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Zoonotic tuberculosis in a high bovine tuberculosis burden area of Ethiopia

Authors :
Sosina Ayalew
Getinet Habtamu
Fantanesh Melese
Bamlak Tessema
Roland T. Ashford
Shubhada K. Chothe
Abraham Aseffa
James L. N. Wood
Stefan Berg
Adane Mihret
for the ETHICOBOTS Consortium
Bizuneh Belachew
Eshcolewyene Fekadu
Gizachew Gemechu
Hawult Taye
Rea Tschopp
Shewit Haile
Tsegaye Hailu
Adam Bekele
Chilot Yirga
Mulualem Ambaw
Tadele Mamo
Tesfaye Solomon
Tilaye Teklewold
Solomon Gebre
Getachew Gari
Abde Aliy
Abebe Olani
Asegedech Sirak
Gizat Almaw
Getnet Mekonnen
Mekdes Tamiru
Sintayehu Guta
James Wood
Andrew Conlan
Alan Clarke
Henrietta L. Moore
Catherine Hodge
R. Glyn Hewinson
Martin Vordermeier
Javier Nunez-Garcia
Gobena Ameni
Berecha Bayissa
Aboma Zewude
Adane Worku
Lemma Terfassa
Mahlet Chanyalew
Temesgen Mohammed
Miserach Zeleke
Source :
Frontiers in Public Health, Vol 11 (2023)
Publication Year :
2023
Publisher :
Frontiers Media S.A., 2023.

Abstract

BackgroundTuberculosis (TB) is a major cause of ill health and one of the leading causes of death worldwide, caused by species of the Mycobacterium tuberculosis complex (MTBC), with Mycobacterium tuberculosis being the dominant pathogen in humans and Mycobacterium bovis in cattle. Zoonotic transmission of TB (zTB) to humans is frequent particularly where TB prevalence is high in cattle. In this study, we explored the prevalence of zTB in central Ethiopia, an area highly affected by bovine TB (bTB) in cattle.MethodA convenient sample of 385 patients with pulmonary tuberculosis (PTB, N = 287) and tuberculous lymphadenitis (TBLN, N = 98) were included in this cross-sectional study in central Ethiopia. Sputum and fine needle aspirate (FNA) samples were obtained from patients with PTB and TBLN, respectively, and cultures were performed using BACTEC™ MGIT™ 960. All culture positive samples were subjected to quantitative PCR (qPCR) assays, targeting IS1081, RD9 and RD4 genomic regions for detection of MTBC, M. tuberculosis and M. bovis, respectively.ResultsTwo hundred and fifty-five out of 385 sampled patients were culture positive and all were isolates identified as MTBC by being positive for the IS1081 assay. Among them, 249 (97.6%) samples had also a positive RD9 result (intact RD9 locus) and were consequently classified as M. tuberculosis. The remaining six (2.4%) isolates were RD4 deficient and thereby classified as M. bovis. Five out of these six M. bovis strains originated from PTB patients whereas one was isolated from a TBLN patient. Occupational risk and the widespread consumption of raw animal products were identified as potential sources of M. bovis infection in humans, and the isolation of M. bovis from PTB patients suggests the possibility of human-to-human transmission, particularly in patients with no known contact history with animals.ConclusionThe detected proportion of culture positive cases of 2.4% being M. bovis from this region was higher zTB rate than previously reported for the general population of Ethiopia. Patients with M. bovis infection are more likely to get less efficient TB treatment because M. bovis is inherently resistant to pyrazinamide. MTBC species identification should be performed where M. bovis is common in cattle, especially in patients who have a history of recurrence or treatment failure.

Details

Language :
English
ISSN :
22962565
Volume :
11
Database :
Directory of Open Access Journals
Journal :
Frontiers in Public Health
Publication Type :
Academic Journal
Accession number :
edsdoj.f6ce67e2a6b48c6bc02b6fdd549fea4
Document Type :
article
Full Text :
https://doi.org/10.3389/fpubh.2023.1204525