Evaluation of Caco-2 cells response to Listeria monocytogenes virulence factors by RT-PCR

Microb Pathog. 2018 Jul:120:79-84. doi: 10.1016/j.micpath.2018.04.059. Epub 2018 Apr 30.

Abstract

Listeria monocytogenes expresses various virulence factors enabling the invasion and multiplying in host cells, and together induces cytokines transcription. In order to explore the relationship between virulence factors of L. monocytogenes wild-type EGD-e and cellular response in human colonic epithelial cell line(Caco-2), we constructed mutant strains with in-frame deletions of critical virulence genes of inlA, inlB, hly, actA and virulence regulatory factor prfA from EGD-e, respectively. Compared with EGD-e, mutant strains showed significantly decreased invasion and apoptosis in Caco-2 cells. However, mutant strains were capable to evoke cytokines transcription of interleukin-8 (IL-8), mononuclear chemoattractant protein-1 (MCP-1), tumor necrosis factor-a (TNF-a), interleukin-1β (IL-1β), interleukin-6 (IL-6) and CXCL-2 production in Caco-2 cells. Interestingly, EGD-e Δhly-infected Caco-2 cells showed a significant decrease of IL-6, IL-8 and MCP-1 transcription compared with EGD-e at 1 h post-infection. Simultaneously, EGD-e ΔinlB-infected cells showed a decrease in IL-6 transcription, while EGD-e ΔactA-infected cells reflected a decrease in MCP-1 transcription. Virulence genes play a role in inflammatory transcription, but the interaction between pathogenic bacteria and the host cells predominates in inflammatory transcription. Overall, the data showed cellular response of Caco-2 cells infected with EGD-e mutant strains.

Keywords: Caco-2; Inflammatory response; Listeria monocytogenes; Virulence factors.

MeSH terms

  • Apoptosis / drug effects
  • Bacterial Proteins / adverse effects
  • Bacterial Toxins / adverse effects
  • Caco-2 Cells / drug effects*
  • Caco-2 Cells / immunology
  • Caco-2 Cells / metabolism*
  • Chemokine CCL2 / metabolism
  • Chemokine CXCL2 / metabolism
  • Cytokines / metabolism
  • Host-Pathogen Interactions / immunology
  • Host-Pathogen Interactions / physiology
  • Humans
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Listeria monocytogenes / metabolism*
  • Listeria monocytogenes / pathogenicity
  • Membrane Proteins / adverse effects
  • Peptide Termination Factors / adverse effects
  • Reverse Transcriptase Polymerase Chain Reaction / methods*
  • Tumor Necrosis Factor-alpha / metabolism
  • Virulence / genetics
  • Virulence Factors / adverse effects*
  • Virulence Factors / genetics

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • CCL2 protein, human
  • CXCL2 protein, human
  • CXCL8 protein, human
  • Chemokine CCL2
  • Chemokine CXCL2
  • Cytokines
  • Interleukin-1beta
  • Interleukin-6
  • Interleukin-8
  • Membrane Proteins
  • Peptide Termination Factors
  • PrfA protein, Listeria monocytogenes
  • Tumor Necrosis Factor-alpha
  • Virulence Factors
  • inlB protein, Listeria monocytogenes
  • internalin protein, Bacteria
  • actA protein, Listeria monocytogenes