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microbiology quiz 2

Apr 14, 2018

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    Quiz 2

    Dr. Ashish Jawarkar

    M.D. Path

    Parul Sevashram Hospital

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    Q-1

    Which class of organisms causes the

    disease in picture

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    Athletes foot

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    A. Bacteria

    B. Fungi

    C. Virus

    D. Protozoa

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    Fungi

    Eukaryotic organisms

    with rigid cell wall

    Yeasts

    Single-celled Reproduce by budding

    Molds

    Large, fuzzy,

    multicelled organisms

    Produce spores

    Superficial infections

    Athletes foot

    Ringworm

    Thrush

    Can cause systemic

    infections

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    Q-2

    Which of the following is semipermeable

    A. cell membrane

    B. cell wall

    C. Nucleus

    D. Ribosomes

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    Cytoplasmic (Plasma)

    membrane Thin layer 5-10 nm, separates cell wall from cytoplasm

    Acts as a semipermeablemembrane: controls theinflow and outflow of metabolites

    Composed of lipoproteins with small amounts of

    carbohydrates

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    Q-3

    What are the contents of Mac Conkeys

    medium?

    A. Peptone B. Lactose

    C. Neutral Red

    D. All of the above

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    Differential media

    A media which has substances incorporated in it

    enabling it to distinguish between bacteria. Eg: Mac Conkeys medium

    Peptone

    Lactose

    Agar

    Neutral red

    Taurocholate

    Distinguish between lactose fermenters & nonlactose fermenters.

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    Lactose fermentersPinkcolonies

    Non lactose fermenterscolourless colonies

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    Q-4

    What is this used for?

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    For removing oxygen, to grow anaerobic

    bacteria

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    ANAEROBIC CULTURE METHODS

    Anaerobic bacteria differ in their requirement

    and sensitivity to oxygen.

    Cl.tetani is a strict anaerobegrows at an

    oxygen tension < 2 mm Hg.

    Methods: Production of vacuum

    Displacement of oxygen with other gases

    Chemical method Biological method

    Reduction of medium

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    Production of vacuum:

    Incubate the cultures in a vacuum desiccator.

    Displacement of oxygen with other gases

    Displacement of oxygen with hydrogen,

    nitrogen, helium or CO2. Eg: Candle jar

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    Chemical method

    Alkaline pyrogallol absorbs oxygen.

    McI ntoshFildes anaerobic jar

    Consists of a metal jar or glass jar with a metallid which can be clamped air tight.

    The lid has 2 tubesgas inlet and gas outlet

    The lid has two terminalsconnected toelectrical supply.

    Under the lidsmall grooved porcelain spool,wrapped with a layer of palladinised asbestos.

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    Working:

    Inoculated plates are placed inside the jar and

    the lid clamped air tight. The outlet tube is connected to a vacuum pump

    and the air inside is evacuated.

    The outlet tap is then closed and the inlet tube is

    connected to a hydrogen supply.

    After the jar is filled with hydrogen, the electric

    terminals are connected to a current supply, so

    that the palladinised asbestos is heated.Act as a catalyst for the combination of hydrogen

    with residual oxygen.

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    Gaspak

    Commercially available disposable envelope.

    Contains chemicals which generate H2and CO2on addition of water.

    Cold catalystin the envelope

    Indicator is usedreduced methylene blue. Colourlessanaerobically

    Blue colouron exposure to oxygen

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    Q-5

    What is resolution

    A. the ability of the microscope to

    enlarge the object B. the ability of the microscope to show

    two nearby placed objects separately

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    Important Vocabulary :

    magnification \mag-ne-fe-'ka-shen\ n1.

    apparent enlargement of an object 2. theratio of image size to actual sizeA magnification of "100x" means that theimage is 100 timesbigger than the actualobject.

    resolution \rez-e-loo-shen\ n1. clarity,sharpness 2. the ability of a microscope toshow two very close points separately

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    Q-6

    Which type of microscope has been

    used for taking this picture?

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    A. Bright field microscope

    B. Dark field microscope

    C. Phase contrast microscopeD. Fluorosence microscope

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    Bright-field MicroscopeContains two lens systems for magnifying

    specimens

    Specimens illuminated directly from above or

    belowAdvantages: convenient, relatively

    inexpensive, available

    Disadvantages: R.P 0.2 m at best; canrecognize cells but not fine details

    Needs contrast. Easiest way to view cells is

    to fix and stain.

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    Different magnifications

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    Special Microscopy

    Applications

    Dark Field

    Phase Con trast

    Fluorescence

    Electron Microscope

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    Dark Field Microscopy

    special condenserdiaphragm

    occludes direct light,passes wide anglelight

    angle too wide toenter objective

    diffractedlight

    diffracted light scattered

    enters objectiveobjects light on dark background

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    Phase Contrast Microscopy

    light rays through objects of different change in

    phase, not intensity

    special ring-shaped condenser diaphragm

    special glass disc in objective

    change phase differences to intensity differences

    can view transparent

    objects as dark on light

    background (without staining)

    Right; human brain glial

    cells

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    Fluorescence Microscopy

    Illuminate specimen with UV visible fluorescence(filter removes harmful UV)

    View auto-fluorescent objects (e.g., chloroplasts)

    Stain with specific fluorescent dyes, which absorb in

    region 230-350 nm & emit orange, yellow or greenishlight

    Images appear coloured against a dark background

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    Electron Microscopy

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    Q-7

    Steps of staining include

    1. primary stain

    2. decolorisation 3. counter stain

    Which dyes are used for these steps?In gram staining and acid fast staining

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    Primary

    staining

    Decolorisation

    Counter

    staining

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    Primary stain

    Decolorisation

    Counter stain

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    Q-8

    What is sterilisation?

    A. Killing all organisms on the object

    B. Removing only pathogenic organisms

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    DEFINITION

    STERILIZATION

    The process of freeing an article frommicroorganisms including their spores.

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    DISINFECTION:

    Reducing the number of

    pathogenic microorganisms to the

    point where they no longer causediseases.

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    Q-9

    Which is true?

    A. Bacteriostatic agent doesnot kill

    bacteria B. Bactericidal agent kills bacteria

    C. All of the above

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    Bacteriostatic Agent:

    An agent that inh ib i tsthe growth of bacteria, but

    does not necessarily kill them.

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    Bactericide:

    An agent that kills bacteria. Most do not killEndospores.

    Sporicide:

    An agent that kills spores.

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    Q-10

    Which method is used to sterilize?

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    A. Hot air oven

    B. Autoclave

    C. PasteurizationD. Ethylene oxide gas

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    Q-11

    Which organism causes plague

    A. streptococcus pneumoniae

    B. mycobacterium tuberculosisC. vibrio cholerae

    D. yersinia pestis

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    Bubonic Plague or the Black

    Death

    Epidemic swept thru Europe in the Middle

    Ages (13th and 14th centuries)

    40 million people were killed About 1/3 of the population of the continent

    Etiological agent:

    Yersinia pestis Gram (-) rod

    2 Vectors

    Rat

    Flea

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    Yersinia pestis - Gram (-) bacillus

    Vectors - Rat and Flea

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    Bubonic Plague Infection

    1. Flea bite with Yersinia pestis

    2. Bacteria multiply in the bloodstream

    Bacteremia 3. Bacteria localize in lymph nodes,

    especially axillary and groin areas

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    4. Hemorrhaging occurs in lymph nodes, resulting in

    black and blue swellings or Buboes (hence the name

    Bubonic Plague or Black Death)

    B b i Pl I f ti

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    Bubonic Plague Infection 5. If untreated, about 50 % Mortality Rate

    6. If bacteria spread to the lungs, it becomesPneumonic Plague and is now highly

    contagious (Almost a 99 % Mortality Rate)

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