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Emmannaemeka avatarEmmannaemeka avatar
Nnaemeka Emmanuel Nnadi

@Emmannaemeka

I am a faculty member at Plateau State University Bokkos and the chief scientific officer at Centre for phage biology and therapeutics(an Emergent venture sponsored project) with a keen focus on biosecurity research as it relates to Resource limited settings

https://www.linkedin.com/in/nnaemeka-emmanuel-nnadi-a39298b5/
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About Me

. My academic pursuits are centered around microbial ecology, exploring the intricate interactions within microbial communities and their evolution into human pathogens. My primary interest lies in employing the one-health approach to unravel the impact of climate change on the development of more resilient pathogens in the environment and their subsequent infection in humans. Additionally, my laboratory is dedicated to advancing phage therapy as a promising alternative to combat drug resistance.

Projects

Combat global antibiotic resistance

Comments

Combat global antibiotic resistance
Emmannaemeka avatar

Nnaemeka Emmanuel Nnadi

7 days ago
Final report

Description of subprojects and results, including major changes from the original proposal

Description of subprojects and results, including major changes from the original proposal

The ACX Grants 2024 award significantly strengthened our capacity for bacteriophage research and development in Nigeria. The funding allowed us to improve our laboratory infrastructure, expand our phage collection, support postgraduate research, and advance several projects from phage isolation toward characterization and potential therapeutic or agricultural applications.

One of the most important infrastructure achievements was the acquisition of an ultracentrifuge. This addressed a major limitation in our laboratory by improving our ability to concentrate and purify bacteriophages locally. Unlike expenditure on individual experiments, this is a long-term investment that will continue to support multiple phage projects, students, and collaborators beyond the grant period.

A major scientific outcome was our work on Salmonella. We isolated and characterized two novel lytic phages, Jerseyvirus ijeoma and Apdecimavirus ayanbimpe, active against Salmonella Typhi. The work progressed to peer-reviewed publication in 2026 in the study “Exploring lytic Salmonella phages as potential alternatives to antibiotics: isolation, characterization, and stability assessment of Jerseyvirus ijeoma and Apdecimavirus ayanbimpe” (Olorundare et al., 2026). The study demonstrated their lytic activity and assessed their stability under different conditions. These phages now provide candidates for the next stage of our work, particularly preclinical evaluation of safety and therapeutic efficacy.

Our work on Pseudomonas aeruginosa also expanded considerably. An MSc research project resulted in the isolation of 34 bacteriophages active against P. aeruginosa, contributing to our growing phage collection. We also completed genomic characterization of the lytic P. aeruginosa phage CSSBELLO(Igwe, Blessing Chidinma, Adesola Olaleka, and Nnaemeka Nnadi. "Isolation and Genomic Characterization of a Novel Lytic Bacteriophage (CSSBELLO) Infecting Multidrug-Resistant Pseudomonas aeruginosa, Isolated from Wastewater in Jos." Frontiera Scientia 1.1 (2026): 10-19, which was subsequently reported in a peer-reviewed publication. These studies have strengthened our ability to move from phage isolation through biological characterization to genome-level analysis. This work is also feeding into our research on a phage-based bandage for infected wounds, particularly as a potential delivery approach for difficult-to-treat wound infections.

Another important development was our expansion into phage-based vaccine research. We developed a multi-serotype Salmonella phage-based vaccine construct intended to provide broader protection across different Salmonella serotypes. Candidate components have undergone computational and experimental work, with in vivo evaluation representing the next major stage of development.

The programme also expanded beyond human health into agricultural phage biotechnology. In our Xanthomonas project, five bacterial isolates were obtained, three of which were demonstrated to be pathogenic. We subsequently isolated seven lytic bacteriophages, with three showing activity against all three pathogenic isolates tested. Plaque assays, enrichment and purification have been undertaken, and the strongest candidates provide the basis for developing a phage cocktail for future evaluation against bacterial disease in tomato. This has broadened the programme toward a One Health approach by applying the same phage expertise to both human health and food production.

We have also strengthened our capacity in phage genomics and bioinformatics. An important outcome has been the development of PhageMine, an open-source bioinformatics workflow for bacteriophage genome analysis. This development helps address one of the challenges we encountered as our phage collection expanded: the need to move beyond isolation and phenotypic characterization to systematic genomic analysis of candidate phages.

The grant has additionally supported a wider capacity-building effect. MSc and PhD students have participated in projects involving Salmonella, Pseudomonas, phage-based wound applications, and agricultural phages. The laboratory infrastructure and expertise developed through these activities are therefore supporting a growing group of researchers rather than a single project.

Major changes from the original proposal

The overall objective of building local capacity for phage research and developing phage-based solutions has remained unchanged. However, the programme became broader than originally anticipated. Our initial emphasis was largely on phage isolation, characterization, storage and therapeutic development. During implementation, this expanded to include phage-based vaccines, wound-delivery applications, agricultural biocontrol, genomic analysis, bioinformatics and postgraduate training.

We also refined our approach to clinical translation. Rather than moving directly from promising laboratory results toward clinical trials, we now recognize the importance of a staged pathway involving comprehensive genomic characterization, candidate selection, preclinical safety and efficacy studies, manufacturing and quality control, regulatory engagement and, ultimately, appropriately approved clinical evaluation.

Overall, the ACX Grants 2024 award has produced both immediate research outputs and longer-term research capacity. The acquisition of the ultracentrifuge, expansion of our phage collection, publication of characterized phages, development of new therapeutic and agricultural applications, bioinformatics capacity and training of postgraduate researchers represent outcomes that will continue beyond the grant period.

Our next phase will build on this foundation by advancing the strongest phage candidates into preclinical studies, further developing the Xanthomonas phage cocktail and phage-based bandage, strengthening the phage bank, and pursuing the manufacturing and regulatory capacity required to translate promising phages into practical applications.


Combat global antibiotic resistance
Emmannaemeka avatar

Nnaemeka Emmanuel Nnadi

3 months ago
Progress update

What progress have you made since your last update?

We published our findings on two novel lytic Salmonella bacteriophages in the paper, Exploring lytic Salmonella phages as potential alternatives to antibiotics: isolation, characterization, and stability assessment of Jerseyvirus ijeoma and Apdecimavirus ayanbimpe (Olorundare et al., 2026). The study demonstrated that both phages are stable under relevant environmental conditions and exhibit strong lytic activity against Salmonella typhi, providing further evidence for their potential as alternatives to antibiotics.

What are your next steps?

Our next step is to evaluate the therapeutic efficacy and safety of these phages in animal models. Successful preclinical studies will position us to advance toward clinical trials and ultimately develop phage-based therapies for patients with multidrug-resistant Salmonella infections.

Is there anything others could help you with?

We are looking for partners to help us take these phages from the laboratory to the clinic. Specifically, we are seeking support to set up the first phage GMP-compliant phage manufacturing facilities and support to conduct early-phase clinical trials.


Combat global antibiotic resistance
Emmannaemeka avatar

Nnaemeka Emmanuel Nnadi

over 1 year ago
Progress update

What progress have you made since your last update?

We have successfully designed a multi-serotype phage-based vaccine construct against Salmonella to provide broad protection across diverse serotypes. While in vivo validation is pending, the immunogenic epitopes have been computationally and experimentally validated for strong protective potential. This innovation could significantly impact typhoid control in endemic regions.

In a complementary effort, my MSc student has isolated 34 bacteriophages active against Pseudomonas aeruginosa, following targeted isolation from local clinical strains. This growing phage library is vital to developing personalized therapy options for drug-resistant infections in our setting. Together, these initiatives demonstrate our capacity to deliver locally relevant, globally significant solutions in infectious disease control.

What are your next steps?

  1. 1. In Vivo Validation of Vaccine
    Our immediate goal is to conduct in vivo studies on the multi-serotype Salmonella phage-based vaccine to assess its efficacy and protective capabilities. This is a crucial step toward validating the vaccine’s potential for widespread use in combating Salmonella infections.

    2. Expanding the Phage Bank
    We will continue expanding our phage bank by isolating additional phages targeting Salmonella, E. coli, and Pseudomonas. Building a well-resourced, diverse phage library is critical for developing effective, locally relevant phage therapy solutions to combat antimicrobial resistance.

    3. Development of Phage-Based Bandages
    My MSc student works on an innovative phage-based bandage designed for diabetic wound care. This project aims to use phage therapy to treat resistant bacterial infections in diabetic wounds, offering a promising new therapeutic option for patients with chronic wounds.

Is there anything others could help you with?

1. Funding for In Vivo Studies
We seek financial support to carry out in vivo testing of our multi-serotype Salmonella phage vaccine. These studies are essential for demonstrating efficacy and advancing toward translational and clinical applications.

2. Resources for Phage Bank Expansion
We welcome collaboration and support in expanding our phage bank, especially in isolating and characterizing new phages targeting Salmonella, E. coli, and Pseudomonas. A strong phage repository is foundational for developing tailored, effective phage therapies in our region.

3. Access to Sequencing Infrastructure
A robust, locally accessible sequencing platform would significantly reduce phage genome characterisation costs and turnaround time. Partnerships enabling affordable high-throughput sequencing through shared infrastructure or sponsored access would dramatically enhance our capacity for rapid, data-driven phage research.

Combat global antibiotic resistance
Emmannaemeka avatar

Nnaemeka Emmanuel Nnadi

about 2 years ago
Progress update

What progress have you made since your last update?

  1. We purchased an ultracentrifuge to support the work and other consumables.

  2. I have supported one MSc student

  3. Submitted one manuscript draft to Nature Scientific

  4. Isolating phages against Pseudomonas and Salmonella


What are your next steps?

  1. Expand our focus to phage vaccines. I am visiting https://www.theraphage.bio/roderick-slavcev. I hope to design a phage vaccine against Salmonella typhi

  2. Sequence the phages we isolated against Pseudomonas and Salmonella.

  3. Host a PhD student on a lab visit.


Is there anything others could help you with?

  1. We would appreciate any support in getting additional funding.


Transactions

ForDateTypeAmount
Manifund Bankover 2 years agowithdraw60000
Combat global antibiotic resistanceover 2 years agoproject donation+60000