<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Alomeir N</submitter><funding>NIDCR NIH HHS</funding><funding>National Institute of Dental and Craniofacial Research</funding><pagination>105582</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9729470</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>145</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To assess the effect of Nystatin on Candida albicans and Streptococcus mutans duo-species biofilms using an in vitro cariogenic biofilm model.&lt;h4>Design&lt;/h4>Biofilms were formed on saliva-coated hydroxyapatite discs under high sugar challenge (1 % sucrose and 1 % glucose), with inoculation of 10&lt;sup>5&lt;/sup>CFU/ml S. mutans and 10&lt;sup>3&lt;/sup>CFU/ml C. albicans. Between 20 and 68 h, biofilms were treated with 28,000 IU Nystatin solution, 5 min/application, 4 times/day, to mimic the clinical application. Biofilm's three-dimensional structure was assessed using multi-photon confocal microscopy. The expression of C. albicans and S. mutans virulence genes was assessed via real-time PCR. Duplicate discs were used in 3 independent repeats. t-test and Mann-Whitney U test were used to compare outcomes between treatment and control group.&lt;h4>Results&lt;/h4>Nystatin treatment eliminated C. albicans in biofilms at 44 h. Nystatin-treated group had a significant reduction of biofilm dry-weight and reduced S. mutans abundance by 0.5 log CFU/ml at 44 and 68 h (p &lt; 0.05). Worth noting that biomass distribution across the vertical layout was altered by Nystatin treatment, resulting in less volume on the substrate layers in Nystatin-treated biofilms compared to the control. Reduction of microcolonies size and volume was also observed in Nystatin-treated biofilms (p &lt; 0.05). Nystatin-treated biofilms formed unique halo-shaped microcolonies with reduced core EPS coverage. Furthermore, Nystatin-treated biofilms had significant down-regulations of S. mutans gtfD and atpD genes (p &lt; 0.05).&lt;h4>Conclusions&lt;/h4>Nystatin application altered the formation and characteristics of C. albicans and S. mutans duo-species biofilms. Therefore, developing clinical regimens for preventing or treating dental caries from an antifungal perspective is warranted.</pubmed_abstract><journal>Archives of oral biology</journal><pubmed_title>Effect of Nystatin on Candida albicans - Streptococcus mutans duo-species biofilms.</pubmed_title><pmcid>PMC9729470</pmcid><funding_grant_id>R01DE031025</funding_grant_id><funding_grant_id>R01 DE031025</funding_grant_id><funding_grant_id>K23 DE027412</funding_grant_id><funding_grant_id>K23DE027412</funding_grant_id><pubmed_authors>Alomeir N</pubmed_authors><pubmed_authors>Fadaak A</pubmed_authors><pubmed_authors>Xiao J</pubmed_authors><pubmed_authors>Malmstrom H</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Wu TT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of Nystatin on Candida albicans - Streptococcus mutans duo-species biofilms.</name><description>&lt;h4>Objective&lt;/h4>To assess the effect of Nystatin on Candida albicans and Streptococcus mutans duo-species biofilms using an in vitro cariogenic biofilm model.&lt;h4>Design&lt;/h4>Biofilms were formed on saliva-coated hydroxyapatite discs under high sugar challenge (1 % sucrose and 1 % glucose), with inoculation of 10&lt;sup>5&lt;/sup>CFU/ml S. mutans and 10&lt;sup>3&lt;/sup>CFU/ml C. albicans. Between 20 and 68 h, biofilms were treated with 28,000 IU Nystatin solution, 5 min/application, 4 times/day, to mimic the clinical application. Biofilm's three-dimensional structure was assessed using multi-photon confocal microscopy. The expression of C. albicans and S. mutans virulence genes was assessed via real-time PCR. Duplicate discs were used in 3 independent repeats. t-test and Mann-Whitney U test were used to compare outcomes between treatment and control group.&lt;h4>Results&lt;/h4>Nystatin treatment eliminated C. albicans in biofilms at 44 h. Nystatin-treated group had a significant reduction of biofilm dry-weight and reduced S. mutans abundance by 0.5 log CFU/ml at 44 and 68 h (p &lt; 0.05). Worth noting that biomass distribution across the vertical layout was altered by Nystatin treatment, resulting in less volume on the substrate layers in Nystatin-treated biofilms compared to the control. Reduction of microcolonies size and volume was also observed in Nystatin-treated biofilms (p &lt; 0.05). Nystatin-treated biofilms formed unique halo-shaped microcolonies with reduced core EPS coverage. Furthermore, Nystatin-treated biofilms had significant down-regulations of S. mutans gtfD and atpD genes (p &lt; 0.05).&lt;h4>Conclusions&lt;/h4>Nystatin application altered the formation and characteristics of C. albicans and S. mutans duo-species biofilms. Therefore, developing clinical regimens for preventing or treating dental caries from an antifungal perspective is warranted.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T12:19:17.787Z</modification><creation>2025-04-04T12:19:17.787Z</creation></dates><accession>S-EPMC9729470</accession><cross_references><pubmed>36395564</pubmed><doi>10.1016/j.archoralbio.2022.105582</doi></cross_references></HashMap>