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Lack of influence of the anaerobic [NiFe] hydrogenase and L-1,2 propanediol oxidoreductase on the outcome of Actinobacillus pleuropneumoniae serotype 7 infection.

Abstract
The genes for the large subunit of [NiFe] hydrogenase 2, (hybB) and for L-1,2 propanediol oxidoreductase (fucO), were identified in an Actinobacillus (A.) pleuropneumoniae serotype 7 strain. Based on the hypothesis that adaptation to anaerobic conditions in damaged lung tissue may play a role in A. pleuropneumoniae persistence in host tissues, deletion mutants with a deletion in the hybB or the fucO gene were constructed and examined in an aerosol infection model. Deletion of the hybB or fucO genes appeared to have no significant effect on A. pleuropneumoniae virulence.
AuthorsNina Baltes, Sunn Kyaw, Isabel Hennig-Pauka, Gerald-F Gerlach
JournalVeterinary microbiology (Vet Microbiol) Vol. 102 Issue 1-2 Pg. 67-72 (Aug 19 2004) ISSN: 0378-1135 [Print] Netherlands
PMID15288928 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Alcohol Oxidoreductases
  • lactaldehyde reductase
  • nickel-iron hydrogenase
  • Hydrogenase
Topics
  • Actinobacillus Infections (immunology, microbiology, veterinary)
  • Actinobacillus pleuropneumoniae (enzymology, immunology, pathogenicity)
  • Alcohol Oxidoreductases (genetics, immunology, metabolism, physiology)
  • Anaerobiosis (immunology)
  • Animals
  • Body Temperature (immunology)
  • Hydrogenase (genetics, immunology, metabolism, physiology)
  • Lung (immunology, microbiology, pathology)
  • Lymphoid Tissue (immunology, microbiology, pathology)
  • Mutagenesis, Insertional
  • Swine
  • Swine Diseases (immunology, microbiology)

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