Species-specific field testing of Entamoeba spp. in an area of high endemicity

被引:27
作者
Heckendorn, F
N'Goran, EK
Felger, I
Vounatsou, P
Yapi, A
Oettli, A
Marti, HP
Dobler, M
Traoré, M
Lohourignon, KL
Lengeler, C
机构
[1] Swiss Trop Inst, Dept Publ Hlth & Epidemiol, CH-4002 Basel, Switzerland
[2] Ctr Suisse Rech Sci, Abidjan 01, Cote Ivoire
[3] Univ Cocody, URF Biosci, Lab Biol Anim, Abidjan 22, Cote Ivoire
关键词
amoebiasis; Entamoeba dispar; Entamoeba histolytica; diagnosis; epidemiology; Cote d'Ivoire;
D O I
10.1016/S0035-9203(02)90426-8
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Entamoeba histolytica has been separated in recent years into 2 morphologically identical species: the apathogenic E. dispar and the pathogenic E. histolytica, only the latter being pathogenic. Although various laboratory techniques allow discrimination between the 2 species there is a lack of field data about the suitability of available diagnostic tests for use in epidemiological studies and few epidemiological studies using species-specific diagnosis have been performed at community level in endemic areas, especially in sub-Saharan Africa. We conducted a repeated cross-sectional study of 967 schoolchildren in central Cote d'Ivoire to compare and evaluate light microscopy, 2 different antigen detection assays, and one polymerase chain reaction (PCR) assay. Microscopy and a non-specific antigen capture Entamoeba enzyme-linked immunosorbent assay (ELISA) were used for the primary screening of all children (time t(0)). The prevalence of the E. histolytica/E. dispar species complex at t(0) was 18.8% by single microscopical examination and 31.4% using the non-specific ELISA. Approximately 2 months after the initial screening, fresh stool specimens were collected on 2 consecutive days (t(1) and t(2)) from (i) all the children who were positive by microscopy at t(0) (n = 182) and (ii) 155 randomly selected children who were negative at the primary screening. These samples were tested with a second antigen detection ELISA specific for E. histolytica (n = 238) and with a species-specific PCR assay (n = 193). The second and third examinations (t(1) and t(2)) revealed an additional 43 infections with the species complex E. histolytica/E dispar, so that the cumulative microscopical prevalence for t(1) and t(2) was 27.7%. The overall prevalence of E. histolytica by species-specific ELISA antigen detection was low (0.83%), while the prevalence of E. dispar was 15%. When analysing only microscopically positive samples by PCR (n = 129), the ratio E. histolytica:E. dispar was very low (1:46), suggesting that the vast majority of Entamoeba infections in this area were apathogenic. Both species-specific tests performed well but the ELISA was easier to use for large-scale field screening.
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页码:521 / 528
页数:8
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