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首页> 外文期刊>Medical mycology: official publication of the International Society for Human and Animal Mycology >RT-PCR analysis of Candida albicans ALS gene expression in a hyposalivatory rat model of oral candidiasis and in HIV-positive human patients.
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RT-PCR analysis of Candida albicans ALS gene expression in a hyposalivatory rat model of oral candidiasis and in HIV-positive human patients.

机译:口腔念珠菌病减唾液大鼠模型和HIV阳性人类患者中白色念珠菌ALS基因表达的RT-PCR分析。

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摘要

ALS gene expression was studied in the hyposalivatory rat model of oral candidiasis and in clinical specimens collected from HIV-positive patients to assess similarities in expression patterns between the model system and clinical isolates. Two Candida albicans strains, SC5314 and OY-2-76, were used in the rat model system and infection progressed for 3 or 5 days. The strains produced similar oral lesions at 3 days. At 5 days, strain OY-2-76 produced more superficial lesions containing relatively more yeast forms compared to invasive hyphal forms observed for strain SC5314. For all infections, the most severe lesions were observed on the tongue and gingiva overlying the mandible. ALS transcripts were easier to detect by RT-PCR later in infection and under other conditions where more fungal cells were present. Expression of ALS1, ALS2, ALS3 and ALS4 was observed in rats infected for 3 days with ALS5 and ALS9 transcripts detected after 5 days of infection. Expression of ALS6 was observed in a single specimen from a 5-day infection while ALS7 transcript was never found. Expression of all ALS genes was observed in oral clinical material collected from HIV-positive patients although ALS6 and ALS7 transcripts required an extra PCR amplification step to be detected. Overall, the patterns of ALS gene expression were similar between the rat model and human clinical specimens, suggesting that the model would be useful for studying the phenotype of al delta/al delta mutant strains.
机译:在口腔念珠菌病低唾液酸大鼠模型以及从HIV阳性患者收集的临床样本中研究了ALS基因表达,以评估模型系统与临床分离株之间表达模式的相似性。在大鼠模型系统中使用了两个白色念珠菌菌株SC5314和OY-2-76,感染过程进行了3或5天。菌株在第3天产生相似的口腔损伤。在第5天,与观察到菌株SC5314的侵入性菌丝形式相比,菌株OY-2-76产生了更多的浅表皮病灶,其中包含相对更多的酵母形式。对于所有感染,在下颌骨上方的舌头和牙龈上观察到最严重的病变。在感染后和存在更多真菌细胞的其他条件下,RT-PCR易于检测ALS转录本。在感染5天后检测到ALS5和ALS9转录本的感染3天的大鼠中观察到ALS1,ALS2,ALS3和ALS4的表达。在感染5天后的单个标本中观察到ALS6的表达​​,而从未发现ALS7转录本。在从HIV阳性患者收集的口腔临床材料中观察到所有ALS基因的表达,尽管ALS6和ALS7转录本需要检测额外的PCR扩增步骤。总体而言,大鼠模型与人类临床标本之间的ALS基因表达模式相似,这表明该模型可用于研究al delta / al delta突变菌株的表型。

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