First report of naturally infected Sergentomyia minuta with Leishmania major in Tunisia

Background Many sand fly species are implicated in the transmission cycle of Leishmania parasites around the world. Incriminating new sand flies species, as vectors of Leishmania is crucial to understanding the parasite–vector transmission cycle in different areas in Tunisia and surrounding countries. Findings Seventy-four unfed females belonging to the genera Sergentomyia and Phlebotomus were collected in South Tunisia between June and November 2014, using sticky papers. PCR-RFLP (Restriction Fragment Length Polymorphism) analysis of the internal transcribed spacer 1 (ITS1) was used for Leishmania parasites detection and identification. Leishmania (L.) major (Yakimoff & Shokkor, 1914) was identified within two Sergentomyia (S.) minuta (Rondani, 1843) and one Phlebotomus papatasi (Scopoli, 1786). Conclusion This is the first report of L. major identified from S. minuta in Tunisia. This novel finding enhances the understanding of the transmission cycle of L. major parasites of cutaneous leishmaniasis in an endemic area in South Tunisia.


Findings
In Tunisia and other Old World countries, sand fly species of the genus Phlebotomus are traditionally regarded as the proven vectors of Leishmania parasites. However, a few studies have recently suggested the possible involvement of some species of the genus Sergentomyia in the transmission of Leishmania, particularly in some African countries [1][2][3]. There Sergentomyia spp. are the predominant sand fly taxa, and appear able to tolerate different biotopes and environmental conditions. Although, Sergentomyia spp. are proven vectors of reptile Leishmania spp. [4] which are non-pathogenic to humans, and at least some of them feed on humans and/or mammalian reservoirs which can contain Leishmania spp. pathogenic to humans [5]. Therefore, their role as vectors in some visceral and cutaneous leishmaniasis foci where Sergentomyia spp. were abundant is suspected. Thus, the exact role of Sergentomyia spp. in transmitting mammalian leishmaniasis remains to be clarified [1,2,[5][6][7].
An epidemiological study was carried out in Gafsa governorate in southwestern Tunisia, an old emerging focus of cutaneous leishmaniasis (CL), with the objective of detecting and characterizing novel vectors of Leishmania parasites in the region.
Sand fly collections were collected from June to November 2014, using sticky papers. Verbal informed consent was obtained from residents in each of the community. Specimens were sorted and transferred to 70 % ethanol before being processed. Species identification was determined using the available morphological keys for sand fly in Tunisia [8]. Sand flies abdomens were transferred to individual sterilized 1.5 ml vials and stored at −20°C. DNA from each individual female was extracted using the QIAamp® DNA Mini Kit (QIAgen, Germany) according to the manufacturer's instructions.
The presence of the Leishmania DNA was tested by the amplification of the ribosomal internal transcribed spacer 1 (ITS1) of these parasites and followed by Restriction Fragment Length Polymorphism (RFLP) analysis in which the ITS1-PCR products were digested by HaeIII restriction enzyme using protocol previously described [9]. The following WHO reference strains of Leishmania (L.) In this study, males were not considered regarding that only females were haematophageous. Indeed, fed females were excluded from the analysis because the presence of Leishmania DNA in these specimens can be an immediate consequence of blood feeding on an infected host. Only seventy-four unfed females belonging to S. minuta (n = 24), S. fallax (n = 26), S. dreyfussi (n = 4) and P. papatasi (n = 20) were tested for the presence of Leishmania parasites DNA which should be considered as the result of the multiplication of the parasites in the gut of the sand fly. Two S. minuta and one P. papatasi were found positive for L. major DNA using the ITS1-PCR-RFLP method (Fig. 1). The detection of L. major in P. papatasi was not unexpected as this species has already been implicated as a vector of L. major in Tunisia [10]. However, our study is the first report of L. major infecting S. minuta in Tunisia, North Africa.
This preliminary finding raises the speculation and highlights the involvement of S. minuta in the zoonotic CL transmission cycle. Our results corroborate the finding in previous reports of L. major detection in S. minuta in Portugal [7] and in Sergentomyia ingrami (Newstead, 1914) in Ghana [3], respectively. L. major and Leishmania donovani (Laveran & Mesnil, 1903) DNA have previously been reported in Indian Sergentomyia spp. [5]. Some authors have reported Sergentomyia spp. as a common human-biting species, including Sergentomyia (S.) schwetzi (Adler, Theodor & Parrot, 1929) in Sudan [11], as well as Sergentomyia (Sintonius) clydei (Sinton, 1928) and Sergentomyia (Parrotomyia) africana (Newstead, 1912) [12]. Furthermore, Parvidens heischi (Kirk & Lewis, 1950) (formerly considered as belonging to the Sergentomyia genus) is a very aggressive human biter [13]. Based on faunistic evidence, another study conducted in Senegal suggesting the implication of S. schwetzi and Sergentomyia dubia (Parrot, Mornet & Cadenat, 1945) in the transmission of canine leishmaniasis [14]. In Mali, several specimens of Sergentomyia (Spelaeomyia) darlingi (Lewis & Kirk, 1954) were found positive for L. major based on DNA screening [1]. Our results, in addition to those previously described, suggest that Sergentomyia species are involved in the transmission cycle of Leishmania parasites. Therefore, the prevailing opinion that leishmaniasis are strictly transmitted by sand The present study demonstrated, for the first time, the detection of L. major DNA in S. minuta from an endemic area of cutaneous leishmaniasis in South Tunisia. This illustrates the potential role of S. minuta in the transmission cycle of L. major in Tunisia, adding useful information to address the key epidemiological questions on this disease control. However, further research should be directed to investigate the actual role of Sergentomyia species in the transmission of Leishmania parasites in different endemic regions including blood meal analysis and parasite isolation, on larger samples of this genus, are now needed to confirm their respective roles as a potential vectors for zoonotic CL caused by L. major in Tunisia.