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Characterization of IcmF of the type VI secretion system in an avian pathogenic Escherichia coli (APEC) strain.

Authors
  • de Pace, Fernanda
  • Boldrin de Paiva, Jacqueline
  • Nakazato, Gerson
  • Lancellotti, Marcelo
  • Sircili, Marcelo Palma
  • Guedes Stehling, Eliana
  • Dias da Silveira, Wanderley
  • Sperandio, Vanessa
Type
Published Article
Journal
Microbiology
Publisher
Microbiology Society
Publication Date
Oct 01, 2011
Volume
157
Issue
Pt 10
Pages
2954–2962
Identifiers
DOI: 10.1099/mic.0.050005-0
PMID: 21778203
Source
Medline
License
Unknown

Abstract

The intracellular multiplication factor (IcmF) protein is a component of the recently described type VI secretion system (T6SS). IcmF has been shown to be required for intra-macrophage replication and inhibition of phagosome-lysosome fusion in Legionella pneumophila. In Vibrio cholerae it is involved in motility, adherence and conjugation. Given that we previously reported that two T6SS genes (hcp and clpV) contribute to the pathogenesis of a septicaemic strain (SEPT362) of avian pathogenic Escherichia coli (APEC), we investigated the function of IcmF in this strain. Further elucidation of the virulence mechanisms of APEC is important because this pathogen is responsible for financial losses in the poultry industry, and is closely related to human extraintestinal pathogenic E. coli (ExPEC) strains, representing a potential zoonotic risk, as well as serving as a reservoir of virulence genes. Here we show that an APEC icmF mutant has decreased adherence to and invasion of epithelial cells, as well as decreased intra-macrophage survival. The icmF mutant is also defective for biofilm formation on abiotic surfaces. Additionally, expression of the flagella operon is decreased in the icmF mutant, leading to decreased motility. The combination of these phenotypes culminates in this mutant being altered for infection in chicks. These results suggest that IcmF in APEC may play a role in disease, and potentially also in the epidemiological spread of this pathogen through enhancement of biofilm formation.

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