Dermatology Made Easy is based on the most popular topics from DermNet NZ's vast array of material. The book combines the essential focus of the ‘Made Easy’ book series with the authority and knowledge base of DermNet NZ's unparalleled resources.
Author: Natasha Lee BSc (Hons), Visiting Medical Student, University of Leeds; Chief Editor: Hon A/Prof Amanda Oakley, Hamilton, New Zealand, August 2014.
Various tests are carried out in a laboratory to establish or confirm the diagnosis of a bacterial skin infection. Although a thorough history and examination of the patient are vital, laboratory tests help the clinician to reach a diagnosis.
Culture of the bacterial species with antibiotic sensitivity testing is considered the gold standard laboratory test.
Skin samples can be collected in the following ways:
Culturing or growing bacteria is most commonly done by brushing the skin swab on sheep blood agar plates and exposing them to different conditions. Which bacteria grow depend on the medium used to culture the specimen, the temperature for incubation, and the amount of oxygen available.
Antibiotic sensitivity testing determines which antibiotics inhibit the growth of the bacteria that have been cultured. This information allows selection of the most suitable antibiotic to treat a particular infection. Antibiotic susceptibility testing is used to determine:
A Gram stain uses a series of stains or dyes on a sample, followed by inspection under a light microscope to detect and identify bacteria as Gram positive or Gram negative. A Gram stain can be done on the original sample, but it is usually done on cultured bacteria after transferring a colony of bacteria from the agar plate to a glass microscope slide.
The Gram stain also identifies the bacterium's shape and behaviour.
*Note palisading/ paralleling of cells in “Chinese lettering” formation
Coagulase is an enzyme produced by certain bacteria that converts fibrinogen to fibrin and is observed as clumping of cells in plasma. The coagulase test differentiates coagulase-positive Staphylococcus aureus from coagulase-negative staphylococci.
Catalase is an enzyme that degrades hydrogen peroxide into hydrogen and oxygen. The bacterial sample is added to a test tube of hydrogen peroxide. The production of bubbles (oxygen) indicates a positive result. The catalase test differentiates catalase-positive staphylococci and micrococci from catalase-negative streptococci.
Blood tests require a sample of blood accessed by a needle from a vein. Examples of those requested for bacterial infection include:
PCR involves isolating and amplifying lengths of bacterial DNA from a sample of skin, blood or other tissue. The DNA is compared to bacterial DNA from known organisms, thus identifying the species. It is useful for slow-growing bacteria such as anaerobic bacteria and mycobacteria (tuberculosis and atypical mycobacteria), as these cannot be cultured by standard methods.
ELISA can test for specific organisms either by detecting bacterial antigen during an infection or antibacterial antibody. The detection of the antibody confirms contact with an organism at some time but it is not necessarily the reason for a current infection.
ELISA is rarely used for the detection of skin bacteria. It may be used to detect:
See the DermNet NZ bookstore
© 2018 DermNet New Zealand Trust.
DermNet NZ does not provide an online consultation service. If you have any concerns with your skin or its treatment, see a dermatologist for advice.