Vengayil Sujith, Panda Anita, Satpathy Gita, Nayak Niranjan, Ghose Supriyo, Patanaik Dipika, Khokhar Sudarshan
Department of Ophthalmology, Dr. Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.
Invest Ophthalmol Vis Sci. 2009 Jan;50(1):152-6. doi: 10.1167/iovs.07-1283. Epub 2008 Aug 8.
To assess the utility of polymerase chain reaction (PCR) in diagnosing fungal keratitis and compare its sensitivity and specificity with those of the conventional microbiologic techniques used in the authors' laboratory.
A prospective nonrandomized investigation was undertaken at a tertiary-care ophthalmic facility to evaluate 40 eyes of 40 patients with presumed fungal keratitis, both fresh and treated. Besides routine bacterial culture and sensitivity, corneal scrapings were evaluated by fungal culture, potassium hydroxide (KOH) wet mount, Gram's stain, and PCR. The conventional PCR technique was followed with minor modifications to suit the setup, using primers targeted to 28S rRNA sequence, which is common to all fungi that cause corneal infections in tropical climes.
Of the 40 presumed cases of mycotic keratitis (30 untreated), PCR showed positivity in 50%, culture in 25%, hyphae in KOH in 40%, and Gram's staining in 35%. The sensitivities of PCR, KOH, and Gram's were 70%, 60%, and 40% and specificities 56.7%, 66.7%, and 66.7%, respectively. Among 10 of 40 eyes pretreated with antifungal agents, PCR was positive in 50%, but culture in 30%. The time taken for PCR assay was 4 to 8 hours, whereas positive fungal cultures took at least 5 to 7 days.
PCR not only proved an effective rapid method for the diagnosis of fungal keratitis, but was also more sensitive in our hands than KOH wetmount and Gram's smear. Barring the potential limitations, PCR remains a promising tool for faster diagnoses of fungal keratitis.
评估聚合酶链反应(PCR)在诊断真菌性角膜炎中的效用,并将其敏感性和特异性与作者所在实验室使用的传统微生物学技术进行比较。
在一家三级眼科医疗机构进行了一项前瞻性非随机研究,以评估40例疑似真菌性角膜炎患者的40只眼睛,包括未经治疗和已治疗的。除了常规细菌培养和药敏试验外,还通过真菌培养、氢氧化钾(KOH)湿片、革兰氏染色和PCR对角膜刮片进行评估。遵循传统的PCR技术并进行了微小修改以适应实验设置,使用针对28S rRNA序列的引物,该序列是热带地区所有引起角膜感染的真菌所共有的。
在40例疑似真菌性角膜炎病例中(30例未经治疗),PCR阳性率为50%,培养阳性率为25%,KOH湿片中发现菌丝的比例为40%,革兰氏染色阳性率为35%。PCR、KOH和革兰氏染色的敏感性分别为70%、60%和40%,特异性分别为56.7%、66.7%和66.7%。在40只眼中,有10只眼在使用抗真菌药物预处理后,PCR阳性率为50%,而培养阳性率为30%。PCR检测所需时间为4至8小时,而真菌培养阳性至少需要5至7天。
PCR不仅被证明是诊断真菌性角膜炎的一种有效的快速方法,而且在我们的操作中比KOH湿片和革兰氏涂片更敏感。尽管存在潜在局限性,但PCR仍然是快速诊断真菌性角膜炎的一个有前景的工具。