Paromomycin is an aminoglycoside antibiotic approved in 2006 for the treatment of visceral leishmaniasis caused by
Leishmania donovani
in Southeast Asia. Although this drug is not approved for the treatment of visceral and cutaneous leishmaniasis in Brazil, it is urgent and necessary to evaluate the potential of this drug as alternative for the treatment against species responsible for these clinical forms of the disease. In Brazil,
Leishmania amazonensis
is responsible for cutaneous and diffuse cutaneous leishmaniasis. The diffuse cutaneous form of the disease is difficult to treat and frequent relapses are reported, mainly when the treatment is interrupted. Here, we evaluated paromomycin susceptibility
in vitro
of a
L. amazonensis
clinical isolate from a patient with cutaneous leishmaniasis and the reference strain
L. amazonensis
M2269, as well as its
in vivo
efficacy in a murine experimental model
.
Although never exposed to paromomycin, a significant differential susceptibility between these two lines was found. Paromomycin was highly active
in vitro
against the clinical isolate in both forms of the parasite, while its activity against the reference strain was less active.
In vivo
studies in mice infected with each one of these lines demonstrated that paromomycin reduces lesion size and parasite burden and a direct correlation between the susceptibility
in vitro
and the effectiveness of this drug
in vivo
was found. Our findings indicate that paromomycin efficacy
in vivo
is dependent on intrinsic susceptibility of the parasite. Beyond that, this study contributes for the evaluation of the potential use of paromomycin in chemotherapy of cutaneous leishmaniasis in Brazil caused by
L. amazonensis
.