Literature DB >> 8140287

Progress towards a higher taxonomy of viruses.

C W Ward1.   

Abstract

The current consensus view is that a higher hierarchical taxonomy of viruses cannot be established for two reasons. Firstly, viruses appear to be polyphyletic in origin, with several sets of viruses arising by different, independent routes at different times. Secondly, subsequent virus adaptation for survival in different host/vector combinations has involved the selective acquisition of additional genes by a process of cassette or modular evolution, with these additional gene modules coming from other viruses or host genetic material. Thus, depending on the gene product used for comparison, different phylogenetic relationships can be deduced. Further virus adaptation can arise by reassortment of segmented genomes, gene duplication, deletions, frameshift mutations, point mutations or de novo development of new gene products from existing, unused reading frames. The solution to the first objection is to place all viruses in a separate kingdom and assign the current viruses to several phyla that reflect these diverse origins. The solution to the second objection is to consider the core module of replication machinery as the major criterion on which to make the initial assignments to classes and orders. For RNA viruses, the major criterion is the sequence identity of the RNA-dependent RNA polymerase. Using this criterion, the positive strand RNA viruses can be assigned to five classes that correspond to the recently recognized supergroups of RNA viruses. These five classes contain four, three, three, three and one order(s) respectively. These fourteen orders contain 31 virus families (including 17 families of plant viruses) and 48 genera (including 30 genera of plant viruses). This approach confirms the separation of the alphaviruses and flaviviruses into two families, the Togaviridae and Flaviridae, but suggests that several other current taxonomic assignments, such as the pestiviruses, hepatitis C virus, rubiviruses, hepatitis E virus and arteriviruses, may be wrong. The coronaviruses and toroviruses appear to be distinct families in distinct orders, not distinct genera of the same family as currently classified. In addition, the luteoviruses are split into two families and apple chlorotic leaf spot virus appears not to be a closterovirus but a new genus of the Potexviridae. From an analysis of the polymerase dendrograms of the dsRNA viruses, it appears that they are not closely related to each other, but belong to four additional classes (Partitiviridae, Reoviridae, Birnaviridae and Cystoviridae) and one additional order (Totiviridae) of one of the classes of positive ssRNA viruses in the same subphylum as the positive strand RNA viruses.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8140287      PMCID: PMC7135741          DOI: 10.1016/s0923-2516(06)80059-2

Source DB:  PubMed          Journal:  Res Virol        ISSN: 0923-2516


  68 in total

Review 1.  Structure and diversity of influenza virus neuraminidase.

Authors:  P M Colman; C W Ward
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2.  Nucleotide sequence of the ononis yellow mosaic tymovirus genome.

Authors:  S W Ding; P Keese; A Gibbs
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3.  Gene overlap results in a viral protein having an RNA binding domain and a major coat protein domain.

Authors:  T Fujimura; R B Wickner
Journal:  Cell       Date:  1988-11-18       Impact factor: 41.582

Review 4.  Structure of the influenza virus hemagglutinin.

Authors:  C W Ward
Journal:  Curr Top Microbiol Immunol       Date:  1981       Impact factor: 4.291

5.  Tricornaviridae - a proposed family of plant viruses with tripartite, single-stranded RNA genomes.

Authors:  L van Vloten-Doting; R I Francki; R W Fulton; J M Kaper; L C Lane
Journal:  Intervirology       Date:  1981       Impact factor: 1.763

6.  Physical and functional heterogeneity in TYMV RNA: evidence for the existence of an independent messenger coding for coat protein.

Authors:  C Klein; C Fritsch; J P Briand; K E Richards; G Jonard; L Hirth
Journal:  Nucleic Acids Res       Date:  1976-11       Impact factor: 16.971

7.  Ambisense segment 4 of rice stripe virus: possible evolutionary relationship with phleboviruses and uukuviruses (Bunyaviridae).

Authors:  T Kakutani; Y Hayano; T Hayashi; Y Minobe
Journal:  J Gen Virol       Date:  1990-07       Impact factor: 3.891

8.  The genome organization of potato virus M RNA.

Authors:  S K Zavriev; K V Kanyuka; K E Levay
Journal:  J Gen Virol       Date:  1991-01       Impact factor: 3.891

9.  The nucleotide sequence of an infectious clone of the geminivirus beet curly top virus.

Authors:  J Stanley; P G Markham; R J Callis; M S Pinner
Journal:  EMBO J       Date:  1986-08       Impact factor: 11.598

Review 10.  Applying the species concept to plant viruses.

Authors:  M H Van Regenmortel
Journal:  Arch Virol       Date:  1989       Impact factor: 2.574

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  16 in total

1.  Sequence analysis of an Indian field isolate of infectious bursal disease virus shows six unique amino acid changes in the VP1 gene.

Authors:  M V Bais; R S Kataria; A K Tiwari; K N Viswas; A V Reddy; N Prasad
Journal:  Vet Res Commun       Date:  2004-10       Impact factor: 2.459

2.  Sequence analyses and a unifying system of virus taxonomy: consensus via consent.

Authors:  C H Calisher; M C Horzinek; M A Mayo; H W Ackermann; J Maniloff
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

3.  Relationships of tailed phages: a survey of protein sequence identity.

Authors:  H W Ackermann; A Elzanowski; G Fobo; G Stewart
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

4.  A reevaluation of the higher taxonomy of viruses based on RNA polymerases.

Authors:  P M Zanotto; M J Gibbs; E A Gould; E C Holmes
Journal:  J Virol       Date:  1996-09       Impact factor: 5.103

5.  Identification and classification of viruses that have not been propagated.

Authors:  J Maniloff
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

6.  Functional genomics analysis of Singapore grouper iridovirus: complete sequence determination and proteomic analysis.

Authors:  Wen Jun Song; Qi Wei Qin; Jin Qiu; Can Hua Huang; Fan Wang; Choy Leong Hew
Journal:  J Virol       Date:  2004-11       Impact factor: 5.103

7.  Evaluation of complete genome sequences and sequences of individual gene products for the classification of hepatitis C viruses.

Authors:  D D Shukla; P A Hoyne; C W Ward
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

8.  Nucleotide sequence of the 3' terminal region of the RNA of two filamentous grapevine viruses.

Authors:  A Minafra; P Saldarelli; F Grieco; G P Martelli
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

9.  Equine rhinovirus 1 is more closely related to foot-and-mouth disease virus than to other picornaviruses.

Authors:  F Li; G F Browning; M J Studdert; B S Crabb
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-06       Impact factor: 11.205

10.  Sequence and phylogenetic analysis of the cytoplasmic inclusion protein gene of zucchini yellow mosaic potyvirus: its role in classification of the Potyviridae.

Authors:  K C Lee; P H Mahtani; C G Chng; S M Wong
Journal:  Virus Genes       Date:  1997       Impact factor: 2.198

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