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

dc.contributor.authorRodrigues, Adriana C.
dc.contributor.authorOrtiz, Paola A.
dc.contributor.authorCosta-Martins, André G.
dc.contributor.authorDas Neves, Luis Carlos Bernardo G.
dc.contributor.authorGarcia, Herakles A.
dc.contributor.authorAlves, João M.P.
dc.contributor.authorCamargo, Erney P.
dc.contributor.authorAlfieri, Silvia C.
dc.contributor.authorGibson, Wendy
dc.contributor.authorTeixeira, Marta M.G.
dc.date.accessioned2015-11-09T06:17:04Z
dc.date.available2015-11-09T06:17:04Z
dc.date.issued2014-04
dc.description.abstractTrypanosoma 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.librarianhb2015en_ZA
dc.description.sponsorshipBrazilian 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.urihttp://www.elsevier.com/locate/meegiden_ZA
dc.identifier.citationRodrigues, 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.issn1567-1348 (print)
dc.identifier.issn1567-7257 (online)
dc.identifier.other10.1016/j.meegid.2014.01.012
dc.identifier.urihttp://hdl.handle.net/2263/50380
dc.language.isoenen_ZA
dc.publisherElsevieren_ZA
dc.relation.requiresAdobe Acrobat Readeren
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.subjectTrypanosoma congolenseen_ZA
dc.subjectCongopainen_ZA
dc.subjectSavannahen_ZA
dc.subjectForestsen_ZA
dc.subjectKilifien_ZA
dc.subjectGenotypingen_ZA
dc.titleCongopain genes diverged to become specific to Savannah, Forest and Kilifi subgroups of Trypanosoma congolense, and are valuable for diagnosis, genotyping and phylogenetic inferencesen_ZA
dc.typePostprint Articleen_ZA

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