Potential Biomarkers in Diagnosis of Renal Acanthamoebiasis

Int J Mol Sci. 2021 Jun 19;22(12):6583. doi: 10.3390/ijms22126583.

Abstract

Recent studies indicate that Acanthamoeba spp. may play a significant role in kidney dysfunction. The aim of the study was to examine the levels of kidney injury molecule 1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), and monocyte chemotactic protein 1 (MCP-1), as well as an activity of matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9, respectively) in the kidneys of immunocompetent and immunosuppressed mice infected with Acanthamoeba spp. The levels of KIM-1, NGAL, and MCP-1 were analyzed by enzyme-linked immunosorbent assay (ELISA), and the activity of MMPs was determined by gelatin zymography. The elevated KIM-1 level was found in the kidneys of immunocompetent mice at the beginning of Acanthamoeba spp. infection. In the immunosuppressed mice, the KIM-1 level was statistically different. The statistically decreased NGAL level was found in the kidneys of immunocompetent mice compared to the uninfected mice. In the immunocompromised mice, we found statistically significant differences in MCP-1 levels between the uninfected and infected groups. There was an increase in the expression of both MMP-2 and MMP-9 in the kidneys of immunocompetent and immunosuppressed mice infected with Acanthamoeba spp. compared to the uninfected mice. The results indicate that KIM-1, NGAL, MCP-1, MMP-2, MMP-9, and MMP-9/NGAL might be promising biomarkers of renal acanthamoebiasis.

Keywords: Acanthamoeba spp.; KIM-1; MCP-1; MMPs; NGAL; kidney.

MeSH terms

  • Acanthamoeba*
  • Amebiasis / diagnosis
  • Amebiasis / metabolism*
  • Amebiasis / parasitology
  • Animals
  • Biomarkers / metabolism*
  • Chemokine CCL2 / metabolism
  • Hepatitis A Virus Cellular Receptor 1 / metabolism
  • Kidney Diseases / diagnosis
  • Kidney Diseases / metabolism*
  • Kidney Diseases / parasitology
  • Lipocalin-2 / metabolism
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Mice
  • Mice, Inbred BALB C

Substances

  • Biomarkers
  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Havcr1 protein, mouse
  • Hepatitis A Virus Cellular Receptor 1
  • Lipocalin-2
  • Lcn2 protein, mouse
  • Matrix Metalloproteinase 2
  • Mmp2 protein, mouse
  • Matrix Metalloproteinase 9
  • Mmp9 protein, mouse