Pseudomonas aeruginosa invades human aortic endothelial cells and induces cell damage in vitro

Rahul Mittal, Vasanti M. Jhaveri, Sae In Samantha Kay, Patricia Blackwelder, Kunal Patel

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background: Cardiovascular diseases such as endocarditis are the second most common cause of death worldwide. Infective Endocarditis (IE) is the most severe infection of the heart associated with significant mortality and morbidity. The binding and invasion of Human Aortic Endothelial Cells (HAECs) by pathogenic microbes can play an important role in the pathogenesis of IE. Objective: Pseudomonas aeruginosa is an emerging pathogen that has been associated with IE. However, it is not known whether P. aeruginosa can bind and interact with HAECs. The aim of this study was to determine whether P. aeruginosa can bind and colonize HAECs. Methods: The invasion of HAECs by P. aeruginosa was assessed by gentamicin protection assay. Cytokine levels were determined by enzyme-linked Immunosorbent Assay (ELISA) kits. Cell damage was determined by Lactate Dehydrogenase (LDH) assay. Results: P. aeruginosa can bind and invade HAECs. Infection of HAECs with P. aeruginosa induces TNF-a IL-1Β, IL-6 and IL-8 cytokine production leading to the generation of inflammatory milieu that can cause tissue damage as observed in human clinical cases of IE. We also observed that P. aeruginosa induces cell damage in HAECs. Conclusion: In this study, we demonstrate for first time that P. aeruginosa can invade and survive inside HAECs. This cell culture model can be of immense importance to determine the efficacy of drug targets against IE.

Original languageEnglish (US)
Pages (from-to)45-50
Number of pages6
JournalCardiovascular and Hematological Disorders - Drug Targets
Volume19
Issue number1
DOIs
StatePublished - 2019

Keywords

  • Cell damage
  • Cytokines
  • Infective endocarditis
  • Lactate dehydrogenase (LDH) assay
  • Pseudomonas aeruginosa

ASJC Scopus subject areas

  • Molecular Medicine
  • Hematology
  • Pharmacology
  • Cardiology and Cardiovascular Medicine

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