Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 15, Number 2—February 2009

Nontuberculous Mycobacteria, Zambia

Patricia C.A.M. BuijtelsComments to Author , Marianne A.B. van der Sande, Cas S. de Graaff, Shelagh Parkinson, Henri A. Verbrugh, Pieter L.C. Petit, and Dick van Soolingen
Author affiliations: Medical Centre Rijnmond-Zuid, Rotterdam, the Netherlands (P.C.A.M. Buijtels); University Medical Center Rotterdam, Rotterdam (P.C.A.M. Buijtels, H.A. Verbrugh); National Institute of Public Health and the Environment, Bilthoven, the Netherlands (M.A.B. van der Sande, D. van Soolingen); Medical Centre Alkmaar, Alkmaar, the Netherlands (C.S. de Graaff); St. Francis Hospital, Katete, Zambia (S. Parkinson); Vlietland Hospital, Schiedam, the Netherlands (P.L.C. Petit)

Cite This Article


Clinical relevance of nontuberculous mycobacteria (NTM) isolated from 180 chronically ill patients and 385 healthy controls in Zambia was evaluated to examine the contribution of these isolates to tuberculosis (TB)–like disease. The proportion of NTM-positive sputum samples was significantly higher in the patient group than in controls; 11% and 6%, respectively (p<0.05). NTM-associated lung disease was diagnosed for 1 patient, and a probable diagnosis was made for 3 patients. NTM-positive patients and controls were more likely to report vomiting and diarrhea and were more frequently underweight than the NTM-negative patients and controls. Chest radiographs of NTM-positive patients showed deviations consistent with TB more frequently than those of controls. The most frequently isolated NTM was Mycobacterium avium complex. Multiple, not previously identified mycobacteria (55 of 171 NTM) were isolated from both groups. NTM probably play an important role in the etiology of TB-like diseases in Zambia.

Tuberculosis (TB) is a problem of enormous dimensions in Africa, and Mycobacterium tuberculosis is the most important causative agent. However, in industrialized countries, nontuberculous mycobacteria (NTM) also play a key role in etiology of TB-like syndromes. In Africa, the contribution of NTM to such disease has been examined on a small scale only (16).

Zambia is a country with historically high prevalence rates of TB. Patients with acid-fast bacilli (AFB)–positive sputum, or those with chest radiographic findings suggestive of active TB, who do not respond to general antimicrobial drugs, are generally presumed to have pulmonary TB. In general, these patients are treated empirically for 6 months with a combination of drugs recommended by the World Health Organization. However, several TB-like syndromes in Africa could be caused by NTM. Thus, inconclusive diagnosis of pulmonary TB would lead to overdiagnosis of TB and in some cases, to inappropriate treatment for NTM infections.

When NTM are isolated from a usually sterile site (e.g., blood, bone marrow, lymph nodes, synovial fluid), diagnosis of true disease is generally straightforward. However, when NTM are isolated from nonsterile sources, such as sputum or bronchoalveolar lavage samples, the diagnosis is less definitive, especially when the colony numbers are low or NTM are isolated from only 1 cultured specimen. Therefore, it is a challenge to differentiate true NTM lung disease from contamination and colonization. Thus, finding AFB by microscopy of respiratory specimens or by culture may pose a diagnostic problem for the clinician. In 1997, the American Thoracic Society (ATS), published useful criteria for determining the clinical relevance of NTM isolates (7). In 2007, the ATS guidelines were revised to include more lenient diagnostic criteria (8). Clinical criteria include a symptomatic patient with pulmonary symptoms, nodular or cavitary opacities on chest radiographs, or a high-resolution computed tomography scan that shows multifocal bronchiectasis with multiple small nodules. In addition, the microbiologic criteria comprise positive culture results from >2 separate sputum samples, or positive culture results from >1 bronchial wash or lavage, or a lung biopsy specimen with mycobacterial histopathologic features (granulomatous inflammation or AFB) and positive culture for NTM, or lung biopsy specimen showing mycobacterial histopathologic features and >1 sputum or bronchial washing culture positive for NTM.

In a pilot study performed in 3 hospitals in Zambia in 2001, high rates of NTM culture–positive sputum samples were obtained (P.C.A.M. Buijtels et al., unpub. data). Therefore, we studied the clinical relevance of and risk factors for isolation of NTM from HIV-positive and HIV-negative patients with chronic productive cough and from randomly selected community controls in Zambia.

Materials and Methods

The study was conducted in St. Francis Hospital in the district of Katete in Zambia from August 2002 through March 2003. Informed consent was obtained from all patients and controls before enrollment. The study was reviewed and approved by the research ethics committee of the University of Zambia, the Central Board of Health, and the Ministry of Health in Zambia.

The study population was composed of adults (>15 years of age) with chronic (defined as >2 weeks) signs and symptoms and a productive cough who were admitted to the department of internal medicine at the hospital. Most (96%) of the included patients had respiratory tract symptoms. The other 4% of the patients had skin infections/abscesses or lymphadenopathy.

For each eligible patient who consented to participate in the study, 2 healthy community controls were recruited randomly from the neighboring community. These controls were not matched for age or other characteristics of the patients. Nested within this case–control study, the characteristics of NTM-positive and NTM-negative persons were analyzed separately.

At the time of enrollment, patients and controls were interviewed in their own language, and their medical records were reviewed by using a standard form. A detailed physical examination was conducted. Chest radiographs were evaluated in a blinded manner in the Netherlands without any additional clinical information. Radiographs were scored for mediastinal adenopathy, cavitation, pleural and pericardial fluid, miliary pathologic changes, alveolar infiltration, interstitial pathologic changes, other lung pathologic changes, or no pathologic changes. Results of the scoring system were chest radiographs with no pathologic changes, pathologic changes not suggestive of TB, and pathologic changes consistent with TB. Over 3 consecutive days, sputum was collected from patients with a productive cough. Controls were asked to gargle with normal saline if they could not produce sputum. The first 2 sputum samples or gargle specimens were cultured for mycobacteria, and a third sample was stored at –20°C until used.

Laboratory Methods

Sputum or gargle specimens were divided into 2 equal parts: half was decontaminated with N-acetyl-l-cysteine–NaOH and half was decontaminated by using 6% sulfuric acid to compare these decontamination procedures for culture of mycobacteria (9). Specimens were cultured in Mycobacteria Growth Indicator Tubes (Becton Dickinson Microbiology Systems, Cockeysville, MD, USA) according to the manufacturer’s instructions and guidelines reported by Master (10). Mycobacterium isolates were identified by using the Accuprobe culture confirmation test for the M. tuberculosis complex (Accuprobe; bioMérieux, Marcy l’Etoile, France) or by 16S rRNA gene sequencing (11). Serologic testing for HIV was performed by using a qualitative immunoassay (Determine HIV-1/2; Abbott Laboratories, Abbott Park, IL, USA) and the Vidas HIV DUO assay (bioMérieux).

Data Analysis

Data were entered into SPSS version 6 software (SPSS Inc., Chicago, IL, USA) and analyzed by using STATA version 8.0 (StataCorp., College Station, TX, USA). Student t-tests were used to assess different means between groups; proportions were compared by using χ2 tests. Univariate odds ratios with 95% confidence intervals were calculated to assess associations of potential risk factors for NTM positivity. A stepwise backward regression approach was used for multivariate analysis.

Body mass index (BMI) was calculated as weight in kilograms divided by squared height in meters. Underweight was defined as a BMI <18.

Clinical Diagnosis of NTM Lung Disease

NTM lung disease was diagnosed if patients had respiratory symptoms, abnormal chest radiographic results suggestive of Mycobacterium infection, and 2 positive sputum cultures with the same NTM. Patients or controls with positive NTM cultures who did not meet these criteria were considered colonized.


From August 2002 through February 2003, 180 patients and 385 controls were enrolled in the study. Two sputum samples were cultured from 154 patients and 383 controls, and from 1 sample of the remaining participants. The median age of the patients and controls was 35 years (range 16–80 years) and 30 years (range 15–78 years), respectively. Female participants represented 55% (99/180) of the patient group and 69% (265/385) of the control group. A total of 128 (71%) of the patients were HIV positive, and 87 (23%) of the controls were HIV positive. Statistically significant differences in age, sex, and HIV status were observed between patients and controls.

Culture Results for Patients

Of 180 patients, 60 (33%) had only M. tuberculosis isolates in their sputum samples, 12 (7%) had M. tuberculosis and NTM, and 19 (11%) had only NTM (Table 1). Microscopic results of Ziehl-Neelsen–stained smears of sputum samples were positive in 46 (67%) of 69 patients with M. tuberculosis isolates and in 1 patient with an NTM-positive culture.

Of the 31 NTM-positive patients, 29 had 2 consecutive sputum samples subjected to culture. In 22 of the 29 patients, only 1 of 2 cultures was positive. Four NTM-positive patients had 2 positive NTM cultures; 1 of these patients had pulmonary disease. M. intracellulare was isolated twice from 2 of these 4 patients, M. avium was isolated from both samples from 1 patient, and NTM of 2 species and M. tuberculosis was isolated from 1 patient. One of 2 sputum cultures from 3 other NTM-positive patients contained mycobacteria that could not be identified. Two of these 3 patients had M. intracellulare in 1 sputum sample; M. porcinum was isolated from 1 patient.

Case Reports for Patients with Suspected NTM Disease

Characteristics of the 4 patients with NTM isolates in both sputum samples and of the 3 NTM-positive patients from whom 1 of the 2 sputum samples contained mycobacteria that could not be identified are shown in Table 2. For 3 patients (1, 2, and 4), NTM-associated disease was suspected because of the combination of symptoms, positive cultures, and pathologic changes consistent with TB seen on chest radiographs. However, only 1 patient (patient 4) fulfilled the ATS criteria for NTM lung disease. M. intracellulare was isolated from all 3 of these patients.

The first patient (patient 4) was a 32-year-old HIV-positive man who reported having had a productive cough with hemoptysis for 17 weeks. He also was vomiting and had diarrhea. His BMI was 15. He had been treated for TB. Results of a chest radiograph were consistent with TB and showed alveolar infiltration and interstitial pathologic changes. His condition did improve after treatment with antimicrobial drugs (chloramphenicol and tetracycline), and he was again given treatment for TB. Mycobacteria were cultured from 2 sputum samples and identified as M. intracellulare. The patient died 5 weeks later.

The second patient (patient 1), who had M. intracellulare pulmonary disease, was a 55-year-old HIV-positive man. He was admitted because of a productive cough with hemoptysis for 17 weeks. Diarrhea was also reported; his BMI was 17. He had been receiving treatment for TB for 4 months. Sputum obtained before treatment was AFB negative. Radiographic investigation of the chest showed cavities and alveolar consolidation. No improvement was seen after he was treated with antimicrobial drugs (chloramphenicol, amoxicillin, gentamicin, and metronidazole). Sputum was examined again and was smear positive for AFB. The first sputum culture showed M. intracellulare. In the second sputum culture, the isolated mycobacteria could not be identified because of logistic reasons. The patient died 3 weeks later.

The third patient (patient 2), who had M. intracellulare pulmonary disease, was a 45-year-old HIV-positive woman who had had respiratory signs and symptoms for >1 year. She was known to have asthma. Physical examination found enlarged submandibular, supraclavicular, and axillary lymph nodes. Her BMI was 20. Alveolar infiltration was seen on a chest radiograph. Treatment with chloramphenicol was started. Culture of the first sputum sample showed mycobacteria that could not be identified; the second sputum showed M. intracellulare. Three days after admission, the patient was taken home by her family and was lost to follow-up.

Culture Results for Controls

M. tuberculosis was cultured from sputum or gargle specimens from 3 (0.8%) of the 385 controls; in 1 of these 3 controls, NTM and M. tuberculosis were isolated (Table 1). In 61 (16%) controls, only NTM were isolated; this number was comparable with the proportion of patients among whom only NTM were isolated (11%; p = 0.2). In 61 of 62 NTM-positive controls, only 1 sputum or gargle specimen was culture positive for NTM. In 1 control, who was HIV negative, 2 mycobacteria, M. porcinum and an unknown Mycobacterium sp., were isolated. No chest radiographs suggestive of TB were observed for any of the controls.

From 383 controls, 2 sputum or gargle samples were cultured for Mycobacterium spp. Significantly fewer controls (1/383) than patients (4/154) had 2 sputum or gargle cultures positive for NTM (p<0.05).

Mycobacterium spp. Isolated

To compare the influence of the decontamination method on the yield of mycobacteria, we divided sputum or gargle samples from all patients and controls into 2 equal parts before decontamination (9). A total of 635 sputum samples were cultured from 180 patients, and 1,532 sputum or gargle samples were cultured from 385 controls. The results of the cultures are shown in Table 3. The number of NTM (72) isolated from 635 sputum samples of patients was significantly higher than the number of NTM (99) isolated from 1,532 sputum or gargle samples from controls (11% and 6%, respectively, (p<0.001).

Mycobacteria were isolated from 273 (43%) of 635 sputum samples from patients; M. tuberculosis isolates were found in 201 (74%) of the 273 positive sputum specimens, and NTM were found in 72 (26%). The most frequently isolated NTM was M. intracellulare, which was found in 12 specimens.

Mycobacteria were isolated from 104 (6.8%) of 1,532 sputum or gargle samples cultured from the controls. M. tuberculosis was found in 5 (4.8%) of the 104 positive cultures, and NTM were found in 99 (95%). The predominant NTM isolated from the controls were M. avium (5 specimens), M. goodii (4 specimens), and M. peregrinum (4 specimens).

A total of 55 (32%) of 171 NTM isolated from patients and controls were not identified because their 16S rDNA sequences were absent in the BLAST (National Center for Biotechnology Information, Bethesda, MD, USA, database. These 55 NTM species were closely related to various Mycobacterium spp. such as M. intracellulare, M. malmoense, M. fortuitum, M. smegmatis, and M. terrae.

Comparison of Persons with and without NTM in Sputum or Gargle Samples

The 93 patients and controls with NTM-positive cultures had different clinical and radiographic features than the 472 patients and controls without NTM in sputum samples (Table 4). These persons were more likely to report vomiting and diarrhea, were more often underweight (BMI<18), more often had general malaise, and their chest radiographs more frequently showed changes consistent with TB, such as consolidation and interstitial changes. HIV status and presence of M. tuberculosis in the sputum culture did not differ between the NTM-positive and NTM-negative groups. There were no significant differences between these groups in terms of age (mean 36.7 years vs. 34.8 years; p = 0.2), sex, smoking habits, alcohol use, and previous treatment for TB (Table 5). The percentages of farmers and of persons in both groups who used unboiled milk were comparable. Moreover, NTM-positive persons used tap water more often than NTM-negative persons (p = 0.004). A subgroup analysis, restricted to patients with NTM and patients without NTM in sputum, yielded similar results (data not shown).

Independent risk factors for NTM culture–positive sputum were determined by using multivariate analysis. Two factors, underweight (BMI<18) and use of tap water, were independently associated with having an NTM-positive sputum culture (Table 6).


The purposes of this study were to compare the prevalence of NTM in sputum between hospitalized chronically ill patients and community controls and to determine the clinical importance of isolation of NTM. The proportions of patients and controls with positive sputum or gargle cultures for NTM were comparable (11% and 15%, respectively). However, the proportion of NTM-positive sputum samples was higher for patients than for controls (11% and 6%, respectively). This finding suggests that persistent NTM are associated with chronic illness in these patients. It is not known whether culture results were influenced by the method of obtaining specimens. A gargle specimen contains flora of the oropharyngeal mucosa, whereas a sputum sample contains flora of the lower airways. In the patient group, more persons were capable of producing sputum, which may have influenced the yield of positive NTM-positive cultures.

NTM lung disease was definitively diagnosed for 1 patient and probable diagnosis was made for 3 patients (nos. 1, 2, and 4; Table 2). M. intracellulare was isolated from the sputum samples of these HIV-positive patients. These patients had respiratory symptoms, and chest radiographs showed pathologic changes compatible with TB. Unfortunately, in 2 of these patients, 1 of 2 sputum samples with mycobacteria could not be identified because of contamination and reculture problems.

The combination of symptoms, positive cultures, and pathologic changes seen on chest radiographs are characteristics of NTM infection and suggestive of NTM pulmonary disease. However, the ATS criteria valid at the time of the study were not completely fulfilled because only 2 sputum samples were cultured for mycobacteria on consecutive days, instead of the 3 samples recommended. Furthermore, 2 of these patients suspected of having NTM lung disease had been treated for TB. Because these sputum samples were not tested with molecular amplification techniques for multidrug-resistant M. tuberculosis, the possibility that they had multidrug-resistant TB could not be excluded (12,13). Conversely, performance of these nucleic acid amplification tests is generally good for clinical respiratory specimens that are AFB smear positive but less so for specimens that contain fewer organisms or are AFB negative. Moreover, because sputum specimens were not cultured on solid medium, it was not possible to count the number of colony-forming units to distinguish colonization and infection from disease.

Many risk factors for NTM have been identified (1416). In this study in a setting in Africa, HIV, sex, and age were not risk factors for NTM. The 2 risk factors for a positive NTM culture were being underweight and having consumed tap water. NTM are natural inhabitants of municipal water systems and soil. A biofilm may form in the water distribution system and be a source of replicating NTM (17). Consequently, availability of clean tap water may introduce a serious danger, in particular, to immunosuppressed human populations. Therefore, tap water in Zambia should be tested for NTM.

In this study, patients and controls with NTM in sputum or gargle samples more often had symptoms and signs of general malaise, including diarrhea, vomiting, and being underweight, and chest radiographs for these NTM-positive persons more often showed pathologic changes than did those for NTM culture-negative persons. These symptoms and signs may not be specific for NTM infection, but they may reflect the patients’ poor health in general.

Differences in geographic distribution of NTM species have been reported (16,18,19). The most commonly encountered NTM from clinical specimens in industrialized countries are M. avium complex (MAC) and M. kansasii (2024). Despite limited studies conducted in Africa, the distribution of NTM is not known. In our study, the most commonly isolated NTM in patients and controls was M. avium complex. However, 32% of NTM found in both groups in Zambia have not been identified on a species level. This study indicates that the distribution of NTM in Africa may differ from that in Europe and the United States. NTM in Africa may have diverged from NTM in industrialized countries. This hypothesis could be tested by extensive DNA sequencing of semiconserved genes such as those for RNA polymerase B and 65-kD heat-shock protein. Unidentified NTM colonize persons in Africa and can cause disease in some instances. The magnitude of this problem, in addition to the problem of TB, is unknown but deserves more attention.

Rates of NTM colonization and disease that have been reported vary in different areas. In North America and Europe, rates of colonization and disease in the general population range from ≈1–15/100,000 persons to 0.1–2/100,000 persons, respectively (2023,2528). These rates are largely unknown for most countries in Africa. In South Africa, prevalence rates of NTM colonization of 1,400–6,700/100,000 persons have been reported (29,30). In gold miners in South Africa, rates of infection were 101/100,000 persons for NTM, 66/100,000 persons for M. kansasii, and 12/100,000 persons for M. scrofulaceum (31,32). Although numbers of cases were small, the estimated rate of colonization in our study in the patient population was 9% (14/154) and the rate of disease was ≈2% (3/154). Two sputum or gargle specimens were collected and cultured from 383 controls in our study. NTM were isolated from both specimens for 1 of 61 controls with >1 sample being culture positive for NTM. This control was not suspected of having NTM pulmonary disease. The estimated rate of colonization in the general population on the basis of this result is 16% (61/383).

NTM probably play a role in the etiology of TB-like disease in Zambia. More extended studies, in terms of duration and size, will be needed to determine the true prevalence of NTM infection in Africa.

Dr Buijtels is a medical microbiologist at the University Medical Centre in Utrecht. Her research interests include the clinical relevance of NTM in Africa.



We thank Shirley Visser-Triep and Astrid Bos-Grit for excellent laboratory assistance, Wouter Tietge and Ilse van den Berg for sampling a subgroup of the controls, the staff of St. Francis Hospital in Katete for their teamwork and cooperation, and Margôth Petit-Vijgen for managing the extended patient database.

This study was supported by the partnership of microbiologists at the Medical Centre Rijnmond-South in Rotterdam and The Netherlands Society of Tropical Medicine and International Health.



  1. Elliott  AM, Halwiindi  B, Hayes  RJ, Luo  N, Mwinga  AG, Tembo  G, The impact of human immunodeficiency virus on response to treatment and recurrence rate in patients treated for tuberculosis: two-year follow-up of a cohort in Lusaka, Zambia. J Trop Med Hyg. 1995;98:921.PubMedGoogle Scholar
  2. Githui  W, Nunn  P, Juma  E, Karimi  F, Brindle  R, Kamunyi  R, Cohort study of HIV-positive and HIV-negative tuberculosis, Nairobi, Kenya: comparison of bacteriological results. Tuber Lung Dis. 1992;73:2039. DOIPubMedGoogle Scholar
  3. Scott  JA, Hall  AJ, Muyodi  C, Lowe  B, Ross  M, Chohan  B, Aetiology, outcome, and risk factors for mortality among adults with acute pneumonia in Kenya. Lancet. 2000;355:122530. DOIPubMedGoogle Scholar
  4. Fordham von Reyn  C, Arbeit  RD, Tosteson  AN, Ristola  MA, Barber  TW, Waddell  R, The international epidemiology of disseminated Mycobacterium avium complex infection in AIDS. International MAC Study Group. AIDS. 1996;10:102532. DOIPubMedGoogle Scholar
  5. Gilks  CF, Brindle  RJ, Mwachari  C, Batchelor  B, Bwayo  J, Kimari  J, Disseminated Mycobacterium avium infection among HIV-infected patients in Kenya. J Acquir Immune Defic Syndr Hum Retrovirol. 1995;8:1958. DOIPubMedGoogle Scholar
  6. Morrissey  AB, Aisu  TO, Falkinham  JO III, Eriki  PP, Ellner  JJ, Daniel  TM. Absence of Mycobacterium avium complex disease in patients with AIDS in Uganda. J Acquir Immune Defic Syndr. 1992;5:4778. DOIPubMedGoogle Scholar
  7. American Thoracic Society. Diagnosis and treatment of disease caused by nontuberculous mycobacteria. Am J Respir Crit Care Med. 1997;156:S125.PubMedGoogle Scholar
  8. Griffith  DE, Aksamit  T, Brown-Elliott  BA, Catanzaro  A, Daley  C, Gordin  F, An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med. 2007;175:367416. DOIPubMedGoogle Scholar
  9. Buijtels  PC, Petit  PL. Comparison of N-acetyl-L-cysteine-NaOH and sulphuric acid decontamination method for recovery of mycobacteria from clinical specimens. J Microbiol Methods. 2005;62:838. DOIPubMedGoogle Scholar
  10. Master  RN. Mycobacteriology. In: Isenberg HD, editor. Clinical microbiology procedures handbook. Washington: American Society for Microbiology; 1994.
  11. Kirschner  P, Bottger  EC. Species identification of mycobacteria using rDNA sequencing. Methods Mol Biol. 1998;101:34961.PubMedGoogle Scholar
  12. Centers for Disease Control and Prevention. Update: nucleic acid amplification tests for tuberculosis. JAMA. 2000;284:826. DOIPubMedGoogle Scholar
  13. Traore  H, van Deun  A, Shamputa  IC, Rigouts  L, Portaels  F. Direct detection of Mycobacterium tuberculosis complex DNA and rifampin resistance in clinical specimens from tuberculosis patients by line probe assay. J Clin Microbiol. 2006;44:43848. DOIPubMedGoogle Scholar
  14. Bloch  KC, Zwerling  L, Pletcher  MJ, Hahn  JA, Gerberding  JL, Ostroff  SM, Incidence and clinical implications of isolation of Mycobacterium kansasii: results of a 5-year, population-based study. Ann Intern Med. 1998;129:698704.PubMedGoogle Scholar
  15. O’Brien  DP, Currie  BJ, Krause  VL. Nontuberculous mycobacterial disease in northern Australia: a case series and review of the literature. Clin Infect Dis. 2000;31:95867. DOIPubMedGoogle Scholar
  16. O’Brien  RJ, Geiter  LJ, Snider  DE Jr. The epidemiology of nontuberculous mycobacterial diseases in the United States. Results from a national survey. Am Rev Respir Dis. 1987;135:100714.PubMedGoogle Scholar
  17. Falkinham  JO III. Nontuberculous mycobacteria in the environment. Clin Chest Med. 2002;23:52951. DOIPubMedGoogle Scholar
  18. Subcommittee of the Joint Tuberculosis Committee of the British Thoracic Society. Management of opportunist mycobacterial infections: Joint Tuberculosis Committee guidelines 1999. Thorax. 2000;55:2108. DOIPubMedGoogle Scholar
  19. Tsukamura  M, Kita  N, Shimoide  H, Arakawa  H, Kuze  A. Studies on the epidemiology of nontuberculous mycobacteriosis in Japan. Am Rev Respir Dis. 1988;137:12804.PubMedGoogle Scholar
  20. Debrunner  M, Salfinger  M, Brandli  O, von Graevenitz  A. Epidemiology and clinical significance of nontuberculous mycobacteria in patients negative for human immunodeficiency virus in Switzerland. Clin Infect Dis. 1992;15:33045.PubMedGoogle Scholar
  21. Good  RC. Isolation of nontuberculous mycobacteria in the United States, 1979. J Infect Dis. 1980;142:77983.PubMedGoogle Scholar
  22. Good  RC, Snider  DE Jr. Isolation of nontuberculous mycobacteria in the United States, 1980. J Infect Dis. 1982;146:82933.PubMedGoogle Scholar
  23. Isaac-Renton  JL, Allen  EA, Chao  CW, Grzybowski  S, Whittaker  EI, Black  WA. Isolation and geographic distribution of Mycobacterium other than M. tuberculosis in British Columbia, 1972–81. CMAJ. 1985;133:5736.PubMedGoogle Scholar
  24. Wayne  LG, Kubica  GP. The mycobacteria. In: Sneath PH, Holt JG, editors. Bergey’s manual of systematic bacteriology. Baltimore: Williams and Wilkins; 1986. p.1435–57.
  25. Bollert  FG, Watt  B, Greening  AP, Crompton  GK. Non-tuberculous pulmonary infections in Scotland: a cluster in Lothian? Thorax. 1995;50:18890. DOIPubMedGoogle Scholar
  26. Lortholary  O, Deniel  F, Boudon  P, Le Pennec  MP, Mathieu  M, Soilleux  M, Mycobacterium kansasii infection in a Paris suburb: comparison of disease presentation and outcome according to human immunodeficiency virus status. Groupe d’Etude Des Mycobacteries de la Seine-Saint-Denis. Int J Tuberc Lung Dis. 1999;3:6873.PubMedGoogle Scholar
  27. Marks  J. “Opportunist” mycobacteria in England and Wales. Tubercle. 1969;50(Suppl):7880. DOIPubMedGoogle Scholar
  28. Robakiewicz  M, Grzybowski  S. Epidemiologic aspects of nontuberculous mycobacterial disease and of tuberculosis in British Columbia. Am Rev Respir Dis. 1974;109:61320.PubMedGoogle Scholar
  29. Arabin  G, Gartig  D, Kleeberg  HH. First tuberculosis prevalence survey in KwaZulu. S Afr Med J. 1979;56:4348.PubMedGoogle Scholar
  30. Fourie  PB, Gatner  EM, Glatthaar  E, Kleeberg  HH. Follow-up tuberculosis prevalence survey of Transkei. Tubercle. 1980;61:719. DOIPubMedGoogle Scholar
  31. Corbett  EL, Hay  M, Churchyard  GJ, Herselman  P, Clayton  T, Williams  BG, Mycobacterium kansasii and M. scrofulaceum isolates from HIV-negative South African gold miners: incidence, clinical significance and radiology. Int J Tuberc Lung Dis. 1999;3:5017.PubMedGoogle Scholar
  32. Corbett  EL, Blumberg  L, Churchyard  GJ, Moloi  N, Mallory  K, Clayton  T, Nontuberculous mycobacteria: defining disease in a prospective cohort of South African miners. Am J Respir Crit Care Med. 1999;160:1521.PubMedGoogle Scholar




Cite This Article

DOI: 10.3201/eid1502.080006

Table of Contents – Volume 15, Number 2—February 2009

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.



Please use the form below to submit correspondence to the authors or contact them at the following address:

Patricia C.A.M. Buijtels, Meander Medical Centre, Location Lichtenberg, Laboratory for Medical Microbiology and Immunology, Utrechtseweg 160, 3818 ES Amersfoort, the Netherlands;

Send To

10000 character(s) remaining.


Page created: December 08, 2010
Page updated: December 08, 2010
Page reviewed: December 08, 2010
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.