Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Helicobacter 1 (1996), S. 0 
    ISSN: 1523-5378
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: BackgroundRapid urease tests (RUTs) provide a simple, sensitive method of detecting Helicobacter pylori infection. Objectives.Our aim, therefore, was to determine whether the yield of detecting H. pylori infection by RUT varied depending on the site of gastric biopsy. Materials and Methods.Gastric biopsies were obtained from 50 patients for RUT by use of hpfast (GI Supply, Camp Hill, PA). Biopsies were taken from the prepyloric greater curve antrum, from the gastric angle, and from the greater curve in mid-corpus. One biopsy specimen was placed in the RUT gel, and the biopsy from the adjacent mucosa was placed in formalin for subsequent histological evaluation by using the Genta stain. RUTs were examined and scored at intervals of 5, 10, 15, 30, and 45 minutes and after 1, 2, 4, and 24 hours. Results.Fifty patients were entered in the test (150 RUTs), 32 having H. pylori infection. There were no false-positive RUTs (specificity, 100%). The gastric angle site was positive in 100%. The prepyloric site was positive in 87%, and the corpus site was positive in 84.4% (p 〈 .052 for angle or prepyloric antrum versus corpus). The most common pattern was for all to be positive (74%). The median time to positivity was similar with angle and prepyloric sites (37.5 and 60 minutes, respectively, p= not significant) and shorter than the corpus biopsy (180 minutes); (p 〈 .05 for angle or prepyloric antrum versus corpus). Conclusion.The maximum probability for detecting H. pylori infection using a RUT is to obtain a biopsy from the gastric angle. To prevent missing a positive result when intestinal metaplasia is present, we recommend that (at a minimum) biopsies be taken from both the angle and the corpus.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1573-2568
    Keywords: REP-PCR FINGERPRINTING ; DISEASE-SPECIFIC DNA FRAGMENTS ; H. PYLORI
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We previously identified four potential putativegastroduodenal disease fragments by using theinterspersed repetitive extragenic palindromic DNAsequence based PCR (REP-PCR) technique. We investigated these fragments with regard to their diseasespecificity. The putative disease-specific REP-PCRfragments were cloned, mapped by restriction enzymes,cross-hybridized, and confirmed by Southernhybridization. The four fragments were also used as probesagainst REP-PCR amplicons from H. pylori isolatesobtained from gastritis (N = 20), duodenal ulcer (N =30), and gastric cancer patients (N = 30). Three ofthese fragments (1.4- and 0.76-kb for gastritis; 1.35kb for duodenal ulcer) were amplified without anydiscrimination between any disease-specific H. pyloriisolates. However, amplification following hybridization with the fourth 0.81-kb fragment was observedonly from gastritis (60%) and duodenal ulcer (52%) butwith none (0%) of gastric cancer patients. Nucleotidesequence analysis of the 0.81-kb fragment revealed that it was an open reading frame of thehypothetical protein HP0373 matched to the position of380,966 to 383,068 nucleotides of the H. pylori completegenome sequence. Hence, the REP-PCR sequence was not a extragenic palindromic DNA sequence. Thehypothetical protein was also present in all the testedisolates. The REP-PCR fingerprinting technique is usefulto differentiate disease-specific H. pylori strains based on the interspersed repetitiveextragenic palindromic DNA sequences; however, it maynot be useful to identify disease-specific virulencedeterminant(s) without being confirmed by DNA sequence analysis and functional studies.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1432-0991
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The galE gene product, UDP-galactose 4-epimerase, mediates the incorporation of galactose in extracellular polysaccharide materials such as the O-side chain of lipopolysaccharide (LPS). The O-side chain in H. pylori LPS has been shown to cross-react with Lewis x and/or y blood group antigens, suggesting its potential involvement in H. pylori-linked autoimmune disease. To study its role in H. pylori LPS biosynthesis, the galE gene was cloned, sequenced, and a galE-knockout H. pylori strain was constructed. The H. pylori galE gene encoded a protein of 344 amino acids with a molecular weight of 39K. The LPS profile from the galE-knockout H. pylori strain showed a lower molecular weight than that of the parental strain, indicating the involvement of the galE gene in LPS biosynthesis of H. pylori.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...