The host-protective effect of arabinosylated lipoarabinomannan against Leishmania donovani infection is associated with restoration of IFN-γ responsiveness

PLoS One. 2015 Feb 6;10(2):e0117247. doi: 10.1371/journal.pone.0117247. eCollection 2015.

Abstract

Visceral leishmaniasis (VL), which is endemic as a major infectious disease in the tropical and subtropical countries, is caused by a protozoan parasite Leishmania donovani. At present, restricted treatment options and lack of vaccines intensify the problem of controlling VL. Therefore, finding a novel immunoprophylactic or therapeutic principle is a pressing need. Here, we report that arabinosylated lipoarabinomannan (Ara-LAM), a TLR2-ligand isolated from Mycobacterium smegmatis, exhibits a strong immunomodulatory property that conferred protection against L. donovani infection. Although, Ara-LAM modulates TLR2 and MAPK signaling, it is not known whether Ara-LAM involves IFN-γ signaling for effective parasite clearance. Because, it is reported that IFN-γ signaling, a principle mediator of NO generation and macrophage and Tcell activation, is hampered during leishmanial pathogenesis. Ara-LAM increases IFN-γ receptor expression and potentiates IFN-γ receptor signaling through JAK-STAT pathway. Moreover, Ara-LAM reciprocally modulates IRF4 and IRF8 expression and reinstates anti-leishmanial Th1 response that eventuates in significantly reduced parasite load in spleen and liver of L. donovani-infected BALB/c mice. IFN-γRα silencing resulted in the suppression of these host-protective mechanisms affected by Ara-LAM. Thus, Ara-LAM-mediated restoration of IFN-γ responsiveness is a novel immuno-modulatory principle for protection against L. donovani susceptible host.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arabinose / metabolism*
  • Female
  • Host-Pathogen Interactions*
  • Interferon-gamma / immunology*
  • Leishmania donovani / physiology*
  • Leishmaniasis, Visceral / immunology*
  • Lipopolysaccharides / metabolism*
  • Macrophages / immunology
  • Male
  • Mice, Inbred BALB C
  • Receptor, Interferon alpha-beta / metabolism*
  • Transcription Factors / metabolism

Substances

  • Lipopolysaccharides
  • Transcription Factors
  • lipoarabinomannan
  • Receptor, Interferon alpha-beta
  • Interferon-gamma
  • Arabinose

Grants and funding

This work was financially supported by Department of Biotechnology, Govt. of India [Grant number BT/PR14435/MED/29/201/2010]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.