J Med Microbiol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Carroll, I. M.
Right arrow Articles by Smyth, C. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Carroll, I. M.
Right arrow Articles by Smyth, C. J.
Agricola
Right arrow Articles by Carroll, I. M.
Right arrow Articles by Smyth, C. J.
J Med Microbiol 53 (2004), 669-677; DOI: 10.1099/jmm.0.05440-0
© 2004 Society for General Microbiology
ISSN 0022-2615

Microevolution between paired antral and paired antrum and corpus Helicobacter pylori isolates recovered from individual patients

Ian M. Carroll1{dagger}, Niyaz Ahmed2, Sarah M. Beesley1, Aleem A. Khan3, Sheikh Ghousunnissa2, Colm A.Ó Moráin4, C. M. Habibullah3 and Cyril J. Smyth1

1Department of Microbiology, Moyne Institute of Preventive Medicine, Trinity College, University of Dublin, Dublin 2, Ireland 2Centre for DNA Fingerprinting and Diagnostics (CDFD), Nacharam, Hyderabad, 50 00076 India 3Owaisi Hospital and Research Centre, Deccan College of Medical Sciences, Kanchanbagh, Santoshnagar, Hyderabad, India 4Department of Gastroenterology, The Adelaide and Meath Hospital, Tallaght, Dublin 24, Ireland

Correspondence Cyril J. Smyth csmyth{at}tcd.ie

Received August 20, 2003
Accepted February 12, 2004

Sequence variations located at the signal sequence and mid-region within the vacA gene, the 3'-end of the cagA gene, the indel motifs at the 3'-end of the cag pathogenicity island and the regions upstream of the vacA and ribA genes were determined by PCR in 19 paired antral or antrum and corpus Helicobacter pylori isolates obtained at the same endoscopic session, and three antral pairs taken sequentially. Random amplification of polymorphic DNA (RAPD)-PCR and fluorescent amplified fragment length polymorphism (FAFLP)-PCR fingerprinting were applied to these paired clinical isolates. The FAFLP-PCR profiles generated were phylogenetically analysed. For the 22 paired isolates there were no differences within pairs at five of the genetic loci studied. However, six pairs of isolates (27 %), of which four were antrum and corpus pairs, showed differences in the numbers of repeats located at the 3'-end of the cagA gene. RAPD-PCR fingerprinting showed that 16 (73 %) pairs, nine of which were antrum and corpus pairs, possessed identical profiles, while six (27 %) displayed distinctly different profiles, indicating mixed infections. Three of the six pairs showing differences at the 3'-end of the cagA gene yielded identical RAPD-PCR fingerprints. FAFLP-PCR fingerprinting and phylogenetic analysis revealed that all 16 pairs that displayed identical RAPD-PCR profiles had highly similar, but not identical, fingerprints, demonstrating that these pairs were ancestrally related but had undergone minor genomic alterations. Two antrum and corpus pairs of isolates, within the latter group, were isolates obtained from two siblings from the same family. This analysis demonstrated that each sibling was colonized by ancestrally related strains that exhibited differences in vacA genotype characteristics.


{dagger}Present Address: Department of Genetics, University of North Carolina, Chapel Hill, NC 27599-7264, USA.

Abbreviation: FAFLP, fluorescent amplified fragment length polymorphism.




This article has been cited by other articles:


Home page
J Med MicrobiolHome page
R. H. Argent, J. L. Hale, E. M. El-Omar, and J. C. Atherton
Differences in Helicobacter pylori CagA tyrosine phosphorylation motif patterns between western and East Asian strains, and influences on interleukin-8 secretion
J. Med. Microbiol., September 1, 2008; 57(9): 1062 - 1067.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
R. H. Argent, R. J. Thomas, F. Aviles-Jimenez, D. P. Letley, M. C. Limb, E. M. El-Omar, and J. C. Atherton
Toxigenic Helicobacter pylori Infection Precedes Gastric Hypochlorhydria in Cancer Relatives, and H. pylori Virulence Evolves in These Families
Clin. Cancer Res., April 1, 2008; 14(7): 2227 - 2235.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
N. R. Salama, G. Gonzalez-Valencia, B. Deatherage, F. Aviles-Jimenez, J. C. Atherton, D. Y. Graham, and J. Torres
Genetic Analysis of Helicobacter pylori Strain Populations Colonizing the Stomach at Different Times Postinfection
J. Bacteriol., May 15, 2007; 189(10): 3834 - 3845.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
M. J. Matteo, G. Granados, C. V. Perez, M. Olmos, C. Sanchez, and M. Catalano
Helicobacter pylori cag pathogenicity island genotype diversity within the gastric niche of a single host
J. Med. Microbiol., May 1, 2007; 56(5): 664 - 669.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 2004 Society for General Microbiology.