Genotyping of Trypanosoma cruzi DTUs and Trypanosoma rangeli genetic groups in experimentally infected Rhodnius prolixus by PCR-RFLP

• Published in: Acta tropica Vol. 156; pp. 115 - 121
• Main Authors: Sá, Amanda R.N., Dias, Greicy B.M., Kimoto, Karen Y., Steindel, Mário, Grisard, Edmundo C., Toledo, Max Jean O., Gomes, Mônica L.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.04.2016
• Subjects: 24Sα rDNA; Animals; Brazil - epidemiology; Chagas Disease - transmission; Colombia - epidemiology; Experimental infection; Genotype; Humans; Insect Vectors - parasitology; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; RFLP-COII; Rhodnius - parasitology; Rhodnius prolixus; Triatomines; Trypanosoma cruzi; Trypanosoma cruzi - genetics; Trypanosoma cruzi - isolation & purification; Trypanosoma rangeli; Trypanosoma rangeli - genetics; Trypanosoma rangeli - isolation & purification; Experimental infection; Trypanosoma rangeli; RFLP-COII; 24Sα rDNA; Trypanosoma cruzi; Triatomines
• ISSN: 0001-706X; 1873-6254
• DOI: 10.1016/j.actatropica.2016.01.006

Experimental infection in R. prolixus with single and mixed infections with T. cruzi (TcI-TcVI) and T. rangeli (KP1+/KP1-) can be detected and genotyped by RFLP-COII/24Sα-rRNA. [Display omitted] •PCR/RFLP-COII and 24Sα rDNA discriminate all groups of T. cruzi and T. rangeli.•All T. cruzi DTUs and T. rangeli KP1+/KP1− were able to be detected in R. prolixus.•In 79.4% mixed infections both parasites were successfully detected.•In six mixed infections selection of genetic groups occurred. The specific detection and genetic typing of trypanosomes that infect humans, mammalian reservoirs, and vectors is crucial for diagnosis and epidemiology. We utilized a PCR-RFLP assay that targeted subunit II of cytochrome oxidase and 24Sα-rDNA to simultaneously detect and discriminate six Trypanosoma cruzi discrete typing units (DTUs) and two genetic groups of Trypanosoma rangeli (KP1+/KP1−) in intestinal contents of experimentally infected Rhodnius prolixus. The PCR assays showed that in 23 of 29 (79.4%) mixed infections with the six T. cruzi DTUs and mixed infections with individual DTUs and/or groups KP1+ and KP1−, both parasites were successfully detected. In six mixed infections that involved TcIII, the TcI, TcII, TcV, and TcVI DTUs predominated to the detriment of TcIII, indicating the selection of genetic groups. Interactions between different genetic groups and vectors may lead to genetic selection over TcIII. The elimination of this DTU by the immune system of the vector appears unlikely because TcIII was present in other mixed infections (TcIII/TcIV and TcIII/KP1+). Both molecular markers used in this study were sensitive and specific, demonstrating their usefulness in a wide geographical area where distinct genotypes of these two species are sympatric. Although the cellular and molecular mechanisms that are involved in parasite-vector interactions are still poorly understood, our results indicate a dynamic selection toward specific T. cruzi DTUs in R. prolixus during mixed genotype infections.