Fungal Specimen Collection And Hand Flashcards

1
Q

Sample Processing Time

A

Process samples within 2 hours from receipt.

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2
Q

Refrigeration for Delayed Testing

A

Delay in testing of intravascular catheter tips, other medical devices (stents, surgical implants, replacement joints, etc.), lower respiratory tract or urine specimens -> Refrigerate at 4°C.

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3
Q

Storage of Dermatologic Specimens

A

Dermatologic specimens (skin, hair, nails) are very sensitive to cold → Hold at room temperature (22-25°C).

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4
Q

Incubation: Blood, Bone marrow, Tissue, Sterile fluids

A

30°C; TAT 21 days.

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5
Q

Incubation: Hair, Skin, Nail scrapings

A

30°C; TAT 21 days.

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6
Q

Incubation: Vaginal, Throat, Mouth samples

A

30°C; TAT 7 days.

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7
Q

General purpose/Routine media for fungi

A

Sabouraud Dextrose Agar (SDA)

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8
Q

Selective media for pathogenic fungi, inhibits saprophytic fungi (for clinically significant)

A

SDA with cycloheximide

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9
Q

Primary recovery of saprobic and pathogenic fungi

A

Brain-Heart Infusion Agar (BHIA), Potato flake agar, Sabouraud dextrose with brain-heart infusion (SABHI) agar

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10
Q

Primary recovery of pathogenic fungi not including dermatophytes (Antibiotics: chloramphenicol, cycloheximide, gentamicin)

A

Brain-Heart Infusion Agar (BHIA) with antibiotics, Yeast-extract phosphate agar with ammonia

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11
Q

Enhances recovery and sporulation of Blastomyces and Histoplasma

A

Yeast extract phosphate

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12
Q

Primary recovery of pathogenic, cycloheximide-sensitive fungi exclusive of dermatophytes

A

Inhibitory mold agar

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13
Q

Primary recovery of dermatophytes; recommended as screening medium

A

Dermatophyte test medium

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14
Q

Primary recovery of Dermatophytes (E.M.T species) = indicator phenol red

A

Mycosel/Mycobiotic agar

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15
Q

Detection of ascospores in ascosporogenous yeasts (e.g., Saccharomyces spp.) = components of yeasts - compounds of yeasts.

A

Acetate Ascospore Agar

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16
Q

Identification of Cryptococcus, Trichosporon, and Rhodotorula spp.; Separation of Trichophyton mentagrophytes from Trichophyton rubrum.

A

Christensen’s Urea Agar

17
Q

Differentiation of Candida spp. by chlamydospore production.

A

Cornmeal Agar with Tween 80 and Trypan Blue

18
Q

Differential identification of Aspergillus spp.

A

Czapek’s Agar / Czapek-Dox Agar

19
Q

Identification of Cryptococcus neoformans and Cryptococcus gattii (creatinine for enhanced melanization).

A

Niger Seed Agar (Birdseed Agar)

20
Q

Demonstration of conidia formation and the pigment production by Trichophyton rubrum; preparation of microslide cultures and sporulation of dermatophytes.

A

Potato Dextrose Agar

21
Q

Identification of yeasts by determining fermentation.

A

Yeast Fermentation Broth

22
Q

Identification of yeasts by determining carbohydrate assimilation.

A

Yeast Nitrogen-Base Agar

23
Q

Enhanced recovery of Malassezia furfur.

A

SDA with Olive/Mineral Oil

24
Q

For Trichophyton mentagrophytes.

A

Hair Baiting in Media

25
Q

Differentiates Microsporum canis (positive) from Microsporum audouinii (negative).

A

Rice Medium

26
Q

Purpose of Lactic Acid and Glycerol

A

Preservation of structure.