New Probiotic on Market: L Reuteri NCIMB 30242 (ONLY)

There are eight PubMed studies on this strain.

  • Significantly changes the size and composition of the circulating bile acid [2015]
  • a greater proportion of L. reuteri-treated subjects showed improved general GI health status (p = 0.042) and improved diarrhea symptoms (p = 0.03). [2013]
  • the first report of increased circulating 25-hydroxyvitamin D in response to oral probiotic supplementation[2013]

For general information about L.Reuteri see my earlier post.

Available from manufacturer and on Amazon.

This stain is also sold as Cardioviva on amazon

I have just ordered some myself.

Probiotics with Demonstrated Health Benefits and Other Gems

Tonight I found two gems that I wish to share

“The major effects of stress on gut physiology include:

  1. alterations in gastrointestinal motility;
  2. increase in visceral perception;
  3. changes in gastrointestinal secretion;
  4. increase in intestinal permeability;
  5. negative effects on regenerative capacity of gastrointestinal mucosa and mucosal blood flow; and
  6. negative effects on intestinal microbiota.

Mast cells (MC) are important effectors of brain-gut axis that translate the stress signals into the release of a wide range of neurotransmitters and proinflammatory cytokines,”[2011]

Histamine released from Mast Cells cause many of the symptoms of a Jarisch-Herxheimer reaction. So I was about to do a quick review of PubMed for candidates that reduced Mast Cell release:

  • Lactobacillus GG (LGG) [2014] – strong impact – Commercial Probiotic: Culturelle
  • L. salivarius HMI001 [2012]
  • L. casei Shirota (LCS)  [2012]
  • Lactobacillus plantarum depends on the specific strain — if not known, avoid
    • LS/07 CCM7766 [2015] – moderate impact
    • L. plantarum WCFS1 – INCREASES Mast Cell release [2012]

At this point of browsing PubMed, I discovered the 2014 article (World J Gastroenterol. 2014 Aug 28; 20(32): 11023–11032.) and it distracted me because it had some nice tables based on recent literature which warrants reposting.

Recommendations for probiotic use from [2014]

Clinical condition Effectiveness Organism

Diarrhea

Infectious-adult-treatment A Saccharomyces boulardi, LGG
Infectious-childhood- treatment A LGG. Lactobacillus reuteri
Prevention of infection B S. boulardii, LGG
Prevention of AAD A S. boulardii, LGG, L. casei, L. bulgaricus, S. thermophilus
Treatment of recurrent CDAD B S. boulardii, LGG
Prevention of CDAD B LGG, S. boulardii
IBD

Pouchitis

Preventing and maintaining remission A VSL#3
Induce remission C VSL#3

Ulcerative colitis

Inducing remission C Escherichia coli Nissle, VSL#3
Maintenance C E. coli Nissle, VSL#3
Crohn’s C E. coli Nissle, S. boulardii, LGG

IBS

B Bifidobacterium infantis
IBS C Bifidobacterium animalis, VSL#3, Lactobacillus plantarum
Immune response A LGG, Lactobacillus acidophilus, L. plantarum, Bifidobacterium lactis, Lactobacillus johnsonii

Allergy

Atopic eczema assoc. with cow milk allergy
Treatment A LGG, B. lactis
Prevention A LGG, B. lactis
Radiation enteritis C VSL#3, L. acidophilus
Vaginosis and vaginitis C L. acidophilus, LGG, L. reuteri

Reproduced with permission from reference Floch et al[31].

  • An ‘‘A’’ recommendation is based on strong, positive, well-conducted, controlled studies in the primary literature, not abstract form;
  • A ’‘B’’ recommendation is based on positive, controlled studies but the presence of some negative studies;
  • A ‘‘C’’ recommendation is based on some positive studies.
  • IBD: Inflammatory bowel disease;
  • LGG: Lactobacillus GG;
  • S. boulardii: Saccharomyces boulardii.

Reflections on the Treatment of Histamine Oversensitivity

I have an ongoing interest in this area, and this is a followup to my Jan 20th post dealing with Histamine Producing Bacteria and their treatment. In that article I found that Cinnamon, Clove, Sage were good candidates for reducing Proteus morganii  (All species) which is likely an overgrowth in sensitive individuals (To confirm that, we will need a population of histamine-sensitive people getting their gut bacteria sequence).

When I did from googling on those and histamines, I found that they were frequently referred to as histamine liberators [Amy Burkhart, M.D.]. That description is probably very correct — the histamine is being released from dead and dying Proteus morganii.

Unfortunately, some cases writers deem them to be histamine producers [ref, ref] which clouds the issue for sufferers and may prevent them from being released from this problem!

Die-Off or the Jarisch-Herxheimer reaction

Wikipedia has a good summary of the “Herx”. I have experienced this on several occasions and actually view it as an indicator that I am taking an effective herb, spice or antibiotic for what was making me sick. The Herx stopped with remission. By moderating the dosage, I could tune the herx to last only a few hours (or at night, all night long) – with the result that after the herx ended, I felt better.

  • “plasma histamine concentrations rose appreciably before and during the clinical phase of the reaction.”[1985 Full Text]

So the question then becomes one of moderating the histamine release. I recently came across G. Pelletier’s “Naturally Occurring Antihistamines in Body Tissue” in Histamine II and Anti-Histaminics Handbuch der experimentellen Pharmakologie / Handbook of Experimental Pharmacology Volume 18 / 2, 1978, pp 369-380

He found that arginine – an amino acid, had significant impact and was the easiest to obtained of items listed. Interestingly, I found that arginine was usually associated with histamine in most online patient-written articles and recommended to be avoided. In other articles, I found that histidine and arginine tend to bind to each other (potentially reducing the risk of histidine being converted to histamine?). Going to PubMed, I found

  • “Our findings reveal that malarial-parasite-infected mice, like humans, develop L-arginine deficiency, which is associated with intestinal mastocytosis, elevated levels of histamine, and enhanced intestinal permeability.” [2013], so arginine deficiency and elevated histamine appears associated. And supplementation can reduce it.
  • Arginine and glutamine attenuate IgE-dependent human mast cell activation” [2013]
  • “while the histamine response in cells cultured in a high Arginine concentration was suppressed” [2013]

Garlic, IBS, CFS, and the Microbiome

A reader wrote “Every time I eat garlic, both cooked and raw, I get a LOT of foul smelling gas… I don’t get this from onions for example…Do you have any idea why this is, what it might indicated as far as the microbiome go? I know garlic is rich in inulin…”

Inulin from garlic is well known, as well as from:

  • artichokes, garlic, beans, oats, onions and asparagus [ref]

I also recall that garlic has anti-biotic characteristics:

fresh garlic, but not aged garlic, can kill certain bacteria such as E. coli, antibiotic-resistant Staphylococcus aureus, and Salmonella enteritidis in the laboratory.” [WebMd]

Historically:

“From Roman antiquity through World War I, garlic poultices were used to prevent wound infections. The famous microbiologist Louis Pasteur performed some of the original work showing that garlic could kill bacteria. In 1916, the British government issued a general plea for the public to supply it with garlic in order to meet wartime needs. Garlic was called Russian penicillin during World War II because, after running out of antibiotics, the Russian government turned to this ancient treatment for its soldiers.

After World War II, Sandoz Pharmaceuticals manufactured a garlic compound for intestinal spasms, and the Van Patten Company produced another for lowering blood pressure.” [NYU]

Going over to PubMed

  • Garlic contains sulfur compounds like allicin, ajoene, allylmethyltrisulfide, diallyltrisulfide, diallyldisulphide and others which exhibit various biological properties like antimicrobial, anticancer, antioxidant, immunomodulatory, antiinflammatory, hypoglycemic, and cardiovascular effects.[2014]
  • ReducesInflammatory bowel disease (IBD) [2014]
  • Reduces  free-living (Hexamita inflata), and parasitic (Spironucleus vortens and Giardia intestinalis).[2014] Spironucleus vortens[2014]
  • garlic exhibits antibacterial activity against probiotic bifidobacteria. The aim of the current study was to elucidate the mechanism of action of garlic clove extract (GCE) on Bifidobacterium bifidum LMG 11041, B. longum LMG 13197 and B. lactis Bb12 [2014] – so do not take garlic with bifidobactra probiotics!

For more follow there links: Intestines and garlic and  garlic and antibiotics

Bottom Line

The foul smelling gas is likely release by species of bacteria being killed. Cross referencing species cited above I found that Giardia intestinalis is garlic sensistive and produces foul smelling faeces  [2014] as one possibility. Other possibilities include Aerococcus urinae [2013], Strongyloides stercoralis [2012] and likely many more.

A suggestion to discuss with your medical professional would be whether to try increasing dosage (fresh garlic – not capsules etc)  and see if the foul smell eventually clears (suggesting that the bacteria has been effectively reduced). It should be discussed with whoever lives with you… you could be a challenge to be around!.

Looking at the current Genova Diagnostics – GI Effects / Stool Profiles

A CFS reader asked me to review his results and provided a  masked copy of their report (Attached).

In looking at the report, I would describe it as better than the ones in the past.

Page 1

Summaries:

  • High IgA levels
  • Imbalance
  • Lower Diversity
  • Signifiant less abundance

Page 2

  • High Triglycerides – the odds of this with CFS is twice that of controls [2010]. It is also associated with some inherited coagulation defects.
    Fecal secretory IgA is in reference range which seems inconsistent with Page 1
  • n-Butyrate is slightly below the normal range, Propionate is higher. – which suggests IBS with CFS
    • “Patients with inflammatory bowel disease have lower numbers of Butyricicoccus bacteria in their stools. Administration of B pullicaecorum attenuates TNBS-induced colitis in rats and supernatant of B pullicaecorum cultures strengthens the epithelial barrier function by increasing the TER.” [2013]
    • ” Elevated levels of amino acids (alanine and pyroglutamic acid) and phenolic compounds (hydroxyphenyl acetate and hydroxyphenyl propionate) were found inIBS” [2011]

Page 3

  • High level of:
  • Low level of:
    •  Bifidobacterium – typical – See my earlier post
    • Firmicutes/Bacteroidetes Ratio – this is almost identical to the results of another CFS patient [Post]
  • Not detectable:
    • Anaerotruncus colihominis – just 3 pub med articles
    • Coprococcus eutactus – IBS marker [2014]
    • faecalibacterium prausnitzii. ” A reduction of enteric microbiota diversity has been observed in UC patients, mainly affecting the butyrate-producing bacteria, such as Faecalibacterium prausnitzii, which can repress pro-inflammatory cytokines [2014] which may explain the low butyrate levels.
    • Colinsella aerofaciens [ just one article]

Page 4

Gastroinstentinal Microbiome – one issue: Klebsiella pneumonia was high as seen in a prior reader’s lab

Page 5

Microscopic Exam Results – no issues

Page 6

Additional results – no issues

Page 7

Prescriptive Agents:

Only Klebsiella pneumonia was listed and the antibiotics effective against it. This is a histamine producing bacteria and thus over population can result in histamine sensitivity and many CFS like symptoms.

Bottom Line

The results are the same pattern of other CFS patients. The strong IBS indicators suggests that Prescript Assist (which has resulted in IBS remission for a significant percentage) is a logical course of treatment.

Anonomous Report Shared With Me