A&P lecture microbiology and immunology/defense

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Last updated 11:12 PM on 4/8/26
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51 Terms

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prokaryotic cell vs eukaryotic cell

prokaryotic has no nucleus or organelles making it smaller, eukaryotic cells have a nucleus and organelles making them much larger and complex.

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different types of bacteria

  • obligate aerobes

  • obligate anaerobes

  • facultative anaerobes (can live in anaerobic and aerobic)

  • live in extreme conditions

  • may form endospores (can survive anything)

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bacteria morphology

unicellular but often live in “groups”

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good vs bad bacteria

small fraction cause infection or illness, most are harmless. Some are opportunistic pathogens (normally not but can become pathogenic).

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normal flora

the bacteria, fungi, and viruses that live in/on our bodies all the time

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bacterial cells of normal flora

body contains same amount of human cells as it does bacterial cells but are not found in urine, blood, lymph, or CSF.

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locations of bacteria in our body

skin, digestive tract, and respiratory tract act as mini ecosystems to bacteria, providing us with specific benefits.

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controlling bacterial infections

  • antiseptics and disinfectant can kill bacteria or inhibit their growth.

  • Antibiotics and antimicrobial drugs prevent growth but are not toxic to host with minimal side effects (can lead to antibiotic resistance)

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antibiotic resistance

one “generation” for bacteria is a short period of time, many generations = more opportunities for random mutations that could make the bacteria resistant to the antibiotics.

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viruses structure

  • acellular (no cell membrane)

  • cant reproduce on their own

  • cant make/use their own energy (invades host cells cellular machinery to copy genetic info and make more particles)

  • genetic info contained in a “protein coat”

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lytic cycle

virus invades host cell, makes new copies of the virus, then causes lysis of the host cell to release the virus.

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lysogenic cycle

virus invades host cell, viral DNA gets incorporated into host genome and stays there until a condition changes (can be long time). Can later re-enter the lytic cycle.

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control of viral infection

  • hand washing

  • avoiding germs

  • masks

  • vaccination

  • antiviral medications disrupt but can be harmful to host

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fungi structure

  • eukaryotic cells but have unique cell wall

  • not always microscopic (mushrooms vs yeast)

  • part of our normal flora but can be opportunistic pathogens

  • common ones: thrush, athletes foot, ring worm

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control of fungal infections

  • anti fungal medication (sometimes toxic to human cells)

  • fungal pathogens develop resistance

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protozoa structure

  • eukaryotic

  • unicellular

  • most aren’t pathogenic but some are important pathogens with serious effects on human health

  • complex lifestyles involving more than one host

  • associated with contaminated drinking water

  • typically have locomotion

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control of protozoan infection

  • avoid contact

  • ensure access to clean drinking water

  • vaccines

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metazoan parasites structure

  • eukaryotic

  • multicellular (bigger, complex)

  • adult form can be large and visible but are often identified by eggs or larval from (microscopic)

  • can include pinworm, tapeworm, filariasis

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control of metazoan infections

  • avoid contact (uncooked meat, skin, fecal-oral route)

  • some medications are available

  • antibiotics to kill bacteria in the gut of the parasite

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ways microorganisms can cause disease

  • consuming nutrients/resources in your body

  • triggering vomiting/diarrhea

  • causing structural damage

  • provoking an immune response

  • disrupting your normal flora

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nosocomial infections

acquired in a clinical setting due to poor hand hygiene, antibiotic resistant strains of bacteria, resistant endospores, patients are more susceptible.

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barrier defences

skin forms a tight barrier, mucous traps pathogens, clotting response prevents pathogens from entering.

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adaptive responses

lymphocytes are capable of response and cells of the immune system use secreted signals and cell-to-cell interactions to communicate

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cells associated with innate defenses

phagocytic cells destroy/engulf pathogens, granular cells harm/kill pathogens, cells of immune system communicate via cytokines

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innate immunity (non-specific)

  • born with it

  • defense against anything foreign/abnormal

  • first line of defense

  • includes physical barriers, NK cells, inflammation, etc.

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adaptive immunity (specific)

  • develops after birth, after exposure to antigen

  • 4 properties (specificity, versatility, memory, tolerance)

  • includes actions of cytotoxic T cells and B cells.

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specificity

ability to target specific cells

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versatility

ability to respond/build defences against things we don’t know exist and adapt to environment

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memory

ready to act quick if exposed again because our body remembers

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tolerance

need to destroy other cells but not our normal ones

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communication across cell membranes

  • antigens are “specific chemical targets” that stimulate immune response and be displayed on surface of cells (MHC)

  • body can detect “self” from “non-self” antigens

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antigen presenting cells

  • pick up and display antigens on their surface without being infected themselves

  • have class II MHC proteins on their membranes

  • activate helper T cells

  • includes dendritic cells, macrophages, microglia.

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NK cells

  • non-specific

  • recognize foreign antigens/abnormal antigens on cells

  • release perforins to create holes in target cells and destroy

  • destroy body cells infected by viruses (including cancer cells)

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T cells/lymphocytes

  • cell-mediated immunity (attack by phagocytosis)

  • formed in bone marrow but developed in thymus

  • T cell receptors and CD markers on membranes

  • includes helper T cells, cytotoxic T cells, memory T cells, regulatory T cells

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B cells/lymphocytes

  • antibody-mediated immunity

  • formed in bone marrow

  • B cell receptors and class II MHC proteins on membrane

  • includes inactive B cells, sensitized B cells, plasma cells, memory B cells

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what happens if there is a “breach” in immune response?

innate defenses keep thing under control until specific defenses are ready where they will destroy the specific antigen.

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class I MHC

  • on all nucleated cells

  • communicates with CD8 T cells (cytotoxic T cells)

  • results in destruction of infected cell

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class II MHC

  • on specialized cells (APCs, B cells)

  • communicates with CD4 T cells (helper T cells)

  • results in stimulation of immune response

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IgG antibodies

largest, account for 80% of antibodies, responsible for resistance against viruses, bacteria, and bacterial toxins.

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IgE antibodies

attaches as an individual molecule to the exposed surfaces of basophils and mast cells. Causes stimulation of a cell to release histamine.

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IgD antibodies

is an individual molecule on the surfaces of B cells where it binds antigens in the extracellular fluid.

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IgM antibodies

first class of antibody secreted after an antigen is encountered, circulates as a five-antibody starburst.

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IgA antibodies

found in glandular secretions such as mucous, tears, saliva, and semen. Attack pathogens. before they gain access to internal tissues.

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primary response

first exposure to specific antigen, takes time to develop; some IgM first then IgG

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secondary response

second exposure to same antigen, much more rapid as you are now “immune” to the pathogen. Some IgM but much more IgG

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artificially acquired active immunity (vaccines)

antigen is administered triggering immune response, individual will produce antibodies against the antigen so youre ready if ever exposed to the “real” antigen

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inflammation

  • non-specific defense

  • innate

  • a response to invasion/infection, tissue damage, or both

  • symptoms include redness, heat, swelling, and pain

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purpose of inflammation

deliver leukocytes and plasma proteins to site of injury to destroy any invaders, clean up the mess, and facilitate healing/repair

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how do cells get to inflammation sites?

mast cells release histamine triggering vasodilation and increased capillary permeability. Neutrophils and monocytes also undergo margination and diapedesis.

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immunological surveillance and cancer

any cell may undergo a mutation that affects its cell division, becoming cancerous. cancer cells are “self” but are abnormal so can be recognized by your body defenses.

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balance between immunity and autoimmunity

immune response is essential to preventing infection but an overactive immune response could lead to autoimmunity.