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Volume 26, Number 3—March 2020
Research Letter

Low Prevalence of Mycobacterium bovis in Tuberculosis Patients, Ethiopia

Author affiliations: Ethiopian Public Health Institute, Addis Ababa, Ethiopia (M. Getahun, W. Senshaw, G. Diriba, H. Mollalign, E. Tesfaye, B. Yenew, M. Taddess); Addis Ababa University, Addis Ababa (M. Getahun, A. Zewdie, K. Dagne, D. Beyene, G. Ameni); Emory University, Atlanta, Georgia, USA (H.M. Blumberg, R.R. Kempker)

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Abstract

An estimated 17% of all tuberculosis cases in Ethiopia are caused by Mycobacterium bovis. We used M. tuberculosis complex isolates to identify the prevalence of M. bovis as the cause of pulmonary tuberculosis. Our findings indicate that the proportion of pulmonary tuberculosis due to M. bovis is small (0.12%).

In 2016, the World Health Organization (WHO) estimated that there were 147,000 cases and 12,500 deaths worldwide from tuberculosis, which is predominantly caused by Mycobacterium bovis. However, because of the lack of comprehensive surveillance data, particularly from developing countries, actual illness and death could exceed this estimate (1,2). To enhance efforts at addressing zoonotic TB, multiple international organizations collaboratively developed and recently released the Roadmap for Zoonotic Tuberculosis (1). The roadmap states 3 objectives, the first of which is to collect more accurate scientific evidence on zoonotic TB through improved surveillance efforts.

In Ethiopia, ≈80% of persons live in rural areas, where most of the population harvests crops or raises livestock (3). Because of the pastoral lifestyle, the burden of zoonotic TB is thought to be high in such rural communities because of a perceived higher risk of acquiring M. bovis infection (2). In 2013, Müller et al. estimated the proportion of all forms of TB cases caused by M. bovis in Ethiopia to be 17% (4). For this study, we evaluated the contribution of M. bovis toward causing pulmonary TB in Ethiopia.

We obtained a total of 1,785 stored M. tuberculosis complex isolates collected from patients testing positive in smear tests. These tests were performed in 32 health facilities across Ethiopia during November 2011–June 2013 as part of a drug resistance survey. Among the 32 sites enrolled in the drug resistance survey, 30 sites had participated in an earlier survey in 2003–2005; two additional sites were selected from the Gambella and Benishangul Gumuz regions to ensure that >1 health facility from each region was included (Table). We included data from all patients with positive results for TB on consecutive sputum smear tests.

To identify species, region of difference (RD) 9- and RD4-based PCR procedures were performed using HVD primers and QIAGEN HotStarTaq Master Mix reagents (QIAGEN, https://www.qiagen.com), which were described in earlier studies (58). The Capilia TB-Neo test (Goffin Molecular Technologies, http://www.goffinmoleculartechnologies.com) was used to distinguish M. tuberculosis–complex species from other nontuberculous mycobacterial (NTM) species. The same standard operating procedures were used to interpret the results.

Of the 1,785 isolates collected, 1,735 were available for typing. Among those typed, 1,599 (92%) yielded visible bands of M. tuberculosis complex. RD9 typing identified 1,597 (99.87%) of 1,599 isolates as M. tuberculosis, and RD4 typing identified only 2 (0.13%) of 1,599 of the isolates as M. bovis. These findings indicate that pulmonary TB due to M. bovis is rare in Ethiopia.

This study has certain limitations. We used M. tuberculosis complex isolates collected from a sentinel drug resistance survey. Data from smears testing negative for pulmonary TB cases, which account for some proportion of PTB and extrapulmonary TB cases, were not included.

One possible alternative explanation for finding few cases of M. bovis as a pathogen in pulmonary TB is that M. bovis may have been acquired through ingestion of food from livestock infected with extrapulmonary TB (7). In that case, sputum might not have been the ideal technique for isolating M. bovis samples. Previous studies in Ethiopia reported variable (0%–16%) prevalence of M. bovis in extrapulmonary TB patients (8,9). A second possible reason could be the low prevalence of bovine TB in zebu cattle, which comprise >95% of the cattle population of Ethiopia (10) and have been reported to have lower infection rates with M. bovis than other types of cattle. In addition, most cattle husbandry in Ethiopia is on extensively managed small farms in open fields, which poses a low risk for the spread of bovine TB (7). Thus, a low prevalence of bovine TB in the Ethiopia cattle population could result in a limited rate of transmission to humans.

This study included samples from all regions of Ethiopia to identify the prevalence of bovine TB among patients with pulmonary TB. We found that M. bovis was an etiologic agent of human pulmonary TB in only a small fraction of cases, a lower proportion than previously estimated. This finding indicates that aerosol transmission of M. bovis from livestock to humans is rare. A useful focus for future efforts might be to implement or strengthen pasteurization programs in M. bovis–prevalent areas to limit possible transmission of bovine TB through the consumption of dairy products.

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Acknowledgments

This work was supported in part by the Ethiopian Public Health Institute, Aklilu Lemma Institute of Pathobiology of Addis Ababa University, and the National Institutes of Health Fogarty International Center (D43TW009127).

This study received ethics approval from the IRBs of the Ethiopian Public Health Institute and Addis Ababa University.

RD9 and RD4 typing were performed at the Ethiopian Public Health Institute (EPHI).

Dr. Getahun works at the national reference laboratory for Ethiopia. Her main areas of work include conducting research on priority public health problems, providing technical assistance on TB research, and providing supportive supervision for surveillance and program evaluation.

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References

  1. World Health Organization, Food and Agriculture Organization of the United Nations, and World Organisation for Animal Health. Roadmap for zoonotic tuberculosis. Geneva: WHO Press; 2017 [cited 2019 Feb 1]. http://www.fao.org/3/a-i7807e.pdf
  2. Olea-Popelka  F, Muwonge  A, Perera  A, Dean  AS, Mumford  E, Erlacher-Vindel  E, et al. Zoonotic tuberculosis in human beings caused by Mycobacterium bovis-a call for action. Lancet Infect Dis. 2017;17:e215. DOIPubMedGoogle Scholar
  3. Central Statistical Agency, World Bank. Ethiopia rural socioeconomic survey. 2013 [cited 2019 Feb 1]. http://siteresources.worldbank.org/INTLSMS/Resources/3358986-1233781970982/5800988-1367841456879/9170025-1367841502220/ERSS_Survey_Report.pdf
  4. Müller  B, Dürr  S, Alonso  S, Hattendorf  J, Laisse  CJ, Parsons  SD, et al. Zoonotic Mycobacterium bovis-induced tuberculosis in humans. Emerg Infect Dis. 2013;19:899908. DOIPubMedGoogle Scholar
  5. Parsons  LM, Brosch  R, Cole  ST, Somoskövi  A, Loder  A, Bretzel  G, et al. Rapid and simple approach for identification of Mycobacterium tuberculosis complex isolates by PCR-based genomic deletion analysis. J Clin Microbiol. 2002;40:233945. DOIPubMedGoogle Scholar
  6. Mamo  G, Bayleyegn  G, Sisay Tessema  T, Legesse  M, Medhin  G, Bjune  G, et al. Pathology of camel tuberculosis and molecular characterization of its causative agents in pastoral regions of Ethiopia. PLoS One. 2011;6:e15862. DOIPubMedGoogle Scholar
  7. Portillo-Gómez  L, Sosa-Iglesias  EG. Molecular identification of Mycobacterium bovis and the importance of zoonotic tuberculosis in Mexican patients. Int J Tuberc Lung Dis. 2011;15:140914. DOIPubMedGoogle Scholar
  8. Firdessa  R, Berg  S, Hailu  E, Schelling  E, Gumi  B, Erenso  G, et al. Mycobacterial lineages causing pulmonary and extrapulmonary tuberculosis, Ethiopia. Emerg Infect Dis. 2013;19:4603. DOIPubMedGoogle Scholar
  9. Alemayehu Regassa , Girmay Medhin , Gobena Ameni . Bovine tuberculosis is more prevalent in cattle owned by farmers with active tuberculosis in central Ethiopia. Vet J. 2008;178:11925. DOIPubMedGoogle Scholar
  10. Sibhat  B, Asmare  K, Demissie  K, Ayelet  G, Mamo  G, Ameni  G. Bovine tuberculosis in Ethiopia: A systematic review and meta-analysis. Prev Vet Med. 2017;147:14957. DOIPubMedGoogle Scholar

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Cite This Article

DOI: 10.3201/eid2603.190473

Original Publication Date: February 04, 2020

Table of Contents – Volume 26, Number 3—March 2020

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Muluwork Getahun, Ethiopian Public Health Institute, National TB Reference Laboratory, Addis Ababa, 1242, Ethiopia

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Page created: February 20, 2020
Page updated: February 20, 2020
Page reviewed: February 20, 2020
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.
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