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Título : Identification of human intestinal parasites affecting an asymptomatic peri-urban Argentinian population using multi-parallel quantitative real-time polymerase chain reaction
Autor : Cimino, Rubén Oscar 
Jeun, Rebecca 
Juarez, Marisa 
Cajal, Pamela S. 
Vargas, Paola 
Echazú, Adriana 
Bryan, Patricia E. 
Nasser, Julio R. 
Krolewiecki, Alejandro J. 
Mejia, Rogelio 
Palabras clave : Intestinal parasites;Molecular diagnostics;Prevalence;Argentina;Hookworm speciation;Real-time PCR
Fecha de publicación : 17-jul-2015
Editorial : Parasit Vectors
Resumen : 
Background: 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.
URI : http://sgc.anlis.gob.ar/handle/123456789/2658
DOI: 10.1186/s13071-015-0994-z
Aparece en las colecciones: Parasitosis intestinales en Argentina

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