Volume 15, Number 1—January 2009
Pulmonary Tuberculosis and Mycobacterium bovis, Uganda
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|EID||Byarugaba F, Etter EM, Godreuil S, Grimaud P. Pulmonary Tuberculosis and Mycobacterium bovis, Uganda. Emerg Infect Dis. 2009;15(1):124-125. https://dx.doi.org/10.3201/eid1501.080487|
|AMA||Byarugaba F, Etter EM, Godreuil S, et al. Pulmonary Tuberculosis and Mycobacterium bovis, Uganda. Emerging Infectious Diseases. 2009;15(1):124-125. doi:10.3201/eid1501.080487.|
|APA||Byarugaba, F., Etter, E. M., Godreuil, S., & Grimaud, P. (2009). Pulmonary Tuberculosis and Mycobacterium bovis, Uganda. Emerging Infectious Diseases, 15(1), 124-125. https://dx.doi.org/10.3201/eid1501.080487.|
To the Editor: In 2005, prevalence of human tuberculosis (TB) in Uganda was 559 cases/100,000 population (1). In 2002, the average number of extrapulmonary TB cases in humans, considered a crude indicator of the level of bovine TB, was 7.5% of TB cases for Uganda and 6% for Mbarara district, the main Ugandan milk basin (2). Worldwide, the proportion of human cases caused by Mycobacterium bovis has accounted for 3.1% of all forms of TB (3). Although zoonotic TB is more often reported as an extrapulmonary disease, recent publications report that 0.4%–10% of sputum isolates from patients in African countries are M. bovis (3). These studies, however, give little information about the cattle environment. A 2002 survey of dairy cattle in Mbarara district reported that 74% of herds and 6% of individual animals were reactive to the single tuberculin test (4). However, this test does not differentiate between Mycobacterium species involved. We therefore explored whether M. bovis might be a major threat to human health in this region.
From September 2004 through January 2005, we surveyed 658 patients who had been admitted to the Mbarara University Teaching Hospital TB ward after positive bacterial findings for at least 3 sputum smears or positive chest radiographs for smear-negative patients. Of 90 randomly selected patients, only 70 samples were available for analysis to differentiate the species in the M. tuberculosis complex; the other samples were excluded because of contamination, lack of mycobacteria growth on culture, or postal delay in transportation of sample. The questionnaire asked about patients’ demographic data (including occupation), association with cattle, and milk consumption habits. Genomic DNA was extracted from the pellet culture of Middlebrook 7H9 broth (Difco; Cergy, France) as described previously (5). DNA samples were used to carry out PCRs and hybridization processes; we used the GenoType MTBC kit (Hain Lifescience GmbH; Nehren, Germany) for differentiation in the M. tuberculosis complex, especially between M. tuberculosis and M. bovis species (6).
Questionnaire responses showed that 27/64 (42.2%; 6 did not answer) patients had a history of raw milk consumption; nevertheless, 20/24 (83%; 3 did not answer) reported that they boiled fresh milk before consuming it, as did 54/60 (90% of all patients; 10 did not answer). Eating undercooked or raw meat was reported by 91% of the patients. Most patients were adult males (ratio 2.14:0.97 male:female for the district population); 8.6% were <18 years old (56% in the district); and average number of persons in household was 5.7 vs. 4.8 for the district (7). Of the samples, 8.6% were from extrapulmonary sites.
After amplification and hybridization of sample DNA, 69 samples were found to be M. tuberculosis, and 1 was not a Mycobacterium species. Our sampling method would detect at least 1 case of M. bovis in n patient specimens if the prevalence of bovine TB was > p(0.033%) according to the formula in which a is the first order error (5%):
Because of the change in sample size, the limit prevalence was redetermined by using the inverse of the formula above:
If at least 1 sample was positive for M. bovis, the prevalence of bovine TB among patients would be >4.2%. However, the prevalence of M. bovis was <4.2% and confirmed the low-level involvement of M. bovis in human TB in Mbarara district. These findings are consistent with previous work in Uganda’s capital, Kampala, and in other African or Asian countries (2,8,9). The estimation of extrapulmonary cases among all TB cases (95% confidence interval 2%–15.2%) did not differ from the official estimate. We can add, using the second formula shown above, that among the 6 extrapulmonary TB cases, the prevalence of M. bovis is <39.3%. Our results come from a population in a highly rural area (91.5% of the population in Mbarara district) (7), where the high prevalence of animal TB has been reported.
These results could be explained by the patients’ consumption habits, which reduce the risk for contamination. Even if bovine TB could also be found in other farm or wild animals, it seems to have a minor effect on public health. Zoonotic TB appeared to not be a major public health problem in Mbarara district. However, this finding could also result from underdiagnosis of extrapulmonary TB, from prevalence of M. tuberculosis being so high that in proportion M. bovis is a minor problem, or from rural populations’ difficult access to TB diagnosis (directly observed therapy case detection rate in Uganda in 2005 was 37%) (1).
We thank the Mbarara University of Science and Technology, the staff of Mbarara University Teaching Hospital, the National Tuberculosis and Leprosy Control Programme, and the French Embassy in Uganda.
This study was funded by the Agricultural Consultation and Sector Structuring Project (French Development Agency).
- World Health Organization. WHO Report 2007, global tuberculosis control, Uganda. WHO/HTM/TB/2007.376 [cited 2008 Apr 9]. Available from http://www.who.int/tb/publications/global_report/2007/pdf/uga.pdf
- STD/AIDS Control Programme Ministry of Health. STD/HIV/AIDS surveillance report, June 2003, Kampala, Uganda [cited 2008 Apr 9]. Available from http://www.health.go.ug/docs/hiv0603.pdf
- Cosivi O, Grange JM, Daborn CJ, Raviglione MC, Fujikura T, Cousins D, Zoonotic tuberculosis due to Mycobacterium bovis in developing countries. Emerg Infect Dis. 1998;4:59–70.
- Bernard F, Cassel V, Lesnoff M, Rutabinda D, Dhalwa J. Tuberculosis and brucellosis prevalence survey on dairy cattle in Mbarara milk basin (Uganda). Prev Vet Med. 2005;67:267–81.
- van Soolingen D, de Haas PE, Hermans PW, van Embden JD. DNA fingerprinting of Mycobacterium tuberculosis. Methods Enzymol. 1994;235:196–205.
- Richter E, Weizenegger S, Rusch-Gerdes S, Niemann S. Evaluation of genotype MTBC assay for differentiation of clinical Mycobacterium tuberculosis complex isolates. J Clin Microbiol. 2003;41:2672–5.
- Uganda Bureau of Statistics. 2002 Uganda population and housing census main report. 2005, Kampala, Uganda [cited 2008 Mar 11]. Available from http://www.ubos.org
- Jou R, Huang WL, Chiang CY. Human tuberculosis caused by Mycobacterium bovis, Taiwan. Emerg Infect Dis. 2008;14:515–7.
- Niemann S, Rusch-Gerdes S, Joloba ML, Whalen CC, Guwatudde D, Ellner JJ, Mycobacterium africanum subtype II is associated with two distinct genotypes and is a major cause of human tuberculosis in Kampala, Uganda. J Clin Microbiol. 2002;40:3398–405.
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Eric Marcel Charles Etter, CIRAD - UR 22 AGIR 3 Animal et Gestion Intégrée des Risques, Campus International de Baillarguet, TA C-22/E, 34398 Montpellier, France;
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