IIBIO   27936
INSTITUTO DE INVESTIGACIONES BIOTECNOLOGICAS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Moving forward Strongyloides stercoralis detection, studying molecular typing as infection follow up strategy in immunocompromised patients
Autor/es:
BATALLA, ESTELA I; ALBA SOTO, CATALINA D.; REPETTO, SILVIA ANALIA; BURGOS, JUAN M.; RISSO, MARIKENA G.; ARGUELLO, LISANA; GONZALEZ-CAPPA, STELLA MARIS; RUYBAL, PAULA
Lugar:
CABA
Reunión:
Congreso; 18th International Congress on Infectious Diseases (ICID), Buenos Aires, Argentina; 2018
Institución organizadora:
Sociedad Argentina de Infectología; International Society for Infectious Diseases
Resumen:
Moving forward Strongyloides stercoralis detection, studying molecular typing as infection follow up strategy in immunocompromised patientsAuthorsS. Repetto1, L. Argüello1, E. Batalla1, J. Burgos2, S. Gonzalez Cappa1, C. Alba Soto1, M. Risso1, P. Ruybal1; 1Universidad de Buenos Aires, Instituto de Investigaciones en Microbiología y Parasitología Médica, Caba/AR, 2Universidad de San Martín, Instituto de Investigaciones Biotecnológicas, San Martín/ARKeywordsStrongyloides stercoralis/ immunocompromised patients/molecular typingBackgroundStrongyloides stercoralis is a geohelminth which affects 10-40% of the world population in tropical and subtropical areas. It produces chronic infections and severe symptoms in immunocompromised patients with high mortality. Although the parasitological cure is defined as the absence of larvae after one year of treatment, we have observed reactivations after the second year. We evaluated genetic diversity and its possible association with the clinical characteristics and evolution of this parasitosis.Methods & MaterialsTwenty-two patients (18 immunocompromised) with diagnosis and follow-up of strongyloidosis from Argentina, Bolivia, Paraguay, Peru and Dominican Republic were evaluated. The DNA extracted from stool sample at the time of diagnosis was used as a template for amplification and sequencing of a 404 bp region of the mitochondrial gene cox1. The analysis of sequences was: consensus assembly (STADEN), alignment (MEGA6), haplotype resolution (PHASE, DNAsp), allele coding and discriminatory power calculation (PD, MLSTest). Sequences were analyzed in the context of sequences of S. stercoralis (581), S. fuelleborni, S. ratti, S. venezuelensis, S. planiceps, S. mirzai and S. papillosus. Results were expressed in frequencies and percentages. Level of significance was p0.05). However, in all immunocompromised patients who reactivated (7/18), the HP24 variant of the parasite was detected. The presence of HP24 increased the risk of reactivation with a RR of 2.16 (p