Genetic characterisation of Helicobacter pylori isolates from an Argentinean adult population based on cag pathogenicity island right-end motifs, lspA-glmM.

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Genetic characterisation of Helicobacter pylori isolates from an Argentinean adult population based on cag pathogenicity island right-end motifs, lspA-glmM polymorphism and iceA and vacA genotypes  A.G. Leanza, M.J. Matteo, O. Crespo, P. Antelo, J. Olmos, M. Catalano  Clinical Microbiology and Infection  Volume 10, Issue 9, Pages 811-819 (September 2004) DOI: 10.1111/j.1198-743X.2004.00940.x Copyright © 2004 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 1 Representative sequences of the right-end junction region of the cag pathogenicity island (PAI) type III motif and iceA gene. (a) Type III motif isolates characterised by 200-bp unk1 (function unknown [9]) gene sequences that replace almost the entire hel (helicase) gene. The GenBank accession numbers of isolates AR-66, AR-312, AR-616 and AR-43 are AY186032, AY186031, AY186030 and AY186033, respectively. (b) Corresponding empty site in isolates that lack a mini-IS605 insertion at the site of the remnant IS606&* in the right-end junction region of the cag PAI. Absence of a mini-IS605 element in the four DNA fragments classified as type IIIa motif. (c) Type IIIa motif isolates with and without a 39-bp deletion; isolates AR-66 and AR-43 lack this 39-bp deletion, as does strain AF190662 (Sweden53 [12]); AR-312 and AR-616 carry this deletion, as does strain AF191011 (JapanHU54 [12]). (d) Representative sequences of the iceA1 gene at the site of the forward universal primer. Primer sequences are in lower-case letters [4,9]. The GenBank accession numbers of isolates AR-25, AR-82 and AR-84 are AY185132, AY185133 and AY185134, respectively. Clinical Microbiology and Infection 2004 10, 811-819DOI: (10.1111/j.1198-743X.2004.00940.x) Copyright © 2004 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 2 Alignments of vacA-s1 DNA sequences. S1a-F (lower-case sequences without shading) and SS3-F: forward primers for vacA-s1a and vacA-s1b detection by PCR-typing, respectively [4,11]. P1S1 and P22S1a, and P2S1b and P2S1b: oligonucleotide probes for vacA-s1a and vacA-s1b detection by reverse hybridisation, respectively [10]. The GenBank accession numbers of isolates AR-312, AR-710, AR-602(III) and AR-609 are AY185131, AY185128, AY185130 and AY185129, respectively. Clinical Microbiology and Infection 2004 10, 811-819DOI: (10.1111/j.1198-743X.2004.00940.x) Copyright © 2004 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 3 Results of analysis by lspA-glmM polymorphism. (a) Similarity among lspA-glmM fingerprints exhibited by isolates recovered from single colonies of the same biopsy and others from different biopsies. Similarity was scored by Dice coefficient [21]. Letters following a case number indicate isolates recovered from the same biopsy. (b) Fingerprints obtained with AluI (lanes 1-5) and HhaI (lanes 6-11). M, 100-kb size marker ladder (Promega). Clinical Microbiology and Infection 2004 10, 811-819DOI: (10.1111/j.1198-743X.2004.00940.x) Copyright © 2004 European Society of Clinical Infectious Diseases Terms and Conditions