Congopain genes diverged to become specific to Savannah, Forest and Kilifi subgroups of Trypanosoma congolense, and are valuable for diagnosis, genotyping and phylogenetic inferences

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dc.contributor.author Rodrigues, Adriana C.
dc.contributor.author Ortiz, Paola A.
dc.contributor.author Costa-Martins, André G.
dc.contributor.author Das Neves, Luis Carlos Bernardo G.
dc.contributor.author Garcia, Herakles A.
dc.contributor.author Alves, João M.P.
dc.contributor.author Camargo, Erney P.
dc.contributor.author Alfieri, Silvia C.
dc.contributor.author Gibson, Wendy
dc.contributor.author Teixeira, Marta M.G.
dc.date.accessioned 2015-11-09T06:17:04Z
dc.date.available 2015-11-09T06:17:04Z
dc.date.issued 2014-04
dc.description.abstract Trypanosoma congolense is the most important agent of nagana, a wasting livestock trypanosomosis in sub-Saharan Africa. This species is a complex of three subgroups (Savannah, Forest and Kilifi) that differ in virulence, pathogenicity, drug resistance, vectors, and geographical distribution. Congopain, the major Cathepsin L-like cysteine protease (CP2) of T. congolense, has been extensively investigated as a pathogenic factor and target for drugs and vaccines, but knowledge about this enzyme is mostly restricted to the reference strain IL3000, which belongs to the Savannah subgroup. In this work we compared sequences of congopain genes from IL3000 genome database and isolates of the three subgroups of T. congolense. Results demonstrated that the congopain genes diverged into three subclades consistent with the three subgroups within T. congolense. Laboratory and field isolates of Savannah exhibited a highly polymorphic repertoire both inter- and intra-isolates: sequences sharing the archetypical catalytic triad clustered into SAV1–SAV3 groups, whereas polymorphic sequences that, in general, exhibited unusual catalytic triad (variants) assigned to SAV4 or not assigned to any group. Congopain homologous genes from Forest and Kilifi isolates showed, respectively, moderate and limited diversity. In the phylogenetic tree based on congopain and homologues, Savannah was closer to Forest than to Kilifi. All T. congolense subgroup nested into a single clade, which together with the sister clade formed by homologues from Trypanosoma simiae and Trypanosoma godfreyi formed a clade supporting the subgenus Nannomonas. A single PCR targeting congopain sequences was developed for the diagnosis of T. congolense isolates of the three subgroups. Our findings demonstrated that congopain genes are valuable targets for the diagnosis, genotyping, and phylogenetic and taxonomic inferences among T. congolense isolates and other members of the subgenus Nannomonas. en_ZA
dc.description.librarian hb2015 en_ZA
dc.description.sponsorship Brazilian agency CNPq within the PROAFRICA and UNIVERSAL programs. Adriana C. Rodrigues is a postdoctoral fellow of PNPD-CAPES, and Paola A. Ortiz and André G. Martins are recipients of scholarships from PROTAX-CNPq. en_ZA
dc.description.uri http://www.elsevier.com/locate/meegid en_ZA
dc.identifier.citation Rodrigues, AC, Ortiz, PA, Costa-Martins, AG, Neves, LCBG, Garcia, HA, Alves, JMP, Camargo, EP, Alfieri, SC, Gibson, W & Teixeira, MMG 2014, 'Congopain genes diverged to become specific to Savannah, Forest and Kilifi subgroups of Trypanosoma congolense, and are valuable for diagnosis, genotyping and phylogenetic inferences', Infection, Genetics and Evolution, vol. 23, pp. 20-31. en_ZA
dc.identifier.issn 1567-1348 (print)
dc.identifier.issn 1567-7257 (online)
dc.identifier.other 10.1016/j.meegid.2014.01.012
dc.identifier.uri http://hdl.handle.net/2263/50380
dc.language.iso en en_ZA
dc.publisher Elsevier en_ZA
dc.relation.requires Adobe Acrobat Reader en
dc.rights © 2014 Elsevier B.V. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in Infection, Genetics and Evolution. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Infection, Genetics and Evolution, vol. 23, pp. 20-31, 2014. doi : 10.1016/j.meegid.2014.01.012. en_ZA
dc.subject Trypanosoma congolense en_ZA
dc.subject Congopain en_ZA
dc.subject Savannah en_ZA
dc.subject Forests en_ZA
dc.subject Kilifi en_ZA
dc.subject Genotyping en_ZA
dc.title Congopain genes diverged to become specific to Savannah, Forest and Kilifi subgroups of Trypanosoma congolense, and are valuable for diagnosis, genotyping and phylogenetic inferences en_ZA
dc.type Postprint Article en_ZA


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