Compositions, methods and uses for inducing viral growth
Embodiments herein report methods, compositions and uses for inducing and/or accelerating viral growth. In certain embodiments, methods, compositions and uses generally related to copolymer compositions for inducing viral growth, reducing lag time and/or increasing viral plaque size. In other embodiments, methods, compositions and uses of copolymer compositions can be for inducing flaviviral growth, reducing lag in growth and/or increasing plaque size.
1. A composition for growing viral cultures comprising:
one or more ethylene oxide propylene oxide (EO-PO) block copolymers, the EO-PO block copolymers comprise poloxamer 407 , poloxamer 403 or a combination thereof wherein the concentration of EO-PO block copolymer is from 0.063% to 3.0%;
a viral culture;
a host cell; and
a media for growing the viral cultures,
wherein the EO-PO block copolymers accelerate growth of viral cultures.
2. The composition of claim 1 , wherein the viral cultures are selected from the group consisting of Flavivirus, Togavirus, Coronavirus, Filovirus, Paramyxovirus, Orthomyxovirus, Bunyavirus, Arenavirus, Retrovirus, Hepadnavirus, Pestivirus, Herpes virus, and Poxvirus.
3. The composition of claim 1 , wherein the viral cultures are Flavivirus cultures.
4. The composition of claim 1 , wherein the viral cultures are Poxvirus cultures.
5. The composition of claim 1 , wherein at least one of the one or more ethylene oxide propylene oxide (EO-PO) block copolymers comprises poloxamer 407 and the media comprises Dulbecco's Modified Eagle Medium (DMEM).
6. A method for increasing viral growth rate comprising, administering to a host cell culture infected with a virus, a composition comprising one or more ethylene oxide propylene oxide (EO-PO) block copolymers , the EO-PO block copolymers comprise poloxamer 407 , poloxamer 403 or a combination thereof wherein the concentration of EO-PO block copolymer is from 0.063% to 3.0% and a viral growth media, wherein the composition increases viral growth rate in the culture.
7. A method for increasing viral growth rate comprising, administering a composition comprising one or more ethylene oxide propylene oxide (EO-PO) block copolymers to a host cell culture, before, during, or after viral infection of the host cell culture and increasing viral growth rate in the host cell culture, wherein the EO-PO block copolymers comprise poloxamer 407 , poloxamer 403 or a combination thereof wherein the concentration of EO-PO block copolymer is from 0.063% to 3.0%.
8. A method for increasing plaque size of a viral culture comprising, administering to a host cell culture infected with a virus, a composition comprising one or more ethylene oxide propylene oxide (EO-PO) block copolymers wherein the composition increases viral plaque size in the host cell culture compared to a control viral culture without administering one or more ethylene oxide propylene oxide (EO-PO) block copolymers, wherein the EO-PO block copolymers comprise poloxamer 407 , poloxamer 403 or a combination thereof wherein the concentration of EO-PO block copolymer is from 0.063% to 3.0%.
9. A method for reducing growth lag time of a viral culture comprising, administering to a host cell culture infected with a virus, a composition comprising one or more ethylene oxide propylene oxide (EO-PO) block copolymers wherein the composition reduces lag time of the viral cultures in the host cell culture compared to a control viral culture without administering one or more ethylene oxide propylene oxide (EO-PO) block copolymers, wherein the EO-PO block copolymers comprise poloxamer 407 , poloxamer 403 or a combination thereof wherein the concentration of EO-PO block copolymer is from 0.063% to 3.0%.
10. The method of claim 9 , wherein the viral cultures are selected from Flaviviral cultures.
11. The method of claim 9 , wherein the viral cultures comprise viral cultures for generating live, attenuated viral vaccines.
12. The method of claim 9 , wherein the reduction in lag time comprises at least a 10 percent reduction in lag time compared to viral cultures without one or more ethylene oxide propylene oxide (EO-PO) block copolymers.
13. A kit for culturing viruses comprising;
at least one container; and
a composition comprising the composition of claim 1 .
14. The kit of claim 13 , wherein the viral culture are one or more Flaviviruses.
15. The kit of claim 13 , further comprising a host cell stock culture comprising Vero (African green monkey Vero cells), LLC-MK2 cells (monkey kidney cells), or C6/36 mosquito cells.
16. The composition of claim 1 , wherein the virus comprises Flavivirus and the host cell culture comprises Vero (African green monkey Vero cells), LLC-MK2 cells (monkey kidney cells), or C6/36 mosquito cells.
17. A composition for growing viral cultures comprising:
an ethylene oxide propylene oxide (EO-PO) block copolymer comprising poloxamer 403 , at a concentration range of 0.063% to 3.0%;
a viral culture;
a host cell; and
a media for growing the viral cultures,
wherein the EO-PO block copolymer induces growth of viral cultures, wherein the host cells are grown to confluence.
18. The composition of claim 17 , further comprising_poloxamer 407 .
19. A composition for growing viral cultures comprising:
one or more ethylene oxide propylene oxide (EO-PO) block copolymers, the EO-PO block copolymers are selected from the group consisting of poloxamer 407 , poloxamer 403 , and a combination thereof wherein the concentration of EO-PO block copolymer is about 0.063% to 3.0%;
a viral culture;
a host cell; and
a media for growing the viral cultures,
wherein the EO-PO block copolymers accelerate growth of viral cultures, wherein the host cells are grown to confluence.
20. The composition of claim 19 , wherein the viral culture titer is from about 1×10 6 pfu/mL to about 1×10 9 pfu/mL.