<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Zhou W</submitter><pubmed_abstract>&lt;i>Candida auris&lt;/i> emerged as a pathogenic species of fungus that causes severe and invasive outbreaks worldwide. The fungus exhibits high intrinsic resistance rates to various first-line antifungals, and the underlying molecular mechanism responsible for its multidrug resistance is still unclear. In this study, a transcriptomic analysis was performed between two &lt;i>C. auris&lt;/i> isolates that exhibited different anti-drug patterns by RNA-sequencing, namely, CX1 (anti-drug sensitive) and CX2 (resistant). Transcriptomic analysis results revealed 541 upregulated and 453 downregulated genes in the resistant &lt;i>C. auris&lt;/i> strain compared with the susceptible strain. In addition, our findings highlight the presence of potential differentially expressed genes (DEGs), which may play a role in drug resistance, including genes involved in ergosterol and efflux pump biosynthesis such as &lt;i>SNQ2&lt;/i>, &lt;i>CDR4&lt;/i>, &lt;i>ARB1&lt;/i>, &lt;i>MDR1&lt;/i>, &lt;i>MRR1&lt;/i>, and &lt;i>ERG&lt;/i> genes. We also found that Hsp related genes were upregulated for expression in the anti-drug-resistant strain. Biofilm formation and growth conditions were also compared between the two isolates. Our study provides novel clues for future studies in terms of understanding multidrug resistance mechanisms of &lt;i>C. auris&lt;/i> strains.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>708009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8330549</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Comparative Transcriptome Between Anti-drug Sensitive and Resistant &lt;i>Candida auris&lt;/i> in China.</pubmed_title><pmcid>PMC8330549</pmcid><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Qiao D</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Jiang S</pubmed_authors><pubmed_authors>Yan W</pubmed_authors><pubmed_authors>Li N</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Comparative Transcriptome Between Anti-drug Sensitive and Resistant &lt;i>Candida auris&lt;/i> in China.</name><description>&lt;i>Candida auris&lt;/i> emerged as a pathogenic species of fungus that causes severe and invasive outbreaks worldwide. The fungus exhibits high intrinsic resistance rates to various first-line antifungals, and the underlying molecular mechanism responsible for its multidrug resistance is still unclear. In this study, a transcriptomic analysis was performed between two &lt;i>C. auris&lt;/i> isolates that exhibited different anti-drug patterns by RNA-sequencing, namely, CX1 (anti-drug sensitive) and CX2 (resistant). Transcriptomic analysis results revealed 541 upregulated and 453 downregulated genes in the resistant &lt;i>C. auris&lt;/i> strain compared with the susceptible strain. In addition, our findings highlight the presence of potential differentially expressed genes (DEGs), which may play a role in drug resistance, including genes involved in ergosterol and efflux pump biosynthesis such as &lt;i>SNQ2&lt;/i>, &lt;i>CDR4&lt;/i>, &lt;i>ARB1&lt;/i>, &lt;i>MDR1&lt;/i>, &lt;i>MRR1&lt;/i>, and &lt;i>ERG&lt;/i> genes. We also found that Hsp related genes were upregulated for expression in the anti-drug-resistant strain. Biofilm formation and growth conditions were also compared between the two isolates. Our study provides novel clues for future studies in terms of understanding multidrug resistance mechanisms of &lt;i>C. auris&lt;/i> strains.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2024-11-19T20:48:02.959Z</modification><creation>2022-02-11T05:13:16.741Z</creation></dates><accession>S-EPMC8330549</accession><cross_references><pubmed>34354695</pubmed><doi>10.3389/fmicb.2021.708009</doi></cross_references></HashMap>