|
|
| (68 intermediate revisions by 11 users not shown) |
| Line 1: |
Line 1: |
| ==Introduction== | | {{Uncurated}} |
| According to the three-domain system, which is a biological classification scheme fabricated by Carl Woese, the cellular organisms that constitute life are divided into archaea, bacteria, and eukarya. Woese devised this categorization scheme by comparing the 16S rRNA sequences of living cells. The use of this specific ribosomal RNA was key to his success, as it was proved to be present in all living organisms. Therefore, comparison of this gene sequence was useful in determining the phylogeny of cellular life. This sequence differed between domains depending on the environment that surrounded the organisms as well as their method of metabolism. As a result, the prokaryotes were split into two domains, the archaea and bacteria, while the eukarya remained in a separate class due to their multicellular characteristics. [http://www.becomehealthynow.com/article/bodydigestive/787/ (1)]
| | ==Classification== |
|
| |
| Despite the common misconception that bacteria are organisms that only cause disease, they play an important role in facilitating our digestion. For example, the large intestine is home to hundreds of bacteria that aid in absorption, excretion, and catalysis of undigested foods. There are also bacteria present in the small intestine that support break down of foods passed down from the stomach as well as nutrient absorption. [http://coloncancer.about.com/od/glossaries/g/Large_Intestine.htm (2)]
| |
|
| |
|
| We will be focusing on prokaryotic, as well as eukaryotic, organisms that reside in the large intestine. The bacteria that will be discussed include the following: Lactobacillus, [[Bifidobacterium]], Methanogens, Sulfate reducing bacteria, [[Bacteroides]], [[Enterococcus]], [[Escherichia coli]], and [[Clostridium]]. In addition, we will discuss a eukaryotic organism, Candida, and see how it effects the large intestine.
| | ===Higher order taxa=== |
| | Bacteria; Phylum; Class; Order; Family; Genus: |
|
| |
|
| ==Description of Niche== | | ===Species=== |
|
| |
|
| The large intestine, commonly known to be the final stage of digestion, is located in the abdominal cavity; specifically, between the small intestine and the anus. The primary functions of the large intestine include the following: absorbing water from the bolus (which is a round mass of organic matter passed down from the small intestine), storing feces in the rectum prior to excretion, and metabolizing undigested polysaccharides to short-chain fatty acids, which are passively absorbed for energy use. [http://en.wikipedia.org/wiki/Large_intestine (3)]
| | Genus species: |
|
| |
|
| The large intestine is divided into three main parts: the cecum, the colon, and the rectum. The cecum, also known as the first part of the large intestine, is a pouch-shaped member that connects the colon to the ileum (which is the last part of the small intestine). The colon, which serves as a storage tube for solid wastes, is divided into four subcategories: the ascending colon, the transverse colon, the descending colon, and the sigmoid colon. The ascending colon, which is continuous with the cecum, extends upward towards the under surface of the liver. Then, the transverse colon, which is the longest part of the colon, passes downward near the lower end of the spleen. Next, the descending colon runs further down along the lateral border of the left kidney. When it reaches the lower end of the kidney, the colon turns toward the lateral border of the psoas muscle, where it will connect to the sigmoid colon. The sigmoid colon forms a loop of about 40 centimeters and lies within the pelvis region. Last but not least, the rectum. The rectum is the final straight portion of the large intestine that terminates in the anus. As mentioned before, this is where the feces are stored before being expelled out of the body. [http://www.becomehealthynow.com/article/bodydigestive/787/ (1)]
| | ==Description and significance== |
|
| |
|
| Moving on, the pH of the large intestine varies between 5.5 and 7.0, which indicates a fairly neutral environment. This is different from that of the small intestine, which exhibits a pH of 8.5, enabling absorption in mild alkaline environments; thus, water absorption in the large intestine occurs optimally around a neutral pH. [http://en.wikipedia.org/wiki/Colon_(anatomy) (4)]
| | ==Include as many headings as are relevant to your microbe (including things like cell metabolism, ecology, pathology, application to biotechnology). Or, if your microbe is very new and not well studied, then include a heading or two with more description about its native environment or something related to its lifestyle.== |
|
| |
|
| In addition, the temperature inside the large intestine tends to be between 37-40°C. This is crucial to the breakdown of undigestible fibers, as hyperthermic or hypothermic temperatures proved to depress the catalysis of these carbohydrates. Therefore, the physical conditions in the large intestine are reasonably stable in order to ensure proper digestion of food. [http://en.wikipedia.org/wiki/Colon_(anatomy) (4)]
| |
|
| |
| ==Who lives there?==
| |
| ===Lactobacillus===
| |
| [[Lactobacillus]] is a microbe that aids in production of lactic acid through
| |
| homolactic fermentation, and can be found in the human gastrointestinal tract. This
| |
| Gram-positive, rod shaped, bacterium is a beneficial bacterium that assists in
| |
| enzymatic production to help with digestion, maintain pH balance and aid in healthy
| |
| bacterium replacement in the gastrointestinal tract. The lactic acid produced by
| |
| carbohydrate fermentation from lactobacillus, aids in maintaining the correct
| |
| homeostatic pH to ensure no phage is able to survive at the low pH. Studies also
| |
| show that it can synthesize necessary vitamins and help lower cholesterol levels
| |
| (Ray). [[Lactobacillus]] also has been observed to degrade carcinogens, reduce or
| |
| prevent carcinogenesis through antimutagenic activities. One of many strains of
| |
| [[Lactobacillus|Lactobacilli]] that is commercially distributed is [[Lactobacillus|Lactobacillus Acidophilus]],
| |
| which is categorized as a probiotic. Probiotics are bacterium that can be taken as
| |
| a supplement to help increase the beneficial bacteria that are normally present in
| |
| their environment. In the case of [[Lactobacillus|Lactobacillus Acidophilus]], it has
| |
| fermentative capabilities, but lacks the ability to synthesize most cofactors and
| |
| vitamins; which are expected normal capacities of microbes living in such a
| |
| nutrient-rich niche such as the human gastrointestinal cavity (Altermann). The
| |
| adherence of [[Lactobacillus|Lactobacillus Acidophilus]] to the cells lining the colon prevents
| |
| binding of enteropathogenic and enterotoxigenic pathogens, promoting healthy
| |
| metabolic activities. [[Lactobacillus|Lactobacillus Acidophilus]] and other strains of [[Lactobacillus|Lactobilli]]
| |
| are widely used for treatment in diarrheal diseases, however the mixed results do
| |
| not allow an exact conclusion on its treatment accuracy (Macfarlene). [http://www.pnas.org/content/102/11/3906.full (5)]
| |
|
| |
| ===Bifidiobacterium===
| |
| [[Image:Bifidobacteria.jpg|frame|Figure 1. Gram-Stained Preparation of [[Bifidobacterium]]
| |
| Adolescentis]]
| |
|
| |
| [[Bifidobacterium]] is also considered a probiotic bacterium that inhabits the
| |
| anaerobic environment of the human gastrointestinal tract. The amount of this
| |
| bacterium present decreases with age; thus, higher amounts are found in infants, and
| |
| lower amounts in adults, which may lead to the needs of a probiotic supplement.
| |
| [[Bifidobacterium]] is also a rod club-shaped (as pictured), Gram-positive cell,
| |
| which has a symbiotic relationship with the host (gastrointestinal tract),
| |
| benefiting both bacteria and host. This symbiotic relationship is seen by its
| |
| adhesive ability to the microflora, the metabolism of undigested dietary
| |
| carbohydrates and prevents pathogen colonization. This type of beneficial bacteria,
| |
| similarly to the [[Lactobacillus|Lactobacilli]], prevents binding of pathogens such as
| |
| [[Escherichia Coli]], and [[Salmonella Typhimurium]], decreasing susceptibility to
| |
| possible illnesses such as [[E. Coli]] poisoning in humans. The microflora normally
| |
| lining the gut serves as a protective barrier against pathogens, however this can be
| |
| compromised due to antibiotic treatments, stress, poor diet or other physiological
| |
| distress. The [[Bifidobacteria]] can serve as resistance mechanism against the
| |
| colonization of pathogens in the large intestine (Macfarlene). It has been observed
| |
| that their competitive nature, against other gastrointestinal bacteria, is due to
| |
| its ability to scavenge for a large variety of nutrients to use for energy (Schell).
| |
| Studies also show that [[Bifidobacterium]] has also has potential to prevent cancer
| |
| by reactivity with certain carcinogens and promotes immune stimulation (O'Sullivan). [http://www.ncbi.nlm.nih.gov/sites/entrez (6)]
| |
|
| |
| ===Methanogens and Sulfur reducing bacteria===
| |
| In addition, methanogenic bacteria (e.g. Methanobrevibacter smithii) also benefit the gastrointestinal tract in that they reduce carbon dioxide and hydrogen gas to produce methane gas and water. This reduction reaction is an imperative characteristic of the large intestine as it aids in the fermentation of organic matter to obtain energy. For example, prior to entering the large intestine, the small intestine cannot digest or absorb dietary fibers for energy production; thus, these carbohydrates prove to be useless up to this point. However, once the indigestible sugars are in the large intestine, they will be fermented by gut organisms to break down the complex polymers (e.g. resistant starches, non-starch polysaccharides, oligosaccharides and etc.) into its monomeric constituents. These monomers are then oxidized to short chain fatty acids (SCFA), lactate, succinate, ethanol, hydrogen gas and carbon dioxide. The resulting SCFA can then enter central metabolic pathways where it can be converted into energy in the host organism. [http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=1 (7)]
| |
|
| |
| An important fact to note here is that hydrogen gas and carbon dioxide are products of the fermentation reaction. Since the large intestine is an anaerobic environment, the reducing energy is stored in the form of ethanol, lactate, succinate, or H<sub>2</sub>, but not in water (as would be the case in an aerobic environment). This poses a problem as accumulation of H<sub>2</sub> inhibits oxidation of pyridine nucleotides, which leads to a redundant amount of substrate level phosphorylation. Therefore, in order to avoid this unnecessary energy expenditure, a balance between fermentation and H<sub>2</sub> removal is imperative; and this where [[methanogens]] come in to save the day. [http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=1 (7)]
| |
|
| |
| [[Methanogens]] live symbiotically with the large intestine. The bacteria grow by reducing carbon dioxide and H<sub>2</sub> to produce methane gas and water; hence, the fermentation products now function as nutrients for these organisms and not inhibitory poisons to the environment. The large intestine benefits from the reducing activity of the [[methanogens]] because methane is an effective pathway for H<sub>2</sub> disposal, which relieves the inhibition of nucleotide oxidation. As a result, superfluous use of energy is avoided. [http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=1 (7)]
| |
|
| |
| An alternative to methanogenesis is the sulfate reducing pathway. The main substrates for sulfate reducing bacteria are also fermentation products; however, the product of this reduction pathway is a highly toxic hydrogen sulfide which can damage the colonic epithelium. The main organisms that perform this reaction include [[Desulfovibrio]], [[Desulfobacter]], Desulfomonas, Desulfobulbus, and Desulfotomaculum. [http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=2#page (8)]
| |
|
| |
| Fermentation experiments in a lab revealed organisms competing for gaseous nutrients, as sulfate reducing bacteria overpowered [[methanogens]] when present in the same environment. However, recent experiments have shown [[methanogens]] displacing other H<sub>2</sub> consuming bacteria in fecal slurries. In such experiments, the expression of sulfate reducing bacteria was probably limited or nonexistent because it is unlikely for [[methanogens]] to competitively overrule them. The reason for this is due to sulfur reducing bacteria having a higher affinity for H<sub>2</sub> relative to that of [[methanogens]]. Therefore, determination of the more predominant organism depends on the sulfate concentration of the environment. The higher the sulfate concentration, the more reduction performed by sulfate reducing bacteria. [http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=2#page (8)]
| |
|
| |
| ===Bacteroides===
| |
| [[Bacteroides]] are anaerobic organisms that are characterized by the gram-negative cellular envelope. These bacteria exist symbiotically with the large intestine because the [[Bacterioides]] support the core metabolic activities (i.e. amino acid biosynthesis, carbon-oxygen lyases, membrane transport, and etc.) while feeding off dietary fibers passing through the colon. The common species of Bacteroides include B. vulgatus, B. distasoni, [[Bacteroides thetaiotaomicron|B. thetaiotaomicron]], and [[Bacteroides fragilis|B. fragilis]].2
| |
|
| |
| These organisms primarily feed off of plant polysaccharides and the host’s mucous glycans.2 Fibrous polymers that pass through the large intestine can be only be broken down by [[Bacteroides]]. Once these sugars are in the large intestine, the Bacteriodes metabolize them into their respective monomers so that they can enter central metabolism for energy synthesis.4 A unique trait of [[Bacteroides thetaiotaomicron|B. thetaiotaomicron]] is that it can use various polysaccharides to survive. The physiological explanation for this is that [[Bacteroides thetaiotaomicron|B. thetaiotaomicron]] possesses 226 glycoside hydrolases and 15 polysaccharide lyases. Note that [[Bacteroides thetaiotaomicron|B. thetaiotaomicron]] does not reside in human intestine; thus, we cannot digest such polysaccharides.
| |
|
| |
| [[Bacteroides]] are also saccharolytic, meaning that they can obtain energy, carbon sources, dietary carbohydrate molecules from the host.3 The products of fermentation reactions include acetate and propionate, which are short chains of fatty acids can then be absorbed via the large intestine.3 B. distasonis are more specific for carbohydrate processing with the enzymes CAZy glycoside hydrolase family 13 and family 73.2 These enzymes aid in breaking down food molecules and supplying vitamins for metabolic purposes.3 It also has more polysaccharide deacetylases, which allow it to deacetylate the O-acetylated sugars of the host’s epithelial glycans to utilize them.
| |
|
| |
| ===Enterococcus===
| |
| Common Species: ''E. avium, E. durans, E. faecalis, E. faecium, E. solitarius''
| |
|
| |
| [[Enterococcus|Enterococci]] are gram-positive cocci that are found in many different places – normally found in the feces of people and many animals. Two major species – [[Enterococcus faecalis|E. faecalis]] and ''E. faecium'' – can cause urinary tract infections and wound infections in human and animals most commonly. [[Enterococcus faecalis|E. faecalis]] contributes about 90-95% of all species and ''E. faecium'' contributes about 5-10%. They can be also the cause of other diseases – bacteraemia (blood stream), endocarditis (heart vales), and meningitis (brain) – which occurs mostly in severely sick people with weak immune system1. Many of these [[Enterococcus]] infections have been commonly found in clinical environment. Healthy people with strong immune system will not be affected by [[Enterococcus|Enterococci]] but they many become potential carriers.
| |
|
| |
| [[Enterococcus|Enterococci]] infections can be treated with various types of antibiotics, but unfortunately some of the [[Enterococcus|Enterococci]] have become resistant to many types of antibiotics. They are resistant to β-lactam-based antibiotics (penicillin and cephalosporin) as well as many aminoglycosides2. In recent time, some of the [[Enterococcus|Enterococci]] are found to be resistant to Vancomycin, and they are called VRE (Vancomycin-Resistant [[Enterococcus]]). VRE are especially dangerous because they can easily transmit the resistant genes from another (transformation or conjugation), so if there is small portion of [[Enterococcus|Enterococci]] that are resistant to antibiotics, then the whole community will become resistant and no other antibiotics are effective3.
| |
|
| |
| [[Enterococcus|Enterococci]] are commensal bacteria inhabiting in the intestines of both humans and animals.
| |
| [[Enterococcus|Enterococci]] are capable of living in extremely hardy conditions that most of other bacteria won’t survive. They are likely to inhabit in the bowels of animlas or humans, and they are also found in soil, vegetation, and surface water (mainly due to contamination by animal feces). [[Enterococcus|Enterococci]] are capable of growing at a range of temperatures from 10-45 °C and can grow in any environmental concentrations – hypotonic or hypertonic – and over broad range of pH – acidic or alkaline. Even though they are anaerobes, they can live in both low and high oxygen environments. In fact, [[Enterococcus|Enterococci]] can survive at 60 °C for half an hour. They are also capable of living under high salt concentration (6.5% NaCl) and in high bile salts (40%). Some of them are naturally antibiotic resistant4.
| |
|
| |
| [[Enterococcus|Enterococci]] are anaerobes. They ferment carbohydrates to produce lactic acids (lactic acid bacteria). [[Enterococcus|Enterococci]] living in large intestine will use undigested sugars from small intestine and indigestible fibers for their fermentation process. Especially for [[Enterococcus faecalis|E. faecalis]], it contains a large number of sugar uptake systems (PTS: phophoenolypyruvate phosphotransferase system) which recognize sugars outside and transport them with phosphorlyation. This process will use energy (ATP) more efficiently as it is compared to sugar transport by other non-PTS system5. [[Enterococcus faecalis|E. faecalis]] can metabolize following types of sugars: D-glucose, D-fructose, lactose, maltose, etc. It also has cation homeostasis mechanism that contributes to its resistance to change in pH, salt concentration, etc. They under go fermentation process usually because they lack ability to process Kreb’s cycle and following electron transport chain reaction6.
| |
|
| |
| ===Escherichia Coli===
| |
| Common Species: ''Escherichia albertii; E. blattae; [[Escherichia Coli|E. coli]]; E. fergusonii; E. hermannii; E. senegalensis; E. senegalensis; E. vulneris; E. sp.''
| |
|
| |
| [[Escherichia coli]], also known as [[Escherichia Coli|E. coli]], is an anaerobic gram-negative bacterium that can be found in large intestine of warm-blooded animals and humans. Even though it is a predominant and consistent organism, it contributes to only small portion of the content of total bacteria in GI tract. It is often used as an indicator to test the fecal contamination in nature such as water since [[Escherichia Coli|E. coli]] is able to survive outside the body for a brief time period.[1][2] Because of its simple nutritional requirement and ability to grow rapidly, [[Escherichia Coli|E. coli]] is also useful in studying the organisms’ essential processes of life.[3]
| |
|
| |
| [[Escherichia Coli|E. coli]] are both pathogenic and nonpathogenic. Some are nonpathogenic, but it might cause infection if the bacterium is introduced to other tissues in a debilitated host; however, the bacteria from contaminated water or undercooked meat may cause infection in a healthy person as well.[5] Some virulent [[Escherichia Coli|E. coli]] can even lead to urinary tract infections, neonatal meningitis, diarrheal disease, and gastroenteritis.[6] They damage the host in several steps: colonizing the intestinal mucosal surface, evading the defenses by the host, and lastly multiplying themselves in numbers.[5] Since the bacterial infections are usually treated with antibiotics, the antibiotic-resistance became problematic. [[Escherichia Coli|E. coli]] often stay with diverse species of bacteria in a form of biofilm and this causes the transfer of antibiotic-resistant plasmids of [[Escherichia Coli|E. coli]] to other bacteria such as [[Staphylococcus aureus]].[7]
| |
|
| |
| Despite the fact that [[Escherichia Coli|E. coli]] is a unicellular organism, it has an amazing ability in interacting with the environment. It can respond to such signals including pH, osmolarity, temperature, and chemicals. With its chemotaxis proteins in cytoplasmic membrane, [[Escherichia Coli|E. coli]] can detect attractants and repellants without any stimuli. With around six flagella, it can swim towards the attractant with counterclockwise flagellar rotation, but bacteria tumbles with clockwise rotation when it senses the repellant.[4] It can also adjust the size of the porins on the outer membrane in order to regulate the temperature and osmolarity by importing or exporting the larger substances such as nutrients. [[Escherichia Coli|E. coli]] can detect the chemicals in the surrounding environment with its complex metabolism mechanism.[4]
| |
|
| |
| [[Escherichia Coli|E. coli]] is able to survive with or without oxygen. Unlike aerobic organisms which use oxygen as the final electron acceptor, [[Escherichia Coli|E. coli]] use nitrate or other molecules. The major determinants of organization of bacterium are the type of terminal electron acceptor and the presence of glucose (Barrett). [[Escherichia Coli|E. coli]] demonstrates only six distinct functional states no matter what carbon source or electron acceptor has been used.[6] Unless the carbon sources are available, they do not wastefully make the enzymes for degradation. If the metabolites are available in the environment as nutrients, they also don’t make the enzymes for synthesis.[1]
| |
|
| |
| ===Clostridium===
| |
| Common Species: Clostridium dfficile, Clostridium tetani, Clostridium perfringens, Clostridium acetobutylicum
| |
|
| |
| [[Clostridium]], is a gram-positive bacteria belonging to the family of [[Clostridiaceae]]. It is capable of forming endospores during extreme environmental conditions. These organisms are capable of surviving in many environments, but are predominantly found in soil and feces; be that as it may, [[Clostridium]] prefer to live in the human body as such an environment provides optimum growth for the organism. [1]
| |
|
| |
| Most of the species in [[Clostridium]] are pathogenic. [[Clostridium deficile]] for instance, may cause inflammation in the colon of the gastrointestinal tract. Ironically, treatment with relevant antibiotics does not kill this organism, but speed its the growth. The only factor that limits its growth is the presence of other bacteria in the colon (i.e. other competitors). [1]
| |
|
| |
| [[Clostridium]] is able to survive without oxygen. Unlike aerobic organisms which use oxygen as the final electron acceptor, [[Clostridium]] use nitrate or other molecules. These organisms are usually pathogens that live freely in our gastrointestinal tract. A trademark characteristic of this organism is that it is the major cause of Pseudomembranous Coliits, an inflammatory disease of the colon characterized by exudative plaques on congested mucosa. [1]
| |
|
| |
| Studies have shown that commercial broiler chickens that were vaccinated with [[Clostridium perfiringens]] type A Toxoid controlled the growth of necrotic enteritis over a 65 week period. Sera and egg yolk that were injected with the vaccine had higher antibody for [[Clostridium perfiringens|C. perfringers]] compared to controls.
| |
|
| |
| ===Staphylococcus===
| |
| Common species: ''S. arlettae, S. aureus, S. auricularis, S. capitis, S. caprae, S. carnosus, S. chromogenes, S. cohnii, S. condimenti, S. croceolyticus, S. delphini, S. epidermidis, S. equorum, S. faecalis, S. felis, S. fleurettii, S. gallinarum, S. haemolyticus, S. hominis, S. hyicus, S. intermedius, S. kloosii, S. lentus, S. lugdunensis, S. lutrae, S. lyticans, S. muscae, S. nepalensis, S. pasteuri, S. pettenkoferi, S. piscifermentans, S. pseudintermedius, S. saccharolyticus, S. saprophyticus, S. schleiferi, S. sciuri, S. simiae, S. simulans, S. succinus, S. vitulinus, S. warneri, S. xylosus''
| |
|
| |
| Staphylococci are immobile Gram-positive bacteria which form the clusters resembling grapes under the microscope.[1] These small components of soil microbial flora are usually harmless and often can be found in human’s mucous membranes. Even though there are around 31 species in Staphylococcus, S. aureus and S. epidermidis are the most significant species in interaction with humans.[2] The colonies formed by S. aureus are yellow and large, but those formed by S. epidermidis are white and somewhat small.[3]
| |
|
| |
| Although most Staphylococci are known as harmless, they also have pathogenic effect by producing various toxins during the stationary phase of their growth. Therefore, the infected site usually doesn’t show any viable Staph cells. The cramps and severe vomiting are caused by the enterotoxin produced by S. aureus. A quick food poisoning is caused by infection from undercooked or contaminated meats. In addition, these microbes also lead to pneumonia, meningitis, boils, arthritis, and osteomyelitis. Most of S. aureus became resistant against penicillin; however, Vancomycin and nafcillin are prominent ones that is used against most strains.[6]
| |
|
| |
| Staphyloccoci are facultative anaerobe that are able to grow in two ways including aerobic respiration and fermentation which produces lactic acid. They are catalase-positive and oxidase-negative.[4] S. aureus normally grows at a temperature between 15 to 45 degrees and at NaCl concentration maximum 15%. They have several secretions associated with adhesions, endotoxins, exoenzymes, and capsular polysaccharide.[5]
| |
|
| |
| S. aureus is capable of producing the catalase enzyme and converting hydrogen peroxide (H2O2) to water and oxygen. The catalase test is then used to differentiate Staphylococci from Enterococci. S. aureus can also be distinguished from the other Staphylococci species by coagulase test. S. aureus is also capable of producing a protein product called a cogulase which is not an enzyme. This production causes a clot formation, but most of all other Staphylococci species are coagulase-negative.[1]
| |
|
| |
| ==What other organisms are present (e.g. plants, fungi, etc.)==
| |
|
| |
| ===Protozoa===
| |
|
| |
| Protozoa are a collection of single celled eukaryotic organisms.They are among the simplest of all living organism. Most protozoans reside in soils and aquatic habitats. Protozoa are usually not present in normal human intestine but some are capable of colonizing the intestine as parasites. The intestinal protozoa predominantly affected individuals living in the tropics causing diarrhea and other symptoms. Due to increasing world travel, increasing number of elderly and immunosuppresed population, and a global economy “intestinal protozoan infections have become important causes of diarrhea in the United States, Canada, and Europe”([http://www.co-gastroenterology.com/pt/re/cogastro/abstract.00001574-200101000-00004.htm;jsessionid=L33YX1sXnQPTWdWJGvnC87pvy2Z68TGnVMvx9VWF1vBJDLrWVhd9!1270838445!181195628!8091!-1 Huston], [http://cmr.asm.org/cgi/content/abstract/10/1/67 Marshall]). The major protozoan parasites are [[Cryptosporidium parvum]], [[Isospora belli]], Cyclospora cayentanensis, [[microsporidia]], and [[Entamoeba histolytica]]. Of all these [[Entamoeba histolytica]] most often resides in the large intestine.
| |
|
| |
| ====Entamoeba Hystolytica====
| |
|
| |
| cellular organisms:
| |
| Eukaryota; Amoebozoa; Archamoebae; Entamoebidae; Entamoeba;
| |
|
| |
| Species:
| |
| [[Entamoeba histolytica]]
| |
|
| |
| [[Entamoeba histolytica]] is a protozoan that usually resides asymptomatically in the large intestine, but when penetrates the intestinal mucosa causes an invasive intestinal or extraintestinal infection called amebiasis. This amoeba was named by Schaudinn in 1903. It was estimated to infect hundreds of millions of people each year, but in 1993 based in epidemiologic, immunologic, biochemical, and genetic data E. histolytica was reclassified as two distinct species E. histolytica as pathogenic and E. dispar as nonpathogenic. It is now believed that the overall prevalence of infection is 90% of E. dispar and 10% of E. histolytica ([http://books.google.com/books?id=a1w1pMa8eksC&pg=PA61&lpg=PA61&dq=Nataro,+James+P.,+and+Cohen+Paul+S.,+Mobley+Harry+L.+T.,+and+Weiser+Jeffrey+N.+Colonization+of+Mucosal+Surfaces.+Washington,+DC:+ASM+Press,+2005&source=web&ots=jjdPAXNV20&sig=7Zmme-4C07ar9FtV7PU0msKyJxw&hl=en&sa=X&oi=book_result&resnum=1&ct=result Nataro], [http://www.co-gastroenterology.com/pt/re/cogastro/abstract.00001574-200101000-00004.htm;jsessionid=L33YX1sXnQPTWdWJGvnC87pvy2Z68TGnVMvx9VWF1vBJDLrWVhd9!1270838445!181195628!8091!-1 Huston]). Also most individuals infected with E. histolytica also remain asymptomatic. Nevertheless E. histolytica remains as a of pathogen interests with major importance in the developing world in where almost 100,000 people die each year due to complications with amebiasis ( [http://www.innovations-report.de/html/berichte/medizin_gesundheit/bericht-66235.html Lindell]).
| |
|
| |
| “Entamoeba parasites have a two-stage life cycle consisting of a disease-causing trophozoite stage and an infectious cyst stage” ( [http://books.google.com/books?id=a1w1pMa8eksC&pg=PA61&lpg=PA61&dq=Nataro,+James+P.,+and+Cohen+Paul+S.,+Mobley+Harry+L.+T.,+and+Weiser+Jeffrey+N.+Colonization+of+Mucosal+Surfaces.+Washington,+DC:+ASM+Press,+2005&source=web&ots=jjdPAXNV20&sig=7Zmme-4C07ar9FtV7PU0msKyJxw&hl=en&sa=X&oi=book_result&resnum=1&ct=result Nataro]). The organism enters the gastrointestinal tract by ingestion from fecal contaminated food and water. The E. histolytica ingested in a cyst stage is resistant to gastric acidity, chlorination, and desiccation. In the intestinal lumen, escape from a cyst or envelope producing trophozoites by asexual reproduction. The intestine has thick and dense mucous layer that is made up of mucin glycoproteins where trophozoites adhere.
| |
| Entamoeba may enclose back to a cyst in the mucin layer and cysts could be excreted in stool to preserve the life with another cycle of spread by ingestion of fecal contamination and oral ingestion. The trophozoites may also invade the tissue of the large intestine. E. histolytica manages to penetrate the mucin layer and contact “colonic epithelial cells via a galactose- and N-acetyl-D-galactosamine (Gal/GalNac)-specific lectin” ([http://books.google.com/books?id=a1w1pMa8eksC&pg=PA61&lpg=PA61&dq=Nataro,+James+P.,+and+Cohen+Paul+S.,+Mobley+Harry+L.+T.,+and+Weiser+Jeffrey+N.+Colonization+of+Mucosal+Surfaces.+Washington,+DC:+ASM+Press,+2005&source=web&ots=jjdPAXNV20&sig=7Zmme-4C07ar9FtV7PU0msKyJxw&hl=en&sa=X&oi=book_result&resnum=1&ct=result Nataro]). The adhered trophozoites cause epithelial cell killing due to secretion of virulence factors such as amoebapores and cysteine proteinase. E. histolytica rarely enter the portal circulation spreading to the rest of the colon, the liver, and other organs. The interaction of bacterial flora affects the invasion of E. histolytica. An enteric flora decreases and luminal proteases bacteria decrease the ability of trophozoites to adhere to the mucin layer and they may prevent invasion of amoeba diseases ([http://www.ncbi.nlm.nih.gov/pubmed/18473835 Wiesner]). Presumably alterations in bowel flora results in outbreak of amebiasis but still the protective role of bacteria needs further study.
| |
|
| |
| ==Fungi==
| |
|
| |
| Species of Candida, such as C. Albicans, C. Glarata, are one of the few fungal organisms that live in the large intestines. Candida is a condition characterized by yeast/fungal overgrowth that can result in symptoms such as incapacitating fatigue, problems with concentration, extreme tightness in shoulders and neck, and etc. They live in its host by adhering to the mucosal lining, which prevents them from dislodgement by secretion of the mucosal lining. Candida are similar to brewers yeast in that they have dimorphic stages (meaning, they are able to grow in two different morphological forms), allowing them to be a yeast cell or in a hyphae form. Depending on the environment (i.e. pH, temperature, or compound availability changes), the organisim can switch between the two forms. If the pH of the environment is about 4.5, the organism will be budding in the yeast form. If the pH is raised to 6.7, the Candida would switch gene expression and begin growing in the hyphae mode. By possessing the ability to switch gene expressions, it ensures the organisms pathogenicity.
| |
|
| |
| Because Candida reside in mucosal communities, they live next to the host tissue and interact with the gut immune system. An important fact to note is that many intestinal organisms have immunomodulatory properties, which allow them to affect the activities of the intestinal epithelial cells (B and T lymphocytes) as well as other accessory cells from the mucosal immune system.
| |
|
| |
| Despite Candida’s extraordinary ability to evade cell death, its growth can be maintained with the presence of bifidobacterias and similar probiotics. The probiotic bacteria interact with Candida by preventing the organism to propagate uncontrollably. This in turn will reduce inflammatory responses of the intestinal tracts and relieve some of the common symptoms. When Candida proliferate exponentially, this is an implication that there is a deprived presence of bifidobacterias and other probiotics.
| |
|
| |
| Candia, like most large intestine residents, are anaerobes due to the oxygen lacking environment. Therefore, their primary metabolism is that of anaerobic metabolism. An interesting fact to note is that Candida are similar to yeast, in that they utilize fermentation.
| |
|
| |
|
| ==Current Research== | | ==Current Research== |
| | | Include information about how this microbe (or related microbes) are being studied and for what purpose |
| | |
| [[Image:ProbioticTable.jpg|frame|Table 1. Alternative strains of bacteria and yeasts that are currently used as probiotics]]
| |
| | |
| ===Probiotics for Irritable Bowel Syndrome: The affects of intestinal bacteria on colonic health===
| |
| As discussed earlier, there are a myriad of bacterium that reside in the human colon and are carried out through various mechanisms to contribute to digestion. [[Lactobacilli]] and [[Bifidobacterium]] are two types of bacteria that benefit the health of the host in a symbiotic relationships with the gut flora lining the colon. These beneficial bacteria have been researched and observed in order to utilize their health benefits on diseased or irritable colons. Diet will always play a factor in maintaining colonic microflora health, however, this may not be a solution for those who suffer from chronic colonic digestion issues.
| |
| | |
| Commercial probiotics have been one of the many pharmaceutical interventions that have been studied to possibly promote better colonic health. These commercially produced probiotics are typically prepared with a mixture of [[lactobacilli]] and [[bifidobacteria]], which are found to aid in break down of carbohydrates to directly interact with the host metabolism. Research has been ongoing in observing the relationship between the immune system and the intestinal microbes in hopes of finding an immune system-bacterium symbiotic relationship. Typically the host's immune system (a human's in this case) has the
| |
| ability to differentiate between normal bacteria and pathogenic bacteria via specific receptors. Toll-like receptors (TLRs) have different types of receptors found on Gram-positive and Gram-negative cells to mediate recognition responses on bacterial DNA sequences. Through this method, the host's immune system holds the initiates protection from infections when pathogens are present. Be that as it may, when the probiotic bacterium is recognized it was observed to have an anti-inflammatory effect on the intestinal mucosal surface through various mechanisms. Studies show that the probiotics have the ability to alter the gut
| |
| flora by increasing the secretion of intestinal mucus and by changing the volume composition of the fermented stool and gas fermented.
| |
|
| |
| Irritable Bowel Syndrome (IBS) is only one of the many colonic irritations that can occur in the human gastrointestinal tract, and it has been hypothesized that probiotics are able to benefit suffering patients. The probiotics also have an antiviral and antibacterial effect, which could potentially benefit the 15-25% of patients who suffer from infectious gastroenteritis. As mentioned above, the change in stool composition and alteration in gut flora activity could aid with IBS treatment.
| |
| | |
| These theoretical ideas of the probiotics benefitting those suffering from IBS by these mechanisms were tested through various clinical trials in order to understandthe actual target. Using a composite probiotic (VSL#3), the first study focused on
| |
| diarrhea-predominant IBS patients who received placebos, or received the VSL#3 powder twice daily over an eight week span. Of the 25 patients in this study, no differences were observed in gastrointestinal transit time, bowel function scores, or overall relief of original symptoms. However, there was a difference observed on abdominal bloating in the placebo versus active group. The second trial included 48 patients, again using the active treatment or placebos for 8 weeks. There was an increase in the number of patients who experienced relief in flatulence, but lower numbers were recorded in relief of symptoms of abdominal pain. 46% of the patients in the active treatment and 33% of the placebo patients reported satisfactory relief for half of the weeks.
| |
|
| |
| A different research group used 362 women with any subtype of IBS to receive one of three doses of [[B. Infantis]] or placebo once daily for 4 weeks. The results showed that in the last week, only one of the active subgroups had reported significant improvements in comparison to baseline standards. Some of these improvements included relief of abdominal pain/discomfort, bloating/distention, and bowel movement difficulty.
| |
| | |
| To study the role of inflammation in probiotics another study was performed focusing on peripheral blood cytokine levels; 75 patients were given [[B. Infantis]] or [[L. Salivarius]] or placebo for 8 weeks. The [[Bifidobacterium]] showed superior
| |
| symptom relief to that of the [[Lactobacillus]] active group; these symptoms include the three dominant symptoms associated with IBS: Bloating/distention, abdominal pain/discomfort and bowel movement difficulty. Levels of interleukin (IL)-10 and
| |
| IL-12 were measured to observe the inflammatory response. The ratio of lower IL-10 and increased IL-12 levels to that of the baseline control, demonstrated a pro-inflammatory cytokine profile. It was reported that the [[bifidobacteria]] treated group had restored a normal IL-10 / IL-12 ratio, but the placebo and [[L. salivarius]] treated group had a persistent pro-inflammatory cytokine profile. This observation was summarized by the authors in saying, "by demonstrating a normalization of the IL-10 / IL-12 ratio in the bifidobacteria-fed subjects alone, and in parallel with symptomatic improvement, we provide the first evidence for efficacy for an anti-inflammatory approach in IBS" (Walsh).
| |
| | |
| ===Microbially Triggered Drug Delivery to the Colon===
| |
| | |
| Oral therapy has been the most popular route for drug delivery. However, colon, the terminal part of the GI track has been recognized a new site for drug delivery including novel therapeutic drugs. Over 400 bacterial species inhabit in the gastrointestinal (GI) tract to have specific niche throughout the tract. Colon is a part of intestine where a large group of gram negative microflora is found. The flora produces numerous enzymes that are excreted for formulation of colon-specific drug delivery systems. This article focused on analyzing various microbially activated drug delivery systems for colon specific drug delivery with specific reference to the microflora of the GI track and their role of targeting drug delivery to the colon.
| |
| | |
| Since the anaerobic bacteria of the colon are capable of reacting with complex carbohydrates entering the colon, many different systems have been established for drug delivery to the colon. So the prodrugs are tested on different systems (the carriers) that are based upon biodegradable polymers and polysaccharides. In conclusion, the biodegradable polymers (azo and other synthetic polymers) need detailed toxicological study to be performed before they are commercially used. Polysaccharides without any toxic properties are an alternate way of coating drugs (carriers for prodrugs). However, polysaccharide with moieties can bind to specific regions (the inflamed colonic lesions or cancer tissues) before it is being effective.
| |
| | |
| ===Increase of Intestinal Bifidobacterium and Suppression of Coliform Bacteria with Short-Term Yogurt Ingestion===
| |
| | |
| A known carcinogen is Coliform bacilli, which produces bile acid degradation products that increase colon cancer. Certain anaerobic bacteria are beneficial to human because they produce short-chain fatty acid, through fermentation of carbohydrates, that lowers the intestinal pH, and thus suppress harmful bacteria like Coliform bacilli. Yogurt consists of large amount of lactic acid bacteria: 107 per milliliter. However, not all bacteria from yogurt can survive the extreme acidic condition of the stomach. Bacteria like Lactobacillaceae and streptococcaceae can’t survive with the presence of gastric acid in stomach and thus will not proliferate in large intestine. Bifidobacteria has shown to survive the acidic condition of human’s stomach and continue to live in the large intestine. The questions were whether we could increase the amount of Bifidobacteria by injection of yogurt, and whether the increase amount of Bifidobacteria in large intestine decreases the amount of Coliform bacilli.
| |
| | |
| This experiment was done on 34 healthy people, 4 males and 30 females from ages 19 to 42. The experiment was carried out for 26 days; subjects consumed AB yogurt containing equal amount of Streptococcus thermophilus, Lactobacillus bulgaricus, Lactobacillus acidophilus, and Bifidobacterium bifidum for the middle 10 days, while received no yogurt for the first and last 8 days. Their stool samples were collected in 3 to 4 days intervals to test for presence of any bacteria in stool; those bacteria that are presented in stool indicate that they were able to get through stomach and live in the large intestine. Only Bifidobacterium bifidum were identified to be in all the stools starting 3 days after the initial yogurt ingestion and till after 8 days of stopped yogurt ingestion. Results showed that during the 10 days of yogurt ingestion, anaerobic bacteria in stool did increase significantly, while after stopping of yogurt consumption, the amount fell back. In contrast, aerobic bacteria and Coliform bacteria amount decreased during yogurt ingestion period, but returned back after stopping of yogurt ingestion.
| |
| | |
| Researchers concluded that Bifidobacteria are able to survive stomach’s low pH and then proliferate in human’s large intestine. It has anti-cancer affect because it can suppress aerobic bacteria Coliform, which contribute to carcinogenesis. Amount of Bifidobacteria in large intestine can be increased by ingestion of yogurt containing such bacteria.
| |
| | |
| ===Ability of Lactobacillus fermentum to overcome host α-galactosidase deficiency, as evidenced by reduction of hydrogen excretion in rats consuming soya α-galacto-oligosaccharides===
| |
| | |
| Soya contains high concentration of α-galacto-oligosaccharides but human and other mammals lack α-galactosidase to digest the oligosaccharide in the small intestine. As these carbohydrates enter the large intestine, α-galactosidase-producing lactobacilli can use them for fermentation. This article was “to assess the ability of α-galactosidase-producing lactobacilli to improve the digestibility of α-galacto-oligosaccharides” by setting up experimental systems on rats.
| |
| | |
| To test their hypothesis, a model experimental system to assess the potential of α-galactosidase-producing lactobacilli to improve α-galacto-oligosaccharides digestion in rats was set up. The rats were fed with soy milk orally and placed in respiratory chambers to monitor their fermentative gas excretion. Gnotobiotic rats with a hydrogen gas producing strain (Clostridium butyricum) were first checked for their validity in this experiment. Significant amount of hydrogen (H2) emission was detected after ingestion of native soy milk, but no significant amount of H2 emission was detected after ingestion of α-galacto-oligosaccharide-free soy milk. This step validated the experimental system.
| |
| The rats did not produce H2 as the native soy milk was fermented using the α-galactosidase-producing Lactobacillus fermentum CRL722 strain. This also validated the bacteria used in the experiment. A significant reduction of H2 emission was found when L. fermentum CRL722 was coadministered with native soy milk (reduced by 50%). This also explained that α-galactosidase from L. fermentum CRL722 remained active in the gastrointestinal tract of rats associated with C. butyricum. L. fermentum CRL722 induced a significant reduction in H2 emission by 70% in human-microbiota associated rats.
| |
| | |
| In conclusion, the results suggest that L. fermentum α-galactosidase is able to relieve α-galactosidase deficiency in rats very partially. That means that this can be used in further applications where “lactic acid bacteria could be used as a vector for delivery of digestive enzymes in man and animals.”
| |
| | |
| Reference:
| |
| LeBlanc, Jean Guy; Ledue-Clier, Florence; Bensaada, Martine, et al. "Increase of Intestinal Bifidobacterium and Suppression of Coliform Bacteria with Short-Term Yogurt Ingestion" BioMed Central Ltd. Vol. 8 Article no. 22. January 29, 2008.
| |
| http://www.biomedcentral.com/1471-2180/8/22
| |
|
| |
|
| ==References== | | ==References== |
| | [Sample reference] [http://ijs.sgmjournals.org/cgi/reprint/50/2/489 Takai, K., Sugai, A., Itoh, T., and Horikoshi, K. "''Palaeococcus ferrophilus'' gen. nov., sp. nov., a barophilic, hyperthermophilic archaeon from a deep-sea hydrothermal vent chimney". ''International Journal of Systematic and Evolutionary Microbiology''. 2000. Volume 50. p. 489-500.] |
|
| |
|
| 1. Medline Plus: "Large Intestine": http://www.becomehealthynow.com/article/bodydigestive/787/
| | Edited by (Insert your name here), student of Rachel Larsen at the University of Southern Maine |
| | |
| 2. About: Colon Cancer: "Large Intestine": http://coloncancer.about.com/od/glossaries/g/Large_Intestine.htm
| |
| | |
| 3. Wikipedia: "Large Intestine": http://www.becomehealthynow.com/article/bodydigestive/787/
| |
| | |
| 4. Wikipedia: "Colon (anatomy)": http://en.wikipedia.org/wiki/Colon_(anatomy)
| |
| | |
| 5. Altermann, Eric. "Complete genome sequence of the probiotic lactic acid bacterium Lactobacillus acidophilus NCFM.": http://www.pnas.org/content/102/11/3906.full
| |
| | |
| 6. Schell, MA. "The genome sequence of Bifidobacterium longum reflects its adaptation to the human gastrointestinal tract"
| |
| Proc Natl Acad Sci U S A. 2002 Oct 29;99(22):14422-7. Epub 2002 Oct 15: http://www.ncbi.nlm.nih.gov/sites/entrez
| |
| | |
| 7. Gibson, G.R.;Macfarlane, G.T.; Cummings, J.H. "Sulphate reducing bacteria and hydrogen metabolism in the human large intestine.": http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=1
| |
| | |
| 8. Gibson, G.R.;Macfarlane, G.T.; Cummings, J.H. "Sulphate reducing bacteria and hydrogen metabolism in the human large intestine.": http://www.pubmedcentral.nih.gov/pagerender.fcgi?artid=1374298&pageindex=2#page
| |
| | |
| | |
|
| |
|
| Edited by [Benjamin Dae Lee, Hilary Otorowski, Julia Son, Rebecca Son, Alexander Pang, Ella Chen, David Araiza]students of [mailto:ralarsen@ucsd.edu Rachel Larsen]
| | <!--Do not edit or remove this line.-->[[Category:Pages edited by students of Rachel Larsen]] |
