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A Molecular Analysis of Sand Fly Blood Meals in a Visceral Leishmaniasis Endemic Region of Northwestern Ethiopia Reveals a Complex Host-vector System

Overview
Journal Heliyon
Specialty Social Sciences
Date 2019 Aug 7
PMID 31384683
Citations 15
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Abstract

Background: Visceral leishmaniasis (VL, or "kala-azar") is a major cause of disability and death, especially in East Africa. Its vectors, sand flies (Diptera: Psychodidae: Phlebotominae), are poorly controlled and guarded against in these regions, owing in part to a lack of understanding about their feeding behavior.

Methods: A total of 746 freshly fed female sand flies were collected in five population centers in Kafta Humera (northwestern Ethiopia), where VL is endemic. Flies were collected from habitats that ranged from inside houses to open fields, using light traps and sticky traps. Sources of sand fly blood meals were identified using enzyme-linked immunosorbent assays (ELISA) and DNA amplification with reverse-line blot analysis (PCR-RLB); 632 specimens were screened using ELISA, 408 of which had identifiable blood meals, and 114 were screened using PCR-RLB, 53 of which yielded identifications. Fly species determinations were based on morphology, and those specimens subjected to PCR-RLB were also screened for parasites using conventional PCR to amplify the nuclear marker ITS1 (internal transcribed spacer 1) with -specific primers.

Results: More than three-fourths of all sand flies collected were , and the remaining portion was comprised of nine other species. Nearly two-thirds of specimens were collected at village peripheries. The most common blood source for all flies was donkey (33.9% of all identifications), followed by cow (24.2%), human (17.6%), dog (11.8%), and goat or sheep (8.6%); mixtures of blood meals from different sources were found in 28.2% of all flies screened. Unidentified blood meals, presumably from wildlife, not domestic animals, were significantly higher in farm fields. parasites were not detected in any of the 114 flies screened, not surprising given an expected infection rate of 1-5 out of 1,000. Meals that included a mixture of human and cow blood were significantly more frequent relative to all cow meals than human blood meals were to non-cow meals, suggesting a zoopotentiative interaction between cows and humans in this system.

Conclusions: Habitat and host preferences of sand fly vectors in Kafta Humera confirmed the finding of previous reports that the main vector in the region, , is a highly opportunistic feeder that prefers large animals and is most commonly found at village peripheries. These results were similar to those of a previous study conducted in a nearby region (Tahtay Adiabo), except for the role of cattle on the prevalence of human blood meals. Preliminary examinations of blood meal data from different settings point to the need for additional surveys and field experiments to understand the role of livestock on biting risks.

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References
1.
GIBSON G, Torr S . Visual and olfactory responses of haematophagous Diptera to host stimuli. Med Vet Entomol. 1999; 13(1):2-23. DOI: 10.1046/j.1365-2915.1999.00163.x. View

2.
Killick-Kendrick R . The biology and control of phlebotomine sand flies. Clin Dermatol. 1999; 17(3):279-89. DOI: 10.1016/s0738-081x(99)00046-2. View

3.
Mukhtar M, Sharief A, el Saffi S, Harith A, Higazzi T, Adam A . Detection of antibodies to Leishmania donovani in animals in a kala-azar endemic region in eastern Sudan: a preliminary report. Trans R Soc Trop Med Hyg. 2000; 94(1):33-6. DOI: 10.1016/s0035-9203(00)90429-2. View

4.
Alexander B . Sampling methods for phlebotomine sandflies. Med Vet Entomol. 2000; 14(2):109-22. DOI: 10.1046/j.1365-2915.2000.00237.x. View

5.
Dinesh D, Ranjan A, Palit A, Kishore K, Kar S . Seasonal and nocturnal landing/biting behaviour of Phlebotomus argentipes (Diptera: Psychodidae). Ann Trop Med Parasitol. 2001; 95(2):197-202. DOI: 10.1080/00034980120041071. View