Nontuberculous mycobacteria
Nontuberculous mycobacteria (NTM), also known as environmental mycobacteria, atypical mycobacteria[1] and mycobacteria other than tuberculosis (MOTT), aremycobacteria which do not cause tuberculosis or leprosy (also known as Hansen’s disease). NTM do cause pulmonary diseases that resemble tuberculosis.[2] Mycobacteriosis is any of these illnesses, usually meant to exclude tuberculosis. They occur in many animals, including humans.
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Introduction[edit]
Mycobacteria are a family of small, rod-shaped bacilli that can be classified into 3 main groups for the purpose of diagnosis and treatment:
- Mycobacterium tuberculosis complex which can cause tuberculosis: M. tuberculosis, M. bovis, M. africanum, M. microti and M. canetti.
- M. leprae and M. lepromatosis‘ which cause Hansen’s disease or leprosy.
- Nontuberculous mycobacteria (NTM) are all the other mycobacteria which can cause pulmonary disease resembling tuberculosis, lymphadenitis, skin disease, or disseminated disease.
Taxonomy[edit]
In 1959, botanist Ernest Runyon put these human disease-associated bacteria into four groups (Runyon classification):[3]
- Photochromogens, which develop pigments in or after being exposed to light. Examples include M. kansasii, M. simiae and M. marinum.[3]
- Scotochromogens, which become pigmented in darkness. Examples include M. scrofulaceum and M. szulgai.[3]
- Non-chromogens, which includes a group of prevalent opportunistic pathogens called M. avium complex (MAC). Other examples are M. ulcerans, M. xenopi, M. malmoense, M. terrae, M. haemophilum and M. genavense.[4]
- Rapid growers include four well recognized pathogenic rapidly growing non-chromogenic species: M. chelonae, M. abscessus, M. fortuitum and M. peregrinum. Other examples cause disease rarely, such as M. smegmatis and M. flavescens.[4]
The number of identified and cataloged NTM species has been increasing rapidly, from about 50 in 1997 to over 125 by January 2007. The surge is mainly due to improved isolation and identification technique.[5]
However, even with these new techniques, the Runyon classification is still sometimes used to organize the mycobacteria into categories.[6]
Epidemiology[edit]
NTM are widely distributed in the environment, particularly in wet soil, marshland, streams, rivers and estuaries. Different species of NTM prefer different types of environment.[7]Human disease is believed to be acquired from environmental exposures, and unlike tuberculosis and leprosy, there has been no evidence of animal-to-human or human-to-human transmission of NTM, hence the alternative label “environmental bacteria”.[8]
NTM diseases have been seen in most industrialized countries, where incidence rates vary from 1.0 to 1.8 cases per 100,000 persons. Recent studies, including one done in Ontario, Canada, suggest that incidence is much higher. Pulmonary NTM is estimated by some experts in the field to be at least ten times more common than TB in the U.S., with at least 150,000 cases per year.
Most NTM disease cases involve the species known as Mycobacterium avium complex or MAC for short, M. abscessus, M. fortuitum and M. kansasii. M. abscessus is being seen with increasing frequency and is particularly difficult to treat.[8]
Mayo Clinic researchers found a three-fold increased incidence of cutaneous NTM infection between 1980 and 2009 in a population-based study of residents of Olmsted County, Minnesota. The most common species were M. marinum, accounting for 45% of cases and M. chelonae and M. abscessus, together accounting for 32% of patients.[9] M. chelonaeinfection outbreaks, as a consequence of tattooing with infected ink, have been reported in the United Kingdom[10] and the United States.[11]
Rapidly growing NTMs are implicated in catheter infections, post-LASIK, skin and soft tissue (especially post-cosmetic surgery) and pulmonary infections.[12]
Pathogenesis[edit]
The most common clinical manifestation of NTM disease is lung disease, but lymphatic, skin/soft tissue, and disseminated disease are also important.[8]
Pulmonary disease caused by NTM is most often seen in post-menopausal women. It is not uncommon for cystic fibrosis, Alpha 1-antitrypsin deficiency, Marfan Syndrome andPrimary ciliary dyskinesia patients to have pulmonary NTM colonization and/or infection. Pulmonary NTM can also be found in individuals with AIDS and malignant disease. It can be caused by many NTM species which depends on region, but most frequently MAC and M. kansasii.[13]
Lymphadenitis can be caused by various species that is different from one place to another; but again, MAC is the main cause worldwide. Most patient are aged less than 5 years, but the incidence is rare for children having BCG vaccine. The disease has a high curability.[14]
Soft tissue disease due to NTM infection include post-traumatic abscesses (caused by rapid growers), swimming pool granuloma (caused by M. marinum) and Buruli ulcer (caused by M. ulcerans or M. shinshuense). Post-traumatic abscesses most commonly occur after injection.[14]
Disseminated mycobacterial disease was common in US and European AIDS patients in the 1980s and early 1990s, though the incidence has declined in developed nations since the introduction of highly active antiretroviral therapy. It can also occur in individuals after having renal transplantation.[13]
Diagnosis[edit]
Diagnosis of opportunistic mycobacteria is made by repeated isolation and identification of the pathogen with compatible clinical and radiological features. Similar to M. tuberculosis, most nontuberculous mycobacteria can be detected microscopically and grow on Löwenstein-Jensen medium.[13] Many reference centres now use a nucleic acid-based method such as sequence differences detection in the gene coding for 16S ribosomal RNA to identify the species.[7]
Pulmonary NTM disease diagnosis requires both identification of the mycobacterium in the patient’s lung(s) as well as a high resolution CT scan of the lungs.
Research[edit]
Virginia Tech conducted a home water supply and patient sputum comparison study to determine source of infection in pulmonary NTM cases. This study was funded by NTM Info & Research and results were made by mid-2009, and the study can be found at the CDC: Nontuberculous Mycobacteria from Household Plumbing of Patients with Nontuberculous Mycobacteria Disease[15]
An epidemiology study on pulmonary NTM was conducted by National Institute of Allergy & Infectious Disease and results published in 2010. This study was funded by NTM Info & Research. The data can be found at PubMed[16]
French researchers finalized the genome sequence of M. abscessus in March 2008. The genome is available at http://www.ncbi.nlm.nih.gov/sites/entrez?db=genome&cmd=search&term=abscessus.
Colorado State University have a massive research department dedicated solely to Mycobacteria research. It is dubbed the MRL, which stands for the Mycobacteria Research Lab.[17] The MRL, among many Mycobacteria species, studies the pathogenesis and drug resistance of NTMs. Specifically, Dr. Mary Ann DeGroote, a researcher at Colorado State University (as of September 2015) is conducting research on novel therapies for nontuberuclous (NTM) mycobacterial infections.[18]
National Jewish Health and NTMir held in 2015 a Lecture Series for Physicians, Patients and Families, of which videos are available.[19]
Notes[edit]
- Jump up^ Atypical Mycobacteria at the US National Library of Medicine Medical Subject Headings (MeSH)
- Jump up^ American Thoracic Society (1997). “Diagnosis and treatment of disease caused by nontuberculous mycobacteria. This official statement of the American Thoracic Society was approved by the Board of Directors, March 1997. Medical Section of the American Lung Association”. American Journal of Respiratory and Critical Care Medicine. 156 (2 Pt 2): S1–25. doi:10.1164/ajrccm.156.2.atsstatement. PMID 9279284.
- ^ Jump up to:a b c Grange, p. 221
- ^ Jump up to:a b Grange, p. 222
- Jump up^ American Thoracic Society, p.369
- Jump up^ Tortoli E (April 2003). “Impact of genotypic studies on mycobacterial taxonomy: the new mycobacteria of the 1990s”. Clinical Microbiology Reviews. 16 (2): 319–54.doi:10.1128/CMR.16.2.319-354.2003. PMC 153139
. PMID 12692101.
- ^ Jump up to:a b Grange, p. 226
- ^ Jump up to:a b c American Thoracic Society, p. 370
- Jump up^ Wentworth, A.B.; Drage L.A.; Wengenack N.L.; Wilson J.W.; Lohse C.M. (4 December 2012). “Increased Incidence of Cutaneous Nontuberculous Mycobacterial Infection, 1980 to 2009: A Population-Based Study.”. Mayo Clinic Proceedings. 88 (1): 38–45.doi:10.1016/j.mayocp.2012.06.029. PMID 23218797.
- Jump up^ Sergeant, A.; Conaglen P.; Laurenson I.F.; Claxton P.; Mathers M.E.; Kavanagh G.M.; Tidman M.J. (25 July 2012). “Mycobacterium chelonae infection: a complication of tattooing.”. Clinical and Experimental Dermatology. 38 (2): 140–2. doi:10.1111/j.1365-2230.2012.04421.x. PMID 22831709.
- Jump up^ Centers for Disease Control and Prevention (CDC) (24 August 2012). “Tattoo-associated nontuberculous mycobacterial skin infections–multiple states, 2011-2012.”.CDC – Morbidity and Mortality Weekly Report (MMWR). 61 (33): 635–6.PMID 22914227.
- Jump up^ De Groote, MA and Huitt G. Infections due to Rapidly Growing Mycobacteria. Clinical Infectious Diseases 2006;42:1756–1763.
- ^ Jump up to:a b c Grange, p. 225
- ^ Jump up to:a b Grange, p. 223
- Jump up^ http://wwwnc.cdc.gov/eid/article/17/3/10-1510_article
- Jump up^ Prevots DR, Shaw PA, Strickland D, Jackson LA, Raebel MA, Blosky MA, Montes de Oca R, Shea YR, Seitz AE, Holland SM, Olivier KN (2010). “Nontuberculous mycobacterial lung disease prevalence at four integrated health care delivery systems”.Am. J. Respir. Crit. Care Med. 182 (7): 970–6. doi:10.1164/rccm.201002-0310OC.PMC 2970866
. PMID 20538958.
- Jump up^ http://mrl.colostate.edu/
- Jump up^ http://mrl.colostate.edu/faculty/
- Jump up^ “Carolyn and Matthew Bucksbaum NTM lectures 2015”. video collection. Retrieved2016-09-20.
References[edit]
- Griffith David E.; Aksamit Timothy; Brown-Elliott Barbara; et al. (2007). “American Thoracic Society Guidelines: Diagnosis, Treatment and Prevention of Nontuberculous Mycobacterial Diseases”. Am. J. Respiratory and Critical Care Medicine. 175 (4): 367–417. doi:10.1164/rccm.200604-571st.
- New BTS Guideline is forthcoming in Nov. 2016, http://www.brit-thoracic.org.uk/guidelines-and-quality-standards/non-tuberculous-mycobacteria/
- Grange, J. M. (2007). “Environmental mycobacteria”. In Greenwood, David; Slack, Richard; Peitherer, John; & Barer, Mike (Eds.), Medical Microbiology (17th ed.), pp. 221–227. Elsevier. ISBN 978-0-443-10209-7.
External links[edit]
- The NTM Handbook: A Guide for Patients with Nontuberculous Mycobacterial Infections Including MAC
- NTM Info & Research, a nonprofit research and patient support organization
- Stop NTM Now
- National Jewish Medical and Research Center
- University of Texas, Tyler Health Center
- Lung, Nontuberculous Mycobacterial Infections from eMedicine Radiology