From Medscape Infectious Diseases > Expert Reviews and Commentary

Mycobacteria: September 2006

John G. Bartlett, MD

Published: 09/12/2006

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De Groote MA, Huitt G. Infections due to rapidly growing mycobacteria. Clin Infect Dis. 2006;42:1756-1763.

The authors provide an "invited article" on rapidly growing mycobacteria.

Definition: The simple definition is that these mycobacteria "form mature colonies on solid agar in 7 days (from subculture)." The main clinically important members are Mycobacterium fortuitum, M chelonae, and M abscessus.

Source: These organisms are ubiquitous in nature and found in a wide range of sources including water, soil, rocks, and bioaerosols. They survive harsh environments, and biofilm formation is one of the strategies to do it.

Infection vs Pseudoinfection: Pseudoinfections are common due to contaminated instruments, contaminated solutions, and laboratory cross-contamination. A pseudo-outbreak should be suspected when there is a cluster from laboratory reporting without true evidence of infection or an atypical host.

Infections: Table 1 summarizes 5 categories of infection: (1) catheter infections, (2) keratomileusis, (3) soft tissue, (4) pulmonary, and (5) disseminated disease.

Treatment: Table 2 summarizes the drugs used for the major 3 pathogens in this group. Skin and soft tissue infections are usually treated for 3-6 months with excellent probability of cure, sometimes with assistance of surgical debridement. Pulmonary disease involving M abscessus is generally treated with intermittent intravenous imipenem or cefoxitin plus a macrolide; this infection is rarely "cured." Pulmonary infection due to M fortuitum, by contrast, is often successfully treated with 2-3 antibiotics given for 12-24 months. A common regimen is sulfamethoxazole, moxifloxacin, and minocycline. Drugs selected for skin and soft tissue infections are usually intravenous imipenem or cefoxitin combined with amikacin.

Table 1. Types of Infections Due to Rapidly Growing Mycobacteria

Infection Comment
Catheters And Devices
Intravenous lines Risks -- immunosuppression, catheter duration, prior antibiotics. Remove catheter .
Pocket infections, pacemaker, etc. Usually Mycobacterium abscessus. Remove device .
Dialysis-peritonitis Usually from contaminated solution to sterilize reusable filters.
Laser In Situ Keratomileusis
(LASIK) surgery
Complication of laser surgery. Presents with crystalline opacities in corneal stroma.
Soft Tissue  
Post injection Adrenal cortex injections -- naturopathic treatments
Furunculosis Whirlpool footbaths
Pulmonary Infection Multiple risks defined,* but many infected hosts do not have these.
May cause hypersensitivity pneumonitis requiring removal of patient source.
Disseminated Disease Occurs in immunocompromised patients: organ transplant, HIV, or patients with defects in cytokine pathways.

*Defined risks include: (1) lung diseases: chronic bronchitis, bronchiectasis, pulmonary fibrosis, radiation lung injury, lung cancer; (2) inherited conditions: alpha-1 antitrypsin deficiency, cystic fibrosis, cilia motility disorder; (3) slender body habitus: women with pectus excavatum or scoliosis; (4) prior lung infections or granulomatous disease: histoplasmosis, coccidioidomycosis, sarcoidosis; (5) aspiration; (6) hypersensitivity pneumonitis; and (7) endocrine or immune disorders: panhypopituitarism, Cushing disease, or gamma-interferon or interleukin-12 deficiency.

Table 2. Antimicrobials Used to Treat the 3 Major Pathogens of Rapidly Growing Mycobacteria

Agent Regimen Mycobacterium abscessus Mycobacterium chelonae Mycobacterium fortuitum
Clarithromycin 500 mg bid po + + +
Azithromycin 250-500 mg qd po + + +
Doxycycline 100 mg bid po + + +
Minocycline 100 mg bid po + + +
Ciprofloxacin 500-750 mg bid po + + +
Cefoxitin 1-2 gm q 6-8 h IV + -- --
Imipenem 1 gm q 12 h IV + + --
Amikacin 12-15 mg/kg 3x/wk IV + -- --
Tobramycin 2.5 mg/kg q 12 h IV -- + --
Linezolid 600 mg/d IV/po -- + --
Tigecycline 50 mg bid IV -- + --

3x/wk = 3 times per week; bid = twice daily; h = hours; IV = intravenous; po = by mouth; q 6-8 h = every 6-8 hours; q 12 h = every 12 hours; qd = once daily.

Authors and Disclosures

John G. Bartlett, MD, Professor of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland

Disclosure: John G. Bartlett, MD, has disclosed that he has served on the HIV advisory board for Bristol-Myers Squibb, Abbott, and GlaxoSmithKline.

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Authors and Disclosures

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