4.4 Article

RstA is required for the virulence of an avian pathogenic Escherichia coli O2 strain E058

Journal

INFECTION GENETICS AND EVOLUTION
Volume 29, Issue -, Pages 180-188

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.meegid.2014.11.022

Keywords

Avian pathogenic Escherichia coli; RstA; Mutant; Virulence

Funding

  1. National Natural Science Foundation of China [31272559, 30972196, 30771604, 30471281]
  2. Special Fund for Agroscientific Research in the Public Interest [201303044]
  3. Natural Science Foundation of the Higher Education Institutions of Jiangsu Province [14KJB230001]
  4. Natural Science Foundation of Jiangsu Province [BK20140485]
  5. Program for Changjiang Scholars and Innovative Research Teams at Universities [PCSIRT0978]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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Certain strains of avian pathogenic Escherichia coli (APEC) cause severe extraintestinal infections in poultry, including acute fatal septicemia, subacute pericarditis, and airsacculitis. These bacteria contain an RstA/RstB regulatory system, a two-component system that may help APEC strains adapt to the extraintestinal environment and survive under stressful conditions. Whether RstA correlates with APEC pathogenesis or acts as an APEC virulence factor has not been established. Here we provide the first evidence for an important role of rstA in APEC virulence. We generated an rstA-deficient mutant from the highly virulent APEC strain E058. Virulence of the mutant strain was evaluated in vivo and in vitro through bird infection assays, a cytotoxicity assay on chicken macrophage cell line HD-11, and a bactericidal assay to serum complement. Based on lethality assays in 1-day-old birds, rstA deletion from APEC E058 reduced. the bacterial virulence in birds. The deletion also deeply impaired the capacity of APEC E058 to colonize deeper tissues of 5-week-old specific pathogen free chickens. No obvious gross or histopathological lesions were observed in the visceral organs of chickens challenged with the rstA-deficient strain. Also, rstA inactivation reduced the survival of APEC E058 within chicken macrophages. However, no significant differences were observed between the mutant and the wild-type strain in resistance to serum. Our data collectively show that the rstA gene functions in the pathogenesis of diseases caused by avian pathogenic E. coli. (C) 2014 Elsevier B.V. All rights reserved.

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