Volume 17, Number 3—March 2011
Epidemiology of Mycobacterium bovis Disease in Humans, the Netherlands, 1993–2007
In the Netherlands, 1.4% of tuberculosis (TB) cases are caused by Mycobacterium bovis. After we admitted 3 patients with M. bovis infections to our reference hospital, we conducted a retrospective analysis of all M. bovis disease in the Netherlands during 1993–2007. We analyzed data from 231 patients for clinical, demographic, treatment, and outcome characteristics and for risk factors. Most patients were native Dutch (n = 138; 59.7%) or Moroccan (n = 54; 23.4%). Disease was mainly extrapulmonary (n = 136; 58.9%). Although 95 patients had pulmonary disease, person-to-person transmission did not occur, as shown by structural DNA fingerprinting analysis. Lymph node TB was more likely to develop in women (p<0.0001), whereas pulmonary M. bovis disease developed more frequently in men (p<0.0001). Diagnosis was accurate but delayed and led to inadequate treatment in 26% of the cases. Proportion of deaths from M. bovis disease was higher than that for M. tuberculosis disease.
Mycobacterium bovis disease was common in the Western world in the era before pasteurization of milk products. In 1938, the percentage of M. bovis disease among all patients with tuberculosis (TB) was 9% in Amsterdam and 11% in the rest of the Netherlands. In 1940, pasteurization became obligatory, and in 1952, the percentage of M. bovis disease had dropped to 1.5%–2.0% in Amsterdam (1,2). From 1945 until the mid-1960s, M. bovis infection was gradually eradicated in livestock in the Netherlands. Nevertheless, during 1973–1975, ≈2.5% of the human TB cases in the Netherlands were still caused by M. bovis (3). Since 1993, only 10 cases of M. bovis infection have occurred in livestock in the Netherlands. All were caused by infected livestock that had been imported (D. Bakker, pers. comm.). Because most M. bovis infections are contracted through the oral route, extrapulmonary manifestations were primarily observed.
Diagnosing extrapulmonary TB is generally difficult, and as the prevalence of TB has declined, the experience of physicians in diagnosing this specific infectious disease has also decreased, and therefore the time to diagnosis has increased (4,5). The difficulties in the diagnosis and treatment of M. bovis infections in 3 female patients at the University Centre for Chronic Diseases Dekkerswald prompted the present study. To investigate the magnitude of M. bovis infection in persons in the Netherlands, we conducted a retrospective study of patients with M. bovis infection and describe the epidemiologic, clinical, and bacteriologic findings.
We retrieved data from 2 databases: one at the National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands, which contains the bacteriologic information of all M. tuberculosis complex isolates in the Netherlands. The other is the Netherlands Tuberculosis Register (NTR), an anonymous case register held by KNCV Tuberculosis Foundation in The Hague, the Netherlands. This database is based on voluntary registration but contains data from virtually all TB patients in the Netherlands.
The patients in the NTR database have been registered by their physicians. This register holds basic demographic, clinical, and some bacteriologic data. Death is registered as TB related or not TB related without further explanation. Treatment and treatment outcome are registered without further details. Exact treatment length could be determined because length was registered in 2 different categories. Therefore, we could categorize treatment length in 6 groups, namely <3 months, 4–5 months, 6 months, 7–9 months, 10–12 months, and >12 months.
We selected all M. bovis cases that occurred during 1993–2007. By using these 2 databases we had information on bacteriologic and clinical factors, demographic data, and risk factors, as well as treatment and outcome. We used the RIVM database for the bacteriologic data and localization of the infections and the NTR database for the demographic and clinical data, including treatment outcome. To distinguish M. bovis caprae and M. bovis bovis infections, we reviewed available data on IS6110 restriction fragment length polymorphism, spoligotyping, and pyrazinamide susceptibility for all M. bovis isolates analyzed in this study (6,7). Because IS6110 typing of all M. tuberculosis complex isolates is routinely performed in the Netherlands, we also analyzed information on possible interhuman transmission of M. bovis.
Associations between localization of infection in the patient, geographic distribution, ethnicity, etc. were evaluated on basis of information from both databases by using the χ2 test. Mortality rates were evaluated by using the NTR database and were correlated with the demographic and clinical data.
A 73-year-old woman sought treatment for nonproductive cough and dyspnea. Medical history included severe rheumatoid arthritis, for which she had received treatment with anti–tumor necrosis factor-α (TNF-α) for 1 year. High-resolution computed tomography (CT) imaging of the thorax showed micronodular lesions in both lungs. CT imaging of the brain indicated several cerebral nodular lesions, suspected to be tuberculomas. Culture of bronchoalveolar lavage fluid yielded M. bovis. The patient was treated with isoniazid, rifampin, and ethambutol. Moxifloxacin and steroids were added, because of the high penetration level through the blood–brain barrier of moxifloxacin and to compensate for the absence of pyrazinamide in the treatment regimen.
An 84-year-old woman with a medical history of myelodysplastic syndrome and diabetes mellitus type 2 sought treatment for a traumatic leg wound that did not heal, and her condition gradually progressed to generalized skin lesions. She was referred to the dermatologist in our hospital. Culture of a skin biopsy specimen grew M. bovis. The patient had lesions on her tongue, typical of TB (Figure 1), and on her the larynx and in her lungs. The patient’s condition resolved after 9 months of treatment with isoniazid, rifampin, and ethambutol. Contact tracing showed no human transmission.
An 87-year-old woman with severe rheumatoid arthritis sought treatment for weight loss, cough, night sweats, and dyspnea 1 year after starting anti–TNF-α treatment. Radiologic imaging showed a single nodular lesion of the lung parenchyma and pleural fluid. Culture of a bronchoalveolar lavage specimen yielded M. bovis. The patient received isoniazid, ethambutol, and moxifloxacin for 18 months because she had an intolerance for rifampin. No contact tracing was performed.
During 1993–2007, a total of 16,059 patients were registered in the NTR with culture-proven TB; 231 (1.4%) patients were registered with M. bovis infection (8) (Figure 2). The number of patients with M. bovis infection born outside the Netherlands (foreign-born) showed an increase in the proportion from 35.1% to 46.3% in the 1ast 5 years of the study period (Figure 3). Over time, the percentage of patients with M. bovis TB who live in major cities increased from 33.3% to 41.8%, with an accompanying decline elsewhere in the Netherlands. No relation was found between outbreaks in livestock and human disease.
Among patients with M. bovis disease, a significant difference in mean age was noted among those born in the Netherlands and immigrants. In native Dutch persons with M. bovis disease, the median age was 64.8 years, whereas among immigrants, the median age was 38.6 years (Figure 4). We observed 58 cases in young foreign-born patients and 16 cases in young Dutch patients (<40 years). Five Dutch patients had a general risk factor for contracting M. tuberculosis complex disease (1 with drug addiction, 1 with alcohol addiction, and 3 with risk factors not specified) and 44 foreign-born had 1 or 2 general risk factors (32 immigrants, 8 with fugitive status, 3 illegal immigrants, and 1 TB contact, 1 in criminal detention, 1 with risk factor not specified).
Most of the patients were native Dutch (138 [59.7%] of 231). Most foreign-born patients came from Morocco (54 [23.4%] of 231). The other immigrants had other places of origin: Europe (n = 6; 2.6%), Africa (n = 15; 6.5%), Asia (n = 9; 3.9%), and South America (n = 3; 1.3%) (Table 1). A distinction between native Dutch and second-generation Dutch immigrants could not be made.
M. bovis TB mainly had appeared as extrapulmonary disease; 136 (58.9%) of 231 patients had extrapulmonary disease alone, 68 (29.4%) of 231 had pulmonary M. bovis disease, and 27 (11.7%) of 231 had both pulmonary and extrapulmonary disease. A significant difference between men and women was found in terms of localization of disease. In women, lymph node TB was more likely to develop, mainly in the cervical region (p<0.0001); men more often had pulmonary M. bovis disease (p<0.0001). This finding was seen in all age groups in both Dutch and foreign-born patients. (Table 1)
Several treatment schedules were used for our study population; 157 of 231 patients received a combination of isoniazid, rifampin, ethambutol, and pyrazinamide, or another pyrazinamide-containing antimicrobial drug combination. Treatment with pyrazinamide-containing regimens had no negative effect on treatment outcome.
According to World Health Organization (WHO) standards, a regimen of isoniazid and rifampin for 9 months and ethambutol for 2 months is indicated for treating M. bovis disease. In our study population, we noted that 113 (52%) of 217 patients were cured and completed treatment according to the WHO standard. Thirty-seven (17%) of 217 patients were considered cured with an insufficient treatment schedule, duration, or both. For 14 patients, outcome data were not available. No significant associations were found between insufficient treatment and particular disease localizations or outcome.
An anonymous questionnaire distributed to the physicians who were caring for the patients at the time of disease (34 sent and 24 returned) showed that most of the physicians followed the Dutch TB guidelines, which are based on the WHO standard. A problem these colleagues faced was the time lag between sampling and the results of culture, identification, and drug susceptibility tests, which sometimes took as long as 4 months.
Treatment outcome comparisons for Dutch and foreign-born patients in the Netherlands are shown in Table 2. The overall proportion of deaths for the infection itself was 5.2% for M. bovis disease, and the proportion of deaths associated with non–TB-related causes (e.g., cardiac disease and hematologic malignancy) for patients with M. bovis disease was 14.7%.
An analysis of the overall deaths from bovine TB according to sex, age, ethnicity, and disease localization is shown in Table 3. A correlation was found between death and age >60 years, Dutch nationality, and miliary disease. When dividing deaths into the categories of TB related and not–TB related, only high age was statistically significant between the groups; all other variables were not significant (Table 4). Cause and rate of death differed between sexes: among women, death was more often related to M. bovis TB; in men, the overall mortality rate was higher, although these differences were not statistically significant.
M. bovis TB comprised 1.4% of all TB cases in the Netherlands during 1993–2007. This finding is comparable to those of studies in other countries where control and corresponding control efforts of M. bovis TB in livestock are present (9–11). During 1993–1997, mainly elderly Dutch persons were found to have bovine TB; later (1998–2007), the infections were divided more equally between the native Dutch and immigrants (Figure 3).
M. bovis TB in the population of the Netherlands shows an age curve with double peaks. The younger patients were mostly foreign-born or first- and second-generation immigrants, who may have (frequently) traveled back to their country of origin or contracted an M. bovis infection by the oral route before coming to the Netherlands. These patients more often had extrapulmonary M. bovis disease, which mainly affected the cervical or abdominal lymph nodes. Ingestion of unpasteurized dairy products is the most likely route of infection (12,13). The 12 Dutch patients, ages 20–40 years, may have been in contact with nonpasteurized food while traveling to developing countries because the chance of contracting a M. bovis infection in the Netherlands is considered low.
The second age peak contains elderly native-born Dutch persons. This result is most likely a birth-cohort effect because these persons most probably had a late endogenous reactivation of latent M. bovis infection contracted in the era before pasteurization of milk was introduced and while M. bovis infection in livestock was still highly prevalent in the Netherlands. Spoligotyping of their isolates showed a single typical pattern, which is considered the old predominant cattle-endemic strain of the Netherlands (14). This epidemiologic trend has also been seen in other European countries, including Norway, Sweden, and Belgium (9,10).
Endogenous reactivation of M. bovis infections in elderly patients follows impairment of immunity from hematologic causes, immune modulation by medication (including anti–TNF-α treatment), other coexisting conditions, or immunosenescence. As the use of anti–TNF-α treatment rises, due to increasing indications of rheumatologic and gastrointestinal diseases, mycobacterial disease will likely become more common (15). Two of the patients we described had negative tuberculin skin test (for M. tuberculosis complex) and chest radiograph results and, therefore did not receive isoniazid prophylaxis before they received anti–TNF-α treatment. This result calls into question the efficacy of the screening protocol used in the Netherlands to evaluate patients before they receive anti–TNF-α treatment. Of note, reactivations of latent TB usually occur in the first 3–4 months of anti–TNF-α therapy (15), although in our 2 M. bovis patients, reactivation occurred after 1 year. This long-term asymptomatic reactivation of disease has been previously observed (16,17) and raises questions involving the role of the bacteriologic virulence factor in the pace of the reactivations.
In the Netherlands, the 2 largest immigrant populations are from Turkey and Morocco (378,330 and 341,528 persons, respectively) (18). A high occurrence of M. bovis disease was observed in Moroccan patients, whereas, to our surprise, M. bovis disease was rare in Turkish patients. Both populations come from agricultural areas where pasteurization of dairy products is not common. Popular raw milk cheeses in Morocco (jben) and Turkey (kasar, tulum) have been found to contain Listeria and Brucella species in as many as 8.2% of the samples tested (19,20). In both studies, cheeses were not tested for M. bovis. However, M. bovis can survive in raw milk cheese and cause an infection after it is eaten, as was described recently for a cluster of infections resulting from consumption of fresh Mexican cheese in New York and San Diego (12,13,21). Besides consumption of fresh cheese and unpasteurized milk, consumption of raw or undercooked meat is also a possible route of oral transmission (10,22,23).
More women than men were infected by M. bovis, contrary to the epidemiology of M. tuberculosis. Other studies about M. bovis do not show this result (9,11). This difference could be an age-related effect for Dutch patients; however, one can also see this difference in the Moroccan patient population (data not shown).
Notably, we also found a difference in disease localization between men and women. More cervical lymph node TB, which was not correlated with age, was diagnosed for female patients. Female sex has in general been considered a risk factor for M. tuberculosis extrapulmonary TB (24–26). However, this finding has not been described for M. bovis TB. Various explanations have been given for this gender difference in TB. One possible explanation could be a difference in the immunity to M. tuberculosis complex infection. Several studies have been conducted in humans to compare the immune response in both sexes. Differences in reaction among others in TNF and interleukin-10 production have been found (27,28). Another explanation for this finding may be related to the route of infection. Men could be more likely to become infected through the tracheal route by aerosols from diseased cattle, whereas women become infected by ingesting M. bovis while preparing or consuming contaminated food. Lastly, smoking has also been identified as a risk factor for pulmonary TB (25), which (assuming a higher percentage of men are smokers) could explain the difference we found in our study that men have more pulmonary M. bovis disease than women. Unfortunately, we could not retrieve smoking status from the databases.
The geographic distribution of M. bovis TB in the Netherlands showed a proportional increase in M. bovis infections in the major cities in the western part of the Netherlands during 1993–2007. This finding probably reflects the population demographics of the Netherlands, where most persons live in and between major cities, but also by the facts that immigrants mainly live in major cities and that the elderly persons who contracted M. bovis TB in the prepasteurization era are undergoing a natural decline in health.
We showed that, in 37 (17.1%) of the 217 patients, treatment of M. bovis disease cases in this study was not compliant with international guidelines. Although all M. tuberculosis complex isolates in the Netherlands undergo drug susceptibility testing, apparently the results of such testing do not reach clinicians. Recognition of M. bovis as the causative agent of TB does not in itself lead to the conclusion that adjustment of the therapy is required; many physicians only make adjustments after receiving the results of drug susceptibility testing, which usually arrive quite late because of the slow growth of M. bovis. Moreover, the quick molecular identification of cultured M. bovis still implies a culture delay of ≈4 weeks. Better education of physicians and increasing future application of direct molecular identification of M. bovis from clinical samples, i.e., sputum or lymph node aspirates, is therefore needed.
The overall proportion of deaths among patients with M. bovis disease was higher (19.9%) than that among patients with M. tuberculosis disease (4.4%) in the Netherlands. The mortality rates during 1993–2007 were 5.2% for M. bovis disease versus 1.9% for M. tuberculosis disease. This result is probably related to the higher prevalence of miliary and central nervous system localization of M. bovis disease. Death rates from other, non–TB-related, causes for patients with M. bovis infection were 14.7% compared with 2.5% for M. tuberculosis infection (8). Subgroup analysis of M. bovis showed that the proportion of deaths was higher among Dutch than among foreign-born patients, but this result most likely correlates with age and impairment of immunity (10,11,29).
We cannot explain the unexpected trend in lower survival of female patients after an episode of M. bovis disease. Previous studies have shown that male sex is a risk factor for unsuccessful treatment (30,31), but the numbers in our study were too small to draw any firm conclusions.
This study had limitations. First, the analysis of the results was hampered by the relatively low number of foreign-born patients (n = 93) and the heterogeneous nature of the study population. Therefore, only data concerning patients from Morocco (n = 54) could be analyzed separately, and differences with the Dutch case-patients were found in terms of age, mortality rate, and primary localization of disease.
Another limitation is that a distinction could not be made between native Dutch and second-generation immigrants born in the Netherlands. This lack of distinction implies that some patients have roots in a foreign country where the risk for M. bovis TB could be higher.
In conclusion, the incidence of M. bovis disease in the Netherlands is comparable to that in other countries in which control programs for M. bovis infection are enforced. Gender differences in clinical features and mortality rates were found in our cohort of patients. The disease now mainly infects immigrants from Morocco and elderly Dutch citizens. Anti-TNF-α treatment is an emerging cause of endogenous reactivation of M. bovis disease in elderly Dutch patients, as occurred in 2 of the recent bovine TB cases described in this article; reactivation may be slower than for M. tuberculosis infection.
Dr Majoor is a pulmonologist in the Academic Medical Center in Amsterdam. His main research interests are asthma, cystic fibrosis, and TB.
- Ruys AC. Tuberculosis caused by M. bovis in humans in the Netherlands [in Dutch]. Ned Tijdschr Geneeskd. 1938;83:1001–7.
- Ruys AC. The treatment of bovine tuberculosis and epidemiological changes in tuberculosis [in Dutch]. Ned Tijdschr Geneeskd. 1952;96:676–81.
- Schönfeld JK. Infection caused by bovine tuberculum bacteria in humans in the Netherlands during the period 1972–1975 [in Dutch]. Ned Tijdschr Geneeskd. 1978;122:217–9.
- Sherman LF, Fujiwara PI, Cook SV, Bazerman LB, Frieden TR. Patient and health care system delays in the diagnosis and treatment of tuberculosis. Int J Tuberc Lung Dis. 1999;3:1088–95.
- Diwakar L, Logan S, Ghaffar N, Hare A, Lynn W, Ash S. Low back pain: think of tuberculosis. BMJ. 2006;333:201.
- Kamerbeek J, Schouls L, Kolk A, van Agterveld M, van Soolingen D, Kuijper S, Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol. 1997;35:907–14.
- Niemann S, Richter E, Rüsch-Gerdes S. Biochemical and genetic evidence for the transfer of Mycobacterium tuberculosis subsp. caprae Aranaz et al. 1999 to the species Mycobacterium bovis Karlson and Lessel 1970 (approved lists 1980) as Mycobacterium bovis subsp. caprae comb. nov. Int J Syst Evol Microbiol. 2002;52:433–6.
- Erkens CGM, Kalisvaart NA, Slump E, Sebek M, van Soolingen D. Tuberculosis in the Netherlands 2007. Surveillance report [in Dutch]. KNCV Tuberculosefonds, Den Haag; Jan 2009. http://www.kncvtbc.nl/Site/Professional.aspx
- Mignard S, Pichat C, Carret G. Mycobacterium bovis infection, Lyon, France. Emerg Infect Dis. 2006;12:1431–3.
- de la Rua-Domenech R. Human Mycobacterium bovis infection in the United Kingdom: incidence, risks, control measures and review of the zoonotic aspects of bovine tuberculosis. Tuberculosis (Edinb). 2006;86:77–109.
- Hlavsa MC, Moonan PK, Cowan LS, Navin TR, Kammerer JS, Morlock GP, Human tuberculosis due to Mycobacterium bovis in the United States, 1995–2005. Clin Infect Dis. 2008;47:168–75.
- Harris NB, Payeur J, Bravo D, Osorio R, Stuber T, Farrell D, Recovery of Mycobacterium bovis from soft fresh cheese originating in Mexico. Appl Environ Microbiol. 2007;73:1025–8.
- Kinde H, Mikolon A, Rodriguez-Lainz A, Adams C, Walker RL, Cernek-Hoskins S, Recovery of Salmonella, Listeria monocytogenes, and Mycobacterium bovis from cheese entering the United States through a noncommercial land port of entry. J Food Prot. 2007;70:47–52.
- van Soolingen D, de Haas PE, Haagsma J, Eger T, Hermans PW, Ritacco V, Use of various genetic markers in differentiation of Mycobacterium bovis strains from animals and humans and for studying epidemiology of bovine tuberculosis. J Clin Microbiol. 1994;32:2425–33.
- van Ingen J, Boeree MJ, Dekhuijzen PNR, van Soolingen D. Mycobacterial disease in patients with rheumatic disease. Nat Clin Pract Rheumatol. 2008;4:649–56.
- Endean L, Barry SM, Young-Min SA. Possible miliary tuberculosis during adalimumab therapy with negative γ-IFN release assays. Rheumatology. 2009;48:319–20.
- Yoo WH. Multiple organ tuberculosis of lung, pleura, and peritoneum in ankylosing spondylitis during adalimumab therapy. Rheumatol Int. 2010 Jan 5 [Epub ahead of print]. http://www.springerlink.com/content/0172-812/31/1/
- Statline. Centraal Bureau voor de Statistiek 2010 [cited 2010 Apr 3]. http://statline.cbs.nl/StatWeb/publication/?VW=T&DM=SLNL&PA=37296ned&D1=a&D2=0,10,20,30,40,50,(l-1)-l&HD=100105-1504&HDR=G1&STB=T
- Benkerroum N, Oubel H, Zahar M, Dlia S, Filali-Maltouf A. Isolation of a bacteriocin-producing Lactococcus lactis subsp. lactis and application to control Listeria monocytogenes in Moroccan jben. J Appl Microbiol. 2000;89:960–8.
- Aygun O, Pehlivanlar S. Listeria spp. in the raw milk and dairy products in Antakya, Turkey. Food Contr. 17:676–9.
- Centers for Disease Control and Prevention. Human tuberculosis caused by Mycobacterium bovis—New York City, 2001–2004. MMWR Morb Mortal Wkly Rep. 2005;54:605–8.
- van der Merwe M, Bekker JL, van der Merwe P, Michel AL. Cooking and drying as effective mechanisms in limiting the zoonotic effect of Mycobacterium bovis in beef. J S Afr Vet Assoc. 2009;80:142–5.
- Thoen C, Lobue P, de Kantor I. The importance of Mycobacterium bovis as a zoonosis. Vet Microbiol. 2006;112:339–45.
- Martinez AN, Rhee JT, Small PM, Behr MA. Sex differences in the epidemiology of tuberculosis in San Francisco. Int J Tuberc Lung Dis. 2000;4:26–31.
- Lin JN, Lai CH, Chen YH, Lee SS, Tsai SS, Huang CK, Risk factors for extra-pulmonary compared to pulmonary tuberculosis. Int J Tuberc Lung Dis. 2009;13:620–5.
- Peto HM, Pratt RH, Harrington TA, LoBue PA, Armstrong LR. Epidemiology of extrapulmonary tuberculosis in the United States, 1993–2006. Clin Infect Dis. 2009;49:1350–7.
- Temple SE, Pham K, Glendenning P, Phillips M, Waterer GW. Endotoxin induced TNF and IL-10 mRNA production is higher in male than female donors: correlation with elevated expression of TLR4. Cell Immunol. 2008;251:69–71.
- van Eijk LT, Dorresteijn MJ, Smits P, van der Hoeven JG, Netea MG, Pickkers P. Gender differences in the innate immune response and vascular reactivity following the administration of endotoxin to human volunteers. Crit Care Med. 2007;35:1464–9.
- Rodwell TC, Moore M, Moser KS, Brodine SK, Strathdee SA. Tuberculosis from Mycobacterium bovis in binational communities, United States. Emerg Infect Dis. 2006;14:909–16.
- Ditah IC, Reacher M, Palmer C, Watson JM, Innes J, Kruijshaar ME, Monitoring tuberculosis treatment outcome: analysis of national surveillance data from a clinical perspective. Thorax. 2008;63:440–6.
- Fok A, Numata Y, Schulzer M, FitzGerald MJ. Risk factors for clustering of tuberculosis cases: a systematic review of population-based molecular epidemiology studies. Int J Tuberc Lung Dis. 2008;12:480–92.
- Figure 1. Mycobacterium bovis lesion on the tongue of patient 2, the Netherlands.
- Figure 2. Mycobacterium tuberculosis and M. bovis infections, the Netherlands, 1993–2007. Data derived from the National Institute for Public Health and the Environment (RIVM) database.
- Figure 3. Percentage of Mycobacterium bovis infections in foreign-born persons and total number of M. bovis infections, the Netherlands, 1993–2007. Data derived from the National Institute for Public Health and the...
- Figure 4. Number of Mycobacterium bovis infections, according to patient age and origin, the Netherlands, 1993–2007. Data derived from the National Tuberculosis Registry database.
- Table 1. Clinical and demographic data for Mycobacterium bovis TB case-patients, by sex, as recorded in the Netherlands Tuberculosis Registry, the Netherlands, 1993–2007
- Table 2. Treatment results according to age, sex, and localization of Mycobacterium bovis disease in Dutch and foreign-born case-patients, as recorded in the National Tuberculosis Registry, the Netherlands, 1993–2007
- Table 3. Correlation of overall deaths from Mycobacterium bovis disease with demographic variables, the Netherlands, 1993–2007
- Table 4. Correlation of TB-related and non–TB-related deaths according to demographic variables, the Netherlands, 1993–2007
Suggested citation for this article: Majoor CJ, Magis-Escurra C, van Ingen J, Boeree MJ, van Soolingen D. Epidemiology of Mycobacterium bovis disease in humans, the Netherlands, 1993–1997. Emerg Infect Dis [serial on the Internet]. 2011 Mar [date cited]. http://dx.doi.org/10.3201/eid1703.101111
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Christof J. Majoor, Department of Pulmonology, Academic Medical Center, PO Box 22660, 1100 DE Amsterdam, the Netherlands
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