Comparison of three PCR‐based methods to detect Loa loa and Mansonella perstans in long‐term frozen storage dried blood spots

• Published in: Tropical medicine & international health Vol. 27; no. 8; pp. 686 - 695
• Main Authors: Ta‐Tang, Thuy‐Huong, Febrer‐Sendra, Begoña, Berzosa, Pedro, Rubio, José Miguel, Romay‐Barja, María, Ncogo, Policarpo, Agudo, Diego, Herrador, Zaida, Fernández‐Soto, Pedro, Muro, Antonio, Benito, Agustín
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.08.2022
• Subjects: Blood; Cytochrome; Cytochrome oxidase I; Cytochromes; Deoxyribonucleic acid; DNA; dried blood spots; Filariae; Filariasis; Loa loa; Mansonella perstans; Mathematical analysis; Microscopy; molecular diagnosis; nested‐PCR; Parasites; Polymerase chain reaction; Real time; real‐time PCR; saponin/Chelex; Saponins; Sensitivity; Mansonella perstans; Nested-PCR; Real-time PCR; saponin/Chelex; Loa loa; microscopy; Filariae; dried blood spots; molecular diagnosis
• ISSN: 1360-2276; 1365-3156
• DOI: 10.1111/tmi.13786

Objectives Loa loa and Mansonella perstans are two very common filarial species in Africa. Although microscopy is the traditional diagnostic method for human filariasis, several polymerase chain reaction (PCR) methods have emerged as an alternative approach for identifying filarial parasites. The aim of this study is to compare three molecular methods and decide which is the most suitable for diagnosing human loiasis and mansonellosis in non‐endemic regions using dried blood spot (DBS) as a medium for sample collection and storage. Methods A total of 100 DBS samples, with their corresponding thin and thick blood smears, were selected for this study. Microscopy was used as the reference method to diagnose and calculate the microfilaraemia. Filarial DNA was extracted using the saponin/Chelex method and the DNA isolated was assayed by Filaria‐real time‐PCR, filaria‐nested PCR, and cytochrome oxidase I PCR. All PCR products were subsequently purified and sequenced. The statistical values for each molecular test were calculated and compared. Results Overall, 64 samples were identified as negative by all tests and a further 36 samples were positive by at least one of the methods used. The sensitivity and specificity were similar for the different molecular methods, all of which demonstrated good agreement with microscopy. Conclusions Based on this study, and from a practical point of view (single and short amplification round), the optimal technique for diagnosing filarial infection in non‐endemic regions is filaria‐real time‐PCR, which presents high sensitivity and specificity and is also able to detect a wide range of human filariae.