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CLINICAL LAB SCIENEC

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392

ESSENTIALS OF CLINICAL LABORATORY SCIENCE

In the Lab

Critical Reminder

Viruses require living cells

on which to be inoculated to

achieve growth. They cannot

be placed in Petri dishes

with nutrient media such as

that designed for bacteria.

Therefore, they take more time

and effort to grow.

There are no antibiotics for

viruses. Cold and influenza

viruses are not affected to the

patient’s advantage when the

physician prescribes antibiotics.

Equipment and Supplies

1. Gloves, disposable paper towels, and disinfectant or other cleaning

solution

2. Swabs tipped with cotton or synthetic material (to be used to transfer

organisms) or reusable or sterile disposable inoculating metal loops and

needles

3. Bacterial incinerator if reusable metal loops and needles are being used,

OR sterile disposable loops and needles

4. Incubator for enhancing growth of bacteria (set at 36°C–37°C)

5. Agar plates (Petri dishes)

6. Source of organisms such as stock cultures on agar plates or in broth

(liquid media) tubes

7. Waterproof sharp marker

8. Disposal containers appropriate for biohazardous waste

Procedure

1. Wash hands and don gloves.

2. Assemble necessary equipment and supplies.

3. If reusable metal loops and needles are being used, turn on incinerator and

check that it has reached the optimum level of heat.

4. Select the proper agar plate (Petri dish) and use the marker to label it with appropriate

identifying information.

5. Introduce the sterile swab or sterilized or disposable metal loop into the broth

tube or pick up an isolated colony of bacteria from an agar plate.

6. Taking care not to touch any other surfaces

with the swab or metal loop, lift the

lid from a sterile agar plate slightly and

inoculate a fourth of the plate by rolling the

swab over the surface, taking care not to

tear the agar.

7. Replace the lid on the agar plate and

dispose of the swab in a biohazard container.

8. Streak the remainder of the agar surface

by touching the sterile loop or a

needle (this takes skill and a light touch)

to the first quadrant and streaking all the

way to the opposite side of the second

quadrant, repeating the process 7 or 8

FIGURE 15-3 Different types of nutrient media required for certain

bacterial organisms.

Source: Delmar/Cengage Learning.

times ( Figure 15-4). This serves to isolate

colonies of bacteria and to allow multiple

strains of organisms to be separated.

Copyright 2010 Cengage Learning. All Rights Reserved. May not be copied, scanned, or duplicated, in whole or in part. Due to electronic rights, some third party content may be suppressed from the eBook and/or eChapter(s).

Editorial review has deemed that any suppressed content does not materially affect the overall learning experience. Cengage Learning reserves the right to remove additional content at any time if subsequent rights restrictions require it.

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