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Rift valley fever: diagnostic challenges and investment needs for vaccine development

Rift valley fever virus (RVFV) is a causative agent of a viral zoonosis that constitutes a major clinical burden in wild and domestic ruminants. The virus causes major outbreaks in livestock (sheep, goats, cattle and camels) and can be transmitted to humans by contaminated animal products or via art...

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Autores principales: Petrova, Velislava, Kristiansen, Paul, Norheim, Gunnstein, Yimer, Solomon A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437696/
https://www.ncbi.nlm.nih.gov/pubmed/32816810
http://dx.doi.org/10.1136/bmjgh-2020-002694
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author Petrova, Velislava
Kristiansen, Paul
Norheim, Gunnstein
Yimer, Solomon A
author_facet Petrova, Velislava
Kristiansen, Paul
Norheim, Gunnstein
Yimer, Solomon A
author_sort Petrova, Velislava
collection PubMed
description Rift valley fever virus (RVFV) is a causative agent of a viral zoonosis that constitutes a major clinical burden in wild and domestic ruminants. The virus causes major outbreaks in livestock (sheep, goats, cattle and camels) and can be transmitted to humans by contaminated animal products or via arthropod vectors. Human-to-human transmission has not been reported to date, but spill-over events from animals have led to outbreaks in humans in Africa and the Arabian Peninsula. Currently, there is no licensed human vaccine against RVFV and the virus is listed as a priority pathogen by the World Health Organisation (WHO) due to the high epidemic potential and the lack of effective countermeasures. Multiple large RVFV outbreaks have been reported since the virus was discovered. During the last two decades, over 4000 cases and ~1000 deaths have been reported. The lack of systematic surveillance to estimate the true burden and incidence of human RVF disease is a challenge for planning future vaccine efficacy evaluation. This creates a need for robust diagnostic methodologies that can be deployed in remote regions to aid case confirmation, assessment of seroprevalence as well as pathogen surveillance required for the different stages of vaccine evaluation. Here, we perform comprehensive landscaping of the available diagnostic solutions for detection of RVFV in humans. Based on the identified gaps in the currently available in-house and commercially available methods, we highlight the specific investment needs for diagnostics that are critical for accelerating the development of effective vaccines against RVFV.
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spelling pubmed-74376962020-08-24 Rift valley fever: diagnostic challenges and investment needs for vaccine development Petrova, Velislava Kristiansen, Paul Norheim, Gunnstein Yimer, Solomon A BMJ Glob Health Analysis Rift valley fever virus (RVFV) is a causative agent of a viral zoonosis that constitutes a major clinical burden in wild and domestic ruminants. The virus causes major outbreaks in livestock (sheep, goats, cattle and camels) and can be transmitted to humans by contaminated animal products or via arthropod vectors. Human-to-human transmission has not been reported to date, but spill-over events from animals have led to outbreaks in humans in Africa and the Arabian Peninsula. Currently, there is no licensed human vaccine against RVFV and the virus is listed as a priority pathogen by the World Health Organisation (WHO) due to the high epidemic potential and the lack of effective countermeasures. Multiple large RVFV outbreaks have been reported since the virus was discovered. During the last two decades, over 4000 cases and ~1000 deaths have been reported. The lack of systematic surveillance to estimate the true burden and incidence of human RVF disease is a challenge for planning future vaccine efficacy evaluation. This creates a need for robust diagnostic methodologies that can be deployed in remote regions to aid case confirmation, assessment of seroprevalence as well as pathogen surveillance required for the different stages of vaccine evaluation. Here, we perform comprehensive landscaping of the available diagnostic solutions for detection of RVFV in humans. Based on the identified gaps in the currently available in-house and commercially available methods, we highlight the specific investment needs for diagnostics that are critical for accelerating the development of effective vaccines against RVFV. BMJ Publishing Group 2020-08-17 /pmc/articles/PMC7437696/ /pubmed/32816810 http://dx.doi.org/10.1136/bmjgh-2020-002694 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Analysis
Petrova, Velislava
Kristiansen, Paul
Norheim, Gunnstein
Yimer, Solomon A
Rift valley fever: diagnostic challenges and investment needs for vaccine development
title Rift valley fever: diagnostic challenges and investment needs for vaccine development
title_full Rift valley fever: diagnostic challenges and investment needs for vaccine development
title_fullStr Rift valley fever: diagnostic challenges and investment needs for vaccine development
title_full_unstemmed Rift valley fever: diagnostic challenges and investment needs for vaccine development
title_short Rift valley fever: diagnostic challenges and investment needs for vaccine development
title_sort rift valley fever: diagnostic challenges and investment needs for vaccine development
topic Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437696/
https://www.ncbi.nlm.nih.gov/pubmed/32816810
http://dx.doi.org/10.1136/bmjgh-2020-002694
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