Phenotype evaluation of human and canine isolates of Leishmania infantum

Comp Immunol Microbiol Infect Dis. 2020 Dec:73:101551. doi: 10.1016/j.cimid.2020.101551. Epub 2020 Sep 17.

Abstract

Human visceral leishmaniasis (VL) and canine leishmaniasis (CanL) in countries of South and Central America are caused by Leishmania infantum and has been endemic in Brazil for several years. The parasite biodiversity as well as the pharmacologic properties of drugs and the host species, are involved in the efficacy or inefficacy of leishmaniasis treatments. Although there are substantial number of reports describing the genetic characterization of the clinical field isolates of L. infantum,the phenotypic parameters have been less studied. In this study isolates from human and canine leishmaniasis (Hum1 and Can1) obtained in Campinas, São Paulo state, Brazil were identified as L. infantum. The Hum1 and Can1 isolates exhibited typical promastigote growth pattern. Regarding morphological features Can1 isolate differed in cell size. The infectivity in vitro of both isolatesis lower compared to the reference strain of L. infantum. Moreover, the in vivo infectivity of the three parasites is similar in Balb/c mice. The Hum1 isolate is more sensitive to leishmanial drugs (amphotericin B, miltefosine and glucantime) than the Can1 isolate when inside human macrophages, but not when inside canine macrophages. These findings indicated that L. infantum isolates differs in some phenotypic characteristics.

Keywords: Canine leishmaniasis; Clinical isolates; Leishmaniainfantum; Macrophage; Mice; Visceral leishmaniasis.

MeSH terms

  • Animals
  • Brazil / epidemiology
  • Cell Line
  • Child
  • Dog Diseases / drug therapy
  • Dog Diseases / epidemiology
  • Dog Diseases / parasitology*
  • Dogs
  • Endemic Diseases
  • Female
  • Humans
  • Leishmania infantum / classification*
  • Leishmania infantum / genetics
  • Leishmania infantum / growth & development
  • Leishmania infantum / isolation & purification
  • Leishmaniasis, Visceral / drug therapy
  • Leishmaniasis, Visceral / epidemiology
  • Leishmaniasis, Visceral / parasitology*
  • Macrophages / cytology
  • Macrophages / parasitology
  • Mice
  • Mice, Inbred BALB C
  • Phenotype
  • Polymerase Chain Reaction