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Laureat2011
 

Rotavirus virus like particles as tracers in environmental studies

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Auteurs :
S.CABALLERO(1), F. X ABAD, F(1). LOISY, F.(2) LE GUYADER(2), J. COHEN(3), R. M. PINTO(1), A. BOSCH(1).


Journal
:
Applied and Environmental Microbiology, July 2004, p. 3904-3909, Vol. 70, No. 7.


Type
:
Publication


Affiliation
:
Enteric Virus Laboratory, Department of Microbiology, University of Barcelona, Barcelona, Spain,1 Microbiology Laboratory, Ifremer, Nantes,2 Molecular and Structural Virology, CNRS-INRA, Gif-sur-Yvette, France3


Résumé
:
Virus-like particles (VLPs) with the full-length VP2 and VP6 rotavirus capsid proteins, produced in the baculovirus expression system, have been evaluated as surrogates of human rotavirus in different environmental scenarios. Green fluorescent protein-labeled VLPs (GFP-VLPs) and particles enclosing a heterologous RNA (pseudoviruses), whose stability may be monitored by flow cytometry and antigen capture reverse transcription-PCR, respectively, were used. After 1 month in seawater at 20°C, no significant differences were observed between the behaviors of GFP-VLPs and of infectious rotavirus, whereas pseudovirus particles showed a higher decay rate. In the presence of 1 mg of free chlorine (FC)/liter both tracers persisted longer in freshwater at 20°C than infectious viruses, whereas in the presence of 0.2 mg of FC/liter no differences were observed between tracers and infectious rotavirus at shortcontact times. However, from 30 min of contact with FC onward, the decay of infectious rotavirus was higher than that of recombinant particles. The predicted Ct value for a 90% reduction of GFP-VLPs or pseudoviruses induces a 99.99% inactivation of infectious rotavirus. Both tracers were more resistant to UV light irradiation than infectious rotavirus in fresh and marine water. The effect of UV exposure was more pronounced on pseudovirus than in GFP-VLPs. In all types of water, the UV dose to induce a 90% reduction of pseudovirus ensures a 99.99% inactivation of infectious rotavirus. Recombinant virus surrogates open new possibilities for the systematic validation of virus removal practices in actual field situations where pathogenic agents cannot be introduced.


Mots Clés
:
Rotavirus, Traceurs, Environnement, Réaction en Chaîne par Polymérase, RT-PCR, NLV