ONRAB® oral rabies vaccine is shed from, but does not persist in, captive mammals.
Administration, Oral
Animals
Animals, Wild
/ immunology
Antibodies, Viral
/ immunology
Disease Reservoirs
/ virology
Enzyme-Linked Immunosorbent Assay
Foxes
Immunization
Immunogenicity, Vaccine
Rabies
/ prevention & control
Rabies Vaccines
/ administration & dosage
Rabies virus
/ immunology
Raccoons
Rats
Sigmodontinae
Vaccines, DNA
/ administration & dosage
Captive trials
Non-target
Quantitative PCR
Rabies vector
Safety
Journal
Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899
Informations de publication
Date de publication:
18 07 2019
18 07 2019
Historique:
received:
20
02
2019
revised:
13
06
2019
accepted:
14
06
2019
pubmed:
30
6
2019
medline:
20
9
2020
entrez:
29
6
2019
Statut:
ppublish
Résumé
ONRAB® is a human adenovirus rabies glycoprotein recombinant vaccine developed to control rabies in wildlife. To support licensing and widespread use of the vaccine, safety studies are needed to assess its potential residual impact on wildlife populations. We examined the persistence of the ONRAB® vaccine virus in captive rabies vector and non-target mammals. This research complements work on important rabies vector species (raccoon, striped skunk, and red fox) but also adds to previous findings with the addition of some non-target species (Virginia opossum, Norway rats, and cotton rats) and a prolonged period of post vaccination monitoring (41 days). Animals were directly inoculated orally with the vaccine and vaccine shedding was monitored using quantitative real-time PCR applied to oral and rectal swabs. ONRAB® DNA was detected in both oral and rectal swabs from 6 h to 3 days post-inoculation in most animals, followed by a resurgence of shedding between days 17 and 34 in some species. Overall, the duration over which ONRAB® DNA was detectable was shorter for non-target mammals, and by day 41, no animal had detectable DNA in either oral or rectal swabs. All target species, as well as cotton rats and laboratory-bred Norway rats, developed robust humoral immune responses as measured by competitive ELISA, with all individuals being seropositive at day 31. Similarly, opossums showed good response (89% seropositive; 8/9), whereas only one of nine wild caught Norway rats was seropositive at day 31. These results support findings of other safety studies suggesting that ONRAB® does not persist in vector and non-target mammals exposed to the vaccine. As such, we interpret these data to reflect a low risk of adverse effects to wild populations following distribution of ONRAB® to control sylvatic rabies.
Identifiants
pubmed: 31248686
pii: S0264-410X(19)30808-4
doi: 10.1016/j.vaccine.2019.06.046
pii:
doi:
Substances chimiques
Antibodies, Viral
0
Rabies Vaccines
0
Vaccines, DNA
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
4310-4317Informations de copyright
Crown Copyright © 2019. Published by Elsevier Ltd. All rights reserved.