Abstract
Mycobacteriosis are infections caused by bacteria of the genus Mycobacterium. The nontuberculous mycobacteria (NTM) are environmental, acid-fast bacilli (AFB), Gram-positive, that cause varied manifestations in different groups of patients. It can be the cause of a broad range of clinical disorders, from cutaneous infections, such as cervical or intrathoracic lymphadenitis in children, to disseminated infections at all ages. NTM infection has been an important cause of morbidity and mortality. Early diagnosis and initiation of treatment with multiple antibiotics for several months and potential use of adjunctive surgery are necessary to achieve the best outcome.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- AFB:
-
Acid-fast bacillus
- AIDS:
-
Acquired immunodeficiency syndrome
- AST:
-
Antimicrobial susceptibility testing
- BCG:
-
Bacillus Calmette-Guérin
- BU:
-
Buruli ulcer
- CLSI:
-
Clinical and Laboratory Standards Institute
- CTB:
-
Cutaneous tuberculosis
- HIV:
-
Human immunodeficiency virus
- IGRA:
-
Interferon-γ release assay
- IL:
-
Interleukin
- INF:
-
Interferon
- MABSC:
-
Mycobacterium abscessus complex
- MAC:
-
M. avium-intracellulare complex
- MIC:
-
Minimum inhibitory concentration in liquid medium
- MMSA:
-
Mycobacteria mobility shift assay
- MTB:
-
Mycobacterium tuberculosis
- MTC:
-
Mycobacterium tuberculosis complex
- NAATs:
-
Nucleic Acid Amplification Tests
- NTM:
-
Nontuberculous mycobacteria
- NTMI:
-
Nontuberculous mycobacteria infection
- NTM-LD:
-
Nontuberculous mycobacterial lung disease
- PCR:
-
Polymerase chain reaction
- PNTM:
-
Pulmonary nontuberculous mycobacterial
- PRA:
-
Polymorphism restriction analysis
- RGM:
-
Rapidly Growing Mycobacteria
- RIPE:
-
Rifampin, isoniazid, pyrazinamide, and ethambutol
- SSTI:
-
Skin disease and soft tissue infection
- TB:
-
Tuberculosis
- TST:
-
Tuberculin skin test
- WHO:
-
World Health Organization
References
Parte AC, Sardà Carbasse J, Meier-Kolthoff JP, Reimer LC, et al. List of prokaryotic names with standing in nomenclature (LPSN) moves to the DSMZ. Int J Syst Evol Microbiol. 2020;70:5607–12. https://doi.org/10.1099/ijsem.0.004332.
Euzéby JP. List of prokaryotic names with standing in nomenclature (LPSN). https://lpsn.dsmz.de/genus/mycobacterium. Accessed 9 Dec 2020.
Turenne CY. Nontuberculous mycobacteria: insights on taxonomy and evolution. Infect Genet Evol. 2019;72:159–68. https://doi.org/10.1016/j.meegid.2019.01.017.
Tortoli E, Meehan CJ, Grottola A, Serpini GF, et al. Genome-based taxonomic revision detects a number of synonymous taxa in the genus Mycobacterium. Infect Genet Evol. 2019;75:103983. https://doi.org/10.1016/j.meegid.2019.103983.
Claeys TA, Robinson RT. The many lives of nontuberculous mycobacteria. J Bacteriol. 2018;200:e00739–17. https://doi.org/10.1128/JB.00739-17.
Gupta RS, Lo B, Son J. Phylogenomics and comparative genomic studies robustly support division of the genus Mycobacterium into an emended genus Mycobacterium and four novel genera. Front Microbiol. 2018;9:67. https://doi.org/10.3389/fmicb.2018.00067.
Pavlik I, Falkinham JO III, Kazda J. Potentially pathogenic mycobacteria. In: Kazda J, Pavlik I, Falkinham III JO, Hruska K, editors. The ecology of mycobacteria: impact on animal’s and human’s health. Dordrecht: Springer; 2009. p. 21–79.
Leao SC, Tortoli E, Euzéby JP, Garcia MJ. Proposal that Mycobacterium massiliense and Mycobacterium bolletii be united and reclassified as Mycobacterium abscessus subsp. bolletii comb. nov., designation of Mycobacterium abscessus subsp. abscessus subsp. nov. and emended description of Mycobacterium abscessus. Int J Syst Evol Microbiol. 2011;61:2311–3.
Jagielski T, van Ingen J, Rastogi N, Dziadek J, et al. Current methods in the molecular typing of Mycobacterium tuberculosis and other mycobacteria. Biomed Res Int. 2014;2014:645802. PMID: 24527454.
Pavlik I, Falkinham JO III, Kazda J. Environments providing Favourable conditions for the multiplication and transmission of mycobacteria. In: Kazda J, Pavlik I, Falkinham III JO, Hruska K, editors. The ecology of mycobacteria: impact on animal’s and human’s health. Netherlands: Springer; 2009. p. 89–197. https://doi.org/10.1007/978-1-4020-9413-2.
Adjemian J, Daniel-Wayman S, Ricotta E, Prevots DR. Epidemiology of nontuberculous mycobacteriosis. Semin Respir Crit Care Med. 2018;39(3):325–35. https://doi.org/10.1055/s-0038-1651491. Epub 2018 Aug 2. PMID: 30071547.
Ramos-e-Silva M, Castro MCR. Mycobacterial infections. In: Bolognia JL, et al., editors. Dermatology. London: Elsevier; 2018. p. 1296–316. isbn:978-0-7020-6275-9.
Bates TR, Keenher T, O’Reilly LC, Heath CH, et al. Extensive cutaneous Mycobacterium abscessus infection due to contaminated insulin delivery system. QJM. 2009;102:881–4.
Slany M, Jezek P, Fiserova V, Bodnarova M, et al. Mycobacterium marinum infections in humans and tracing of its possible environmental sources. Can J Microbiol. 2012;58(1):39–44.
Sousa PP, Cruz RCS, Schettini AP, Westphal DC. Mycobacterium abscessus skin infection after tattooing—case report. An Bras Dermatol. 2015;90(5):741–3.
Thomson RM. Changing epidemiology of pulmonary nontuberculous mycobacteria infections. Emerg Infect Dis. 2010;16(10):1576–83.
Marras TK, Daley CL. Epidemiology of human pulmonary infection with nontuberculous mycobacteria. Clin Chest Med. 2002;23(3):553–67. https://doi.org/10.1016/s0272-5231(02)00019-9.
Falkingham JO III, Norton CD, Le Chavallier MW. Factors influencing numbers of Mycobacterium avium, Mycobacterium intracellulare, and other mycobacteria in drinking water distribution systems. Appl Environ Microbiol. 2001;67:1225–31.
du Moulin GC, Stottmeier KD, Pelletier PA, Tsang AY, Hedley-Whyte J. Concentration of Mycobacterium avium by hospital hot water systems. JAMA. 1988;260(11):1599–601.
Peters M, Müller C, Rüsch-Gerdes S, Seidel C, et al. Isolation of atypical mycobacteria from tap water in hospitals and homes: is this a possible source of disseminated MAC infection in AIDS patients? J Infect. 1995;31(1):39–44.
Ross BC, Johnson PD, Oppedisano F, Marino L, et al. Detection of Mycobacterium ulcerans in environmental samples during an outbreak of ulcerative disease. Appl Environ Microbiol. 1997;63(10):4135–8. https://doi.org/10.1128/AEM.63.10.4135-4138.1997.
Kubalek I, Mysak J. The prevalence of environmental mycobacteria in drinking water supply systems in a demarcated region in Czech Republic in the period 1984–1989. Eur J Epidemiol. 1996;12(5):471–4.
Vaerewijck MJM, Huys G, Palomino JC, Swings J, et al. Mycobacteria in drinking water distribution systems: ecology and significance for human health. FEMS Microbiol Rev. 2005;29(5):911–34.
Schulze-Röbbecke R, Feldmann C, Fischeder R, Janning B, et al. Dental units: an environmental study of sources of potentially pathogenic mycobacteria. Tuber Lung Dis. 1995;76(4):318–23.
Ashford DA, Whitney E, Raghunathan P, Cosivi O. Epidemiology of selected mycobacteria that infect humans and other animals. Rev Sci Tech. 2001;20(1):325–37. https://doi.org/10.20506/rst.20.1.1266.
Cardona PJ. Pathogenesis of tuberculosis and other mycobacteriosis. Enferm Infecc Microbiol Clin. 2018;36(1):38–46. https://doi.org/10.1016/j.eimc.2017.10.015. PMID: 29198784.
Faria S, Joao I, Jordao L. General overview on nontuberculous mycobacteria, biofilms, and human infection. J Pathog. 2015;2015:809014.
Kuritsky JM, Bullen MG, Broome CV, Silcox VA, Good RC, Wallace RJ Jr. Sternal wound infections and endocarditis due to organisms of the Mycobacterium fortuitum complex. Ann Intern Med. 1983;98:938–9.
Laussucq S, Baltch AL, Smith RP, et al. Nosocomial Mycobacterium fortuitum colonization from a contaminated ice machine. Am Rev Respir Dis. 1988;138:891–4.
Panwalker AP, Fuhse E. Nosocomial Mycobacterium gordonae pseudoinfection from contaminated ice machines. Infect Control. 1986;7(2):67–70. https://doi.org/10.1017/s0195941700063918.
Burns DN, Wallace RJ Jr, Schultz ME, Zhang YS, et al. Nosocomial outbreak of respiratory tract colonization with Mycobacterium fortuitum: demonstration of the usefulness of pulsed-field gel electrophoresis in an epidemiologic investigation. Am Rev Respir Dis. 1991;144(5):1153–9.
Ide S, Nakamura S, Yamamoto Y, Kohno Y, et al. Epidemiology and clinical features of pulmonary nontuberculous mycobacteriosis in Nagasaki, Japan. PLoS One. 2015;10(5):e0128304.
Tebruegge M, Pantazidou A, MacGregor D, Gonis G, et al. Nontuberculous mycobacterial disease in children—epidemiology, diagnosis & management at a tertiary center. PLoS One. 2016;11(1):e0147513.
Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med. 2007;175(4):367–416.
Lima CT, Magalhães V. Abscess resulting from Mycobacterium kansasii in the left thigh of AIDS patient. An Bras Dermatol. 2014;89(3):478–80.
Macente S, Helbel C, Souza SFR, Siqueira VLD, et al. Disseminated folliculitis by Mycobacterium fortuitum in an immunocompetent woman. An Bras Dermatol. 2013;88(1):102–4.
Serra C, Loi G, Saddi B, Pautasso M, Manzin A. Unusual clinical presentation of Mycobacterium fortuitum infection in an immunocompetent woman. J Clin Microbiol. 2007;45:1663–5.
Wildner LM, Bazzo ML, Liedke SC, Nogueira CL, et al. Mycobacteria mobility shift assay: a method for the rapid identification of Mycobacterium tuberculosis and nontuberculous mycobacteria. Mem Inst Oswaldo Cruz. 2014;109(3):356–61.
Chung J, Ince D, Ford BA, Wanat KA. Cutaneous infections due to nontuberculosis Mycobacterium: recognition and management. Am J Clin Dermatol. 2018;19(6):867–78. https://doi.org/10.1007/s40257-018-0382-5. PMID: 30168084.
Gonzalez-Santiago TM, Drage LA. Nontuberculous mycobacteria: skin and soft tissue infections. Dermatol Clin. 2015;33(3):563–77. https://doi.org/10.1016/j.det.2015.03.017. PMID: 26143432.
Porvaznik I, Solovič I, Mokrý J. Non-tuberculous mycobacteria: classification, diagnostics, and therapy. Adv Exp Med Biol. 2017;944:19–25. https://doi.org/10.1007/5584_2016_45. PMID: 27826888.
Coros A, DeConno E, Derbyshire KM. IS6110, a Mycobacterium tuberculosis complex-specific insertion sequence, is also present in the genome of Mycobacterium smegmatis, suggestive of lateral gene transfer among mycobacterial species. J Bacteriol. 2008;190(9):3408–10. https://doi.org/10.1128/JB.00009-08.
Rivitti EA. Tuberculose e Micobacterioses Atípicas. In: Rivitti EA, editor. Dermatologia de Sampaio e Rivitti. São Paulo: Artes Médicas; 2018. p. 627–42. isbn:788536702759.
Paredes CF, Marcos LA, Martínez AFH, Morales AJR, et al. Cutaneous mycobacterial infections. Clin Microbiol Rev. 2018;32(1):e00069–18. https://doi.org/10.1128/CMR.00069-18.
Nguyen HH, Fadul N, Ashraf MS, Siraj DS. Osteomyelitis infection of Mycobacterium marinum: a case report and literature review. Case Rep Infect Dis. 2015;2015:905920.
Oh HW, Youn SH, Kim MS, Na CH, et al. Mycobacterium marinum infection on the face diagnosed by polymerase chain reaction amplification and direct sequencing. Ann Dermatol. 2015;27(5):639–41.
Yano Y, Kitada S, Mori M, Kagami S, et al. Pulmonary disease caused by rapidly growing mycobacteria: a retrospective study of 44 cases in Japan. Respiration. 2013;85(4):305–11.
Zhang X, Liu W, Liu W, Jiang H, et al. Cutaneous infections caused by rapidly growing mycobacteria: case reports and review of clinical and laboratory aspects. Acta Derm Venereol. 2015;95(8):985–9.
Uslan DZ, Kowalski TJ, Wengenack NL, Virk A, Wilson JW. Skin and soft tissue infections due to rapidly growing mycobacteria: comparison of clinical features, treatment, and susceptibility. Arch Dermatol. 2006;142(10):1287–92. https://doi.org/10.1001/archderm.142.10.1287.
Suvanasuthi S, Wongpraparut C, Pattanaprichakul P, Bunyaratavej S. Mycobacterium fortuitum cutaneous infection from amateur tattoo. J Med Assoc Thail. 2012;95(6):834–7.
Quiñones C, Ramalle-Gómara E, Perucha M, Lezaun ME, et al. An outbreak of Mycobacterium fortuitum cutaneous infection associated with mesotherapy. J Eur Acad Dermatol Venereol. 2010;24(5):604–6.
Uslu U, Böhm O, Heppt F, Sticherling M. Skin and soft tissue infections caused by Mycobacterium chelonae: more common than expected? Acta Derm Venereol. 2019;99(10):889–93. https://doi.org/10.2340/00015555-3230. PMID: 31141157.
Hammoudi N, Cassagne C, Armstrong N, Ranque S, Henrissat B, Drancourt M, Bouam A. Mycobacterium ulcerans mycolactones-fungi crosstalking. Sci Rep. 2019;9(1):3028. https://doi.org/10.1038/s41598-019-39927-3. PMID: 30816261.
Olivares L, Fandiño M, Pardal PF, Cortiñas MEP, et al. Infección cutánea por Mycobacterium chelonae. Dermatol Argent. 2011;17(6):446–50.
Murback ND, Higa Júnior MG, Pompílio MA, Cury ESJ, et al. Disseminated cutaneous atypical mycobacteriosis by M. chelonae after sclerotherapy of varicose veins in a immunocompetent patient: a case report. An Bras Dermatol. 2015;90(3 Suppl 1):S138–42.
Bechara C, Macheras E, Heym B, Pages A, et al. Mycobacterium abscessus skin infection after tattooing: first case report and review of the literature. Dermatology. 2010;221(1):1–4.
Wongkitisophon P, Rattanakaemakorn P, Tanrattanakorn S, Vachiramon V. Cutaneous Mycobacterium abscessus infection associated with mesotherapy injection. Case Rep Dermatol. 2011;3(1):37–41.
Wu TS, Yang CH, Brown-Elliott BA, Chao AS, et al. Postcesarean section wound infection caused by Mycobacterium massiliense. J Microbiol Immunol Infect. 2016;49(6):955–61. S1684-1182(15):00821-X.
Deshayes C, Angala SK, Marion E, Brandli I, et al. Regulation of mycolactone, the Mycobacterium ulcerans toxin, depends on nutrient source. PLoS Negl Trop Dis. 2013;7(11):e2502.
Adu EJ. Management of complications of Mycobacterium ulcerans disease: a three-year review. Int J Mycobacteriol. 2013;2(4):206–10.
Pszolla N, Sarkar MR, Strecker W, Kern P, et al. Buruli ulcer: a systemic disease. Clin Infect Dis. 2003;37(6):e78–82. https://doi.org/10.1086/377170.
Kassi K, Kouame K, Allen W, Kouassi LA, et al. Squamous cell carcinoma secondary to Buruli ulcer: a clinical case report in a young girl. Bacteriol Virusol Parazitol Epidemiol. 2010;55(1):25–8. PMID: 21033631.
Kaplan JE, Benson C, Holmes KK, Brooks JT, et al.; CDC. Guidelines for prevention and treatment of opportunistic infections in HIV-infected adults and adolescents. Atlanta. 2009;1–198. Accessed 25 Dec 2020.
Lawn SD, Bekker LG, Miller RF. Immune reconstitution disease associated with mycobacterial infections in HIV-infected individuals receiving antiretrovirals. Lancet Infect Dis. 2005;5(6):361–73.
Kollipara R, Richards K, Tschen J, Campbell L, et al. Disseminated Mycobacterium avium complex with cutaneous lesions. J Cutan Med Surg. 2016;20:272.
Richards CJ, Olivier KN. Nontuberculous mycobacteria in cystic fibrosis. Semin Respir Crit Care Med. 2019;40(6):737–50. https://doi.org/10.1055/s-0039-1693706. PMID: 31659731.
Heraud D, Carr RD, McKee J, Dehority W. Nontuberculous mycobacterial adenitis outside of the head and neck region in children: a case report and systematic review of the literature. Int J Mycobacteriol. 2016;5(3):351–3. https://doi.org/10.1016/j.ijmyco.2016.04.006. PMID: 27847024.
Formanoy E, Lam HY, Arends JE. Tenosynovitis of the right hand. Mycobacterium kansasii. Neth J Med. 2013;71(10):526–30. PMID: 24394739.
Shaaban H, Layne T, Sensakovic JW, Boghossian J. Mycobacterium kansasii septicemia in an AIDS patient complicated by acute respiratory distress syndrome and acute liver failure. Int J STD AIDS. 2014;25(2):152–4.
Wolinsky E. Mycobacterial lymphadenitis in children: a prospective study of 105 nontuberculous cases with longterm follow-up. Clin Infect Dis. 1995;20(4):954–63.
Amir J. Non-tuberculous mycobacterial lymphadenitis in children: diagnosis and management. Isr Med Assoc J. 2010;12(1):49–52. PMID: 20450132.
Raffaldi I, Scolfaro C, Garazzino S, Peradotto F, et al. An atypical deep neck infection in a two-year-old child. Infez Med. 2014;22(2):136–9. PMID: 24955801.
Nolt D, Michaels MG, Wald ER. Intrathoracic disease from nontuberculous mycobacteria in children: two cases and a review of the literature. Pediatrics. 2003;112(5):e434. https://doi.org/10.1542/peds.112.5.e434.
van Ingen J, Boeree MJ, de Lange WC, de Haas PE, et al. Clinical relevance of Mycobacterium szulgai in the Netherlands. Clin Infect Dis. 2008;46(8):1200–5.
Bartolf A, Cosgrove CA. Mycobacterium szulgai infection in the flexor sheath of the right index finger in an immunocompetent patient. BMJ Case Rep. 2017;2017:bcr2016217722. https://doi.org/10.1136/bcr-2016-217722. PMID: 28288996.
Singh AK, Marak RS, Maurya AK, Das M, et al. Mixed cutaneous infection caused by Mycobacterium szulgai and Mycobacterium intermedium in a healthy adult female: a rare case report. Case Rep Dermatol Med. 2015;2015:607519.
Nookeu P, Angkasekwinai N, Foongladda S, Phoompoung P. Clinical characteristics and treatment outcomes for patients infected with Mycobacterium haemophilum. Emerg Infect Dis. 2019;25(9):1648–52. https://doi.org/10.3201/eid2509.190430. PMID: 31441427; PMCID: PMC6711220.
Lindeboom JA, Bruijnesteijn van Coppenraet LES, van Soolingen D, Prins JM, et al. Clinical manifestations, diagnosis, and treatment of Mycobacterium haemophilum infections. Clin Microbiol Rev. 2011;24(4):701–17.
Atiya N, Sulaiman H, Chong J, Ng KP. First report of cervicofacial lymphadenitis due to Mycobacterium haemophilum in an immunocompromised adult patient. J Infect Dev Ctries. 2015;9(3):313–6.
Forbes BA, Hall GS, Miller MB, et al. Practice guidelines for clinical microbiology laboratories: mycobacteria. Clin Microbiol Rev. 2018;31(2):e00038–17. https://doi.org/10.1128/CMR.00038-17.
Bachmeyer C, Blum L, Stelianides S, Benchaa B, et al. Mycobacterium xenopi pulmonary infection in an HIV infected patient under highly active antiretroviral treatment. Thorax. 2001;56(12):978–9.
Pigem R, Cairó M, Martínez-Lacasa X, Irigoyen D, et al. Disseminated infection with cutaneous involvement caused by Mycobacterium malmoense in an immunocompromised patient. J Am Acad Dermatol. 2013;69(4):e192–3.
Lhuillier E, Brugière O, Veziris N, Danel C, et al. Relapsing Mycobacterium genavense infection as a cause of late death in a lung transplant recipient: case report and review of the literature. Exp Clin Transplant. 2012;10(6):618–20.
Charles P, Lortholary O, Dechartres A, Doustdar F, et al. Mycobacterium genavense infections: a retrospective multicenter study in France, 1996–2007. Medicine (Baltimore). 2011;90(4):223–30.
Tuchinda C, Puavilai S, Sathapatayavongs B, Sungkanuparph S, et al., et al. Sweet’s syndrome: a reaction to non-tuberculous mycobacterial infections. J Med Assoc Thail. 2004;87(5):567–72. PMID: 15222531.
Chetchotisakd P, Kiertiburanakul S, Mootsikapun P, Assanasen S, et al. Disseminated nontuberculous mycobacterial infection in patients who are not infected with HIV in Thailand. Clin Infect Dis. 2007;45(4):421–7. https://doi.org/10.1086/520030.
Martin A, Colmant A, Verroken A, Rodriguez-Villalobos H. Laboratory diagnosis of nontuberculous mycobacteria in a Belgium hospital. Int J Mycobacteriol. 2019;8:157–61. https://doi.org/10.4103/ijmy.ijmy_40_19.
Goren MB, Cernich M, Brokl O. Some observations of mycobacterial acid-fastness. Am Rev Respir Dis. 1978;118:151–4. https://doi.org/10.1164/arrd.1978.118.1.151.
Staropoli JF, Branda JA. Cord formation in a clinical isolate of Mycobacterium marinum. J Clin Microbiol. 2008;46:2814–6. https://doi.org/10.1128/JCM.00197-08.
Clinical and Laboratory Standards Institute. M48-A: laboratory detection and identification of mycobacteria. https://clsi.org/standards/products/microbiology/documents/m48/. Accessed 18 Dec 2020.
Esteban J, Garcia-Pedrazuela M, Muñoz-Egea MC, Alcaide F. Current treatment of nontuberculous mycobacteriosis: an update. Expert Opin Pharmacother. 2012;13(7):967–86.
Wildner LM, Nogueira CL, Souza BS, Senna SG, Silva RM, Bazzo ML. Mycobacteria: epidemiology and diagnosis. J Trop Pathol. 2011;40(3):207–30. https://doi.org/10.5216/rpt.v40i3.15972.
Pfyffer GE. Mycobacterium: general characteristics, laboratory detection, and staining procedures. In: Jorgensen JH, Pfaller MA, Carroll KC, Funke G, Landry ML, et al., editors. Manual of clinical microbiology. 11th ed. Washington: ASM Press; 2015. p. 536–69. https://doi.org/10.1128/9781555817381.ch30.
Brown-Elliott BA, Nash KA, Wallace RJ Jr. Antimicrobial susceptibility testing, drug resistance mechanisms, and therapy of infections with nontuberculous mycobacteria. Clin Microbiol Rev. 2012;25(3):545–82.
Clinical and Laboratory Standards Institute. M24-A2: susceptibility testing of mycobacteria, Nocardia spp, and other aerobic Actinomycetes. https://clsi.org/standards/products/microbiology/documents/m24/. Accessed 18 Dec 2020.
Yotsu RR, Murase C, Sugawara M, Suzuki K, et al. Revisiting Buruli ulcer. J Dermatol. 2015;42(11):1033–41.
World Health Organization (WHO). Buruli ulcer (Mycobacterium ulcerans infection). https://www.who.int/news-room/fact-sheets/detail/buruli-ulcer-(mycobacterium-ulcerans-infection). Accessed 25 Dec 2020.
Soini H, Musser JM. Molecular diagnosis of mycobacteria. Clin Chem. 2001;47(5):809–14. PMID: 11325882.
Escobar-Escamilla N, Ramírez-González JE, González-Villa M, Torres-Mazadiego P, et al. Hsp65 phylogenetic assay for molecular diagnosis of nontuberculous mycobacteria isolated in Mexico. Arch Med Res. 2014;45(1):90–7.
Zelazny AM, Root JM, Shea YR, Colombo RE, et al. Cohort study of molecular identification and typing of Mycobacterium abscessus, Mycobacterium massiliense, and Mycobacterium bolletii. J Clin Microbiol. 2009;47:1985–95. https://doi.org/10.1128/JCM.01688-08.
Clinical and Laboratory Standards Institute. MM18-A: interpretive criteria for identification of bacteria and fungi by DNA target sequencing. https://clsi.org/standards/products/molecular-diagnostics/documents/mm18/. Accessed 18 Dec 2020.
Bartralot R, Pujol RM, García-Patos V, Sitjas D, et al. Cutaneous infections due to nontuberculous mycobacteria: histopathological review of 28 cases. Comparative study between lesions observed in immunosuppressed patients and normal hosts. J Cutan Pathol. 2000;27(3):124–9. https://doi.org/10.1034/j.1600-0560.2000.027003124.x.
Song H, Lee H, Choi G, Shin J. Cutaneous nontuberculous mycobacterial infection: a clinicopathological study of 7 cases. Am J Dermatopathol. 2009;31(3):227–31.
Dodiuk-Gad R, Dyachenko P, Ziv M, Shani-Adir A, et al. Nontuberculous mycobacterial infections of the skin: a retrospective study of 25 cases. J Am Acad Dermatol. 2007;57(3):413–20.
Bau AEK. Micobacterioses Não Tuberculosas. In: Lupi O, Santos JB, Cunha PR, editors. Rotinas de Diagnóstico e Tratamento da Sociedade Brasileira de Dermatologia. 1st ed. São Paulo: GEN; 2010. p. 326–31. isbn:9788581140841.
Li JJ, Beresford R, Fyfe J, Henderson C. Clinical and histopathological features of cutaneous nontuberculous mycobacterial infection: a review of 13 cases. J Cutan Pathol. 2017;44:433–43. https://doi.org/10.1111/cup.12903.
Lan NPH, Kolader ME, Dung NV, Campbell JI, et al. Mycobacterium fortuitum skin infections after subcutaneous injections with Vietnamese traditional medicine: a case report. BMC Infect Dis. 2014;14:550.
Wi YM. Treatment of Extrapulmonary nontuberculous mycobacterial diseases. Infect Chemother. 2019;51(3):245–55. https://doi.org/10.3947/ic.2019.51.3.245.
Philips RC, Hoyer PE, White SM, Tinkey KT, Loeffelholz M, Andersen CR, Wilkerson MG, Gibson BR, Kelly BC. Cutaneous nontuberculous mycobacteria infections: a retrospective case series of 78 patients from the Texas Gulf Coast region. J Am Acad Dermatol. 2019;81(3):730–9.
Franco-Paredes C, Marcos LA, Henao-Martínez AF, Rodríguez-Morales AJ, Villamil-Gómez WE, Gotuzzo E, Bonifaz A. Cutaneous mycobacterial infections. Clin Microbiol Rev. 2018;32(1):e00069–18. https://doi.org/10.1128/CMR.00069-18.
Strnad L, Winthrop KL. Treatment of Mycobacterium abscessus complex. Semin Respir Crit Care Med. 2018;39(3):362–76. https://doi.org/10.1055/s-0038-1651494. PMID: 30071551.
Shen GH, Wu BD, Hu ST, Lin CF, et al. High efficacy of clofazimine and its synergistic effect with amikacin against rapidly growing mycobacteria. Int J Antimicrob Agents. 2010;35(4):400–4. https://doi.org/10.1016/j.ijantimicag.2009.12.008.
Yotsu RR, Richardson M, Ishii N. Drugs for treating Buruli ulcer (Mycobacterium ulcerans disease). Cochrane Database Syst Rev. 2018;8(8):CD012118. https://doi.org/10.1002/14651858.CD012118.pub2. PMID: 30136733; PMCID: PMC6513118.
Akram SM, Rawla P. Mycobacterium kansasii. [Updated 2020 Aug 13]. In: StatPearls [Internet]. Treasure Island: StatPearls Publishing; 2020. Accessed 26 Dec 2020.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Glossary
- Nontuberculous Mycobacteria (NTM)
-
Are generally considered to be environmental saprophytes widely distributed in nature and can be found in numerous niches including soil, water, wild and domestic animals, fish, dust, and family and hospital settings. Mycobacteria are widespread in the environment, particularly in aquatic reservoirs.
- Mycobacterium fortuitum, M. abscessus, M. chelonae, M. smegmatis (RGM)
-
These species of Rapidly Growing Mycobacteria (RGM) are capable of producing various diseases in humans ranging from cutaneous infection to disseminated infection; hematogenously disseminated infection is usually seen only in immunocompromised hosts. The majority of infections are due to accidental inoculation from trauma, surgery, injection, or cannulation.
- Buruli ulcer (BU)
-
Is a disease affecting the skin, tissues, and in some cases the bones, caused by the environmental pathogen Mycobacterium ulcerans. Its mode of transmission is still elusive and controversial. Infection with this agent leads to extensive destruction of the tissues with the formation of large ulcers particularly on exposed parts of the body, such as the limbs, head, and neck.
- Immune reconstitution inflammatory syndrome (IRIS)
-
Is an inflammatory reaction resulting from restored immunity to specific infectious or noninfectious antigens. It is a frequent complication of MAC disease, most commonly presenting with fever and lymphadenitis after the CD4 count increases in response to antiretroviral therapy (ART), in persons with AIDS. Localized manifestations of MAC disease have been reported most often in patients who are receiving and have responded to ART.
- Mycobacterium avium-intracellulare complex (MAC)
-
Includes both M. avium and M. intracellulare and represents the most frequent bacterial opportunistic infection in persons with HIV/AIDS.
- Marjolin’s ulcer
-
Consists of the malignant transformation of a chronic ulcerative lesion. Over many years, these scars may develop into squamous cell carcinoma.
Rights and permissions
Copyright information
© 2023 The Author(s), under exclusive license to Springer Nature Switzerland AG
About this chapter
Cite this chapter
dos Santos, J.B., Ferraz, C.E., de Araújo, J.G., de Oliveira, M.H., da Silva, P.G., de Medeiros, V.L.S. (2023). Other Mycobacterioses. In: Rangel Bonamigo, R. (eds) Dermatology in Public Health Environments. Springer, Cham. https://doi.org/10.1007/978-3-031-13505-7_7
Download citation
DOI: https://doi.org/10.1007/978-3-031-13505-7_7
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-031-13504-0
Online ISBN: 978-3-031-13505-7
eBook Packages: MedicineMedicine (R0)