Emergence of Nontuberculous Mycobacteria at the Human–Livestock–Environment Interface in Zambia

Author:

Zulu Mildred123ORCID,Malama Sydney34,Monde Ngula235,Kainga Henson36,Tembo Rabecca13,Mwaba Florence13,Saad Shereen Ahmed37,Daka Victor38,Mukubesa Andrew N.2,Ndebe Joseph2,Shambaba Obi5,Munyeme Musso23ORCID

Affiliation:

1. Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka P.O. Box 50110, Zambia

2. Department of Disease Control, School of Veterinary Medicine, University of Zambia, Lusaka P.O. Box 32379, Zambia

3. Africa Center of Excellence for Infectious Diseases of Humans and Animals, University of Zambia, Lusaka P.O. Box 32379, Zambia

4. Department of Biological Sciences, School of Natural Science, University of Zambia, Lusaka P.O. Box 32379, Zambia

5. Department of Biomedical Sciences, Tropical Diseases Research Centre, Ndola P.O. Box 71769, Zambia

6. Department of Veterinary Epidemiology and Public Health, Faculty of Veterinary Medicine, Lilongwe University of Agriculture and Natural Resources, Lilongwe 207203, Malawi

7. Department of Clinical Studies, College of Veterinary Science, University of Bahr El Ghazal, Wau P.O. Box 10739, South Sudan

8. Department of Public Health, School of Medicine, Copperbelt University, Ndola P.O. Box 71191, Zambia

Abstract

The prevalence of nontuberculous mycobacteria (NTM) infections and disease is rising worldwide due to increased research, diagnostics capabilities, and awareness of the disease. There is limited prevalence data for NTM from different sources in Zambia. The aim of this study was to determine the prevalence and species distribution of NTM at the human–livestock–environment interface. A cross-section study was conducted in Namwala, Chipata, and Lundazi Districts of Zambia from April 2020 to December 2021. Sputum samples were collected from tuberculosis presumptive patients from different health centers, cattle tissues were collected from different abattoirs during routine post-mortem, and water samples were collected from different drinking points for humans and animals such as taps, boreholes, wells, rivers, dams and ponds, and then cultured following standard mycobacteriology procedures. Capilia TB-Neo assay was used to identify NTM from the positive cultures. DNA was extracted and the 16S to 23S rRNA (internal transcribed spacer region) (ITS) was amplified and sequenced to identify the species. The overall prevalence of NTM from humans, cattle, and water was 9.1% (72/794, 95% CI 7.2–11.3). The prevalence in humans was 7.8% (33/421, 95% CI 5.54–10.94), in cattle it was 10.6% (15/142, 95% CI 6.2–17.1), and in water it was 10.4% (24/231, 95% CI 6.9–15.2). Our study has shown, for the first time in Zambia, simultaneous isolation of NTM at the human–livestock–environment interface; M. avium complex and M. fortuitum were the most commonly isolated species. M. fortuitum and M. gordonae were isolated from all three sources, while M. abscessus was isolated from humans and water. The isolation of similar NTM species at the interface which are potentially pathogenic is a public health problem which merits further investigation.

Funder

African Centre of excellence for Infectious Diseases in Humans and Animals

World Bank

ACEIDHA

Publisher

MDPI AG

Subject

Microbiology (medical),Molecular Biology,Microbiology

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