<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Sun C</submitter><pubmed_abstract>&lt;i>Candida albicans&lt;/i>, a common commensal and opportunistic fungal pathogen in humans, can occasionally progress to disseminated candidiasis which is a serious condition with a high morbidity and fatality rate. The emergence of drug-resistant fungal strains compels us to look for an efficient treatment solution. Our earlier studies have demonstrated that the unique antimicrobial peptide AMP-17 from &lt;i>Musca domestica&lt;/i> has a strong antifungal impact on &lt;i>C. albicans in vitro&lt;/i>. Here, we verified the therapeutic effects of AMP-17 on systemic candidiasis &lt;i>in vivo&lt;/i> and the peptide interacts with fluconazole, a common antifungal medication, to treat systemic candidiasis. In the disseminated candidiasis model of &lt;i>Galleria mellonella&lt;/i> and mice challenged with &lt;i>C. albicans&lt;/i>,</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>1480808</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11564183</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Antimicrobial peptide AMP-17 induces protection against systemic candidiasis and interacts synergistically with fluconazole against &amp;lt;i&amp;gt;Candida albicans&amp;lt;/i&amp;gt; biofilm.</pubmed_title><pmcid>PMC11564183</pmcid><pubmed_authors>Tian Z</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Zhu L</pubmed_authors><pubmed_authors>Sun C</pubmed_authors><pubmed_authors>Guo G</pubmed_authors><pubmed_authors>Huang M</pubmed_authors><pubmed_authors>Jiao Z</pubmed_authors><pubmed_authors>Peng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antimicrobial peptide AMP-17 induces protection against systemic candidiasis and interacts synergistically with fluconazole against &amp;lt;i&amp;gt;Candida albicans&amp;lt;/i&amp;gt; biofilm.</name><description>&lt;i>Candida albicans&lt;/i>, a common commensal and opportunistic fungal pathogen in humans, can occasionally progress to disseminated candidiasis which is a serious condition with a high morbidity and fatality rate. The emergence of drug-resistant fungal strains compels us to look for an efficient treatment solution. Our earlier studies have demonstrated that the unique antimicrobial peptide AMP-17 from &lt;i>Musca domestica&lt;/i> has a strong antifungal impact on &lt;i>C. albicans in vitro&lt;/i>. Here, we verified the therapeutic effects of AMP-17 on systemic candidiasis &lt;i>in vivo&lt;/i> and the peptide interacts with fluconazole, a common antifungal medication, to treat systemic candidiasis. In the disseminated candidiasis model of &lt;i>Galleria mellonella&lt;/i> and mice challenged with &lt;i>C. albicans&lt;/i>,</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-18T12:50:25.556Z</modification><creation>2025-04-06T22:13:18.737Z</creation></dates><accession>S-EPMC11564183</accession><cross_references><pubmed>39552641</pubmed><doi>10.3389/fmicb.2024.1480808</doi></cross_references></HashMap>