Development and evaluation of real-time loop-mediated isothermal amplification assay for rapid detection of cystic echinococcosis. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Ahmed, Mohamed; Eldigail, Mawahib; Elamin, Fatima; Ali, Ibtisam; Grobusch, Martin; Aradaib, Imadeldin
• Is Part Of: BMC veterinary research. Volume 12:Issue 1(2016)
• Page Start: 1
• Page End: 10
• Publication Date: 2016-12
• Subjects: LAMP -- Cystic echinococcosis -- Echinococcus granulosus-complex -- Hydatid cysts -- Sudan; Veterinary medicine -- Research -- Periodicals; Veterinary medicine -- Periodicals; 636.0890724
• DOI: 10.1186/s12917-016-0809-2
• Languages: English
• ISSNs: 1746-6148

Abstract

Abstract Background Cystic echinococcosis (CE) or hydatidosis, caused by the larval stage ofEchinococcus granulosus (EG)-complex, is a neglected parasitic disease of public health importance. The disease is endemic in many African and Mediterranean countries including the Sudan. The objective of the present study was to develop and evaluate a real-time loop-mediated isothermal amplification (LAMP) assay for simple and rapid detection of CE in humans and domestic live stock in Sudan. Methods A set of six LAMP primers, designed from the mitochondrial NADH-1 gene of EG cattle strain of genotype 5 (G5), was used as a target for LAMP assay. The assay was performed at a constant temperature (63 °C), with a real-time follow-up using a LightCycler and fluorochrome dye. Following amplification cycles in a simple water bath, LAMP products were observed for color change by naked eye and were visualized under UV light source using agarose gel electrophoresis. Results The real-time LAMP assay identified a variety of hydatid cysts strains recovered in the Sudan, includingEchinococcus canadenses (G6)and Echinococcus ortleppi (G5). Real-time LAMP positive results were detected by the presence of an amplification curve, whereas negative results were indicated by absence of fluorescence detection. Positive LAMP results appeared as a bluish-colored reaction as observed by naked eye, whereas negative LAMP results were observed as purple-colored reaction. The sensitivity studies indicated that the LAMP assay detected as little as a 10 fg of parasite DNA. There was 100 % agreement between results of the LAMP assay and our previously described nested PCR when testing 10-fold serial dilution of DNA extracted from EG-complex hydatid cyst. However, there was no cross-reactivity with other parasites includingcysticercus bovis, Fasciola gigantica, and Schistosoma bovis and nucleic acid free samples. Conclusion The developed LAMP assay would be expected to prove highly significant in epidemiological surveys of CE in developing countries or areas of resource-poor settings for both ease of use and cost.