Conserved amino acid markers from past influenza pandemic strains

<p>Abstract</p> <p>Background</p> <p>Finding the amino acid mutations that affect the severity of influenza infections remains an open and challenging problem. Of special interest is better understanding how current circulating influenza strains could evolve into a new...

Full description

Bibliographic Details
Main Authors: Vitalis Elizabeth A, Gardner Shea N, Allen Jonathan E, Slezak Tom R
Format: Article
Language:English
Published: BMC 2009-04-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/9/77
id doaj-819789be31d94a28818654004318f810
record_format Article
spelling doaj-819789be31d94a28818654004318f8102020-11-24T22:24:48ZengBMCBMC Microbiology1471-21802009-04-01917710.1186/1471-2180-9-77Conserved amino acid markers from past influenza pandemic strainsVitalis Elizabeth AGardner Shea NAllen Jonathan ESlezak Tom R<p>Abstract</p> <p>Background</p> <p>Finding the amino acid mutations that affect the severity of influenza infections remains an open and challenging problem. Of special interest is better understanding how current circulating influenza strains could evolve into a new pandemic strain. Influenza proteomes from distinct viral phenotype classes were searched for class specific amino acid mutations conserved in past pandemics, using reverse engineered linear classifiers.</p> <p>Results</p> <p>Thirty-four amino acid markers associated with host specificity and high mortality rate were found. Some markers had little impact on distinguishing the functional classes by themselves, however in combination with other mutations they improved class prediction. Pairwise combinations of influenza genomes were checked for reassortment and mutation events needed to acquire the pandemic conserved markers. Evolutionary pathways involving H1N1 human and swine strains mixed with avian strains show the potential to acquire the pandemic markers with a double reassortment and one or two amino acid mutations.</p> <p>Conclusion</p> <p>The small mutation combinations found at multiple protein positions associated with viral phenotype indicate that surveillance tools could monitor genetic variation beyond single point mutations to track influenza strains. Finding that certain strain combinations have the potential to acquire pandemic conserved markers through a limited number of reassortment and mutation events illustrates the potential for reassortment and mutation events to lead to new circulating influenza strains.</p> http://www.biomedcentral.com/1471-2180/9/77
collection DOAJ
language English
format Article
sources DOAJ
author Vitalis Elizabeth A
Gardner Shea N
Allen Jonathan E
Slezak Tom R
spellingShingle Vitalis Elizabeth A
Gardner Shea N
Allen Jonathan E
Slezak Tom R
Conserved amino acid markers from past influenza pandemic strains
BMC Microbiology
author_facet Vitalis Elizabeth A
Gardner Shea N
Allen Jonathan E
Slezak Tom R
author_sort Vitalis Elizabeth A
title Conserved amino acid markers from past influenza pandemic strains
title_short Conserved amino acid markers from past influenza pandemic strains
title_full Conserved amino acid markers from past influenza pandemic strains
title_fullStr Conserved amino acid markers from past influenza pandemic strains
title_full_unstemmed Conserved amino acid markers from past influenza pandemic strains
title_sort conserved amino acid markers from past influenza pandemic strains
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2009-04-01
description <p>Abstract</p> <p>Background</p> <p>Finding the amino acid mutations that affect the severity of influenza infections remains an open and challenging problem. Of special interest is better understanding how current circulating influenza strains could evolve into a new pandemic strain. Influenza proteomes from distinct viral phenotype classes were searched for class specific amino acid mutations conserved in past pandemics, using reverse engineered linear classifiers.</p> <p>Results</p> <p>Thirty-four amino acid markers associated with host specificity and high mortality rate were found. Some markers had little impact on distinguishing the functional classes by themselves, however in combination with other mutations they improved class prediction. Pairwise combinations of influenza genomes were checked for reassortment and mutation events needed to acquire the pandemic conserved markers. Evolutionary pathways involving H1N1 human and swine strains mixed with avian strains show the potential to acquire the pandemic markers with a double reassortment and one or two amino acid mutations.</p> <p>Conclusion</p> <p>The small mutation combinations found at multiple protein positions associated with viral phenotype indicate that surveillance tools could monitor genetic variation beyond single point mutations to track influenza strains. Finding that certain strain combinations have the potential to acquire pandemic conserved markers through a limited number of reassortment and mutation events illustrates the potential for reassortment and mutation events to lead to new circulating influenza strains.</p>
url http://www.biomedcentral.com/1471-2180/9/77
work_keys_str_mv AT vitaliselizabetha conservedaminoacidmarkersfrompastinfluenzapandemicstrains
AT gardnershean conservedaminoacidmarkersfrompastinfluenzapandemicstrains
AT allenjonathane conservedaminoacidmarkersfrompastinfluenzapandemicstrains
AT slezaktomr conservedaminoacidmarkersfrompastinfluenzapandemicstrains
_version_ 1725759719927185408