Long Covid Study – VERY early data

This post is intended for researchers by pointing to bacteria whose genetics are likely significant for long COVID. The raw data is below. Preliminary z-scores indicated that they are significant (Pr < 0.01) and no filtering has occurred for False Detection Rate. Users are advised to perform their own statistics.

Note: These results are lab-specific, using the data provided by BiomeSight.

The reference site for the study is: http://longcovid.microbiomeprescription.com/, the raw data is available at: http://citizenscience.microbiomeprescription.com/

Symptom ObsNo Symptom ObsLabSymptomName
152998biomesightOfficial Diagnosis: COVID19 (Long Hauler
The sample population
Bacteriatax_rankNo Symptom CountSymptom CountNo Symptom Frequency %Symptom Frequency %
Lactococcusgenus62013662.189.5
Negativicoccusgenus4618646.256.6
Pedobacter kwangyangensisspecies3547635.550
Hydrogenophilaceaefamily4809048.159.2
Nostocgenus3446834.544.7
Veillonella montpellierensisspecies5179451.861.8
Rhodothermalesorder24362.423.7
Gillisia limnaeaspecies58611458.775
Tetragenococcusgenus60110760.270.4
Gillisiagenus59211459.375
Paenibacillaceaefamily77113377.387.5
Tetragenococcus halophilusspecies1015510.136.2
Rhodothermiaclass24362.423.7
Hydrogenophilaliaclass479904859.2
Bifidobacterium brevespecies4318243.253.9
Thermosediminibacteralesorder72557.236.2
Bifidobacterium choerinumspecies65411765.577
Bifidobacterium longumspecies71512971.684.9
Hydrogenophilalesorder4809048.159.2
Hydrogenophilusgenus4308143.153.3
Rhodothermaeotaphylum24362.423.7
Items deem significant based on Bernoulli distribribution
Bacteriatax_rankNo Symptom MeanSymptom MeanNo Symptom StdDevSymptom Std DevSymptom ObsNo Symptom Obs
Porphyromonas bennonisspecies3177131435.92361.143288
Clostridiaclass618307487672199278.7150542.1152995
Insolitispirillum peregrinumspecies82591219815534.521217.596593
Sphingobacteriumgenus112515901432.31764.9150938
Sphingobacteriiaclass296344221929577.839150.6152995
Lelliottia amnigenaspecies9222052676.6592.238301
Roseburia faecisspecies13441712219243.98796.5152978
Leptolyngbyaceaefamily67266152.61051.535232
cellular organismsnorank9940549883959012.55355.3152996
Opitutaeclass142315447.2759.379604
Caloramator mitchellensisspecies81621358019886.927582.2145925
Leptolyngbyagenus67266152.21051.535230
Sphingobacteriaceaefamily259593736226540.835832.1152994
Cytophagiaclass9482232289911229.4150960
Aphanizomenonaceaefamily222124374.4152.8108653
Betaproteobacteriaclass282712148026518.817465.6151993
Pseudanabaenalesorder110230274973.341297
Pseudanabaenaceaefamily68230141.9973.441297
Spirosomaceaefamily73022823089.712178.6127791
Tenericutesphylum250763955922.116841.5147957
Puniceicoccaceaefamily139301443741.779599
Sutterella wadsworthensisspecies64181049110990.413485.8108636
Eubacterialesorder614586482370199230.3150329.8152995
Dolichospermumgenus217125371.1153.2107646
Dialister invisusspecies479680359328.110909.7105622
Mollicutesclass250763955922.116841.5147957
Coprococcus catusspecies12568681371850136804
Treponemataceaefamily1604544813832.332843.837235
Dorea formicigeneransspecies143491415911112.9142902
Bacteroides eggerthiispecies85451538521533.530777.757394
Cytophagalesorder9482232289911229.4150960
Spirochaetalesorder1551544813579.132843.837244
Terrabacteria groupclade721047521084231350.3165314.8152996
Cytophagaceaefamily78521892917.911452.3144907
Caloramatorgenus88591412620084.927641.6151972
Spirochaetesphylum90337431012027201.354441
Emticiciagenus78425533286.612937.6112693
Leptolyngbya laminosaspecies66266152.81051.535228
Burkholderialesorder279632130526363.517380.9151993
Pedobactergenus8642130411010617703.6151980
Burkholderiaceaefamily361197598.7409.8135886
Eubacteriales incertae sedisnorank375161837.1256.6139895
Butyrivibrio proteoclasticusspecies4962031108.1350.589657
Dolichospermum curvumspecies20197393.5137.787505
Desulfovibrio fairfieldensisspecies7202631789.350843284
Bacteroidaceaefamily300654238983181167141573.4152995
Bacteroidiaclass426327369089188681.8168273.3152995
Acidaminococcusgenus98423044664.69773.8105707
Bacteroidalesorder426327369089188681.8168273.3152995
Spirochaetaceaefamily1598544813805.732843.837236
Porphyromonas asaccharolyticaspecies3141553970.48744.843238
Erysipelotrichaceaefamily6385347510831.84414.9152993
Roseburiagenus300331920134050.417905.1152991
FCB groupclade448905391426199421.4186334152996
Dialistergenus466879129234.310868.1107646
Lachnospiraceaefamily219269176420109155.381234.8152995
Cerasicoccusgenus249650650.71037.434250
Sphingobacterialesorder296344221929577.839150.6152995
Eubacteriaceaefamily354315557588.14328.8152989
Synechococcaceaefamily68230141.6973.441299
Acidaminococcus intestinispecies3007991051.32292.137222
Acholeplasma hippikonspecies4268121052.52058.935260
Treponemagenus1604544813832.332843.837235
Firmicutesphylum657764502820205065.5155846.7152997
Caloramator indicusspecies37310652091.53540.544373
Faecalibacterium prausnitziispecies10010914176677192.187778152986
Spirochaetiaclass903374310119.827201.354441
Prevotella stercoreaspecies50771001018648.525185.554406
Insolitispirillumgenus82591219815534.521217.596593
Emticicia oligotrophicaspecies78525533291.112937.7112691
Lelliottiagenus9222052676.6592.238301
Sphingobacterium bambusaespecies316506452.11018.8140825
Items deemed significant based on mean and standard deviation

Bacteria to Hand-Pick for Autism with Ombre/Thryve samples

Some recent work has identified bacteria that are associated with Autism. For a summary of method, see this post. The following are the list of bacteria seen with Ombre/Thryve samples that are annotated with Autism. There are not sufficient samples yet for specific autism characteristics – so please check your uploaded samples and update the symptoms.

Note the list is Ombre/Thryve specific and cannot be applied to other microbiome reports. There is also Bacteria to Hand-Pick for Autism with Biomesight samples

These are bacteria that you want to reduce (with one caveat — the suggestions algorithm requires the percentile to be 50%ile or more). How to hand pick them? See below the list.

Note: you may only have a few of these. They are shown in the same sequence as seen on Microbiome Tree. The LAST item is what was found to be statistically significant.

  1. Proteobacteria Gammaproteobacteria Gammaproteobacteria incertae sedis
  2. Pectobacteriaceae Brenneria Brenneria alni
  3. Enterobacterales Enterobacteriaceae Klebsiella/Raoultella group
  4. Enterobacteriaceae Klebsiella/Raoultella group Klebsiella
  5. Alphaproteobacteria Hyphomicrobiales Devosiaceae
  6. Alphaproteobacteria Hyphomicrobiales Hyphomicrobiaceae
  7. Betaproteobacteria Neisseriales Neisseriaceae
  8. Betaproteobacteria Rhodocyclales Zoogloeaceae
  9. Burkholderiales Burkholderiaceae Burkholderia
  10. Sutterellaceae Sutterella Sutterella wadsworthensis
  11. Bacteria Proteobacteria delta/epsilon subdivisions
  12. Proteobacteria delta/epsilon subdivisions Deltaproteobacteria
  13. Desulfovibrionaceae Desulfovibrio Desulfovibrio piger
  14. PVC group Verrucomicrobia Opitutae
  15. Flavobacteriia Flavobacteriales Cryomorphaceae
  16. Flavobacteriales Cryomorphaceae Cryomorpha
  17. Cryomorphaceae Cryomorpha Cryomorpha ignava
  18. Bacteroidetes/Chlorobi group Bacteroidetes Sphingobacteriia
  19. Bacteroidetes Sphingobacteriia Sphingobacteriales
  20. Sphingobacteriia Sphingobacteriales Sphingobacteriaceae
  21. Bacteroidales Porphyromonadaceae Porphyromonas
  22. Clostridia Eubacteriales Defluviitaleaceae
  23. Eubacteriales Defluviitaleaceae Defluviitalea
  24. Clostridia Eubacteriales Proteinivoraceae
  25. Eubacteriales Proteinivoraceae Anaerobranca
  26. Eubacteriales Lachnospiraceae Butyrivibrio
  27. Lachnospiraceae Butyrivibrio Butyrivibrio crossotus
  28. Lachnospiraceae Butyrivibrio Butyrivibrio fibrisolvens
  29. Eubacteriaceae Eubacterium Eubacterium coprostanoligenes
  30. Eubacteriales Peptococcaceae Desulfosporosinus
  31. Eubacteriales Clostridiaceae Alkaliphilus
  32. Clostridiaceae Clostridium Clostridium oryzae
  33. Clostridiaceae Clostridium Clostridium lundense
  34. Clostridiaceae Clostridium Clostridium intestinale
  35. Eubacteriales Clostridiaceae Lactonifactor
  36. Eubacteriales Clostridiaceae Caloramator
  37. Eubacteriales Eubacteriales incertae sedis Natranaerovirga
  38. Eubacteriales Eubacteriales incertae sedis [Bacteroides] pectinophilus
  39. Clostridia Thermosediminibacterales Thermosediminibacteraceae
  40. Terrabacteria group Firmicutes Firmicutes sensu stricto incertae sedis
  41. Firmicutes Firmicutes sensu stricto incertae sedis Hydrogenispora
  42. Selenomonadales Sporomusaceae Anaerospora
  43. Sporomusaceae Anaerospora Anaerospora hongkongensis
  44. Selenomonadales Selenomonadaceae Megamonas
  45. Bacilli Bacillales Listeriaceae
  46. Bacillales Listeriaceae Listeria
  47. Bacilli Bacillales Bacillales incertae sedis
  48. Bacillales Bacillales incertae sedis Bacillales Family X. Incertae Sedis
  49. Bacillales incertae sedis Bacillales Family X. Incertae Sedis Thermicanus
  50. Lactobacillales Lactobacillaceae Limosilactobacillus
  51. Lactobacillaceae Limosilactobacillus Limosilactobacillus fermentum
  52. Lactobacillales Lactobacillaceae Liquorilactobacillus
  53. Lactobacillaceae Liquorilactobacillus Liquorilactobacillus vini
  54. Cyanobacteria/Melainabacteria group Cyanobacteria Oscillatoriophycideae
  55. Cyanobacteria Oscillatoriophycideae Oscillatoriales
  56. Bacteria Terrabacteria group Chloroflexi
  57. Terrabacteria group Chloroflexi Chloroflexia
  58. Bacteria Terrabacteria group Actinobacteria
  59. Terrabacteria group Actinobacteria Actinomycetia
  60. Actinobacteria Actinomycetia Bifidobacteriales
  61. Actinomycetia Bifidobacteriales Bifidobacteriaceae
  62. Bifidobacteriales Bifidobacteriaceae Bifidobacterium
  63. Bifidobacteriaceae Bifidobacterium Bifidobacterium bifidum
  64. Bifidobacteriaceae Bifidobacterium Bifidobacterium asteroides
  65. Bifidobacteriaceae Bifidobacterium Bifidobacterium subtile
  66. Actinomycetia Propionibacteriales Nocardioidaceae
  67. Actinobacteria Coriobacteriia Coriobacteriales
  68. Coriobacteriia Coriobacteriales Coriobacteriaceae
  69. Coriobacteriales Coriobacteriaceae Senegalimassilia
  70. Coriobacteriaceae Senegalimassilia Senegalimassilia anaerobia
  71. Tenericutes Mollicutes Entomoplasmatales
  72. Mollicutes Entomoplasmatales Spiroplasmataceae
  73. Entomoplasmatales Spiroplasmataceae Spiroplasma
  74. Tenericutes Mollicutes Anaeroplasmatales
  75. Mollicutes Anaeroplasmatales Anaeroplasmataceae
  76. Anaeroplasmatales Anaeroplasmataceae Anaeroplasma
  77. Acidobacteria Acidobacteriia Acidobacteriales
  78. Acidobacteriia Acidobacteriales Acidobacteriaceae
  79. cellular organisms Bacteria Elusimicrobia
  80. Bacteria Elusimicrobia Elusimicrobia

To make a selection, just check the appropriate checkboxes.

Using Frequency of Detection in Samples

This is a technical note. Recently I came across this doing analysis of Long COVID data.

Thermosediminibacterales(order)

  • With Long COVID: 55/152 samples or 36.2%
  • Reference (excluding Long COVID samples): 72/996 or 7.2%

This present an interesting insight on possible blinkered thinking when seeing such data. Some examples are:

  • Don’t brother looking —
    • It’s a rare bacteria (just 7% of people have it…)
    • It does not occur in most Long COVID patients, not interesting
  • I computed the means and standard deviations, and the difference is not sufficiently significant, so do not mention

My take is simple, it occurs FIVE times more often. I view microbiome dysbiosis are the result of the “perfect storm” or should I say “imperfect storm”. The wrong concentrations of compounds and enzymes coming together from a host of bacteria. With that dysbiosis view, a rare bacteria oddity like this, hints at a subset. This is contrary to the common view that dysbiosis is caused by a single or small group of bacteria and you can make simple either/or decisions based on their presence or lack of presence.

In the case of the long COVID data, I observed some odd (by traditional thinking) situation. A few examples:

  • A 10 fold difference of frequency with the higher frequency having a higher average – the traditional expectation. More of this bacteria is growing, hence we find more often.
  • A 10 fold difference of frequency with the higher frequency having a lower average, with statistical significance. This is what stopped me to re-examine my perspective, including the need to re-evaluate some blinkers.

The natural question: Determining Significance!

For most people dealing with biological data, presence or non-presence is typically a dependent factor. For example, here are some means for bacteria with the outcome being Crohn’s disease detected or not (the control case). The data will often be dropped into logistic regression.

I went back to flipping bias coins thinking and raise a beer to the memory of Bernoulli. In the above case, the expected bias is that 7.2% of the time the coin will land with a head. We try a new coin and toss it 152 times and get heads 36.2% of the time…

The hypothesis to test is whether the coin is equivalent?

  • The standard deviation of the population is a simple calculation – except we need to change .50 to .362 in formula below. (P.S. The Std Dev of the population is about 1%, so a range of .342 to .382 could be tried safety)
From http://20bits.com/article/hypothesis-testing-the-basics

The result is a z-score of -7.43, or clearly significant well beyond a 0.01 level. Thus the presence or lack of presence is statistically significant and should be included in any analysis (but rarely seems to be in most papers)

Using Diet Style Information

One of the goal of Microbiome Prescription is to stay true to source data / study. There are many studies that deal with a diet style or atypical food elements, like ‘high milk fat’. Below these wide sweeping terms may be concrete specific items that are reported in a different manner. A simple examples:

Underneath the covers of this complex microbiome engine in the human body, the impact of more beef or more milk is an increased availability of Vitamin B2.

Diets are complex concepts subject to regional interpretation. A high beef diet means more beef than a typical person… so how much is that [source]?

  • If you are in China, it’s more than 1 pound of beef a month.
  • If you are in Russia, it’s more than 2 pound of beef a month.
  • If you are in USA, it’s more than 3.5 ounces of beef a day (so, more than a MacDonald’s Quarter Pounder every day).
  • If you are in Uruguay or Argentina, it’s more than 5.5 ounces of beef a day.

When we go over to items like a Mediterranean Diet, often it can mean many things with a wide range of contents. Both of the following would meet that criteria for many people:

  • One serving of cereal, two servings of citrus fruits, one servings each of eggplant, okra , green beans
  • 13 servings of cereal and breads, one half apple, five servings of potatoes, 3 servings of carrots, 1 serving of onions.

The MedDiet contained three to nine serves of vegetables, half to two serves of fruit, one to 13 serves of cereals and up to eight serves of olive oil daily. It contained approximately 9300 kJ, 37% as total fat, 18% as monounsaturated and 9% as saturated, and 33 g of fibre per day.

Definition of the Mediterranean Diet; a Literature Review [2015]

The majority of studies emphasized the same key dietary components and principles: an increased intake of vegetables, wholegrains, and the preferential consumption of white meat in substitute of red and processed meat and abundant use of olive oil. However, the reporting of specific dietary recommendations for fruit, legumes, nuts, bread, red wine, and fermentable dairy products were less consistent or not reported

Differences in the interpretation of a modernized Mediterranean diet prescribed in intervention studies for the management of type 2 diabetes: how closely does this align with a traditional Mediterranean diet? [2019]

To me, a medDiet is eating traditional Greek — stuffed grape leaves, Tomato Fritters, etc with a glass of Ouzo [example] – in my younger days while I was teaching, I would have this 3-4 nights of the week.

At this point, we find that most studies involving diet deteriorates into vague hand-waving.

Can you use diet style?

This is a two sided coin. If you take recommendation for items like Luteolin, it can be translated into diet such as more celery seed, olives, blueberries. Quercetin into Cranberries and Blueberries. etc. While a high meat diet is vague — does it mean beef? pork? chicken? fish? – how much?

A logical solution is to decompose the diet into an itemized list of what the diet means by component. Then using the wonderful databases at the US Department of Agriculture develop a profile of what you are getting with this style of diet. Usually there are multiple diet suggestions, so you need to intersect them to get the true bottom line on what the diet changes should be.

Bottom Line — Use Diet Style with caution!

IMHO, it is so close to saying “Buy tech stocks for your retirement”. Without doing due diligence, you may end up with a worthless portfolio. At the bottom of the suggestions is a Flavonoid section which could be translated into food specific items.

Antibiotic Apocalypse on the Microbiome

This is an interesting case which appears to illustrate well that microbiome-agnostic prescription of antibiotics can produce horrible results. Doing a yearly 16s microbiome test will allow you to potentially negotiate with your MD to pick antibiotics that both address the MD concerns and potentially improve your microbiome as a side effect. See this post: Negotiations with your Medical Professional

My backstory:

I have used FQ antibiotics many times in the last 15 years for Chronic bacterial prostatitis..

During the last few years I was diagnosed with diverticula and had an episode of diverticulitis 3 years ago which also required antibiotics.. In the last 2 years my bloating was so severe that I was like a pregnant woman.. I am a male 40 years old.. So last July I went to the beach and caught E.Coli once again from the water or the beach.. This gave me acute infection with fever the next day.. This is where the drama starts as I ended up going to 4 different labs giving me different results and switching antibiotics for 5 months.. My gut was so bad that I’ve spend one night at the WC and another day I was stuck in traffic and I didn’t come back in time.. So embarrassing..

So January I stopped the FQs since I got a severe reaction with a set of symptoms that almost took my life.. My calf tore while being in bed, not even walking, swollen joints with fluid, tinnitus, diarrhea for 1 month, stomach ache and spasms, neuropathy, brain fog, insomnia and more..

I was sure that everything started from my gut, something triggered auto-immune along with toxicity from the drugs.. 2 months in bed.. 4 months and I barely walk with many symptoms.. What saved me initially I think was homemade Kefir I had and making myself..

Then I did the test at Biomesight and understood why and what happened.. Now I know very well that life or death starts from the gut.. 

Current State

First, I like to get a feel for where the microbiome is at from a high level. Looking at the usual health measures:

  • Dr. Jason Hawrelak Recommendations guidance puts the person at the 35%ile, definitely in the concerning space
  • On the Potential Medical Conditions Detected, 14 items were flagged, again concerning
  • In the Bacteria deemed Unhealthy list, the following stood out
NameRankPercentileCountCommentMore Info
[Ruminococcus] gnavusspecies95.227410Not Healthy PredictorCitation
Anaerotruncus colihominisspecies97.95200Not Healthy PredictorCitation
Bacteroides fragilisspecies86.317220H02076 Bacteroides infectionCitation

Looking at the distribution by frequency, nothing really stands out.

PercentileGenusSpecies
0 – 91418
10 – 191934
20 – 291919
30 – 391214
40 – 49157
50 – 59915
60 – 691313
70 – 79815
80 – 89109
90 – 991518

Looking at the antibiotics list taken, I went over to the Antibiotics List for MDs page for this sample. We are using this to see which antibiotics likely helped the dysbiosis of the gut to happen.

The following were the antibiotics that he had been prescribed. I put after each the positive and negative estimates from the above page. We see a -.266 for something taken for 84 days…

  • IV Cipro 1 time in hospital
  • Cipro oral cycles (21 days) : 5x –  (0.194)
  • Norfloxacin cycles (14 days) 6x (0.282)
  • Levofloxacin : 10 days – no data
  • Fosfomycin: 8 sachets – no impact
  • Cefaclor cycle (14 days): 12x – negative impact (Take Estimate:  35.1, Avoid Estimate:  39) (0.079)
  • Amoxicillin / Clavulanic Acid cycles (21 days): 4x  ( – 0.266 )
  • Cefixime cycle (24 days) : 1x  ( – 0.114 )
  • Trimethoprim / Sulfamethoxazole : 3 days  (0.128) /   ( – 0.604 )
  • Doxycycline: 2 days  ( – 0.173 )

In this case, it is clear from the data above that the antibiotics were a factor for his problems. if he must take antibiotics again (or can persuade his MD to do a trial), the best ones suggested by the Artificial Intelligence algorithms are:

  1. rifaximin (antibiotic)s   (1)
  2. metronidazole (antibiotic)s   (0.887)
  3. ampicillin trihydrate (antibiotic)   (0.834)

Action Plan Going Forward

The KEGG AI Computed Probiotics had the HIGHEST VALUES that I have ever seen with the top items being, I would go for three of these (2 weeks of one, then rotate to the next, repeat): Something that lists bacillus subtilis as the first ingredient, miyarisan (jp) / miyarisan, something that is just lactobacillus plantarum (i.e. 299v)

Bacteria NameWeight
BIO-BOTANICAL RESEARCH / Megacidin [bacillus coagulans, bacillus subtilis]4285.54
miyarisan (jp) / miyarisan [clostridium butyricum miyairi]4130.42
enviromedica terraflora sbo probiotic [bacillus clausii, bacillus coagulans,bacillus megaterium
bacillus pumilus, bacillus subtilis]
3724.82
INVIVO THERAPEUTICS / Bio.Me IB + [bacillus subtilis, enterococcus faecium]3716.08
CustomProbiotics.com / L. Plantarum Probiotic Powder [lactobacillus plantarum]3324.66
Of the bacillus, bacillus subtilis seems to be the best

For supplements, we have (even at 20%) a short list. Usually supplements can be taken consistently.

  • beta-alanine – Percentile: 5.2
  • Glycine – Percentile: 3
  • L-Cysteine – Percentile: 10.4
  • L-glutamine – Percentile: 15.5
  • Magnesium – Percentile: 3.7
  • Molybdenum – Percentile: 0.9

Building Consensus Suggestions

Remember, no one knows how to pick the best bacteria to target. We apply multiple criteria and then work from what is agreed upon with the different approaches (i.e. consensus).

The consensus list is long with 534 items (typical). My main take away

Bottom Line

Given the severity of this person, I suggest trying suggestions for 2-3 months and then gets retested. I expect significant changes — but that is likely just a course correction. We need to do more course corrections to get back to a safe harbor.

ALWAYS REVIEW WITH YOUR MEDICAL PROFESSIONAL BEFORE STARTING

Bacteria Shifts Seen in Chronic Fatigue Syndrome

Using novel technics for my earlier post Bacteria Shifts Seen in Long COVID caused me to look at it’s sibling: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Since we have a much large sample size, we can get more rigorous and be lab specific (see The taxonomy nightmare before Christmas…). The result are the three tables below. The criteria for shift was a difference of 4 percentile or more.

Biomesight

Tax_nameTax_rankSample Frequency
of Detection
Population Frequency
of Detection
Shift
Phocaeicola plebeiusspecies125.2Lower
Oscillatorialesorder13.55.1Lower
Bacteroides gallinarumspecies13.54.5Lower
Aerococcaceaefamily14.14.5Lower
Phocaeicola coprocolaspecies15.15.4Lower
Desulfovibriogenus22.98.8Lower
Collinsellagenus258.7Lower
Hathewayagenus30.210.6Higher
Bacteroides ovatusspecies30.210.6Higher
Anaerotruncus colihominisspecies30.210.4Higher
Bacteroides rodentiumspecies30.210.6Higher
Sample Size: 58

OmbreLabs / Thryve

Tax_nameTax_rankSample Frequency
of Detection
Population Frequency
of Detection
Shift
Alteromonadaceaefamily9.43.4Lower
Paenibacillusgenus126.6Lower
Phocaeicola plebeiusspecies127.1Lower
Bacteroides gallinarumspecies13.57.3Lower
Oscillatorialesorder13.54.8Lower
Planococcaceaefamily13.56.7Lower
Aerococcaceaefamily14.16.8Lower
Phocaeicola coprocolaspecies15.17.5Lower
Turicibacter sanguinisspecies15.15.1Lower
Sarcinagenus19.30.4Lower
[Ruminococcus] torquesspecies19.88.1Lower
Desulfovibriogenus22.97.2Lower
Ruminiclostridiumgenus22.98.2Lower
Peptostreptococcaceaefamily248.2Lower
Collinsellagenus257.2Lower
Anaerostipesgenus26.68.3Lower
Eubacteriumgenus29.28.3Lower
Eubacteriales incertae sedisnorank29.78Lower
Clostridiumgenus30.28.2Higher
Sphingobacterialesorder30.24.8Higher
Blautia hanseniispecies30.25.3Higher
Oscillospiragenus30.20Higher
Bacteroides ovatusspecies30.27.2Higher
Anaerotruncus colihominisspecies30.26.7Higher
Blautia wexleraespecies30.28.3Lower
Bacteroides rodentiumspecies30.27.4Higher
Sphingobacteriiaclass30.24.8Higher
Sphingobacteriaceaefamily30.24.8Higher
Hathewayagenus30.24.1Higher
Anaerofilumgenus30.24.2Higher
Actinobacteriaphylum30.28.3Lower
Sample Size 51

uBiome

Tax_nameTax_rankSample Frequency
of Detection
Population Frequency
of Detection
Shift
Planococcaceaefamily13.50.3Lower
Bacteroides gallinarumspecies13.50.1Lower
Oscillatorialesorder13.50.1Lower
Aerococcaceaefamily14.10.6Lower
Phocaeicola coprocolaspecies15.10.4Lower
Turicibacter sanguinisspecies15.13.3Lower
Sarcinagenus19.35.4Lower
Ruminiclostridiumgenus22.90.2Higher
Adlercreutzia equolifaciensspecies22.93.8Lower
Desulfovibriogenus22.92.7Lower
Peptostreptococcaceaefamily245.6Lower
Collinsellagenus255.5Lower
Anaerostipesgenus26.65.6Lower
Eubacteriumgenus29.21.1Higher
Eubacteriales incertae sedisnorank29.75.5Lower
Oscillospiragenus30.24.2Higher
Anaerotruncus colihominisspecies30.22.1Higher
Blautia wexleraespecies30.25.4Lower
Bacteroides rodentiumspecies30.20.1Higher
Sphingobacteriiaclass30.20.1Higher
Sphingobacteriaceaefamily30.20Higher
Anaerofilumgenus30.21.8Higher
Actinobacteriaphylum30.25.6Lower
Bacteroides ovatusspecies30.22.9Higher
Clostridiumgenus30.25.5Higher
Sphingobacterialesorder30.20.1Higher
Blautia hanseniispecies30.21.8Higher

Common across all labs

Amount of Bacteria

For the amount of shift, the nightmare described in The taxonomy nightmare before Christmas… comes true!

Tax_nameTax_rankOmbreBiomesightuBiome
PaenibacillusgenusLowerHigherHigher
Phocaeicola plebeiusspeciesLowerHigherHigher
OscillatorialesorderLowerHigherHigher
PlanococcaceaefamilyLowerHigherHigher
Phocaeicola coprocolaspeciesLowerHigherHigher
Turicibacter sanguinisspeciesLowerHigherHigher
SarcinagenusLowerHigherHigher
Bacteroides gallinarumspeciesLowerLowerHigher
The shift in bacteria count observed

Frequency of Detection

Here we have agreement across all of the labs

Tax_nameTax_rankOmbreBiomesightuBiome
PaenibacillusgenusMoreMoreMore
Phocaeicola plebeiusspeciesMoreMoreMore
Bacteroides gallinarumspeciesMoreMoreMore
OscillatorialesorderMoreMoreMore
PlanococcaceaefamilyMoreMoreMore
Phocaeicola coprocolaspeciesMoreMoreMore
Turicibacter sanguinisspeciesMoreMoreMore
SarcinagenusMoreMoreMore
AerococcaceaefamilyMoreMore
DesulfovibriogenusMoreMore
RuminiclostridiumgenusMoreMore
PeptostreptococcaceaefamilyMoreMore
CollinsellagenusMoreMore
AnaerostipesgenusMoreMore
EubacteriumgenusMoreMore
Eubacteriales incertae sedisnorankMoreMore
ClostridiumgenusMoreMore
SphingobacterialesorderMoreMore
Blautia hanseniispeciesMoreMore
OscillospiragenusMoreMore
Bacteroides ovatusspeciesMoreMore
Blautia wexleraespeciesMoreMore
SphingobacteriiaclassMoreMore

What does all of this mean?

It means that the bacteria count may be a little bit of a red herring. It is the frequency of detection that may be a better criteria for what is significant.

To put this in human terms, for a political movement, looking at the bank account may not be the best way of detecting if it is significant; it is the number of different types of people that turns up at meetings!

The mathematics and number crunching becomes more complex… but we are dealing with a complex system. For example, if you are using uBiome and many of the following was detected, then the odds of having ME/CFS is significant. It suggests a different criteria for selecting bacteria to generate suggestions.

  • Planococcaceae
  • Bacteroides gallinarum
  • Oscillatoriales
  • Aerococcaceae
  • Phocaeicola coprocola
  • Turicibacter sanguinis

Returning to Long COVID

Below is NOT the amount of bacteria, it is the frequency that these bacteria were detected in the samples. In other words, there is a group of bacteria that blooms – they show up more frequently, not necessarily in larger numbers, just there — trouble makers!

Bacteria Identified in Long COVIDOmbre
ME/CFS
Biomesight
ME/CFS
Ubiome
ME/CFS
MicrococcaceaeMoreMoreMore
PeptostreptococcaceaeMoreMoreMore
Butyricimonas virosaMoreMoreMore
SarcinaMoreMoreMore
EnterobacterMoreMoreMore
LactobacillaceaeMoreMoreMore
CoriobacteriiaMoreMoreMore
Slackia faecicanisMoreMore
RhodovibrionaceaeMoreMore
Blautia wexleraeMoreMore
Salinicoccus luteusMoreMore
StaphylococcaceaeMoreMore
BifidobacterialesMoreMore
Holdemanella biformisMoreMore
CoriobacterialesMoreMore
HoldemanellaMoreMore
Eubacteriales incertae sedisMoreMore
FusobacteriiaMoreMore

This analysis shows a very similar pattern in the microbiome between Long COVID and ME/CFS.

FMT (7x) failed, SIBO failed… next step?

The back story for this person is long and detailed — with a massive number of tests and conditions done! This is a much shorten version

Back Story

Male, 40yrs of age. Very physically active and successful engineer & businessman prior to illness onset 7 years ago at 33yrs of age.

Illness onset summary:

  • July 2014 I had bad flu symptoms: very fatigued and bad cough, which took a couple of months to seemly recover from, albeit still had bouts of mild fatigue and random mild cough.
  • September 2014 I moved into a moldy / water damage building.
  • October 2014 I had the flu again. Did seem to recover.
  • 2015 On-going random fatigue and insomnia, which is persistent to today.
  • Sometime during this 2014/2015 period whilst living in moldy house I had a circular red rash (similar to erythema migrans) on my forearm indicating insect bite mark. Took 2 weeks to go away. Did not take photo and did not notice any symptoms during this time. I had not travelled anywhere during this time.
  • I have for +7yrs managed my symptoms by predominately eating carnivore diet, regular fasts, and having daily water enemas as it is the only way I can pass stool. Start of 2020 I had to stop working all together due to extreme fatigue and brain fog. I have dedicated 100% of my limited energy to my treatment ever since.

I have seen over 17 Health Professionals of various specialities, with numerous treatments with no real improvement. First four years was predominately about treating the gut (which is still my main symptom) with various SIBO treatments, including herbs (e.g. oregano), antibiotics (Erythromycin, Rifaximin & Vancomycin), antifungals (nystatin) and seven Faecal Matter Transplants (FMT), with no success. Have had multiple endoscopy and colonoscopies with no major findings other than removal of some polyps, and negative to Whipple’s PCR albeit +ve antibodies. Many stool samples with no detected parasites.

End of 2019 I identified that Lyme and/or mycotoxin (mold) toxicity could be the cause, and in 2020 was diagnosed with Chronic Inflammatory Response Syndrome (CIRS) from mycotoxin toxicity due to various test results, and subsequently also Mast Cell Activation Syndrome (MCAS) and Cell Danger Response (CDR). I have been treating this for +24 months via various treatments e.g. binders and antifungles, although can’t tolerate most e.g. CSM, nystatin, Amphotericin B, Itranconazole. I did see some initial improvement with charcoal & bentonite which I occasionally still take when herxing, but no noteworthy improvements in symptoms.

My Lyme antibody test results are equivocal with only some IgM +ve results. I did initially respond well to doxycycline but these improvements only lasted 2 weeks. After using it on and off for other a year I can’t tolerate it for longer than 5 days or so. Cannot tolerate azithromycin and erythromycin cause severe large bowel pain, as do many other herbs e.g. Cowden protocol.

Often my bowel pain gets bad enough that pain killers are not enough so I go back on doxy as that has been the only thing helps, but I can’t stay on doxy as it makes me feel horrible after eating (which is when I take it).

Multiple hair analysis indicate that mercury distribution could be an issue, and I have had negative cognitive symptoms to single thiol chelators i.e. chlorella and EDTA. EDTA does make me feel like I’m loosing my mind. Recently start 5mg dosage of OSR which does make me more fatigued and worsen digestion.

My condition only seems to get worse and am not able to tolerate any treatments anymore.

Reinvestigating my gut biome I have taken Biomesight stool sample (whilst taking doxycycline) to see if there is any pre/probiotics I can take that will help, and considering Phage therapy and or retrying FMT treatment.

Note I’ve tried many prebiotics all of which have exacerbated my symptoms e.g. bloating, toxicity, bowel pain fatigue, brain fog etc as do most plants, hence carnivore diet, and many probiotics most of which make no difference or make me very fatigued e.g. Megaspore (presumably due to histamine).

Analysis

See the YouTube for more information and walk thru.

Using Health Analysis Page

  • Health Status – 2 Healthy, 9 Unhealthy
  • Jason Hawrelak – at 56%ile , significant issues
  • Potential Medical Conditions Detected – a massive list!!!
This is only the top of the list!

In short, OUCH!

Looking at the bacteria called out especially:

First Probiotics

I am finding that this is a friendly start point because we have multiple logics available to determine them (which, of course, can result in disagreement). The list is very close to the common pattern seen with ME/CFS patients:

Looking at probiotics based on dominant symptoms we see one is on the list above

From top of the Safest Take list from Consensus Report below

The lists are effectively identical! One list was obtain solely by looking at the DNA of the bacteria in your sample and the DNA of the bacteria in the probiotics. The last list was generated from clinical trails reporting shifts of bacteria from taking probiotics. It appears to confirm that the novel experimental DNA produces good results.

I am pleased with that, because our depth of knowledge is actually far greater with DNA. This also allows us to evaluate new probiotics quickly without needing to wait for clinical studies and publications.

Consensus Report

As has become my custom, I whipped thru all of the suggestions using expert criteria.

  •  Use JasonH (15 Criteria) – 10 matches
  •  Use Medivere (54 Criteria) – 10 matches
  •  Use Metagenomics (59 Criteria) – 10 matches
  •  Use Nirvana/CosmosId (36 Criteria) – 10 matches
  •  Use XenoGene (22 Criteria) – 10 matches
  •  Standard Lab Ranges (+/- 2 Std Dev) – 15 matches
  •  Box Plot Whisker – 47 matches (10%)
  •  Kaltoft-Moltrup Normal Ranges – 111 matches (23%)
  •  Percentile in top or bottom 10%ile – 122 matches (25%)

Looking at the consensus number of suggestions for the above, the numbers were similar, suggesting that despite the differences number of bacteria selected, the suggestions were likely similar.

Takes

My personal pick of the top suggestions are below (excluding probiotics cited above):

This leads to the regular suggestion frequently seen with ME/CFS patients: Start each day with barley porridge with walnuts and appropriate yogurt. Note: Oats is on the safest list too, but less studied.

As a side note: meat and beef do not occur anywhere on the safest list. milk-derived saturated,fat and high saturated milk fat diet does — which suggests that whole milk should be the preferred milk (if milk is taken)

Avoids

The following items caught my eye on the highest risk items:

I must point out that many items above are on the “internet-myth” always good to fix the gut list.

The avoid probiotics are:

It is left to the reader to go thru the lists. The list suggestion counts, from safest to most avoid, was (258, 88, 33, 52, 33,101) – so full of strongly to take…

I should point out that the complete list is available for download. I would suggest downloading it and then check everything in the diet against the list.

The land of Supplements

The AI Kegg items detected as being low are:

  • Glycine – Percentile: 3
  • L-glutamine – Percentile: 2.1
  • L-Threonine – Percentile: 9
  • magnesium – Percentile: 0.7
  • Molybdenum – Percentile: 3.8

I downloaded the list from consensus and put their results below

  • Glycine – Take: 9, Avoid:0
  • L-glutamine – Take: 0, Avoid 4
  • L-Threonine – No information
  • magnesium – Take: 9, Avoid 0
  • Molybdenum – No information

So two are clear additions, two are good candidates to try as an experiment, one has some risk.

Vitamins – Consensus]

To save typing I am using (Take/Avoid) counts

The following have higher Avoid counts than take counts, and should likely be avoided

Remember — beware people telling you what is good for you! A mother recently message me. She started the suggestions and everything was going ok and then she listened to a random suggestion.

Prescription Drugs

I decided to do a consensus report on prescription items. This is done on Advance Suggestions page. I checked the following items:

And then went thru the same expert choices as above.

The results are actually more items as shown below’

I would suggest downloading and placing the list on your mobile phone to have handy when discussing prescription drugs with your physician. Sometimes, you find alternative drugs would satisfy the MD and be better for your gut… it is negotiation!

I was amused, with some of these results for the alternative substances:

He mentions some antibiotics that he was on without apparent success

  • Erythromycin, – a mild take (5/0), impact ratio is 4:1
  • Rifaximin – a stronger take (7/0) impact ratio is 2:1
  • Vancomycin – a mix result (6/1) impact ratio is 2:1
  • Doxycycline – (3/4), impact ratio is 3:2 (net positive)
    • Minocycline – (7/0) impact ratio is 2.5:1 and is suggested as a replacement. I checked all of the tetracycline family and this was the best one.

The nice thing is that none made him worst. I leave it to him to lookup the use, side-effects of the best suggestions and then see if he can persuade his MD to do off-label prescriptions. My usual suggestion is to follow Cecile Jadin approach and do rotation: 7-10 days on, 2 weeks off, take a different one, repeat.

Bottom Line

My intent is to show you how to use the data available. “To teach you to fish“. As you try fishing your skill level will improve and you may be able to teach others to fish.

All of these are suggestions coming from mathematical models and not clinical experience. Suggestions should be reviewed by a knowledgeable medical professional before starting.

I am a computer scientist and a statistician. I am not licensed to practice medicine, and where I live has strict laws about ‘appearing to practice medicine’. What I can do for readers is to write a public blog (anonymous) from your data and back story as an education post on using the software and the statistics it produces. I cannot consult. The content should be reviewed by a medical professional before implementing.

Bottom line, my time is better spent for everyone in building the data and the methods, not in dealing with a small number of clients (thus relationships will go undiscovered and/or data becoming stale). If you want or need hand holding — there are many that will gladly do it for a fee, some uses this site and others use University Training from 1990.

Bacteria Shifts Seen in Long COVID

There is a Long COVID Study in progress via the cooperation BiomeSight.com and Microbiome Prescrption. The data is not yet processed for the study, but we have some interest results already from those that uploaded their samples and marked Long COVID as a symptom.

BacteriaTaxonomy
Rank
Average
Percentile
Frequency Seen
in this Group
Frequency Seen
in All Samples
Micrococcaceaefamily1945.836.5
Actinobacteriaphylum19.710099.7
cellular organismsnorank2010099.9
Adlercreutzia equolifaciensspecies20.162.542.8
Peptostreptococcaceaefamily22.895.896.5
Butyricimonas virosaspecies23.341.738.8
Sarcinagenus24.745.852.4
Enterobactergenus25.141.723.6
Lactobacillaceaefamily2695.894.9
Coriobacteriiaclass2710099
Actinomycetiaclass27.610099.2
Adlercreutziagenus27.866.745.3
Slackia faecicanisspecies2837.511.8
Bifidobacterium adolescentisspecies28.179.231.4
Rhodovibrionaceaefamily28.437.50
Blautia wexleraespecies29.210094.4
Anaerostipesgenus29.795.896.1
Salinicoccus luteusspecies30.937.512.6
Staphylococcaceaefamily30.962.540.4
Bifidobacterialesorder31.210089.7
Holdemanella biformisspecies31.366.732.7
Coriobacterialesorder31.310095.7
Holdemanellagenus31.466.732.8
Eubacteriales incertae sedisnorank31.595.889.5
Bifidobacteriaceaefamily31.710089.6
Fusobacteriaphylum31.745.840.8
Fusobacteriiaclass31.845.840.7
Eggerthellalesorder31.810097
Eggerthellaceaefamily31.910097
Terrabacteria groupclade31.910099.9
Fusobacterialesorder3245.840.7
Collinsellagenus3291.789.4
Leuconostocaceaefamily3262.554.4
Coriobacteriaceaefamily32.710094.7
Bifidobacteriumgenus3310088.2
Pseudobutyrivibriogenus33.279.281.6
Turicibacter sanguinisspecies33.862.555.5
Bacteroides denticanumspecies34.270.821.9
Fusobacteriumgenus34.241.733.9
Erysipelotrichaceaefamily34.410098.8
Doreagenus34.410098.3
Natranaerobialesorder34.554.221
Actinomycetaceaefamily34.687.582.5
Roseburia faecisspecies34.895.880.9
Veillonella montpellierensisspecies34.937.514.6
Holdemaniagenus65.795.877.6
Chlorobaculumgenus67.45020.2
Bacteroides ovatusspecies67.610073.9
Anaerotruncus colihominisspecies69.110065.8
Oscillospiragenus75.17555.5
Data on a Sample Size of 24

What is striking is not higher counts, but certain bacteria are being seen a lot more often. In fact, no bacteria is seen less often with Long COVID people but the amount may be less. That is more types of bacteria but with lower levels than average.

Note: Percentile means the percentile ranking of samples for a specific bacteria. The expected percentile for a random sample of people is 50%ile. Thus a lower percentile means that the median of the group is less than the median of the population. A higher percentile means that the median of the group is higher than the median of the population. The severe skewness of bacteria distribution does not mean the the average of the sample is lower or higher than the average of the population — in fact, they may be the same. (Welcome to statistical gymnastics 301!!!)

The ME/CFS Connection

This type of novel analysis (using frequency of detection and not amount of bacteria) results in Long COVID and Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). being very similar at the microbiome level. see Bacteria Shifts Seen in Chronic Fatigue Syndrome.

2 Samples for Autistic Child

Backstory

My son is born in 2009 and diagnosed with autism in 2011. When he was 3 months old he has lot of reflux and unable to digest milk always used to throw up and we ended up using antibiotics because of mucus forming issues and at 10 months he had few words.

  • And at 18 months he got diagnosis’s of autism and was completely Non-Verbal.
  • After removing gluten and dairy from his diet at age 3.5 he started saying words
  • he also got diagnosed with Lyme and coinfections like bartonella and Babesia .
  • Now he is 11 years still having lot of issues like his weight is just 55 Lbs  he has focus issues and lot/severe OCDs and tantrums and lot of rigidity and not conversational yet ,cognitive issues cannot understand abstract concepts and has lot of echolilia and  no social skills and gets head pain all of a sudden which might be PANS will last for few minutes and will be fine again.
  • And he has lot of Gut issues like  failure to thrive even though his diet his healthy he does not gain weight at all and he has leaky gut and always have constipation issues  and poor digestion issues and picky eating and he complaints some times that his stomach hurts and some times his stomach gets very tight like gas forming. And he has brain and Gut inflammation.
  • Very recently from couple of months  he started having Acid Reflux issues after eating he will be spitting for an hour as if something is coming back from his stomach. 
    • We also noticed that when ever he eats chicken and eggs he is more constipated. We did the GI work up and everything came up normal except one thing that he does not have enzymes to digest lactose and also we make sure he is not constipated and his bowls are moving everyday with some laxative.

We have two samples for this person, while we will use the last one for suggestions, a comparison may be spark insights.

Basic Analysis

Looking at the two samples, we see that things are very different than with the ME/CFS person in this post. Instead of over representation in rare bacteria, there is over representation in common bacteria (i.e. the bacteria that most people have).

EarlierSampleLatestSample
PercentileGenusSpeciesGenusSpecies
0 – 910177
10 – 19109912
20 – 2969813
30 – 391018710
40 – 49129612
50 – 591215918
60 – 69107812
70 – 7910161016
80 – 8925392238
90 – 991031494064
Std Dev29.3144.0010.6517.61
  • Looking at “Potential Medical Conditions Detected” for both samples we see a very long list of candidate conditions for both samples
  • For “Bacteria deemed Unhealthy”, again we have some long lists
  • For “Dr. Jason Hawrelak Recommendations”, we have the earlier sample at 75%ile and the latest sample at 98.8%ile, i.e. “no issues”
  • AI Computer Probiotics.
  • AI Computed supplements at 10% level: Neither sample had any.

There is the appearance of improvement between the sample. This may be solely due to the changes due to age (18 months between samples), or moving further away from microbiome disruptive events of the past.

Going Forward

We need to go with some caution because the child microbiome is different than an adult’s and most of the data we are using are from adults.

I am going to build the consensus in a slightly different way than usual:

  •  Use JasonH (15 Criteria) – 6 bacteria picked
  •  Standard Lab Ranges (+/- 2 Std Dev) – 17 bacteria picked
  •  Box Plot Whisker – 59 bacteria picked
  •  Kaltoft-Moltrup Normal Ranges – 92 bacteria picked
  •  Percentile in top or bottom  10 % – 160 bacteria picked
  • Canned Autism using U.S. Nation Library of Medicine Data – 8 bacteria picked
  • Using Experimental Page using Official Diagnosis Autism only – 9 bacteria picked

Looking at Consensus Items

I scanned the top items and picked items that I suspect will be acceptable, easy to obtain and reasonable cost:

Take / Add to regime

There were some interesting AVOIDS (very different than ME/CFS people)

Avoid / Remove or Reduce use of

Seeing lactulose as a very strong to be avoid agrees so much with no tolerance for milk. I checked the antibiotics positive/negative benefit and was actually surprise to see on the positive impact many of the antibiotics used for ME/CFS and Lyme: fluoroquinolone (antibiotic)s, tetracycline (antibiotic)s, minocycline (antibiotic)s with the best one being vancomycin (antibiotic). This was interesting because “Vancomycin is used to treat colitis (inflammation of the intestine caused by certain bacteria) that may occur after antibiotic treatment.”[MedlinePlus]

Questions And Answers

  1. Do you mean your current recommendations is not to use any probiotics or use only Lactobacillus salivarius strain of probiotics ?
    1. Only a very small number of probiotics appear to have a positive impact, less than 18. The other 39 came out with a negative effect. You need to read the labels carefully.
  2. I also for the earlier sample you mentioned the PDF use of prescript assist soil based probiotic and also lactobacillus bulgaricus (probiotics) and lactobacillus kefiri . I have not used these so now do you think using them might be helpful based on the analysis 
    1. Those are on the recommended list, so YES
  3. And based on your analysis what is most pathogenic bacteria that I need to address from the sample which is problematic such that I research and see how to reduce it?
    1. Unlike most people, this child has a huge amount of Lactobacillus bacteria, he has 98% more than anyone else in the database. Clicking on the link above (and those below) are the worst offenders where his levels are higher than 95% of peoples
    2. [Ruminococcus] gnavus, Actinomyces, Bacillus, Dorea, Erysipelatoclostridium ramosum, Shigella (especially Shigella dysenteriae),Streptococcus pyogenes, Streptococcus sanguinis
    3. In the video, I will show how you can find suggestions EXPLICIT for these.
  4. What key strains of good bacteria do you think is missing for weight gain or in general ?
    1. Every good strain becomes bad if there are too many of them, for example Lactobacillus above. The microbiome should be viewed as “Yin/Yang” and not good and bad. I really do not have a clean answer for that question.
  5. Which Lactobacillus strains does he have has 95% which I need to avoid further is it Lactobacillus Reutri and Lactobacillus Johnson and Lactobacillus planetarium are those the ones which I need to avoid completely to give or any other list?
    1. ALL Lactobacillus are similar with only small changes between them. They are a family. As with human families, they cross support each other. You want to lower all of the Lactobacillus, ideally have no lactobacillus probiotics.
  6. Currently I started using sauerkraut , thinking he needs more Lactobacillus strains and I read sauerkraut has lot of different good strains. Would it be still okay to use it?
    1. He DOES NOT need more Lactobacillus strains — he needs a lot less!
    2. In my humble opinion NO. Two main reasons:
      1. You have no idea of which bacteria are in. Commercial versions usually do not list the
        species. On the few that do, it is very questionable if the label is correct.
        ” the species of lactic acid bacteria present in sauerkraut fermentations are more diverse than previously reported and include Leuconostoc citreum, Leuconostoc argentinum, Lactobacillus paraplantarum, Lactobacillus coryniformis, and Weissella sp.” [2007]
        For Weissella, he is at 90%ile — too high. He does not need more
  7. Do I need to do anything to reduce Lactobacillus strains that are high?
    1. There is no studies that target explicit strains.
    2. melatonin supplement, B-vitamins reduce it too.
    3. A word of caution here. Are you going to target just one item of concern in several dozens by focusing on this item (with the potential cost of many other things becoming worst); or work from suggestions that are targeted to improve the microbiome as a whole?

In response to question #3, I did a hand picked of all of those over 95%ile on the Health Summary with the results shown below

In response to quest 5-7, the Lactobacillus tree. Note that of 65,000 Lactobacillus bacteria — less than 1,400 ( 2%) had the species identified. We do not know the species that he is high in.

A short list of Suggestions

To be discussed with family MD before starting

Items to AVOID (You may wish to read the full list

One of the easiest modern ways to do it, is to download this data as a CSV and save on your smart phone when shopping.

REMINDER: The items indicate odds/confidence in shifting the microbiome is the intended direction. It is NOT how effective it is. Each item in the take likely improves your odds of improving when taken; keep taking items the avoid list — continuing likely increase the odds of not changing.

Evidence of ME/CFS improving using Microbiome Data

Short bio: 35yr Male have had ME/CFS for about 7 years, see A review of a ME/CFS Microbiome for prior review plus backstory. This was my review for “A – Thryve:2021-11-21 self” below.

This person has had done three samples, so we will both look at the latest sample and across samples.

  • A – Thryve:2021-11-21 self
  • B – Thryve:2022-03-15 self (he used the microbiome prescription site himself to get next course adjustment)
  • C – Thryve:2022-05-16 self (this review)

The key questions focus on objective improvement and subjective improvement.

General Health Issues

The evenness of Genus and Species across percentile is shown below

AABBCC
PercentileGenusSpeciesGenusSpeciesGenusSpecies
0 – 91116691115
19-Oct123015301927
20 – 29193120241231
30 – 39183523451633
40 – 49162420371830
50 – 59213125452133
60 – 69182017301422
70 – 79162311281623
80 – 8951416241321
90 – 993141320514
Total139238166292145249
Std.Dev.6.057.715.7211.104.607.02

My reading is that at the Genus level, the microbiome is stablizing. An ideal microbiome would have a Standard Deviation of 0.0 (i.e. the appropriate percentage is in each class). We see for Genus move from 6.0 -> 5.7 -> 4.6. Species have a far greater degree of randomness because may species are not identified, most genus are identified.

Potential Medical Conditions Detected

The count has been similar: A:3 B:6 C:2 with the one items in common being Allergies.

Unhealth Bacteria

The counts were similar between all samples: A:18, B:20, C:21

Dr. Jason Hawrelak Recommendations

We had significant improvement between the first two samples and a slight loss going to the third: A: 56.5%(5) B:95.5% (8) C: 89% (7)

AI Computed Probiotics

Sample A
Sample B
Sample C — NOTHING!!!

AI Suggested Supplements

Using the default 10% level, we found samples A and B only suggested one supplement. C suggested 2 (L-Histidine and manganese). I looked up the item from A and B and saw that it had continued to improve. 🙂

SupplementsABC
beta-alanine 7.39.217.3

Has there been positive change?

My reading of the above objective numbers is yes in several vectors. There was nothing show a clear negative change. Somethings stayed put — that is fine, it is small steps. As the picture below illustrates, it is not a direct line/tunnel through the mountain ranges of dysbiosis, we have to work our way across passes and valleys.

The “I don’t feel better” quicksand

I have too often seen — especially with people suffering from Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) — patients giving up on a course of action because they reached a point where they may state “I don’t feel better from doing this, so I am changing…”. For these people, this is often caused by several factors:

  • They do not remember how they were actually 2 weeks or 2 months ago…
  • Their MD have no objective tests to show progress
  • They expect significant constant change constantly (they are frustrated waiting for improvement)

Using the microbiome and repeated testing, they can get objective measurement of changes instead of relying on subjective measurement being done under the influence of brain fog with memory problems.

In this person case, we do see objective improvement of the dysbiosis. What about subjective?

“You’re welcome to mention I have noticed improved sleep and lower anxiety despite my good and bad bacteria shifting around “

From the reader

Moving Forward

As reviewed above, we have no KEGG suggested probiotics, but do have these supplements suggested:

On a personal note, I used NADH during my 1999-2000 relapse (1st time diagnosis). I eventually switched to 400 mg of flushing niacin twice a day (after MD checked my liver function see facts) and have continue to do so (with liver being tested every year).

Getting suggestions based on US National Library of Medicine Studies

As is my pro forma approach, I did each of the following (with number of bacteria picked after):

The new layout of the consensus page is shown below

Remember these are blindfolded suggestions, items like polysorbate 80 as a supplement is not recommended by any MD, it is in many supplements. [src]

My suggestion for 3 probiotics to rotate thru are:

For more information on probiotics see the bottom section of this recent review.

For supplements, there are only 3 easily accessed items that are positive, everything else is negative impact!!: Ferric citrate (iron supplement), magnesium (commonly used for ME/CFS) and vitamin k2

For other things, see the video or the suggestions on your microbiome.

Bottom Line

You are making objective progress. A word of caution, if some of the items that you are currently taking on the avoid list, slowly remove them by reducing amount and watching for potential adverse effect. Some of the positive objective changes may be due to them (there is a risk of a feedback loop: if you are taking them, they are not needed BUT it you stop taking them, your microbiome may devolve to a state needing them).

Last – Using Symptoms

This is EXPERIMENTAL. It is a thought experiment and I am still learning it’s behavior. For some symptoms it may reduce awesome results, for others it may improve one set of symptoms at a cost of other symptoms getting worst. I picked two of the more unusual symptoms that he had:

  • Comorbid: Methylation issues (MTHFR)
  • Immune: Chronic Sinusitis

This resulted in this list being selected with a very strong Filter (first time I have seen this)

RankNameYour valuePercentile
class Flavobacteriia217
order Chromatiales219.4
order Flavobacteriales217
order Marinilabiliales2113.5
phylum Tenericutes429.5
species Bifidobacterium bohemicum2111.8
species Eubacterium ramulus872095.5
species Prevotella disiens94684.1

With the top suggestions for this small subset being:

ModifierConfidence
  daesiho-tang0.982
  chicory (prebiotic)0.955
  inulin (prebiotic)0.955
  jerusalem artichoke (prebiotic)0.955  📏
  resveratrol (grape seed/polyphenols/red wine)0.955  📏
  glycyrrhizic acid (licorice)0.509  📏
All of the prebiotics listed are similar, any one would do.

I would suggest using it to increase the priority of some items that are positive suggestions in the consensus list, I would not go with using this set of suggestions alone.

Questions from Reader

  • Ferric Citrate ,  haven’t been able to find this type?🤔 Have you seen it anywhere? Also how would one figure out the dose for gut bacteria shifting?
    • I am an ex-science teacher and thus know it more common name, Iron Citrate. Swanson and others sells it.
  • Bacillus- taking terraflora , think I’m up to 6 caps. I saw in a study I need to get to 20 !!😅 …I also have prescript on hand BUT that has a lot of other SBO strains. Would you stuck to TERRAflora for now?  
    • I would keep the Prescript Assist on the shelf, and keep to Terraflora, I would keep increasing the dosage every second day until the bottle was finished. I would look around for ones with similar probiotics for the next cycle, for example Youtheory, Spore Probiotic, 6 Billion CFU, 60 Vegetarian Capsules – for two reasons:
      • Cheaper per BCFU (and also higher BCFU per dosage)
      • Different strains often helps because they produce slightly different products
  • Miyarisan , I thought I saw this in my results somewhere , maybe it was far down the list…would you save or finish if you had my results?
    • It is on the list, I would finish it before starting the next cycle of probiotics (REMEMBER: we want to be rotating the probiotics – not take them continuously)
  • Akkermansia – I have 2 bottle of this stuff actually from pendulum . I read you and your wife has taken it. How much did you take or I know it’s a new product but if you’ve seen a study with dosing please let me know. 
    • The one existing study used 10 BCFU/day, and the bottle reads 0.4 gm. Lacking more information, I would just keep to the bottle recommended dosage.
  • NADH- I have the flush stuff and cq10? Do you think that combo works or does it have to be Nadh?
    • Personally, I found flush niacin had greater impact and still look forward to my morning flush to get the mind working (it improves oxygen delivery because it’s a vascular dilator). Assuming you can tolerate the flush.

ALWAYS REVIEW WITH YOUR MEDICAL PROFESSIONAL FIRST