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Host alternation is necessary to maintain the genome stability of rift valley Fever virus.
Moutailler S., Roche B., Thiberge J.-M., Caro V., Rougeon F., Failloux A.-B.
PLoS Neglected Tropical Diseases 5, 5 (2011) e1156 - http://hal-pasteur.archives-ouvertes.fr/pasteur-00597944
(21629727)
Host alternation is necessary to maintain the genome stability of rift valley Fever virus.
Sara Moutailler1, Benjamin Roche2, Jean-Michel Thiberge3, Valérie Caro3, François Rougeon2, Anna-Bella Failloux () 1
1 :  Génétique Moléculaire des Bunyavirus
Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
2 :  Génétique et Biochimie du Développement
Institut Pasteur de Paris – CNRS : URA2581
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
3 :  PF8 - Génotypage des Pathogènes et Santé Publique (Plate-forme)
Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
Genome stability of RVFV
Background: Most arthropod-borne viruses (arboviruses) are RNA viruses, which are maintained in nature by replication cycles that alternate between arthropod and vertebrate hosts. Arboviruses appear to experience lower rates of evolution than RNA viruses that replicate in a single host. This genetic stability is assumed to result from a fitness trade-off imposed by host alternation, which constrains arbovirus genome evolution. To test this hypothesis, we used Rift Valley fever virus (RVFV), an arbovirus that can be transmitted either directly (between vertebrates during the manipulation of infected tissues, and between mosquitoes by vertical transmission) or indirectly (from one vertebrate to another by mosquito-borne ransmission). Methodology/Principal Findings: RVFV was serially passaged in BHK21 (hamster) or Aag2 (Aedes aegypti) cells, or in alternation between the two cell types. After 30 passages, these single host-passaged viruses lost their virulence and induced protective effects against a challenge with a virulent virus. Large deletions in the NSs gene that encodes the virulence factor were detectable from the 15th serial passage onwards in BHK21 cells and from the 10th passage in Aag2 cells. The phosphoprotein NSs is not essential to viral replication allowing clones carrying deletions in NSs to predominate as they replicate slightly more rapidly. No genetic changes were found in viruses that were passaged alternately between arthropod and vertebrate cells. Furthermore, alternating passaged viruses presenting complete NSs gene remained virulent after 30 passages. Conclusions/Significance: Our results strongly support the view that alternating replication is necessary to maintain the virulence factor carried by the NSs phosphoprotein.
Sciences du Vivant/Ecologie, Environnement/Interactions entre organismes
Anglais
24/05/2011

Articles dans des revues avec comité de lecture
10.1371/journal.pntd.0001156
PLoS Neglected Tropical Diseases (PLoS Negl Trop Dis)
Publisher Public Library of Science
ISSN 1935-2727 (eISSN : 1935-2735)
internationale
24/05/2011
5
5
e1156

Evolution – Virulence – Gene deletion – Cell adaptation
ACIP grants (AC-2004 and A-25-2006) and the Infravec program (UE-228421).
Numéro Cordis 228421
Acronyme INFRAVEC
Titre Research capacity for the implementation of genetic control of mosquitoes
Financé par INFRA
Début 2009-09-01
Date de fin 2013-08-31
Identifiant de l'appel FP7-INFRASTRUCTURES-2008-1
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