Comparative genomic analysis of human infective Trypanosoma cruzi lineages with the bat-restricted subspecies T. cruzi marinkellei

• Published in: BMC genomics Vol. 13; no. 1; p. 531
• Main Authors: Franzén, Oscar, Talavera-López, Carlos, Ochaya, Stephen, Butler, Claire E, Messenger, Louisa A, Lewis, Michael D, Llewellyn, Martin S, Marinkelle, Cornelis J, Tyler, Kevin M, Miles, Michael A, Andersson, Björn
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 05-10-2012; BioMed Central; BMC
• Subjects: Acetyltransferases - genetics; Animals; Bioinformatics; Cell culture; Cells; Chagas Disease - parasitology; Chiroptera - parasitology; Comparative analysis; Computational Biology; DNA Copy Number Variations; DNA, Protozoan - genetics; Experiments; Genes; Genetic aspects; Genetic diversity; Genetic Linkage; Genetic research; Genomes; Genomics; Humans; Medicin och hälsovetenskap; Parasites; Physiological aspects; Protozoa; Retroelements - genetics; Tropical diseases; Trypanosoma; Trypanosoma - classification; Trypanosoma - genetics; Trypanosoma cruzi; Trypanosoma cruzi - classification; Trypanosoma cruzi - genetics; United Kingdom; Sweden
• ISSN: 1471-2164; 1471-2164
• DOI: 10.1186/1471-2164-13-531

Trypanosoma cruzi marinkellei is a bat-associated parasite of the subgenus Schizotrypanum and it is regarded as a T. cruzi subspecies. Here we report a draft genome sequence of T. c. marinkellei and comparison with T. c. cruzi. Our aims were to identify unique sequences and genomic features, which may relate to their distinct niches.
The T. c. marinkellei genome was found to be ~11% smaller than that of the human-derived parasite T. c. cruzi Sylvio X10. The genome size difference was attributed to copy number variation of coding and non-coding sequences. The sequence divergence in coding regions was ~7.5% between T. c. marinkellei and T. c. cruzi Sylvio X10. A unique acetyltransferase gene was identified in T. c. marinkellei, representing an example of a horizontal gene transfer from eukaryote to eukaryote. Six of eight examined gene families were expanded in T. c. cruzi Sylvio X10. The DGF gene family was expanded in T. c. marinkellei. T. c. cruzi Sylvio X10 contained ~1.5 fold more sequences related to VIPER and L1Tc elements. Experimental infections of mammalian cell lines indicated that T. c. marinkellei has the capacity to invade non-bat cells and undergo intracellular replication.
Several unique sequences were identified in the comparison, including a potential subspecies-specific gene acquisition in T. c. marinkellei. The identified differences reflect the distinct evolutionary trajectories of these parasites and represent targets for functional investigation.