Sufei Tian, Chen Rong, Hailong Li, Yusheng Wu, Na Wu, Yunzhuo Chu, Ning Jiang, Jingping Zhang, Hong Shang
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All five patients received 24-hour AmB (5 mg/L) bladder irrigation treatment. Evolutionary analyses revealed an <i>ERG3</i> (c923t) mutation in AmB<sup>1</sup> <i>C. auris</i>. Additionally, AmB<sup>2</sup> <i>C. auris</i> was found to contain a t2831c mutation in the <i>RAD2</i> gene. In the AmB<sup>1</sup> group, membrane lipid-related gene expression (<i>ERG1, ERG2, ERG13,</i> and <i>ERG24</i>) was upregulated, while in the AmB<sup>2</sup> group, expression of DNA-related genes (e.g. <i>DNA2</i> and <i>PRI1</i>) was up-regulated. In a series of <i>C.auris</i> strains with reduced susceptibility to AmB, five key genes were identified: two upregulated (<i>IFF9</i> and <i>PGA6)</i> and three downregulated (<i>HGT7, HGT13,</i>and <i>PRI32)</i>. In this study, we demonstrate the microevolution of reduced AmB sensitivity in vivo and further elucidate the relationship between reduced AmB sensitivity and low-concentration AmB bladder irrigation. These findings offer new insights into potential antifungal drug targets and clinical markers for the \"super fungus\", <i>C. auris</i>.</p>","PeriodicalId":11602,"journal":{"name":"Emerging Microbes & Infections","volume":" ","pages":"2398596"},"PeriodicalIF":8.4000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11385638/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genetic microevolution of clinical <i>Candida auris</i> with reduced Amphotericin B sensitivity in China.\",\"authors\":\"Sufei Tian, Chen Rong, Hailong Li, Yusheng Wu, Na Wu, Yunzhuo Chu, Ning Jiang, Jingping Zhang, Hong Shang\",\"doi\":\"10.1080/22221751.2024.2398596\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The global rate of Amphotericin B (AmB) resistance in <i>Candida auris</i> has surpassed 12%. However, there is limited data on available clinical treatments and microevolutionary analyses concerning reduced AmB sensitivity. In this study, we collected 18 <i>C. auris</i> isolates from five patients between 2019 and 2022. We employed clinical data mining, genomic, and transcriptomic analyses to identify genetic evolutionary features linked to reduced AmB sensitivity in these isolates during clinical treatment. We identified six isolates with a minimum inhibitory concentration (MIC) of AmB below 0.5 µg/mL (AmB<sup>0.5</sup>) and 12 isolates with an AmB-MIC of 1 µg/mL (AmB<sup>1</sup>) or ≥ 2 µg/mL (AmB<sup>2</sup>). All five patients received 24-hour AmB (5 mg/L) bladder irrigation treatment. Evolutionary analyses revealed an <i>ERG3</i> (c923t) mutation in AmB<sup>1</sup> <i>C. auris</i>. Additionally, AmB<sup>2</sup> <i>C. auris</i> was found to contain a t2831c mutation in the <i>RAD2</i> gene. In the AmB<sup>1</sup> group, membrane lipid-related gene expression (<i>ERG1, ERG2, ERG13,</i> and <i>ERG24</i>) was upregulated, while in the AmB<sup>2</sup> group, expression of DNA-related genes (e.g. <i>DNA2</i> and <i>PRI1</i>) was up-regulated. In a series of <i>C.auris</i> strains with reduced susceptibility to AmB, five key genes were identified: two upregulated (<i>IFF9</i> and <i>PGA6)</i> and three downregulated (<i>HGT7, HGT13,</i>and <i>PRI32)</i>. In this study, we demonstrate the microevolution of reduced AmB sensitivity in vivo and further elucidate the relationship between reduced AmB sensitivity and low-concentration AmB bladder irrigation. 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引用次数: 0
摘要
全球白色念珠菌对两性霉素 B(AmB)的耐药率已超过 12%。然而,现有的临床治疗数据和关于AmB敏感性降低的微进化分析却很有限。在本研究中,我们从 2019 年至 2022 年期间的五名患者中收集了 18 个念珠菌分离株。我们采用临床数据挖掘、基因组和转录组分析来确定这些分离株在临床治疗期间与AmB敏感性降低相关的基因进化特征。我们发现了6株AmB最低抑菌浓度(MIC)低于0.5微克/毫升(AmB0.5)的分离株和12株AmB-MIC为1微克/毫升(AmB1)或≥2微克/毫升(AmB2)的分离株。所有五名患者都接受了 24 小时 AmB(5 毫克/升)膀胱冲洗治疗。进化分析表明,AmB1 C. auris 中存在 ERG3(c923t)突变。此外,还发现 AmB2 C. auris 包含 RAD2 基因 t2831c 突变。在 AmB1 组中,膜脂质相关基因(ERG1、ERG2、ERG13 和 ERG24)的表达上调,而在 AmB2 组中,DNA 相关基因(如 DNA2 和 PRI1)的表达上调。在一系列对 AmB 敏感性降低的 C.auris 菌株中,发现了五个关键基因:两个上调(IFF9 和 PGA6),三个下调(HGT7、HGT13 和 PRI32)。在这项研究中,我们证明了体内 AmB 敏感性降低的微观演变,并进一步阐明了 AmB 敏感性降低与低浓度 AmB 膀胱灌注之间的关系。这些发现为 "超级真菌 "C. auris 的潜在抗真菌药物靶点和临床标记物提供了新的见解。
Genetic microevolution of clinical Candida auris with reduced Amphotericin B sensitivity in China.
The global rate of Amphotericin B (AmB) resistance in Candida auris has surpassed 12%. However, there is limited data on available clinical treatments and microevolutionary analyses concerning reduced AmB sensitivity. In this study, we collected 18 C. auris isolates from five patients between 2019 and 2022. We employed clinical data mining, genomic, and transcriptomic analyses to identify genetic evolutionary features linked to reduced AmB sensitivity in these isolates during clinical treatment. We identified six isolates with a minimum inhibitory concentration (MIC) of AmB below 0.5 µg/mL (AmB0.5) and 12 isolates with an AmB-MIC of 1 µg/mL (AmB1) or ≥ 2 µg/mL (AmB2). All five patients received 24-hour AmB (5 mg/L) bladder irrigation treatment. Evolutionary analyses revealed an ERG3 (c923t) mutation in AmB1C. auris. Additionally, AmB2C. auris was found to contain a t2831c mutation in the RAD2 gene. In the AmB1 group, membrane lipid-related gene expression (ERG1, ERG2, ERG13, and ERG24) was upregulated, while in the AmB2 group, expression of DNA-related genes (e.g. DNA2 and PRI1) was up-regulated. In a series of C.auris strains with reduced susceptibility to AmB, five key genes were identified: two upregulated (IFF9 and PGA6) and three downregulated (HGT7, HGT13,and PRI32). In this study, we demonstrate the microevolution of reduced AmB sensitivity in vivo and further elucidate the relationship between reduced AmB sensitivity and low-concentration AmB bladder irrigation. These findings offer new insights into potential antifungal drug targets and clinical markers for the "super fungus", C. auris.
期刊介绍:
Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses.
The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries.
This journal addresses topics of critical biological and clinical importance, including but not limited to:
- Epidemic surveillance
- Clinical manifestations
- Diagnosis and management
- Cellular and molecular pathogenesis
- Innate and acquired immune responses between emerging microbes and their hosts
- Drug discovery
- Vaccine development research
Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.