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Whole Genome Sequence and Phylogenetic Analysis Show Strains from Latin America Have Followed a Unique Evolution Pathway

Abstract

(HP) genetics may determine its clinical outcomes. Despite high prevalence of HP infection in Latin America (LA), there have been no phylogenetic studies in the region. We aimed to understand the structure of HP populations in LA mestizo individuals, where gastric cancer incidence remains high. The genome of 107 HP strains from Mexico, Nicaragua and Colombia were analyzed with 59 publicly available worldwide genomes. To study bacterial relationship on whole genome level we propose a virtual hybridization technique using thousands of high-entropy 13 bp DNA probes to generate fingerprints. Phylogenetic virtual genome fingerprint (VGF) was compared with Multi Locus Sequence Analysis (MLST) and with phylogenetic analyses of virulence island sequences. With MLST some Nicaraguan and Mexican strains clustered close to Africa isolates, whereas European isolates were spread without clustering and intermingled with LA isolates. VGF analysis resulted in increased resolution of populations, separating European from LA strains. Furthermore, clusters with exclusively Colombian, Mexican, or Nicaraguan strains were observed, where the Colombian cluster separated from Europe, Asia, and Africa, while Nicaraguan and Mexican clades grouped close to Africa. In addition, a mixed large LA cluster including Mexican, Colombian, Nicaraguan, Peruvian, and Salvadorian strains was observed; all LA clusters separated from the Amerind clade. With sequence analyses LA clades clearly separated from Europe, Asia and Amerind, and Colombian strains formed a single cluster. A NeighborNet analyses suggested frequent and recent recombination events particularly among LA strains. Results suggests that in the new world, has evolved to fit mestizo LA populations, already 500 years after the Spanish colonization. This co-adaption may account for regional variability in gastric cancer risk.

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References
1.
Devi S, Ahmed I, Khan A, Rahman S, Alvi A, Sechi L . Genomes of Helicobacter pylori from native Peruvians suggest admixture of ancestral and modern lineages and reveal a western type cag-pathogenicity island. BMC Genomics. 2006; 7:191. PMC: 1553449. DOI: 10.1186/1471-2164-7-191. View

2.
Bubendorfer S, Krebes J, Yang I, Hage E, Schulz T, Bahlawane C . Genome-wide analysis of chromosomal import patterns after natural transformation of Helicobacter pylori. Nat Commun. 2016; 7:11995. PMC: 4917963. DOI: 10.1038/ncomms11995. View

3.
Leal-Herrera Y, Torres J, P Monath T, Ramos I, Gomez A, Madrazo-de la Garza A . High rates of recurrence and of transient reinfections of Helicobacter pylori in a population with high prevalence of infection. Am J Gastroenterol. 2003; 98(11):2395-402. DOI: 10.1111/j.1572-0241.2003.07708.x. View

4.
Bjorkholm B, Sjolund M, Falk P, Berg O, Engstrand L, Andersson D . Mutation frequency and biological cost of antibiotic resistance in Helicobacter pylori. Proc Natl Acad Sci U S A. 2001; 98(25):14607-12. PMC: 64729. DOI: 10.1073/pnas.241517298. View

5.
Achtman M, Azuma T, Berg D, Ito Y, Morelli G, Pan Z . Recombination and clonal groupings within Helicobacter pylori from different geographical regions. Mol Microbiol. 1999; 32(3):459-70. DOI: 10.1046/j.1365-2958.1999.01382.x. View