II. THE PROKARYOTIC CELL: BACTERIA
B. PROKARYOTIC CELL ANATOMY
2b. The Gram-Negative Cell Wall
Fundamental Statements for this Learning Object:
1. Because of the naure of their cell wall, Gram-negative bacteria stain pink after Gram staining.
2. The Gram-negative cell wall consists of 2-3 interconnected layers of peptidoglycan surrounded by an outer membrane.
3. Peptidoglycan prevents osmotic lysis in the hypotonic environment in which most bacteria live.
4. The outer membrane is a semipermeable structure that contains pore-forming proteins called porins that allow nutrients to pass through the outer membrane.
5. Surface proteins embedded in the cell wall can function as adhesins, secretion systems, and enzymes.
6. The Gram-negative cell wall activates both the body's innate immune defenses and its adaptive immune defenses.
7. The body activates innate immunity by recognizing molecules unique to microorganisms that are not associated with human cells called pathogen-associated molecular patterns or PAMPs. PAMPs bind to Pattern-recognition receptors (PRRs) on defense cells to trigger the production of inflammatory cytokines.
8. Inflammation is the means by which the body delivers defense cells and defense molecules to an infection site, however, excessive inflammation, can be harmful and even deadly to the body.
9. PAMPs associated with the Gram-negative cell wall include peptidoglycan monomers, lipopolysaccharide (LPS), porins, and mannose-rich sugar chains.
10. An antigen is a molecular shape that reacts with antigen receptors on lymphocytes to initiate an adaptive immune response.
11. Cell wall molecules can also trigger adaptive immunity such as the production of antibody molecules against bacterial cell wall antigens.
LEARNING OBJECTIVES FOR THIS SECTION
In this section
on Prokaryotic Cell Anatomy we are looking at the various anatomical parts that make up a bacterium. As mentioned in the introduction to this section,
a typical bacterium usually consists of:
There are three primary types of bacterial cell wall: Gram-positive, Gram-negative, and acid-fast. We will now look at the Gram-negative bacterial cell wall.
The Gram-Negative Cell Wall (def)
As mentioned in the previous section on peptidoglycan, Gram-negative bacteria are those that decolorize during the Gram stain procedure, pick up the counterstain safranin, and appear pink.
Flash animation illustrating the interaction of the Gram's stain reagents at a molecular level
© Daniel Cavanaugh, Mark Keen, authors, Licensed for use, ASM MicrobeLibrary.
Common Gram-negative bacteria of medical importance include Salmonella species, Shigella species, Neisseria gonorrhoeae, Neisseria meningitidis, Haemophilus influenzae, Escherichia coli, Klebsiella pneumoniae, Proteus species, and Pseudomonas aeruginosa.
Click on this link, read the description of urinary tract infections (UTIs), and be able to match the infection with its description on an exam.
A. Structure and Composition of the Gram-Negative Cell Wall
In electron micrographs, the Gram-negative cell wall (see Figs. 1A and 1B) appears multilayered. It consists of:
1. A thin, inner wall composed of peptidoglycan
The peptidoglycan portion of the Gram-negative cell wall is generally 2-3 nanometers (nm) thick and contains just 2-3 layers of peptidoglycan (see Fig. 1C). Chemically, only 10 to 20% of the Gram-negative cell wall is peptidoglycan.
2. An outer membrane
The outer membrane of the Gram-negative cell wall appears as a lipid bilayer about 7 nm thick. It is composed of phospholipids, lipoproteins, lipopolysaccharides (LPS), and proteins. Phospholipids are located mainly in the inner layer of the outer membrane, as are the lipoproteins that connect the outer membrane to the peptidoglycan (see Figs. 1A and 1B). The lipopolysaccharides, located in the outer layer of the outer membrane, consist of a lipid portion called lipid A embedded in the membrane and a polysaccharide portion extending outward from the bacterial surface. The LPS portion of the outer membrane is also known as endotoxin.
In addition, pore-forming proteins called porins (see Fig. 1B) span the outer membrane. The porins function as channels for the entry and exit of solutes through the outer membrane of the Gram-negative cell wall.
3. The outer membrane of the Gram-negative cell wall is studded with surface proteins that differ with the strain and species of the bacterium (see Fig. 1B).
4. The periplasm (def) is the gelatinous material between the outer membrane, the peptidoglycan, and the cytoplasmic membrane. This periplasmic space is about 15nm wide and contains a variety of hydrolytic enzymes fot nutrient breakdown, periplasmic binding proteins for transport via the ATP-binding cassette (ABC) system, and chemoreceptors for chemotaxis (discussed under Bacterial Flagella later in this Unit).
B. Functions of the Gram-Negative Cell Wall Components
1. The peptidoglycan in the Gram-negative cell wall prevents osmotic lysis (def).
2. The outer membrane of the Gram-negative cell wall confers several functions:
a. Like the cytoplasmic membrane discussed previously in Unit 1, is semipermeable and acts as a coarse molecular sieve. Many small molecules may pass through due to pores running through the membrane. These pores are composed of proteins called porins (see Fig. 1B).
b. Because of its semipermeable nature, the outer membrane helps retain certain enzymes and prevents some toxic substances, such as penicillin G and lysozyme, from entering.
c. The LPS from the outer membrane of the Gram-negative cell wall (see Fig. 1B) is thought to add strength to the outer membrane, in a manner similar to the glycopeptides and teichoic acids of the gram-positive cell wall.
d. The outer membrane may also form vesicles that contain quorum signaling molecules, enzymes, toxins, virulence factors, and even antibiotic resistance genes. These vesicles can then fuse with the outer membrane of other Gram-negative bacteria enabling them to communicate, obtain virulence factors, pick up resistance genes, or deliver toxins to human cells.
3. The surface proteins in the bacterial peptidoglycan (see Fig. 1B), depending on the strain and species, carry out a variety of activities.
a. Some surface proteins function as enzymes.
b. Other proteins serve as adhesins (def). Adhesins enable the bacterium to adhere intimately to host calls and other surfaces in order to colonize those cells and resist flushing (See Fig. 2 ).
c. Many bacteria involved in infection have the ability to co-opt the functions of host cells for the bacterium's own benefit. This is done by way of bacterial secretions systems that enable the bacterium to directly inject bacterial effector molecules into the cytoplasm of the host cell in order to alter its cellular machinery or cellular communication to the benefit of the bacteria. They do this by producing secretion systems such as the type 3 secretion system that produces hollow, needle-like tubes called injectosomes (def). Certain bacteria, for example, inject invasins (def) into the cytoplasm of the host cell that enable the bacterium to enter that cell.
The role of these cell wall surface proteins will be discussed in greater detail later in Unit 3 under Bacterial Pathogenicity.
4. The periplasm (def) contains enzymes for nutrient breakdown as well as periplasmic binding proteins to facilitate the transfer of nutrients across the cytoplasmic membrane.
C. The Role of Gram-Negative Cell Wall Components to the Initiation of Body Defenses
The body has two immune systems: the innate immune system and the adaptive immune system.
1. Innate immunity is an antigen-nonspecific (def) defense mechanisms that a host uses immediately or within several hours after exposure to almost any microbe. This is the immunity one is born with and is the initial response by the body to eliminate microbes and prevent infection.
2. Adaptive (acquired) immunity refers to antigen-specific (def) defense mechanisms that take several days to become protective and are designed to react with and remove a specific antigen. This is the immunity one develops throughout life.
Initiation of Innate Immunity
In order to protect against infection, one of the things the body must initially do is detect the presence of microorganisms. The body does this by recognizing molecules unique to microorganisms that are not associated with human cells. These unique molecules are called pathogen-associated molecular patterns or PAMPS (def). (Because all microbes, not just pathogenic microbes, possess PAMPs, pathogen-associated molecular patterns are sometime referred to as microbe-associated molecular patterns or MAMPs.)
LPS, porins, and fragments of peptidoglycan are PAMPs associated with the cell wall of Gram-negative bacteria. In addition, bacteria and other microorganisms also possess mannose-rich glycans (short carbohydrate chains with the sugar mannose or fructose as the terminal sugar) that function as PAMPs. These mannose-rich glycans are common in microbial glycoproteins and glycolipids but rare in those of humans (see Fig. 3).
These PAMPS bind to pattern-recognition receptors or PRRs (def) on a variety of defense cells of the body and triggers innate immune defenses such as inflammation (def), fever, and phagocytosis.
Inflammation (def) is the first response to infection and injury and is critical to body defense. Basically, the inflammatory response is an attempt by the body to restore and maintain homeostasis (def) after injury. Most of the body defense elements are located in the blood, and inflammation is the means by which body defense cells and body defense chemicals leave the blood and enter the tissue around an injured or infected site.
Body defense cells called macrophages (def), and dendritic cells (def) have pattern recognition receptors such as toll-like receptors on their surface that are specific for the peptidoglycan fragments and LPS in the Gram-negative cell wall and/or to NODs in their cytoplasm that are specific for peptidoglycan fragments. The binding of these cell wall components to their corresponding pattern recognition receptors triggers the macrophages to release various defense regulatory chemicals called cytokines (def), including IL-1, IL-6, IL-8, TNF-alpha, and PAF. The cytokines then bind to cytokine receptors on target cells and initiate inflammation and activate both the complement pathways (def) and the coagulation pathway (see Fig. 4).
The LPS binds to a LPS-binding protein circulating in the blood and this complex, in turn, binds to a receptor molecule (CD14) found on the surface of body defense cells called macrophages. This is thought to promote the ability of the toll-like receptor pair TLR-4/TLR4 to respond to the LPS. The binding of these cell wall components to their corresponding pattern recognition receptors triggers macrophages to release various defense regulatory chemicals called cytokines (def), including IL-1, IL-6, IL-8, TNF-alpha, and PAF. The cytokines then bind to cytokine receptors on target cells and initiate inflammation and activate both the complement pathways (def) and the coagulation pathway (def) (see Fig. 4).
The LPS aso activates the alternative complement pathway and the lectin pathway (def), innate defense pathways that play a variety of roles in body defense.
Innate immunity will be discussed in greater detail in Unit 5.
Initiation of Adaptive Immunity
Proteins and polysaccharides associated with the Gram-negative cell wall function as antigens and initiate adaptive immunity. An antigen (def) is defined as a molecular shape that reacts with antibody molecules and with antigen receptors on lymphocytes. We recognize those molecular shapes as foreign or different from our body's molecular shapes because they fit specific antigen receptors on our B-lymphocytes and T-lymphocytes, the cells that carry out adaptive immunity.
The actual portions or fragments of an antigen that react with antibodies and with receptors on B-lymphocytes and T-lymphocytes are called epitopes (def). An epitope is typically a group of 5-15 amino acids with a unique shape that makes up a portion of a protein antigen, or 3-4 sugar residues branching off of a polysaccharide antigen. A single microorganism has many hundreds of different shaped epitopes that our lymphocytes can recognize as foreign and mount an adaptive immune response against.
The body recognizes an antigen as foreign when epitopes of that antigen bind to B-lymphocytes (def) and T-lymphocytes (def) by means of epitope-specific receptor molecules having a shape complementary to that of the epitope. The epitope receptor on the surface of a B-lymphocyte is called a B-cell receptor and is actually an antibody molecule. The receptor on a T-lymphocyte is called a T-cell receptor (TCR).
There are two major branches of the adaptive immune responses: humoral immunity and cell-mediated immunity.
1. Humoral immunity (def): Humoral immunity involves the production of antibody molecules in response to an antigen (def) and is mediated by B-lymphocytes. Through a variety of mechanisms, these antibodies are able to remove or neutralize microorganisms and their toxins after binding to their epitopes. For example, antibodies made against cell wall antigens can stick bacteria to phagocytes, a process called opsonization (def). Antibodies made against cell wall adhesins can prevent bacteria from adhering to and colonizing host cells.
2. Cell-mediated immunity (def): Cell-mediated immunity involves the production of cytotoxic T-lymphocytes, activated macrophages, activated NK cells, and cytokines in response to an antigen (def) and is mediated by T-lymphocytes. These defense cells help to remove infected cells and cancer cells displaying foreign epitopes.
Adaptive immunity will be discussed in greater detail in Unit 6.
D. Significance of Gram-Negative Cell Wall Components to Bacterial Pathogenicity
The lipid A portion of the LPS portion in the outer membrane is also known as endotoxin. During severe systemic infections with large numbers of bacteria present, high levels of LPS are released resulting in excessive cytokine production by the macrophages and other cells and this, in turn, can harm the body (see Fig. 5).
Medscape article on infections associated with organisms mentioned in this Learning Object. Registration to access this website is free.
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Updated: April, 2014
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