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Lecture Notes - Chapter 27 of Microbiology: An Evolving Science

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Typed lecture notes covering chapter 27 of Microbiology: An Evolving Science, the textbook used in the "General Microbiology" course (BioM122) at UCI. Aligns with lecture 24 (last lecture of course).










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Uploaded on
August 7, 2024
Number of pages
5
Written in
2019/2020
Type
Class notes
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Dr. katrine whiteson
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All classes

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Vaccines & Antibiotics (Ch. 27, Lec. 24)
Thursday, December 10, 2020 12:00 PM
LEC24 RQ
The primary antibody response differs from the secondary antibody response in that
• Terms of disease occurrence: in the primary response, plasma cells differentiate from naive B cells, whereas in
• Endemic disease: occurs at a steady, predictable freq. the secondary response, plasma cells may differentiate from memory B cells.
• Epidemic disease: sudden INC in disease occurrence above the expected level, usually in
clusters. Ex. B. Pertussis(whooping cough) in OC area. The oral polio vaccine is an example of a __________ vaccine.
○ Outbreak: a local epidemic. Ex. Salmonella food poisoning. live attenuated
• Pandemic disease: a worldwide epidemic. Ex. Influenza virus. -Some vaccines, such as the polio vaccine, need to provide a live microbe to produce
• Index case: the first case of the disease in an epidemic. Patient zero.
an immune response in the correct compartment to ensure that the virus cannot be
• Public health surveillance:
○ In early 1900s, leading cause of death in the US was infectious disease. shed from the gut if feces contamination of the water supply is a concern.
○ Yet surveillance identified sources/risks of infection. -> PH measures reduced
disease prevalence: water treatment, strict sanitation, antimicrobials, beginning A(n) __________ vaccine will produce a cell-mediated immune response.
vaccine development. live, attenuated organism
○ Today, the US leading cause of death is heart disease and other vascular/metabolic
diseases. Penicillin inhibits peptidoglycan synthesis in bacterial cell walls. Humans do not have
• Tracking infectious disease: cell walls. This is an example of
○ In 1940s, PH effort extended to population-based methods of monitoring disease. -> selective toxicity.
Can see trends in disease, then disseminate information to reduce spread.
○ Now, response to an outbreak: (1) epidemiologist correlate the disease w/ an Suppose an exponentially growing culture of bacteria is treated with a potential
infectious organism, (2) physicians/nurses collect pt specimens, (3) clinical
antimicrobial compound. Over the next few hours, cell doubling stops (untreated, control
microbiologists isolate /identify the causative organism.
• Out of all the individuals in a population: cultures continue doubling), but the cells remain metabolically active. This antimicrobial
○ Incidence: # of new cases. compound is
○ Prevalence: total # of cases. bacteriostatic.
○ Even if incidence is low, prevalence can be high (newly infected people are living
longer).
• Recent INC in mortality rates, esp in the US. Outlier is the Spanish Flu of 1918.
• The US PH System is composed of:
○ Local and State level: public health laboratories, county health dept.
○ National level: CDC--Center of Disease Control and Prevention
• Control of epidemic:
1. Reduction/elimination of the source: treat/quarantine infected individuals, reduce likelihood
of transmission, control/remove reservoirs.
2. INC level of herd immunity: vaccination programs.
a. Herd immunity: pop resistance to infection bc large percentage(>70%) of said pop is
immune.
b. Factors that affect her immunity: introduction of new susceptible individuals,
antigenic shift or drift in pathogen-- individuals that may not be immune to these new
strains.
3. Sanitation methods: food safety(pasteurization, food inspection), water purification and
chlorination, insect vector control.
○ Dr. James in UCI molecular Bio dept has genetically-engineered male mosquitoes.
When males mate w/ females, daughters (female offspring) cannot fly due to wing
mutation. -> flightless females die, reducing the mosquito population. Can control
dengue fever!
• Smallpox is the only human disease to be eradicated. Only present in humans, no
reservoirs to cause incidence.
• Vaccine: microbial Ag used to induce protective immunity.
○ Goal is to induce Ab and T cell-mediated responses to protect the host from future
infection.
○ Administered w an adjuvant(vaccine ingredient) to maximally stimulate immunity. Ex.
Heat-killed bacteria.
○ Immunization: result achieved by successful delivery of a vaccine that has stimulated
immunity.
• Edward Jenner and Vaccine Development:
○ Dr. Jenner observed that ppl who had cowpox(vaccinia) never became sick w/
smallpox(variola), i.e. milkmaids w/ cowpox infection.

, ○ First case of vaccination: In 1796, Jenner injected cowpox-infected skin tissue into
the arm of James Phipps--causing mild symptoms of cowpox. Then inoculated
Phipps w/ smallpox, and Phipps did NOT develop the disease. -> Vaccination
process known as variolation!
• Types of vaccine:
○ Whole cell: consists of a whole microorganism (bacteria/virus).
• Inactivated: microbe is killed by heat/formaldehyde. Ex. Flu shot injection
• Epitopes present on killed antigen are used for immunity.
• Attenuated/Weakened: live microbes that have been altered for reduced
virulence. Ex. Flu mist
○ Subunit: consists of purified macromolecules from pathogens(polysaccharides,
surface antigens, toxoids).
○ Recombinant vector / DNA: consist of individual genes or DNA from pathogens. Ex.
HBV/Herpes B.
• Primary and secondary Ab responses:
○ Primary antibody response:
• Via disease or vaccination.
• Ab appear in the serum after several days.
• B cells that bind Ag make the Ab.
• Some B cells become memory B cells.
○ Secondary antibody response:
• Via second exposure to pathogen to pathogen or booster does.
• Ab appear in blood within hours. -> much larger and quicker response!









• Generation of Attenuated Vaccines:
○ Methods for generating attenuated(avirulent) vaccines:
• Deletion of specific virulence genes.
• Serial passage in a dif host organism -> adaptation to the new host and
reduced virulence in the orig host.
○ Benefit: induce stronger immunity than inactivated vaccines by providing more Ag.
(Viral copies are made via replication that immune system can fight against.)
○ Drawback: risk of reversion to virulence; can NOT be given to immunocompromised
hosts.
• How is the flu virus vaccine produced?
○ (Inactivated) Live virus of a chosen strain is injected into embryonated chicken eggs.
○ Virus infectivity is destroyed using formalin and disrupted using detergents to release
Ag(w/ specific epitopes that we can develop Ab for) that are used for vaccine.
• Detergent can disrupt the actual structure of the HA(hemagglutinin) that is
recognized by antibodies…have to consider during vaccine development.
○ (Attenuated) Same procedure, but would use a strain that does not cause disease.




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I have a Biological Sciences degree from UC Irvine class of 2021. Most of my documents will be from courses I've taken during my time at UCI. No answers to exams or quizzes, just study guides and lecture notes.

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