Uses non-pathogenic forms, products or antigens of micro-organisms to stimulate an immune response, which confers protection against subsequent infection
Organisms with the same or very similar antigens on the surface. Such types are subgroups or strains of a microbial species, which may be used to trace infections. They are usually identified by using antibodies from serum
1. Viral DNA/RNA instructs the cell to make virus particles, when full cell lysis occurs, and the virus escapes the cells to infect other cells/organisms (shedding)
2. Production of toxic substances
3. Viral cell transformation, where they can trigger cells to become cancerous
4. Viruses infecting white blood cells suppress the immune system (e.g. HIV)
Have a thin peptidoglycan cell wall with a layer of lipopolysaccharide. Gram negative bacteria stain red using Gram staining technique. The additional layer of lipopolysaccharide protects the bacterial cells from lysozyme and from penicillin type antibiotics
Have a thick peptidoglycan cell wall and no lipopolysaccharide layer. Gram positive bacteria stain purple using Gram staining technique. Gram positive bacteria are susceptible to lysozyme and penicillin
These are produced by white blood cells called lymphocytes. Antibodies are proteins (globulins). They are Y shaped and formed from four polypeptide chains with two binding sites. They are specific to the antigen and they bind to form an antigen-antibody complex. This renders the antigen inactive by agglutination or marking for phagocytosis
1. Bacteria divide rapidly and have a high mutation rate. Bacteria can also obtain plasmids that carry antibiotic resistance genes from other resistant bacteria by conjugation
2. Some mutations confer resistance to antibiotics. Overuse of these antibiotics gives the resistant strain a selective advantage
3. Numbers of the resistant strain increase, making infections more difficult to treat with the usual antibiotics
Peptidoglycan bacterial cell walls are strengthened by polysaccharide cross-linked by amino acids. This stops osmotic lysis. Penicillin affects the formation of the cross links by inhibiting the enzyme that makes them. The wall is weakened and osmotic changes can cause cells to burst. Gram negative bacteria have an outer lipopolysaccharide layer that protects the cells from penicillin
Tetracycline acts as a competitive inhibitor of the second anticodon-binding site on the 30S subunit of bacterial ribosomes. It prevents the binding of a tRNA molecule to its complementary codon. This prevents protein synthesis common to all bacteria
1. Stem cells in the bone marrow make B lymphocytes that mature in the spleen and lymph nodes and have receptors for the detection of specific antigens on the surface of foreign cells
2. When the B lymphocytes are activated by a corresponding antigen, they divide rapidly forming antibody secreting plasma cells. This clonal expansion is increased by the cytokines from the cell mediated response
3. B lymphocytes also make memory cells that remain in the bloodstream and divide rapidly if the antigen is encountered again
1. On first exposure to the antigen, there is a latent period when antigen presenting cells (including macrophages) carry out phagocytosis and incorporate foreign antigen into their cell membranes (antigen presentation)
2. T helper cells detect these antigens and secrete cytokines that stimulate B cells to undergo clonal expansion and stimulate macrophages to carry out phagocytosis
3. Some B cells then differentiate to become antibody-secreting plasma cells with short lives. Others become long-lived memory cells that retain the ability to undergo mitosis in case of secondary infection
1. Following re-exposure to the same antigen, there is a very short latent period due to the presence of memory cells
2. Only a very small amount of antigen is required to stimulate rapid production of plasma cells
3. Antibody levels increase to between 10 and 100 times greater than the initial response in a very short time frame. Antibody levels stay high for longer and no symptoms develop
Individual receives antibodies from someone else. Protection is short lived as no memory cells are produced and the antibodies themselves identified as foreign and destroyed
1. Stem cells in the bone marrow make T lymphocytes, which are activated in the thymus gland
2. Detecting a foreign antigen causes proliferation of T lymphocytes as: T killer cells cause lysis of target cells, T memory cells remain in bloodstream, T helper cells release cytokines
3. Cytokines stimulate the clonal expansion of B cells and to produce antibodies. Cytokines activate phagocytes to engulf and digest the foreign cells