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Peer-reviewedCC BY-NC-NDBMC public health

Mathematical modelling of malaria-typhoid co-infection: human-vector-environment dynamics and implications for integrated disease control.

5 affiliations
  1. 1Department of Mathematics, Enugu State University of Science and Technology, Enugu, Nigeria. [email protected].
  2. 2Department of Industrial Mathematics and Health Statistics, David Umahi Federal University of Health Sciences, Uburu, Ebonyi, Nigeria.
  3. 3Department of Mathematical Sciences, Bingham University, Karu, Nassarawa, Nigeria.
  4. 4Department of Mathematics, National Open University, Abuja, Nigeria.
  5. 5Department of Mathematics, Enugu State University of Science and Technology, Enugu, Nigeria.

Abstract

Background: Malaria and typhoid fever remain major public health challenges across many low- and middle-income countries, where their overlapping clinical presentation frequently complicates diagnosis and management. Despite numerous epidemiological studies, relatively few mathematical models have jointly examined the transmission dynamics of malaria–typhoid co-infection while simultaneously accounting for vector transmission, environmental bacterial contamination, chronic carriers, treatment, and disease interaction. This study develops and analyzes a deterministic co-infection model to investigate the transmission dynamics of malaria and typhoid fever and to identify the epidemiological factors that most strongly influence disease persistence and control.

Methods: A deterministic compartmental model consisting of human, mosquito, and environmental bacterial compartments was formulated and analyzed. The disease-free equilibrium was established, and the basic reproduction numbers for malaria (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R0M\end{document}) and typhoid (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R0T\end{document}) were derived using the next-generation matrix approach. Local stability, bifurcation behavior, and sensitivity analyses were performed to characterize disease dynamics. Local sensitivity indices and Latin Hypercube Sampling coupled with Partial Rank Correlation Coefficients (LHS–PRCC) were employed to identify the dominant transmission drivers, while numerical simulations were conducted to examine the temporal evolution of the epidemiological compartments and intervention contour analyses.

Results: The model admits a locally asymptotically stable disease-free equilibrium whenever the final reproduction threshold satisfies \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R0<1\end{document}, where \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R0=max {R0M,R0T}\end{document}. Numerical evaluation yielded \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R0M=1.6556\end{document} and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R0T=1.5909\end{document}, indicating that malaria constitutes the dominant transmission pathway. Bifurcation analysis revealed backward bifurcation for the malaria subsystem and forward bifurcation for the typhoid subsystem, demonstrating that reducing \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}ℛ0M\end{document} below unity alone may not guarantee malaria elimination, whereas typhoid elimination follows the classical threshold condition. Local and global sensitivity analyses consistently identified mosquito biting rate, mosquito mortality, malaria transmission probabilities, human recruitment, typhoid transmission rate, environmental sanitation, bacterial carrying capacity, and treatment-related parameters as the principal determinants of disease transmission. Numerical simulations showed rapid early epidemic growth followed by convergence to an endemic equilibrium, with the co-infected population remaining substantially lower than the mono-infected populations. Contour analyses further demonstrated that simultaneous vector control and environmental sanitation substantially enlarge the parameter regions where \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}ℛ0<1\end{document}, emphasizing the importance of integrated intervention strategies.

Conclusion: The proposed malaria–typhoid co-infection model demonstrates that sustained transmission is driven by distinct but interacting vector and environmental pathways. The coexistence of backward bifurcation in malaria and forward bifurcation in typhoid highlights the need for disease-specific control strategies, while the sensitivity and intervention analyses show that combining effective vector management, environmental sanitation, prompt treatment, and reduction of chronic bacterial carriage provides the greatest potential for reducing disease burden and interrupting transmission in endemic settings.

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BibTeX
@article{nwachukwu2026mathematical,
  title = {{Mathematical modelling of malaria-typhoid co-infection: human-vector-environment dynamics and implications for integrated disease control.}},
  author = {Queeneth Ojoma Nwachukwu and Patrick Agwu Okpara and Emmanuel Azuaba and Aondona Christopher Fanyam and Donald Chukwuma Ugo},
  journal = {BMC public health},
  year = {2026},
  month = aug,
  doi = {10.1186/s12889-026-28980-z},
  url = {https://europepmc.org/article/MED/43009912},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Mathematical modelling of malaria-typhoid co-infection: human-vector-environment dynamics and implications for integrated disease control.
AU  - Queeneth Ojoma Nwachukwu
AU  - Patrick Agwu Okpara
AU  - Emmanuel Azuaba
AU  - Aondona Christopher Fanyam
AU  - Donald Chukwuma Ugo
PY  - 2026
DA  - 2026/08/14
JO  - BMC public health
DO  - 10.1186/s12889-026-28980-z
UR  - https://europepmc.org/article/MED/43009912
AB  - Background: Malaria and typhoid fever remain major public health challenges across many low- and middle-income countries, where their overlapping clinical presentation frequently complicates diagnosis and management. Despite numerous epidemiological studies, relatively few mathematical models have jointly examined the transmission dynamics of malaria–typhoid co-infection while simultaneously accounting for vector transmission, environmental bacterial contamination, chronic carriers, treatment, and disease interaction. This study develops and analyzes a deterministic co-infection model to investigate the transmission dynamics of malaria and typhoid fever and to identify the epidemiological factors that most strongly influence disease persistence and control.  Methods: A deterministic compartmental model consisting of human, mosquito, and environmental bacterial compartments was formulated and analyzed. The disease-free equilibrium was established, and the basic reproduction numbers for malaria (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R_0M\end{document}) and typhoid (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R_0T\end{document}) were derived using the next-generation matrix approach. Local stability, bifurcation behavior, and sensitivity analyses were performed to characterize disease dynamics. Local sensitivity indices and Latin Hypercube Sampling coupled with Partial Rank Correlation Coefficients (LHS–PRCC) were employed to identify the dominant transmission drivers, while numerical simulations were conducted to examine the temporal evolution of the epidemiological compartments and intervention contour analyses.  Results: The model admits a locally asymptotically stable disease-free equilibrium whenever the final reproduction threshold satisfies \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R_0<1\end{document}, where \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R_0=max {R_0M,R_0T}\end{document}. Numerical evaluation yielded \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R_0M=1.6556\end{document} and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}R_0T=1.5909\end{document}, indicating that malaria constitutes the dominant transmission pathway. Bifurcation analysis revealed backward bifurcation for the malaria subsystem and forward bifurcation for the typhoid subsystem, demonstrating that reducing \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}ℛ_0M\end{document} below unity alone may not guarantee malaria elimination, whereas typhoid elimination follows the classical threshold condition. Local and global sensitivity analyses consistently identified mosquito biting rate, mosquito mortality, malaria transmission probabilities, human recruitment, typhoid transmission rate, environmental sanitation, bacterial carrying capacity, and treatment-related parameters as the principal determinants of disease transmission. Numerical simulations showed rapid early epidemic growth followed by convergence to an endemic equilibrium, with the co-infected population remaining substantially lower than the mono-infected populations. Contour analyses further demonstrated that simultaneous vector control and environmental sanitation substantially enlarge the parameter regions where \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}ℛ_0<1\end{document}, emphasizing the importance of integrated intervention strategies.  Conclusion: The proposed malaria–typhoid co-infection model demonstrates that sustained transmission is driven by distinct but interacting vector and environmental pathways. The coexistence of backward bifurcation in malaria and forward bifurcation in typhoid highlights the need for disease-specific control strategies, while the sensitivity and intervention analyses show that combining effective vector management, environmental sanitation, prompt treatment, and reduction of chronic bacterial carriage provides the greatest potential for reducing disease burden and interrupting transmission in endemic settings.
SN  - 1471-2458
ER  -