Infection and Immunity · 2003 · 40 citations · 42 references
Life SciencesMicrobiologyMolecular BiologyDiagnostic MicrobiologyMicrobial GeneticsProtein BiochemistryBacterial Virulence FactorsMicrobial Virulence FactorsPathogen BiologyPathogen Virulence FactorsVirulence Gene RegulationFunctional Genomics Of PathogenicityInsertional MutagenesisMolecular Basis Of VirulencePathogenicity MechanismsPilus StructureVirulence Variation
Pili of pathogenic Neisseria are major virulence factors associated with adhesion, cytotoxicity, twitching motility, autoaggregation, and DNA transformation. Pili are modified posttranslationally by the addition of phosphorylcholine. However, no genes involved in either the biosynthesis or the transfer of phosphorylcholine in Neisseria meningitidis have been identified. In this study, we identified five candidate open reading frames (ORFs) potentially involved in the biosynthesis or transfer of phosphorylcholine to pilin in N. meningitidis. Insertional mutants were constructed for each ORF in N. meningitidis strain C311#3 to determine their effect on phosphorylcholine expression. The effect of the mutant ORFs on the modification by phosphorylcholine was analyzed by Western analysis with phosphorylcholine-specific monoclonal antibody TEPC-15. Analysis of the mutants showed that ORF NMB0415, now defined as pptA (pilin phosphorylcholine transferase A), is involved in the addition of phosphorylcholine to pilin in N. meningitidis. Additionally, the phase variation (high frequency on-off switching of expression) of phosphorylcholine on pilin is due to changes in a homopolymeric guanosine tract in pptA.
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Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
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Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
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