Department of Microbiology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
MTA-SZTE "Lendület" Fungal Pathogenicity Mechanisms Research Group, Department of Microbiology, University of Szeged, Szeged, Hungary.
Front Cell Infect Microbiol. 2021 Apr 14;11:660347. doi: 10.3389/fcimb.2021.660347. eCollection 2021.
Mucormycosis is a life-threatening opportunistic infection caused by certain members of the fungal order Mucorales. This infection is associated with high mortality rate, which can reach nearly 100% depending on the underlying condition of the patient. Treatment of mucormycosis is challenging because these fungi are intrinsically resistant to most of the routinely used antifungal agents, such as most of the azoles. One possible mechanism of azole resistance is the drug efflux catalyzed by members of the ATP binding cassette (ABC) transporter superfamily. The pleiotropic drug resistance (PDR) transporter subfamily of ABC transporters is the most closely associated to drug resistance. The genome of encodes eight putative PDR-type transporters. In this study, transcription of the eight genes has been analyzed after azole treatment. Only the showed increased transcript level in response to all tested azoles. Deletion of this gene caused increased susceptibility to posaconazole, ravuconazole and isavuconazole and altered growth ability of the mutant. In the deletion mutant, transcript level of and significantly increased. Deletion of and was also done to create single and double knock out mutants for the three genes. After deletion of and , growth ability of the mutant strains decreased, while deletion of resulted in increased sensitivity against posaconazole, ravuconazole and isavuconazole. Our result suggests that the regulation of the eight genes is interconnected and and participates in the resistance of the fungus to posaconazole, ravuconazole and isavuconazole.
毛霉病是一种由毛霉目真菌引起的危及生命的机会性感染。这种感染与高死亡率相关,死亡率取决于患者的基础疾病状况,可达近 100%。毛霉病的治疗具有挑战性,因为这些真菌对大多数常规使用的抗真菌药物(如大多数唑类药物)具有内在耐药性。唑类耐药的一个可能机制是 ATP 结合盒(ABC)转运蛋白超家族成员催化的药物外排。ABC 转运蛋白的多药耐药(PDR)转运子亚家族与耐药性最密切相关。的基因组编码 8 个推定的 PDR 型转运蛋白。在这项研究中,分析了唑类药物处理后这 8 个 基因的转录情况。只有 基因在所有测试的唑类药物作用下表现出转录水平升高。该基因的缺失导致对泊沙康唑、拉夫康唑和伊曲康唑的敏感性增加,并改变了突变体的生长能力。在 缺失突变体中, 和 的转录水平显著增加。还进行了 和 的缺失,以创建这三个基因的单和双敲除突变体。 和 的缺失后,突变菌株的生长能力下降,而 的缺失导致对泊沙康唑、拉夫康唑和伊曲康唑的敏感性增加。我们的结果表明,这 8 个 基因的调控是相互关联的, 和 参与了真菌对泊沙康唑、拉夫康唑和伊曲康唑的耐药性。