Literature DB >> 2319644

Evolution of the nucleoprotein gene of influenza A virus.

O T Gorman1, W J Bean, Y Kawaoka, R G Webster.   

Abstract

Nucleotide sequences of 24 nucleoprotein (NP) genes isolated from a wide range of hosts, geographic regions, and influenza A virus serotypes and 18 published NP gene sequences were analyzed to determine evolutionary relationships. The phylogeny of NP genes was determined by a maximum-parsimony analysis of nucleotide sequences. Phylogenetic analysis showed that NP genes have evolved into five host-specific lineages, including (i) Equine/Prague/56 (EQPR56), (ii) recent equine strains, (iii) classic swine (H1N1 swine, e.g., A/Swine/Iowa/15/30) and human strains, (iv) gull H13 viruses, and (v) avian strains (including North American, Australian, and Old World subgroups). These NP lineages match the five RNA hybridization groups identified by W. J. Bean (Virology 133:438-442, 1984). Maximum nucleotide differences among the NPs was 18.5%, but maximum amino acid differences reached only 10.8%, reflecting the conservative nature of the NP protein. Evolutionary rates varied among lineages; the human lineage showed the highest rate (2.54 nucleotide changes per year), followed by the Old World avian lineage (2.17 changes per year) and the recent equine lineage (1.22 changes per year). The per-nucleotide rates of human and avian NP gene evolution (1.62 x 10(-3) to 1.39 x 10(-3) changes per year) are lower than that reported for human NS genes (2.0 x 10(-3) changes per year; D. A. Buonagurio, S. Nakada, J. D. Parvin, M. Krystal, P. Palese, and W. M. Fitch, Science 232:980-982, 1986). Of the five NP lineages, the human lineage showed the greatest evolution at the amino acid level; over a period of 50 years, human NPs have accumulated 39 amino acid changes. In contrast, the avian lineage showed remarkable conservatism; over the same period, avian NP proteins changed by 0 to 10 amino acids. The specificity of the H13 NP in gulls and its distinct evolutionary separation from the classic avian lineage suggests that H13 NPs may have a large degree of adaptation to gulls. The presence of avian and human NPs in some swine isolates demonstrates the susceptibility of swine to different virus strains and supports the hypothesis that swine may serve as intermediates for the introduction of avian influenza virus genes into the human virus gene pool. EQPR56 is relatively distantly related to all other NP lineages, which suggests that this NP is rooted closest to the ancestor of all contemporary NPs. On the basis of estimation of evolutionary rates from nucleotide branch distances, current NP lineages are at least 100 years old, and the EQPR56 NP is much older.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2319644      PMCID: PMC249282     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  28 in total

1.  Is the gene pool of influenza viruses in shorebirds and gulls different from that in wild ducks?

Authors:  Y Kawaoka; T M Chambers; W L Sladen; R G Webster
Journal:  Virology       Date:  1988-03       Impact factor: 3.616

2.  Origin of the hemagglutinin gene of H3N2 influenza viruses from pigs in China.

Authors:  H Kida; K F Shortridge; R G Webster
Journal:  Virology       Date:  1988-01       Impact factor: 3.616

3.  Two subtypes of nucleoproteins (NP) of influenza A viruses.

Authors:  M Gammelin; J Mandler; C Scholtissek
Journal:  Virology       Date:  1989-05       Impact factor: 3.616

4.  Evolution of human influenza A viruses over 50 years: rapid, uniform rate of change in NS gene.

Authors:  D A Buonagurio; S Nakada; J D Parvin; M Krystal; P Palese; W M Fitch
Journal:  Science       Date:  1986-05-23       Impact factor: 47.728

5.  Comparison of the nucleoprotein genes of a chicken and a mink influenza A H 10 virus.

Authors:  U Reinhardt; C Scholtissek
Journal:  Arch Virol       Date:  1988       Impact factor: 2.574

6.  Distinct lineages of influenza virus H4 hemagglutinin genes in different regions of the world.

Authors:  R O Donis; W J Bean; Y Kawaoka; R G Webster
Journal:  Virology       Date:  1989-04       Impact factor: 3.616

7.  Localisation of the temperature-sensitive defect in the nucleoprotein of an influenza A/FPV/Rostock/34 virus.

Authors:  J Mandler; C Scholtissek
Journal:  Virus Res       Date:  1989-02       Impact factor: 3.303

8.  Nucleotide sequence analysis of the nucleoprotein gene of an avian and a human influenza virus strain identifies two classes of nucleoproteins.

Authors:  A J Buckler-White; B R Murphy
Journal:  Virology       Date:  1986-12       Impact factor: 3.616

9.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

10.  Avian-to-human transmission of the PB1 gene of influenza A viruses in the 1957 and 1968 pandemics.

Authors:  Y Kawaoka; S Krauss; R G Webster
Journal:  J Virol       Date:  1989-11       Impact factor: 5.103

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  66 in total

1.  Matrix gene of influenza a viruses isolated from wild aquatic birds: ecology and emergence of influenza a viruses.

Authors:  Linda Widjaja; Scott L Krauss; Richard J Webby; Tao Xie; Robert G Webster
Journal:  J Virol       Date:  2004-08       Impact factor: 5.103

2.  Sequence of the nucleoprotein (NP) gene of the influenza Alanas acuta/Primorje/695/76 (H2N3) virus.

Authors:  J Mandler; M S Kunerl; S Ludwig; M E Herget; C Scholtissek
Journal:  Nucleic Acids Res       Date:  1991-06-25       Impact factor: 16.971

3.  Interspecific exchange of avian influenza virus genes in Alaska: the influence of trans-hemispheric migratory tendency and breeding ground sympatry.

Authors:  John M Pearce; Andrew B Reeves; Andrew M Ramey; Jerry W Hupp; Hon S Ip; Mark Bertram; Michael J Petrula; Bradley D Scotton; Kimberly A Trust; Brandt W Meixell; Jonathan A Runstadler
Journal:  Mol Ecol       Date:  2010-11-12       Impact factor: 6.185

4.  Mechanism of antigenic variation in an individual epitope on influenza virus N9 neuraminidase.

Authors:  G M Air; W G Laver; R G Webster
Journal:  J Virol       Date:  1990-12       Impact factor: 5.103

5.  Hemagglutinin mutations related to antigenic variation in H1 swine influenza viruses.

Authors:  S M Luoh; M W McGregor; V S Hinshaw
Journal:  J Virol       Date:  1992-02       Impact factor: 5.103

6.  Phylogenic analysis of the M genes of influenza viruses isolated from free-flying water birds from their Northern Territory to Hokkaido, Japan.

Authors:  Rashid Manzoor; Yoshihiro Sakoda; Aaron Mweene; Yoshimi Tsuda; Noriko Kishida; Gui-Rong Bai; Ken-Ichiro Kameyama; Norikazu Isoda; Kosuke Soda; Michiko Naito; Hiroshi Kida
Journal:  Virus Genes       Date:  2008-07-10       Impact factor: 2.332

7.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1990-08-25       Impact factor: 16.971

Review 8.  Evolution and ecology of influenza A viruses.

Authors:  R G Webster; W J Bean; O T Gorman; T M Chambers; Y Kawaoka
Journal:  Microbiol Rev       Date:  1992-03

9.  Perpetuation of influenza A viruses in Alaskan waterfowl reservoirs.

Authors:  T Ito; K Okazaki; Y Kawaoka; A Takada; R G Webster; H Kida
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

10.  Genetic reassortment in pandemic and interpandemic influenza viruses. A study of 122 viruses infecting humans.

Authors:  L P Shu; G B Sharp; Y P Lin; E C Claas; S L Krauss; K F Shortridge; R G Webster
Journal:  Eur J Epidemiol       Date:  1996-02       Impact factor: 8.082

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