Humans Are Holobionts
Microbiome—all the (1).
* Microbiota—all the (2) in and on an organism.
(3)—hosts and microbes live together and evolve together.
* Each microbial niche is related to a variety of factors such as body location, age, sex, diet and environment.
Microbiome Dev’s from Birth to Adulthood Dev’t of a Stable Microbiome
Microbiota community is (1).
* Begins developing at (2) and changes as we age.
* A stable community of microbes adopted by age (3).
* It is important to develop a (4) microbiome.
Early Colonization
Newborn colonization important.
* (1) provides exposure to microbes from the (2), whereas cesarean delivery provides microbe exposure from initial caretakers.
Bifidobacteria
* Transport (3) directly across their plasma membrane.
* Fermentation of these sugars provides (4) and lowers gut pH, limiting (5).
Adult Human Microbiota
Relatively stable over time.
* Only change due to physical or lifestyle changes.
Variable from person to person and at different sites within a person.
Bacteria common to human skin, the intestinal tract, and the other
mucosal surfaces include six major phyla: (6)
Some archaea, fungi, and viruses are also present.
Microbiota Vary by Body Site
Skin
Environment:
* Slightly (1) pH.
* High concentration of (2).
* Some areas lack (3).
* Some bathed in oily lubricant (4).
Some microbes are temporarily present and are typically unable to multiply on the skin.
Three environmental niches: (5)
Staphylococcus epidermidis
Colonize the skin and generally nonpathogenic.
* (1) of healthy skin.
Modulate (2) gene expression, stimulating (3).
* Secreting products of fermentation called (4).
* Binding to the pattern recognition receptor (5).
(6)–inhibits growth of pathogens.
Respiratory Tract
(1)—nostrils, sinuses, pharynx, and oropharynx.
* Colonized by a diverse group of microbes.
(2)—larynx below the vocal cords, trachea, bronchi, and lungs.
* Not sterile as previously thought.
Lower Respiratory Tract
Difficult to sample lungs without (1).
Microbes are introduced principally from the (2).
* Stay temporary—expelled and replaced by new transients
Eye and External Ear
Eye
* Small number of bacteria are found on the (1) of the eye.
* Predominant bacterium is (2).
External ear
* Similar to (3), with nonpathogenic staphylococci and Corynebacterium spp. predominating.
Mouth
Soon after birth, the mouth is colonized by microorganisms from (1).
(2) become dominant due to the anoxic nature of the space between the teeth and gums.
As teeth grow, Streptococcus parasanguis and S. mutans attach to enamel surfaces; S. salivarius attaches to the buccal (that is, inside the cheeks) and gum epithelial surfaces and colonizes the saliva.
* Produce a (3) that enable them to attach to oral surfaces.
* Contribute to dental plaque, caries, gingivitis, and periodontal disease.
Stomach
Most microbes killed by acidic conditions.
* (1) can survive.
Microorganisms may survive:
* If they pass through stomach (2).
* If ingested with food particles and are (3).
Small Intestine
Divided into three areas:
* (1)—contains few organisms due to stomach acid, bile, and pancreatic secretions; Gram-positive bacteria comprise most of the microbiota.
* (2)—Enterococcus faecalis, lactobacilli, diphtheroids, and the yeast Candida albicans found.
* (3)—flora similar to that in colon; pH becomes more alkaline; anaerobic Gram-negative bacteria and members of the family Enterobacteriaceae become established.
Large Intestine (Colon)
A Functional Core Microbiome Is Required for Host Homeostasis
()
Microbes that provide the host with a suite of activities required for health and homeostasis.
* Provision of vitamin K by E. coli.
* Emerging role of gut microbiota in human behavior.
* Rapidly advancing field.
Functional Core Microbiome
Host Metabolism
Gut microbiota converts food into calories that we can use.
Overweight people:
* Higher concentrations of gut bacteria belonging to the phylum (1) compared to bacteria belonging to the phylum (2).
* Several other gut microbiota population changes.
Impact of Fermentation End Products on Host Metabolism
Bacteria ferment monomers into short chain fatty acids, some of which promote weight gain.
Has refocused attention from the individual species in the gut microbiome to the ()
metabolome (products these microorganisms secrete).
Immunity
(1) disrupt the gut microbial community.
* Following (1) treatment, people are at higher risk of (2).
* (3)—based on competitive exclusion.
Microbiome releases (4) that target pathogens.
Microbiome Sig’s Influence Immune Cell Func @ Sites Distant from the Gut
Germ-free mice discovered to have () that mature in the bone marrow.
limited development of white blood cells
Gut Microbiota Metabolites Regulate Inflammation
Gut Microbiota Affects Central Nervous System
Specific behavioral traits (that is, inquisitiveness, sociability) and feelings (that is, anxiety, depression) differ when comparing GF mice and conventional mice.
* Influence is heritable.
We can predict three ways the
microbiome can influence the CNS:
* Microbiome impacts the (1).
* Direct pathway from gut to brain (2) which transmit signals to the brain via the vagus nerve.
* (3) cross the blood brain barrier.
Metabolic Syndrome
Condition characterized by at least three of the following:
(1-5)
Associated with chronic, low-level (6).
* Linked to the microbiome as explained by (7).
1-5:
* Large waist circumference.
* High blood triglyceride level.
* High blood pressure.
* Elevated low-density lipoprotein.
* High fasting blood glucose levels.
Cardiovascular Disease
Diet consumed by a person with cardiovascular disease: (1)
* Little (2) for gut microbes to produce anti-inflammatory SCFAs.
* Promotes growth of a “meat-eating” microbial population that metabolizes (3) resulting in the production of (4).
* (4) is absorbed into the bloodstream, travels to the liver where it is enzymatically oxidized by liver cells to (5).
* Acceleration of (6).
Cancer
Microbes are involved in about 20% of malignancies.
* Certain viruses cause host cells to become cancerous.
* Alter the host cell cycle to (1) and prevent host cells from (2), thereby increasing mutation rates.
* (3) dysregulate host cell cycling.
* Bacteria can be involved in metastasis of tumors to distant sites.
* Many cancers linked to microorganisms are driven by the inflammatory state associated with (4).