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   Is PCR the next reference standard for the diagnosis of schistosoma in stool? A comparison with microscopy in Senegal and Kenya  
   
نویسنده meurs l. ,brienen e. ,mbow m. ,ochola e.a. ,mboup s. ,karanj d.m.s. ,secor w.e. ,polman k. ,van lieshout l.
منبع plos neglected tropical diseases - 2015 - دوره : 9 - شماره : 7 - صفحه:1 -16
چکیده    Background the current reference test for the detection of s. mansoni in endemic areas is stool microscopy based on one or more kato-katz stool smears. however,stool microscopy has several shortcomings that greatly affect the efficacy of current schistosomiasis control programs. a highly specific multiplex real-time polymerase chain reaction (pcr) targeting the schistosoma internal transcriber-spacer-2 sequence (its2) was developed by our group a few years ago,but so far this pcr has been applied mostly on urine samples. here,we performed more in-depth evaluation of the its2 pcr as an alternative method to standard microscopy for the detection and quantification of schistosoma spp. in stool samples. methodology/principal findings microscopy and pcr were performed in a senegalese community (n = 197) in an area with high s. mansoni transmission and co-occurrence of s. haematobium,and in kenyan schoolchildren (n = 760) from an area with comparatively low s. mansoni transmission. despite the differences in schistosoma endemicity the pcr performed very similarly in both areas; 13–15% more infections were detected by pcr when comparing to microscopy of a single stool sample. even when 2–3 stool samples were used for microscopy,pcr on one stool sample detected more infections,especially in people with light-intensity infections and in children from low-risk schools. the low prevalence of soil-transmitted helminthiasis in both populations was confirmed by an additional multiplex pcr. conclusions/significance the its2-based pcr was more sensitive than standard microscopy in detecting schistosoma spp. this would be particularly useful for s. mansoni detection in low transmission areas,and post-control settings,and as such improve schistosomiasis control programs,epidemiological research,and quality control of microscopy. moreover,it can be complemented with other (multiplex real-time) pcrs to detect a wider range of helminths and thus enhance effectiveness of current integrated control and elimination strategies for neglected tropical diseases. © 2015,plos neglected tropical diseases. all rights reserved.
آدرس department of parasitology,leiden university medical center,leiden,netherlands,department of biomedical sciences,institute of tropical medicine,antwerp, Belgium, department of parasitology,leiden university medical center,leiden, Netherlands, laboratory of bacteriology and virology,aristide le dantec teaching hospital,dakar, Senegal, center for global health research,kenya medical research institute,kisumu, Kenya, laboratory of bacteriology and virology,aristide le dantec teaching hospital,dakar, Senegal, center for global health research,kenya medical research institute,kisumu, Kenya, division of parasitic diseases and malaria,centers for disease control and prevention,atlanta,ga, United States, department of biomedical sciences,institute of tropical medicine,antwerp, Belgium, department of parasitology,leiden university medical center,leiden, Netherlands
 
     
   
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