Ana Luque

Gut flora, or intestinal bacteria, are the bacteria that normally live in the digestive tract and perform a number of useful functions involving digestion for their hosts.

Gut Flora
From Wikipedia, the free encyclopedia

The average human body, consisting of about 10 trillion cells, has about ten times that number of microorganisms in the gut. Bacterial cells make up most of the material in the colon and 60% of the mass of feces. Somewhere between 300 and 1000 different species live in the gut, with most estimates at about 500. However, it is probable that 99% of the bacteria come from about 30 or 40 species.

Research suggests that the relationship between gut flora and humans is not merely commensal, i.e. a non-harmful coexistence, but rather symbiotic or mutualistic, having a mutually beneficial relationship. Though people can survive even with no gut flora, the bacteria perform a host of useful functions, such as fermenting unused material to provide energy, training the immune system, and preventing growth of harmful species. However, gut flora are not always purely helpful; the bacteria are thought to cause some diseases.

Localization
The upper stomach and small intestine do not have many bacteria. The colon has the greatest numbers of bacteria and the most different species, and the activity of these bacteria make the colon the most metabolically active organ in the body. Most of the bacteria in the small intestine are Gram-positive, while those in the colon are mostly Gram-negative. The first part of the colon is mostly responsible for fermenting carbohydrates, while the latter part mostly breaks down proteins and amino acids. Bacterial growth is rapid in the cecum and ascending colon, which has a low pH, and slow in the descending colon, which has an almost neutral pH. The body maintains the proper balance and locations of species by manipulating pH, the activity of the immune system, and peristalsis.

Types
Not all the species in the gut have been identified because some cannot be cultured and DNA isolation and identification is difficult. Populations of species vary widely among different individuals but stay fairly constant within an individual over time.

Most bacteria come from the genera Bacteroides, Clostridium, Fusobacterium, Eubacterium, Ruminococcus, Peptococcus, Peptostreptococcus, and Bifidobacterium. Facultative anaerobes such as Escherichia and Lactobacillus are also present to a lesser extent. Species from the genus Bacteroides alone constitute about 30% of all bacteria in the gut, suggesting that that genus is especially important in the functioning of the host.

Roles
Bacteria in the gut fulfil a host of important functions for humans, including breaking down and aiding in the absorption of otherwise undigestible food; stimulating cell growth; repressing the growth of harmful bacteria, training the immune system to respond only to pathogens; and defending against some diseases.

Carbohydrate fermentation and absorption
Without gut flora, the human body would be unable to break down and use some of the carbohydrates it consumes, because some types of gut flora have enzymes that human cells lack for breaking down polysaccharides. Rodents raised in a sterile environment and lacking in gut flora need to eat 30% more calories just to remain the same weight as their normal counterparts. Carbohydrates that humans cannot digest without bacterial help include starches; fiber; oligosaccharides and sugars that the body failed to absorb like lactose and alcohols; mucus produced by the gut; and proteins.

Bacteria turn carbohydrates they ferment into short chain fatty acids, or SCFAs. These materials can be used by host cells, providing a major source of useful energy and nutrients for humans. They increase the gut's absorption of water, reduce counts of damaging bacteria, increase growth of human gut cells, and are also used for the growth of indigenous bacteria. The SCFAs are produced by a form of fermentation called saccharolytic fermentation and include acetic acid, propionic acid, and butyric acid. Gases and organic acids like lactic acid are also produced by saccahrolytic fermentation. Acetic acid is used by muscle, propionic acid helps the liver produce ATP, and butyric acid provides energy to gut cells and may prevent cancer.

Another, less favorable type of fermentation, proteolytic fermentation, breaks down proteins like enzymes, dead host and bacterial cells, and collagen and elastin found in food, and can produce toxins and carcinogens in addition to SCFAs. Thus a diet lower in protein lowers exposure to toxins.

Evidence also suggests that bacteria enhance the absorption and storage of lipids. Bacteria also produce and help the body absorb needed vitamins like vitamin K. In addition, the SCFAs they produce help the body absorb nutrients such as calcium, magnesium, and iron.

Trophic Effects
Another benefit of SCFAs is that they increase growth of intestinal epithelial cells and control their proliferation and differentiation. They may also cause lymphoid tissue near the gut to grow. Bacterial cells also alter intestinal growth by changing the expression of cell surface proteins such as sodium/glucose transporters. In addition, changes they 

Repression of pathogenic bacterial growth
Another important role of helpful gut flora is that they prevent species that would harm the host from colonizing the gut, an activity termed the “barrier effect”. Yeasts and harmful bacterial species such as Clostridium difficile are unable to grow too much due to competition from helpful gut flora species, thus animals without gut flora are infected very easily. The barrier effect protects humans from both invading species and species normally present in the gut at low numbers, whose growth is usually inhibited by the gut flora.

Helpful bacteria prevent the growth of pathogenic species by competing for nutrition and attachment sites to the epithelium of the colon. Symbiotic bacteria are more at home in this ecological niche and are thus better at the competition. The indigenous bacteria send chemical signals to the host about how many nutrients they need, and the host provides only that much, so harmful bacteria are starved out. Indigenous gut flora also produce bacteriocins, substances which kill harmful microbes and the levels of which can be regulated by enzymes produced by the host.

The process of fermentation, since it produces fatty acids, also serves to lower the pH in the colon, preventing the proliferation of harmful species of bacteria and facilitating that of helpful species. The pH may also enhance the excretion of carcinogens.

Immunity
Gut flora have a continuous and dynamic effect on the host's gut and systemic immune systems. The bacteria are key in promoting the early development of the gut's mucosal immune system both in terms of its physical components and function and continue to play a role later in life in its operation. The bacteria stimulate the lymphoid tissue associated with the gut mucosa to produce antibodies to pathogens. The immune system recognizes and fights harmful bacteria, but leaves the helpful species alone, a tolerance developed in infancy.

As soon as an infant is born, bacteria begin colonizing its digestive tract. The first bacteria to settle in are able to affect the immune response, making it more favorable to their own survival and less so to competing species; thus the first bacteria to colonize the gut are important in determining the person's lifelong gut flora makeup. However, there is a shift at the time of weaning from predominantly facultative aerobic species such as Streptococci and Escherichia coli to mostly obligate anaerobic species.

Recent findings have shown that gut bacteria play a role in the expression of Toll-like receptors (TLRs) in the intestines, molecules that help the host repair damage due to injury. TLRs cause parts of the immune system to repair injury caused for example by radiation.

Bacteria can influence the phenomenon known as oral tolerance, in which the immune system is less sensitive to an antigen (including those produced by gut bacteria) once it has been ingested. This tolerance, mediated in part by the gastrointestinal immune system and in part by the liver, can reduce an overreactive immune response like those found in allergies and auto-immune disease.

Some species of gut flora, such as some of those in the Bacteroides genus, are able to change their surface receptors to mimic those of host cells in order to evade immune response. Bacteria with neutral and harmful effects on the host can also take advantage of these strategies. The host immune system has also adapted to this activity, preventing overgrowth of harmful species.

Preventing allergy
Bacteria are also implicated in preventing allergies, an overreaction of the immune system to non-harmful antigens. Studies on the gut flora of infants and young children have shown that those who have or later develop allergies have different gut flora compositions, with higher chances of having the harmful species C. difficile and S. aureus and lower prevalence of Bacteroides and Bifidobacteria. One explanation is that since helpful gut flora stimulate the immune system and train it to respond properly to antigens, a lack of these bacteria in early life leads to an inadequately trained immune system which overreacts to antigens. Of course, the differences in flora could be a result, not a cause, of the allergies.

Preventing Inflammatory Bowel Disease
Another indicator that bacteria help train the immune system is the epidemiology of Inflammatory Bowel Disease, or IBD, such as Crohn's Disease (CD). Some authors suggest that SCFAs prevent IBD. In addition, some forms of bacteria can prevent inflammation. The incidence and prevalence of IBD is high in industrialized countries with a high standard of living and low in less economically developed countries, having increased in developed countries throughout the twentieth century. The disease is also linked to good hygiene in youth; lack of breastfeeding; and consumption of large amounts of sucrose and animal fat. Its incidence is inversely linked with poor sanitation during the first years of life and consumption of fruits, vegetables, and unprocessed foods. Also, the use of antibiotics, whicative gut flora and harmful infectious pathogens alike, especially during childhood, is associated with irritable bowel syndrome. On the other hand, using probiotics, bacteria consumed as part of the diet that impart health benefits (aside from just nutrition), helps treat IBD. All of these factors could indicate that IBD is caused by inadequate amounts of gut flora colonizing a person’s gut.

Effects of antibiotics
Because bacteria play such an important role in the health of the host, altering their numbers, for example by taking broad-spectrum antibiotics, may affect the host's health and ability to digest food. People may take the drugs to cure bacterial illnesses or may unintentionally consume significant amounts of antibiotics by eating the meat of animals to which they were fed.[citation needed] Antibiotics can cause antibiotic-associated diarrhea (AAD) by irritating the bowel directly, changing the levels of gut flora, or allowing pathogenic bacteria to grow. Another harmful effect of antibiotics is the increase in numbers of antibiotic-resistant bacteria found after their use, especially if used incorrectly. When they invade the host, the resistant bacteria cause illnesses that are more difficult to treat.

Changing the numbers and species of gut flora can reduce the body's ability to ferment carbohydrates and metabolize bile acids and may cause diarrhea. Carbohydrates that are not broken down may absorb too much water and cause runny stools, or lack of SCFAs produced by gut flora could cause the diarrhea.

A reduction in innate bacteria also abrogates their ability to inhibit the growth of harmful species such as C. difficile and Salmonella kedougou, and these species can get out of hand, though their overgrowth may be incidental and not be the true cause of diarrhea.

Gut flora composition also changes in severe illnesses, due not only to antibiotic use but also to such factors as ischemia of the gut, failure to eat, and immune compromise. Negative effects from this have led to interest in selective digestive tract decontamination (SDD), a treatment to kill only pathogenic bacteria and allow the reestablishment of healthy ones.

Probiotics and prebiotics
Since the lack of gut flora can have such harmful health effects, the use of probiotics has anti-inflammatory effects in the gut and may be useful for improving health. Prebiotics, dietary components that are not bacteria themselves but stimulate the growth of helpful bacteria, may also have a positive health effect.

Role in disease
Bacteria in the digestive tract have pathogenic properties in addition to their health-inducing ones: they can produce toxins and carcinogens and have been implicated in such conditions as multisystem organ failure, sepsis, colon cancer, and IBD. A major factor in health is the balance of bacterial numbers; if the numbers grow too high or low, it will result in harm to the host. The host has enzymes to regulate this balance.

Cancer
Some genera of bacteria, such as Bacteroides and Clostridium, have been associated with an increase in tumor growth rate, while other genera like Lactobacillus and Bifidobacteria are known to prevent tumor formation.

Translocation
Helpful bacteria can be very harmful to the host if they get outside of the intestinal tract. Translocation, which occurs when bacteria leave the gut through its mucosal lining, the border between the lumen of the gut and the inside of the body, can occur in a number of different diseases. It can be caused by too much growth of bacteria in the small intestine, reduced immunity of the human, or increased gut lining permeability. The gut can become more permeable in diseases like cirrhosis, which is damaging due in part to the activity of gut flora.

If the gut is perforated, bacteria can invade the body, causing a potentially fatal infection. Aerobic bacteria can make infection by anaerobes worse by using up all available oxygen and creating an environment favorable to anaerobes.

Inflammatory Bowel Disease
Some suspect that IBD is due to a reduction in immune tolerance and subsequent overreaction of the host's immune system to harmful or non-harmful bacteria. IBD may be caused by all of the gut flora together or some specific types.

It has been noted that though colitis and Crohn's disease (two types of IBD) probably have genetic components, they are not inherited in a Mendelian fashion and are thus probably due to a complex set of factors rather than solely to a gene. Though neither bacterial colonization nor genetics is sufficient to cause the disease, bacteria probably play a role in these disorders.

Some suspect that inflammation in IBD is due to increased permeability of the inner lining of the colon, which may allow bacteria to invade the tissues and cause an immune reaction that leads prolonged inflammation. Abnormal tight junctions, which are supposed to prevent permeability, have been found in cells of patients with IBD. Because of the potentially harmful role of these bacteria, antibiotics are frequently prescribed to treat Crohn’s disease. However, inflammation could occur first and cause the increased intestinal permeability found in diseases such as Crohn's, so the causative role of bacteria is not clear.

Colitis
It has been suggested that commensal bacteria are responsible for the development of colitis, since mice raised in a sterile environment do not get the disease. However, while some bacterial strains such as C. difficile and even normal gut bacteria cause colitis, others prevent the disease in mice.

References 
1.	Beaugerie L and Petit JC. 2004. Antibiotic-associated diarrhoea. Best Practice & Research Clinical Gastroenterology, Volume 18, Issue 2, Pages 337-352.
2.	Björkstén B, Sepp E, Julge K, Voor T, and Mikelsaar M. 2001. Allergy development and the intestinal microflora during the first year of life. Journal of Allergy and Clinical Immunology, Volume 108, Issue 4, Pages 516-520. Abstract available.
3.	Carman RJ, Simon MA, Fernández H, Miller MA, and Bartholomew MJ. 2004. Ciprofloxacin at low levels disrupts colonization resistance of human fecal microflora growing in chemostats. Regulatory Toxicology and Pharmacology, Volume 40, Issue 3, December, Pages 319-326.
4.	Garcia-Tsao G and Wiest R. 2004. Gut microflora in the pathogenesis of the complications of cirrhosis. Best Practice & Research Clinical Gastroenterology, Volume 18, Issue 2, Pages 353-372.
5.	Gibson RG. 2004. Fibre and effects on probiotics (the prebiotic concept). Clinical Nutrition Supplements, Volume 1, Issue 2, Pages 25-31.
6.	Guarner F and Malagelada JR. 2003a. Role of bacteria in experimental colitis. Best Practice & Research Clinical Gastroenterology, Volume 17, Issue 5, October 2003, Pages 793-804.
7.	Guarner F and Malagelada JR. 2003b. Gut flora in health and disease. The Lancet, Volume 361, Issue 9356, 8 February 2003, Pages 512-519. Abstract available.
8.	Hugot JP. 2004. Inflammatory bowel disease: a complex group of genetic disorders. Best Practice & Research Clinical Gastroenterology, Volume 18, Issue 3, Pages 451-462.
9.	Jewell AP. 2005. Is the liver an important site for the development of immune tolerance to tumours? Medical Hypotheses, Volume 64, Issue 4, Pages 751-754.
10.	Keeley J. 2004. Good bacteria trigger proteins to protect the gut. Howard Hughes Medical Institute. EurekAlert.
11.	Knight DJW and Girling KJ. 2003. Gut flora in health and disease. The Lancet, Volume 361, Issue 9371, Page 1831.
12.	Nordgård L, Traavik T, and Nielsen KM. 2005. Nucleic Acid Isolation from Ecological Samples—Vertebrate Gut Flora. Methods in Enzymology, Volume 395, Pages 38-48.
13.	Riordan SM, McIver CJ, Wakefield D, Duncombe VM, Thomas MC, and Bolin TD. 2001. Small intestinal mucosal immunity and morphometry in luminal overgrowth of indigenous gut flora. The American Journal of Gastroenterology, Volume 96, Issue 2, Pages 494-500.
14.	Sears CL. 2005. A dynamic partnership: Celebrating our gut flora. Anaerobe, Volume 11, Issue 5, Pages 247-251.
15.	Shanahan F. 2002. The host–microbe interface within the gut. Best Practice & Research Clinical Gastroenterology, Volume 16, Issue 6, Pages 915-931.
16.	Steinhoff U. 2005. Who controls the crowd? New findings and old questions about the intestinal microflora. Immunology Letters, Volume 99, Issue 1, 15 June , Pages 12-16.
17.	Suenaert P, Bulteel V, Lemmens L, Noman M, Geypens B, Assche GV, Geboes K, Ceuppens JL and Rutgeert P. 2002. Anti-tumor necrosis factor treatment restores the gut barrier in Crohn’s disease. The American Journal of Gastroenterology, Volume 97, Issue 8, Pages 2000-2004.
18.	University of Glasgow. 2005. The normal gut flora.
19.	Vedantam G and Hecht DW. 2003. Antibiotics and anaerobes of gut origin. Current Opinion in Microbiology, Volume 6, Issue 5, Pages 457-461.
20.	Veltkamp C, Tonkonogy SL, De Jong YP, Albright C, Grenther WB, Balish E, Terhorst C, and Sartor RB. 2001. Continuous Stimulation by Normal Luminal Bacteria Is Essential for the Development and Perpetuation of Colitis in Tgsmall epsilon, Greek26 Mice. Gastroenterology, Volume 120, Issue 4, Pages 900-913.
21.	Wynne AG, McCartney AL, Brostoff J, Hudspith BN, Glenn GR and Gibson G. 2004. An in vitro assessment of the effects of broad-spectrum antibiotics on the human gut microflora and concomitant isolation of a Lactobacillus plantarum with anti-Candida activities. Anaerobe, Volume 10, Issue 3, Pages 165-169.

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About Ana Luque


Author of The Yogurt Diet, Ana has led the movement toward better health and weight loss through the use of probioticsthe healthy bacteria that live in the gut and are so necessary to perform many of the body’s functions, including proper digestion and assimilation of nutrients.  She has been a consultant and spokesperson for the probiotic and yogurt industries, and provides wellness coaching to the workforces of corporate clients.

Nutritionist, writer, wellness coach, chef, spokesperson and researcher, Ana has been featured in major media outlets as the pioneer expert in the use of yogurt and probiotics for health and weight loss.  She has worked with clients from all walks of life, including celebrities, Royal family members in Europe, corporations and top executives worldwide.

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