Micro

    Cards (115)

    • The methods of microbial control used outside of the body are designed to result in 4 possible outcomes 

      sanitization, disinfection, antisepsis, and sterilization
    • sanitization
      Sanitizing kills bacteria on surfaces using chemicals, it is not intended to neutralize viruses
    • Disinfection
      Disinfecting neutralizes viruses and kills bacteria on surfaces using chemicals(does not kill bacterial endospores)
    • asepsis
      Any practice that prevents the entry of infectious agents into sterile tissues and thus preventsinfection
    • sterilization
      Process that destroys or removes all viable microorganisms (including viruses and endospores)
    • Bacterial endospores havetraditionally been considered themost resistant microbial entities

      The goal of sterilization is thedestruction of bacterial endospores
    • Bacteristatic
      chemical agents that prevent the growth ofbacteria on tissues or on objects in the environment
    • Fungistatic
      chemicals that inhibit fungal growth
    • Bactericidal
      destroys bacteria except for those in theendospore stage
    • Fungicidal:

      kills fungal spores, hyphae, yeasts
    • Virucidal
      inactivates viruses, especially on living tissue
    • Sporicidal
      destroys bacterial endospores (achieves sterility)
    • Mechanical, Filtration
      Pore sizes can be controlled to permit truesterilization by trapping viruses or large proteins• Pore size 0.2 μm (micron) filters out mostbacteria• Pore size 0.02 μm filters out most viruses
    • Filtration is important to water purification
      unable to remove toxins
    • physical, heat
      Lower temperatures are microbistatic (slows activities- enzymes or metabolic reactions), Elevated temperatures are microbicidal(moist or dry)
    • Moist heat- water+heat
      boiling water- disinfection not sterilize (does not kill endospores)
      pasteurization- disinfection not sterilize
      autoclaving- steam under pressure ( WILL STERILIZE)
    • Dry heat-killing microbes using heat- no water involved 

      IncinerationDirect exposure of bacteria to intense heat (several thousand °C),burns microbes to ashes and gases
      Hot air oven-sterilization needs 3 hours, destroys endospores
    • Moist vs dry heat
      Moist heat:Operates at lower temperatures and shorter exposuretimes to achieve the same effectiveness as dry heatMicrobicidal effect is the coagulation (clotting) anddenaturation of proteins
      Dry heat:Dehydrates the cell, removing waternecessary for metabolic reactionsAt very high temperatures, oxidizes cells,burning them to ashes and gases
    • Physical- ultraviolet radiation
      Causes damage to cells through two main pathways:• formation of thymine dimers in DNA and• generation of reactive oxygen species
      Disadvantages• UV does not penetrate glass, plastic or water very well• Not good for surfaces with lots of “hiding places”
      DOES STERILIZE
    • prevention of uv related damage
      1. DNA repair enzymes e.g. Photolyase2. Antioxidant enzymes e.g. superoxide dismutase,catalase3. Pigments e.g. carotenoids, melanin• ROS scavenging• Dissipation of excitation energy as heat4. Negative phototaxisnavigate away from light
    • Ionizing Radiation
      Causes double strand DNA breaks
    • Chemical control- alcohol
      Work by denaturing proteins and disrupting cell walls & membranes
      Effective against vegetative cells
    • Chemical control-Halogens
      They generally disrupt microbial enzyme function
      Effective against vegetative cells and some endospores
    • Chemical Control- Oxidizing Agents
      Work by oxidizing enzymes thus shutting down the microbe’s metabolism
      Bactericidal, virucidal, and fungicidal; sporicidal in higher concentrationsEspecially effective against anaerobic organisms
    • Chemical Control- Phenol
      They denature proteins and disrupt cell membranes
      Effective against vegetative cells but not spores
    • Chemical control - Surfactants

      Work by disrupting the cell membrane structure
      Generally, work well against vegetative cells but not endospores
    • Chemical control - Heavy Metals
      Bind to proteins, inhibit enzymatic activity
      work well against vegetative cells but not endospores
    • Chemical control - Aldehydes
      Work by: denaturing proteins inactivating nucleic acids inactivating membranes
      Effective at sterilization
    • Biological Control of Microorganisms
      emerging field that shows great promise- natural control
    • selective toxicity
      kill or inhibit microbial cells without damaging host tissues
    • Drugs with excellent selective toxicity block the synthesis of the bacterial cell wall(penicillins and cephalosporins)

      Human cells lack the chemical peptidoglycan and are unaffected by the drug
    • Antibiotics are natural metabolic products of bacteria and fungi

      Produced to inhibit the growth of competing microbes inthe same habitat (antagonism)
    • Goals of chemotherapy: disrupt the structure or function of an organism to thepoint where it can no longer survive
      Antimicrobial drug categories:• Inhibition of cell wall synthesis• Inhibition of nucleic acid structure and function• Inhibition of protein synthesis• Interference with cytoplasmic membrane structure and function• Inhibition of folic acid synthesis
    • Drugs That Target the Cell Wall
      Most drugs that target the cell wall contain a beta-lactam ring in their molecular structureβ-lactams inhibit the synthesis of the peptidoglycan layer of bacterial cell wallsEspecially useful against Gram positive organisms
    • Penicillin resistant bacteria
      Microbes resistant to penicillin have β-lactamase or penicillinase which hydrolyzes the β-lactam ring and inactivates its antibacterial properties
      Some bacteria, e.g. E. coli, produce an enzyme called extended spectrum beta-lactamase(ESBL), this enzyme makes ESBL bacteria harder to treat with antibiotics
      Methicillin-resistant Staphylococcus aureus (MRSA) are resistant to all beta-lactamantibiotics including penicillins and cephalosporins
    • Drugs That Target Protein Synthesis
      Aminoglycosides: stick to ribosomes and causethe misreading of the mRNA, leading to abnormalproteins
      Tetracyclines: block the attachment of tRNA onribosomes and stop further protein synthesis
      Macrolides: stick to ribosomes inhibit movement oftRNAs during protein synthesis
    • Drugs That Target Folic Acid Synthesis, DNA or RNA
      Sulfonamides (sulfa): interfere with folate metabolism by blocking enzymesrequired for the synthesis of tetrahydrofolate (B9), which is needed by the cells forfolic acid synthesis and eventual production of DNA, RNA, and amino acids
    • Drugs That Target Cytoplasmic or Cell Membranes
      Polymyxins (colistins): interact with membranephospholipids; distort the cell surface and cause leakageof protein and nitrogen bases, particularly in gram-negative bacteria
    • Spectrum of Activity
      Broad-spectrum drugs: effective against more than one group of bacteria
      Narrow-spectrum drugs: target a specific group
    • Bacteria in Biofilms
      Bacteria in biofilms are often unaffected by antimicrobials, Antibiotics often cannot penetrate the sticky extracellularmaterial surrounding biofilms Different gene expressionprofiles during free-livingvs. biofilm stages
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