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Title: Defence against infectious diseases
Description: International Baccalaureate Biology SL Topic 6.3 2017 Clear and detailed notes of topic 6.3 from the book and lecture

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Defence against infectious diseases

Topic 6
...
3

Biology SL

Urethra

Tube that carries urine from the bladder to

Vagina

The reproductive tract leading from the

the outside

uterus to the outside

Blood clotting
➢ When small blood vessels are broken, blood escapes from the closed circulatory
system and so pathogens have a way to gain access to the body, as these blood
vessels are often in the skin


The body responds creating a clot that seals the damaged blood vessel
preventing excessive blood loss and helping prevent pathogens from
entering the body

➢ Circulating in the blood plasma are a variety of molecules called plasma proteins
some of which are involved in clotting


Two of them are prothrombin and fibrinogen

➢ Also circulating in the bloodstream are cell fragments known as platelets


They form in the bone marrow along with erythrocytes and leukocytes



They don’t remain as entire cells but instead, one very large cell breaks
down into many fragments and each of the fragments becomes a platelet



They don’t have a nucleus but they have a short cellular life span of about
8-10 days

➢ Steps


The damaged cells of the blood vessel release chemicals that stimulate
platelets to adhere to the damaged area



The damaged tissue and platelets release chemicals called clotting factors
that convert prothrombin into thrombin


Thrombin is an active enzyme that catalyses the conversion of
soluble fibrinogen into the relatively insoluble fibrin



Fibrin, a fibrous protein, forms a mesh-like network that helps to stabilize
the platelet plug



More and more cellular debris becomes trapped in the fibrin mesh and soon
a stable clot has formed

2

Defence against infectious diseases

Topic 6
...
, it’s known as the secondary, tertiary, etc
...
3

Biology SL

Antibodies

➢ Antibodies are Y-shaped proteins that are produced by the body and that can bind
to the surface of pathogens
➢ Each type of antibody is different, because each type has been produced in response
to a different pathogen
➢ Each pathogen is made up of either cells with cell membranes or in case of a virus, a
protein coat called capsid


The cellular invaders have proteins that are embedded in their outer surface
called antigens


Non-specific proteins = antigens

➢ Each antibody at the end of the forks of the Y is a binding site


The binding site is where an antibody attaches itself to an antigen, meaning
that it attaches to the pathogen

➢ The leukocytes that produce the antibodies are a type of cell called plasma cells


Each of has has many different types of antibody-producing plasma cells
and each type can produce only one type of antibody



Each cell produces a relatively small number of antibodies but our immune
response has a way of producing many when they are needed

➢ Steps


A specific antigen type/pathogen is detected and identified by a white blood
cell



A specific plasma cell, called lymphocyte, that can produce an antibody that
will bind to the antigen is identified



The specific plasma cell type clones itself by mitosis to increase rapidly in
number



The specific plasma cells begin to produce antibodies



The antibodies circulate in the bloodstream and eventually find their
antigen match



Using various mechanisms, the antibodies help eliminate the pathogen



Some of the plasma cells remain in the bloodstream and provide immunity
against a second infection by the same pathogen




These long-lived cells are called memory cells

Memory plasma cells of this type respond quickly if the same antigen is
encountered again

➢ Vaccines are weakened or non-pathogenic forms of pathogens that cause a primary
immune response producing the same lymphocytes as the actual disease
4

Defence against infectious diseases

Topic 6
...
3

Biology SL

➢ Antibiotics are chemicals that take advantage of the differences between
prokaryotic and eukaryotic cells and selectively block some of the biochemistry
needed by bacteria


They have no effect on animal cells

➢ Many categories of antibiotics


One may block protein synthesis in bacteria



Or may inhibit the production of a new cell wall by bacteria blocking the
ability to grow and divide

➢ Antibiotics have no effect on viruses since they have no metabolism of their own


Antibiotics often target specific metabolic pathways



Since viruses use our own cells against us, a medicine against the virus
would also harm our body cells

Penicillin
➢ One of the most famous antibiotics, produced by the fungus Penicillium


The effect was first discovered by Alexander Fleming in 1928


A petri dish where bacteria grew were inhibited by penicillin and no bacteria
continued to exist

➢ Fleming was unable to isolate the chemical produced by the fungus, but around
1940 Ernst Chain and Howard Florey were able to do it and tested the chemical on
mice


They infected 8 mice with deadly bacteria
...
The penicillin was given in high dose to an
ill person who nearly died

Resistance
➢ A growing problem today is the resistance of some bacteria to antibiotics


In a bacterial population there are millions of individuals



Bacteria reproduce rapidly



Mutations occur and these mutations can lead to resistance to antibiotics


A bacterium which is resistant to an antibiotic due to mutation can
reproduce fast and build a colony of resistant bacteria

➢ The long-term use and overuse of antibiotics has led many pathogens to be
resistant to nearly all of the antibiotics today
➢ MRSA (pronounced mersa) are strains of Staphylococcus aureus, a pathogen which
has developed a resistance to many types of antibiotics
6


Title: Defence against infectious diseases
Description: International Baccalaureate Biology SL Topic 6.3 2017 Clear and detailed notes of topic 6.3 from the book and lecture