Literature DB >> 11773120

Phenotypic variation of Helicobacter pylori isolates from geographically distinct regions detected by lectin typing.

Sean O Hynes1, Nathalie Broutet, Torkel Wadström, Marika Mikelsaar, Paul W O'Toole, John Telford, Lars Engstrand, Shigeru Kamiya, Andreas F Mentis, Anthony P Moran.   

Abstract

A total of 309 Helicobacter pylori isolates from 18 different countries were analyzed with a previously developed lectin typing system. The system was developed by using a proteolytic pretreatment to enhance the carbohydrate fraction of the sample. Four lectins from Ulex europaeus, Lotus tetragonolobus, Erythrina cristigali, and Triticum vulgaris were used to type the strains. The lectins were chosen for their specificities for sugars commonly encountered in the lipopolysaccharide of H. pylori. The isolates were received from their parent institutions as pellets of biomass and were typed at one of three centers (in Ireland, Sweden, and Estonia). All 16 possible lectin reaction patterns were observed in the study, with the isolates with the predominant pattern exhibiting reactions with all the lectins in the panel. For European patients suffering from gastritis, an association was noted between lectin reaction pattern MH4 and atrophic chronic gastritis; isolates with lectin reaction pattern MH4 were isolated from patients with atrophic chronic gastritis, whereas isolates with this pattern were not isolated from patients with chronic gastritis (P = 0.0006). In addition, statistically significant relationships were noted between the lectin reaction pattern and the associated pathology of isolates from the Swedish population. Isolates with patterns MH13 and MH16, which had low lectin reactivities, correlated with nonulcer disease (P = 0.0025 and P = 0.0002, respectively), and all four isolates from adenocarcinoma patients were characterized as possessing reaction pattern MH16. In contrast, isolates with lectin reaction patterns MH1 and MH10, which had high lectin reactivities, were associated with ulcer disease (P = 0.046 and P = 0.0022, respectively).

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Year:  2002        PMID: 11773120      PMCID: PMC120102          DOI: 10.1128/JCM.40.1.227-232.2002

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  35 in total

1.  Lectin typing of Campylobacter isolates.

Authors:  N O'Sullivan; J Benjamin; M B Skirrow
Journal:  J Clin Pathol       Date:  1990-11       Impact factor: 3.411

2.  Analysis and typing of the vacA gene from cagA-positive strains of Helicobacter pylori isolated in Japan.

Authors:  Y Ito; T Azuma; S Ito; H Miyaji; M Hirai; Y Yamazaki; F Sato; T Kato; Y Kohli; M Kuriyama
Journal:  J Clin Microbiol       Date:  1997-07       Impact factor: 5.948

3.  Expression of the human cell surface glycoconjugates Lewis x and Lewis y by Helicobacter pylori isolates is related to cagA status.

Authors:  H P Wirth; M Yang; M Karita; M J Blaser
Journal:  Infect Immun       Date:  1996-11       Impact factor: 3.441

Review 4.  The role of Helicobacter pylori in pathogenesis: the spectrum of clinical outcomes.

Authors:  R H Hunt
Journal:  Scand J Gastroenterol Suppl       Date:  1996

5.  Lectin typing of Pseudomonas aeruginosa strains of different serogroups, Habs and Fisher types.

Authors:  B P Chatterjee; A K Guha; R Pal; M Bhattacharyya
Journal:  Zentralbl Bakteriol       Date:  1989-09

6.  Typing of Helicobacter pylori with monoclonal antibodies against Lewis antigens in lipopolysaccharide.

Authors:  I M Simoons-Smit; B J Appelmelk; T Verboom; R Negrini; J L Penner; G O Aspinall; A P Moran; S F Fei; B S Shi; W Rudnica; A Savio; J de Graaff
Journal:  J Clin Microbiol       Date:  1996-09       Impact factor: 5.948

7.  Allelic variation in the cagA gene of Helicobacter pylori obtained from Korea compared to the United States.

Authors:  S Miehlke; K Kibler; J G Kim; N Figura; S M Small; D Y Graham; M F Go
Journal:  Am J Gastroenterol       Date:  1996-07       Impact factor: 10.864

8.  Clinical and pathological importance of heterogeneity in vacA, the vacuolating cytotoxin gene of Helicobacter pylori.

Authors:  J C Atherton; R M Peek; K T Tham; T L Cover; M J Blaser
Journal:  Gastroenterology       Date:  1997-01       Impact factor: 22.682

9.  Antigenicity of Helicobacter pylori lipopolysaccharides.

Authors:  S D Mills; L A Kurjanczyk; J L Penner
Journal:  J Clin Microbiol       Date:  1992-12       Impact factor: 5.948

10.  Agglutination of "Streptococcus milleri" by lectins.

Authors:  J T Kellens; J A Jacobs; W J Peumans; E E Stobberingh
Journal:  J Med Microbiol       Date:  1994-07       Impact factor: 2.472

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