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Test Code MMLSA Antimicrobial Susceptibility, Anaerobic Bacteria, Minimal Inhibitory Concentration, Varies

Infectious

Reporting Name

Susceptibility, Anaerobic, MIC

Useful For

Determining the in vitro susceptibility on isolates of anaerobic bacteria involved in human infections

 

Directing antimicrobial therapy for anaerobic bacterial infections

Additional Tests

Test ID Reporting Name Available Separately Always Performed
BATTA Anaerobe Suscep Battery No Yes

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
ANAID Anaerobe Ident No, (Bill Only) No
RMALA Id MALDI-TOF Mass Spec Anaerobe No, (Bill Only) No
ISAN Anaerobe Ident by Sequencing No, (Bill Only) No
PCRID Identification by PCR No, (Bill Only) No
BLA Beta Lactamase No, (Bill Only) No
SANA Anaerobe Suscep per agent No, (Bill Only) No
ANIDE Organism Ref for ID, Anaerobic Bact Yes No
MECAB mecA PCR Test, Bill Only No, (Bill Only) No

Testing Algorithm

When this test is ordered, the reflex tests may be performed at an additional charge. All anaerobic bacterial organisms recovered will automatically have susceptibility testing performed and billed as appropriate. Antimicrobial agents appropriate to the organism and specimen source will be tested according to Mayo Clinic's practice and the laboratory's standard operating procedures.

 

For a listing of the antimicrobials routinely tested in this laboratory as well as antimicrobials that may be tested upon request, see Anaerobic Bacteria Antimicrobials. If the organism or antimicrobial agent of interest is not listed in this table, call 800-533-1710 and ask to speak to the Bacteriology Anaerobe Laboratory.

 

If organism identification is not provided within 72 hours of specimen receipt, referred anaerobic bacteria identification will be performed at an additional charge.

Method Name

Minimal Inhibitory Concentration (MIC) by Agar Dilution

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Varies


Shipping Instructions


For shipping information, see Infectious Specimen Shipping Guidelines.



Necessary Information


Organism identification and specimen source are required.



Specimen Required


Specimen Type: Organism in pure culture

Acceptable Sources: Isolates from blood cultures, bone and joint infections, or brain abscesses, and organisms isolated in pure culture from other sources

Supplies:

Anaerobic Transport Tube (T588)

Infectious Container, Large (T146)

Container/Tube:

Preferred: Anaerobic transport tube

Acceptable: Thioglycollate broth or any other suitable anaerobic transport system

Collection Instructions :

1. Organism must be in pure culture and actively growing. Do not submit mixed cultures.

2. Place specimen in a large infectious container and label as an etiologic agent/infectious substance if appropriate


Specimen Minimum Volume

See Specimen Required

Specimen Stability Information

Specimen Type Temperature Time Special Container
Varies Ambient

Reject Due To

Agar plate Reject

Reference Values

Susceptibility results are reported as minimal inhibitory concentration (MIC) in mcg/mL. Breakpoints (also known as clinical breakpoints) are used to categorize an organism as susceptible, susceptible-dose dependent, intermediate, resistant, or nonsusceptible according to breakpoint setting organizations, either the Clinical and Laboratory Standards Institute (CLSI) or the European Committee on Antimicrobial Susceptibility Testing (EUCAST), as applicable.

 

In some instances, an interpretive category cannot be provided based on available data; therefore, the following comment will be included on the report: There are no established interpretive guidelines for agents reported without interpretations.

 

For information regarding CLSI and EUCAST susceptibility interpretations, see Susceptibility Interpretative Category Definitions.

Day(s) Performed

Monday through Sunday

CPT Code Information

87186-Antimicrobial Susceptibility, Anaerobic Bacteria, MIC

87076-Organism Ref for ID, Anaerobic Bact (if appropriate)

87076-Anaerobe Ident (if appropriate)

87076-Id MALDI-TOF Mass Spec Anaerobe (if appropriate)

87153-Anaerobe ident by sequencing (if appropriate)

87150-Identification by PCR (if appropriate)

87185-Beta Lactamase (if appropriate)

87181-Anaerobe Susceptibility per Agent (if appropriate)

87150-mecA PCR (if appropriate)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
MMLSA Susceptibility, Anaerobic, MIC 50545-3

 

Result ID Test Result Name Result LOINC Value
MMLSA Susceptibility, Anaerobic, MIC 50545-3

Clinical Information

Anaerobic bacteria are the greatest component of the human body's normal bacterial flora. Anaerobic bacteria colonize the skin, oral cavity, and genitourinary and lower gastrointestinal tracts and generally do not cause infection. Their presence is important for vitamin and other nutrient absorption and in preventing infection with disease-causing bacteria.

 

When usual skin and mucosal barriers are compromised, in an anaerobic environment, these bacteria can behave as pathogens. Typical anaerobic infections include periodontitis, abdominal or pelvic abscesses, endometritis, pelvic inflammatory disease, aspiration pneumonia, empyema and lung abscesses, sinusitis, brain abscesses, gas gangrene, and other soft tissue infections.

 

Anaerobic bacteria grow aggressively in the body under anaerobic conditions and may possess a variety of virulence factors, including capsules and extracellular enzymes. They also can develop resistance to antimicrobials by producing beta-lactamase and other modifying enzymes, and by alterations in membrane permeability and structure of penicillin-binding proteins. Susceptibility testing results are useful to clinicians because anaerobic bacteria are a significant cause of human infection, and they are often resistant to commonly used antimicrobials. Bacteroides and Parabacteroides species produce beta-lactamases. Ertapenem, metronidazole, and clindamycin are generally effective agents, although resistance to clindamycin, and occasionally ertapenem, is increasing.

 

The minimal inhibitory concentration (MIC) obtained during antimicrobial susceptibility testing is helpful in indicating the concentration of antimicrobial agent required at the site of infection necessary to inhibit the infecting organism. For each organism-antimicrobial agent combination, the Clinical and Laboratory Standards Institute and/or the European Committee on Antimicrobial Susceptibility Testing provides interpretive criteria for determining whether the MIC should be interpreted as susceptible, susceptible dose dependent, intermediate, nonsusceptible, resistant, or epidemiological cutoff value.

Interpretation

A "susceptible" category result and a low minimal inhibitory concentration value indicates in vitro susceptibility of the organism to the antimicrobial tested.

 

For interpretation of various antimicrobial susceptibility interpretive categories (ie, susceptible, intermediate, resistant, or epidemiological cutoff value), see Reference Values.

Cautions

In vitro susceptibility does not guarantee clinical response. Therefore, the decision to treat with a particular agent should not be based solely on the antimicrobial susceptibility testing result.

Method Description

An agar dilution method is used for routine testing. The antimicrobial is added to agar in various concentrations depending upon levels attainable in serum. A standardized suspension of the organism is applied to the agar plates, which are incubated anaerobically for 42 to 48 hours at 35 to 37° C. The end point is that in which a marked reduction occurs in the appearance of growth on the test plate as compared to that of growth on the control plate. Examples of marked change include a change from confluent growth to a haze, less than 10 tiny colonies, or 1 to 3 normal-sized colonies.(Clinical and Laboratory Standards Institute [CLSI]: Methods for Antimicrobial Susceptibility Testing of Anaerobic Bacteria. 9th ed. CLSI standard M11. CLSI; 2018)

Report Available

8 to 14 days

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.