Abstract

Doc number: 25

Abstract

Background: Helicobacter pylori is a Gram-negative bacterium that persistently infects the human stomach inducing chronic inflammation. The exact mechanisms of pathogenesis are still not completely understood. Although not a natural host for H. pylori , mouse infection models play an important role in establishing the immunology and pathogenicity of H. pylori . In this study, for the first time, the genome sequences of clinical H. pylori strain UM032 and mice-adapted derivatives, 298 and 299, were sequenced using the PacBio Single Molecule, Real-Time (SMRT) technology.

Result: Here, we described the single contig which was achieved for UM032 (1,599,441 bp), 298 (1,604,216 bp) and 299 (1,601,149 bp). Preliminary analysis suggested that methylation of H. pylori genome through its restriction modification system may be determinative of its host specificity and adaptation.

Conclusion: Availability of these genomic sequences will aid in enhancing our current level of understanding the host specificity of H. pylori .

Details

Title
Comparing the genomes of Helicobacter pylori clinical strain UM032 and Mice-adapted derivatives
Author
Khosravi, Yalda; Rehvathy, Vellaya; Wee, Wei Yee; Wang, Susana; Baybayan, Primo; Singh, Siddarth; Ashby, Meredith; Ong, Junxian; Amoyo, Arlaine Anne; Seow, Shih Wee; Choo, Siew Woh; Perkins, Tim; Chua, Eng Guan; Tay, Alfred; Marshall, Barry James; Loke, Mun Fai; Goh, Khean Lee; Pettersson, Sven; Vadivelu, Jamuna
Publication year
2013
Publication date
2013
Publisher
BioMed Central
e-ISSN
1757-4749
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1428186775
Copyright
© 2013 Khosravi et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.