Urbanization of congenital transmission of Trypanosoma cruzi: prospective polymerase chain reaction study in pregnancy

• Published in: Transactions of the Royal Society of Tropical Medicine and Hygiene 2011-10, Vol.105 (10), p.543-549
• Main Authors: Bisio, Margarita, Seidenstein, María Elena, Burgos, Juan M., Ballering, Griselda, Risso, Marikena, Pontoriero, Rosa, Moreau, Marcelo, Altcheh, Jaime, Leguizamón, María Susana, Freilij, Hector, Marceillac, Marta, Schijman, Alejandro G.
• Format: Article
• Language: English
• Subjects: Adult; Argentina - epidemiology; Biological and medical sciences; Blotting, Western; Chagas Disease - epidemiology; Chagas Disease - genetics; Chagas Disease - transmission; Chronic Disease; Congenital infection; Discrete typing units; DNA, Kinetoplast - genetics; Enzyme-Linked Immunosorbent Assay; Female; General aspects; Humans; Infant, Newborn; Medical sciences; Minicircle signatures; Placenta; Placenta Diseases - epidemiology; Placenta Diseases - parasitology; Polymerase Chain Reaction; Pregnancy; Pregnancy Complications, Parasitic - epidemiology; Pregnancy Complications, Parasitic - genetics; Prospective Studies; Trypanosoma cruzi; Trypanosoma cruzi - genetics; Trypanosoma cruzi - pathogenicity; Urbanization
• ISSN: 0035-9203; 1878-3503
• DOI: 10.1016/j.trstmh.2011.07.003

Chagas disease ranks among the world's most neglected tropical diseases and congenital transmission is increasingly responsible for urbanization of Chagas disease in non-endemic areas. Molecular assays for amplification and profiling of parasite minicircle DNA (kDNA) and identification of discrete typing units (DTUs) were prospectively conducted in bloodstream and placental samples from pregnant women cursing chronic Chagas disease residing in Buenos Aires city. Sensitivity of kDNA-PCR increased from 75.6% to 95.6% when one to three sequential blood samples were analysed. Congenital infection (CI) was diagnosed in 3 neonates born to kDNA-PCR positive mothers, one who had transmitted CI in a previous gestation, pointing to family clustering of congenital transmission. Fourteen of 44 placental samples were kDNA-PCR positive, all from non-CI transmitting women, indicating that placental PCR is not useful for CI diagnosis. Placental PCR positivity was not related to maternal bloodstream PCR positivity and placental parasitic subpopulations not observed in bloodstream were detected by minicircle signatures. PCR targeted to intergenic regions of spliced-leader genes and serological tests using trypomastigote small surface recombinant antigens showed predominance of DTU group TcII/V/VI and only one patient infected with TcI. To our knowledge, this is the first PCR-based follow-up study of bloodstream and placental T. cruzi infections during pregnancy, including identification of DTUs. kDNA-PCR assays in serial blood samples provided high sensitivity for detection of T. cruzi DNA in pregnant women with chronic Chagas disease.