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. 2026 Jun 11;6(6):e0004945. doi: 10.1371/journal.pgph.0004945

Spatio-temporal modelling of COVID-19 infection and associated risk factors in Dakar, Senegal

Assane Niang Gadiaga 1,2,*, Mame Wodji Tine 2,3, Aminata Niang Diene 2,3, Catherine Linard 4, Niko Speybroeck 5, Ortis Yankey 1, Somnath Chaudhuri 1,6, Chibuzor Christopher Nnanatu 1, Eimear Cleary 1, Shengjie Lai 1, Attila N Lazar 1, Andrew J Tatem 1
Editor: Julia Robinson7
PMCID: PMC13257971  PMID: 42275303

Abstract

Infectious diseases are a major threat to global health and economy and the recent COVID-19 pandemic is a perfect example of this. Appropriate modelling and accurate prediction of the outcome of disease spread over time and across space are critical steps towards informed development of effective strategies for public health interventions. In low and middle-income countries, however, the scarcity of spatially disaggregated time-series infectious diseases data often limits the analysis of the burden of infectious disease at a broad-scale, and the effects of the contextual risk factors is not often fully captured. In this study, we investigate the spatio-temporal patterns of COVID-19 infection in Dakar at the neighbourhood level, and evaluate the impact of potential risk factors. Geostatistical models based on COVID-19 infection data were used to explain and predict the spatio-temporal distribution of infections between June 2020 and June 2021. We specified a Bayesian regression model that incorporates a spatio-temporally autocorrelated random effect in order to quantify the evolution of the spatial patterns of the COVID-19 infection overtime. Results show significant strong spatial heterogeneity but relatively small temporal variations of the COVID-19 distribution, and a positive association between adjusted population density (mean of the posterior probability: 0.29, credible interval: 0.24-0.34) and residential areas (mean of the posterior probability: 1.25, credible interval: 0.66-1.83) with COVID-19 infection. Western areas are at higher risk of COVID-19 infection compared to eastern and less densely populated peripheral neighbourhoods. Measuring the role of contextual risk factors and mapping the at-risk areas can provide valuable insights for policymakers, enabling more targeted public health interventions. These efforts also support the management of endemic diseases and preparedness for future outbreaks.

1. Introduction

The COVID-19 pandemic has had profound health, economic, and social consequences worldwide throughout the year 2020 until now. Since its emergence in late 2019, the disease has spread rapidly, leading to unprecedented public health responses such as lockdowns, social distancing measures, and mass vaccination campaigns [1]. As of April 2024, the global related death toll had risen to more than 7 million from more than 700 million reported infections [2]. While widespread vaccination efforts have significantly reduced transmission and mortality [3], the containment of the virus is challenging because of the biological features of the virus [4], involving mutating variants that mitigate the effectiveness of the vaccine, leading to sustained rates of infection throughout the community.

Given the persistent risk of COVID-19 variants worldwide, assessing the disease spread and understanding its spatio-temporal patterns are key to effective monitoring, prevention and control. This is particularly true in many LMICs, where fragile disease surveillance systems were unable to monitor the progress of COVID-19 and formulate appropriate responses. Recent studies have explored the role of various contextual factors in shaping the spread of COVID-19, including population density, landscape connectivity, human mobility, socioeconomic characteristics, environmental conditions, pollution and smoking [5–11]. Population density, in particular, has been widely investigated as a risk factor of disease transmission, given the fact that people’s proximity to each other increases likelihood of infection [12]. In many cases, the relationship was positive, with more densely populated areas having higher rates of infections or experiencing early outbreaks [5,10,13,14]. Highly connected areas also face earlier and higher COVID-19 infection rates [15–18], and socioeconomic factors such as residential characteristics drive disparities in COVID-19 cases and deaths [7,19–21].

Several statistical approaches have been used to investigate the role of the aforementioned risk factors on the spread of the COVID-19 disease. They are either classical and frequentist methods, which remain at the core of most practical statistical applications [22], or Bayesian methods, which have been increasingly used in the field of spatial epidemiology due to their ability to incorporate spatial and temporal dependencies [23,24].

Although the scientific community is deploying efforts to understand contextual factors invloved in the spread of COVID-19, existing epidemiological data are not often resolved at spatial levels that allows for in-depth analyses; they are in most cases available at a large scale (i.e., regional or national levels) and the patterns of the disease at finer levels (i.e., at the intra-urban levels) remains unknown.

In Senegal, the first case of COVID-19 was reported in early March 2020, and the majority of subsequent Senegalese cases were reported in Dakar, the capital city. According to the Ministry of Health, as of May 29, 2020, the Dakar region accounted for nearly three quarter (2525 cases out of the 3429 detected in the country; 73.6%) of reported COVID-19 infections in Senegal [25]. Public health authorities classified the source of the COVID-19 infection as one of the following four categories: (1) contact cases; (2) community cases; (3) imported cases and (4) evacuated cases. An infection was termed as a community case when the source of infection was unknown [26], making efforts to control the pandemic more challenging. Against this backdrop, the present study analysed the spatio-temporal dynamics of COVID-19 disease in Dakar, with a focus on the COVID-19 infection which arose from community transmission, and using COVID-19 time-series data at the finest administrative level.

Through a spatio-temporal Bayesian framework we evaluate the impact of population density, temperature, distance to marketplaces, non-pharmaceutical interventions such as ease of social distancing index, and residential characteristics on COVID-19 spread. Distance to marketplaces is used here as a proxy of mobility [27], while residential and non-residential areas indicate differences in living conditions and is a useful proxy on poverty levels [28]. In addition to the widely used population density (count of people per total area), adjusted population density that refers to the count of people per built-up area was also considered. This approach seeks to better capture the effect of crowding, because, although density expresses a ratio between population and an unit of area, these units are not uniformly distributed over the space. Our aim is to understand the spatio-temporal dynamic of COVID-19 spread in Dakar as well as related potential drivers. In a context of fragile health system, as in many low- and middle-income countries, having detailed time-series epidemiological data at the finest administrative level for Dakar offers a unique opportunity to explore advanced spatial statistical modelling approach and improve our understanding of localised transmission patterns. Understanding these localised transmission patterns is essential for designing targeted public health interventions, optimizing resource allocation, and mitigating the impact of future outbreaks.

2. Materials and methods

2.1. Study area and data

2.1.1. Study area.

Dakar is the capital city of Senegal (Fig 1) and an example of African city that combines several aspects of Africa’s urban growth: rapid urbanization, land cover and land use changes, inequalities in living conditions [29] that have led to different health status [28]. Located in the westernmost part of the African continent (Fig 1), Dakar is the driving force of the Senegalese economy and through its markets, banks and industrial sector remains a magnet for migrants from all over the country. According to the last national census conducted in 2023, the region had a population of 4 million inhabitants, nearly a quarter of the Senegalese population (22%) in an area representing only 0.3% of the country [30]. The availability of georeferenced fine scale census information [28] and high quality, very-high resolution remote sensing land cover and land use products [31,32] has improved our knowledge on health inequalities and associated socioeconomic and environmental risk factors [28,33].

Fig 1. Geographical location of Dakar.

Fig 1

The underlying base layer is republished from https://doi.org/10.4081/gh.2021.910, under a CC BY license, with permission from the ASSESS project, original copyright Gadiaga et al. 2021.

2.1.2. Data.

The epidemiological data used in this study were obtained from the daily reports of COVID-19 infection in Dakar produced by the Ministry of health [25]. Data cover the period from 01/06/2020 to 30/06/2021 and record the number of confirmed COVID-19 infections from community-based transmission. Each anonymised record includes the date of the confirmed infection, the location of the infection and the number of new infections. There can be more than one record per date, with similar or different locations. The location of the infection often refers to the neighbourhood, which is the smallest administrative unit in an urban area. However, in some situations, the location can refer to a higher administrative extent, i.e., the commune, or a lower level spatial extent such as the housing unit. Geographic coordinates of each infection record were obtained by joining the excel-based disease data file with the neighbourhood shapefile. To do this, the unique identifier availabe in the latter was assigned to the disease record when there is a matching between the location of the infection and the polygon shapefile. When the location of the infection was referring to a Commune or a housing unit, a fuzzy-matching algorithm was used to merge the infection record with the neighbourhood shapefile. After the geocoding of the infection records, the daily cases were aggregated by month for each neighbourhood. Thus, each neighbourhood has an aggregated count spanning the study period, providing an idea of the basic severity status of the neighborhood during the pandemic (covid19_Dakar).

Although the neighborhood-level data offer an opportunity to examine the intra-urban variation of COVID-19 infection in Dakar, it is important to note that this does not provide a complete picture of the status of the pandemic in the city, as only infections from community transmission are analysed. In fact, only community based transmission can be used to reconstruct the spatio-temporal dynamic of the pandemic because, unlike the other type of infection, it includes information about the location of the infection (patient’s residence).

Furthermore, just as there are multiple records for some dates, there are also days with no reported infections from community transmission. This might weaken the quality of the study, although it remains unclear whether the absence of reported infections is due to a lack of such cases among tested patients on the corresponding dates. The cumulative incidence and temporal distribution of COVID-19 infections over the study period are illustrated in Fig 2 and Fig 3, respectively.

Fig 2. Aggregated incidence of COVID-19 confirmed infection from community transmission from June 2020 to June 2021.

Fig 2

The underlying base layer is republished from https://doi.org/10.4081/gh.2021.910, under a CC BY license, with permission from the ASSESS project, original copyright Gadiaga et al. 2021.

Fig 3. Monthly distribution of COVID-19 infection from community transmission in Dakar from June 2020 to June 2021.

Fig 3

As predictors of COVID-19 infection, we used two high resolution satellite derived land use [32] and gridded population datasets [34], with a spatial resolution of 10m for the population data and street block level for the land use map. Additionally, distance to marketplaces, ease of social distancing index, and temperature data obtained from the WorldPop data repository were used [35]. The land use map depicts several spatial metrics, such as residential built-up areas (planned or unplanned), non-residential built-up areas (administrative, commercial and service areas), agricultural vegetation, natural vegetation, water bodies and baresoil areas. It provides a detailed representation of Dakar’s urban landscape, with an overall accuracy of 79% [32], and is useful for understanding inequalities in health and living conditions [28,33]. In the present study, however, this accuracy may be hampered by the mismatch between the year the satellite data were collected (2015) and the year in which the COVID-19 data were obtained (2020–2021). Although built and settlement layers are time-variant, we assume that this 5 year gap is negligible in the particular context of Dakar. To further assess this, we used the world settlement footprint data [36] and calculated the average percentage of change in the built-up areas at the neighbourhood level from 2015 to 2019. On average, built-up areas per neighbourhood in Dakar increased by 5% during the period 2015–2019, indicating minimal changes. It is important to note that the land use data does not cover Goree and Ngor islands as well as some parts of eastern Dakar. Thus, to ensure a full overlap between the COVID-19 data and the geospatial predictors, the spatial extent of the study area was reduced and sparsely built-up areas in the eastern urbanisation front were excluded from the analysis.

Using these remotely sensed data sources, we first extracted the average residential built-up areas, non-residential built-up areas, temperature, and distance to marketplaces for each neighborhood. The total gridded population per neighborhood was divided by the neighborhood’s total area to calculate population density. We then computed the adjusted population density by dividing the gridded population counts by the total built-up area for each neighborhood. Additionally, built-up area was divided by the neighborhood’s total area to calculate built-up density. The covariates used for the modeling are listed in Table 1.

Table 1. List of covariates used for the modelling.
Variable Description Source
Temperature Annual average temperature WorldPop
Built-up density Built-up area per total area MAUPPa
Distance to marketplaces Average distance to marketplaces WorldPop
Population density Count of people per total area MAUPP
Adjusted population density Count of people per built-up area MAUPP
Residential areas Proportion of land use (LU) used for residential purposes MAUPP
Non-residential ACS areas Proportion of LU without residences used for administrative, commercial and services (ACS) purposes MAUPP
Ease of social distancing index Score index that evaluates the feasibility of social distancing measure WorldPop

aMAUPP = Modelling and forecasting African Urban Population Patterns for vulnerability and heath assessments (https://maupp.ulb.ac.be/).

Statistical analyses were performed to check for multicollinearity among the covariates and to remove any covariates that were not statistically significant. To address this, we used the Variance Inflation Factor (VIF) to measure the level of collinearity. Covariates with a VIF greater than 5 were considered to have high multicollinearity and were therefore removed from the analysis [37,38]. Only covariates with a VIF less than 5 and those that were statistically significant were selected for the final model. Among the 8 variables considered for this analysis and introduced in Table 1, built-up density and ease of social distancing index were found showing multicollinearity issue and further dropped. In the following section, the Bayesian statistical modelling approach we developed to conduct this research is presented.

2.2. Modelling COVID-19 infection risk

The spread of infectious diseases like COVID-19, involves complex patterns over both space and time. This complexity arises from the interactions between human behaviour, environmental factors, and disease transmission. To analyse COVID-19 cases in Dakar, Senegal, we have used a Bayesian spatio-temporal modelling approach. This method allows us to account for both spatial and temporal autocorrelation structures in the data. Spatial autocorrelation refers to the way disease cases are clustered in certain areas, while temporal autocorrelation deals with how cases change over time. Our modelling approach is important because COVID-19 cases are not evenly distributed across different locations or time periods, as illustrated in Fig 2 and Fig 3.

In this study, we applied three distinct modelling approaches to analyse the spread of COVID-19 in Dakar, as summarized in table 2. Our first approach focused on identifying monthly trends across the entire city. For this, we used both first-order and second-order random walk models (RW1 and RW2) to capture temporal randomness. To account for neighbourhood-level variations, we included an independent and identically distributed (IID) random effect. In this approach, we aggregated the total number of COVID-19 cases across Dakar for each month, using these monthly totals as the response variable.

Table 2. Overview of the three modelling approaches with their specificities.

Model Type Spatial structure Space-time interaction Model equation Description
Model 1 Temporal None None log(qt)= β0+ ZtTβ+ ui+ γt Temporal AR model without spatial structure
Model 2 Spatio-temporal SPDE Separable log(qit)= β0+ ZitTβit+ S(xi)+ ui+ γt Combine AR temporal structure with spatial SPDE model and separate space and time effects (no interaction)
Model 3 Spatio-temporal SPDE Yes log(qit)= β0+ ZitTβit+ S(xi)+ ui+ γt+ δit Combines AR temporal structure with spatial SPDE model and space-time interaction

In the second approach, we examined COVID-19 case counts at the neighbourhood level, capturing spatial variations within Dakar in addition to temporal trends. This separate spatio-temporal model included spatial randomness based on individual neighbourhoods, temporal randomness, and the IID effect of each neighbourhood. Finally, our third approach also involved spatio-temporal modelling, but with an added spatio-temporal interaction effect. This term represented an unobserved independent effect for each combination of neighbourhood and month, allowing us to capture unique patterns in each area over time.

The rationale for constructing a temporal regression and spatio-temporal approaches is that temporal patterns often occur in different aspects of health, particularly in infectious disease transmission [39]. Furthermore, infectious disease diffusion and spread is an intrinsically spatial process, as it involves complex interactions between human andseveral landscapes attributes. Therefore, this study uses temporal, spatial and spatiotemporal modelling approaches to evaluate possible temporal and spatio-temporal correlation in the COVID-19 infection and spread.

2.2.1. Temporal modelling of COVID-19 infection.

In the first approach, we have employed a temporal Poisson regression framework to analyse the temporal dynamics of COVID-19 in Dakar. In this model, the number of confirmed cases at each time point was represented using a Poisson likelihood, as we are dealing with count data. The temporal resolution of the analysis has been set to one month, allowing us to explore trends and changes in the number of infected cases over time. Additionally, we incorporated geospatial variables to assess their potential correlations with the infection rates.

Let Yt and Et represent the number of observed and expected COVID-19 cases in the population at time t, where t=1,…,T. We assume that, given the relative risk qt, the number of observed cases follows a Poisson distribution:

Yt ∣ qt ~ Poisson (λt= Et qt)

where Et is the total population for the study area, and the log-risk is modelled as:

log(qt)= β0+ ZtTβ+ ui+ γt (1)

where, the relative risk qt expresses the probability of infection given there is a contact to an infected person, and Zt represents the matrix of covariates used to account for various factors influencing the infection rates. The term ui is an IID random effect that captures unobserved variability across the neighbourhoods. Additionally, γt represents the temporal effects, which can be modelled using either a RW1 or a RW2 to account for the temporal structure and potential trends over time. In the case of the RW1, the temporal effects γt are modeled such that the increments Δγt= γt− γt−1 follow a Gaussian distribution with zero mean and precision τ. On the other hand, for a RW2, the temporal effects are modeled as Δ2 γt= γt−2 γt−1+ γt−2 also follow a Gaussian distribution with zero mean and precision τ. This RW2 model provides a smoother temporal evolution over time compared to the RW1 model, making it particularly useful for capturing complex temporal patterns such as trends, cycles, or deviations from simple linear temporal patterns.

For prior selection, we have used penalized complexity (PC) priors [39]. For the IID random effect, the PC prior on the precision was set to [0.5, 0.01], where 0.5 is the central tendency and 0.01 controls the spread or uncertainty around it. For the RW1 or RW2 model on the monthly data, the PC prior on the precision with parameters [1, 0.01] represents a location parameter of 1 and a scale parameter of 0.01, indicating a prior belief that the precision is centered around 1 with relatively low uncertainty. The prior for the coefficient vector β = (β0,…,βp) which follows a zero-mean Gaussian distribution with a precision of 0.001. All log-precision parameters followed inverse gamma distributions with shape parameter α=1 and scale parameter β= 0.00005.

2.2.2. Spatio-temporal modelling of COVID-19 infection.

In the second approach, we employed a spatio-temporal Poisson regression framework to analyze the spread of COVID-19 in Dakar. In this model, the number of confirmed cases at each spatial unit (neighborhood) and time point was represented using a Poisson likelihood. Similar to the first approach, the temporal resolution of the spatio-temporal analysis was set to one month, allowing us to observe trends and changes in case numbers over time (months). The spatio-temporal model included spatial random effects to account for the influence of neighboring regions on case numbers. It also incorporated temporal random effects to capture trends and seasonal variations over time. Additionally, geospatial covariates were included to explore their potential associations with infection rates.

Let Yit and Eit represent the number of observed and expected COVID-19 infected cases in the i-th area (neighbourhood) and the t-th period (month), where t=1,…,T. We assume that, given the relative risk qit, the number of observed cases follows a Poisson distribution:

Yit ∣ qit ~ Poisson (λit= Eit qit)

where,  Eit are the total population for individual neighbourhood of the study area and the log-risk is modelled as in Equation (2) for spatio-temporal separable model and in Equation (3) for spatio-temporal interaction model.

log(qit)= β0+ ZitTβit+ S(xi)+ ui+ γt (2)
log(qit)= β0+ ZitTβit+ S(xi)+ ui+ γt+ δit (3)

where in both Equation (2) and (3), S(.) represents the spatially structured random effects, and Zit represents the matrix of covariates used in the model. The temporally structured effect has been represented by γt. In Equation (3), δit represents the spatio-temporal interaction between the two structured effects. The IID random effect ui is added to the model to capture neighbourhood-level variability with a penalized complexity (PC) prior on the precision set as [0.5,0.01] where we assumed a prior mean of 0.5 and a prior precision of 0.01.

The matrix of covariates was built by stacking the covariate values for every space-time combination, and separate random effect mapping matrices link these observations to spatial, temporal or spatio-temporal latent effects. We have modelled temporal trends using a RW1 for the monthly data. This model was scaled for identifiability, and we applied a PC prior on the precision with parameters [1,0.01] with a prior mean of 1 and a prior precision of 0.01. For all prior selections, we used PC priors following the framework proposed by Simpson et al. [39]. We have assigned a vague prior to the vector of coefficients β = (β0,…,βp) which follows a zero-mean Gaussian distribution with a precision of 0.001. Finally, all parameters associated with log-precisions are assigned inverse Gamma distributions with shape parameter α=1 and scale parameter β= 0.00005.

The default prior distributions for all parameters in R-INLA were selected based on commonly used priors in previous studies [40–42]. Our findings demonstrated robustness to alternative priors. We have tested multiple scenarios with different priors and consistently obtained the same results. As shown in Equation (3), we introduced a spatio-temporal interaction effect as an unobserved, independent term for each region-period combination (i,t), modelled as δit~Normal(0,1τδ). This interaction term assumes no additional structure, representing independent variations from the main spatial and temporal effects when those are included in the model. It captures global space-time heterogeneity and is typically modeled as white noise, as discussed in previous studies [40]. This interaction term offers a more flexible structure, capturing localized deviations from the main spatial and temporal patterns. To compare modelling strategies, we constructed the third model set that incorporates all covariates, using both spatio-temporal interactions and PC priors. A summary of these competing models is presented in Table 2 in the Results Section.

The dataset used in this study shows zero inflation. As such, zero-inflated Poisson (ZIP) and Poisson Hurdle models can be used to accommodate zero-inflated discrete distributions. While ZIP models add extra probability mass to the zero outcome [43], Poisson hurdle models, on the other hand, are characterized by a mixture of zero and non-zero outcomes [44,45]. In a ZIP model, the response variable Yit is zero with probability π, and follows a Poisson distribution with parameter λit with probability 1−π. In particular,

Yit=0,with prob π+(1−π)e−λitk,      with prob (1−π) λitke−λitk!, k≥1   (4)

Conversely, in a Poisson hurdle model, the response variable Yit is zero with probability π, and follows a truncated Poisson distribution with parameter λit with probability 1−π. Mathematically,

Yit=0,with prob  πk,  with prob  (1−π)1−e−λit(λitke−λitk!), k≥1    (5)

In the model fitting process, Bayesian inference typically employs Markov Chain Monte Carlo (MCMC) methods to estimate the joint posterior distribution of model parameters [46,47]. However, for large datasets such as the time-series data used in this study, this can be computationally intensive. As a faster alternative, the integrated nested Laplace approximation (INLA) approximates posterior marginal distributions efficiently, especially for models represented as latent Gaussian Markov random fields (GMRF) [42,48]. In the current study, we have applied INLA along with a stochastic partial differential equation (SPDE) method. The SPDE method allows us to model a continuous spatial process, such as a Gaussian field (GF), using a discretely indexed spatial random process like a GMRF [49,50].

In particular, the spatial random process represented by S(.) explicitly denotes dependence on the spatial field, follows a zero-mean Gaussian process with Matérn covariance function [51] represented as:

 Cov(S(xi),S(xj))=σ22ν−1Γ(ν)(κ∥xi−xj∥)ν Kν(κ∥xi−xj∥)

The parameter σ2 represents the process variance, indicating the variability of the values around the mean. The smoothness parameter ν> 0 influences the rate of decay of correlations with distance, while the scaling parameter κ> 0 governs the overall range of the covariance. The term ∥xi−xj∥  denotes the Euclidean distance between locations. The modified Bessel function of the second kind, Kν(.), defines the covariance structure, and Γ(ν) is the gamma function, normalizing the covariance for scaling purposes.

The parameterized model we follow is of the form:

(κ2−Δ)(α/2)(τS)=W on Rd

where Δ=∑i=1d∂2∂xi2 is the Laplacian, α=(ν+d/2)  is the smoothness parameter, τ  is inversely proportional to σ, W is Gaussian white noise and κ> 0 is the scale parameter, related to range r, defined as the distance at which the spatial correlation becomes negligible. For each ν, we have r=8ν/κ, with r corresponding to the distance where the spatial correlation is close to 0.1. Note that we have d=2 for a two-dimensional process, and we fix ν=1, so that α=2 in this case [40–42]. It is worth noting that the spatial range parameters were adopted from the empirical study conducted by [50].

In the current study, we have applied the PC priors [39] for the Matérn model, which helps prevent overfitting by supporting simpler models. The Matérn covariance function was adopted because it provides a flexible and interpretable description of spatial dependence and is standard within the SPDE-INLA framework. Fixing the spatial dimension as 2 and the smoothness parameter as 1 to define the structure of the spatial field ensure computational stability [49,50]. The prior for the marginal standard deviation is set as [1,0.1] where we assumed a prior mean of 1 and a prior precision of 0.1. This allows some flexibility around a mean of 1 based on our expectations of spatial variation.

We utilized the centroids of each neighborhood as the target locations for SPDE mesh construction. According to Verdoy [52], an optimal mesh should possess a sufficient number of vertices to facilitate effective predictions, and within a limit to have control over computational time. Following this principle, the triangulated mesh has been generated using inla.mesh.2d function from R-INLA package, based on Delaunay triangulation method [50], with the best fitting mesh having 7365 vertices for the 1078 neighbourhoods considered in this study. S1 Fig depicts the SPDE mesh designed for the study area with 1078 neighborhood centroid locations highlighted as red points and the blue line marks the boundary of the study area. We have created a projection matrix to transfer the spatially continuous Gaussian random field from the observations to the mesh nodes. The centroids of the neighbourhoods and the triangulation in the mesh are used to develop this projection matrix.

In a nutshell, all models assume that the number of COVID-19 cases follows a Poisson likelihood, with the expected count determined by population size and relative risk. The models differ in how spatial and temporal dependencies are incorporated. The temporal model includes monthly random effects modelled as either RW1 or RW2 processes, while the spatio-temporal models incorporate both spatially structured effects (using SPDE approach) and temporally structured effects (RW1). The interaction model further includes an independent spatio-temporal interaction term to capture unobserved localized deviations. It is important to note that the smoothness parameter (ν) of the Matérn covariance function, and the spatial dimension are treated as fixed model components. In contrast, the hyperparameters associated with the PC priors for the random effects (u), the temporal effects, and the spatial range parameter in the SPDE model are assumed parameters. The modelling framework also includes several quantities that are estimated from the data, such as the regression coefficients (β), the independent and identically distributed (IID) random effects (u), the structured temporal random effects, the spatiotemporal interaction terms (δ), and the values of the spatial Gaussian field (S(x)). These parameters are inferred from the data, and their uncertainty is characterised by their posterior distributions. A summary of the model parameters and priors is presented in Table 3. A summary of estimated parameters and priors is presented in Table 3.

Table 3. Description of the parameters of the spatio-temporal models.
Parameter Description Model(s) Used Prior Distribution
β₀, β Fixed effects (intercept, covariates) All models Normal(0, 0.001)
uᵢ IID random effect (neighbourhood-level variability) Spatio-temporal PC prior [0.5, 0.01]
γₜ Temporal random effect (RW1 or RW2) Temporal, Spatio-temporal PC prior [1, 0.01]
δᵢₜ Spatio-temporal interaction term Interaction model only Normal(0, 1/τδ)
S(xᵢ) Spatially structured effect (SPDE) Spatio-temporal Matérn covariance, PC prior [1, 0.1]
τ Precision parameters (for random effects) All models Inverse Gamma(1, 0.00005)
ν Smoothness parameter in SPDE Spatio-temporal Fixed at 1
κ Scale parameter in SPDE Spatio-temporal Derived from range r

In the model fitting process, we have included eight covariates, such as population density, adjusted population density, built-up density, average value of temperature, residential built-up areas, non-residential built-up areas, distance to marketplaces, ease of social distancing index, as outlined in Section 2.1. The variable month spans from 1 to 12, representing each month of the year, and month is treated as factor in the model. We used data on COVID-19 cases from June 2020 to May 2021 (a total of 12 months) to fit the model described in Equation (2). To assess prediction accuracy, we held out data from the following month, June 2021, as a test set. Using this fitted model, INLA then predicted the COVID-19 cases for these held-out months by computing the predictive distributions based on the posterior distributions of the model parameters and latent variables. This approach allows INLA to provide both point predictions and uncertainty estimates, making it suitable for evaluating model accuracy on out of sample data. Finally, we compared the predicted values with the original observed COVID-19 cases from June 2021 to evaluate the predictive performance of the model, with detailed comparison results and performance metrics discussed in Section 3. All the analyses were conducted in R statistical software (v.4.2.2). Specifically, the INLA package (https://www.r-inla.org/) was used to implement Bayesian regression modelling strategies described above. Model ouputs were subsequently extracted, postprocessed and visualised using INLAutils (https://github.com/timcdlucas/INLAutils), the companion package to INLA, which provides specialised tools for model diagnostics and result interpretation.

3. Results

The following results summarize the outcomes of our Bayesian spatio-temporal modelling approaches, highlighting the temporal dynamics, spatial heterogeneity, and zero-inflation characteristics of COVID-19 case distributions in Dakar. For the latter, a ZIP hurdle distribution is used in the modelling, and the parameter significance as well as the goodness of fit of the three fitted Bayesian ZIP hurdle models are presented in Table 3. It appears that the spatio-temporal interaction model was the best model to fit the data. Indeed, the best fitting spatio-temporal interaction model (M3) has the lowest Deviance Information Criterion (DIC) and Watanabe-Akaike information Criterion (WAIC) values compared to the temporal (M1) and separable spatio-temporal model (M2). The DIC and WAIC values varied slightly from the temporal to the separable spatial-temporal models (37050 and 37049 DIC values for M1 and M2, respectively, then 37061 and 37060 WAIC values for M1 and M2, respectively). When a spatio-temporal interaction is specified, the DIC and WAIC has significantly dropped, indicating higher predictability when the space-time interaction is accounted for (Table 4).

Table 4. Posterior estimates of model parameters of temporal and spatio-temporal models of COVID-19 in Dakar.

Spatio-temporal Model
Temporal Model (M1) Separable Model (M2) Interaction model (M3)
Variable Mean 95% BCI a Mean 95% BCI Mean 95% BCI
Intercept -10.23 -55.38,-34.91 -10.25 -55.42,34.92 -10.27 -55.46,34.92
Residential areas 1.25 0.67,1.83 1.25 0.67,1.83 1.25 0.66,1.83
Non-residential areas -0.66 -1.29,-0.04 -0.66 -1.29,-0.04 -0.67 -1.29,-0.04
Population density -0.003 -0.003,-0.002 -0.003 -0.003,-0.002 -0.003 -0.003,-0.002
Adjusted population density 0.29 0.24,0.34 0.29 0.24,0.34 0.29 0.24,0.34
Temperature 0.03 -0.12,-0.18 0.03 -0.12,0.18 0.03 -0.12,0.18
Distance to marketplaces 0.00 0.00,0.00 0.00 0.00,0.00 0.00 0.00,0.00
DIC b 37044 37043 36711
WAIC c 37056 37055 36885

a BCI: Bayesian Credible Interval

b DIC: Deviance Information Criterion

c WAIC: Watanabe-Akaike Information Criterion

For the models specified in Equations (2) and (3), we examine the posterior distributions of fixed and random effects for both the separable spatio-temporal model and the spatio-temporal interaction model. These posterior distributions are presented in S2 Fig, S3 Fig, and S4 Fig, S5 Fig. For both models, the posterior distribution of the fixed effects provides insights into the impact of covariates on the outcome across space and time.

The results indicate that the covariates month number, distance to marketplace, and temperature are non-significant in both models, with null posterior mean or zero included within the range of the 95% credible interval. Conversely, population density and non-residential ACS areas show a significant negative effect, suggesting a negative association in the model. As the proportion of non-residential areas, and the count of people per hectare per neighbourhood’s total area increase, the expected mean of the COVID-19 infection decrease by 0.003 and 0.67, respectively. These expected values fall within the 95% credible interval for both the effect of non-residential areas (-1.29, -0.04) and population density (-0.003, -0.002). Adjusted population density and residential areas exhibit a significant positive effect, indicating a strong positive influence. When the proportion of residential areas increases, the expected mean of COVID-19 infection increases by 0.29. Similarly, an increase in the count of people per built-up area leads to an increase in the expected mean of COVID-19 infection by 1.25.. Also there is a 95% probability this effect lies between 0.66 and 1.83 for residential areas, and between 0.24 and 0.34 for adjusted population density. For both spatio-temporal models, the fixed effects demonstrate a similar trend and nature.

On the other hand, the posterior distribution of the random effects captures underlying spatial, temporal, and spatio-temporal variability. In the separable model (M2), spatial and temporal effects are modeled independently, assuming no interaction between them. In contrast, the spatio-temporal (M3) interaction model includes an additional interaction term, allowing for unique variations in each region-period combination. S2 Fig depicts the marginal posterior mean of spatial, IID and temporal random effects with 95% credible intervals. The random effects analysis indicates that the IID random effect (neigh_id_index) has a stronger influence compared to the spatial random effect (denoted as i) and the temporal random effect (rw1_month_all), with the latter two exhibiting minimal variability. In the top panel, the spatial random effect remains close to zero across all observed SPDE mesh vertices, with very narrow credibility intervals. This suggests that the variability introduced by this random effect is minimal, and that it does not contribute significantly to the outcome. The middle panel displays the IID random effect for individual neighbourhood, representing individual-level variability. Here, substantial fluctuations are observed, with several indices showing large deviations from zero, accompanied by wider credibility intervals for specific sections of the index. This finding highlights the significant role that the IID random effect associated with neighbourhood factors plays in the model, contributing considerable variability to the outcome. The steep changes in mean values for certain neighbourhoods highlight strong spatial heterogeneity, suggesting that specific neighborhoods possess unique characteristics that drive differences in the outcome. In the bottom panel, the random effect for rw1_month_all, which captures temporal variation across months, remains relatively stable around zero. However, the wider credibility intervals, particularly at the extremes of the plot, suggest uncertainty in the estimation of this effect. This suggests that while there is some variability over time, the overall effect is small, and the wide intervals indicate uncertainty in how the model captures monthly fluctuations. The wider band towards the ends may reflect more uncertainty in the estimation for early and later months, which could result from less data or greater variability in those periods.

In contrast, S5 Fig depicts the random effects for the spatio-temporal interaction model. This figure contains four panels, with the final plot representing the spatio-temporal interaction effect. Notably, the IID random effect remains consistent across both models. However, the credible intervals for the spatial and temporal random effects are wider in the spatio-temporal interaction model, though the variation remains close to zero. This indicates increased uncertainty in these random effects estimates but suggests that their overall contribution remains minimal. In the last panel, the spatio-temporal interaction effect displays minimal variation, with values remaining relatively stable around zero. This stability indicates that the interaction effect contributes little additional variability to the model, suggesting limited region-period-specific deviations beyond those captured by the main spatial and temporal effects.

For the spatio-temporal separable model, the spatial effect parameters of κ and τ have mean values of 53.70 and 0.29, respectively. These values represent the marginal posterior distributions of the two hyperparameters for the spatial random field. Using these parameters, we calculated the spatial range r to be 0.452 km, or 452 meters. In contrast, for the spatio-temporal interaction model, we found of κ to be 35.62 and of τ to be 1.149, resulting in a spatial range of 0.064 km, or 64 meters. Notably, the spatio-temporal separable model shows a larger spatial range and higher κ value compared to the interaction model, indicating a broader influence of spatial correlations. To further assess the goodness-of-fit of our best-fitting model, we evaluated its predictive performance at unsampled locations [53]. Fig 4 reports the comparison between predicted COVID-19 infections derived from the best-fitting model and observed data. The Pearson correlation coefficient is 97%, which indicates a strong positive association between the predicted and the observed COVID-19 infections.

Fig 4. Comparison between the predicted and observed infection for the testing records.

Fig 4

A dynamic map that depicts the prediction from the spatio-temporal interaction model has been developed in an R-shiny app and accessible through this link (covid19_Dakar). A sample view of the shiny app is presented in S6 Fig.

The risk of COVID-19 infection is higher in the western Dakar, particularly in the neighbourhoods of the following Communes: Fann-Point-E, Amitie, Plateau, Mermoz Sacre Coeur, Ngor, Sicap Liberte, Dieuppeul, Grand Yoff and Patte d’Oie. Central and Eastern peripheral areas have the lowest probabilities of COVID-19 infection.

4. Discussion

In this study, we developed Bayesian spatio-temporal models to examine the role of contextual risk factors in the spread of COVID-19 infection at the neighborhood level in Dakar. In addition to assessing the influence of these risk factors, we quantified the uncertainties associated with both the fixed effects of covariates and the random effects of spatial, temporal, and spatio-temporal components. A key outcome of this study is the mapping of areas at higher risk of COVID-19 infection in Dakar. Furthermore, the strong correlation between the predicted values from the model and the observed values underscores the high predictive accuracy of the best-fitted spatio-temporal interaction model.

To investigate the relationship between the covariates and COVID-19 infection, various contextual factors were considered. These factors were extracted from remote sensing images, which have proven useful for obtaining environmental and socioeconomic information. Remotely sensed socioeconomic and environmental variables have been widely applied to enhance our understanding of the local epidemiology of infectious diseases [54–59], including COVID-19 disease [60]. Population density is a very important feature of compact cities and an important proxy of socio-economic conditions along with land use characteristics such as built-up residential areas and built-up non-residential areas examined in this study.

Regarding the contrasting statistical correlations that were previously found in the literature, showing a positive [10,14], then a negative correlation [5,8] between COVID-19 infection and population density, this study was an opportunity to further investigate this issue, by using very detailed data, and a more rigorous analytical approach. Our results confirm evidence of contrasting statistical correlations and highlight the impact of the scale of measurement on these correlations. On the one hand, COVID-19 infection was found to be significantly negatively associated with population density when no further adjustments were made and when population density was calculated using the total area of the spatial units as the denominator. On the other hand, when using adjusted population density, which considers only the built-up area as the denominator, a significant positive association with COVID-19 infection was observed. Therefore, adjusting population density before its application in our spatial statistical analysis has addressed issues related to the intrinsic properties of raw, non-adjusted population density such as the implicit assumption of uniformity over spatial units [13], the varying definitions of boundaries and the effect of varying scale of measurements [61]. Since the early stages of the pandemic, areas with high population density have experienced the greatest burden of COVID-19 infections [62,63]. Population density has significantly influenced the spatial distribution of COVID-19 [64], and has been a key indicator for implementing control measures such as physical distancing [65] that aimed to combat the spread of the disease. Our findings link negative correlation between COVID-19 infection and population density to the omission of important methodological considerations. Conversely, the positive association that emerges following further adjustements confirms the role of population density as a primary risk factor for infectious diseases [61], including COVID-19 diseases.

Similarly, we found a significant positive association between residential areas and COVID-19 infection. In contrast, COVID-19 infection was negatively associated with non-residential areas, which include ACS areas. The distance to marketplaces was found to be not significant, suggesting that the effect of mobility was not fully captured by the geospatial predictors used in this study. Despite the complexities surrounding the influence of neighborhood features on the spread of COVID-19 [66], the positive association between COVID-19 infection and residential areas provides insights into local exposure in relation to built-up areas and land use characteristics. Additional information about residential dwellers, such as household social composition and income levels, could further reveal significant disparities in the spread of COVID-19 across residential areas [67,68].

The spatio-temporal model with space-time interaction demonstrated higher predictive performance compared to the non-spatial model and the spatio-temporal model with separable space-time effects. Including the space-time interaction improved the model performance as it accounts for specific local spikes, which cannot be explained by overall spatial or temporal effects alone. Indeed, the spatio-temporal interaction term has the benefit of capturing localised deviations in the infection risk, which is particularly valuable for identifying transient, area-specific surges, thereby enhancing model’s sensitivity to local heterogeneity [40,41]. It is worthy to mention that, INLA provides fast and accurate approximations for posterior marginal distributions in latent Gaussian models, but it does not generate exact joint posterior samples as in MCMC [41–43,48]. The performance may be limited in models with highly non-Gaussian posteriors or complex dependence structures; however, for spatial and spatio-temporal Poisson models, the INLA-SPDE framework can yield results comparable to MCMC with substantially lower computational cost [42,43,50]. In particular, the SPDE-INLA framework has been extensively validated for spatial data and is known to produce results that closely match MCMC-based inference while being computationally much more efficient [41–43,49,50]. In the present study, the primary objective was to compare multiple temporal and spatio-temporal model specifications, including different random-effect structures and interaction terms. As a result, INLA was chosen to enable comparison of multiple competing model structures using alternative priors and model specifications.

There is an important limitation that deserves to be highlighted. The epidemiological data provided by the Ministry of Health includes only the location of cases resulting from community transmission, therefore total case counts in some areas could be underrepresented. No information is available on the spatial distribution of other types of infection, such as the so-called “contact cases”. Including these in the analysis could have refined our results. Furthermore, despite the low mortality rate from COVID-19, data on COVID-19 related-deaths could have provided additionnal insigths into the role of contextual risk factors in the spread of the disease. Notwithstanding the higher predictability of the spatio-temporal model, the link between COVID-19 infection and identified contextual factors may not be direct, as we are dealing with empiric observational data and satellite-derived variables that carry a certain degree of uncertainty. Consequently, caution is needed when drawing conclusions from the results, as causal inference from the model findings is limited. In this study, we aggregated the number of confirmed infections by months, which in turn smooths the daily reporting noise. Nonetheless, missing data, under-reporting and uneven testing across neighbourhoods may still affect the results. For instance, areas with better testing access might report more cases, which could confound the association with contextual risk factors. Potential data biases may arise from incomplete reporting or spatial variations in the detection of the infection, although greater concentration of health facilities and shared testing infrastructure in Dakar may limit these differences. Lastly, it is worth mentioning that, although remotely-sensed variables are useful proxies that capture meaningful landscape characteristics, census or survey-based household-level crowding and socioeconomic variables are useful indicators that could further refine our spatio-temporal model, and improve our understanding on the influence of contextual risk factors on COVID-19 infection.

5. Conclusion

The COVID-19 related social, health and economic impact has been gradually lessened, thanks to various efforts notably the rapid deployment of various vaccines that prompted a high level of population immunity. But in the post-pandemic era, the disease is still circulating and the end of the global health emergency has led to the emergence of a new global health threat. The risk of COVID-19 infection, or re-infection persists, as new virus variants can emerge, causing new surges in cases and deaths.

From a public health perspective, the research findings gained from this study can be valuable resources for health systems in low- and middle-income countries, for geographically targeted interventions. These outputs can serve as support tools for the optimised distribution and less-labour intensive delivery of the COVID-19 vaccine. They can support disease surveillance system through the monitoring of the potential COVID-19 outbreaks. Testing or vaccination efforts should prioritize high-risk western neighbourhoods, or dense residential areas.

Furthermore, the model can be adapted for the study of other infectious diseases, including malaria, tuberculosis and other neglected tropical diseases. Here we can leverage the flexibility of Bayesian spatio-temporal models, which has gained more popularity due to their capacity to incorporate spatial and temporal dependencies, uncertainties and intricate interactions. Bayesian computing has long been a complex task, but in the era of big data and the rapid advancement of computer technology, the Bayesian framework has been enhanced enough to allow in-depth investigations of epidemiological data, and the study of different diseases with a different and more extensive set of regressors.

Supporting information

S1 Fig. SPDE triangulation of the study area.

The underlying base layer is republished from https://doi.org/10.4081/gh.2021.910, under a CC BY license, with permission from the ASSESS project, original copyright Gadiaga et al. 2021.

(TIF)

pgph.0004945.s001.tif (2.7MB, tif)
S2 Fig. Marginal posterior distributions of covariate coefficients for the separable spatio-temporal model.

(TIF)

pgph.0004945.s002.tif (100.3KB, tif)
S3 Fig. Marginal posterior distributions of covariate coefficients for the spatio-temporal interaction model.

(TIF)

pgph.0004945.s003.tif (98KB, tif)
S4 Fig. Marginal posterior distribution of the random effects components for the separable spatio-temporal model.

Top: Marginal posterior mean of the spatial random effect S(.). Middle: Marginal posterior mean of the iid effect ui. Bottom: Marginal posterior mean of the temporal random effect.γt

(TIF)

pgph.0004945.s004.tif (1.1MB, tif)
S5 Fig. Marginal posterior distribution of the random effects components for the spatio-temporal interaction model.

Top panel: Marginal posterior mean of the spatial random effect S(.). Second panel: Marginal posterior mean of the iid effect ui. Third panel: Marginal posterior mean of the temporal random effect γt. Bottom panel: Spatio-temporal interaction effect.

(TIF)

pgph.0004945.s005.tif (988.2KB, tif)
S6 Fig. Overview of the R-Shiny App that visualizes the comparison between the observed and predicted COVID-19 prevalence.

The underlying base layer is republished from https://doi.org/10.4081/gh.2021.910, under a CC BY license, with permission from the ASSESS project, original copyright Gadiaga et al. 2021.

(TIF)

pgph.0004945.s006.tif (1.4MB, tif)

Data Availability

The epidemiological data used in this study is publicly available through a request from the Ministry of Health of Senegal (https://www.sante.gouv.sn/. The following geospatial predictors that we utilised to perform the analyses are freely available through the WorldpPop database: Temperature: https://hub.worldpop.org/geodata/summary?id=62208; Distance to marketplaces: https://hub.worldpop.org/doi/10.5258/SOTON/WP00644; Ease of social distancing index: https://data.worldpop.org/repo/wopr/_MULT/SocialDistancing/v1.0/ The rest of the data may be found in MAUPP data repositories https://maupp.ulb.ac.be/page/grippa2018/. The neighbourhood shapefile used as base layer is accessible upon request through the following repository: https://github.com/assanenian/INLA_Bayesian_Spatiotemporal Lastly, the imagery underlying the base layer in the shiny app is derived from the leaflet package in the R statistical software.

Funding Statement

This study was financially supported by the Gates Foundation in the form of a grant awarded to AG, OY, SC, CN, and AL (INV-044979). This study was also financially supported by the National Institutes of Health in the form of a grant awarded to SL and AT (R01AI160780). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004945.r001

Decision Letter 0

Helen Howard

24 Aug 2025

PGPH-D-25-01352

Spatio-temporal modelling of COVID-19 infection and associated risk factors in Dakar, Senegal

PLOS Global Public Health

Dear Dr. Gadiaga,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please note that we have only been able to secure a single reviewer to assess your manuscript. We are issuing a decision on your manuscript at this point to prevent further delays in the evaluation of your manuscript. Please be aware that the editor who handles your revised manuscript might find it necessary to invite additional reviewers to assess this work once the revised manuscript is submitted. However, we will aim to proceed on the basis of this single review if possible.

Could you please revise the manuscript to carefully address the concerns raised?

Please submit your revised manuscript by Oct 08 2025 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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We look forward to receiving your revised manuscript.

Kind regards,

Helen Howard

Staff Editor

PLOS Global Public Health

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[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

-->Comments to the Author

1. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.-->

Reviewer #1: Partly

**********

-->2. Has the statistical analysis been performed appropriately and rigorously?-->

Reviewer #1: N/A

**********

-->3. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.-->

Reviewer #1: Yes

**********

-->4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.-->

Reviewer #1: Yes

**********

-->5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)-->

Reviewer #1: The study develops geostatistical models to examine the spatiotemporal distribution of COVID-19 at the neighborhood level, incorporating risk factors such as population density, temperature, mobility, etc. Its goal is to evaluate key determinants of COVID-19 transmission risk and provide insights for targeted interventions.

Comments

1. The manuscript would benefit from a clearer and more detailed description of the modeling methods/tools, assumptions, and numerical implementation.

The rationale for using a temporal Poisson regression framework in Model 1, and spatiotemporal approaches in Models 2 and 3 should be explained. The authors should clarify the motivation for constructing multiple models and whether direct comparisons between them are appropriate. Additionally, details on how the simulations were numerically implemented are needed to ensure reproducibility.

2. The models rely on several assumptions, including assumed parameter values, priors, etc. How sensitive are the results to these assumptions? It would also be helpful to clearly outline the three models in the methodology, explicitly stating the assumptions for each, and distinguishing which parameters are estimated versus assumed. A summary table listing all parameters and their values would improve clarity.

3. In Section 2.2.2, the construction of the covariate matrices and the spatially structured random effects S(⋅) is unclear. Provide details on how these were formulated. It may also be good to mention the number of neighborhoods included in the analysis.

4. Clarify which quantities were fitted during the model fitting process and describe how this was done. Further details are needed on the use of INLA and SPDE, how these were implemented to obtain the results.

5. The clarity of the results in Table 2 should be improved, as it currently does not provide meaningful interpretation. For instance, what does a (negative) -0.003 mean population density represent? What does intercept refer to in the model and what does it describe? What does 1.25 mean residential areas represent?

6. It is unclear whether the results in Table 2 are derived from the model fitting. The manuscript may benefit from a figure illustrating how well the best fit model compare with the observed data.

7. Non-pharmaceutical interventions (NPIs) such as social distancing or school closures substantially changed human behavior and hence, are expected to have a significant effect on the COVID-19 transmission during the study period. How are NPIs accounted for in the modeling framework?

8. One motivation for the modeling study is to provide targeted interventions, once the drivers of the disease spread are identified. Based on the results, provide insights into what specific targeted interventions may or might have helped mitigate COVID-19 transmission in the study area.

**********

-->6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Reviewer #1: No

**********

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PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004945.r003

Decision Letter 1

Katrien Janin

15 Dec 2025

PGPH-D-25-01352R1

Spatio-temporal modelling of COVID-19 infection and associated risk factors in Dakar, Senegal

PLOS Global Public Health

Dear Dr. Gadiaga,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

The manuscript has been evaluated by two reviewers, and their comments are available below.

The reviewers have raised a number of concerns. The reviews request clarification regarding the choice of parameters for the Bayesian model, to more clearly distinguish between the considered models, and expand on the limitations (e.g. address that the model is not a causal model.). Could you please carefully review the comments and revise the manuscript to address all comments raised?

Please submit your revised manuscript by Jan 11 2026 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Katrien G. Janin, PhD

Staff Editor

PLOS Global Public Health

Journal Requirements:

If the reviewer comments include a recommendation to cite specific previously published works, please review and evaluate these publications to determine whether they are relevant and should be cited. There is no requirement to cite these works unless the editor has indicated otherwise.

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Additional Editor Comments (if provided):

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Reviewers' comments:

Reviewer's Responses to Questions

-->Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.-->

Reviewer #1: All comments have been addressed

Reviewer #2: (No Response)

**********

-->2. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.-->

Reviewer #1: Yes

Reviewer #2: Yes

**********

-->3. Has the statistical analysis been performed appropriately and rigorously?-->

Reviewer #1: Yes

Reviewer #2: Yes

**********

-->4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.-->

Reviewer #1: Yes

Reviewer #2: Yes

**********

-->5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.-->

Reviewer #1: Yes

Reviewer #2: Yes

**********

-->6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)-->

Reviewer #1: (No Response)

Reviewer #2: Dear authors,

congratulations on this very interesting project and manuscript! My primary impression is that this study is really valuable, particularly because it integrates geographical and infection data by an advanced methodology. This is already reason for me to promote this type of work.

However, there are a few things that I recommend to consider (that is why I will opt for 'minor revision') that in my opinion can make this very good manuscript into a great manuscript.

Please consider:

1. I consider language & wording to be overall very good. There are some places where singular/plural is grammatically wrong, and at least one sentence that seems to be incomplete.

2. Regarding the choice of parameters for the Bayesian model, you mainly motivate it by literature. I think it would yet be better to provide further information on the meaning of the parameter choices as some of them appear arbitrary without further context. For example, in line 356, one parameter is set to sqrt(8v)/k. What is the rationale behind this and what is the potential impact of this parameter?

3. Regarding the implementation, you provide the Github link, which is great. I checked the code and was a bit surprised that it had relatively few lines. In any case, I recommend listing the used R packages in the manuscript as well.

4. Pacing: In several parts of the manuscript, there are long paragraphs, some of them with multiple ideas/aspects. Please consider inserting more line breaks. Also, in general, following the ideas along the main dimensions (what/why/how) could be improved.

5. Presentation of modeling approaches: You consider a range of different model (specifications). On first reading, I found it challenging to clearly distinguish between the considered models. I was wondering whether it would be good to present the models incl. their specifications in a table?

6. The variable qt is introduced as 'relative risk'. I think this should be defined more clearly; do you mean the probability of a transmission/infection given there is a contact to an infected person?

7. The analysis is based on empiric/observational data and therefore causal interpretation of the modeling results is limited. You do not explicitly claim in the article that the results are directly to be understood as causal. However, I think it would be better to address the issue within the manuscript (discussion) that the model is not a causal model.

8. Regarding INLA, can you discuss in the manuscript what the drawbacks and potential risks are for the considered model? How reliable is the approximation for spatial data? Is it possible to do a (partial) robustness check by using an actual MCMC posterior simulation (or another method of more accurately representing the posterior distribution)?

9. In lines 340 until 360, a rather complex series of parameters is introduced. Please specify more clearly in the manuscript why these are chosen (e.g., what is the motivation behind the Matern covariance) and which parameters are set by you and which are estimated within the model.

Kind Regards

**********

-->7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy.-->

Reviewer #1: No

Reviewer #2: Yes: Achim Doerre

**********

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Attachment

Submitted filename: PGPH-D-25-01352_R1_reviewer_AD_comments.pdf

pgph.0004945.s008.pdf (5.7MB, pdf)
PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004945.r005

Decision Letter 2

Julia Robinson

25 May 2026

Spatio-temporal modelling of COVID-19 infection and associated risk factors in Dakar, Senegal

PGPH-D-25-01352R2

Dear Dr Gadiaga,

We are pleased to inform you that your manuscript 'Spatio-temporal modelling of COVID-19 infection and associated risk factors in Dakar, Senegal' has been provisionally accepted for publication in PLOS Global Public Health.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they'll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact globalpubhealth@plos.org.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Global Public Health.

Best regards,

Julia Robinson

Executive Editor

PLOS Global Public Health

***********************************************************

Reviewer Comments (if any, and for reference):

Reviewer's Responses to Questions

-->Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.-->

Reviewer #1: All comments have been addressed

**********

-->2. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.-->

Reviewer #1: Yes

**********

-->3. Has the statistical analysis been performed appropriately and rigorously?-->

Reviewer #1: Yes

**********

-->4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.-->

Reviewer #1: Yes

**********

-->5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.-->

Reviewer #1: Yes

**********

-->6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)-->

Reviewer #1: (No Response)

**********

-->7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy.-->

Reviewer #1: No

**********

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Fig. SPDE triangulation of the study area.

    The underlying base layer is republished from https://doi.org/10.4081/gh.2021.910, under a CC BY license, with permission from the ASSESS project, original copyright Gadiaga et al. 2021.

    (TIF)

    pgph.0004945.s001.tif (2.7MB, tif)
    S2 Fig. Marginal posterior distributions of covariate coefficients for the separable spatio-temporal model.

    (TIF)

    pgph.0004945.s002.tif (100.3KB, tif)
    S3 Fig. Marginal posterior distributions of covariate coefficients for the spatio-temporal interaction model.

    (TIF)

    pgph.0004945.s003.tif (98KB, tif)
    S4 Fig. Marginal posterior distribution of the random effects components for the separable spatio-temporal model.

    Top: Marginal posterior mean of the spatial random effect S(.). Middle: Marginal posterior mean of the iid effect ui. Bottom: Marginal posterior mean of the temporal random effect.γt

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    S5 Fig. Marginal posterior distribution of the random effects components for the spatio-temporal interaction model.

    Top panel: Marginal posterior mean of the spatial random effect S(.). Second panel: Marginal posterior mean of the iid effect ui. Third panel: Marginal posterior mean of the temporal random effect γt. Bottom panel: Spatio-temporal interaction effect.

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    S6 Fig. Overview of the R-Shiny App that visualizes the comparison between the observed and predicted COVID-19 prevalence.

    The underlying base layer is republished from https://doi.org/10.4081/gh.2021.910, under a CC BY license, with permission from the ASSESS project, original copyright Gadiaga et al. 2021.

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    Data Availability Statement

    The epidemiological data used in this study is publicly available through a request from the Ministry of Health of Senegal (https://www.sante.gouv.sn/. The following geospatial predictors that we utilised to perform the analyses are freely available through the WorldpPop database: Temperature: https://hub.worldpop.org/geodata/summary?id=62208; Distance to marketplaces: https://hub.worldpop.org/doi/10.5258/SOTON/WP00644; Ease of social distancing index: https://data.worldpop.org/repo/wopr/_MULT/SocialDistancing/v1.0/ The rest of the data may be found in MAUPP data repositories https://maupp.ulb.ac.be/page/grippa2018/. The neighbourhood shapefile used as base layer is accessible upon request through the following repository: https://github.com/assanenian/INLA_Bayesian_Spatiotemporal Lastly, the imagery underlying the base layer in the shiny app is derived from the leaflet package in the R statistical software.


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