par Herrera, Claudia;Truyens, Carine ;Dumonteil, Eric;Alger, Jackeline;Sosa-Estani, Sergio;Cafferata, Maria-Luisa;Gibbons, Luz;Ciganda, Alvaro;Matute, Maria Luisa;Zúniga, Concepcion;Carlier, Yves ;Buekens, Pierre
Référence The Journal of molecular diagnostics, 21, 6, page (1095-1105)
Publication Publié, 2019-11-01
Référence The Journal of molecular diagnostics, 21, 6, page (1095-1105)
Publication Publié, 2019-11-01
Article révisé par les pairs
Résumé : | Trypanosoma cruzi, the causative agent of Chagas disease, exhibits a high genetic variability and has been classified into six discrete typing units (DTUs) named TcI through TcVI. This genetic diversity is believed to be associated with clinical characteristics and outcomes, but evidence supporting such associations has been limited. Herein, we performed a phylogenetic analysis of T. cruzi sequences of the mini-exon intergenic region obtained from a large cohort of pregnant women and newborns from Argentina, Honduras, and Mexico, to assess parasite genetic diversity and possible associations with congenital transmission. Analysis of 105 samples (including five paired samples) from maternal and umbilical cord blood indicated that T. cruzi DTU distribution was similar among pregnant women and newborns from these three countries, with a high frequency of TcII-TcV-TcVI DTUs, including mixed infections with TcI. However, phylogenetic analysis revealed that although the same parasite haplotypes circulated in these three countries, they were present at different frequencies, leading to significant geographic differences. Of importance, a strong association was observed between parasite haplotypes and congenital infection of newborns. Thus, the identification of parasite haplotypes in pregnant women, but not of parasite DTUs, may help predict congenital transmission of T. cruzi. |