2. Lecture 1: The Microbial World Edith Porter, M.D. 1

3.  Definition of Microbiology  Size dimensions  Classification of microbial agents  Microbial diversity  Role of microbes in nature  Beneficial ▪ Environment ▪ Normal microbiota ▪ Commercial use and industrial applications  Harmful ▪ Disease causing  History of Microbiology 2

4.  Micro  Small (micrometer range)  Not visible with the unaided eye  Bio  Living  Able to reproduce 3

5. 1 inch 1 cm 1 mm (1/10 of 1 cm) 1  m (1/1000 of 1 mm) 1 nm (1/1000 of 1  m) Human Egg cell (almost 1 mm) Erythrocyte (7  m) Bacterium (2 –4  m) Large Virus (200 nm) 4

6.  Cellular organisms  Eukaryotes (have a nucleus)  Prokaryotes (do not have a nucleus)  Acellular agents  Viruses (nucleic acid + protein)  Viroids (nucleic acid)  Prions (protein) Cell membrane Nucleus with genetic material Nuclear membrane Cell membrane Genetic material in cytoplasm 5

7. Domain Bacteria Domain Archaea Domain Eukarya Animals Helminths Plants Fungi Protozoa Algae Prokaryotes Protists Slime molds 6 Eukaryotes

8. 7  Bacteria  Peptidoglycan cell walls  Binary fission  For energy, use organic chemicals, inorganic chemicals, or photosynthesis  Some produce molecular oxygen  Archaea  No peptidoglycan  Often in extreme environments  Diverse metabolic pathways  Not known to cause disease

9.  Cellulose cell walls  Use photosynthesis for energy  Produce molecular oxygen and organic compounds 8

10.  Chitin cell walls  Use organic chemicals for energy  Two forms  Molds ▪ Multicellular ▪ Consisting of masses of mycelia composed of filaments called hyphae  Yeasts ▪ Unicellular  Dimorphic shift 9

11.  Unicellular  Absorb or ingest organic chemicals  May be motile via pseudopods, cilia, or flagella 10

12.  Multicellular animals  Parasitic flatworms and roundworms are called helminths  Microscopic stages in life cycles Dirofilaria immitis

13.  Viruses are replicated only when they are in a living host cell  Consist of DNA or RNA core  Core is surrounded by a protein coat  Coat may be enclosed in a lipid envelope (from host cell)  Not all viruses are harmful!

14.  Proteinaceous infectious particles  Consist of protein only  Prions induce conformation changes of normal counter parts  Body’s response leads to symptomatic disease  Neurodegenerative disorders  CJD  BSE Brain section of animal with BSE

15.  Genus name followed by species name  Typically relate to the discoverer, habitat, properties of the organism or its role  Genus name capitalized, species name lower case  In italic (or underlined) 14

16.  Escherichia coli or E. coli  Neisseria meningitidis or N. meningitidis spaceDiscoverer was Escherich lives in colon Discoverer was Neisser causes meningitis 15 space

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18.  Plankton  Geochemical cycling  Microbes recycle carbon, nutrients, sulfur, and phosphorus that can be used by plants and animals  Oxygen production  Normal flora: digestion, vitamin production etc  Cellulose digestion by protozoa in termite gut  Vitamin K production by human intestinal flora 17 Microbes on human tongue in a healthy individual

19.  A small percentage of all microorganisms are involved in diseases  Humans, animals and plants can be affected  Opportunistic and obligate pathogens  Diseases linked to  microbial proliferation (e.g. pus, pneumonia)  toxic substances (e.g. botulism, liver cancer) 18

20. An organism that contains a nucleus and a cell membrane is: a. Virus b. Prokaryote c. Helminth d. Archaea 19

21. Choose the correct form of naming a microbe: a. Pseudomonas maltophilia b. P. maltophilia c. Pseudomonas m. d. P. m. 20

22.  Development of tools to study microbes  Microbes exist  Microbes cause disease  Humans have a defense system  Drugs that kill microbes can be developed  Microbes can be exploited to the benefit of humans 21

23.  For identification  Optics (microscope)  Glass slides  Dyes  Culture media, inoculation material  Biochemical and molecular genetic assays  Advanced tools to study their role  In vitro models  Animal models 22

24.  ~ 1600 Galilei: Lenses for use in a microscope  1665: Robert Hooke described cells  1676 Van Leeuwenhoek: first recorded description of microbes called “animacules”  17 th /18 th century: spontaneous generation  Living things arise from non living matter  1858 Virchow proposes concept of biogenesis  Cells arise from living cells  1861 Pasteur disproves theory of spontaneous generation (and proves concept of biogenesis) 23

25. Fermentation, Pasteurization 24  Pasteur’s S-shaped flask kept microbes out but let air in

26.  1847 Semmelweis  childbed fever  1867 Lister  antiseptic surgery with phenol  1876 Koch  First proof that microbes cause disease: Bacillus anthracis causes anthrax  1884 Gram stain developed, Koch’s postulates formulated http://www.acponline.org/bioterro/anthrax/graphics/cutaneous.jpg http://www.cdc.gov/ncidod/eid/vol7no2/images/cover_final_rgb.jpg http://www.chemistryexplained.com/images/chfa_03_img0510.jpg 25

27.  Microbe must be present in every case of disease and not in the healthy one.  Microbe must be isolated in pure culture.  When inoculated into a healthy tissue the same disease must arise.  From this diseased tissue the same microbe must be re-isolated in pure culture. 26

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29.  1798 Jenner: cow pox vaccination  1884 Metchnikoff: phagocytosis  1890 Ehrlich: theory of antibodies  1921 Fleming: lysozyme 28

30.  End of 19 th century: dyes  1910 Ehrlich: First chemotherapeuticum (salvarsan: arsenic compound to treat syphilis)  1928 Fleming: first antibiotic (penicillin)  First successful treatment in 1942 29

31. Food preparation (fermentation) Bread, yogurt, kim-chi, cheese, beer, wine and many more Production of Chemicals acetone, butanol, alcohol, organic acids and many more Drugs Antibiotics, some cancer drugs Biotechnology Bioremediation Clean up of BP oil spill Genetic engineering Recombinant drugs Immunoassays Rebecca Lancefield: serotyping of Streptococcus spec. 30

32.  Emerging infectious diseases and topics  Avian Flue (H5N1) and swine flu  West Nile virus encephalitis  Mad cow diseases (prions)  E. coli O157:H7  Biofilm ▪ On teeth, mucosal surfaces, rocks, medical devices ▪ Hard to penetrate, source of recurrent infections  Emerging antibiotic resistance  Vancomycin resistant staphylococci and enterococci  Multidrug resistant tuberculosis strains  Resistance among malaria strains 31 S. aureus Biofilm

33.  Microbial agents include prokaryotes, eukaryotes and acellular agents  Prokaryotes are cells without nucleus  Bacteria, archaea, fungi, algae, and protozoa are in the MICROMETER range (  m)  Viruses, acellular agents, are in the NANOMETER range (nm) 32