Host competence of the African rodents Arvicanthis neumanni, A. niloticus and Mastomys natalensis for Leishmania donovani from Ethiopia and L. (Mundinia) sp. from Ghana

. 2020 Apr ; 11 () : 40-45. [epub] 20191206

Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid31879594
Odkazy

PubMed 31879594
PubMed Central PMC6920283
DOI 10.1016/j.ijppaw.2019.12.002
PII: S2213-2244(19)30244-5
Knihovny.cz E-zdroje

Visceral leishmaniasis caused by Leishmania donovani is regarded as mostly anthroponotic, but a role for animal reservoir hosts in transmission has been suggested in East Africa. Field studies in this region have shown the presence of this parasite in several mammalian species, including rodents of the genera Arvicanthis and Mastomys. Further, the natural reservoirs of Leishmania (Mundinia) sp. causing human cutaneous disease in Ghana, West Africa, are unknown. This study assessed the potential role of the Sub-Saharan rodents Arvicanthis neumanni, A. niloticus and Mastomys natalensis as hosts of L. donovani and L. sp. from Ghana, based on experimental infections of animals and xenodiagnoses. The distribution and load of parasites were determined post mortem using qPCR from the blood, skin and viscera samples. The attractiveness of Arvicanthis and Mastomys to Phlebotomus orientalis was tested by pair-wise comparisons. None of the animals inoculated with L. donovani were infectious to P. orientalis females, although, in some animals, parasites were detected by PCR even 30 weeks post infection. Skin infections were characterized by low numbers of parasites while high parasite burdens were present in spleen, liver and lymph nodes only. Therefore, wild Arvicanthis and Mastomys found infected with L. donovani, should be considered parasite sinks rather than parasite reservoirs. This is indirectly supported also by results of host choice experiments with P. orientalis in which females preferred humans over both Arvicanthis and Mastomys, and their feeding rates on rodents ranged from 1.4 to 5.8% only. Therefore, the involvement of these rodents in transmission of L. donovani by P. orientalis is very unlikely. Similarly, poor survival of Leishmania parasites in the studied rodents and negative results of xenodiagnostic experiments do not support the involvement of Arvicanthis and Mastomys spp. in the transmission cycle of L. sp. from Ghana.

Zobrazit více v PubMed

Ashford R.W. Leishmaniasis reservoirs and their significance in control. Clin. Dermatol. 1996;14:523–532. PubMed

Ashford R.W. The leishmaniases as emerging and reemerging zoonoses. Int. J. Parasitol. 2000;30:1269–1281. PubMed

Borja L.S., de Sousa O.M.F., da Silva Solcà M., Bastos L.A., Bordoni M., Magalhães J.T., Larangeira D.F., Barrouin-Melo S.M., Fraga D.B.M., Veras P.S.T. Parasite load in the blood and skin of dogs naturally infected by Leishmania infantum is correlated with their capacity to infect sand fly vectors. Vet. Parasitol. 2016;229:110–117. PubMed

Chance M.L., Schnur L.F., Thomas S.C., Peters W. Biochemical and serological taxonomy of Leishmania from Ethiopian zoogeographical region of Africa. Ann. Trop. Med. Parasitol. 1978;72:533–542. PubMed

Chaves L.F., Hernandez M.J., Dobson A.P., Pascual M. Sources and sinks: revisiting the criteria for identifying reservoirs for American cutaneous leishmaniasis. Trends Parasitol. 2007;23:311–316. PubMed

Courtenay O., Carson C., Calvo-Bado L., Garcez L.M., Quinnell R.J. Heterogeneities in Leishmania infantum infection: using skin parasite burdens to identify highly infectious dogs. PLoS Neglected Trop. Dis. 2014;8:26. PubMed PMC

Dereure J., El-safi S.H., Bucheton B., Boni M., Mohamed M., Davoust B., Pratlong F., Feugier E., Lambert M., Dessein A., Dedet J. Visceral leishmaniasis in eastern Sudan: parasite identification in humans and dogs; host-parasite relationships. Microbes Infect. 2003;5:1103–1108. PubMed

El-Hassan A.M., Zijlstra E.E., Meredith S.E.O., Ghalib H.W., Ismail A. Identification of Leishmania donovani using a polymerase chain reaction in patient and animal material obtained from an area of endemic kala-azar in the Sudan. Acta Trop. 1993;55:87–90. PubMed

Elnaiem D.A., Ward R.D., Hassan H.K., Miles M.A., Frame I.A. Infection rates of Leishmania donovani in Phlebotomus orientalis from a focus of visceral leishmaniasis in eastern Sudan. Ann. Trop. Med. Parasitol. 1998;92:229–232. PubMed

Elnaiem D.A., Hassan M.M., Maingon R., Nureldin G.H., Mekawi A.M., Miles M., Ward R.D. The egyptian mongoose, Herpestes ichneumon, is a possible reservoir host of visceral leishmaniasis in eastern Sudan. Parasitology. 2001;122:531–536. PubMed

Espinosa O.A., Serrano M.G., Camargo E.P., Teixeira M.M.G., Shaw J.J. An appraisal of the taxonomy and nomenclature of trypanosomatids presently classified as Leishmania and Endotrypanum. Parasitology. 2016;145(Special Issue 4):430–442. PubMed

Gebresilassie A., Abbasi I., Aklilu E., Yared S., Kirstein O.D., Moncaz A., Tekie H., Balkew M., Warburg A., Hailu A., Gebre-michael T. Host-feeding preference of Phlebotomus orientalis (Diptera: Psychodidae) in an endemic focus of visceral leishmaniasis in northern Ethiopia. Parasites Vectors. 2015;8:270. PubMed PMC

Gebresilassie A., Yared S., Aklilu E., Kirstein O.D., Moncaz A., Tekie H., Balkew M., Warburg A., Hailu A., Gebre-Michael T. Host choice of Phlebotomus orientalis (Diptera: Psychodidae) in animal baited experiments: a field study in Tahtay Adiyabo district, northern Ethiopia. Parasites Vectors. 2015;8:1–10. PubMed PMC

Granjon L., Ducroz J.-F. Genus Arvicanthis Grass rats. In: Happold D.C.D., editor. Mammals of Africa: Volume III. Bloomsbury Publishing; London: 2013. pp. 379–380.

Hoogstraal H., Heyneman D. Leishmaniasis in the Sudan republic. 30. Final epidemiological report. Am. J. Trop. Med. Hyg. 1969;18:1091–1210.

Howard M.K., Sayers G., Miles M.A. Leishmania donovani metacyclic promastigotes: transformation in vitro, lectin agglutination, complement resistance, and infectivity. Exp. Parasitol. 1987;64:147–156. PubMed

Kassahun A., Sadlova J., Dvorak V., Kostalova T., Rohousova I., Frynta D., Aghova T., Yasur-Landau D., Lemma W., Hailu A., Baneth G., Warburg A., Volf P., Votypka J. Detection of Leishmania donovani and L. tropica in Ethiopian wild rodents. Acta Trop. 2015;145:39–44. PubMed

Killick-Kendrick M., Killick-Kendrick R. The initial establishment of sandfly colonies. Parassitologia. 1991;33:313–320. PubMed

Kwakye-Nuako G., Mosore M.T., Duplessis C., Bates M.D., Puplampu N., Mensah-Attipoe I., Desewu K., Afegbe G., Asmah R.H., Jamjoom M.B., Ayeh-Kumi P.F., Boakye D.A., Bates P.A. First isolation of a new species of Leishmania responsible for human cutaneous leishmaniasis in Ghana and classification in the Leishmania enriettii complex. Int. J. Parasitol. 2015;45:679–684. PubMed

Leirs H. Genus Mastomys multimammate mice. In: Happold D.C.D., editor. Mammals of Africa: Volume III. Bloomsbury Publishing; London: 2013. pp. 460–471.

Quinnell R.J., Courtenay O. Transmission, reservoir hosts and control of zoonotic visceral leishmaniasis. Parasitology. 2009;136:1915–1934. PubMed

Sadlova J., Price H.P., Smith B.A., Votypka J., Volf P., Smith D.F. The stage-regulated HASPB and SHERP proteins are essential for differentiation of the protozoan parasite Leishmania major in its sand fly vector. Phlebotomus papatasi. Cell. Microbiol. 2010;12 PubMed PMC

Sadlova J., Seblova V., Votypka J., Warburg A., Volf P. Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model. Parasites Vectors. 2015;8:158. Article number. PubMed PMC

Sadlova J., Myskova J., Lestinova T., Votypka J., Yeo M., Volf P. Leishmania donovani development in Phlebotomus argentipes: comparison of promastigote and amastigote-initiated infections. Parasitology. 2017;144:403–410. PubMed PMC

Sadlova J., Vojtkova B., Hrncirova K., Lestinova T., Spitzova T., Becvar T., Votypka J., Bates P., Volf P. Host competence of African rodents Arvicanthis neumanni, A. niloticus and Mastomys natalensis for Leishmania major. Int. J. Parasitol. Parasites Wildl. 2019;8:118–126. PubMed PMC

Volf P., Volfova V. Establishment and maintenance of sand fly colonies. J. Vector Ecol. 2011;36:1–9. PubMed

Yared S., Gebresilassie A., Abbasi I., Aklilu E., Kirstein O.D., Balkew M., Brown A.S., Clouse R.M., Warburg A., Hailu A., Gebre-michael T. A molecular analysis of sand fly blood meals in a visceral leishmaniasis endemic region of northwestern Ethiopia reveals a complex host-vector system. Heliyon. 2019;5 PubMed PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...