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The new coronavirus disease 2019 (COVID-19) infection is a double challenge for people infected with comorbidities such as cardiovascular and cerebrovascular diseases and diabetes. Comorbidities have been reported to be risk factors for the complications of COVID-19. In this work, we develop and analyze a mathematical model for the dynamics of COVID-19 infection in order to assess the impacts of prior comorbidity on COVID-19 complications and COVID-19 re-infection. The model is simulated using data relevant to the dynamics of the diseases in Lagos, Nigeria, making predictions for the attainment of peak periods in the presence or absence of comorbidity. The model is shown to undergo the phenomenon of backward bifurcation caused by the parameter accounting for increased susceptibility to COVID-19 infection by comorbid susceptibles as well as the rate of re-infection by those who have recovered from a previous COVID-19 infection. Sensitivity analysis of the model when the population of individuals co-infected with COVID-19 and comorbidity is used as response function revealed that the top ranked parameters that drive the dynamics of the co-infection model are the effective contact rate for COVID-19 transmission, $\beta\sst{cv}$, the parameter accounting for increased susceptibility to COVID-19 by comorbid susceptibles, $\chi\sst{cm}$, the comorbidity development rate, $\theta\sst{cm}$, the detection rate for singly infected and co-infected individuals, $\eta_1$ and $\eta_2$, as well as the recovery rate from COVID-19 for co-infected individuals, $\varphi\sst{i2}$. Simulations of the model reveal that the cumulative confirmed cases (without comorbidity) may get up to 180,000 after 200 days, if the hyper susceptibility rate of comorbid susceptibles is as high as 1.2 per day. Also, the cumulative confirmed cases (including those co-infected with comorbidity) may be as high as 1000,000 cases by the end of November, 2020 if the re-infection rates for COVID-19 is 0.1 per day. It may be worse than this if the re-infection rates increase higher. Moreover, if policies are strictly put in place to step down the probability of COVID-19 infection by comorbid susceptibles to as low as 0.4 per day and step up the detection rate for singly infected individuals to 0.7 per day, then the reproduction number can be brought very low below one, and COVID-19 infection eliminated from the population. In addition, optimal control and cost-effectiveness analysis of the model reveal that the the strategy that prevents COVID-19 infection by comorbid susceptibles has the least ICER and is the most cost-effective of all the control strategies for the prevention of COVID-19.

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This paper considers and analyzes a fractional order model for COVID-19 and tuberculosis co-infection, using the Atangana-Baleanu derivative. The existence and uniqueness of the model solutions are established by applying the fixed point theorem. It is shown that the model is locally asymptotically stable when the reproduction number is less than one. The global stability analysis of the disease free equilibrium points is also carried out. The model was simulated using data relevant to both diseases in New Delhi, India. Fitting the model to the cumulative confirmed COVID-19 cases for New Delhi from March 1, 2021 to June 26, 2021, COVID-19 and TB contact rates and some other important parameters of the model are estimated. The numerical method used combines the two-step Lagrange polynomial and the fundamental theorem of fractional calculus and has been shown to be highly accurate and efficient, user-friendly and converges quickly to the exact solution even with a large step of discretization. Simulations of the Fractional order model revealed that reducing the risk of COVID-19 infection by latently-infected TB individuals will not only bring down the burden of COVID-19, but will also reduce the co-infection of both diseases in the population. Also, the conditions for the co-existence or elimination of both diseases from the population are established.

A two-sex deterministic model for Human Papillomavirus (HPV) that assesses the impact of treatment and vaccination on its transmission dynamics is designed and rigorously analyzed. The model is shown to exhibit the phenomenon of backward bifurcation, caused by the imperfect vaccine as well as the re-infection of individuals who recover from a previous infection, when the associated reproduction number is less than unity. Analysis of the reproduction number reveals that the impact of treatment on effective control of the disease is conditional, and depends on the sign of a certain threshold unlike when preventive measures are implemented (i.e. condom use and vaccination of both males and females). Numerical simulations of the model showed that, based on the parameter values used therein, a vaccine (with 75% efficacy) for male population with about 40% condom compliance by females will result in a significant reduction in the disease burden in the population. Also, the numerical simulations of the model reveal that with 70% condom compliance by the male population, administering female vaccine (with 45% efficacy) is sufficient for effective control of the disease.

a b s t r a c tThis work investigates entropy generation in a steady flow of viscous incompressible fluids between two infinite parallel porous plates. The fluid temperature variation is due to asymmetric heating of the porous plates as well as viscous dissipation. Two different physical situations are discussed with their entropy generation profiles: (i) Couette flow with suction/injection and (ii) pressure-driven Poiseuille flow with suction/injection. In each case, closed form expressions for entropy generation number and Bejan number are derived in dimensionless form by using the expressions for velocity and temperature which are derived by solving the resulting momentum and energy equations by the method of undetermined coefficient. The effect of the governing parameters on velocity, temperature, entropy generation and Bejan number are extensively discussed with the help of graphs. It is interesting to remark that entropy generation number increases with suction on one porous plate while it decreases on the other porous plate with injection.

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In this work, a co-infection model for human papillomavirus (HPV) and Chlamydia trachomatis with cost-effectiveness optimal control analysis is developed and analyzed. The disease-free equilibrium of the co-infection model is shown not to be globally asymptotically stable, when the associated reproduction number is less unity. It is proven that the model undergoes the phenomenon of backward bifurcation when the associated reproduction number is less than unity. It is also shown that HPV re-infection (ε p = 0) induced the phenomenon of backward bifurcation. Numerical simulations of the optimal control model showed that: (i) focusing on HPV intervention strategy alone (HPV prevention and screening), in the absence of Chlamydia trachomatis control, leads to a positive population level impact on the total number of individuals singly infected with Chlamydia trachomatis, (ii) Concentrating on Chlamydia trachomatis intervention controls alone (Chlamydia trachomatis prevention and treatment), in the absence of HPV intervention strategies, a positive population level impact is observed on the total number of individuals singly infected with HPV. Moreover, the strategy that combines and implements HPV and Chlamydia trachomatis prevention controls is the most cost-effective of all the control strategies in combating the co-infections of HPV and Chlamydia trachomatis.