Variability of the response of human vaginal Lactobacillus crispatus to 17β-estradiol

被引:0
作者
Maximilien Clabaut
Amine M. Boukerb
Amine Ben Mlouka
Amandine Suet
Ali Tahrioui
Julien Verdon
Magalie Barreau
Olivier Maillot
Agathe Le Tirant
Madina Karsybayeva
Coralie Kremser
Gérard Redziniak
Cécile Duclairoir-Poc
Chantal Pichon
Julie Hardouin
Pascal Cosette
Sylvie Chevalier
Marc G. J. Feuilloley
机构
[1] Rouen Normandie Université,Laboratory of Microbiology Signals and Microenvironment (LMSM EA 4312)
[2] Proteomic Platform PISSARO University of Rouen Normandy,Laboratory «Polymères, Biopolymères, Surfaces» (UMR 6270 CNRS)
[3] UPR4301 French National Centre for Scientific Research,Centre de Biophysique Moléculaire
[4] Université de Poitiers,Laboratoire EBI, UMR CNRS 7267
[5] Seqens Cosmetics,undefined
[6] Remedials Laboratory,undefined
[7] GymoPharm,undefined
[8] Cosmetic Inventions,undefined
来源
Scientific Reports | / 11卷
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摘要
We previously showed that the physiological concentration of 17β-estradiol in the vaginal environment is sufficient to affect the membrane dynamics and adhesion phenotype of the Lactobacillus crispatus strain CIP104459. However, L. crispatus is a heterogeneous species. Here, we investigated the effect of 17β-estradiol on the recently isolated L. crispatus vaginal strain V4, related to a cluster distant from CIP104459 and at the limit of being a different subspecies. Grown in the same medium, the two strains expressed a highly similar pool of proteins. However, in contrast to CIP104459, L. crispatus V4 showed high aggregation potential and 17β-estradiol promoted this phenotype. This effect was associated with large changes in cell-surface polarity and Lewis acid/base properties. In addition, we observed no effect on the membrane dynamics, contrary to CIP104459. These results can be explained by differences in the properties and organization of the S layer between the two strains. However, as for CIP104459, 17β-estradiol increased biosurfactant production of L. crispatus V4 and their adhesion to vaginal cells. This suggests that 17β-estradiol agonists would be valuable tools to favor a stable re-implantation of L. crispatus in the vaginal mucosa.
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