Please use this identifier to cite or link to this item:
http://sgc.anlis.gob.ar/handle/123456789/2658
DC Field | Value | Language |
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dc.contributor.author | Cimino, Rubén Oscar | es |
dc.contributor.author | Jeun, Rebecca | es |
dc.contributor.author | Juarez, Marisa | es |
dc.contributor.author | Cajal, Pamela S. | es |
dc.contributor.author | Vargas, Paola | es |
dc.contributor.author | Echazú, Adriana | es |
dc.contributor.author | Bryan, Patricia E. | es |
dc.contributor.author | Nasser, Julio R. | es |
dc.contributor.author | Krolewiecki, Alejandro J. | es |
dc.contributor.author | Mejia, Rogelio | es |
dc.date.accessioned | 2025-08-07T16:21:28Z | - |
dc.date.available | 2025-08-07T16:21:28Z | - |
dc.date.issued | 2015-07-17 | - |
dc.identifier.uri | http://sgc.anlis.gob.ar/handle/123456789/2658 | - |
dc.description.abstract | 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. | es |
dc.language.iso | en_US | es |
dc.publisher | Parasit Vectors | es |
dc.subject | Intestinal parasites | es |
dc.subject | Molecular diagnostics | es |
dc.subject | Prevalence | es |
dc.subject | Argentina | es |
dc.subject | Hookworm speciation | es |
dc.subject | Real-time PCR | es |
dc.title | Identification of human intestinal parasites affecting an asymptomatic peri-urban Argentinian population using multi-parallel quantitative real-time polymerase chain reaction | es |
dc.type | Artículo | es |
dc.identifier.doi | 10.1186/s13071-015-0994-z | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.fulltext | With Fulltext | - |
item.languageiso639-1 | en_US | - |
item.grantfulltext | open | - |
item.openairetype | Artículo | - |
Appears in Collections: | Parasitosis intestinales en Argentina |
Files in This Item:
File | Description | Size | Format | |
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03. Cimino et al. Parasites & Vectors (2015) 8,380.pdf | 616.82 kB | Adobe PDF | View/Open |
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