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Altered Expression of Selectable Marker URA3 in Gene-Disrupted Candida albicans Strains Complicates Interpretation of Virulence Studies

机译:在基因破坏的白色念珠菌菌株中选择标记URA3的表达变化使毒力研究的解释复杂化。

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摘要

The ura-blaster technique for the disruption of Candida albicans genes has been employed in a number of studies to identify possible genes encoding virulence factors of this fungal pathogen. In this study, the URA3-encoded orotidine 5′-monophosphate (OMP) decarboxylase enzyme activities of C. albicans strains with ura-blaster-mediated genetic disruptions were measured. All strains harboring genetic lesions via the ura-blaster construct showed reduced OMP decarboxylase activities compared to that of the wild type when assayed. The activity levels in different gene disruptions varied, suggesting a positional effect on the level of gene expression. Because the URA3 gene of C. albicans has previously been identified as a virulence factor for this microorganism, our results suggest that decreased virulence observed in strains constructed with the ura-blaster cassette cannot accurately be attributed, in all cases, to the targeted genetic disruption. Although revised methods for validating a URA3-disrupted gene as a target for antifungal drug development could be devised, it is clearly desirable to replace URA3 with a different selectable marker that does not influence virulence.
机译:用于破坏白色念珠菌基因的ura-blaster技术已用于许多研究中,以鉴定编码这种真菌病原体毒力因子的可能基因。在这项研究中,测量了URA3编码的具有乌拉-blaster介导的遗传破坏的白色念珠菌菌株的尿苷5'-单磷酸(OMP)脱羧酶活性。与野生型相比,所有通过ura-blaster构建体携带遗传损伤的菌株均显示出与野生型相比降低的OMP脱羧酶活性。不同基因破坏中的活性水平各不相同,表明对基因表达水平有位置影响。由于以前已将白色念珠菌的URA3基因鉴定为该微生物的致病因子,因此我们的结果表明,在所有情况下,用ura-blaster盒构建的菌株中观察到的致病力下降均不能准确地归因于靶向遗传破坏。尽管可以设计出用于验证将URA3破坏的基因作为抗真菌药物开发目标的修订方法,但显然希望用不影响毒力的不同选择标记替代URA3。

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