Evaluation of a real-time two-step RT-PCR assay for quantitation of Chronic bee paralysis virus (CBPV) genome in experimentally-infected bee tissues and in life stages of a symptomatic colony.

Philippe Blanchard 1, * Magali Ribière 1 Olivier Celle 1 Perrine Lallemand 1 Frank Schurr 1 Violaine Olivier 1 Anne Laure Iscache 1 Jean Paul Faucon 1
* Auteur correspondant
1 AFSSA - Agence Française de Sécurité Sanitaire des Aliments
Abstract : A two-step real-time RT-PCR assay, based on TaqMan technology using a fluorescent probe (FAM-TAMRA) was developed to quantify Chronic bee paralysis virus (CBPV) genome in bee samples. Standard curves obtained from a CBPV control RNA and from a plasmid containing a partial sequence of CBPV showed that this assay provided linear detection over a 7-log range (R(2)>0.99) with a limit of detection of 100 copies, and reliable inter-assay and intra-assay reproducibility. Standardisation including RNA purification and cDNAs synthesis was also validated. The CBPV TaqMan methodology was first evaluated by quantifying the CBPV genomic load in bee samples from an experimental infection obtained by topical application. Up to 1.9 x 10(10) CBPV copies per segment of insect body (head, thorax and abdomen) were revealed whereas a lower CBPV genomic load was detected in dissected organs such as mandibular and hypopharyngeal glands, brain and alimentary canal (up to 7.2 x 10(6) CBPV copies). The CBPV genomic loads in different categories of bees from a hive presenting the trembling symptoms typical of Chronic paralysis were then quantified. Significantly higher CBPV loads were found in guard, symptomatic and dead bees (up to 1.9 x 10(13) CBPV copies) than in forager, drones and house bees (up to 3.4 x 10(6) CBPV copies). The results obtained for symptomatic or dead bees support the correlation between high CBPV genomic load and pathology expression. Moreover, the high CBPV genomic load revealed in guard bees highlights the possible pivotal role played by this category of bees in CBPV infection.
Keywords : Chronic bee paralysis virus (CBPV) Real-time PCR Quantitation Infection dynamics Apis mellifera
Type de document :
Article dans une revue
Journal of Virological Methods, Elsevier, 2007, 141 (1), pp.7-13. 〈10.1016/j.jviromet.2006.11.021〉
Liste complète des métadonnées
https://hal-anses.archives-ouvertes.fr/anses-00414768
Contributeur : Philippe Blanchard <>
Soumis le : vendredi 11 septembre 2009 - 22:14:03
Dernière modification le : lundi 14 septembre 2009 - 09:35:55
Document(s) archivé(s) le : mardi 15 juin 2010 - 23:24:07

Fichiers

Blanchard_PCRQuantiCBPV_Versio...
Fichiers produits par l'(les) auteur(s)

Identifiants

Collections

ANSES

Citation

Philippe Blanchard, Magali Ribière, Olivier Celle, Perrine Lallemand, Frank Schurr, et al.. Evaluation of a real-time two-step RT-PCR assay for quantitation of Chronic bee paralysis virus (CBPV) genome in experimentally-infected bee tissues and in life stages of a symptomatic colony.. Journal of Virological Methods, Elsevier, 2007, 141 (1), pp.7-13. 〈10.1016/j.jviromet.2006.11.021〉. 〈anses-00414768〉

Exporter

BibTeX TEI DC DCterms EndNote

Partager

Métriques

Consultations de la notice

275

Téléchargements de fichiers

431

Contact

support.ccsd.cnrs.fr
hal.support@ccsd.cnrs.fr
Logo CCSD