Coronary heart disease (caused by high fat, high salt diet coupled with stressful and sedentary lifestyle)
Sickle cell anaemia (caused by mutation that changed the structure of haemoglobin A (HbA) gene in chromosome 11, resulting in a variant of haemoglobin that is less soluble and does not bind readily with oxygen)
1. At day 0, the body had its first exposure to a pathogen with antigen A
2. Lymphocytes that are exposed to antigen A undergo cell differentiation and cell division to produce effector lymphocytes and memory lymphocytes
3. Time is needed for cell differentiation and cell division, hence, a primary immune response appears only after a lag period of several days (around 8 days)
4. Effector lymphocytes are short-lived, actively produce and secrete anti-A antibodies, and cause agglutination of pathogens and signal phagocytes to carry out phagocytosis
5. Memory lymphocytes are long-lived, remain in the blood stream for months or even years, and are more easily and more quickly induced to become effector cells by a later encounter with the same antigen
1. At day 40, when the pathogen with antigen A infects the body again, memory lymphocytes recognize the specific antigen A and triggers a secondary immune response with shorter lag time and higher intensity (more anti-A antibodies produced and released into the bloodstream)
2. This results in a more sensitive and rapid immune response against the pathogen resulting in reinfection with less severe signs and symptoms / immunity against this specific strain of pathogen
Are chemicals that block metabolic pathways of bacteria, hence bacteriostatic (preventing growth/reproduction) or bactericidal (causing bacterial cell death)
Inhibit enzymes involved in DNA replication, DNA transcription and RNA synthesis, protein synthesis by bacteria ribosomes, cell surface membrane functions, and bacteria cell wall synthesis
Ineffective against viruses due to structural and reproductive differences
1. Random gene mutation and plasmid transfer results in genetic variation in antibiotic resistance among bacteria cells in the population
2. Antibiotics exert a selection pressure, bacteria cells which are antibiotic resistant are better adapted because they have membrane proteins that are able to pump antibiotics out of the cell, while the bacteria cells which are sensitive to antibiotics die off from the antibiotics
3. Antibiotic resistant bacteria survive longer and reproduce more offspring which inherits the allele for antibiotic resistance
4. Hence, the proportion of the population having the allele for antibiotic resistance will increase gradually over many generations, leading to the evolution of the population to become antibiotic resistant