Infection of ILeishmania donovani/I in IPhlebotomus orientalis/I Sand Flies at Different Microhabitats of a Kala-Azar Endemic Village in Eastern Sudan

• Published in: Tropical medicine and infectious disease Vol. 9; no. 2
• Main Authors: Khogali, Altayeb, Elnaiem, Dia-Eldin A, Díaz-Regañón, Ramón, Jibreel, Tayseer, Nour, Bakri Y. M, Abdelrahman, Samira Hamid, Molina, Ricardo, Jiménez, Maribel
• Format: Journal Article
• Language: English
• Published: MDPI AG 01.02.2024
• Subjects: DNA sequencing; Infection; Nucleotide sequencing; South Sudan; Ethiopia; Sudan; Spain
• ISSN: 2414-6366; 2414-6366
• DOI: 10.3390/tropicalmed9020040

A study was carried out to compare the infection rates of Leishmania donovani in Phlebotomus orientalis sandflies at different microhabitats of a VL endemic village in Gedarif state, Sudan. DNA extracts of 1078 P. orientalis sand fly females sampled by CDC light traps from indoor, outdoor, peri-domestic, and sylvatic sites, in three transmission seasons, March–June 2016–18, in Helat-Belo village, were subjected to independent PCR amplifications targeting Leishmania kDNA and the cpb gene followed by ITS1 region sequencing. Leishmania kDNA was detected in 1.4% of the 1078 P. orientalis females captured in the area. Two of these specimens showed a characteristic 741 bp band of L. donovani after cpb gene amplification. The DNA sequence of the ITS1 region of the parasites matched the ITS1 L. donovani genotype F. There were no signficant differences between rates of infection of L. donovani in P. orientalis captured at different sites. Blood meals found in infected flies origninated from human (5 specimens), cattle (4 specimens) and donkey (2 specimens). The finding of fresh cow and donkey blood in the infected flies suggests the possible role of these animals in the zoopotentiation and/or zooprophylaxis against VL. The study provides important information for VL transmission models and control programs in East Africa.