Analysis of Endothelial Adherence of Bartonella henselae and Acinetobacter baumannii Using a Dynamic Human Ex Vivo Infection Model

Infect Immun. 2015 Dec 28;84(3):711-22. doi: 10.1128/IAI.01502-15.

Abstract

Bacterial adherence determines the virulence of many human-pathogenic bacteria. Experimental approaches elucidating this early infection event in greater detail have been performed using mainly methods of cellular microbiology. However, in vitro infections of cell monolayers reflect the in vivo situation only partially, and animal infection models are not available for many human-pathogenic bacteria. Therefore, ex vivo infection of human organs might represent an attractive method to overcome these limitations. We infected whole human umbilical cords ex vivo with Bartonella henselae or Acinetobacter baumannii under dynamic flow conditions mimicking the in vivo infection situation of human endothelium. For this purpose, methods for quantifying endothelium-adherent wild-type and trimeric autotransporter adhesin (TAA)-deficient bacteria were set up. Data revealed that (i) A. baumannii binds in a TAA-dependent manner to endothelial cells, (ii) this organ infection model led to highly reproducible adherence rates, and furthermore, (iii) this model allowed to dissect the biological function of TAAs in the natural course of human infections. These findings indicate that infection models using ex vivo human tissue samples ("organ microbiology") might be a valuable tool in analyzing bacterial pathogenicity with the capacity to replace animal infection models at least partially.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acinetobacter Infections / microbiology*
  • Acinetobacter baumannii / genetics
  • Acinetobacter baumannii / physiology*
  • Angiomatosis, Bacillary / microbiology*
  • Animals
  • Bacterial Adhesion*
  • Bartonella henselae / genetics
  • Bartonella henselae / physiology*
  • Endothelial Cells / microbiology*
  • Humans
  • In Vitro Techniques
  • Umbilical Cord / microbiology*

Grants and funding

This work was supported by grants from the Deutsche Forschungsgemeinschaft (DFG-FOR 2251 to V. Kempf, S. Göttig, B. Averhoff, G. Wilharm, and V. Müller and DFG-SFB 815 to V. Kempf and R. Brandes).