A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.

The His274→Tyr (H274Y) oseltamivir (Tamiflu) resistance mutation causes a substantial decrease in the total levels of surface-expressed neuraminidase protein and activity in early isolates of human seasonal H1N1 influenza, and in the swine-origin pandemic H1N1. In seasonal H1N1, H274Y only became wi...

Full description

Bibliographic Details
Main Authors: Jesse D Bloom, Jagannath S Nayak, David Baltimore
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3140507?pdf=render
_version_ 1819161213981949952
author Jesse D Bloom
Jagannath S Nayak
David Baltimore
author_facet Jesse D Bloom
Jagannath S Nayak
David Baltimore
author_sort Jesse D Bloom
collection DOAJ
description The His274→Tyr (H274Y) oseltamivir (Tamiflu) resistance mutation causes a substantial decrease in the total levels of surface-expressed neuraminidase protein and activity in early isolates of human seasonal H1N1 influenza, and in the swine-origin pandemic H1N1. In seasonal H1N1, H274Y only became widespread after the occurrence of secondary mutations that counteracted this decrease. H274Y is currently rare in pandemic H1N1, and it remains unclear whether secondary mutations exist that might similarly counteract the decreased neuraminidase surface expression associated with this resistance mutation in pandemic H1N1. Here we investigate the possibility of predicting such secondary mutations. We first test the ability of several computational approaches to retrospectively identify the secondary mutations that enhanced levels of surface-expressed neuraminidase protein and activity in seasonal H1N1 shortly before the emergence of oseltamivir resistance. We then use the most successful computational approach to predict a set of candidate secondary mutations to the pandemic H1N1 neuraminidase. We experimentally screen these mutations, and find that several of them do indeed partially counteract the decrease in neuraminidase surface expression caused by H274Y. Two of the secondary mutations together restore surface-expressed neuraminidase activity to wildtype levels, and also eliminate the very slight decrease in viral growth in tissue-culture caused by H274Y. Our work therefore demonstrates a combined computational-experimental approach for identifying mutations that enhance neuraminidase surface expression, and describes several specific mutations with the potential to be of relevance to the spread of oseltamivir resistance in pandemic H1N1.
first_indexed 2024-12-22T17:08:47Z
format Article
id doaj.art-ff26077fb5344b0c9e1f93793811eda4
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-22T17:08:47Z
publishDate 2011-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-ff26077fb5344b0c9e1f93793811eda42022-12-21T18:19:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2220110.1371/journal.pone.0022201A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.Jesse D BloomJagannath S NayakDavid BaltimoreThe His274→Tyr (H274Y) oseltamivir (Tamiflu) resistance mutation causes a substantial decrease in the total levels of surface-expressed neuraminidase protein and activity in early isolates of human seasonal H1N1 influenza, and in the swine-origin pandemic H1N1. In seasonal H1N1, H274Y only became widespread after the occurrence of secondary mutations that counteracted this decrease. H274Y is currently rare in pandemic H1N1, and it remains unclear whether secondary mutations exist that might similarly counteract the decreased neuraminidase surface expression associated with this resistance mutation in pandemic H1N1. Here we investigate the possibility of predicting such secondary mutations. We first test the ability of several computational approaches to retrospectively identify the secondary mutations that enhanced levels of surface-expressed neuraminidase protein and activity in seasonal H1N1 shortly before the emergence of oseltamivir resistance. We then use the most successful computational approach to predict a set of candidate secondary mutations to the pandemic H1N1 neuraminidase. We experimentally screen these mutations, and find that several of them do indeed partially counteract the decrease in neuraminidase surface expression caused by H274Y. Two of the secondary mutations together restore surface-expressed neuraminidase activity to wildtype levels, and also eliminate the very slight decrease in viral growth in tissue-culture caused by H274Y. Our work therefore demonstrates a combined computational-experimental approach for identifying mutations that enhance neuraminidase surface expression, and describes several specific mutations with the potential to be of relevance to the spread of oseltamivir resistance in pandemic H1N1.http://europepmc.org/articles/PMC3140507?pdf=render
spellingShingle Jesse D Bloom
Jagannath S Nayak
David Baltimore
A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.
PLoS ONE
title A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.
title_full A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.
title_fullStr A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.
title_full_unstemmed A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.
title_short A computational-experimental approach identifies mutations that enhance surface expression of an oseltamivir-resistant influenza neuraminidase.
title_sort computational experimental approach identifies mutations that enhance surface expression of an oseltamivir resistant influenza neuraminidase
url http://europepmc.org/articles/PMC3140507?pdf=render
work_keys_str_mv AT jessedbloom acomputationalexperimentalapproachidentifiesmutationsthatenhancesurfaceexpressionofanoseltamivirresistantinfluenzaneuraminidase
AT jagannathsnayak acomputationalexperimentalapproachidentifiesmutationsthatenhancesurfaceexpressionofanoseltamivirresistantinfluenzaneuraminidase
AT davidbaltimore acomputationalexperimentalapproachidentifiesmutationsthatenhancesurfaceexpressionofanoseltamivirresistantinfluenzaneuraminidase
AT jessedbloom computationalexperimentalapproachidentifiesmutationsthatenhancesurfaceexpressionofanoseltamivirresistantinfluenzaneuraminidase
AT jagannathsnayak computationalexperimentalapproachidentifiesmutationsthatenhancesurfaceexpressionofanoseltamivirresistantinfluenzaneuraminidase
AT davidbaltimore computationalexperimentalapproachidentifiesmutationsthatenhancesurfaceexpressionofanoseltamivirresistantinfluenzaneuraminidase