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浮游态和生物膜态临床分离株 与 之间的相关性。

Correlation between and in clinical strains of at planktonic and biofilm states.

机构信息

Department of Dermatovenereology, The Second Hospital, Shanxi Medical University, Taiyuan030001, Shanxi, China.

Department of Blood Transfusion, The Second Hospital, Shanxi Medical University, Taiyuan030001, Shanxi, China.

出版信息

Can J Microbiol. 2022 Dec 1;68(12):722-730. doi: 10.1139/cjm-2022-0139. Epub 2022 Sep 26.

DOI:10.1139/cjm-2022-0139
PMID:36162133
Abstract

This study aimed to explore the influences of and on itraconazole (ITR) resistance of at different states. A total of 10 ITR-resistant strains and 10 ITR-sensitive strains were used for sequencing and sequencing. sequencing showed no missense mutation, and three synonymous mutations. gene sequencing identified two missense mutations M140I (8) and K191Q (4), and 14 synonymous mutations G201A (1), A246C (5), C282T (6), G288A (6), C321T (7), A399C (16), C432T (16), C465T (11), G552A (16), G669T (1), G672A (1), G681T (2), T783C (1), and T819A (2). The biofilm formation capacity of resistant strains, including the ∆/∆ strain, was stronger. Afterward, real-time quantitative PCR was used to analyze the expression of and . Compared with the sensitive strains, and expressions were both significantly upregulated in resistant strains at planktonic and biofilm states ( < 0.05). Compared with the strains at planktonic state, was significantly upregulated, while was significantly downregulated at biofilm states ( < 0.05). Additionally, expression in the knocked down strain of was significantly upregulated, and expression was evidently downregulated in the ∆/∆ strain at biofilm states compared with that at planktonic states ( < 0.05). Loss of can increase level and may influence the biofilm formation of , thus increasing ITR resistance of.

摘要

本研究旨在探讨不同状态下 和 对伊曲康唑(ITR)耐药的影响。共使用了 10 株 ITR 耐药株和 10 株 ITR 敏感株进行 测序和 测序。 测序未发现错义突变,仅有 3 个同义突变。 基因测序鉴定出两个错义突变 M140I(8)和 K191Q(4),以及 14 个同义突变 G201A(1)、A246C(5)、C282T(6)、G288A(6)、C321T(7)、A399C(16)、C432T(16)、C465T(11)、G552A(16)、G669T(1)、G672A(1)、G681T(2)、T783C(1)和 T819A(2)。耐药 株,包括 ∆/∆ 株,的生物膜形成能力更强。随后,使用实时定量 PCR 分析 和 的表达。与敏感株相比,耐药株在浮游和生物膜状态下 和 的表达均显著上调( < 0.05)。与浮游状态下的菌株相比,生物膜状态下 显著上调,而 显著下调( < 0.05)。此外,与浮游状态相比, 敲低株的 表达显著上调,而 ∆/∆ 株的 表达在生物膜状态下明显下调( < 0.05)。 缺失可增加 水平,可能影响 的生物膜形成,从而增加 的 ITR 耐药性。

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