KDNA genetic signatures obtained by LSSP-PCR analysis of Leishmania (Leishmania) infantum isolated from the new and the old world

PLoS One. 2012;7(8):e43363. doi: 10.1371/journal.pone.0043363. Epub 2012 Aug 17.

Abstract

Background: Visceral Leishmaniasis (VL) caused by species from the Leishmania donovani complex is the most severe form of the disease, lethal if untreated. VL caused by Leishmania infantum is a zoonosis with an increasing number of human cases and millions of dogs infected in the Old and the New World. In this study, L. infantum (syn. L.chagasi) strains were isolated from human and canine VL cases. The strains were obtained from endemic areas from Brazil and Portugal and their genetic polymorphism was ascertained using the LSSP-PCR (Low-Stringency Single Specific Primer PCR) technique for analyzing the kinetoplastid DNA (kDNA) minicircles hypervariable region.

Principal findings: KDNA genetic signatures obtained by minicircle LSSP-PCR analysis of forty L. infantum strains allowed the grouping of strains in several clades. Furthermore, LSSP-PCR profiles of L. infantum subpopulations were closely related to the host origin (human or canine). To our knowledge this is the first study which used this technique to compare genetic polymorphisms among strains of L. infantum originated from both the Old and the New World.

Conclusions: LSSP-PCR profiles obtained by analysis of L. infantum kDNA hypervariable region of parasites isolated from human cases and infected dogs from Brazil and Portugal exhibited a genetic correlation among isolates originated from the same reservoir, human or canine. However, no association has been detected among the kDNA signatures and the geographical origin of L. infantum strains.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Brazil
  • DNA Primers / genetics
  • DNA, Kinetoplast / chemistry
  • DNA, Kinetoplast / genetics*
  • DNA, Protozoan / genetics*
  • Dog Diseases / parasitology
  • Dogs
  • Genotype
  • Humans
  • Leishmania infantum / classification
  • Leishmania infantum / genetics*
  • Leishmania infantum / isolation & purification
  • Leishmaniasis, Visceral / parasitology
  • Leishmaniasis, Visceral / veterinary
  • Molecular Sequence Data
  • Phylogeny
  • Polymerase Chain Reaction / methods*
  • Portugal
  • Sequence Analysis, DNA
  • Sequence Homology, Nucleic Acid
  • Species Specificity
  • Zoonoses / parasitology

Substances

  • DNA Primers
  • DNA, Kinetoplast
  • DNA, Protozoan

Associated data

  • GENBANK/JQ609524
  • GENBANK/JQ609525
  • GENBANK/JQ609526
  • GENBANK/JQ609527
  • GENBANK/JQ609528
  • GENBANK/JQ609529
  • GENBANK/JQ609530
  • GENBANK/JQ609531
  • GENBANK/JQ609532
  • GENBANK/JQ609533
  • GENBANK/JQ609534
  • GENBANK/JQ609535
  • GENBANK/JQ609536
  • GENBANK/JQ609537
  • GENBANK/JQ609538
  • GENBANK/JQ609539
  • GENBANK/JQ609540
  • GENBANK/JQ609541

Grants and funding

For this study, the authors received financial support from the European Community (EpiLeishNetSA - Contract n° 015407) and from Brazilian funding agencies Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG). JSCA was supported by a PhD scholarship from the Coordenaçao de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brazil. CML was supported by an undergraduate scholarship from the FAPEMIG, Brazil. The funders had no role in the study design, the data collection and analysis, the decision to publish, or preparation of the manuscript.