Tularemia laboratory findings: Difference between revisions
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*F. tularensis cells are smaller than Haemophilus influenzae. | *F. tularensis cells are smaller than Haemophilus influenzae. | ||
*Bipolar staining is not a distinctive feature of F. tularensis cells. | *Bipolar staining is not a distinctive feature of F. tularensis cells. | ||
*Additional work: Another smear may be prepared for referral to your state public health laboratory. | *Additional work: Another smear may be prepared for referral to your state public health laboratory. <ref name= "ID FT"> Protocol for the Presumptive Identification of Francisella tularensis. https://www.ok.gov/health2/documents/Francisella_tularensis%202-15-13.pdf Accessed March 8, 2016. </ref> | ||
===Cultures=== | ===Cultures=== | ||
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*These organisms require cysteine supplementation; therefore, ''F. tularensis'' may at first grow on SBA, but upon subsequent passage will fail to grow on standard SBA. *On cysteine supplemented agar plates, it is a gray-white, opaque colony, usually too small to be seen at 24 h on most general media such as CA, TM, and BCYE. | *These organisms require cysteine supplementation; therefore, ''F. tularensis'' may at first grow on SBA, but upon subsequent passage will fail to grow on standard SBA. *On cysteine supplemented agar plates, it is a gray-white, opaque colony, usually too small to be seen at 24 h on most general media such as CA, TM, and BCYE. | ||
*After incubation for 48 h or more, colonies are about 1-2 mm in diameter, white to grey to bluish-grey, opaque, flat, with an entire edge, smooth, and have a shiny surface. | *After incubation for 48 h or more, colonies are about 1-2 mm in diameter, white to grey to bluish-grey, opaque, flat, with an entire edge, smooth, and have a shiny surface. | ||
*''F. tularensis'' will not grow on MacConkey or EMB plates. | *''F. tularensis'' will not grow on MacConkey or EMB plates. <ref name= "ID FT"> Protocol for the Presumptive Identification of Francisella tularensis. https://www.ok.gov/health2/documents/Francisella_tularensis%202-15-13.pdf Accessed March 8, 2016. </ref> | ||
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*Procedure: Use established laboratory procedures for [[catalase]], [[oxidase]],[[beta-lactamase]], XV (or satellite), and [[urease]] tests. | *Procedure: Use established laboratory procedures for [[catalase]], [[oxidase]],[[beta-lactamase]], XV (or satellite), and [[urease]] tests. | ||
*Interpretation: According to established laboratory practice. | *Interpretation: According to established laboratory practice. | ||
*Additional notes: Commercial biochemical identification systems are not recommended at this stage. | *Additional notes: Commercial biochemical identification systems are not recommended at this stage. <ref name= "ID FT"> Protocol for the Presumptive Identification of Francisella tularensis. https://www.ok.gov/health2/documents/Francisella_tularensis%202-15-13.pdf Accessed March 8, 2016. </ref> | ||
==References== | ==References== | ||
Revision as of 20:03, 8 March 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
There are a variety of lab diagnostic tests used to diagnose tularemia including gram stains, bacteria cultures,biochemical,and antibody fluorescence tests. Gram stains and bacteria cultures are useful in identifying F.tularensis. Unfortunately, these diagnostics offer difficult interpretations with extensive procedures. Antibody fluorescence allows for quick and effective testing. This method is extraordinarily important in diagnosing pneumonic variations of tularemia, as these variations are often associated with a higher mortality rate.
Laboratory Findings
Stains and smears
Gram stain
- Staining of F. tularensis often reveals the presence of tiny, 0.2-0.5-μm X 0.7-1.0 μm, pleomorphic, poorly staining, gram-negative coccobacilli seen mostly as single cells.
- The gram stain interpretation may be difficult because the cells are minute and faintly staining.
- F. tularensis cells are smaller than Haemophilus influenzae.
- Bipolar staining is not a distinctive feature of F. tularensis cells.
- Additional work: Another smear may be prepared for referral to your state public health laboratory. [1]
Cultures
- Established inoculation and plating procedures are used. For tissues, established laboratory procedure is used to inoculate media (e.g., grind, touch-preparation, or a sterile wood stick). Plates are taped shut in 2 places to prevent inadvertent opening (alternate to taping is acceptable).
- Incubation of cultures.
- Temperature: 35-37°C
- Atmosphere: Ambient, use of 5% CO2 is acceptable.
- Length of incubation: primary plates are held for 5 days. If it is known that patient has been treated with bacteriostatic antibiotics, then plates are held for up to 7 days to allow bacteria recovery time.
- F. tularensis grows in commercial blood culture media.
- These organisms require cysteine supplementation; therefore, F. tularensis may at first grow on SBA, but upon subsequent passage will fail to grow on standard SBA. *On cysteine supplemented agar plates, it is a gray-white, opaque colony, usually too small to be seen at 24 h on most general media such as CA, TM, and BCYE.
- After incubation for 48 h or more, colonies are about 1-2 mm in diameter, white to grey to bluish-grey, opaque, flat, with an entire edge, smooth, and have a shiny surface.
- F. tularensis will not grow on MacConkey or EMB plates. [1]
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Biochemical reactions/tests
- Procedure: Use established laboratory procedures for catalase, oxidase,beta-lactamase, XV (or satellite), and urease tests.
- Interpretation: According to established laboratory practice.
- Additional notes: Commercial biochemical identification systems are not recommended at this stage. [1]
References
- ↑ 1.0 1.1 1.2 Protocol for the Presumptive Identification of Francisella tularensis. https://www.ok.gov/health2/documents/Francisella_tularensis%202-15-13.pdf Accessed March 8, 2016.