Comparative genomic analysis of three Leishmania species that cause diverse human disease
By C. Peacock, K. Seeger, D. Harris, L. Murphy, J. Ruiz, M. Quail, N. Peters, E. Adlem, Adrian R. N. Tivey, M. Aslett and 32 more. Nature Genetics, 2007
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Leishmania parasites cause a broad spectrum of clinical disease. Here we report the sequencing of the genomes of two species of Leishmania: Leishmania infantum and Leishmania braziliensis. The comparison of these sequences with the published genome of Leishmania major reveals marked conservation of synteny and identifies only ∼200 genes with a differential distribution between the three species. L. braziliensis, contrary to Leishmania species examined so far, possesses components of a putative RNA-mediated interference pathway, telomere-associated transposable elements and spliced leader–associated SLACS retrotransposons. We show that pseudogene formation and gene loss are the principal forces shaping the different genomes. Genes that are differentially distributed between the species encode proteins implicated in host-pathogen interactions and parasite survival in the macrophage.
Subfields: Epidemiology, Parasitology, Public Health, Environmental and Occupational Health
View Paper: https://www.semanticscholar.org/paper/736a95f8b3fa0e1212df3eba1abe1607a6643b37
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Citations in the corpus
- TriTrypDB: a functional genomic resource for the Trypanosomatidae (2009, background): “braziliensis Viannia strain (35 chromosomes, 32Mb) (9); and L.”