Proteome profiling of cutaneous leishmaniasis lesions due to dermotropic Leishmania donovani in Sri Lanka.
Nuwani H ManamperiNimesha Madhushani EdirisingheHarshima WijesingheLakmali PathirajaNishantha PathiranaVishmi Samudika WanasingheChamalka Gimhani de SilvaW AbeyewickremeNadira Darshani KarunaweeraPublished in: bioRxiv : the preprint server for biology (2024)
Characterization of the host response in cutaneous leishmaniasis (CL) through proteome profiling has gained limited insights in leishmaniasis research, in comparison to that of the parasite. The primary objective of this study was to comprehensively analyze the proteomic profile of the skin lesions tissues in patients with CL, by mass spectrometry, and subsequent validation of these findings through immunohistochemical methods. Sixty-seven proteins exhibited significant differential expression between tissues of CL lesions and healthy controls (p<0.01), representing numerous enriched biological processes within the lesion tissue, as evident by both the Kyoto Encyclopedia of Genes and Genomes (KEGG) and Reactome databases. Among these, the integrated endoplasmic reticulum stress response (IERSR) emerges as a pathway characterized by the up-regulated proteins in CL tissues compared to healthy skin. Expression of endoplasmic reticulum (ER) stress sensors, inositol-requiring enzyme-1 (IRE1), protein kinase RNA-like ER kinase (PERK), and activating transcription factor 6 (ATF6) in lesion tissue was validated by immunohistochemistry. In conclusion, proteomic profiling of skin lesions carried out as a discovery phase study revealed a multitude of probable immunological and pathological mechanisms operating in patients with CL in Sri Lanka, which needs to be further elaborated using more in-depth and targeted investigations.
Keyphrases
- endoplasmic reticulum
- transcription factor
- single cell
- protein kinase
- mass spectrometry
- gene expression
- soft tissue
- endoplasmic reticulum stress
- wound healing
- poor prognosis
- high resolution
- randomized controlled trial
- small molecule
- genome wide
- high throughput
- signaling pathway
- liquid chromatography
- drug delivery
- ms ms
- genome wide identification
- capillary electrophoresis
- dna binding
- toxoplasma gondii
- life cycle