Usa Lek-UthaiRangsima PassaraKosol RoongruangchaiPrayute BuddhirakkulNitaya ThammapalerdMahidol UniversityFaculty of Medicine, Thammasat University2018-09-132018-09-132009-04-01Experimental Parasitology. Vol.121, No.4 (2009), 342-34510902449001448942-s2.0-61349101762https://repository.li.mahidol.ac.th/handle/20.500.14594/27723A method employing loop-mediated isothermal amplification (LAMP) of 18S ribosomal RNA gene was developed to detect Acanthamoeba in contact lens cases. A prevalence of 7% (10/150) was detected, with 100% sensitivity and 100% specificity when compared with the standard culture technique. Using visual inspection of turbidity a minimum of 10 pg of Acanthamoeba DNA could be detected, 10 times more sensitive than quantitative PCR employing two of the LAMP primers. The production of LAMP amplicons was confirmed by gel-electrophoresis and ethidium bromide staining. The LAMP procedure takes less than 2 h to perform and will be useful for incorporation into a point-of-care screening of suspected Acanthamoeba infection. © 2008 Elsevier Inc. All rights reserved.Mahidol UniversityImmunology and MicrobiologyArticleSCOPUS10.1016/j.exppara.2008.12.009