Negative-strand RNA viruses: The plant-infecting counterparts

While a large number of negative-strand (−)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organizat...

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Vydáno v:Virus research Ročník 162; číslo 1; s. 184 - 202
Hlavní autoři: Kormelink, Richard, Garcia, Maria Laura, Goodin, Michael, Sasaya, Takahide, Haenni, Anne-Lise
Médium: Journal Article
Jazyk:angličtina
Vydáno: Netherlands Elsevier B.V 01.12.2011
Témata:
Amino Acid Sequence
Animals
Biological Evolution
Bunyaviridae
Bunyaviridae - genetics
Bunyaviridae - pathogenicity
Cell-to-cell movement
Evolution
genome
Genome, Viral
host plants
Host-Pathogen Interactions
Humans
insects
Molecular Sequence Data
Negative-strand RNA plant viruses
Ophiovirus
Peribunyaviridae
Phylogeny
Plant Diseases - immunology
Plant Diseases - virology
plant viruses
Plant Viruses - classification
Plant Viruses - genetics
Plant Viruses - pathogenicity
Plant-adapted rhabdovirus
Plants - immunology
Plants - virology
plasmodesmata
Reverse Genetics
Rhabdoviridae
Rhabdoviridae - genetics
Rhabdoviridae - pathogenicity
Rhabdoviridae Infections - immunology
Rhabdoviridae Infections - virology
RNA
RNA Interference
RNA silencing suppressor
RNA Viruses - genetics
RNA Viruses - pathogenicity
RNA, Viral - genetics
RNAi-mediated resisance
Sequence Homology, Amino Acid
Tenuivirus
Tenuivirus - genetics
Tenuivirus - pathogenicity
Tospovirus
Tospovirus - genetics
Tospovirus - pathogenicity
Varicosavirus
Viral Proteins - genetics
Viral Proteins - immunology
viruses
RNAi-mediated resisance
Negative-strand RNA plant viruses
Tospovirus
Varicosavirus
Reverse genetics
Ophiovirus
Bunyaviridae
Rhabdoviridae
RNA silencing suppressor
Evolution
Tenuivirus
Cell-to-cell movement
Plant-adapted rhabdovirus
ISSN:0168-1702, 1872-7492, 1872-7492
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Abstract While a large number of negative-strand (−)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organization, while others have just recently been/or are still classified in floating genera. In most cases, at least two striking differences can still be discerned between the animal/human-infecting viruses and their plant-infecting counterparts which for the latter relate to their adaptation to plants as hosts. The first one is the capacity to modify plasmodesmata to facilitate systemic spread of infectious viral entities throughout the plant host. The second one is the capacity to counteract RNA interference (RNAi, also referred to as RNA silencing), the innate antiviral defence system of plants and insects. In this review an overview will be presented on the negative-strand RNA plant viruses classified within the families Bunyaviridae, Rhabdoviridae, Ophioviridae and floating genera Tenuivirus and Varicosavirus. Genetic differences with the animal-infecting counterparts and their evolutionary descendants will be described in light of the above processes.
AbstractList While a large number of negative-strand (-)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organization, while others have just recently been/or are still classified in floating genera. In most cases, at least two striking differences can still be discerned between the animal/human-infecting viruses and their plant-infecting counterparts which for the latter relate to their adaptation to plants as hosts. The first one is the capacity to modify plasmodesmata to facilitate systemic spread of infectious viral entities throughout the plant host. The second one is the capacity to counteract RNA interference (RNAi, also referred to as RNA silencing), the innate antiviral defence system of plants and insects. In this review an overview will be presented on the negative-strand RNA plant viruses classified within the families Bunyaviridae, Rhabdoviridae, Ophioviridae and floating genera Tenuivirus and Varicosavirus. Genetic differences with the animal-infecting counterparts and their evolutionary descendants will be described in light of the above processes.While a large number of negative-strand (-)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organization, while others have just recently been/or are still classified in floating genera. In most cases, at least two striking differences can still be discerned between the animal/human-infecting viruses and their plant-infecting counterparts which for the latter relate to their adaptation to plants as hosts. The first one is the capacity to modify plasmodesmata to facilitate systemic spread of infectious viral entities throughout the plant host. The second one is the capacity to counteract RNA interference (RNAi, also referred to as RNA silencing), the innate antiviral defence system of plants and insects. In this review an overview will be presented on the negative-strand RNA plant viruses classified within the families Bunyaviridae, Rhabdoviridae, Ophioviridae and floating genera Tenuivirus and Varicosavirus. Genetic differences with the animal-infecting counterparts and their evolutionary descendants will be described in light of the above processes.
While a large number of negative-strand (-)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organization, while others have just recently been/or are still classified in floating genera. In most cases, at least two striking differences can still be discerned between the animal/human-infecting viruses and their plant-infecting counterparts which for the latter relate to their adaptation to plants as hosts. The first one is the capacity to modify plasmodesmata to facilitate systemic spread of infectious viral entities throughout the plant host. The second one is the capacity to counteract RNA interference (RNAi, also referred to as RNA silencing), the innate antiviral defence system of plants and insects. In this review an overview will be presented on the negative-strand RNA plant viruses classified within the families Bunyaviridae, Rhabdoviridae, Ophioviridae and floating genera Tenuivirus and Varicosavirus. Genetic differences with the animal-infecting counterparts and their evolutionary descendants will be described in light of the above processes.
While a large number of negative-strand (−)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organization, while others have just recently been/or are still classified in floating genera. In most cases, at least two striking differences can still be discerned between the animal/human-infecting viruses and their plant-infecting counterparts which for the latter relate to their adaptation to plants as hosts. The first one is the capacity to modify plasmodesmata to facilitate systemic spread of infectious viral entities throughout the plant host. The second one is the capacity to counteract RNA interference (RNAi, also referred to as RNA silencing), the innate antiviral defence system of plants and insects. In this review an overview will be presented on the negative-strand RNA plant viruses classified within the families Bunyaviridae, Rhabdoviridae, Ophioviridae and floating genera Tenuivirus and Varicosavirus. Genetic differences with the animal-infecting counterparts and their evolutionary descendants will be described in light of the above processes.
While a large number of negative-strand (−)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have been classified within families together with animal/human infecting viruses due to similarities in particle morphology and genome organization, while others have just recently been/or are still classified in floating genera. In most cases, at least two striking differences can still be discerned between the animal/human-infecting viruses and their plant-infecting counterparts which for the latter relate to their adaptation to plants as hosts. The first one is the capacity to modify plasmodesmata to facilitate systemic spread of infectious viral entities throughout the plant host. The second one is the capacity to counteract RNA interference (RNAi, also referred to as RNA silencing), the innate antiviral defence system of plants and insects. In this review an overview will be presented on the negative-strand RNA plant viruses classified within the families Bunyaviridae, Rhabdoviridae, Ophioviridae and floating genera Tenuivirus and Varicosavirus. Genetic differences with the animal-infecting counterparts and their evolutionary descendants will be described in light of the above processes.
Author Garcia, Maria Laura
Haenni, Anne-Lise
Kormelink, Richard
Sasaya, Takahide
Goodin, Michael
Author_xml – sequence: 1
  givenname: Richard
  surname: Kormelink
  fullname: Kormelink, Richard
  email: richard.kormelink@wur.nl
  organization: Laboratory of Virology, Wageningen University, Droevendaalsesteeg 1, 6708PB Wageningen, The Netherlands
– sequence: 2
  givenname: Maria Laura
  surname: Garcia
  fullname: Garcia, Maria Laura
  organization: Facultad de Ciencias Exactas, Instituto de Biotecnología y Biología Molecular, CONICET – Universidad Nacional de La Plata, Calle 115 e/49 y 50, 1900 La Plata, Argentina
– sequence: 3
  givenname: Michael
  surname: Goodin
  fullname: Goodin, Michael
  organization: Department of Plant Pathology, University of Kentucky, Lexington, Kentucky, 40546-0312, USA
– sequence: 4
  givenname: Takahide
  surname: Sasaya
  fullname: Sasaya, Takahide
  organization: Divison of Plant Protection, National Agricultural Research Center, Tsukuba 305-8666, Japan
– sequence: 5
  givenname: Anne-Lise
  surname: Haenni
  fullname: Haenni, Anne-Lise
  organization: Institut Jacques Monod, CNRS – Université 7-Paris-Diderot, 15 rue Hélène Brion, 75205 Paris Cedex 13, France
BackLink https://www.ncbi.nlm.nih.gov/pubmed/21963660$$D View this record in MEDLINE/PubMed
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10.1099/0022-1317-75-12-3585
10.1128/JVI.77.7.3922-3928.2003
10.1016/j.virusres.2008.02.003
10.1099/vir.0.010488-0
10.1007/s10327-005-0239-7
10.1016/j.virol.2006.06.037
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Issue 1
Keywords RNAi-mediated resisance
Negative-strand RNA plant viruses
Tospovirus
Varicosavirus
Reverse genetics
Ophiovirus
Bunyaviridae
Rhabdoviridae
RNA silencing suppressor
Evolution
Tenuivirus
Cell-to-cell movement
Plant-adapted rhabdovirus
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Snippet While a large number of negative-strand (−)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have...
While a large number of negative-strand (-)RNA viruses infect animals and humans, a relative small number have plants as their primary host. Some of these have...
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SubjectTerms Amino Acid Sequence
Animals
Biological Evolution
Bunyaviridae
Bunyaviridae - genetics
Bunyaviridae - pathogenicity
Cell-to-cell movement
Evolution
genome
Genome, Viral
host plants
Host-Pathogen Interactions
Humans
insects
Molecular Sequence Data
Negative-strand RNA plant viruses
Ophiovirus
Peribunyaviridae
Phylogeny
Plant Diseases - immunology
Plant Diseases - virology
plant viruses
Plant Viruses - classification
Plant Viruses - genetics
Plant Viruses - pathogenicity
Plant-adapted rhabdovirus
Plants - immunology
Plants - virology
plasmodesmata
Reverse Genetics
Rhabdoviridae
Rhabdoviridae - genetics
Rhabdoviridae - pathogenicity
Rhabdoviridae Infections - immunology
Rhabdoviridae Infections - virology
RNA
RNA Interference
RNA silencing suppressor
RNA Viruses - genetics
RNA Viruses - pathogenicity
RNA, Viral - genetics
RNAi-mediated resisance
Sequence Homology, Amino Acid
Tenuivirus
Tenuivirus - genetics
Tenuivirus - pathogenicity
Tospovirus
Tospovirus - genetics
Tospovirus - pathogenicity
Varicosavirus
Viral Proteins - genetics
Viral Proteins - immunology
viruses
Title Negative-strand RNA viruses: The plant-infecting counterparts
URI https://dx.doi.org/10.1016/j.virusres.2011.09.028
https://www.ncbi.nlm.nih.gov/pubmed/21963660
https://www.proquest.com/docview/2000041011
https://www.proquest.com/docview/905677318
https://www.proquest.com/docview/911160887
Volume 162
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