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Updated: May 5, 2026

Protocols for Vaginal Inoculation and Sample Collection in the Experimental Mouse Model of Candida vaginitis
Published on: December 8, 2011
β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and
Anneli M L Edström Hägerwall1, Victoria Rydengård, Per Fernlund
1Division of Infection Medicine, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Abstract:
The innate immune factors controlling Candida albicans are mostly unknown. Vulvovaginal candidiasis is common in women and affects approximately 70-75% of all women at least once. Despite the propensity of Candida to colonize the vagina, transmission of Candida albicans following sexual intercourse is very rare. This prompted us to investigate whether the post coital vaginal milieu contained factors active against C. albicans. By CFU assays, we found prominent candidacidal activity of post coital seminal plasma at both neutral and the acid vaginal pH. In contrast, normal seminal plasma did not display candidacidal activity prior to acidification. By antifungal gel overlay assay, one clearing zone corresponding to a protein band was found in both post coital and normal seminal plasma, which was subsequently identified as β-microseminoprotein. At neutral pH, the fungicidal activity of β-microseminoprotein and seminal plasma was inhibited by calcium. By NMR spectroscopy, amino acid residue E(71) was shown to be critical for the calcium coordination. The acidic vaginal milieu unleashed the fungicidal activity by decreasing the inhibitory effect of calcium. The candidacidal activity of β-microseminoprotein was mapped to a fragment of the C-terminal domain with no structural similarity to other known proteins. A homologous fragment from porcine β-microseminoprotein demonstrated calcium-dependent fungicidal activity in a CFU assay, suggesting this may be a common feature for members of the β-microseminoprotein family. By electron microscopy, β-microseminoprotein was found to cause lysis of Candida. Liposome experiments demonstrated that β-microseminoprotein was active towards ergosterol-containing liposomes that mimic fungal membranes, offering an explanation for the selectivity against fungi. These data identify β-microseminoprotein as an important innate immune factor active against C. albicans and may help explain the low sexual transmission rate of Candida.
Insights
Seminal plasma contains β-microseminoprotein, an innate immune factor that kills Candida albicans. This protein
Area of Science:
- Immunology
- Microbiology
- Biochemistry
Background:
- Vulvovaginal candidiasis affects most women, yet Candida albicans transmission via sexual intercourse is rare.
- The innate immune factors controlling Candida albicans in the vaginal environment are largely unknown.
Purpose of the Study:
- To investigate factors in the post-coital vaginal milieu with activity against Candida albicans.
- To identify and characterize the candidacidal components of seminal plasma.
Main Methods:
- Colony-forming unit (CFU) assays to measure candidacidal activity.
- Antifungal gel overlay assay and protein identification (mass spectrometry implied).
- Nuclear Magnetic Resonance (NMR) spectroscopy, electron microscopy, and liposome experiments.
Main Results:
- Post-coital seminal plasma exhibits candidacidal activity at vaginal pH, unlike normal seminal plasma.
- β-microseminoprotein was identified as a key candidacidal factor, with activity dependent on pH and calcium.
- β-microseminoprotein causes Candida lysis and targets fungal membranes, explaining its selectivity.
Conclusions:
- β-microseminoprotein is an innate immune factor effective against Candida albicans.
- The mechanism involves calcium-dependent activity modulated by vaginal acidity.
- This finding may explain the low sexual transmission rate of Candida.
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