4.6 Article

Central Asian Rodents as Model Animals forLeishmaniamajorandLeishmania donovaniResearch

Journal

MICROORGANISMS
Volume 8, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms8091440

Keywords

Phodopus sungorus; Cricetulus griseus; Lagurus lagurus; model animals; cutaneous leishmaniasis; visceral leishmaniasis; infectiousness; xenodiagnosis; Phlebotomus; sand fly

Categories

Funding

  1. ERD Funds, project CePaViP [CZ.02.1.01/0.0/0.0/16_019/0000759]
  2. Czech Science Foundation [17-01911S]
  3. Charles University [UNCE 204072, GAUK 688217]
  4. European Commission Horizon 2020 Research and Innovation Programme, Marie-Sklodowska Curie grant [642609]

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The clinical manifestation of leishmaniases depends on parasite species, host genetic background, and immune response. Manifestations of human leishmaniases are highly variable, ranging from self-healing skin lesions to fatal visceral disease. The scope of standard model hosts is insufficient to mimic well the wide disease spectrum, which compels the introduction of new model animals for leishmaniasis research. In this article, we study the susceptibility of three Asian rodent species (Cricetulus griseus, Lagurus lagurus,andPhodopus sungorus) toLeishmania majorandL. donovani.The external manifestation of the disease, distribution, as well as load of parasites and infectiousness to natural sand fly vectors, were compared with standard models, BALB/c mice andMesocricetus auratus. No significant differences were found in disease outcomes in animals inoculated with sand fly- or culture-derived parasites. All Asian rodent species were highly susceptible toL. major.Phodopus sungorusshowed the non-healing phenotype with the progressive growth of ulcerative lesions and massive parasite loads.Lagurus lagurusandC. griseusrepresented the healing phenotype, the latter with high infectiousness to vectors, mimicking best the character of natural reservoir hosts. Both,L. lagurusandC. griseuswere also highly susceptible toL.donovani,having wider parasite distribution and higher parasite loads and infectiousness than standard model animals.

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