Cargando…

993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus

BACKGROUND: The Live Attenuated Influenza Virus (LAIV) used in the United States is based on the cold-passaged A/AnnArbor/6/60 strain (AA). An alternative LAIV (Len), developed from the cold-passaged A/Leningrad/134/17/57 strain, has also been used in some countries outside the United States. Recent...

Descripción completa

Detalles Bibliográficos
Autores principales: Smith, Andrew, Rodriguez-Garcia, Laura, Ghouayel, Maya El, Martinez-Sobrido, Luis, Dewhurst, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253618/
http://dx.doi.org/10.1093/ofid/ofy210.830
_version_ 1783373537706246144
author Smith, Andrew
Rodriguez-Garcia, Laura
Ghouayel, Maya El
Martinez-Sobrido, Luis
Dewhurst, Stephen
author_facet Smith, Andrew
Rodriguez-Garcia, Laura
Ghouayel, Maya El
Martinez-Sobrido, Luis
Dewhurst, Stephen
author_sort Smith, Andrew
collection PubMed
description BACKGROUND: The Live Attenuated Influenza Virus (LAIV) used in the United States is based on the cold-passaged A/AnnArbor/6/60 strain (AA). An alternative LAIV (Len), developed from the cold-passaged A/Leningrad/134/17/57 strain, has also been used in some countries outside the United States. Recent concerns with the efficacy and safety of the current US LAIV warrant the development of an improved LAIV. METHODS: We used in vitro minireplicon and multicycle viral growth assays to analyze the combined effects of polymerase mutations from LAIV (AA) and LAIV (Len) on the phenotype of PR8. Mini-replicon assays were performed in HEK-293T cells with firefly luciferase under the control of the influenza virus NP promoter; we controlled for cell density with a constitutively active Renilla luciferase. Multicycle growth curve experiments were performed at 33°C, 37°C, and 39°C in MDCK cells with an m.o.i. of 0.001. Mean values for triplicate infections at 12, 24, 48, and 72 hours were plotted as TCID50/mL. RESULTS: Control experiments showed replication of PR8 (AA) and PR8 (Len) in MDCK cells was significantly decreased as compared with WT PR8 at 37°C and 39°C at 24–48 hour time points, but not at 33C (the temperature of nasal passages). We found that polymerase activity was up to 3 logs more temperature-sensitive (ts) at 37°C and 39°C with the combined Len and AA mutations using the mini-replicon assay. In the growth curve experiments, the combined Len and AA mutations conferred up to a 4-log decrease in replication levels at 37°C as compared with PR8 (Len) and an even greater decrease compared with PR8 (AA). CONCLUSION: Our findings suggest combining the AA and Len LAIV polymerase mutations decreases LAIV replication at body temperature (37°C), as compared with either LAIV alone. This could be useful in developing an improved LAIV that is safer in vulnerable hosts (e.g., children under the age of 2 who may be vulnerable to wheezing), while also permitting dose escalation that might result in greater efficacy. Minireplicon assay. [Image: see text] Polymerase activity of combination mutants. [Image: see text] Multicycle replication kinetics of combination mutants (red) against PR8 Len (black) at 33C (solid), 37C (dashed) and 39C (dotted). [Image: see text] DISCLOSURES: All authors: No reported disclosures.
format Online
Article
Text
id pubmed-6253618
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-62536182018-11-28 993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus Smith, Andrew Rodriguez-Garcia, Laura Ghouayel, Maya El Martinez-Sobrido, Luis Dewhurst, Stephen Open Forum Infect Dis Abstracts BACKGROUND: The Live Attenuated Influenza Virus (LAIV) used in the United States is based on the cold-passaged A/AnnArbor/6/60 strain (AA). An alternative LAIV (Len), developed from the cold-passaged A/Leningrad/134/17/57 strain, has also been used in some countries outside the United States. Recent concerns with the efficacy and safety of the current US LAIV warrant the development of an improved LAIV. METHODS: We used in vitro minireplicon and multicycle viral growth assays to analyze the combined effects of polymerase mutations from LAIV (AA) and LAIV (Len) on the phenotype of PR8. Mini-replicon assays were performed in HEK-293T cells with firefly luciferase under the control of the influenza virus NP promoter; we controlled for cell density with a constitutively active Renilla luciferase. Multicycle growth curve experiments were performed at 33°C, 37°C, and 39°C in MDCK cells with an m.o.i. of 0.001. Mean values for triplicate infections at 12, 24, 48, and 72 hours were plotted as TCID50/mL. RESULTS: Control experiments showed replication of PR8 (AA) and PR8 (Len) in MDCK cells was significantly decreased as compared with WT PR8 at 37°C and 39°C at 24–48 hour time points, but not at 33C (the temperature of nasal passages). We found that polymerase activity was up to 3 logs more temperature-sensitive (ts) at 37°C and 39°C with the combined Len and AA mutations using the mini-replicon assay. In the growth curve experiments, the combined Len and AA mutations conferred up to a 4-log decrease in replication levels at 37°C as compared with PR8 (Len) and an even greater decrease compared with PR8 (AA). CONCLUSION: Our findings suggest combining the AA and Len LAIV polymerase mutations decreases LAIV replication at body temperature (37°C), as compared with either LAIV alone. This could be useful in developing an improved LAIV that is safer in vulnerable hosts (e.g., children under the age of 2 who may be vulnerable to wheezing), while also permitting dose escalation that might result in greater efficacy. Minireplicon assay. [Image: see text] Polymerase activity of combination mutants. [Image: see text] Multicycle replication kinetics of combination mutants (red) against PR8 Len (black) at 33C (solid), 37C (dashed) and 39C (dotted). [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253618/ http://dx.doi.org/10.1093/ofid/ofy210.830 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Smith, Andrew
Rodriguez-Garcia, Laura
Ghouayel, Maya El
Martinez-Sobrido, Luis
Dewhurst, Stephen
993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus
title 993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus
title_full 993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus
title_fullStr 993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus
title_full_unstemmed 993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus
title_short 993. Combining Key Residues of the Russian and US Live-Attenuated Influenza Viruses for a More Attenuated Virus
title_sort 993. combining key residues of the russian and us live-attenuated influenza viruses for a more attenuated virus
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253618/
http://dx.doi.org/10.1093/ofid/ofy210.830
work_keys_str_mv AT smithandrew 993combiningkeyresiduesoftherussianandusliveattenuatedinfluenzavirusesforamoreattenuatedvirus
AT rodriguezgarcialaura 993combiningkeyresiduesoftherussianandusliveattenuatedinfluenzavirusesforamoreattenuatedvirus
AT ghouayelmayael 993combiningkeyresiduesoftherussianandusliveattenuatedinfluenzavirusesforamoreattenuatedvirus
AT martinezsobridoluis 993combiningkeyresiduesoftherussianandusliveattenuatedinfluenzavirusesforamoreattenuatedvirus
AT dewhurststephen 993combiningkeyresiduesoftherussianandusliveattenuatedinfluenzavirusesforamoreattenuatedvirus