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  3. Contagious Bovine and Caprine Pleuropneumonia: a research community's recommendations for the development of better vaccines.
 

Contagious Bovine and Caprine Pleuropneumonia: a research community's recommendations for the development of better vaccines.

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BORIS DOI
10.7892/boris.152074
Date of Publication
July 2020
Publication Type
Article
Division/Institute

Department of Infecti...

Institut für Veterinä...

Contributor
Jores, Jörgorcid-logo
Institut für Veterinärbakteriologie (IVB)
Baldwin, Cynthia
Blanchard, Alain
Browning, Glenn F
Colston, Angie
Gerdts, Volker
Goovaerts, Danny
Heller, Martin
Juleff, Nick
Labroussaa, Fabien
Institut für Veterinärbakteriologie (IVB)
Liljander, Anne
Muuka, Geoffrey
Nene, Vish
Nir-Paz, Ran
Sacchini, Flavio
Summerfield, Arturorcid-logo
Department of Infectious Diseases and Pathobiology (DIP)
Thiaucourt, François
Unger, Hermann
Vashee, Sanjay
Wang, Xiumei
Salt, Jeremy
Subject(s)

600 - Technology::630...

500 - Science::570 - ...

600 - Technology::610...

Series
npj vaccines
ISSN or ISBN (if monograph)
2059-0105
Publisher
Nature Publishing Group
Language
English
Publisher DOI
10.1038/s41541-020-00214-2
PubMed ID
32728480
Uncontrolled Keywords

Bacterial infection V...

Description
Contagious bovine pleuropneumonia (CBPP) and contagious caprine pleuropneumonia (CCPP) are major infectious diseases of ruminants caused by mycoplasmas in Africa and Asia. In contrast with the limited pathology in the respiratory tract of humans infected with mycoplasmas, CBPP and CCPP are devastating diseases associated with high morbidity and mortality. Beyond their obvious impact on animal health, CBPP and CCPP negatively impact the livelihood and wellbeing of a substantial proportion of livestock-dependent people affecting their culture, economy, trade and nutrition. The causative agents of CBPP and CCPP are Mycoplasma mycoides subspecies mycoides and Mycoplasma capricolum subspecies capripneumoniae, respectively, which have been eradicated in most of the developed world. The current vaccines used for disease control consist of a live attenuated CBPP vaccine and a bacterin vaccine for CCPP, which were developed in the 1960s and 1980s, respectively. Both of these vaccines have many limitations, so better vaccines are urgently needed to improve disease control. In this article the research community prioritized biomedical research needs related to challenge models, rational vaccine design and protective immune responses. Therefore, we scrutinized the current vaccines as well as the challenge-, pathogenicity- and immunity models. We highlight research gaps and provide recommendations towards developing safer and more efficacious vaccines against CBPP and CCPP.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/201412
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File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
b152074.pdftextAdobe PDF1.1 MBAttribution (CC BY 4.0)publishedOpen
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