Fall Semester 2025: Final Exam Study Guide Part 3 of 3
FINAL EXAM STUDY GUIDE PART 3 OF 3: NEW MATERIAL
New Disease Note Cards
Understand the causative agents for the following diseases:
Bubonic Plague: Yersinia pestis
Toxoplasmosis: Toxoplasma gondii
Cat Scratch Disease: Bartonella henselae
Historical Figures of Microbiology
Review significant historical figures in microbiology and their contributions:
Robert Hooke:
Known for his pioneering work in cell theory, he coined the term "cell" after observing cork under a microscope.
Antoni van Leeuwenhoek:
First to observe and describe microscopic organisms, known as the "father of microbiology".
John Needham:
Conducted experiments pertaining to spontaneous generation which claimed that microbes could arise from non-living matter.
Francesco Redi:
Challenged the idea of spontaneous generation with his meat jar experiments, demonstrating that maggots came from eggs laid by flies.
Lazzaro Spallanzani:
Supported the biogenesis theory and disproved Needham’s conclusions by showing that sealed containers with broth did not develop microbial life.
Louis Pasteur:
Developed the germ theory of disease and pasteurization; demonstrated that microorganisms could cause disease.
Robert Koch:
Established a series of principles known as Koch's postulates that are used to establish a causative relationship between a microbe and a disease.
John Snow:
Investigated the cholera outbreak in London, establishing epidemiology as a field of study and linking water supply to disease spread.
Ignaz Semmelweis:
Advocated for hand hygiene in medical settings to reduce maternal deaths from puerperal fever.
Joseph Lister:
Introduced antiseptic techniques in surgery, significantly reducing infection rates.
Remak vs. Virchow:
Discuss the debate between Remak and Virchow concerning cellular pathology and the origin of cells. Virchow famously stated, "Omnis cellula e cellula" (All cells come from cells).
Germ Theory of Disease
Be familiar with the Germ Theory of Disease:
The theory posits that specific microorganisms are the cause of specific diseases. This marked a significant advancement in understanding the link between microbes and illness.
Biosafety Levels (BSL)
Understand the biosafety levels established by the Centers for Disease Control and Prevention (CDC):
BSL-1:
Non-pathogenic E. coli (K12 = the classic common, harmless lab strain)
BSL-2:
Includes Staphylococcus aureus, Pseudomonas aeruginosa, and HIV. These organisms pose moderate hazards to personnel and the environment.
BSL-3:
Mycobacterium tuberculosis (causes TB which can be transmitted through aerosols).
BSL-4:
Highly pathogenic and dangerous agents such as Ebola virus, Hantavirus, and Marburg virus.
Personal Protective Equipment (PPE)
Understand the escalation of required PPE corresponding to increasing biosafety levels.
Recognize the additional features and instrumentation necessary to outfit an infectious disease lab appropriately as the BSL increases.
Biofilm Formation
Refer to Part 1 of the Study Guide for details on biofilm formation, as it may be relevant for questions pertaining to this topic.
Hemolysis Patterns
Understand the function of Red Blood Cells (RBCs) and the structure of hemoglobin:
RBCs transport oxygen from the lungs to body tissues and bring carbon dioxide back to the lungs.
Hemoglobin is the protein in RBCs that carries oxygen; it consists of four subunits (two alpha and two beta chains), each bound to a heme group that contains iron.
Be able to distinguish between the various types of hemolysis:
Alpha Hemolysis: Partial hemolysis; characterized by a greenish coloration in the agar due to the reduction of hemoglobin to methemoglobin.
Beta Hemolysis: Complete hemolysis; shown as clear zones around colonies as the bacteria fully lyse the RBCs and degrade hemoglobin.
Gamma Hemolysis: No hemolysis; the medium remains unchanged.
Important to recognize each type of hemolysis and what it implies:
Hemolysis patterns are crucial for bacterial identification in clinical settings, aiding in determining treatment strategies for patients.
Control of Microorganisms by Heat
Familiarize with methods for controlling microorganisms by heat:
Direct Flame: Excellent for sterilizing instruments; high effectiveness in killing microbes, especially spores.
Boiling: Effective for most pathogens, but not necessarily for spores.
Dry Heat (Oven): Generally requires higher temperatures for extended periods.
Moist Heat Under Pressure (Autoclave):
Related temperature: 121°C
Required time exposure: 15-30 minutes at this temperature
Extent of pressure: 15 psi (pounds per square inch)
This method is very successful at killing microorganisms, including spores.
Markers for effective sterilization methods include:
“Does it kill spores?”
Other Methods of Control
Types of filters:
Understand pros and cons related to various filtering methods used in microbiology.
UV Light:
Typical uses include surface disinfection; effective against many microbes but generally not effective for spores.
Ultrasonic Waves (US):
Commonly used for cleaning delicate instruments; can break down microbial populations effectively.