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North African gundis (Ctenodactylus gundi) were trapped in the Leishmania (L.) tropica focus of cutaneous leishmaniasis, situated in southeast Tunisia and evaluated for Leishmania infection by real-time kinetoplast DNA polymerase chain reaction (PCR). Species identification was performed by internal transcribed spacer one (ITS1)-PCR-restriction fragment length polymorphism (RFLP) and high-resolution melting (HRM) analysis of the 7SL RNA gene. Real-time PCR on blood was positive in 6 of 13 (46.2%) tested gundis. Leishmania tropica was identified in five infected gundis and Leishmania major in one specimen. Alignments of the ITS-1 DNA sequences and 7S-HRM curves analysis indicated that similar genotypes were present in humans, a sandfly, and gundis from the same region suggesting a potential role of this rodent as reservoir host of L. tropica in southeast Tunisia.
Financial support: This study was supported by the network of Pasteur Institutes (Actions Concertées Inter-Pasteuriennes, ACIP A 04 2007).
Authors' addresses: Nadia Bousslimi, Soumaya Ben-Ayed, Imène Ben-Abda, Karim Aoun, and Aïda Bouratbine, Laboratoire de Parasitologie, Institut Pasteur de Tunis, Tunis Belvédère, Tunisia, E-mails: nguetari@gmail.com, Soumayatba@yahoo.fr, benabda.imen@gmail.com, karim.aoun@pasteur.rns.tn, and aida.bouratbine@pasteur.rns.tn.