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Advisor(s)
Abstract(s)
Recombination is one of the main mechanisms contributing to Helicobacter pylori genomic variability. homB
and homA are paralogous genes coding for H. pylori outer membrane proteins (OMPs). Both genes display
allelic variation yielded by polymorphisms of the genes’ middle regions, with six different alleles. This study
used bioinformatic and statistical analyses to evaluate whether the allelic diversity of homB and homA is
generated by recombination. A detailed molecular analysis of the most prevalent homB allelic variant was also
performed to establish its molecular profile. The two most prevalent homB and homA allelic variants resulted
from interallelic homologous recombination between the rarest allelic variants of each gene, with a crossover
point localized in the middle of the genes, containing the allelic region. Molecular analysis of the most
prevalent homB allele revealed a geographic partition among Western and East Asian strains, more noticeable
for the 5 and 3 homB regions than for the middle allelic regions. In conclusion, the diversity of the 5 and 3
homB regions reflect the strains’ geographical origin, and variants likely occur via the accumulation of single
nucleotide polymorphisms. On the other hand, homologous recombination seems to play an important role in
the diversification of the highly polymorphic homB and homA allele-defining regions, where the most prevalent
alleles worldwide result from genomic exchange between the rarest variants of each gene, suggesting that the
resulting combinations confer biological advantages to H. pylori. This phenomenon illustrates an evolutionary
scenario in which recombination appears to be associated with ecological success.
Description
Keywords
Helicobacter pylori Outer membrane proteins Allelic diversity Recombination Infecções Gastrentestinais
Pedagogical Context
Citation
J Bacteriol. 2010 Aug;192(15):3961-8. Epub 2010 Jun 4
Publisher
American Society for Microbiology
