Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 145 (1999), 1289-1298; DOI  10.1099/13500872-145-6-1289
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Dundon, W. G.
Right arrow Articles by Smyth, C. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dundon, W. G.
Right arrow Articles by Smyth, C. J.
Agricola
Right arrow Articles by Dundon, W. G.
Right arrow Articles by Smyth, C. J.

A novel tRNA-associated locus (trl) from Helicobacter pylori is co-transcribed with tRNAGly and reveals genetic diversity

William G. Dundon1,{dagger}, David G. Marshall1, Colm A. Ó. Moráin2 and Cyril J. Smyth1

1 Department of Journal of General Microbiology, Trinity College, Dublin 2, Ireland
2 Department of Gastroenterology, The Adelaide and Meath Hospital, Tallaght, Dublin 24, Ireland

ABSTRACT

To date several genes have been identified in Helicobacter pylori that are expressed in only a proportion of strains, some of which are correlated with the pathogenicity of the bacterium. With this in mind, the present study was undertaken to identify other genes that are not expressed in all clinical isolates of H. pylori. Using arbitrarily primed PCR of RNA, a cDNA fragment of 187 bp (designated trl for transfer RNA-associated locus) was identified that was expressed in only one of two clinical isolates being tested. The fragment was purified, cloned and sequenced. A search of public databases prior to the release of the complete genome sequence of H. pylori strain 26695 showed no similarity with any other known genes or gene products. Inverse PCR was used to obtain further nucleotide sequence information surrounding the trl locus. A DNA probe derived from the trl locus hybridized with 32 (50%) of 64 clinical H. pylori isolates tested. Comparison of the nucleotide sequences of a trl-positive and trl-negative isolate showed that the locus is situated between two tRNA genes, tRNAGly and tRNALeu, in H. pylori. Primer extension analysis showed that the trl locus is co-transcribed with tRNAGly. Analysis of the region between tRNAGly and tRNALeu in trl-negative isolates revealed additional genetic diversity among these isolates.

Author for correspondence: William G. Dundon. Tel: +39 049 8276056. Fax: +39 049 8276049. e-mail: dundon@civ.bio.unipd.it


Keywords: arbitrarily primed PCR, ddiversity, dtRNA, horizontal transfer

{dagger} Present address: Centro CNR Biomembrane e Dipartimento di Scienze Biomediche, Università di Padova, Via G. Colombo 3, 35121, Padova, Italy.




This article has been cited by other articles:


Home page
J. Clin. Microbiol.Home page
S. M. Alexander, T. H. Grayson, E. M. Chambers, L. F. Cooper, G. A. Barker, and M. L. Gilpin
Variation in the Spacer Regions Separating tRNA Genes in Renibacterium salmoninarum Distinguishes Recent Clinical Isolates from the Same Location
J. Clin. Microbiol., January 1, 2001; 39(1): 119 - 128.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1999 Society for General Microbiology.