Alexandrakis G, Jalali S, Gloor P
Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06520-8061, USA.
Br J Ophthalmol. 1998 Mar;82(3):306-11. doi: 10.1136/bjo.82.3.306.
AIMS/BACKGROUND: The purpose of this study was apply the polymerase chain reaction (PCR) to develop a sensitive, specific, and rapid test to diagnose Fusarium keratitis. Fusarium is the most common cause of fungal corneal infection in some parts of the world. It is often difficult to establish that a keratitis is due to fungal infection.
Fusarium solani keratitis was induced in three eyes of three rabbits by injection of a suspension of the fungus into the anterior corneal stroma. In one rabbit the contralateral eye served as a control. From four to 28 days after inoculation, the corneas were scraped for culture, then scraped and swabbed for PCR analysis. The PCR was performed with primers directed against a portion of the Fusarium cutinase gene, and the presence or absence of this amplified target sequence was determined by agarose gel.
The amplified DNA sequence was detected in 25 of 28 samples from the corneas infected with Fusarium, for a sensitivity of 89%. Only three of the 14 samples from these eyes with Fusarium keratitis were positive by culture, for a sensitivity of 21%. Seven of eight control samples were negative by the PCR based test, for a specificity of 88%.
This PCR based test holds promise of being an effective method of diagnosing Fusarium keratitis as well as Fusarium infections at other sites.
目的/背景:本研究的目的是应用聚合酶链反应(PCR)开发一种灵敏、特异且快速的检测方法,以诊断镰刀菌性角膜炎。在世界某些地区,镰刀菌是真菌性角膜感染最常见的病因。通常很难确定角膜炎是否由真菌感染引起。
通过向前房角膜基质注射真菌悬液,在三只兔子的三只眼睛中诱发茄病镰刀菌角膜炎。在一只兔子中,对侧眼作为对照。接种后4至28天,刮取角膜进行培养,然后刮取并擦拭角膜用于PCR分析。使用针对镰刀菌角质酶基因一部分的引物进行PCR,并通过琼脂糖凝胶确定是否存在该扩增的靶序列。
在28份感染镰刀菌的角膜样本中,有25份检测到扩增的DNA序列,灵敏度为89%。在这些患有镰刀菌性角膜炎的眼睛的14份样本中,只有3份培养呈阳性,灵敏度为21%。基于PCR的检测中,8份对照样本中有7份为阴性,特异性为88%。
这种基于PCR的检测方法有望成为诊断镰刀菌性角膜炎以及其他部位镰刀菌感染的有效方法。