Reverse genetics systems

US9821052B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9821052-B2
Application numberUS-201013388033-A
CountryUS
Kind codeB2
Filing dateJul 30, 2010
Priority dateJul 31, 2009
Publication dateNov 21, 2017
Grant dateNov 21, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention provides various reverse genetics systems for producing segmented RNA viruses, wherein the systems do not require bacteria for propagation of all of their expression constructs.

First claim

Opening claim text (preview).

The invention claimed is: 1. A non-bacterial DNA construct comprising a promoter and coding sequences for expressing at least two different genome segments of a segmented RNA virus, wherein the construct lacks both a bacterial origin of replication and a bacterial selection marker, wherein the at least two segments are selected from the group of segments consisting of PB2, PB1, PA, HA, NP, NA, M and NS, wherein the construct is linear, and, wherein the promoter is operatively linked for transcription in an eukaryotic host cell, wherein the eukaryotic host cell is a mammalian cell or avian cell. 2. A eukaryotic host cell comprising the non-bacterial construct of claim 1 . 3. A method for producing a segmented RNA virus, comprising a step of culturing a host cell of claim 2 such that expression of the RNA virus segments occurs to produce the virus. 4. The host cell of claim 2 , wherein the cell is a MDCK cell. 5. The non-bacterial DNA construct of claim 1 , wherein the coding sequences are for influenza virus A or B genome segments PB2, PB1, PA, NP, and NS. 6. A method for producing a segmented RNA virus, comprising a) transfecting a host cell with the construct of claim 1 , and b) culturing the host cell such that expression of the RNA virus segments occurs to produce the virus; wherein the host cell is a mammalian or avian host cell. 7. A non-bacterial DNA construct comprising a promoter and coding sequences for expressing all eight genome segments of an influenza A or B virus, wherein the construct lacks both a bacterial origin of replication and a bacterial selection marker, wherein the promoter is operatively linked for transcription in an eukaryotic host cell, wherein the eukaryotic host cell is a mammalian cell or avian cell, and wherein the construct is linear. 8. A eukaryotic host cell comprising the non-bacterial construct of claim 7 . 9. A method for producing a segmented RNA virus, comprising a step of culturing a host cell of claim 8 such that expression of the RNA virus segments occurs to produce the virus. 10. The host cell of claim 8 , wherein the cell is a MDCK cell.

Assignees

Inventors

Classifications

  • Viral antigens · CPC title

  • A61K39/145Primary

    Orthomyxoviridae, e.g. influenza virus · CPC title

  • New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title

  • for animal cells · CPC title

  • Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title

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Frequently asked questions

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What does patent US9821052B2 cover?
The invention provides various reverse genetics systems for producing segmented RNA viruses, wherein the systems do not require bacteria for propagation of all of their expression constructs.
Who is the assignee on this patent?
Dormitzer Philip, Franti Michael, Mason Peter, and 1 more
What technology area does this patent fall under?
Primary CPC classification A61K39/145. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).