In-depth genome analyses of viruses from vaccine-derived rabies cases and corresponding live-attenuated oral rabies vaccines.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
02 08 2019
Historique:
received: 27 06 2017
revised: 19 01 2018
accepted: 28 01 2018
pubmed: 15 2 2018
medline: 28 7 2020
entrez: 15 2 2018
Statut: ppublish

Résumé

Live-attenuated rabies virus strains such as those derived from the field isolate Street Alabama Dufferin (SAD) have been used extensively and very effectively as oral rabies vaccines for the control of fox rabies in both Europe and Canada. Although these vaccines are safe, some cases of vaccine-derived rabies have been detected during rabies surveillance accompanying these campaigns. In recent analysis it was shown that some commercial SAD vaccines consist of diverse viral populations, rather than clonal genotypes. For cases of vaccine-derived rabies, only consensus sequence data have been available to date and information concerning their population diversity was thus lacking. In our study, we used high-throughput sequencing to analyze 11 cases of vaccine-derived rabies, and compared their viral population diversity to the related oral rabies vaccines using pairwise Manhattan distances. This extensive deep sequencing analysis of vaccine-derived rabies cases observed during oral vaccination programs provided deeper insights into the effect of accidental in vivo replication of genetically diverse vaccine strains in the central nervous system of target and non-target species under field conditions. The viral population in vaccine-derived cases appeared to be clonal in contrast to their parental vaccines. The change from a state of high population diversity present in the vaccine batches to a clonal genotype in the affected animal may indicate the presence of a strong bottleneck during infection. In conclusion, it is very likely that these few cases are the consequence of host factors and not the result of the selection of a more virulent genotype. Furthermore, this type of vaccine-derived rabies leads to the selection of clonal genotypes and the selected variants were genetically very similar to potent SAD vaccines that have undergone a history of in vitro selection.

Identifiants

pubmed: 29439868
pii: S0264-410X(18)30156-7
doi: 10.1016/j.vaccine.2018.01.083
pii:
doi:

Substances chimiques

RNA, Viral 0
Rabies Vaccines 0
Vaccines, Attenuated 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4758-4765

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Florian Pfaff (F)

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany. Electronic address: Florian.Pfaff@fli.de.

Thomas Müller (T)

Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany. Electronic address: Thomas.Mueller@fli.de.

Conrad M Freuling (CM)

Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany. Electronic address: Conrad.Freuling@fli.de.

Christine Fehlner-Gardiner (C)

Centre of Expertise for Rabies, Ottawa Laboratory-Fallowfield, Canadian Food Inspection Agency, Ottawa, Canada. Electronic address: Christine.Fehlner-Gardiner@inspection.gc.ca.

Susan Nadin-Davis (S)

Centre of Expertise for Rabies, Ottawa Laboratory-Fallowfield, Canadian Food Inspection Agency, Ottawa, Canada. Electronic address: Susan.Nadin-Davis@inspection.gc.ca.

Emmanuelle Robardet (E)

Nancy Laboratory for Rabies and Wildlife, French Agency for Food, Environmental and Occupational Health & Safety, Malzéville, France. Electronic address: Emmanuelle.ROBARDET@anses.fr.

Florence Cliquet (F)

Nancy Laboratory for Rabies and Wildlife, French Agency for Food, Environmental and Occupational Health & Safety, Malzéville, France. Electronic address: Florence.CLIQUET@anses.fr.

Vlad Vuta (V)

Institute for Diagnosis and Animal Health, University of Agronomic Study and Veterinary Medicine, Faculty of Veterinary Medicine, Bucharest, Romania. Electronic address: vuta.vlad@idah.ro.

Peter Hostnik (P)

Virology Unit, Veterinary Faculty, Institute of Microbiology and Parasitology, University of Ljubljana, Ljubljana, Slovenia. Electronic address: peter.hostnik@vf.uni-lj.si.

Thomas C Mettenleiter (TC)

Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany. Electronic address: ThomasC.Mettenleiter@fli.de.

Martin Beer (M)

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany. Electronic address: Martin.Beer@fli.de.

Dirk Höper (D)

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Germany. Electronic address: Dirk.Hoeper@fli.de.

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Classifications MeSH