Common Contaminant
This section covers the characteristics that help identify a common contaminant, Mycobacterium gordonae, and differentiate it from true pathogens
General Principles
- Ubiquitous in the Environment: M. gordonae is widely distributed in the environment, particularly in water sources (tap water, distilled water, etc.). This makes it a common contaminant in clinical specimens
- Low Pathogenicity: M. gordonae is generally considered to be of low pathogenicity, meaning it rarely causes disease in humans. Most isolates represent colonization or contamination rather than true infection
- Clinical Significance: Distinguishing M. gordonae from pathogenic mycobacteria is crucial to avoid unnecessary treatment and anxiety for patients
Mycobacterium gordonae
- Common Name: “Tap water bacillus”
- Clinical Significance: Typically a contaminant; rarely causes disease
- Diseases: Very rarely, M. gordonae has been implicated in pulmonary infections, skin infections, and disseminated infections, primarily in immunocompromised individuals
Acid-Fast Reaction
- Acid-Fast: Strongly acid-fast. Stains readily with carbolfuchsin and resists decolorization with acid-alcohol
Colony Morphology
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Egg-Based Media (e.g., Löwenstein-Jensen)
- Smooth, round, dome-shaped colonies
- Typically produce a deep yellow to orange pigment, even in the dark (scotochromogenic)
- The intensity of the pigment can vary between strains
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Agar-Based Media (e.g., Middlebrook 7H10/7H11)
- Similar to egg-based media, but the colonies may appear slightly more transparent
Differentiation from Pathogenic Mycobacteria
- Clinical Context: The most important factor is the clinical context. M. gordonae is unlikely to be a true pathogen unless there is strong evidence of infection (e.g., consistent isolation from multiple specimens, histopathological evidence of tissue invasion)
- Scotochromogenicity: The deep yellow to orange pigment produced in the dark is a key characteristic. While some other mycobacteria can produce pigment, M. gordonae’s pigment is typically more intense and consistent
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Biochemical Tests
- Tween 80 Hydrolysis: This test differentiates M. gordonae from other scotochromogenic mycobacteria
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Molecular Methods
- PCR and Sequencing: These methods provide definitive identification and can differentiate M. gordonae from closely related species
- Lipid analysis (HPLC): useful in identifying different mycobacteria
When to Suspect Contamination
- Single Positive Culture: A single positive culture of M. gordonae, especially from a non-sterile site (e.g., sputum), is highly suggestive of contamination
- Lack of Clinical Correlation: If the patient has no signs or symptoms of mycobacterial infection, contamination is more likely
- Isolation from Water Sources: If the same strain of M. gordonae is isolated from laboratory water sources, contamination is highly probable
Laboratory Practices to Minimize Contamination
- Sterile Water: Use only sterile, distilled water for media preparation and other laboratory procedures
- Regular Water Testing: Routinely test laboratory water sources for mycobacteria
- Proper Specimen Collection: Emphasize proper specimen collection techniques to minimize environmental contamination
- Quality Control: Implement strict quality control procedures to monitor for contamination in media and reagents
Key Terms
- Contaminant: A microorganism that is unintentionally introduced into a specimen or culture
- Scotochromogen: A microorganism that produces pigment in the dark
- Pathogenicity: The ability of a microorganism to cause disease
- Colonization: The presence of a microorganism on or in a host without causing disease
- Tween 80 Hydrolysis: A biochemical test used to determine the ability of an organism to hydrolyze Tween 80, a nonionic surfactant
- Catalase Test: A biochemical test used to detect the presence of the enzyme catalase, which catalyzes the decomposition of hydrogen peroxide into water and oxygen
- Urease Test: A biochemical test used to determine the ability of an organism to produce the enzyme urease, which hydrolyzes urea into ammonia and carbon dioxide
- PCR (Polymerase Chain Reaction): A molecular biology technique used to amplify specific DNA sequences
- Sequencing: A molecular biology technique used to determine the nucleotide sequence of DNA
- HPLC (High-Performance Liquid Chromatography): An analytical chemistry technique used to separate, identify, and quantify the components in a mixture