Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.18/1688
Título: Proteome variability among Helicobacter pylori isolates clustered according to genomic methylation
Autor: Vitoriano, Inês
Vítor, Jorge
Oleastro, Mónica
Roxo-Rosa, Mónica
Vale, Filipa
Palavras-chave: Helicobacter pylori
Proteomics
Genomic Methylation
Phylogenetics
Infecções Gastrointestinais
Data: Jun-2013
Editora: Wiley-Blackwell
Citação: J Appl Microbiol. 2013 Jun;114(6):1817-32. doi: 10.1111/jam.12187. Epub 2013 Apr 4
Resumo: Aims: To understand whether the variability found in the proteome of Helicobacter pylori relates to the genomic methylation, virulence and associated gastric disease. Methods and Results: We applied the Minimum-Common-Restriction- Modification (MCRM) algorithm to genomic methylation data of 30 Portuguese H. pylori strains, obtained by genome sensitivity to Type II restriction enzymes’ digestion. All the generated dendrograms presented three clusters with no association with gastric disease. Comparative analysis of twodimensional gel electrophoresis (2DE) maps obtained for total protein extracts of 10 of these strains, representative of the three main clusters, revealed that among 70 matched protein spots (in a universe of 300), 16 were differently abundant (P < 0 05) among clusters. Of these, 13 proteins appear to be related to the cagA genotype or gastric disease. The abundance of three protein species, DnaK, GlnA and HylB, appeared to be dictated by the methylation status of their gene promoter. Conclusions: Variations in the proteome profile of strains with common geographic origin appear to be related to differences in cagA genotype or gastric disease, rather than to clusters organized according to strain genomic methylation. Significance and Impact of the Study: The simultaneous study of the genomic methylation and proteome is important to correlate epigenetic modifications with gene expression and pathogen virulence.
Peer review: yes
URI: http://hdl.handle.net/10400.18/1688
ISSN: 1364-5072
doi: 10.1128/JCM.00302-13
Versão do Editor: http://onlinelibrary.wiley.com/doi/10.1111/jam.12187/abstract;jsessionid=2236FA47F8D01A4D273CAE5BD294A935.d01t02
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