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    Recombinant Mycoplasma mycoides proteins elicit protective immune responses against contagious bovine pleuropneumonia

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    Authors
    Nkando, I.
    Pérez Casal, J.
    Mwirigi, M.
    Prysliak, T.
    Townsend, H.
    Berberov, E.
    Kuria, J.
    Mugambi, J.
    Soi, R.
    Liljander, Anne M.
    Jores, Joerg
    Gerdts, V.
    Potter, A.
    Naessens, Jan
    Wesonga, H.O.
    Date Issued
    2016-03
    Language
    en
    Type
    Journal Article
    Review status
    Peer Review
    ISI journal
    Accessibility
    Limited Access
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    Citation
    Nkando, I., Perez-Casal, J., Mwirigi, M., Prysliak, T., Townsend, H., Berberov, E., Kuria, J., Mugambi, J., Soi, R., Liljander, A., Jores, J., Gerdts, V., Potter, A., Naessens, J. and Wesonga, H. 2016. Recombinant Mycoplasma mycoides proteins elicit protective immune responses against contagious bovine pleuropneumonia. Veterinary Immunology and Immunopathology 171:103–114.
    Permanent link to cite or share this item: https://hdl.handle.net/10568/72741
    DOI: https://doi.org/10.1016/j.vetimm.2016.02.010
    Abstract/Description
    Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia (CBPP), a devastating respiratory disease mainly affecting cattle in sub-Saharan Africa. The current vaccines are based on live-attenuated Mmmstrains and present problems with temperature stability, duration of immunity and adverse reactions, thus new vaccines are needed to overcome these issues. We used a reverse vaccinology approach to identify 66 Mmm potential vaccine candidates. The selection and grouping of the antigens was based on the presence of specific antibodies in sera from CBPP-positive animals. The antigens were used to immunize male Boran cattle (Bos indicus) followed by a challenge with the Mmm strain Afadé. Two of the groups immunized with five proteins each showed protection after the Mmm challenge (Groups A and C; P < 0.05) and in one group (Group C) Mmm could not be cultured from lung specimens. A third group (Group N) showed a reduced number of animals with lesions and the cultures for Mmm were also negative. While immunization with some of the antigens conferred protection, others may have increased immune-related pathology. This is the first report that Mmm recombinant proteins have been successfully used to formulate a prototype vaccine and these results pave the way for the development of a novel commercial vaccine.
    CGIAR Author ORCID iDs
    Jan Naessenshttps://orcid.org/0000-0002-7075-9915
    Anne Liljanderhttps://orcid.org/0000-0002-7543-5493
    Joerg Joreshttps://orcid.org/0000-0003-3790-5746
    AGROVOC Keywords
    animal diseases; disease control
    Subjects
    ANIMAL DISEASES; CBPP; DISEASE CONTROL; LIVESTOCK; VACCINES;
    Organizations Affiliated to the Authors
    Kenya Agricultural and Livestock Research Organization; Vaccine Infectious Disease Organization; International Livestock Research Institute; University of Nairobi; University of Bern
    Collections
    • ILRI articles in journals [6643]
    • ILRI vaccine biosciences program outputs [99]

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