Abstract

Since leishmaniases are zoonotic vector-borne diseases transmitted through the bites of infected female sand flies, identification of the sources of imbibed blood meals and the detection and identification of leishmanial DNA in them are important in discerning animal reservoirs, clarifying the epidemiology and facilitating control of local leishmaniases. CDC light traps, aspirators and sticky paper traps were used to collect sand flies in four Palestinian foci of both, CL and VL. Phlebotomine species identification was based on morphological keys. Female specimens were screened to detect and identify leishmanial infections, using kDNA-PCR and ITS1-PCR, and engorged female specimens were analyzed to identify the origin of their blood meals, using an RDB blood meal assay based on the amplification of the cytochrome b gene (cytb) of vertebrate mitochondrial DNA (mtDNA). Twenty sand fly species, 11 of the genus Phlebotomus and nine the genus Sergentomyia, were identified. The most abundant species was Ph. papatasi (33.7%), followed by Ph. sergenti (21%). Among the 691 female sand fly specimens, 18.5% (128/691) were positive for leishmanial DNA, using the kDNA-PCR and 6.4% (44/691) were positive using the ITS1-PCR. DNA from parasites of the genus Leishmania was identified in only 1.5% of the infected sand flies. That of Leishmania tropica parasites was detected in six female specimens of Ph. sergenti and that of L. major parasites in two female specimens of Ph. papatasi. Interestingly, two engorged females of the species Se. (Neophlebotomus) sp. were positive for L. tropica DNA. Ninety engorged female sand flies of Ph. papatasi and 104 of Ph. sergenti had fed on a large variety of vertebrate hosts such as humans, hyraxes, rats, cows, goats and birds. Regarding blood-meals showing a mixture from different species of animal host, hyrax and rat blood was revealed in 8/104 (7.7%) females of Ph. sergenti. Detection of hyrax blood in engorged female sand flies of the species Ph. sergenti supports the role of hyraxes being a potential reservoir of L. tropica in Palestinian regions. Rat blood meals might be significant since a few strains L. tropica and L. infantum were isolated from rats. Further studies must be undertaken before conclusions could be drawn.

Highlights

  • In the Palestinian Authority, zoonotic cutaneous leishmaniasis (CL) caused mainly by L. tropica and L. major is considered a public health problem

  • The transmission cycle of CL caused by L. tropica has not been fully elucidated and relatively little information is available on its epidemiology in the Palestinian Authority

  • For the first time, we report the presence of DNA from parasites of the species L. tropica in a female sand fly of the genus Sergentomyia and subgenus Neophlebotomus but of unidentified species, where the identification was based on morphological characteristics of spermathecae, cibarium teeth and the length of A3 (Antennal segment 3)

Read more

Summary

Introduction

In the Palestinian Authority, zoonotic cutaneous leishmaniasis (CL) caused mainly by L. tropica and L. major is considered a public health problem. Vectorial competence of Ph. sergenti has been studied and compared with the three Old World species of Leishmania L. tropica, L. major and L. infantum [1]. Ph. sergenti showed high specificity for strains of L. tropica and lost artificially fed infections of L. major and L. infantum after voiding the remnants of the digested blood meals. This and similar findings in neighbouring regions suggest that Ph. sergenti is, probably, the vector of L. tropica in the Palestinian Authority [2]. Identification of blood meals ingested by hematophagous arthropods is important for determining their preferred reservoir hosts and, their vectorial capacity for pathogens [3]. Several molecular biological methods have been applied successfully to blood meal analysis of different haematophagous insects in elucidating their natural host-feeding preferences and host-feeding arrays [5,6,7]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call