Antibody response to the 45 kDa Candida albicans antigen in an animal model and potential role of the antigen in adherence

Author:

Bujdáková Helena1,Paulovičová Ema2,Borecká-Melkusová Silvia1,Gašperík Juraj3,Kucharíková Soňa1,Kolecka Anna1,Lell Claudia4,Jensen Dorthe B.4,Würzner Reinhard4,Chorvát Dušan5,Pichová Iva6

Affiliation:

1. Department of Microbiology and Virology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia

2. Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovakia

3. Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia

4. Department of Hygiene, Microbiology and Social Medicine, Innsbruck Medical University, Austria

5. Department of Biophotonics, International Laser Centre, Bratislava, Slovakia

6. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic

Abstract

The Candida antigen CR3-RP (complement receptor 3-related protein) is supposed to be a ‘mimicry’ protein because of its ability to bind antibody directed against the α subunit of the mammalian CR3 (CD11b/CD18). This study aimed to (i) investigate the specific humoral isotypic response to immunization with CR3-RP in vivo in a rabbit animal model, and (ii) determine the role of CR3-RP in the adherence of Candida albicans in vitro using the model systems of buccal epithelial cells (BECs) and biofilm formation. The synthetic C. albicans peptide DINGGGATLPQ corresponding to 11 amino-acids of the CR3-RP sequence DINGGGATLPQALXQITGVIT, determined by N-terminal sequencing, was used for immunization of rabbits to obtain polyclonal anti-CR3-PR serum and for subsequent characterization of the humoral isotypic response of rabbits. A significant increase of IgG, IgA and IgM anti-CR3-RP specific antibodies was observed after the third (P<0.01) and the fourth (P<0.001) immunization doses. The elevation of IgA levels suggested peptide immunomodulation of the IgA1 subclass, presumably in coincidence with Candida epithelial adherence. Blocking CR3-RP with polyclonal anti-CR3-RP serum reduced the ability of Candida to adhere to BECs, in comparison with the control, by up to 35 % (P<0.001), and reduced biofilm formation by 28 % (P<0.001), including changes in biofilm thickness and integrity detected by confocal laser scanning microscopy. These properties of CR3-RP suggest that it has potential for future vaccine development.

Publisher

Microbiology Society

Subject

Microbiology (medical),General Medicine,Microbiology

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