Cargando…
Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease
BACKGROUND: Nipah virus (NiV) is a highly pathogenic zoonotic agent in the family Paramyxoviridae that is maintained in nature by bats. Outbreaks have occurred in Malaysia, Singapore, India, and Bangladesh and have been associated with 40 to 75% case fatality rates. There are currently no vaccines o...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878732/ https://www.ncbi.nlm.nih.gov/pubmed/24330654 http://dx.doi.org/10.1186/1743-422X-10-353 |
_version_ | 1782297855134793728 |
---|---|
author | Mire, Chad E Versteeg, Krista M Cross, Robert W Agans, Krystle N Fenton, Karla A Whitt, Michael A Geisbert, Thomas W |
author_facet | Mire, Chad E Versteeg, Krista M Cross, Robert W Agans, Krystle N Fenton, Karla A Whitt, Michael A Geisbert, Thomas W |
author_sort | Mire, Chad E |
collection | PubMed |
description | BACKGROUND: Nipah virus (NiV) is a highly pathogenic zoonotic agent in the family Paramyxoviridae that is maintained in nature by bats. Outbreaks have occurred in Malaysia, Singapore, India, and Bangladesh and have been associated with 40 to 75% case fatality rates. There are currently no vaccines or postexposure treatments licensed for combating human NiV infection. METHODS AND RESULTS: Four groups of ferrets received a single vaccination with different recombinant vesicular stomatitis virus vectors expressing: Group 1, control with no glycoprotein; Group 2, the NiV fusion protein (F); Group 3, the NiV attachment protein (G); and Group 4, a combination of the NiV F and G proteins. Animals were challenged intranasally with NiV 28 days after vaccination. Control ferrets in Group 1 showed characteristic clinical signs of NiV disease including respiratory distress, neurological disorders, viral load in blood and tissues, and gross lesions and antigen in target tissues; all animals in this group succumbed to infection by day 8. Importantly, all specifically vaccinated ferrets in Groups 2-4 showed no evidence of clinical illness and survived challenged. All animals in these groups developed anti-NiV F and/or G IgG and neutralizing antibody titers. While NiV RNA was detected in blood at day 6 post challenge in animals from Groups 2-4, the levels were orders of magnitude lower than animals from control Group 1. CONCLUSIONS: These data show protective efficacy against NiV in a relevant model of human infection. Further development of this technology has the potential to yield effective single injection vaccines for NiV infection. |
format | Online Article Text |
id | pubmed-3878732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38787322014-01-03 Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease Mire, Chad E Versteeg, Krista M Cross, Robert W Agans, Krystle N Fenton, Karla A Whitt, Michael A Geisbert, Thomas W Virol J Research BACKGROUND: Nipah virus (NiV) is a highly pathogenic zoonotic agent in the family Paramyxoviridae that is maintained in nature by bats. Outbreaks have occurred in Malaysia, Singapore, India, and Bangladesh and have been associated with 40 to 75% case fatality rates. There are currently no vaccines or postexposure treatments licensed for combating human NiV infection. METHODS AND RESULTS: Four groups of ferrets received a single vaccination with different recombinant vesicular stomatitis virus vectors expressing: Group 1, control with no glycoprotein; Group 2, the NiV fusion protein (F); Group 3, the NiV attachment protein (G); and Group 4, a combination of the NiV F and G proteins. Animals were challenged intranasally with NiV 28 days after vaccination. Control ferrets in Group 1 showed characteristic clinical signs of NiV disease including respiratory distress, neurological disorders, viral load in blood and tissues, and gross lesions and antigen in target tissues; all animals in this group succumbed to infection by day 8. Importantly, all specifically vaccinated ferrets in Groups 2-4 showed no evidence of clinical illness and survived challenged. All animals in these groups developed anti-NiV F and/or G IgG and neutralizing antibody titers. While NiV RNA was detected in blood at day 6 post challenge in animals from Groups 2-4, the levels were orders of magnitude lower than animals from control Group 1. CONCLUSIONS: These data show protective efficacy against NiV in a relevant model of human infection. Further development of this technology has the potential to yield effective single injection vaccines for NiV infection. BioMed Central 2013-12-13 /pmc/articles/PMC3878732/ /pubmed/24330654 http://dx.doi.org/10.1186/1743-422X-10-353 Text en Copyright © 2013 Mire et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Mire, Chad E Versteeg, Krista M Cross, Robert W Agans, Krystle N Fenton, Karla A Whitt, Michael A Geisbert, Thomas W Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease |
title | Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease |
title_full | Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease |
title_fullStr | Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease |
title_full_unstemmed | Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease |
title_short | Single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal Nipah virus disease |
title_sort | single injection recombinant vesicular stomatitis virus vaccines protect ferrets against lethal nipah virus disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878732/ https://www.ncbi.nlm.nih.gov/pubmed/24330654 http://dx.doi.org/10.1186/1743-422X-10-353 |
work_keys_str_mv | AT mirechade singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease AT versteegkristam singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease AT crossrobertw singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease AT aganskrystlen singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease AT fentonkarlaa singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease AT whittmichaela singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease AT geisbertthomasw singleinjectionrecombinantvesicularstomatitisvirusvaccinesprotectferretsagainstlethalnipahvirusdisease |