Sifting through the core-genome to identify putative cross-protective antigens against Riemerella anatipestifer
Infectious serositis of ducks, caused by Riemerella anatipestifer , is one of the main infectious diseases that harm commercial ducks. Whole-strain-based vaccines with no or few cross-protection were observed between different serotypes of R. anatipestifer , and so far, control of infection is hampe...
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Veröffentlicht in: | Applied microbiology and biotechnology 2023-05, Vol.107 (9), p.3085-3098 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Infectious serositis of ducks, caused by
Riemerella anatipestifer
, is one of the main infectious diseases that harm commercial ducks. Whole-strain-based vaccines with no or few cross-protection were observed between different serotypes of
R. anatipestifer
, and so far, control of infection is hampered by a lack of effective vaccines, especially subunit vaccines with cross-protection. Since the concept of reverse vaccinology was introduced, it has been widely used to screen for protective antigens in important pathogens. In this study, pan-genome binding reverse vaccinology, an emerging approach to vaccine candidate screening, was used to screen for cross-protective antigens against
R. anatipestifer
. Thirty proteins were identified from the core-genome as potential cross-protective antigens. Three of these proteins were recombinantly expressed, and their immunoreactivity with five antisera (anti-serotypes 1, 2, 6, 10, and 11) was demonstrated by Western blotting. Our study established a method for high-throughput screening of cross-protective antigens against
R. anatipestifer
in silico, which will lay the foundation for the development of a cross-protective subunit vaccine controlling
R. anatipestifer
infection.
Key points
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Pan-genome binding reverse vaccine approach was first established in R. anatipestifer to screen for subunit vaccine candidates.
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Thirty potential cross-protective antigens against R. anatipestifer were identified by this method.
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The reliability of the method was verified preliminarily by the results of Western blotting of three of these potential antigens. |
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ISSN: | 0175-7598 1432-0614 |
DOI: | 10.1007/s00253-023-12479-3 |