The Department of Dermatovenereology, The Second Hospital, Shanxi Medical University, NO.382, Wuyi Road, Taiyuan, 030001, Shanxi, China.
The Department of Bluttranfusion, The Second Hospital, Shanxi Medical University, Taiyuan, 030001, Shanxi, China.
Braz J Microbiol. 2023 Jun;54(2):619-627. doi: 10.1007/s42770-023-00961-z. Epub 2023 Apr 22.
This study aimed to explore the roles of SAP2 and GCN4 in itraconazole (ITR) resistance of C. albicans under different conditions, and their correlations. A total of 20 clinical strains of C. albicans, including 10 ITR resistant strains and 10 sensitive strains, were used. Then, SAP2 sequencing and GCN4 sequencing were performed, and the biofilm formation ability of different C. albicans strains was determined. Finally, real-time quantitative PCR was used to measure the expression of SAP2 and GCN4 in C. albicans under planktonic and biofilm conditions, as well as their correlation was also analyzed. No missense mutations and three synonymous mutation sites, including T276A, G543A, and A675C, were found in SAP2 sequencing. GCN4 sequencing showed one missense mutation site (A106T (T36S)) and six synonymous mutation sites (A147C, C426T, T513C, T576A, G624A and C732T). The biofilm formation ability of drug-resistant C. albicans strains was significantly higher than that of sensitive strains (P < 0.05). Additionally, SAP2 and GCN4 were up-regulated in the ITR-resistant strains, and were both significantly higher in C. albicans under biofilm condition. The mRNA expression levels of SAP2 and GCN4 had significantly positive correlation. The higher expression levels of SAP2 and GCN4 were observed in the ITR-resistant strains of C. albicans under planktonic and biofilm conditions, as well as there was a positive correlation between SAP2 and GCN4 mRNA expression.
本研究旨在探讨 SAP2 和 GCN4 在不同条件下白念珠菌伊曲康唑(ITR)耐药中的作用及其相关性。共收集了 20 株临床白念珠菌,包括 10 株 ITR 耐药株和 10 株敏感株。然后进行 SAP2 测序和 GCN4 测序,测定不同白念珠菌菌株的生物膜形成能力。最后,采用实时定量 PCR 法检测浮游和生物膜条件下白念珠菌中 SAP2 和 GCN4 的表达,并分析其相关性。SAP2 测序未发现错义突变和三个同义突变位点,包括 T276A、G543A 和 A675C。GCN4 测序显示一个错义突变位点(A106T(T36S))和六个同义突变位点(A147C、C426T、T513C、T576A、G624A 和 C732T)。耐药白念珠菌菌株的生物膜形成能力明显高于敏感菌株(P<0.05)。此外,ITR 耐药株中 SAP2 和 GCN4 上调,生物膜条件下白念珠菌中 SAP2 和 GCN4 均显著上调。SAP2 和 GCN4 的 mRNA 表达水平呈显著正相关。在浮游和生物膜条件下,白念珠菌 ITR 耐药株中 SAP2 和 GCN4 的表达水平较高,且 SAP2 和 GCN4 mRNA 表达之间呈正相关。