Open AccessIdentification, cloning and characterization of rfaE of Actinobacillus pleuropneumoniae serotype 1, a gene involved in lipopolysaccharide inner‐core biosynthesis
Author(s) -
Provost Marilou,
Harel Josée,
Labrie Josée,
Sirois Marc,
Jacques Mario
Publication year - 2003
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1016/s0378-1097(03)00247-7
Subject(s) - actinobacillus pleuropneumoniae , complementation , salmonella enterica , biology , microbiology and biotechnology , mutant , virulence , novobiocin , salmonella , gene , lipid a , escherichia coli , serotype , genetics , bacteria , antibiotics
Actinobacillus pleuropneumoniae is the causative agent of porcine pleuropneumonia and its lipopolysaccharides (LPS) have been identified as important adhesins involved in adherence to host cells. To better understand the role of LPS core in the virulence of this organism, the aim of the present study was to identify and clone genes involved in LPS core biosynthesis by complementation with Salmonella enterica serovar Typhimurium mutants ( rfaC , rfaD , rfaE and rfaF ). Complementation with an A. pleuropneumoniae 4074 genomic library was successful with Salmonella mutant SL1102. This Salmonella deep‐rough LPS mutant is defective for the rfaE gene, which is an ADP–heptose synthase. Novobiocin was used to select transformants that had the smooth‐LPS type, since Salmonella strains with wild‐type smooth‐LPS are less permeable, therefore more resistant to hydrophobic antibiotics like novobiocin. We obtained a clone that was able to restore the wild‐type smooth‐LPS Salmonella phenotype after complementation. The wild‐type phenotype was confirmed using phage (Felix‐O, P22c.2 and Ffm) susceptibility and SDS–PAGE (sodium dodecyl sulfate–polyacrylamide gel electrophoresis). One of the open reading frames contained in the 3.3‐kb insert in the plasmid encoded a 475‐amino‐acid protein with 71% identity and 85% similarity to the RfaE protein of S. enterica . We then attempted to generate an A. pleuropneumoniae rfaE mutant by gene replacement. The rfaE gene seems essential in A. pleuropneumoniae viability as we were unable to isolate a heptose‐less knockout mutant.