Leishmania donovani reduces the levels of retinoic acid-synthesizing enzymes in infected macrophages and favoring its own survival

Parasitol Res. 2019 Jan;118(1):63-71. doi: 10.1007/s00436-018-6115-0. Epub 2018 Oct 18.

Abstract

People suffering from malnutrition become susceptible to the infection like Leishmania sp., as it results in a compromised immune response. Retinoic acid (RA), an important constituent of nutrition, shows an immune-modulatory activity. However, its role in the containment of infection is not yet ascertained, particularly in case of visceral leishmaniasis (VL). VL patients (n = 10) and healthy endemic controls (n = 9) were recruited to measure the serum levels of RA. An in vitro model of Leishmania infection using the murine mφ cell line J774.1 was used to investigate the RA-synthesizing enzymes (RALDH-1 and RALDH-2). Parasite loads among infected mφ were measured by quantitative expression of kDNA in the presence of an inhibitor of the RALDH-2 enzyme. We found a significant decrease in the serum levels of RA in VL cases. Importantly, we observed decreased levels of RALDH-1 and RALDH-2 among L. donovani-infected mφ along with simultaneous decrease as well as increase in the Th-1 and Th-2-associated factors, respectively. Furthermore, the pretreatment of mφ with an RALDH-2 inhibitor improved parasite in vitro infection. Our findings show impaired RA pathway among infected mφ and indicate that an intact RA pathway is critical for anti-Leishmania immune response. Graphical abstract ᅟ.

Keywords: Immune suppression; Leishmania; Retinoic acid; Retinoic acid–synthesizing enzymes; Visceral leishmaniasis.

MeSH terms

  • Animals
  • Cell Line
  • Down-Regulation
  • Gene Expression Regulation
  • Humans
  • Immunologic Factors / blood*
  • Leishmania donovani / physiology*
  • Leishmaniasis, Visceral / blood
  • Leishmaniasis, Visceral / immunology
  • Leishmaniasis, Visceral / parasitology*
  • Macrophages / enzymology
  • Macrophages / parasitology*
  • Male
  • Mice
  • Retinal Dehydrogenase / metabolism*
  • Tretinoin / blood*
  • Tretinoin / immunology
  • Tretinoin / metabolism

Substances

  • Immunologic Factors
  • Tretinoin
  • Retinal Dehydrogenase