Early molecular diagnosis of acute Chagas disease after transplantation with organs from Trypanosoma cruzi-infected donors.

TitleEarly molecular diagnosis of acute Chagas disease after transplantation with organs from Trypanosoma cruzi-infected donors.
Publication TypeJournal Article
Year of Publication2013
AuthorsCura CI, Lattes R, Nagel C, Gimenez MJ, Blanes M, Calabuig E, Iranzo A, Barcan LA, Anders M, Schijman AG
JournalAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons//Am J Transplant
Volume13
Issue12
Pagination3253 - 61
Date Published2013
ISBN Number1600-6143
Other Numbers100968638
Keywords*Chagas Disease/di [Diagnosis], *Organ Transplantation/ae [Adverse Effects], Adolescent, Adult, Aged, Algorithms, DNA, Kinetoplast/ge [Genetics], Female, Genotype, Humans, Male, Middle Aged, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length, Time Factors, Tissue Donors, Trypanosoma cruzi/ge [Genetics], Young Adult
Abstract

Organ transplantation (TX) is a novel transmission modality of Chagas disease. The results of molecular diagnosis and characterization of Trypanosoma cruzi acute infection in naive TX recipients transplanted with organs from infected deceased donors are reported. Peripheral blood and cerebrospinal fluid samples from the TX recipients of organs from infected donors were prospectively and sequentially studied for detection of T. cruzi by means of kinetoplastid DNA polymerase chain reaction (kDNA-PCR). In positive blood samples, a PCR algorithm for identification of T. cruzi Discrete Typing Units (DTUs) and quantitative real-time PCR (qPCR) to quantify parasitic loads were performed. Minicircle signatures of T. cruzi infecting populations were also analyzed using restriction fragment length polymorphism (RFLP)-PCR. Eight seronegative TX recipients from four infected donors were studied. In five, the infection was detected at 68.4 days post-TX (36-98 days). In one case, it was transmitted to two of three TX recipients. The comparison of the minicircle signatures revealed nearly identical RFLP-PCR profiles, confirming a common source of infection. The five cases were infected by DTU TcV. This report reveals the relevance of systematic monitoring of TX recipients using PCR strategies in order to provide an early diagnosis allowing timely anti-trypanosomal treatment.© Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.

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