Streptococcal Syndrome?

Discussion in 'Fibromyalgia and ME & Chronic Fatigue Syndrome' started by RadioFM, Jun 23, 2014.

  1. RadioFM

    RadioFM Member

    Radio: I have had problems with streptococcal infections in my family for many years. My sister develop meningitis at 5 years old. My brother develop myocarditis at 25 and my grandmother rheumatic fever at age 19. I feel that streptococcal infections needs more research in relation with chronic diseases.

    Please review these links below.

    "Post streptococcal syndromes may manifest in multiple organs including the musculoskeletal, central nervous, urinary, integumentary, and circulatory systems. The commonly described post streptococcal syndromes include acute rheumatic fever, post streptococcal glomerulonephritis, post streptococcal arthritis, and pediatric autoimmune neuropsychiatric disorders. Classically, these complications occur more often in children. While much is written in the pediatric literature regarding these syndromes, a compilation of information is difficult to find. This article summarizes some of the frequently described post streptococcal syndromes and associations." See more here:

    "Post streptococcal related myalgia/myositis
    : Myalgias are reported in association with streptococcal and/or post streptococcal syndromes. Clinical presentations include severe muscle pain and/or tenderness.37,38 Laboratory data may show elevation in sedimentation rates and leukocytosis, but muscle enzymes and muscle biopsies may be normal. Several cases of post streptococcal polymyalgias have responded to penicillin, NSAIDs or steroid therapy.38-40 " See more here:

    Polymyalgia Rheumatica - CRASH! USMLE Step 2 and 3

    Dysbiosis toxins and other chronic infections can be possible contributing factors as well... Such as: Enterococcus, Mycoplasma, Klebsiella and many others....See link below.

    Last edited: Sep 11, 2014
  2. Mikie

    Mikie Moderator

    No one knows for sure the cause of our conditions. Many are convinced that whatever triggered their CFIDS/ME or FMS is the cause, but cause is not the same as relationship. It's a common assumption people make. I do not believe we can heal until we address our chronic infections but even after or infections are under control, most of us are not cured. Physical or emotional trauma, stress, injury, etc. are known to trigger our conditions. There can be many triggers.

    Love, Mikie
  3. RadioFM

    RadioFM Member

    Radio: I feel we need to identify these possible chronic infections in order to have a chance of keeping them under control.

    Yes, there many contributing factors related to FM. Such as: Inadequate hormone production, HPA axis dysfunction and dysbiosis. But, I have not seen Post Streptococcal Syndrome discussed as a possible factor? This type of chronic infection will not go away with a few courses of antibiotics. There is also molecular mimicry aspect as well as a genetic component to consider related to this possible syndrome.

    See links below...

    Infectious Causes

    Infection may be the most common trigger leading to vasculitis. As a model, vasculitis due to infection is mediated through a type III or immune-complex reaction where the antigens are the infectious agents or antigenic portions of them.[36] After the zone of equivalence is reached, the immune complexes precipitate and become trapped within vessel walls, stimulating an immune response that ultimately leads to vascular injury. Candida polysaccharides and fragments of gram-positive and gram-negative organisms can activate the alternate pathway and also lead to the inflammatory reaction characteristic of vasculitis. Alternatively, direct endothelial cell invasion can be the main pathogenic process in infections caused by cytomegalovirus, herpes simplex, rickettsiae, fungi, and bacteria. Recent concepts suggest other mechanisms may be at work as well in the development of vasculitis within the context of infection. Cytokines, such as tumor necrosis factor and various interleukins, are produced directly by the stimulation from the infectious agents. Subsequently, recruitment of neutrophils to the small vessels occurs and leads to the development of vasculitis. Vasculitis related to infection due to streptococcus and staphylococcus has been associated with this mechanism of vascular injury. See more here:

    The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Pay it forward and never give up the fight!
    Last edited: Sep 1, 2014
  4. Mikie

    Mikie Moderator

    Some bacteria do not go away. People with Lyme or mycoplasma infections may have the bacteria go into a cyst form deep inside body tissue. Getting injured, sick or being stressed can allow these latent cysts to become active again. I have a chronic mycoplasma infection which has been latent for a long time (knocking on wood :) Unfortunately, many docs do not realize that just a couple of courses of ABX will not stop these infections. It takes at least a six-month course of ABX to deal with mycoplasma infections and, even then, one may have to pulse off and on the ABX for a much longer time. I was on Doxycycline for 2 1/2 years to drive my mycoplasma infection into latency. That's likely because it went untreated for so long until I found Dr. Nicolson.

    Herpes-Family viral infections also never go away and can reactivate under the same conditions as above. Keeping everything latent may be the best we can do with some of these chronic infections. Building up a healthy immune system is absolutely necessary to keeping these infections at bay. Our treatments have to be multi-faceted. Transfer Factors can really help with this. I also took them and they were much stronger than either ABX or AVs.

    Love, Mikie
    RadioFM likes this.
  5. RadioFM

    RadioFM Member

    Yes, I agree with you 100%....Lyme disease is a hug factor to consider and needs to be evaluated. Yes, we need to build up the immune system and it will be necessary in-order to help keep these infection under control.

    I feel that streptococcal infection may be inside lymphatic system as well and deep inside body tissue. Please review these threads as there is some great research links on this topic.

    Last edited: Sep 15, 2014
  6. Abdulrahman

    Abdulrahman Member

    Hello Radio,

    I am responding to your first message. Wth regard to those that have repeated and long term bacterial infections as you stated such as Myocarditis [ Heart Tissue Infection] and Menigitis there is an important factor i discovered; and that is that the immune deficiency is not the only cause of such infections. A very important cause is the serious deficiency in human tissues of critical minerals that are anti-viral and anti-bacterial.

    The following minerals exhibit anti-bacterial resitance when incorporated in tissues such as heart tissue, Kidney tissue, Liver, Brain....: Copper, Selenium, Iodine

    For those with a deficiency in the body of the above minerals, there will be a low resistance to bacterial attack, and this is dangerous to the critical organs. The proof of the above statement is that if you study the concentration of the above minerals in Heart Tissue, Liver, and Kidneys the levels are far higher than found in other tissues. The body is incorporating a high concentration of these minerals in such critical organs to act as an anti-viral and anti-bacterial shield.

    The majority of people have little idea of how much Copper or Selenium should be stored in the body and where are the highest food sources.
    RadioFM likes this.
  7. Abdulrahman

    Abdulrahman Member

    The antibacterial effects of lithium, selenium, and germanium were evaluated with respect to growth, biofilm formation, and mutational frequencies (MF), of Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. Selenium showed the highest antimicrobial and bactericidal activities as shown by zone of inhibition assay and scanning electron microscopy imaging (SEM). The SEM images showed that the metals in culture media led to cell disintegration that could have resulted in the leakage of cytoplasmic constituents, and cell dehydration. In biofilms, the combination of metal and antibiotics increased oxidative stress, mutational frequencies(MF), and formation of mutator phenotypes. Adding the antioxidant ascorbic acid reduced the S. aureus biofilm MF, but increased the MF of P. aeruginosa biofilm. Image analysis showed that metal and ascorbic acid cooperated in destroying cell structure pointing to the effectiveness of the antioxidant to prevent the formation of reactive oxygen species, oxidative stress, and bacterial DNA mutation rates. Generally, results showed that the antibacterial effect depended on the combinations of metal, antibiotic and antioxidant different and the bacterial strain being tested. Biofilm cultures yielded adherent colony variants that differed in appearance and in the capability of the variants to form hypermutator phenotypes with relatively high MFs. There was perfect sequence alignment of an approximately 500 bases of the P. aeruginosa 16S rDNA fragment of the wild-type and colony variants. In contrast, the 16S rDNA sequence of S. aureus variant showed several mutations, deletions, and insertions, implying the high mutability of S. aureus when exposed to external factors. Further studies should be conducted on the molecular basis of the antibacterial action and possible applications of selenium, germanium, and lithium in reducing antibiotic resistance, and biofilm infection. In addition, there is a need to understand bacterial adaptation to metals and their interaction with other antimicrobial agents in order to design effective drug therapies.
    RadioFM likes this.
  8. Abdulrahman

    Abdulrahman Member

    Mechanisms of antibacterial action of copper[edit]
    In 1973, researchers at Battelle Columbus Laboratories[4] conducted a comprehensive literature, technology and patent search that traced the history of understanding the “bacteriostatic and sanitizing properties of copper and copper alloy surfaces” which demonstrated that copper, in very small quantities, has the power to control a wide range of molds, fungi, algae and harmful microbes. Of the 312 citations mentioned in the review across the time period 1892–1973, the observations below are noteworthy:
    A subsequent paper [11] probed some of copper’s antimicrobial mechanisms and cited no fewer than 120 investigations into the efficacy of copper’s action on microbes. The authors noted that the antimicrobial mechanisms are very complex and take place in many ways, both inside cells and in the interstitial spaces between cells.
    Examples of some of the molecular mechanisms noted by various researchers include the following:
    • The 3-dimensional structure of proteins can be altered by copper, so that the proteins can no longer perform their normal functions. The result is inactivation of bacteria or viruses [11]
    • Copper complexes form radicals that inactivate viruses.[12][13]
    • Copper may disrupt enzyme structures, and functions by binding to sulfur- or carboxylate-containing groups and amino groups of proteins.[14]
    • Copper may interfere with other essential elements, such as zinc and iron.
    • Copper facilitates deleterious activity in superoxide radicals. Repeated redox reactions on site-specific macromolecules generate OH- radicals, thereby causing “multiple hit damage” at target sites.[15][16]
    • Copper can interact with lipids, causing their peroxidation and opening holes in the cell membranes, thereby compromising the integrity of cells.[17] This can cause leakage of essential solutes, which in turn, can have a desiccating effect.
    • Copper damages the respiratory chain in Escherichia coli cells.[18] and is associated with impaired cellular metabolism.[19]
    • Faster corrosion correlates with faster inactivation of microorganisms. This may be due to increased availability of cupric ion, Cu2+, which is believed to be responsible for the antimicrobial action.[20]
    • In inactivation experiments on the flu strain, H1N1, which is nearly identical to the H5N1 avian strain and the 2009 H1N1 (swine flu) strain, researchers hypothesized that copper’s antimicrobial action probably attacks the overall structure of the virus and therefore has a broad-spectrum effect.[21]
    • Microbes require copper-containing enzymes to drive certain vital chemical reactions. Excess copper, however, can affect proteins and enzymes in microbes, thereby inhibiting their activities. Researchers believe that excess copper has the potential to disrupt cell function both inside cells and in the interstitial spaces between cells, probably acting on the cells’ outer envelope.[22]
  9. Abdulrahman

    Abdulrahman Member

    Warning: Please note that the above minerals should be taken only in their organic state otherwise when in their mineral chemical form, they are looked upon by the body as pollutants, not as critical minerals to be used for physiological functions. Therfeore, mineral Copper is damaging to your health, and the same applies to Selenium.

    But when eaten through high concentration organic sources, the result is instant absorption by the body and very great health benefits. Plants absorb the minerals from soils and then transform the minerals into organic molecules which the human body will absorb well. In addition, animals eat such plants and will concentrate the minerals in some organs. For example, liver is the highest source of copper in animals and humans because it is stored there by the animal body. The Highest plant sources in the world for the anti-bacterial and anti-viral minerals are:

    Copper: Tamarind Fruit ----------------- 20 mg Copper/100 g Fruit , Extremely High Concentration, about 100 x typical concentrations in foods

    Selenium: Brazil Nuts -------------------- 550 mcg/Ounce or six to eight nuts, Extremely High about 20 x other highest selenium foods

    Sulfur: Mustard Seed or Mustard Sauce -------------- 10,000 mg Sulfur/100 g seed extremely High, about 20 x other high Sulfur Foods

    Iodine: Seaweed -------------------Varies from seaplant to seaplant but can be averaged at 1000 mcg Iodine/1 grams dried seaweed

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  10. RadioFM

    RadioFM Member

    Last edited: Sep 15, 2014