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烟曲霉中由于 G448S 突变(cyp51A 基因)导致伏立康唑耐药的体外-体内相关性。

In vitro-in vivo correlation of voriconazole resistance due to G448S mutation (cyp51A gene) in Aspergillus fumigatus.

机构信息

John D. Dingell VA Medical Center, Detroit, MI, USA.

出版信息

Diagn Microbiol Infect Dis. 2012 Nov;74(3):272-7. doi: 10.1016/j.diagmicrobio.2012.06.030. Epub 2012 Aug 14.

Abstract

Invasive pulmonary aspergillosis continues to be associated with a high mortality despite timely and appropriate therapy. Although host immunity plays a major role in poor clinical response, antifungal drug resistance cannot be ignored. Our studies were aimed 1) to study the mechanism of drug resistance in voriconazole strains of Aspergillus fumigatus, 2) to establish a causal relationship between cyp51A mutation and voriconazole resistance (VRC-R), and 3) to determine whether VRC-R due to cyp51A mutation correlated with in vivo resistance. A point mutation (G448S) involving cyp51A gene in VRC-R isolate was associated with resistance to VRC but not to posaconazole (POS); POS had superior activity to VRC in reducing lung fungal burden and mortality in mice infected with a VRC-R mutant of A. fumigatus. Our study demonstrated that azole resistance is based on specific site of cyp51A mutation and that in vitro VRC-R correlates with in vivo resistance.

摘要

尽管及时和适当的治疗,侵袭性肺曲霉病仍然与高死亡率相关。尽管宿主免疫在不良临床反应中起主要作用,但不能忽视抗真菌药物耐药性。我们的研究旨在:1)研究烟曲霉伏立康唑耐药株的耐药机制,2)建立 cyp51A 突变与伏立康唑耐药(VRC-R)之间的因果关系,3)确定由于 cyp51A 突变导致的 VRC-R 是否与体内耐药性相关。VRC-R 分离株中 cyp51A 基因的点突变(G448S)与 VRC 耐药相关,但与泊沙康唑(POS)无关;POS 在降低烟曲霉 VRC-R 突变感染小鼠肺部真菌负担和死亡率方面比 VRC 更有效。我们的研究表明,唑类耐药性基于 cyp51A 突变的特定部位,体外 VRC-R 与体内耐药性相关。

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