Experimentally revised repertoire of putative contingency loci in Neisseria meningitidis strain MC58: evidence for a novel mechanism of phase variation

Analysis of the genome sequence of Neisseria meningitidis strain MC58 revealed 65 genes associated with simple sequence repeats. Experimental evidence of phase variation exists for only 14 of these 65 putatively phase variable genes. We investigated the phase variable potential of the remaining 51 genes. The repeat tract associated with 20 of these 51 genes was sequenced in 26 genetically distinct strains. This analysis provided circumstantial evidence for or against the phase variability of the candidate genes, based on the sequence and the length of the repeated motif. These predictions of phase variability were substantiated for three of these candidate genes using colony immunoblotting or β‐galactosidase as a reporter. This investigation identified a novel phase variable gene (NMB1994 or nadA) associated with a repeat tract (TAAA) not previously reported to be associated with phase variable genes in N. meningitidis. Analysis of the nadA transcript revealed that the repeat tract was located upstream of the putative −35 element of the nadA promoter. Semiquantitative RT‐PCR showed that variation in the number of repeats was associated with changes in the level of expression of nadA, findings consistent with a model whereby the variable number of (TAAA) repeats modulates the promoter strength.

[1]  R. Rappuoli,et al.  NadA, a Novel Vaccine Candidate of Neisseria meningitidis , 2002, The Journal of experimental medicine.

[2]  D. Caugant Faculty Opinions recommendation of Comparative whole-genome analyses reveal over 100 putative phase-variable genes in the pathogenic Neisseria spp. , 2001 .

[3]  Lori A. S. Snyder,et al.  Comparative whole-genome analyses reveal over 100 putative phase-variable genes in the pathogenic Neisseria spp. , 2001, Microbiology.

[4]  S. Busby,et al.  Activation and repression of transcription initiation in bacteria. , 2001, Essays in biochemistry.

[5]  J. Dankert,et al.  Multiple Mechanisms of Phase Variation of PorA inNeisseria meningitidis , 2000, Infection and Immunity.

[6]  H. Tettelin,et al.  Repeat‐associated phase variable genes in the complete genome sequence of Neisseria meningitidis strain MC58 , 2000, Molecular microbiology.

[7]  D. Graham,et al.  A M(r) 34,000 proinflammatory outer membrane protein (oipA) of Helicobacter pylori. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[8]  A. Oliver,et al.  High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. , 2000, Science.

[9]  S. Carson,et al.  Phase variation of the gonococcal siderophore receptor FetA , 2000, Molecular microbiology.

[10]  E. Moxon,et al.  Enzyme linked immunosorbent assay (ELISA) for the detection of serum antibodies to the inner core lipopolysaccharide of Neisseria meningitidis group B. , 2000, Journal of immunological methods.

[11]  J. Venter,et al.  Identification of vaccine candidates against serogroup B meningococcus by whole-genome sequencing. , 2000, Science.

[12]  S. Salzberg,et al.  Complete genome sequence of Neisseria meningitidis serogroup B strain MC58. , 2000, Science.

[13]  D. Field,et al.  The length of a tetranucleotide repeat tract in Haemophilus influenzae determines the phase variation rate of a gene with homology to type III DNA methyltransferases , 2000, Molecular microbiology.

[14]  E. Moxon,et al.  The genetic basis of the phase variation repertoire of lipopolysaccharide immunotypes in Neisseria meningitidis. , 1999, Microbiology.

[15]  I. Henderson,et al.  Molecular switches — the ON and OFF of bacterial phase variation , 1999, Molecular microbiology.

[16]  F. Moreau,et al.  Mutational analysis of the promoter region of the porA gene of Neisseria meningitidis. , 1999, Gene.

[17]  M. Gipson,et al.  Phase variation of HpuAB and HmbR, two distinct haemoglobin receptors of Neisseria meningitidis DNM2 , 1999, Molecular microbiology.

[18]  A. Richardson,et al.  HmbR, a Hemoglobin-Binding Outer Membrane Protein of Neisseria meningitidis, Undergoes Phase Variation , 1999, Journal of bacteriology.

[19]  E. Moxon,et al.  Identification of a novel gene involved in pilin glycosylation in Neisseria meningitidis , 1998, Molecular microbiology.

[20]  Alex van Belkum,et al.  Short-Sequence DNA Repeats in Prokaryotic Genomes , 1998, Microbiology and Molecular Biology Reviews.

[21]  M. Achtman,et al.  Multilocus sequence typing: a portable approach to the identification of clones within populations of pathogenic microorganisms. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[22]  R. Fleischmann,et al.  DNA repeats identify novel virulence genes in Haemophilus influenzae. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Ende,et al.  Invasion of primary nasopharyngeal epithelial cells by Neisseria meningitidis is controlled by phase variation of multiple surface antigens , 1996, Infection and immunity.

[24]  S. Hammerschmidt,et al.  Capsule phase variation in Neisseria meningitidis serogroup B by slipped‐strand mispairing in the polysialyltransferase gene (siaD): correlation with bacterial invasion and the outbreak of meningococcal disease , 1996, Molecular microbiology.

[25]  C. Nickerson,et al.  Role of curved DNA in binding of Escherichia coli RNA polymerase to promoters , 1995, Journal of bacteriology.

[26]  Ende,et al.  Variable expression of class 1 outer membrane protein in Neisseria meningitidis is caused by variation in the spacing between the -10 and -35 regions of the promoter , 1995, Journal of bacteriology.

[27]  M. Achtman,et al.  Variable expression of the Opc outer membrane protein in Neisseria meningitidis is caused by size variation of a promoter containing poly‐cytidine , 1994, Molecular microbiology.

[28]  M. Nowak,et al.  Adaptive evolution of highly mutable loci in pathogenic bacteria , 1994, Current Biology.

[29]  R. Gourse,et al.  A third recognition element in bacterial promoters: DNA binding by the alpha subunit of RNA polymerase. , 1993, Science.

[30]  F. Mooi,et al.  Phase variation of H. influenzae fimbriae: Transcriptional control of two divergent genes through a variable combined promoter region , 1993, Cell.

[31]  S. Normark,et al.  Phase variation of gonococcal pili by frameshift mutation in pilC, a novel gene for pilus assembly. , 1991, The EMBO journal.

[32]  L. Bracco,et al.  Synthetic curved DNA sequences can act as transcriptional activators in Escherichia coli. , 1989, The EMBO journal.

[33]  S. Morrison,et al.  Expression and phase variation of gonococcal P.11 genes in Escherichia coli involves ribosomal frameshifting and slipped‐strand mispairing , 1989, Molecular microbiology.

[34]  R. Wartell,et al.  Sequence distributions associated with DNA curvature are found upstream of strong E. coli promoters. , 1987, Nucleic acids research.

[35]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .