Abstract
Leishmaniasis is caused by members of the
species and constitute a group of infective diseases that range from cutaneous lesions to lethal visceral forms. In infected persons, macrophages recognize and eliminate the parasites via phagocytosis. In order to change a hostile environment into an environment adequate for survival and reproduction, the engulfed Leishmania species needs to modulate the function of its host macrophage. The expression patterns of cytokine genes such as interleukin-12 (
), tumour necrosis factor-alpha
and interferon-gamma (
) represent the immune response. In this study, we employed an RNA-seq approach for human monocyte-derived macrophages infected with Leishmania major (
) to decipher cytokine gene expression alterations in host macrophages.
In this descriptive study, human monocytes were isolated by magnetic activated cell sorting (MACS) and cultured in the presence of monocyte colony stimulating factor (M-CSF) to obtain the macrophages. Monocyte-derived macrophages were then co-cultured with metacyclic promastigotes of
for 4 hours. RNA isolation was performed using TRIzol reagent. RNA sequencing was performed using the Illumina sequencing platforms. Gene expression analysis was performed using a Bioconductor DESeq2 package.
Our data revealed significant changes in immune response gene expressions in macrophages infected with
, with an up-regulation of cytokines and mostly down-regulation of their receptors.
The obtained data could shed more light on the biology of
and how the host cell responds to leishmaniasis.
