Real-time PCR for detection of Strongyloides stercoralis in human stool samples from Cote d'Ivoire: Diagnostic accuracy, inter-laboratory comparison and patterns of hookworm co-infection

被引:45
|
作者
Becker, Soeren L. [1 ,2 ,3 ]
Piraisoody, Nivetha [3 ]
Kramme, Stefanie [2 ,4 ]
Marti, Hanspeter [2 ,4 ]
Silue, Kigbafori D. [5 ,6 ]
Panning, Marcus [7 ]
Nickel, Beatrice [2 ,4 ]
Kern, Winfried V. [8 ]
Herrmann, Mathias [3 ]
Hatz, Christoph F. [2 ,4 ,9 ]
N'Goran, Eliezer K. [5 ,6 ]
Utzinger, Juerg [1 ,2 ]
von Mueller, Lutz [3 ]
机构
[1] Swiss Trop & Publ Hlth Inst, Dept Epidemiol & Publ Hlth, CH-4002 Basel, Switzerland
[2] Univ Basel, CH-4003 Basel, Switzerland
[3] Univ Saarland, Inst Med Microbiol & Hyg, D-66421 Homburg, Germany
[4] Swiss Trop & Publ Hlth Inst, Dept Med Serv & Diagnost, CH-4002 Basel, Switzerland
[5] Univ Felix Houphouet Boigny, Unite Format & Rech Biosci, Abidjan 02, Cote Ivoire
[6] Ctr Suisse Rech Sci Cote Ivoire, Dept Environm & Sante, Abidjan 01, Cote Ivoire
[7] Univ Med Ctr Freiburg, Inst Virol, D-79104 Freiburg, Germany
[8] Univ Med Ctr Freiburg, Dept Internal Med, Div Infect Dis, D-79106 Freiburg, Germany
[9] Univ Zurich, Epidemiol Biostat & Prevent Inst, CH-8001 Zurich, Switzerland
关键词
Baermann technique; Diagnostic accuracy; Hookworm; Koga agar plate culture; Real-time PCR; Strongyloides stercoralis; ETHER CONCENTRATION TECHNIQUE; SOIL-TRANSMITTED HELMINTHS; ANCYLOSTOMA-DUODENALE; MOLECULAR DIAGNOSIS; INFECTIONS; PARASITES; FLOTAC;
D O I
10.1016/j.actatropica.2015.07.019
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Human infections with the helminth species Strongyloides stercoralis encompass a wide clinical spectrum, ranging from asymptomatic carriage to life-threatening disease. The diagnosis of S. stercoralis is cumbersome and the sensitivity of conventional stool microscopy is low. New molecular tools have been developed to increase sensitivity. We compared the diagnostic accuracy of real-time PCR with microscopy for the detection of S. stercoralis and hookworm in human stool samples, and investigated the inter-laboratory agreement of S. stercoralis-specific real-time PCR in two European laboratories. Stool specimens from 256 randomly selected individuals in rural Cote d'Ivoire were examined using three microscopic techniques (i.e. Kato-Katz, Koga agar plate (MAP) and Baermann (BM)). Additionally, ethanol-fixed stool aliquots were subjected to molecular diagnosis. The prevalence of S. stercoralis and hookworm infection was 21.9% and 52.0%, respectively, whilst co-infections were detected in 35 (13.7%) participants. The diagnostic agreement between real-time PCR and microscopy was excellent when both MAP and BM tested positive for S. stercoralis, but was considerably lower when only one microscopic technique was positive. The sensitivity of KAP, BM and real-time PCR for detection of S. stercoralis as compared to a combination of all diagnostic techniques was 21.4%, 37.5% and 76.8%, respectively. The inter-laboratory agreement of S. stercoralis-specific PCR was substantial (kappa = 0.63, p <0.001). We conclude that a combination of real-time PCR and stool microscopy shows high accuracy for S. stercoralis diagnosis. Besides high sensitivity, PCR may also enhance specificity by reducing microscopic misdiagnosis of morphologically similar helminth larvae (i.e. hookworm and S. stercoralis) in settings where both helminth species co-exist. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:210 / 217
页数:8
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