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CAMP test

From Wikipedia, the free encyclopedia
Microbiological method for identification
This is an example of a positive CAMP test indicated by the formation of dark arrowheads where the Strep group B (Streptococcus agalactiae) meets theStaphylococcus aureus (light-yellow/golden middle streak with surrounding dark hemolysis).
Example of a workup algorithm of possible bacterial infection in cases with no specifically requested targets (non-bacteria, mycobacteria etc.), with most common situations and agents seen in a New England community hospital setting. CAMP test is shown at bottom left.

TheCAMP test (Christie–Atkins–Munch-Petersen) is a test to identify group Bβ-hemolyticstreptococci (Streptococcus agalactiae)[1][2] based on their formation of a substance,CAMP factor,[3] that enlarges the area ofhemolysis formed by the β-hemolysin elaborated fromStaphylococcus aureus.

CAMP factor

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Although the test is usually used to identify group B streptococcus, there is some evidence that the CAMP factor gene is present in several groups of streptococci, includinggroup A.[4]

A similar factor has been identified inBartonella henselae.[5]

Uses

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The CAMP test can be used to identifyStreptococcus agalactiae. Though not strongly beta-hemolytic on its own,[6] group B strep presents with wedge-shaped colonies in the presence ofStaphylococcus aureus.[7]

It can also be used to identifyListeria monocytogenes which produces a positive CAMP reaction.[8]

Setup

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  1. Streak a beta-lysin–producing strain ofaureus down the center of a sheep blood agar plate.
  2. The test organism streak should be 3 to 4 cm long.
  3. Streak test organisms across the plate perpendicular to the S.aureus streak within 2 mm. (Multiple organisms can be tested on a single plate).
  4. Incubate at 35°-37°C in ambient air for 18-24 hours.
  5. Wedge shaped pattern radiating from the test organism near theS. aureus indicates positivity

Reverse CAMP test

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The reverse CAMP test is a method to identifyClostridium perfringens using β-hemolytic streptococci. The CAMP factor produced byS. agalactiae and thealpha toxin produced byC. perfringens act synergistically to produce enhanced hemolysis. Streaking these two organisms perpendicular to each other on a blood agar plate will yield a “bow tie” shaped zone of hemolysis which indicates a positive test.[9][10]

History

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CAMP is an acronym for "Christie–Atkins–Munch-Peterson",[11][12][13] for the three researchers who discovered the phenomenon.[14]

It is often incorrectly reported as the product offour people (counting Munch-Petersen as two people).[15] The true relationship (three people) is the reason for twoen dashes and then onehyphen in Christie–Atkins–Munch-Petersen.

The name of the test bears no relationship to the name of thesecond messengercyclic adenosine monophosphate (commonly referred to as cAMP).

References

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  1. ^Phillips EA, Tapsall JW, Smith DD (August 1980)."Rapid tube CAMP test for identification of Streptococcus agalactiae (Lancefield group B)".J. Clin. Microbiol.12 (2):135–7.doi:10.1128/jcm.12.2.135-137.1980.PMC 273541.PMID 7014603.
  2. ^Wilkinson HW (July 1977)."CAMP-disk test for presumptive identification of group B streptococci".J. Clin. Microbiol.6 (1):42–5.doi:10.1128/jcm.6.1.42-45.1977.PMC 274694.PMID 328534.
  3. ^"Laboratory Demonstrations". Archived fromthe original on September 28, 2008. Retrieved2008-12-12.
  4. ^Gase K, Ferretti JJ, Primeaux C, McShan WM (September 1999)."Identification, cloning, and expression of the CAMP factor gene (cfa) of group A streptococci".Infect. Immun.67 (9):4725–31.doi:10.1128/IAI.67.9.4725-4731.1999.PMC 96801.PMID 10456923.
  5. ^Litwin CM, Johnson JM (July 2005)."Identification, cloning, and expression of the CAMP-like factor autotransporter gene (cfa) of Bartonella henselae".Infect. Immun.73 (7):4205–13.doi:10.1128/IAI.73.7.4205-4213.2005.PMC 1168562.PMID 15972511.
  6. ^"Microbiology Primer: Hemolysis". Archived fromthe original on 2008-12-11. Retrieved2008-12-12.
  7. ^"Streptococcaceae Answers". Archived fromthe original on 2008-10-05. Retrieved2008-12-12.
  8. ^Aryal S (19 April 2016)."CAMP Test- Principle, Uses, Procedure and Result Interpretation".Microbiology Info.com. Retrieved2019-09-04.
  9. ^Anne Hanson (2006-10-09)."CAMP Test Protocols"(PDF).American Society for Microbiology. Archived fromthe original(PDF) on 2023-02-18.
  10. ^Pratiksha Pokhrel (2015-09-24)."Reverse CAMP test for the identification of Clostridium perfringens".Microbiology Notes. Archived fromthe original on 2021-01-24.
  11. ^Ratner HB, Weeks LS, Stratton CW (August 1986)."Evaluation of spot CAMP test for identification of group B streptococci".J. Clin. Microbiol.24 (2):296–7.doi:10.1128/jcm.24.2.296-297.1986.PMC 268893.PMID 3528214.
  12. ^Nsagha DS, Bello CS, Kandakai-Olukemi YT (January 2000)."Hippurate hydrolysis and Christie, Atkins, Munch-Peterson tests as epidemiological diagnostic tools for Streptococcus agalactiae carriage in pregnancy".East Afr Med J.77 (1):34–6.doi:10.4314/eamj.v77i1.46373.PMID 10944837.
  13. ^Valanne S, McDowell A, Ramage G, et al. (May 2005)."CAMP factor homologues in Propionibacterium acnes: a new protein family differentially expressed by types I and II".Microbiology.151 (Pt 5):1369–79.doi:10.1099/mic.0.27788-0.PMID 15870447.
  14. ^Christie, R., Atkins, NE and Munch-Petersen, E. (1944). A note on a lytic phenomenon shown by group B streptococci. Aust. J. Exp. Biol. Med. Sci. 22, 197-200
  15. ^"Streptococci". Retrieved2008-12-12.
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