Recombination and mutation during long-term gastric colonization by Helicobacter pylori: Estimates of clock rates, recombination size, and minimal age

The bacterium Helicobacter pylori colonizes the gastric mucosa of half of the human population, resulting in chronic gastritis, ulcers, and cancer. We sequenced ten gene fragments from pairs of strains isolated sequentially at a mean interval of 1.8 years from 26 individuals. Several isolates had acquired small mosaic segments from other H. pylori or point mutations. The maximal mutation rate, the import size, and the frequency of recombination were calculated by using a Bayesian model. The calculations indicate that the last common ancestor of H. pylori existed at least 2,500–11,000 years ago. Imported mosaics have a median size of 417 bp, much smaller than for other bacteria, and recombination occurs frequently (60 imports spanning 25,000 bp per genome per year). Thus, the panmictic population structure of H. pylori results from very frequent recombination during mixed colonization by unrelated strains.

[1]  M. Floch Helicobacter pylori: Molecular and Cellular Biology , 2001 .

[2]  R. Rappuoli,et al.  Living dangerously: how Helicobacter pylori survives in the human stomach , 2001, Nature Reviews Molecular Cell Biology.

[3]  M. Gail,et al.  Re: Chemoprevention of gastric dysplasia: randomized trial of antioxidant supplements and anti-helicobacter pylori therapy. , 2001, Journal of the National Cancer Institute.

[4]  P. Deloukas,et al.  Comparison of human genetic and sequence-based physical maps , 2001, Nature.

[5]  M. Achtman,et al.  Helicobacter pylori: molecular and cellular biology. , 2001 .

[6]  François Taddei,et al.  Evolutionary Implications of the Frequent Horizontal Transfer of Mismatch Repair Genes , 2000, Cell.

[7]  M. Nachman,et al.  Estimate of the mutation rate per nucleotide in humans. , 2000, Genetics.

[8]  M. Schenker,et al.  Frequent interspecific genetic exchange between commensal neisseriae and Neisseria meningitidis , 2000, Molecular microbiology.

[9]  D. Posada,et al.  Population genetics of the porB gene of Neisseria gonorrhoeae: different dynamics in different homology groups. , 2000, Molecular biology and evolution.

[10]  E. Kuipers,et al.  Quasispecies development of Helicobacter pylori observed in paired isolates obtained years apart from the same host. , 2000, The Journal of infectious diseases.

[11]  B. Spratt,et al.  Extensive variation in the ddl gene of penicillin-resistant Streptococcus pneumoniae results from a hitchhiking effect driven by the penicillin-binding protein 2b gene. , 1999, Molecular biology and evolution.

[12]  M. Z. Humayun,et al.  Mutation as an origin of genetic variability in Helicobacter pylori. , 1999, Trends in microbiology.

[13]  J. Peden,et al.  Absence in Helicobacter pylori of an uptake sequence for enhancing uptake of homospecific DNA during transformation. , 1999, Microbiology.

[14]  M Achtman,et al.  Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[15]  S. Schbath,et al.  Characteristics of Chi distribution on different bacterial genomes. , 1999, Research in microbiology.

[16]  N. Moran,et al.  Calibrating bacterial evolution. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[17]  C. Josenhans,et al.  In Vivo Distribution of Helicobacter felis in the Gastric Mucus of the Mouse: Experimental Method and Results , 1999, Infection and Immunity.

[18]  M. Achtman,et al.  Recombination and clonal groupings within Helicobacter pylori from different geographical regions , 2012 .

[19]  D. Berg,et al.  Emergence of recombinant strains of Helicobacter pylori during human infection , 1999, Molecular microbiology.

[20]  J. M. Smith,et al.  Free recombination within Helicobacter pylori. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[21]  F. Ayala,et al.  Malaria's Eve: evidence of a recent population bottleneck throughout the world populations of Plasmodium falciparum. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[22]  B. Tümmler,et al.  Large chromosomal inversions occur in Pseudomonas aeruginosa clone C strains isolated from cystic fibrosis patients. , 2006, FEMS microbiology letters.

[23]  Mark Borodovsky,et al.  The complete genome sequence of the gastric pathogen Helicobacter pylori , 1997, Nature.

[24]  B. Tümmler,et al.  Large chromosomal inversions occur in clone C strains isolated from cystic fibrosis patients , 1997 .

[25]  E. Betrán,et al.  The estimation of the number and the length distribution of gene conversion tracts from population DNA sequence data. , 1997, Genetics.

[26]  H. Ochman,et al.  Amelioration of Bacterial Genomes: Rates of Change and Exchange , 1997, Journal of Molecular Evolution.

[27]  Jared M. Diamond,et al.  Guns, germs and steel : how the inequalities of wealth and power among modern peoples were moulded by prehistory , 1997 .

[28]  D. Berg,et al.  Long-term colonization with single and multiple strains of Helicobacter pylori assessed by DNA fingerprinting , 1995, Journal of clinical microbiology.

[29]  R. Milkman,et al.  Transduction, restriction and recombination patterns in Escherichia coli. , 1995, Genetics.

[30]  D. Dykhuizen,et al.  Clonal divergence in Escherichia coli as a result of recombination, not mutation. , 1994, Science.

[31]  G Harauz,et al.  Meiotic gene conversion tract length distribution within the rosy locus of Drosophila melanogaster. , 1994, Genetics.

[32]  S. Goodman,et al.  Factors influencing the specific interaction of Neisseria gonorrhoeae with transforming DNA , 1991, Journal of bacteriology.

[33]  R Milkman,et al.  Molecular evolution of the Escherichia coli chromosome. III. Clonal frames. , 1990, Genetics.

[34]  L. van Alphen,et al.  Antigenic drift of Haemophilus influenzae in patients with chronic obstructive pulmonary disease , 1989, Infection and immunity.

[35]  M. Fox,et al.  Electron microscope visualization of the products of Bacillus subtilis transformation. , 1977, Journal of molecular biology.

[36]  S. Lacks,et al.  Transformation and DNA size: two controlling parameters and the efficiency of the single strand intermediate. , 1968, Cold Spring Harbor symposia on quantitative biology.

[37]  N. Metropolis,et al.  Equation of State Calculations by Fast Computing Machines , 1953, Resonance.