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PROMOTING A HEALTHY MICROBIOME WITH
FOOD AND PROBIOTICS
DEFINITIONS
Prebiotic: The food that probiotics need to sustain themselves (e.g.,
fructooligosaccharides)
Probiotic: A living organism that benefits the health of the host (e.g., bacteria and
yeast)
Synbiotic: A supplement that contains both a prebiotic and a probiotic
Postbiotic: A metabolic byproduct of probiotics (e.g., n-butyrate from fermentation
of fiber and bacteria)
NUTRITION: THE ULTIMATE PREBIOTIC
Although a person’s population of bacteria originates at the time of birth, most of the
microbiome is established in the human gut with the introduction of food. Breast milk
includes milk oligosaccharides (MOS) that provide bacteria with nutrients to grow,
particularly Bifidobacteria. Diets that contain the most fiber, fruit, and vegetables are
known to engender the most diversity and richness of bacteria growth in the gut. Healthy
bacteria produce short-chain fatty acids, such as n-butyrate, that support the health of the
intestinal lining.[1]
Foods rich in choline and carnitine (e.g., red meat and eggs) are metabolized by the
intestinal microbiota to form the gas trimethylamine (TMA). TMA is converted by the liver
to trimethylamine oxide (TMAO). This substance (an unhealthy postbiotic) has been
strongly linked to the development of atherosclerosis and coronary artery disease.[2]
Eating a diet low in red meat and animal fat and rich in fibrous plants has been found to
support bacteria in the gut that can reduce how much energy the body stores; our gut’s
microbiome can influence one’s risk of obesity.[3] When humans were hunters and
gatherers, it was harder to kill wild game, so eating meat and animal fat was less common.
It may have been advantageous in the past to have a gut that contained bacteria able to
maximize energy storage when such foods were available. Unfortunately, in modern times,
when animal-based foods are easy to obtain, it may be that our gut bacteria increase our
risk of obesity.
The number of studies investigating associations between our gut microbiome and various
health conditions continues to grow exponentially. Positive changes in our gut flora have
now been associated with improvements in conditions ranging from acne, nonalcoholic
fatty liver disease, and chronic kidney disease,[4-6] to the conditions listed in Table 1,
below.
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Unfortunately, only 5% of Americans consume recommended amounts of daily fiber (21-38
gm per day depending on sex and age), as the average daily American intake is only 16.2
gm. “Whole grains” are often considered by consumers to be a surrogate for fiber, though
the fiber content of whole grains various widely by grain and type of processing.[7]
A good rule of thumb to optimize one’s fiber intake is to examine food labels and determine
the “total carbohydrate to fiber ratio.” A ratio of less than 10 is good, and a ratio of less
than 5 is ideal. For example, if a serving of cereal has 20 gm of total carbohydrates and 4
gm of fiber, this ratio would be 20/4=5; this would be an excellent choice.
Nutrition is the main therapeutic tool to positively influence the microbiome. A diet rich in
fiber, vegetables, and fruit helps establish a diverse and rich microbiome that promotes the
health of the host.
Prebiotic foods: Asparagus, artichokes, bananas, oatmeal, leeks, chicory root, red wine,
honey, and beans. Soluble fiber, such as guar gum and psyllium, is also a good prebiotic.
FOOD SOURCES OF PROBIOTICS
Fermentation occurs when a food interacts with a microorganism or enzyme and
undergoes anaerobic biochemical change. This process can prolong the shelf life, promote
the growth of healthy bacteria, enhance taste, and improve digestibility of the food.
Microbes that promote fermentation can produce postbiotics that suppress the growth of
harmful bacteria that could otherwise cause spoilage and disease. An example of this is
Lactobacillus. Lactobacillus species produce lactic acid, which facilitates the digestion of
lactose in milk. Fermentation produces antimicrobial substances such as acids, carbon
dioxide, and alcohol. It is one of the oldest methods for preserving food and an excellent
way to populate the gut with healthy bacteria. The byproducts of probiotic fermentation
maintain a balanced ecosystem while also supporting digestion.
Fermentation is self-limited, based on the amount of bacteria found in a given food. Take
wine, for example. When the sugar in the grape is fermented, alcohol is produced, reducing
the amount of bacteria in the wine.
Red wine is a good prebiotic. A 2012 study of 10 men given 9 oz (270 ml) of red wine daily
found that their fecal microbiome was altered. There was more growth of species of
Bifidobacteria, Bacteroides, and Enterococcus. The increase in Bifidobacteria was linked to
lower levels of cholesterol and changes in C-reactive protein, a marker of inflammation
levels. Benefits were attributed to the polyphenols (e.g., resveratrol) found in wine.[8]
Fermented foods contain a broad spectrum of beneficial bacteria, supporting overall
microbiome health. Eating fermented foods has been showed to enhance immune function,
metabolic health, and improve intestinal permeability. Studies have provided positive
associations with improvements in metabolic syndrome, colon cancer incidence,
depression, stress hormones, anxiety, and even anger.[9]
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COMMON PROBIOTIC FOODS
The following list includes types of probiotics and which foods they can be found in.
Unfortunately, the high temperatures involved in pasteurization kills probiotics. Look for
labeling that says, “contains live cultures” or “contains active cultures.”
PLANTS
Probiotics: Lactobacillus, Leuconostoc, Pediococcus
Foods: Sauerkraut (cabbage), miso (soy paste), tempeh (soy), pickles (cucumber)
Notes: Avoid pickling with vinegar as this can reduce the growth of bacteria.
DAIRY
Probiotics: Lactobacillus, Streptococcus, Saccharomyces (yeast)
Foods: Yogurt, milk, kefir
Notes: Yogurt with live cultures is one of the most accepted methods to obtain
probiotics.
TEA
Probiotics: Lactobacillus, Pediococcus, Acetobacter, Saccharomyces (yeast),
Brettanomyces (yeast)
Foods: Kombucha
Notes: Although the tea leaf is a plant, kombucha is mentioned separately because it
is a good source of a variety of probiotics. Also, it is important to be mindful of the
added sugar content (often from adding juice after fermentation) of many
commercially available products.
PROBIOTIC SUPPLEMENTS
Note: Please refer to the Passport to Whole Health, Chapter 15 on Dietary Supplements for
more information about how to determine whether or not a specific supplement is
appropriate for a given individual. Supplements are not regulated with the same degree of
oversight as medications, and it is important that clinicians keep this in mind. Products
vary greatly in terms of accuracy of labeling, presence of adulterants, and the legitimacy of
claims made by the manufacturer.
Prescribing probiotics can be challenging, as there are thousands of products, each
claiming superiority over the other. Many products have a “special recipe,” a patented
strain, or a mixture of multiple different organisms (a sort of microbiologic shotgun
approach). It is difficult to say whether one probiotic type is superior to another. Studies
indicate that certain microorganisms work better for different illnesses, but it may just be a
matter of which probiotics have been studied and which ones have not.
The goal is to populate the gastrointestinal ecosystem with a healthy balance of
microorganisms that optimally supports the host. At this time, it is not clear what that
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balance should be. In fact, it is probably highly individualized, based on geographic
location, food choices, and even the company one keeps.
WHAT TO LOOK FOR IN A PROBIOTIC
First, look at what genus, species, and strain(s) are in the product. Probiotics’ names have
three parts, usually listed in order. The first part is the name of the genus, the second part
is the species, and the third part is the name of the strain. For example, Lactobacillus
rhamnosus GG is from the genus Lactobacillus and has the species name rhamnosus. GG is
the name of the strain. Different companies patent different strains that they develop.
Lactobacillus is usually abbreviated with an L, and Bifidobacterium is usually abbreviated
with a B. Lactobacilli work in the small intestine, and Bifidobacteria work in the large
intestine. Because antibiotics can kill the bacteria along the entire intestinal tract, it is
important to add back both of these types of bacteria for people who have just taken
antibiotics.
A general rule of thumb is to make sure the product you recommend contains species from
both Lactobacilli and Bifidobacteria. The yeast Saccharomyces boulardii has also shown
benefit for a number of conditions.
Some of the most-researched probiotics are:
Lactobacillus rhamnosus GG (available as the brand Culturelle)
Bifidobacterium lactis BB12 (abbreviated as B. lactis BB12)
L. acidophilus NAS (sometimes just called Acidophilus)
L. bulgaricus LB-51
L. gasseri
L. plantarum
B. bifidum Malyoth strain
B. longum
L. acidophilus DDS1
Saccharomyces boulardiithis is actually a yeast that has been found to have several
benefits
Others, which have been studied less but are often taken, are L. johnsonii, L. reuteri, L.
rhamnosus, B. breve, B. infantis, E. faecalis, and Streptococcus salivarius.
DOSING
Usually 1x10
9
, or 1 billion, colony-forming units (CFUs) is a good daily dose. For Crohn’s
disease or irritable bowel, 1x10
11
,
or 100 billion, CFUs is recommended daily by some
experts. For treating bacterial infections in the vagina, vaginal suppositories with 1 billion
CFUs of lactobacillus organisms are typically used. Many experts recommend taking
probiotics on an empty stomach, when there is less stomach acid present. Children are
Promoting a Healthy Microbiome with Food and Probiotics
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often given doses in the 1x10
8
range. Many products that are tailored to infants or young
children are available.
GUIDELINES FOR PRESCRIBING PROBIOTICS
Take on an empty stomach.
Heat-dried formulations should be kept refrigerated. Lyophilized ones can handle
room temperature.
Most doses range from 1 to 10 billion (10
8
-10
9
) CFUs 1-2 two times daily.
If taking with antibiotics, separate the antibiotic and the probiotic dosing time by 2 hours.
DURATION OF TREATMENT
This is controversial. Some would say that once a healthy gut ecosystem is established,
continued use of probiotics is not necessary and would be similar to seeding an already
seeded garden. But others argue that the therapeutic benefit of the bacteria may be
beneficial after the microbiome is established. The focus should always be on improving
the whole ecosystem so the individual is not dependent on bacteria in pill form.
Various sources recommend taking probiotics daily anywhere from 2 weeks to 2 months to
fully recolonize the bowel’s healthy bacteria. After the initial course, it may be possible to
back off to 2-3 doses per week. In Crohn’s disease or irritable bowel syndrome (IBS),
people often need daily doses for longer time periods. Improvement in symptoms can help
guide this decision. Many of the studies, where probiotics were given to prevent diarrhea
after antibiotic treatment, had subjects take them at the same time as the antibiotic. It is
best to take them 2 hours apart from each other and continue the probiotic for 1-2 weeks
after the antibiotic course is completed.
WHAT TO TREAT?
Table 1 lists conditions that have the strongest evidence in support of using probiotics for
prevention and treatment. For more information, check out the Probiotics Chapter in
Rakel’s Integrative Medicine textbook, which is available through the national VA
Library.[10]
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TABLE 1. CONDITIONS WITH THE STRONGEST EVIDENCE FOR BENEFIT FROM
PROBIOTICS
Indication Bacteria Strains
Used
Comments Key
Study
Prevention of
upper respiratory
infection (URI) in
children
Lactobacillus
acidophilus +/-
Bifidobacteria
animalis
Benefits seen with Lactobacillus
alone or combined with
Bifidobacteria given twice daily
for 6 months.
[11]
Prevention of
colic, reflux, and
constipation in
infants
Lactobacillus reuteri
DSM 17938 during
the first 3 months of
life
Mean duration of crying time
was 38 minutes for the probiotic
group versus 71 minutes in the
placebo group (P < .01).
[12]
Prevention of
diarrhea in
preschoolers
Lactobacillus reuteri
DSM 17938 1 x 10
8
CFUs given daily for
3 months
Not only reduces the incidence
and duration of diarrhea but also
reduced the incidence of URI.
[13]
Prevention of
atopic dermatitis
in infants
Lactobacillus
rhamnosus strain GG
(Culturelle)
When this was given to mothers
prenatally and then to their
offspring for 6 months, the
benefit persisted after a 4-year
follow-up.
[14]
Ability to store fat Bacteria from
human twins
(overweight and
normal weight)
were transplanted
into sterile mice.
Bacteria from overweight twin
caused mice to gain more
weight. Eating a high-fiber, low-
fat diet negated the effect.
[3]
Irritable bowel
syndrome
Bifidobacteria
infantis 35624
The dose of 1 x 10
8
CFUs worked
best in this study of women. The
available data supports
bifidobacteria to be more
effective than lactobacillus at
reducing gas and bloating.
[15,16]
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Indication Bacteria Strains
Used
Comments Key
Study
C. difficile colitis Donor stool infusion
Single-strain
probiotic (no clear
recommended
species)
Significant benefits have
resulted in this becoming the
therapy of choice for drug-
resistant cases.
>50% reduction among
hospitalized individuals if
started[17] within 2 days of
antibiotic initiation
[18]
RESOURCE LINKS
Passport to Whole Health:
https://www.va.gov/WHOLEHEALTHLIBRARY/docs/Passport_to_WholeHealth_FY
2020_508.pdfAuthorS
“Promoting a Healthy Microbiome with Food and Probiotics” was written by David Rakel,
MD and updated by David Lessens, MD, MPH (2014, updated 2020). Sections were adapted
from Probiotics and Prebiotics: Frequently Asked Questions by J. Adam Rindfleisch,
MPhil, MD.
This Whole Health tool was made possible through a collaborative effort between the
University of Wisconsin Integrative Health Program, VA Office of Patient Centered Care and
Cultural Transformation, and Pacific Institute for Research and Evaluation.
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promotes cardiovascular disease. Nature. 2011;472(7341):57-63.
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