infectious reverse genetics system for a norovirus, and should provide approaches to address fundamental questions in norovirus molecular biology and replication
0027-8424
11050-11055
Ward, V.K.
2bf9252a-8435-40a1-af0f-b55df3c3f383
McCormick, C.J.
0fce14bf-2f67-4d08-991f-114dd1e7f0bd
Clarke, I.N.
ff6c9324-3547-4039-bb2c-10c0b3327a8b
Salim, O.
a8a00604-9e57-4638-8c96-5b37e75fee90
Wobus, C.F.
1154165a-5cf3-43fe-8ddd-eb9a1f65fcba
Thackray, L.B.
a86cd752-80fe-4ec0-ba31-dbdf5167207d
Virgin, H.W.
0d3c05f8-11a0-4db3-a60b-1059b7210452
Lambden, P.R.
e99ecc21-50d7-4a43-9e79-efba46592c77
Ward, V.K.
2bf9252a-8435-40a1-af0f-b55df3c3f383
McCormick, C.J.
0fce14bf-2f67-4d08-991f-114dd1e7f0bd
Clarke, I.N.
ff6c9324-3547-4039-bb2c-10c0b3327a8b
Salim, O.
a8a00604-9e57-4638-8c96-5b37e75fee90
Wobus, C.F.
1154165a-5cf3-43fe-8ddd-eb9a1f65fcba
Thackray, L.B.
a86cd752-80fe-4ec0-ba31-dbdf5167207d
Virgin, H.W.
0d3c05f8-11a0-4db3-a60b-1059b7210452
Lambden, P.R.
e99ecc21-50d7-4a43-9e79-efba46592c77

Ward, V.K., McCormick, C.J., Clarke, I.N., Salim, O., Wobus, C.F., Thackray, L.B., Virgin, H.W. and Lambden, P.R. (2007) Recovery of infectious murine norovirus using pol II-driven expression of full-length cDNA. Proceedings of the National Academy of Sciences of the United States of America, 104 (26), 11050-11055. (doi:10.1073/pnas.0700336104).

Record type: Article

Abstract

Noroviruses are the major cause of nonbacterial gastroenteritis in humans. These viruses have remained refractory to detailed molecular studies because of the lack of a reverse genetics system coupled to a permissive cell line for targeted genetic manipulation. There is no permissive cell line in which to grow infectious human noroviruses nor an authentic animal model that supports their replication. In contrast, murine norovirus (MNV) offers a tractable system for the study of noroviruses with the recent discovery of permissive cells and a mouse model. The lack of a reverse genetic system for MNV has been a significant block to understanding the biology of noroviruses. We report recovery of infectious MNV after baculovirus delivery of viral cDNA to human hepatoma cells under the control of an inducible DNA polymerase (pol) II promoter. Recovered virus replicated in murine macrophage (RAW264.7) cells, and the recovery of MNV from DNA was confirmed through recovery of virus containing a marker mutation. This pol II promoter driven expression of viral cDNA also generated infectious virus after transfection of HEK293T cells, thus providing both transduction and transfection systems for norovirus reverse genetics. We used norovirus reverse genetics to demonstrate by mutagenesis of the protease-polymerase (pro-pol) cleavage site that processing of pro-pol is essential for the recovery of infectious MNV. This represents the first infectious reverse genetics system for a norovirus, and should provide approaches to address fundamental questions in norovirus molecular biology and replication

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Published date: 2007
Organisations: Infection Inflammation & Immunity

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Local EPrints ID: 48477
URI: http://eprints.soton.ac.uk/id/eprint/48477
ISSN: 0027-8424
PURE UUID: a053d0e1-217c-4144-ad7a-a0a60a215bcf
ORCID for C.J. McCormick: ORCID iD orcid.org/0000-0002-6155-9161
ORCID for I.N. Clarke: ORCID iD orcid.org/0000-0002-4938-1620
ORCID for O. Salim: ORCID iD orcid.org/0000-0002-2562-4827

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Date deposited: 25 Sep 2007
Last modified: 16 Mar 2024 03:47

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Contributors

Author: V.K. Ward
Author: C.J. McCormick ORCID iD
Author: I.N. Clarke ORCID iD
Author: O. Salim ORCID iD
Author: C.F. Wobus
Author: L.B. Thackray
Author: H.W. Virgin
Author: P.R. Lambden

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