Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/2658
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dc.contributor.authorCimino, Rubén Oscares
dc.contributor.authorJeun, Rebeccaes
dc.contributor.authorJuarez, Marisaes
dc.contributor.authorCajal, Pamela S.es
dc.contributor.authorVargas, Paolaes
dc.contributor.authorEchazú, Adrianaes
dc.contributor.authorBryan, Patricia E.es
dc.contributor.authorNasser, Julio R.es
dc.contributor.authorKrolewiecki, Alejandro J.es
dc.contributor.authorMejia, Rogelioes
dc.date.accessioned2025-08-07T16:21:28Z-
dc.date.available2025-08-07T16:21:28Z-
dc.date.issued2015-07-17-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/2658-
dc.description.abstractBackground: In resource-limited countries, stool microscopy is the diagnostic test of choice for intestinal parasites (soil-transmitted helminths and/or intestinal protozoa). However, sensitivity and specificity is low. Improved diagnosis of intestinal parasites is especially important for accurate measurements of prevalence and intensity of infections in endemic areas. Methods: The study was carried out in Orán, Argentina. A total of 99 stool samples from a local surveillance campaign were analyzed by concentration microscopy and McMaster egg counting technique compared to the analysis by multi-parallel quantitative real-time polymerase chain reaction (qPCR). This study compared the performance of qPCR assay and stool microscopy for 8 common intestinal parasites that infect humans including the helminths Ascaris lumbricoides, Ancylostoma duodenale, Necator americanus, Strongyloides stercoralis, Trichuris trichiura, and the protozoa Giardia lamblia, Cryptosporidium parvum/hominis, and Entamoeba histolytica, and investigated the prevalence of polyparasitism in an endemic area. Results: qPCR showed higher detection rates for all parasites as compared to stool microscopy except T. trichiura. Species-specific primers and probes were able to distinguish between A. duodenale (19.1 %) and N. americanus (36.4 %) infections. There were 48.6 % of subjects co-infected with both hookworms, and a significant increase in hookworm DNA for A. duodenale versus N. americanus (119.6 fg/μL: 0.63 fg/μL, P < 0.001) respectively. qPCR outperformed microscopy by the largest margin in G. lamblia infections (63.6 % versus 8.1 %, P < 0.05). Polyparasitism was detected more often by qPCR compared to microscopy (64.7 % versus 24.2 %, P < 0.05). Conclusions: Multi-parallel qPCR is a quantitative molecular diagnostic method for common intestinal parasites in an endemic area that has improved diagnostic accuracy compared to stool microscopy. This first time use of multi-parallel qPCR in Argentina has demonstrated the high prevalence of intestinal parasites in a peri-urban area. These results will contribute to more accurate epidemiological survey, refined treatment strategies on a public scale, and better health outcomes in endemic settings.es
dc.language.isoen_USes
dc.publisherParasit Vectorses
dc.subjectIntestinal parasiteses
dc.subjectMolecular diagnosticses
dc.subjectPrevalencees
dc.subjectArgentinaes
dc.subjectHookworm speciationes
dc.subjectReal-time PCRes
dc.titleIdentification of human intestinal parasites affecting an asymptomatic peri-urban Argentinian population using multi-parallel quantitative real-time polymerase chain reactiones
dc.typeArtículoes
dc.identifier.doi10.1186/s13071-015-0994-z-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en_US-
item.grantfulltextopen-
item.openairetypeArtículo-
Appears in Collections:Parasitosis intestinales en Argentina
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