Could non-tuberculous mycobacteria infections explain the high mortality rates among TB patients in Kilifi, Kenya?

Pwani University, Kenya
BiologyMedicine
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About This Project

Mortality rate is significantly higher among clinically diagnosed Tuberculosis (TB) patients than the ones bacteriologically confirmed. Epidemiological studies have shown the emergence of Non-Tuberculous Mycobacteria (NTMs) causing lung damage and disease. This study aims to determine the proportion of NTM infections among TB patients. We hypothesize that the proportion of clinically diagnosed TB patients did not actually have TB but other serious lung conditions masquerading as TB.

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What is the context of this research?

Diagnosis remains the biggest gap in the Tuberculosis (TB) care cascade; early and accurate diagnosis is key in attaining global TB targets of eliminating TB as a public health concern. A considerable proportion of patients with presumed TB are found not to have Mycobacterium tuberculosis (MTB) following clinical and subsequent bacteriological investigation. Even though, clinical presentation of Non-Tuberculous Mycobacteria (NTMs) infection is quite similar to MTB, NTMs often go undetected or considered clinically irrelevant. Several NTM species cause lung damage and diseases contributing to substantial morbidity and mortality. Clinical diagnosis of TB is very common in high TB burden settings and remains a cause of high mortality rates among TB patients. Poor TB treatment outcomes especially death is strongly associated with clinically diagnosed TB patients.

What is the significance of this project?

The similarity of MTB and NTMs in clinical presentation and initial laboratory diagnosis confers a possibility of an unintended treatment. Treatment of NTMs is complicated and associated with higher liver toxicity compared to MTB treatment. It has been reported that there is a two- to five- fold higher mortality risk in clinically diagnosed TB cases compared to the bacteriologically confirmed cases in Kilifi County, Kenya. The high mortality raises concerns of misdiagnosis, where some patients treated for MTB may have had NTM infections. Results from this study shall demonstrate that TB diagnosis based solely on signs and symptoms, without bacteriological confirmation, is associated with poor treatment outcomes. Therefore, a clear understanding of the clinical presentation of MTB infection and a well-defined, systematic diagnostic approach are essential for effective TB control strategies.

What are the goals of the project?

In this ongoing study, we're recruiting TB patients from TB clinics around the county of Kilifi, Kenya. This is a prospective cohort study where the target is 383 participants (both clinically diagnosed and bacteriologically confirmed TB patients). The study participant shall produce sputum sample (thick mucus coughed up from the lower airways in the lungs) that is dedicated for molecular detection of NTMs and then advised to come to the clinic for monitoring after two (2) months where another sputum sample shall be taken. The treatment outcome shall be noted at the end of the full treatment course. Epidemiological, microbiological and transcriptomic data will be collected. For transcriptome sequence analysis, RNA from immune cells shall be extracted from three (3) categories of TB patients together with healthy controls. The objective is to establish if there is differential expression of specific immune related genes in MTB / NTM disease versus healthy controls.

Budget

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Seed funding for this project was provided by IDeAL - KEMRI / Wellcome trust which covered a significant amount of TB patient (study participant) recruitment into the study, preliminary PCR tests and some hospital diagnostic tests for most of the study participants. The requested budget items will cover the remaining study participant recruitment and the last part of transcriptomics work. This is RNA extraction work and sequencing costs that shall involve shipment of RNA samples for sequencing and bioinformatics analysis. These resources shall ensure a comprehensive execution of the project's goal of acquisition of epidemiological, microbiological and transcriptomic data. This tripartite approach is relevant in demonstrating the impact of these neglected Non-Tuberculous Mycobacteria infections in TB patients on anti-TB drug administration.

Endorsed by

Prophet is my mentee who is currently working on this important research to understand the reasons for high deaths rates among TB patients in Kilifi. This work is timely and the knowledge obtained from it will be a great addition to the understanding and designing of public health interventions against tuberculosis.
TB is a major cause of morbidity and mortality in sub-Saharan Africa and this work by Prophet in very important and will go a long way in providing key information to help better in understanding and management. I therefore strongly endorse this work and the efforts being made to bridge the financial gaps experienced during its implementation.
I am pleased to strongly endorse this project - it is an important and timely study. TB-related mortality in Kenya remains worryingly high and is not always fully explained by current diagnoses. Investigating whether non-tuberculous mycobacterial infections contribute to these deaths could be truly transformative for diagnosis and care. I know Prophet and the team well: they are accomplished, rigorous scientists with a rare commitment to solving African health problems. This project deserves support.

Project Timeline

Study participant recruitment began in August 2025 and is expected to reach the target of 383 by July 2026. In June to July 2026 RNA extraction, shipment of the RNA samples and sequencing should be completed. In July and September all the baseline sputum samples and the second month sputum samples will be processed and analyzed respectively. In December, the TB treatment outcomes for all the study participants shall have been obtained and analyzed.

Jun 18, 2026

Project Launched

Jul 17, 2026

Study participant recruitment

Jul 31, 2026

RNA extraction, shipment of RNA samples, sequencing and bioinformatics

Sep 30, 2026

Molecular detection of NTMs from all the sputum samples

Dec 18, 2026

Analysis of TB treatment outcomes from all the study participants

Meet the Team

Prophet Ingosi Mulega
Prophet Ingosi Mulega

Affiliates

Pwani University, Kenya
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Team Bio

Osman Abdullahi is a consultant epidemiologist, currently an associate professor in Pwani University, Kenya. He pioneered the tuberculosis research program in Kilifi County, Kenya.

https://www.researchgate.net/profile/Osman-Abdullahi-2


Faiz Shee is an Immunologist and molecular biologist, and currently a lecturer in Pwani University, Kilifi, Kenya. He has experience in MTB Molecular biology as well as Malaria Immunology and Antigenic Variation.

https://scholar.google.com/cit...

Prophet Ingosi Mulega

My name is Prophet Ingosi Mulega born and raised in the coastal parts of Kenya but natively from the western parts of the country. I am currently a PhD student registered in Pwani University, Kenya under IDeAL_KEMRI / Wellcome trust studentship. I hold a Diploma in Medical Laboratory Science, Bachelor of Science in Medical laboratory science and a Master of Science in Microbiology. I am registered and licensed to practice in Kenya and East Africa by the Kenya Medical Laboratory Technicians and Technologists Board (A04134). I developed interest in tropical infectious diseases while working in a public sub county hospital in Mombasa, Kenya. Here I was charged with the responsibility of laboratory investigations for Tuberculosis (TB) patients with HIV / AIDS. Many years back I believed in precision in laboratory diagnostics to safeguard public health. Today I am now actively involved in a prospective cohort research study that shall justify laboratory bacteriological confirmation to avoid misdiagnosis of TB as a PhD student.

Publications

https://pmc.ncbi.nlm.nih.gov/articles/PMC8079137

My systematic review and meta analysis; Epidemiology of Non-Tuberculous Mycobacteria Among Presumptive TB Cases in Africa, is submitted for publication and is currently under peer review in the journal submitted in.

Additional Information

This is the process of extraction Mycobacterial DNA from the sputum samples, the technique is called Genolyse method


After extraction of Mycobacterial DNA, the amplification on the 23rRNA gene region ready for staining with Reverse hybridization method


The machine used during Reverse hybridization where specific oligonucleotide probes immobilized on membrane strips are stained. The results are then interpreted according to a combination of banding patterns for different NTM species.


The stained banding patterns on the membrane strips are interpreted using this chart

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