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You should discuss various treatment options, their risks and benefits, with your own doctor . Be aware that treatment of H. pylori is not always recommended by all experts on H. pylori , or in all patients with H. pylori . Each patient is an individual and decisions must be made in concert with his or her own medical practitioner on a case-by-case basis. The Helicobacter Foundation makes a good faith attempt to ensure that information provided is accurate and up-to date, but answers posted by persons on this board are opinions of that person. You should check the credentials of the person making the posting. Ideally, information supplied through these forums has been published or presented at national and international scientific meetings. The Helicobacter Foundation makes no guarantees about the accuracy of this information which is given free of charge to whomever requests it.

Basic Science / Molecular Epidemiology / Evolution

Scientific questions might be discussed here - maybe someone technical can answer them and provide special insights.
Moderators: Toni, barjammar, stomach
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  • Toxins (esp. CagA and VacA)
    CagA was the first protein antigen identified as a marker for the more evil type of H.pylori. cagA is one of about 30 genes in Cag pathogenicity island (cagPAI). These genes form a secretion system which injects CagA protein into cells where it causes disorganised cellular structure due to "growth factor like" effects.
    VacA is a toxin which causes vacuolation of epithelial cells (bubbles within) when H.pylori attaches. VacA is a activated in acid to form a membrane pore which causes cells to become leaky, especially to urea. It also suppresses some of the immune response allowing H.pylori to persist.
    Moderators: Toni, barjammar, stomach
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  • Other Evil Genes (babA, dupA, NAP etc)
    Numerous other genes increase attachment, invasion, neutrophil attraction, survival and/or persistance of H.pylori in the gastric mucosa.
    Moderators: Toni, barjammar, stomach
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  • Genomics of Helicobacters
    One of the first bugs to be sequenced, H.pylori has a small genome (1.6 MD) befitting its lifestyle in a hostile acidic mucosal niche. Of the 1500 genes, 750-1000 are essential, the others are different in each strain. Hp has an "open pan-Genome" which means the more strains you look at the more genes you will find - i.e. you will never have a complete set of all its possible genes!
    Moderators: Toni, barjammar, stomach
    3 Topics
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    Last post by stomach View the latest post
    Fri May 28, 2010 9:59 am
  • Animal Models of Hp
    The initial animals infected with human Hp were germ free piglets. After that beagle puppies, pigs, mice, cats and, best of all, Mongolian Gerbils. The latter animals develop ulcers and stomach tumours in the presence of salt and carcinogens - similar to humans. There is much work to be done in this area.
    Moderators: Toni, barjammar, stomach
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  • Other Basic Sciences of Hp
    Many more basic science categories can be added. If we have some good entries here we can expand the topic list.
    Moderators: Toni, barjammar, stomach
    3 Topics
    12 Posts
    Last post by barjammar View the latest post
    Wed May 19, 2010 6:20 am
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