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Mycobacterium fortuitum

Mycobacterium fortuitum is a rapidly growing nontuberculous mycobacterium (NTM) classified within Runyon group IV, characterized by its environmental ubiquity in soil, water, and dust worldwide.^[1] This aerobic, non-spore-forming, Gram-positive bacterium grows on solid media within one week, distinguishing it from slower-growing mycobacteria like M. tuberculosis.^[2] Originally isolated from frogs and initially named M. ranae, it encompasses at least 50 identified strains and is part of the M. fortuitum complex, which includes related species like M. peregrinum.^[1] As an opportunistic pathogen, M. fortuitum primarily causes infections in immunocompetent individuals following trauma or exposure to contaminated sources, rather than through person-to-person transmission.^[3] It accounts for up to 15% of rapidly growing mycobacteria (RGM) isolates in the United States, with no specific endemic regions or predilections based on sex, race, or geography.^[2] Outbreaks have been linked to contaminated water in settings such as pedicure footbaths, whirlpools, tattoo inks, and surgical procedures, highlighting its role in healthcare-associated infections.^[1] The increasing isolation rates reflect greater awareness and environmental persistence rather than rising incidence.^[4] Clinically, M. fortuitum most commonly manifests as skin and soft tissue infections, often presenting as abscesses or cellulitis after minor trauma or surgery, and can involve bones or joints in disseminated cases.^[2] Pulmonary disease, though rarer, occurs predominantly in patients with underlying lung conditions such as prior tuberculosis, interstitial lung disease, or chronic aspiration, where it may lead to cavitary or nodular lesions.^[4] It is also implicated in infections related to prosthetic devices and catheters, underscoring its significance in post-surgical wound complications.^[1] The nonchromogenic nature of its colonies and broad in vitro susceptibility to agents like fluoroquinolones and imipenem aid in its identification and management.^[2]

Overview and Taxonomy

General Characteristics

Mycobacterium fortuitum is a species of nontuberculous mycobacteria, named in 1938 by José da Costa Cruz after isolating it from pus in a leg abscess of a Brazilian patient following subcutaneous injections; the name reflects the fortuitous nature of the discovery. The species was first isolated from frogs in 1905 and named M. ranae (now a synonym).^[5]^[6] This bacterium belongs to the phylum Actinomycetota and is classified as a rapidly growing mycobacterium (RGM) within Runyon Group IV, characterized by visible colony growth within 3 to 7 days on standard laboratory media.^[7]^[8] As an environmental opportunist, M. fortuitum is ubiquitous worldwide in natural and man-made settings such as water, soil, and dust, where it persists as a saprophyte.^[9] It manifests as acid-fast, non-spore-forming rods and is strictly aerobic, catalase-positive, distinguishing it from the causative agent of tuberculosis, Mycobacterium tuberculosis.^[10]^[11] While generally non-pathogenic, it can cause opportunistic infections in humans, most commonly affecting skin and soft tissues, but also leading to pulmonary or disseminated disease, particularly in individuals with predisposing factors like trauma or immunosuppression.^[3]

Taxonomic Classification

Mycobacterium fortuitum belongs to the phylum Actinomycetota, class Actinomycetia, order Mycobacteriales, family Mycobacteriaceae, and genus Mycobacterium.^[12]^[13] The species M. fortuitum encompasses two recognized subspecies: M. fortuitum subsp. fortuitum and M. fortuitum subsp. acetamidolyticum.^[12] The latter was established based on distinct phenotypic traits, including acetamide hydrolysis and intermediate growth rates compared to the nominate subspecies.^[14] Historically, the third biovariant complex within M. fortuitum—comprising sorbitol-negative and sorbitol-positive strains—was reclassified in 2004 into four novel species: Mycobacterium boenickei, Mycobacterium houstonense, Mycobacterium neworleansense, and Mycobacterium brisbanense, using a polyphasic approach involving 16S rRNA gene sequencing, DNA-DNA hybridization, and biochemical profiles.^[15] Identification of M. fortuitum often relies on sequencing the 16S rRNA gene, which provides phylogenetic resolution within the genus.^[16] Genomes of M. fortuitum type strains measure approximately 6.3 Mb with a G+C content of 66%, consistent with other rapidly growing mycobacteria (RGMs).^[17] This species is nonchromogenic and clusters phylogenetically with other RGMs such as M. abscessus and M. chelonae in Runyon group IV, distinguished by its rapid growth.^[1] The type strain is ATCC 6841 (equivalent to DSM 46621, CIP 104534, and JCM 6387), originally isolated from a human cold abscess.^[18]^[12]

Microbiology and Habitat

Morphological and Growth Properties

Mycobacterium fortuitum is a slender, rod-shaped bacterium, typically measuring 1–3 μm in length and 0.2–0.4 μm in width. It is nonmotile and non-spore-forming, with a lipid-rich cell wall that renders it Gram-positive but resistant to standard Gram staining, resulting in poor visualization. The bacterium is acid-fast, staining positively with the Ziehl-Neelsen method due to the presence of mycolic acids in its cell wall.^[19]^[5]^[2] In laboratory culture, M. fortuitum produces smooth, nonpigmented colonies that appear cream-white or buff-colored, often reaching 1–2 mm in diameter. These colonies form rapidly, typically within 3–5 days on solid media. Rough colonial variants can also occur, reflecting phenotypic diversity among isolates.^[20]^[2] As a member of the rapidly growing mycobacteria group, M. fortuitum exhibits accelerated proliferation compared to slow-growing species like M. tuberculosis, which require 2–6 weeks for visible colony development; in contrast, M. fortuitum achieves detectable growth in 3–7 days. Optimal cultivation occurs at 28–37°C on enriched media such as Löwenstein-Jensen or Middlebrook 7H10/7H11 agars, with no growth observed at 5°C, though some strains grow up to 45°C. The bacterium is strictly aerobic, showing no microaerophilic adaptation, and demonstrates tolerance to 5% NaCl, enabling growth in saline-supplemented environments.^[5]^[21]^[22]

Biochemical and Genetic Features

Mycobacterium fortuitum exhibits distinct biochemical properties that facilitate its identification among rapidly growing mycobacteria (RGMs). It is positive for catalase activity, including heat-stable catalase at 68°C, which decomposes hydrogen peroxide into water and oxygen, aiding in differentiation from slow-growing species. Urease activity is also positive, hydrolyzing urea to ammonia and carbon dioxide, producing a detectable pH change. Nitrate reduction is positive, converting nitrate to nitrite via enzymatic action. Pyrazinamidase activity is variable, hydrolyzing pyrazinamide to pyrazinoic acid inconsistently across strains. In contrast, niacin production is negative, with no accumulation of nicotinic acid detectable in culture extracts, and Tween 80 hydrolysis is variable, with some strains showing degradation of the emulsifier polyoxyethylene sorbitan monooleate. Additionally, M. fortuitum does not produce pigmentation and is classified as scotochromogen-negative, forming non-pigmented colonies regardless of light exposure.^[23]^[24]^[25] Intrinsic antibiotic susceptibility patterns further characterize M. fortuitum and distinguish it from other RGMs. The species demonstrates inherent resistance to pyrazinamide due to limited conversion to its active form, pyrazinoic acid, rendering standard antituberculous agents ineffective and highlighting its opportunistic nature. This resistance profile, combined with variable susceptibility to other drugs like macrolides via inducible erm genes, is crucial for species-level differentiation within RGMs.^[26]^[27] Genetic identification relies on molecular techniques targeting conserved genes. Polymerase chain reaction (PCR) amplification and sequencing of the 16S rRNA gene provide broad phylogenetic placement, while hsp65 and rpoB genes offer higher resolution for species confirmation, achieving identification rates exceeding 80% in clinical isolates. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) enables rapid proteomic profiling after cell wall disruption, correlating spectral patterns with M. fortuitum databases for accurate, same-day identification.^[28]^[29]^[30] Virulence in M. fortuitum is linked to genes maintaining cell wall integrity, notably mmpL4, which encodes a membrane protein transporter essential for exporting lipids such as glycopeptidolipids to the outer membrane. This export process reinforces the lipid-rich cell wall, enhancing resistance to host defenses and environmental stresses, thereby contributing to pathogenesis in opportunistic infections.^[31]^[32]

Natural Habitat and Distribution

Mycobacterium fortuitum is a ubiquitous environmental bacterium primarily found in natural and man-made water systems, including freshwater bodies such as rivers, lakes, and groundwater, as well as soil, dust, and sewage. It thrives in low-nutrient conditions and has been isolated from tap water, municipal water distribution systems, and biofilms within plumbing infrastructure. These habitats provide ideal conditions for its persistence as a saprophytic organism, with frequent detections in household plumbing, showerheads, and hospital water networks.^[33]^[34] The bacterium exhibits robust survival adaptations that enable its persistence in diverse environments. It forms protective biofilms in water pipes and surfaces, which shield it from environmental stresses and antimicrobial agents. M. fortuitum demonstrates significant resistance to disinfectants, including chlorine at concentrations up to 2 μg/ml free chlorine, where it can survive exposure for 60 minutes with up to 60% viability; this resistance is enhanced in low-nutrient media typical of drinking water. Additionally, it tolerates desiccation, moderate temperatures, and interactions with protozoa, further aiding its environmental resilience; its rapid growth rate contributes to this persistence by allowing quick colonization of new niches. Recent genomic studies (as of 2024) have identified genes contributing to biofilm formation and enhanced resistance to disinfectants, aiding its persistence in water systems.^[35]^[34]^[33]^[36] Globally distributed, M. fortuitum occurs worldwide without specific endemic hotspots, though isolation rates are higher in temperate regions and urban water systems. It has been reported across continents, including North America (e.g., United States, Mexico), Europe (e.g., Netherlands, Finland), Asia (e.g., India, Afghanistan), Africa (e.g., Zambia, Malawi, South Africa), and Australia. Recent studies up to 2024 highlight its continued prevalence in aquatic environments, such as fishponds and hospital supplies, underscoring ongoing environmental detections.^[33]^[34]^[37] Beyond water and soil, M. fortuitum is associated with non-human sources, including animals like fish (e.g., goldfish, common bass), pigs, camels, manatees, and earthworms, as well as plants in aquarium settings and peat-rich soils. While it can cause infections in these hosts, it primarily functions as an environmental saprophyte rather than a obligate pathogen.^[37]^[33]

Pathogenesis and Epidemiology

Mechanisms of Infection

Mycobacterium fortuitum primarily gains entry into the human body through breaches in the skin or mucous membranes caused by trauma, surgical procedures, or contaminated medical devices such as catheters and prosthetic implants, with additional routes including inhalation of aerosolized particles from environmental sources like water systems.^[38] Unlike tuberculous mycobacteria, infections are opportunistic and do not involve person-to-person transmission, relying instead on environmental exposure to initiate colonization in susceptible hosts.^[39] Key virulence factors enabling persistence include the bacterium's thick, lipid-rich cell wall composed of mycolic acids and arabinogalactan, which resists degradation and impairs phagocytosis by host macrophages, allowing initial survival within phagosomes.^[40] Additionally, M. fortuitum possesses type VII secretion systems, notably ESX-1, which export effector proteins homologous to ESAT-6 that disrupt phagosomal membranes, facilitating escape into the cytosol and evasion of lysosomal fusion.^[41] Genes such as phoP, relA, and icl further contribute to stress tolerance and intracellular persistence by regulating adaptive responses to host oxidative and nutrient stresses.^[41] The pathogen evades innate immunity by inhibiting interferon-gamma (IFN-γ)-induced signaling in macrophages, notably restricting nitric oxide (NO) production to levels insufficient for bacterial killing (3.9–4.8 μM versus 23.1–37.7 μM in controls), thereby limiting phagosome-lysosome fusion to approximately 45% compared to over 75% for avirulent strains.^[42] This results in disorganized granuloma formation, where infected macrophages aggregate but fail to fully contain the bacteria, mirroring but less structured than tuberculous responses.^[43] Biofilm formation, mediated by factors like FabG4 in lipid biosynthesis, enhances chronicity by creating protective matrices on host tissues and devices, promoting intracellular survival in non-phagocytic cells such as epithelial layers.^[44]^[45] Infection susceptibility is heightened by host factors including immunosuppression from conditions like HIV or corticosteroid therapy, which impair macrophage activation and granuloma integrity, as well as physical barrier disruptions from trauma or underlying lung diseases such as cystic fibrosis. Emerging risks include post-COVID-19 immunosuppression, as noted in case reports of coinfections as of 2025.^[46]^[47]^[48] These elements collectively enable M. fortuitum to establish persistent, low-grade infections in otherwise resilient tissues.

Clinical Manifestations and Risk Factors

Mycobacterium fortuitum primarily causes localized skin and soft tissue infections, often presenting as abscesses, cellulitis, nodules, or ulcers following trauma or surgical procedures.^[49] These infections typically manifest as single erythematous papules that progress to fluctuant, painful boils or draining sinuses over weeks to months.^[50] Osteomyelitis and arthritis are common musculoskeletal complications, particularly after penetrating injuries or joint surgeries, with tenosynovitis and spondylodiscitis occurring less frequently.^[51] Ocular involvement, such as keratitis or corneal ulcers, arises from direct trauma to the eye.^[50] Pulmonary disease is observed in patients with pre-existing structural lung damage, including chronic obstructive pulmonary disease (COPD) or post-gastrectomy states leading to aspiration, and may present with migratory infiltrates, cough, sputum production, or hemoptysis.^[52] The incubation period varies from days to months, with infections becoming chronic if untreated.^[19] Rare manifestations include disseminated disease in immunocompromised individuals, such as those with transplants, chemotherapy, or HIV, often involving catheter-related bacteremia or multiple organ involvement.^[53] Endocarditis is an uncommon but serious complication, typically affecting prosthetic heart valves.^[54] Key risk factors encompass trauma, surgical interventions, and nosocomial exposure to contaminated water or injectables, which facilitate bacterial entry through breaches in the skin or mucosa.^[49] Immunosuppression heightens susceptibility to severe or widespread infections, while chronic lung conditions predispose to respiratory involvement.^[52] Recent trends indicate increasing cases linked to cosmetic procedures, such as mesotherapy, with outbreaks reported in Asia and Latin America due to contaminated equipment or solutions, resulting in clusters of cutaneous abscesses and nodules.^[55]^[56]

Epidemiological Patterns

Mycobacterium fortuitum infections are rare overall, representing approximately 0.1-0.5% of all nontuberculous mycobacterial (NTM) cases globally, though it accounts for up to 15% of rapidly growing mycobacteria (RGM) isolates in the United States.^[1] In pulmonary disease, M. fortuitum is an uncommon cause, comprising about 5-10% of RGM-associated lung infections, with one study identifying it in only 40 out of 6,800 patients tested for acid-fast bacilli.^[1] Incidence is higher in endemic regions such as India and Brazil, particularly for skin and soft-tissue infections, where M. fortuitum constitutes around 31.5% of RGM cases in reviewed reports from these areas.^[57]^[58] Outbreaks of M. fortuitum are typically nosocomial or community-associated, often linked to contaminated medical devices or water sources. Notable examples include a 2004 outbreak in the United States involving over 100 cases of furunculosis from pedicure whirlpools at nail salons, and a cluster of 17 prosthetic joint infections in 2025 traced to surgical site contamination during hip and knee procedures.^[59]^[60] Other clusters have arisen from hemodialyzers, ice machines, bronchoscopes, and tattoo inks, highlighting the role of waterborne dissemination in healthcare and cosmetic settings.^[61]^[62]^[63] Transmission occurs primarily through environmental exposure rather than airborne spread like tuberculosis, with M. fortuitum entering via trauma, surgery, or contact with contaminated water and soil.^[64] It thrives in biofilms within water systems, resisting chlorination, and cases show seasonal peaks in warm months, lagging 2-6 weeks behind rainfall increases, often tied to heightened water-related activities.^[34]^[65] Vulnerable populations include the elderly, diabetics, post-surgical patients, and immunocompromised individuals, with children also at risk for lymphadenitis.^[1] Infections are underreported in developing countries due to limited diagnostic capabilities.^[66] Case reports of coinfections with SARS-CoV-2 have been documented as of 2025.^[48]

Diagnosis and Management

Diagnostic Techniques

Diagnosis of Mycobacterium fortuitum infections relies on a combination of clinical suspicion and laboratory confirmation, with specimen collection tailored to the infection site. Common specimens include pus from abscesses or wounds, tissue biopsies from skin or soft tissue lesions, sputum for pulmonary cases, and blood cultures for disseminated disease.^[67]^[68] These samples undergo decontamination using N-acetyl-L-cysteine-sodium hydroxide (NALC-NaOH) at a concentration of 0.25-2% to reduce contaminating flora while minimizing damage to mycobacteria, particularly important for rapidly growing mycobacteria (RGMs) that are more susceptible to harsh processing.^[69]^[68] The rapid growth properties of M. fortuitum aid in culture recovery post-decontamination compared to slower-growing nontuberculous mycobacteria (NTM).^[70] Microscopic examination begins with acid-fast bacilli (AFB) smears using fluorochrome or Ziehl-Neelsen staining to detect mycobacteria, providing a rapid preliminary indication of infection.^[68] However, AFB smears exhibit low sensitivity for RGMs such as M. fortuitum, often below 50-60% due to lower organism burdens in clinical specimens compared to Mycobacterium tuberculosis.^[71]^[72] Culture remains the cornerstone for definitive diagnosis, employing automated liquid systems like the Mycobacteria Growth Indicator Tube (MGIT) or solid media such as Lowenstein-Jensen agar, with M. fortuitum typically detectable in 3-7 days at 28-37°C incubation.^[70]^[69] Once growth occurs, species identification proceeds via traditional biochemical tests (e.g., nitrate reduction, iron uptake) or commercial molecular probes targeting ribosomal RNA.^[68]^[73] Advanced molecular diagnostics enhance specificity and speed, particularly for distinguishing M. fortuitum from M. tuberculosis. The GeneXpert MTB/RIF assay, designed for tuberculosis detection, yields negative results for NTM like M. fortuitum, prompting further testing.^[74] Polymerase chain reaction (PCR) targeting the hsp65 gene, followed by sequencing or restriction enzyme analysis, provides accurate species-level identification.^[75]^[68] Next-generation sequencing (NGS) is increasingly utilized for comprehensive resistance profiling, detecting mutations associated with antimicrobial resistance in clinical isolates.^[76] Imaging modalities support diagnosis by delineating disease extent, with computed tomography (CT) or magnetic resonance imaging (MRI) revealing pulmonary nodules, cavitary lesions, or osteoarticular involvement such as vertebral abscesses in M. fortuitum cases.^[77]^[78] Histopathologic examination of biopsies often shows granulomatous inflammation with detectable AFB, confirming mycobacterial etiology when correlated with culture results.^[68]^[79] Key challenges in diagnosing M. fortuitum include its clinical and radiographic mimicry of tuberculosis or other NTM infections, leading to potential misdiagnosis without species-specific identification.^[68] The American Thoracic Society/Infectious Diseases Society of America (ATS/IDSA) guidelines stress the importance of rapid species identification through molecular methods to differentiate RGMs and inform appropriate management, as delays can complicate outcomes in healthcare-associated outbreaks.^[68]^[69]

Treatment Strategies

Mycobacterium fortuitum exhibits a characteristic susceptibility profile among rapidly growing mycobacteria, generally showing sensitivity to amikacin, cefoxitin, ciprofloxacin, linezolid, and trimethoprim-sulfamethoxazole (TMP-SMX), while demonstrating intrinsic resistance to isoniazid and rifampin.^[3]^[80]^[81] Susceptibility testing is essential to guide therapy due to variability in isolate responses.^[3] Treatment regimens typically involve dual antibiotic therapy to minimize resistance development, such as amikacin combined with ciprofloxacin for initial intravenous (IV) administration in severe cases, transitioning to oral agents like ciprofloxacin or TMP-SMX for milder infections.^[80]^[3] Duration is generally 4-6 months for skin and soft tissue infections, with a minimum of 12 months recommended for osteomyelitis or disseminated disease to ensure sustained clearance.^[80]^[3] Surgical intervention plays a critical role, particularly debridement for abscesses and biofilms in localized infections, with total excision reserved for refractory cases involving extensive tissue involvement or foreign bodies.^[80]^[3] Removal of prosthetic materials or catheters is often necessary to eradicate biofilms.^[80] Resistance trends include emerging inducible clarithromycin resistance mediated by the erm(39) gene, necessitating routine susceptibility testing as per updates in NTM management from 2019-2024.^[82]^[83] Monitoring for macrolide resistance is particularly important, as initial susceptibility may not predict long-term efficacy.^[82] Clinical outcomes with combined medical and surgical therapy yield cure rates of 80-95%, though relapse is common with monotherapy or inadequate duration.^[84]^[80] Success is higher in non-disseminated cases treated promptly.^[84] The American Thoracic Society (ATS) and Infectious Diseases Society of America (IDSA) 2020 guidelines for nontuberculous mycobacteria (NTMs) emphasize personalized drug susceptibility testing (DST) to tailor regimens for rapidly growing species like M. fortuitum.^[69]^[85]

Prevention and Control

Preventing infections caused by Mycobacterium fortuitum, a rapidly growing nontuberculous mycobacterium (NTM), primarily involves mitigating exposure to contaminated water and environmental sources in healthcare and community settings. In hospitals, implementing comprehensive water management programs is essential to reduce the risk of nosocomial transmission, as M. fortuitum thrives in aqueous environments like plumbing systems, faucets, and showerheads. These programs include regular monitoring and maintenance to prevent water stagnation, which fosters bacterial growth. Filtration systems, such as point-of-use membrane filters, have been shown to effectively limit exposure to rapidly growing mycobacteria in potable water supplies, particularly in vulnerable populations like residents of skilled nursing facilities. Additionally, ultraviolet (UV) treatment, including pulsed-xenon UV light, demonstrates high efficacy in reducing M. fortuitum viability on surfaces and in water, offering a practical disinfection method for healthcare facilities. Avoiding the use of tap water or non-sterile ice during invasive procedures, such as injections or catheter insertions, further minimizes contamination risks from potentially harboring M. fortuitum. Contaminated medical devices, including injectables and heater-cooler units, should be avoided or rigorously sterilized according to manufacturer guidelines to prevent outbreaks. Infection prevention strategies emphasize strict adherence to sterile techniques during high-risk procedures. In surgical settings, maintaining aseptic protocols and avoiding exposure of wounds or injection sites to tap water are critical, as M. fortuitum can colonize surgical sites through contaminated irrigation solutions or equipment. For aesthetic procedures like pedicures, using properly disinfected whirlpool footbaths and advising against leg shaving prior to treatment reduces skin breaches that facilitate bacterial entry, as evidenced by outbreaks linked to inadequate salon hygiene. Screening high-risk patients, such as immunocompromised individuals undergoing dialysis or chemotherapy, for prior environmental exposures can guide targeted precautions, though routine screening is not universally recommended due to the opportunistic nature of infections. Outbreak management requires prompt identification and intervention to contain clusters of M. fortuitum infections. Upon detection of cases, healthcare facilities should initiate contact tracing to identify shared exposures, such as common water sources or procedures, and collaborate with public health departments for investigation. For water systems implicated in transmission, hyperchlorination exceeding 2 ppm, combined with flushing and filtration, has been effective in inactivating atypical mycobacteria, though M. fortuitum's resistance necessitates higher concentrations and validation of residual levels. Surveillance of healthcare-associated infections, including reporting clusters to infection control teams, enables early source remediation and prevents wider spread. Public health measures focus on education and surveillance to curb community-acquired infections. Healthcare providers and the public should be educated on proper trauma care to avoid contamination from soil or water during wound management, as M. fortuitum is ubiquitous in natural environments. In endemic areas, enhanced surveillance for NTM infections supports trend monitoring and resource allocation, with no vaccine currently available for prevention. Recent advances up to 2025 include biofilm-disrupting protocols tailored for high-risk settings like dialysis units, where M. fortuitum peritonitis has been reported. Humanized monoclonal antibodies targeting bacterial DNABII proteins rapidly disperse NTM biofilms, enhancing susceptibility to disinfectants and antibiotics in preclinical models, with potential applications in peritoneal dialysis systems. Additionally, a 2025 outbreak investigation in a Tennessee surgery center underscored the need for stricter oversight in outpatient facilities, leading to updated infection prevention protocols emphasizing regular water testing and staff training.

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A protective immune response against pathogenic mycobacterial infections is dependent on the granuloma formation. Within the granuloma, the macrophage ...Missing: evasion | Show results with:evasion
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Mycobacterium fortuitum fabG4 knockdown studies: Implication as ...
Jun 23, 2022 · MFfabG4 knockdown resulted in diminished pellicle and attenuated biofilm formation, along with impaired sliding motility, and reduced cell ...
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Mycobacterium biofilms - PMC - NIH
Feb 7, 2023 · A majority of the species of the genus Mycobacterium (probably almost all of them) can form biofilms, both in vitro and, probably, in vivo.
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Disseminated Coinfection by Mycobacterium fortuitum and ... - NIH
Sep 7, 2021 · Mycobacterium fortuitum is a rapidly growing non-tuberculous mycobacterium (NTM) with weak pathogenicity. Here, we present a rare case of ...Missing: growth | Show results with:growth
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CFTR Depletion Confers Hypersusceptibility to Mycobacterium ...
Jul 16, 2020 · Using the zebrafish model, we show that embryos are susceptible to M. fortuitum infection in a dose-dependent manner.
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Cutaneous Mycobacterial Infections | Clinical Microbiology Reviews
Nov 14, 2018 · Mycobacteria may seed the skin and soft tissues during systemic dissemination in immunosuppressed individuals (24, 25, 37, 42–44). There is some ...
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Mycobacterium Fortuitum Clinical Presentation - Medscape Reference
Dec 6, 2024 · Eye: Keratitis or corneal ulcers may be present. Lungs: Rales or rhonchi may be present. Heart: Valvular murmur with endocarditis may be present ...
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Clinical manifestations and outcomes of musculoskeletal ... - PubMed
Jul 27, 2019 · The most common MSK manifestation was arthritis (61%), followed by osteomyelitis (50%), tenosynovitis (25%), and spondylodiscitis (14%).
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Natural history of Mycobacterium fortuitum pulmonary infection ...
Jan 2, 2018 · Mycobacterium fortuitum is one of the rapidly growing mycobacteria, which are mainly present in soil and water [6, 7]. M. fortuitum mainly ...Missing: habitat | Show results with:habitat
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Disseminated infection with rapidly growing mycobacteria - PubMed
Disseminated infection with the rapidly growing mycobacteria Mycobacterium chelonae and Mycobacterium fortuitum is uncommon. Only eight cases were diagnosed ...
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Mycobacterium fortuitum complex endocarditis-case report and ...
Here we present a case of a female who developed an endocarditis due to Mycobacterium chelonae after valve replacement as well as a review of the literature.Missing: osteomyelitis keratitis
[52]
Mesotherapy and cutaneous Mycobacterium fortuitum infection
This case demonstrates the importance of suspecting mycobacterial etiology in patients with nodules and abscesses in the areas of mesotherapy treatment.Missing: outbreaks procedures
[53]
Clinical Management of Rapidly Growing Mycobacterial Cutaneous ...
Cutaneous infections are the most commonly cited complication of mesotherapy and are mainly related to rapidly growing mycobacteria (RGM). There are increasing ...
[54]
Skin and Soft-Tissue Infections Due to Rapidly Growing Mycobacteria
Rapidly growing mycobacteria (RGM) are increasingly being recognized as potential pathogens. RGM, particularly Mycobacterium abscessus, Mycobacterium ...
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Epidemic of Postsurgical Infections Caused by Mycobacterium ... - NIH
In Brazil, outbreaks caused by RGM have been detected since 1998, mainly in the cities of Rio de Janeiro and São Paulo. Eight outbreaks following laser in situ ...Primary Isolation Of... · Results · Clonal Diversity
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An Outbreak of Mycobacterial Furunculosis Associated with ...
We identified a large outbreak of rapidly growing mycobacterial infections among persons who had had footbaths and pedicures at one nail salon.
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Investigation of a Mycobacterium fortuitum prosthetic joint infection ...
Oct 14, 2025 · This study outlines the investigation into an outbreak of Mycobacterium fortuitum infections involving 17 cases undergoing hip or knee surgeries ...Missing: incidence | Show results with:incidence
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Nosocomial outbreaks/pseudo-outbreaks caused by nontuberculous ...
Disease outbreaks usually involve sternal wound infections, plastic surgery wound infections, or postinjection abscesses. Pseudo-outbreaks most commonly relate ...
[59]
Nosocomial Mycobacterium fortuitum Colonization from a ...
Nov 3, 1987 · M. fortuitum was isolated only from the ice machine in Ward 8A. The ice machine was disconnected, and no additional patients became colonized.
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Outbreak of Nontuberculous Mycobacteria Joint Prosthesis ... - CDC
Mar 14, 2019 · We investigated a cluster of Mycobacterium fortuitum and M. goodii prosthetic joint surgical site infections occurring during 2010–2014.
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[PDF] mycobacteria: drinking water fact sheet | epa
Mycobacteria are rod-shaped bacteria, with over 20 species causing disease, found in various water sources, and are transmitted from environmental sources.
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Seasonality of clinical isolation of rapidly growing mycobacteria - PMC
the summer and fall RGM peaks lagged behind their corresponding peaks of rainfall in the late spring and early autumn by 2–6 weeks;
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[PDF] Nontuberculous mycobacteria: An Emerging Public Health Concern
Aug 1, 2025 · Nontuberculous mycobacteria (NTM) infections are an increasing public health concern. This document establishes the need to improve the ...Missing: vulnerable | Show results with:vulnerable
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SARS-CoV-2 and Mycobacterium Fortuitum Coinfection: A Case ...
Sep 6, 2025 · Multiple sclerosis patients receiving anti-CD20 therapy are at particular risk of a wave-like course of COVID-19, caused by immunosuppression, ...Missing: vulnerable post-
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Mycobacterium Fortuitum Workup - Medscape Reference
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An Official ATS/IDSA Statement: Diagnosis, Treatment, and ...
The minimum evaluation of a patient suspected of nontuberculous mycobacterial (NTM) lung disease should include the following: (1) chest radiograph or, in the ...
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Treatment of Nontuberculous Mycobacterial Pulmonary Disease
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[PDF] Mycobacterial Culture Final - APHL
Typical Growth Rates. • Rapid Growers will grow in 3–7 days. • MTBC is detected in an average of 14 days using MGIT versus 25 days on LJ. • Detection may be ...
[69]
Characteristics and Comparison of Rapidly Growing and Slowly
Of the AFB staining, it could not identify the specimens of NTM and had low sensitivity. 15 In recent years, metagenomic next-generation sequencing (mNGS) is ...Introduction · Clinical Features · Discussion
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Sensitivity of Fluorochrome Microscopy for Detection of ... - PMC
Smears were positive for acid-fast bacilli (AFB) in 63% (677 of 1,082) of specimens growing M. tuberculosis and 56% (638 of 1,148) of specimens growing the four ...
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Laboratory Diagnosis and Susceptibility Testing for Mycobacterium ...
Cultured isolates are identified far less commonly by traditional biochemical profiling and more commonly by molecular methods, such as DNA probes and broad- ...Staining Procedures And... · Nonphenotypic Methods Of... · Nucleic Acid Amplification...
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Misdiagnosis of non-tuberculous mycobacteria as ... - PMC - NIH
GeneXpert detects Mycobacterium tuberculosis complex (MTBC) at low bacterial loads, exhibiting high sensitivity and specificity for smear-negative samples.
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(PDF) Identification of Significant Pathogenic Nontuberculous ...
Oct 30, 2023 · For identifying NTM from different clinical specimens, hsp-65 PCR Restriction fragment length polymorphism Analysis (hsp65-PRA) is the widely ...<|control11|><|separator|>
[74]
Comparative genome analysis reveals high-level drug resistance ...
The size of the MF GZ001 genome is 6413573 bp. The final assembly of the genome was circularized with a high G+C content of 66.18% ( Figure 2 , Table 1 ). It ...
[75]
Approach to the diagnosis and treatment of non-tuberculous ...
For skin and soft tissue NTM infections, radiographic imaging studies are not routinely required for diagnosis. However, imaging studies such as sonography, CT, ...
[76]
A Case Report: Mycobacterium fortuitum Spondylodiscitis
Molecular biology techniques are crucial for early detection, particularly in mycobacterial infections. In spondylodiscitis, MRI findings are nonspecific and ...Missing: histopathology | Show results with:histopathology
[77]
Pathology of Granulomatous Pulmonary Diseases - Allen Press
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Mycobacterium Fortuitum Treatment & Management
Dec 6, 2024 · Mycobacterium fortuitum is a nontuberculous mycobacterium (NTM), a grouping that encompasses all mycobacteria outside of the Mycobacterium ...
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Nationwide surveillance of antimicrobial susceptibility of 509 rapidly ...
Jun 9, 2021 · Although M. fortuitum was resistant to macrolides, it was susceptible to amikacin, imipenem, fluoroquinolones, and trimethoprim/sulfamethoxazole ...
[80]
Species Distribution and Macrolide Susceptibility of Mycobacterium ...
Clarithromycin-resistant M. fortuitum isolates exhibited common mutations of erm(39), potentially involved in clarithromycin resistance. INTRODUCTION. The ...Introduction · Fig 1 · Table 2
[81]
Species Distribution and Macrolide Susceptibility of Mycobacterium ...
Most M. fortuitum, M. porcinum, and M. septicum isolates were inducibly resistant to clarithromycin, whereas two-thirds of ...Missing: antibiotic | Show results with:antibiotic
[82]
Clinical Characteristics and Treatment Outcomes of Mycobacterium ...
Jul 10, 2023 · Mycobacterium fortuitum (M. fortuitum) is a rapidly growing mycobacterium that causes M. fortuitum-pulmonary disease (PD).
[83]
Guideline Implementation Tools - American Thoracic Society
Treatment of Nontuberculous Mycobacterial Pulmonary Disease: An Official ATS/ERS/ESCMID/IDSA Clinical Practice Guideline Implementation Tools.Missing: fortuitum | Show results with:fortuitum