β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism.

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism. / Edström Hägerwall, Anneli; Rydengård, Victoria; Fernlund, Per; Mörgelin, Matthias; Baumgarten, Maria; Cole, Alexander M.; Malmsten, Martin; Kragelund, Birthe; Sørensen, Ole E.

In: P L o S Pathogens, Vol. 8, No. 4, e1002625, 2012, p. 1-12.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Edström Hägerwall, A, Rydengård, V, Fernlund, P, Mörgelin, M, Baumgarten, M, Cole, AM, Malmsten, M, Kragelund, B & Sørensen, OE 2012, 'β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism.', P L o S Pathogens, vol. 8, no. 4, e1002625, pp. 1-12. https://doi.org/10.1371/journal.ppat.1002625

APA

Edström Hägerwall, A., Rydengård, V., Fernlund, P., Mörgelin, M., Baumgarten, M., Cole, A. M., Malmsten, M., Kragelund, B., & Sørensen, O. E. (2012). β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism. P L o S Pathogens, 8(4), 1-12. [e1002625]. https://doi.org/10.1371/journal.ppat.1002625

Vancouver

Edström Hägerwall A, Rydengård V, Fernlund P, Mörgelin M, Baumgarten M, Cole AM et al. β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism. P L o S Pathogens. 2012;8(4):1-12. e1002625. https://doi.org/10.1371/journal.ppat.1002625

Author

Edström Hägerwall, Anneli ; Rydengård, Victoria ; Fernlund, Per ; Mörgelin, Matthias ; Baumgarten, Maria ; Cole, Alexander M. ; Malmsten, Martin ; Kragelund, Birthe ; Sørensen, Ole E. / β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism. In: P L o S Pathogens. 2012 ; Vol. 8, No. 4. pp. 1-12.

Bibtex

@article{dd3befd47ce64df88229c111b5a1f929,
title = "β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism.",
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.",
author = "{Edstr{\"o}m H{\"a}gerwall}, Anneli and Victoria Rydeng{\aa}rd and Per Fernlund and Matthias M{\"o}rgelin and Maria Baumgarten and Cole, {Alexander M.} and Martin Malmsten and Birthe Kragelund and S{\o}rensen, {Ole E.}",
year = "2012",
doi = "10.1371/journal.ppat.1002625",
language = "English",
volume = "8",
pages = "1--12",
journal = "P L o S Pathogens",
issn = "1553-7366",
publisher = "Public Library of Science",
number = "4",

}

RIS

TY - JOUR

T1 - β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism.

AU - Edström Hägerwall, Anneli

AU - Rydengård, Victoria

AU - Fernlund, Per

AU - Mörgelin, Matthias

AU - Baumgarten, Maria

AU - Cole, Alexander M.

AU - Malmsten, Martin

AU - Kragelund, Birthe

AU - Sørensen, Ole E.

PY - 2012

Y1 - 2012

N2 - 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.

AB - 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.

U2 - 10.1371/journal.ppat.1002625

DO - 10.1371/journal.ppat.1002625

M3 - Journal article

VL - 8

SP - 1

EP - 12

JO - P L o S Pathogens

JF - P L o S Pathogens

SN - 1553-7366

IS - 4

M1 - e1002625

ER -

ID: 47459999