Ghosh Abhrajyoti, Basu Sayan, Datta Himadri, Chattopadhyay Dhrubajyoti
Dr. B C Guha Centre for Genetic Engineering and Biotechnology, University of Calcutta, Kolkata, India.
Am J Ophthalmol. 2007 Sep;144(3):396-403. doi: 10.1016/j.ajo.2007.05.017. Epub 2007 Jul 12.
To evaluate the polymerase chain reaction (PCR) and sequencing-based ribosomal deoxyribonucleic acid (rDNA) typing technique for rapid and sensitive diagnosis of fungal keratitis.
Laboratory investigation.
The present study included culture-based methods along with PCR and ITS2/5.8S rDNA sequencing to evaluate fungal infections in 32 corneal scrapings from patients with suspected mycotic keratitis.
Good correlation was found between the culture and PCR rDNA sequencing-based methods. We also identified fungal strains that were noncultivable in routine culture medium and fungal strains, which have been reported scarcely in previous reports from eastern Indian studies.
The PCR and rDNA sequencing-based approaches may be useful alternatives to culture-based techniques for the rapid and sensitive diagnosis of fungal keratitis. We found that clinically significant pathogenic fungal strains can be detected and differentiated by this method in a short period. This method therefore is useful for the early treatment of fungal infection.
评估基于聚合酶链反应(PCR)和测序的核糖体脱氧核糖核酸(rDNA)分型技术用于快速、灵敏诊断真菌性角膜炎的效果。
实验室研究。
本研究采用基于培养的方法以及PCR和ITS2/5.8S rDNA测序,以评估32例疑似真菌性角膜炎患者角膜刮片的真菌感染情况。
基于培养的方法与基于PCR rDNA测序的方法之间存在良好的相关性。我们还鉴定出了在常规培养基中无法培养的真菌菌株以及在印度东部以往研究报告中鲜有报道的真菌菌株。
基于PCR和rDNA测序的方法可能是基于培养的技术的有用替代方法,用于快速、灵敏地诊断真菌性角膜炎。我们发现,通过该方法可在短时间内检测和区分具有临床意义的致病真菌菌株。因此,该方法有助于真菌感染的早期治疗。