A phylogenetic and evolutionary justification for three genera of Geminiviridae

SummaryGene-by-gene phylogenetic analyses of all of the viruses for which sequences are known, as well as analysis of the coding capacities, clearly demonstrated that there are two major groups of viruses in the taxonomic familyGeminiviridae. These are of the Subgroup I type, with one genomic component, which mainly infect monocots and are leafhopper-transmitted; and of the Subgroup III type, with one or two genomic components, which infect dicots and are whitefly-transmitted. The existence of “New World” and “Old World” clusters of Subgroup III viruses was confirmed, as well as the possession by the latter of an AV1 ORF not present in New World viruses. A third minor generic group is defined by viruses of the Subgroup II type, which have a single genomic component, infect dicots, and are leafhopper-transmitted. The latter group appear to be the result of an ancient recombination event between a Subgroup III-like and a Subgroup I-like virus. The question of whether one- and two-component Subgroup III viruses should be in the same taxon appears hard to resolve: the only distinguishing feature of the one-component Subgroup III viruses is that they apparently have no second component, as gene-for-gene comparisons of the “A” components of the viruses with other Subgroup III viruses place them within a larger Old World group of viruses, most of which are two component. The possibility exists that these viruses may either have independently lost their B components, or possess a B component that has simply not yet been found. Possible nomenclatural changes to accommodate viruses with the same name which are not closely related to one another, and possible evolutionary scenarios to account for the observed familial, generic and specific diversity of geminiviruses, are discussed.

[1]  T. Miyata,et al.  Sequence similarity between putative gene products of geminiviral DNAs , 1984, Nature.

[2]  B. Harrison,et al.  Advances in Geminivirus Research , 1985 .

[3]  R. Coutts,et al.  Geminivirus coat protein gene promoter sequences can function in Escherichia coli. , 1986, Nucleic acids research.

[4]  J. Rao Sequence homology between the coat proteins of DNA and RNA plant viruses. , 1986 .

[5]  D. Bisaro,et al.  Tomato golden mosaic virus A component DNA replicates autonomously in transgenic plants , 1986, Cell.

[6]  H. Jeske,et al.  Single-stranded DNA from abutilon mosaic virus is present in the plastids of infected Abutilon sellovianum. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[7]  R. H. Markham,et al.  Characterization of maize streak virus: description of strains; symptoms , 1988 .

[8]  C. Ward,et al.  Amino Acid Sequence Homology of Coat Proteins as a Basis for Identification and Classification of the Potyvirus Group , 1988 .

[9]  P. Ahlquist,et al.  Sequence of cowpea chlorotic mottle virus RNAs 2 and 3 and evidence of a recombination event during bromovirus evolution. , 1989, Virology.

[10]  J. Julia,et al.  Nesoclutha declivata Homoptera Cicadellidae, vector of Digitaria Streak Virus (Geminivirus) in Vanuatu , 1989 .

[11]  G. Vandemark,et al.  Phylogeny of geminiviruses. , 1989, The Journal of general virology.

[12]  E. Rybicki,et al.  Detection and typing of maize streak virus and other distantly related geminiviruses of grasses by polymerase chain reaction amplification of a conserved viral sequence. , 1990, The Journal of general virology.

[13]  R. Briddon,et al.  Geminivirus coat protein gene replacement alters insect specificity. , 1990, Virology.

[14]  R. Beachy,et al.  Systemic movement and symptom production following agroinoculation with a single DNA of tomato yellow leaf curl geminivirus (Thailand). , 1990, Virology.

[15]  J. Stanley,et al.  Encapsidation and spread of African cassava mosaic virus DNA A in the absence of DNA B when agroinoculated to Nicotiana benthamiana. , 1990 .

[16]  E. Koonin,et al.  Diverse groups of plant RNA and DNA viruses share related movement proteins that may possess chaperone-like activity. , 1991, The Journal of general virology.

[17]  D. Bisaro,et al.  Replicational release of geminivirus genomes from tandemly repeated copies: evidence for rolling-circle replication of a plant viral DNA. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[18]  E. Rybicki,et al.  Genome typing of southern African subgroup 1 geminiviruses. , 1992, The Journal of general virology.

[19]  E. Koonin,et al.  Geminivirus replication proteins are related to prokaryotic plasmid rolling circle DNA replication initiator proteins. , 1992, The Journal of general virology.

[20]  L. Hanley-Bowdoin,et al.  A geminivirus replication protein is a sequence-specific DNA binding protein. , 1992, The Plant cell.

[21]  E. Rybicki,et al.  Coat protein phylogeny and systematics of potyviruses. , 1992, Archives of virology. Supplementum.

[22]  K. Richardson,et al.  The nucleotide sequence of the infectious cloned DNA component of tobacco yellow dwarf virus reveals features of geminiviruses infecting monocotyledonous plants. , 1992, Virology.

[23]  J. Latham,et al.  A symptom variant of beet curly top geminivirus produced by mutation of open reading frame C4. , 1992, Virology.

[24]  L. Wu,et al.  Sequence-specific interaction with the viral AL1 protein identifies a geminivirus DNA replication origin. , 1992, The Plant cell.

[25]  S. Lazarowitz,et al.  Geminiviruses: Genome structure and gene function , 1992 .

[26]  Yiguo Hong,et al.  Nucleotide sequence evidence for the occurrence of three distinct whitefly-transmitted geminiviruses in cassava. , 1993, The Journal of general virology.

[27]  S. Hormuzdi,et al.  Genetic analysis of beet curly top virus: evidence for three virion sense genes involved in movement and regulation of single- and double-stranded DNA levels. , 1993, Virology.

[28]  R. Dietzgen,et al.  Nucleotide sequence of one component of the banana bunchy top virus genome contains a putative replicase gene. , 1993, The Journal of general virology.

[29]  L. Herrera-Estrella,et al.  Complete nucleotide sequence of pepper huasteco virus: analysis and comparison with bipartite geminiviruses. , 1993, The Journal of general virology.

[30]  H. Jeske,et al.  DNA B facilitates, but is not essential for, the spread of abutilon mosaic virus in agroinoculated Nicotiana benthamiana. , 1993, Virology.

[31]  Yves Van de Peer,et al.  TREECON: a software package for the construction and drawing of evolutionary trees , 1993, Comput. Appl. Biosci..

[32]  R F Doolittle,et al.  Convergent evolution: the need to be explicit. , 1994, Trends in biochemical sciences.

[33]  C. Fauquet,et al.  Complete nucleotide sequence of the geminivirus tomato yellow leaf curl virus, Thailand isolate. , 1994, The Journal of general virology.

[34]  W. J. Lucas,et al.  Two proteins of a plant DNA virus coordinate nuclear and plasmodesmal transport , 1994, Cell.

[35]  L. Hanley-Bowdoin,et al.  Interaction between a geminivirus replication protein and origin DNA is essential for viral replication. , 1994, The Journal of biological chemistry.

[36]  A. Gibbs,et al.  Molecular Basis of Virus Evolution: Molecular systematics of the Potyviridae, the largest plant virus family , 1995 .

[37]  H. Jeske,et al.  Replicative form DNA of abutilon mosaic virus is present in plastids , 1990, Molecular and General Genetics MGG.

[38]  E. Koonin,et al.  Cell-to-cell movement of plant viruses , 1993, Archives of Virology.

[39]  C. Fauquet,et al.  Geminivirus nomenclature: the need to set taxonomic standards , 2005, Archives of Virology.

[40]  R. Kirby,et al.  Complete nucleotide sequence of sugarcane streak Monogeminivirus , 2005, Archives of Virology.