Next Article in Journal
Multi-Source Data-Driven Personalized Recommendation and Decision-Making for Automobile Products Based on Basic Uncertain Information Order Weighted Average Operator
Previous Article in Journal
Superconductivity and the Sustainable Development Goals (SDGs): A Challenge for Researchers in Superconductivity
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Systematic Review

Urban, Architectural, and Socioeconomic Factors Contributing to the Concentration of Potential Arbovirus Vectors and Arbovirosis in Urban Environments from a One Health Perspective: A Systematic Review

1
Department of Public Health & Infectious Diseases, Sapienza University of Rome, 00185 Rome, Italy
2
Department of Prevention, ASL Roma 1, 00193 Rome, Italy
3
Department of Health and Social Care, ASL Roma 1, 00193 Rome, Italy
*
Authors to whom correspondence should be addressed.
Sustainability 2025, 17(9), 4077; https://doi.org/10.3390/su17094077
Submission received: 28 March 2025 / Revised: 23 April 2025 / Accepted: 29 April 2025 / Published: 30 April 2025

Abstract

:
Today, urbanisation and environmental changes are increasingly influencing the social and biological landscape of our planet. This systematic review aims to assess the relationship between urban–architectural and socioeconomic factors and vector concentrations in the urban environment. Following the Preferred Reporting Methodology for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, the PubMed, Scopus, and Cochrane libraries were screened for studies conducted in urban contexts and those involving only arboviruses and potential exposure to arboviral vectors in urban environments, published from the beginning to 22 April 2025. Out of a total of 171 identified studies, 132 were selected for further analysis. Of these, 14 studies were eligible. The included studies reported different ways of measuring vector density and different considerations of the urban–architectural or socio-demographic factors related to it. The studies were set in different urban contexts: Asia, Central and South America, Africa and Oceania. Among the vector species, Aedes aegypti was the most analysed, often with Aedes albopictus. Socioeconomic status emerges as a determining factor. Low-income areas experience higher mosquito densities due to overcrowding, sub-optimal infrastructure, and environmental neglect. This review highlights the importance of implementing a standardised and effective global approach in urban health planning.

1. Introduction

Today, urbanisation and environmental changes are increasingly influencing the social and biological landscape of our planet. This systematic review aims to assess the relationship between urban–architectural and socioeconomic factors and the proliferation and spread of arboviruses. The factors considered include the type of construction, the presence of green spaces and their maintenance status, and population density.
Since the 19th century, global population growth has been accompanied by increasing urbanisation. Whereas most of the world’s population previously lived in rural areas, urban settlements have progressively expanded, with large cities becoming more common [1]. Today, however, while urbanisation is slowing down in the old, industrialised countries of Europe and North America, it is growing strongly in the south. Cities have grown significantly over the past 60 years, making urban areas the new dominant ecology on a global scale, where 70% of the population will live by the 2030s [1,2]. The two main factors changing the social and biological landscape of the planet today are urbanisation and environmental changes. On many levels, urban areas are hotspots for environmental change [2,3].
Rapid and unplanned urbanisation, along with a high population density, promotes the spread of Aedes mosquitoes. Densely populated areas—over 1000 inhabitants per km2—are consistently associated with higher rates of arboviral diseases [4]. High-rise buildings and urban density also influence the presence of mosquitoes, with higher numbers found in outdoor environments and lower floors of buildings [5].
The WHO predicts that urbanisation will lead to new vector-borne diseases and a further increase in others, particularly viral communicable diseases caused by Aedes mosquitoes [6]. Controlling Aedes species is a complex process, and it necessitates the risk of an epidemic to be reduced by implementing standard control measures and quality control activities, monitoring protocols, community-wide actions, and firefighting plans [7].
Implementing these interventions can be particularly challenging due to other growing social problems, such as population movements and rapid unplanned urbanisation [8]. Socioeconomic status significantly influences mosquito distribution, with lower-income neighbourhoods experiencing 63% higher mosquito densities and related diseases due to factors like abandoned properties, waste accumulation, and poor sanitation [9]. Moreover, the presence of garbage, trash, and plastic containers is significantly higher in low-income areas, contributing to mosquito breeding sites [10]. The presence of mosquitoes is influenced by environmental conditions such as vegetation, stagnant water, and decaying infrastructure.
Vegetation and water containers in urban areas provide breeding sites for mosquitoes, while decaying infrastructure in abandoned areas exacerbates the problem [11]. The presence of decorative vegetation and entry points for mosquitoes into households are associated with a higher Aedes density [12].
Temperature, humidity, and rainfall also influence mosquitooes’ distribution, with higher numbers found during the summer and autumn [5,13]. Microclimate variables, including temperature and humidity, strongly predict mosquito abundance.
Urban planning that considers these factors can help mitigate the presence of mosquitoes. For instance, models incorporating microclimate data and larval habitat density can predict adult mosquito abundance, aiding in targeted vector control [14].
Furthermore, the consumption of raw materials by humans, and their constant demand for more advanced goods, have caused an exponential and inevitable increase in industrial production, which has a significant impact on water systems, biodiversity, land use, and cover [15].
The extreme weather events that devastated every continent in 2021 and 2022 put additional strain on health services that were already struggling to cope with the impact of the COVID-19 pandemic’s after-effects. The spread of infectious diseases is being affected by climate change, increasing the risk of co-epidemics and emerging diseases for populations [16]. Zika, dengue, and chikungunya are among the arboviruses that are closely linked to climate change. In recent years, these diseases have led to an increase in local epidemics. Climate change affects the distribution and cycle of vector mosquitoes, such as Aedes aegypti and Aedes albopictus, which are responsible for the transmission of Zika, dengue, chikungunya, and yellow fever [17,18,19,20]. High temperatures and humidity promote the proliferation of these mosquitoes and increase arboviral infection rates [13,21]. Moreover, extreme weather events such as El Niño and La Niña have been associated with an increase in infection cases [21].
Italy, located in a temperate zone, has seen an increase in outbreaks of arboviruses. Estimates of the basic breeding number (R0) for these diseases vary by climate zone, with lower values in temperate zones than tropical and subtropical zones. However, with global warming, the R0 is also expected to increase in temperate regions, including Italy [20]. Italy has recorded cases of Zika infection, especially among travellers returning from endemic areas [22]. There have also been cases of dengue, with local epidemics, especially in the summer months, when the weather conditions favour the proliferation of vector mosquitoes [20,22].
In addition, Italy has recorded cases of chikungunya, with a significant outbreak in 2017 that affected several regions, where favourable climatic conditions, as well as the presence of Aedes Albopictus, have favoured the spread of the virus [20,22]. Understanding infectious disease dynamics in urban areas requires considering spatial heterogeneity in socioeconomic, demographic, and physical city characteristics. Studies conducted in the past ten years have demonstrated that variations in socioeconomic characteristics (such as income, poverty, and access to healthcare), demographic characteristics (such as population density), and the physical characteristics of cities (such as growth patterns and slum density) can have both independent and combined effects on the spread of disease [23,24,25].
The population dynamics of infectious diseases in urban environments require an integrated approach that takes into account rapid advances in surveillance and the design of cities to control factors favouring the proliferation of infectious vectors, without focusing on ecological differences among vectors, which are secondary to the relationship between socioeconomic, urban, and behavioural factors. In order to undertake preventive medicine and urban hygiene procedures to reduce the spread of arbovirosis, we questioned how the complex urban environment affects the transmission of disease and what factors can be addressed. This study therefore focuses on identifying factors associated with the prevalence of vectors in urban environments, with the aim of providing potential tools for urban planning and the prioritisation of interventions to control arboviral diseases.

2. Materials and Methods

2.1. Selection Protocol and Search Strategy

The Preferred Reporting Methodology for Systematic Reviews and Meta-Analyses (PRISMA) was followed in the conduct of the current systematic review. The associated protocol, CRD42024613799, has been registered in PROSPERO [26].
Three distinct databases (PubMed, Scopus, and Web of Science) were used in this research. The search string (“vector density” OR “mosquito* density” OR “mosquito* development”) AND (“urban determinant*” OR “social determinant*” OR urbanization OR “urban development”) was then used to find all articles published up until the 22 April 2025.

2.2. Inclusion and Exclusion Criteria for the Study

Furthermore, all of the found articles were then filtered, first by abstract and title and then by full text. Following that, each author (L.C., M.S., L.P., M.A.D., C.D.P., S.D.G.) selected the articles independently. All the publications were reviewed by the same authors (L.C., M.S., L.P., M.A.D., C.D.P., S.D.G.) separately. Following a thorough debate, all the authors came to unanimous agreement if any concerns, doubts, or contradictions were discovered.
All studies that focused on controlling the concentration of arboviral vectors in the urban environment and that presented specific data with a focus on socioeconomic, urban planning, and behavioural factors and their influence were considered eligible. All research that merely measured vector density without linking it to environmental or urban factors was excluded. This study did not take into account reviews, case reports, meta-analyses, symposia, editorials, or any other type of literature. Only articles written in Italian or English were included.

2.3. Data Extraction and Quality Assessment

All of the included papers were then analysed in order to extract information. This includes information regarding author, year, country, socioeconomic and demographic characteristics, urban and architectural factors, natural factors, vector density, and study methodology.
The data were then arranged according to several evaluation and intervention methodologies. The Newcastle–Ottawa Quality evaluation Scale (NOS) was used to conduct a quality evaluation. A collection of questions is used by the NOS for observational studies to assess their research quality, and each study can receive up to nine points in three different categories. The study group selection, sample size, responder profile, and clarity of the various risk factors were all taken into account in the first area, “SELECT” (4 points). The comparability of various result groups and the presence or absence of confounding variables were included in the second category, “COMPARATIVITY” (2 points). The last area, “RESULTS” (3 points), looked at whether exposure and outcome verification was evaluated clearly or if the statistical testing was suitable when it was applied. Following the summation of the scores, the quality was classified as “good” if the final score was higher than 7, “fair” if it was between 5 and 7, or “poor” if it was lower than 5 [27].

3. Results

Out of a total of 171 identified studies on databases, after having removed duplicates, 132 articles were evaluated for their title and abstract, and then 43 were selected for further analysis, and 14 were finally analysed after applying all the inclusion and exclusion criteria, as depicted in Figure 1.
The main explanatory variables used to associate different urban contexts with epidemiological/entomological results were as follows: socioeconomic and demographic factors, including social health determinants (education level, income, employment status, population density, overcrowding); urban factors (building fabric, compact/compact city, dispersed/suburban, formal or informal urbanisation); naturalistic factors (presence and care of green and blue areas); vector density; and the type of measurement of vectors (direct, estimated, indirect).
Fourteen studies were included, reporting one or more of the following elements when comparing different areas: socio-demographic, urban–architectural, and natural characteristics. The selected studies focused on urban contexts in Asia (n = 7), with a clear prevalence in Indian (n = 3) and Chinese (n = 2) contexts, Central and South America (n = 4) (Colombia, n = 2, Brazil, n = 2), Africa (n = 2), and Oceania (n = 1), as reported in Table 1. This prevalence highlights a stronger interest among endemic countries in vector-borne diseases such as dengue, Zika, and malaria. Most urban contexts analysed featured significant socioeconomic disparities, reflected in pronounced differences in urban quality. These cities often include well-serviced neighbourhoods with high-quality infrastructure and informal settlements or slums, characterised by extensive self-construction and lack of regulation.
Due to the high heterogeneity in the content of the included studies, the evaluation was entirely qualitative. This choice is justified by the highly diverse objectives and methods across the studies. Not all the studies provided detailed methodologies for assessing vector density, with some limiting their analysis to counting vectors captured in containers or using specific traps, including direct aspiration when vectors were identified in specific locations. Twelve studies [28,29,30,31,32,33,34,35,36,37,38,39] measured vector density or abundance using direct methods involving vector capture. One study [40] estimated vector density based on contextual conditions, and another [41] inferred density from dengue incidence cases (see Table 1).
Studies employing direct measurements utilised a variety of methods, including the Container Index (CI) [28,33,38], Breteau Index (BI) [29,33,38,39], Human Landing Index (HLI) [28], Standard Space Index (SSI) [29], Adult Density Index (ADI) [29], pupae per person index (PPI) [33,39], Egg Density Index (EDI) [30], and House Index (HI) [33,38]. These methods reflect a significant variability in the calculation of vector density, aiming to produce specific spatial indices for area comparisons. The choice of methodology often depended on the study’s objectives, such as density within drinking water containers (CI), inside homes (HI), generalised density based on sampling and trapping (BI, HLI), or vector density in specific life stages (PPI, EDI). This variability highlights the complexity of studying vector density.
Regarding vector species, Aedes aegypti was the most analysed, appearing in 9 out of 14 studies [31,33,35,36,37,38,39,40,41], often alongside Aedes albopictus [31,36]. The importance of these vectors lies in their high transmission capacity for arboviruses and their notable affinity for urbanised contexts, as underlined in all the studies.
As for the analysed factors, considerable heterogeneity emerged. Most studies were ecological, associating these factors with specific areas or inferring them from contextual descriptions related to vector density analyses. This evidence necessitates further evaluation and specific studies.
Table 1 summarises the number of studies providing the information targeted by this review.
Socio-demographic factors: 11 studies;
Urban–architectural factors: 13 studies;
Natural factors: 12 studies (including temperature and humidity).
Table 1. Included studies and data extraction.
Table 1. Included studies and data extraction.
Authors
Year
Country
Socioeconomic and Demographic Factors Urban and Architectural
Factors
Natural FactorsCarrier Types/SpeciesType of Measurement (Direct, Estimated, Indirect)Quality
Liu et al.
2013
China
[28]
Low socioeconomic level and high population density associated with higher carrier densityLeakage from pipes and wetlands associated with higher presence; tree-lined courtyards, moderate presence; absence of greenery but with drainage systems very low presence; affluent residential area but with private courtyards and proximity to large park, high vector densityVegetation and lake with fish associated with lower occurrence; trees and irrigated areas associated with higher occurrenceCulex pipiens complexDirect measurement (bed net trap; light trap; labour hour method)Good
Wu et al.
2020
China
[29]
Low socioeconomic status and overcrowding, high carrier densityHeavily urbanised areas, lower density; sparsely urbanised areas with haphazard urbanisation, overcrowding, and density with low socioeconomic level, very high densityProximity to waterways but with low socioeconomic level, very high vector density; vegetated areas, intermediate vector density; unused areas (unfinished construction sites, wasteland, or vacant lots), urban—assimilated to urban voids—and suburban lowest density of allAedes albopictusDirect measurement: Breteau Index (BI); Standard Space Index (SSI); Adult Density Index (ADI)Good
Romeo-Aznar et al.
2018
India
[41]
Low socioeconomic level and high population density with overcrowding, high carrier densityHigh building density in deprived areas (and thus poor quality), sheet metal, use of plastic roofing, lack of planning and drainage systems, functional mix (although it is correlated with poor control, open water containers), heat islands, and shaded areas (narrow alleys or lots of vegetation), high vector densityNot describedAedes aegyptiIndirect estimation (from dengue incidence)Good
Santos J.P.C. et al.
2020
Brazil
[30]
Net demographic density Percentage of occupied area; percentage of residential area; percentage of area of
substandard clusters; percentage of area with strategic points; mean verticalisation; number of neighbouring districts; border perimeter with neighbouring districts; percentage of households with unpaved streets; percentage of households with no tree-lined streets; percentage of households with streets without manholes; percentage of households with
streets with exposed trash; percentage of households with
streets with open sewage
Percentage of vegetation; mean daytime
surface temperature; mean night-time
surface temperature; monthly cumulative rainfall
Incidence of dengue cases and Aedes Egg Density Index (EDI)Mean number of incident cases in the study period to the mean population
over the same period multiplied by 100,000 inhabitants. The Aedes Egg Density Index (EDI) is calculated for each neighbourhood from 2013 to 2014 through entomological
monitoring by ovitraps.
Good
French M.A. et al.
2021
Australia
[31]
Head of household; number of members, number
living in household; name, date of birth, sex, marital status, relationship to
head of household, education level, literacy; symptoms, healthcare utilisation, mental health; height and weight for children; haemoglobin; soil-transmitted helminths; individual primary activities and time use, household
assets, self-assessed socioeconomic status and life
satisfaction
Floor, wall, and roof materials; number of rooms; land ownership/tenure, occupation tenure; water sources, access, treatment methods, and cost; sanitation access, type, ownership, and disposal; garbage disposal; local flooding events; child environmental exposureE. coli, nitrogen, pH, temperature, turbidity,
conductivity, dissolved oxygen in water; E. Coli in soil; local agricultural (foodstock), domestic, or feral
animals in animal faeces; temperature and humidity in thermal environment; mosquito species and relative abundance; small mammalian pest species and relative abundance
Culex quinquefasciatus (94⋅7%) and Aedes aegypti (4.9%).
Small numbers of other species were caught, including Anopheles species,
Aedes albopictus, Culex sitiens, a Uranotaenia species, and a Mansonia
species
Counting and identification of mosquitoes caught in trapsGood
Kigozi S.P. et al.
2015
Uganda
[32]
Number of participants; mean age in years during follow-up; total number of routine blood slides; parasite prevalence; person-years of observation; total episodes of malaria; incidence of malaria per person-yearHousehold density, and night-time light brightnessLand cover,
vegetation amount
Anopheles
mosquitoes
Household density of mosquitoes (number of female Anopheles mosquitoes captured)Good
Wai et al.
2012
India, Myanmar, Thailand, Indonesia, Philippines, Sri Lanka
[33]
Subjects aged >25 years.
Middle class neighbourhoods and good to reasonable access to public services
Rainwater reservoirs, unplanned construction, low buildings in deprived areas, accumulation of materials in streets, unmaintained public or private spaces, all associated with higher vector densityAnnual rainfall dataAedes aegyptiDirect measurement: Breteau Index (BI); House Index (HI), Container Index (CI), pupae per person index (PPI)Good
Kang et al.
2018
Uganda
[34]
Not describedConcrete walls, brick floors, screened gutters and vents, tiled roofs, protective factors; incomplete houses, exposed brick, architectural elements that promote stagnation and vector densityTemperature, humidity, rainfallAnopheles spp.Direct measurement (trap)Good
Ferdousi et al.
2015
Bangladesh
[40]
Not describedBrick or concrete houses, brick houses and bamboo roofs, shacks, 111 different types of indoor, outdoor, or rooftop water containersNot describedAedes aegyptiEstimatedGood
Xavier et al., 2023 Brazil
[35]
Not describedMostly single-family houses with basic sanitation and mutual geographic isolation: about 2.5 km apart and separated by stretches of unbuilt environment Possible temporal variations due to monthly weather conditions (precipitation or temperature) or insecticide spraying are consideredAedes aegypti e Culex quinquefasciatusThe density of adult mosquitoes measured directly by active aspiration of adult mosquitoes and indices based on the presence of eggs of Aedes females in traps and the abundance of eggs in trapsFair
Micanaldo E.F. et al.
2021
Philippines
[36]
Low to middle, high population density, inadequate sanitary conditionsEntomological, epidemiological, and landscape data from the rainy season; lack of drainage infrastructure, which contributes to flooding deteriorating infrastructure, agriculture, water bodies, commercial, residential Landscape and climate variables, strong monsoon rain and tropical
storms. Heavy rain
Aedes aegypti and Aedes albopictusDirect and indirectGood
Gómez-Vargas W. et al.
2024
Colombia
[37]
High population density,
low to middle
Unregulated urbanisation, regulated urbanisation deteriorating infrastructure, agriculture, water bodies, commercial, residential, drainage system,
3 different municipalities
Landscape,
monthly records of precipitation (mm), relative humidity (%),
and temperature (˚C)
Aedes aegyptiDirect and indirect. Mean density
of Ae. aegypti was 1.47 females/dwelling and 0.51 females/inhabitant,
Prokopack aspirators
Good
Telle O. et al.
2021
India
[38]
Low socioeconomic level and high population density associated with higher carrier densityTaller buildings (in affluent neighbourhoods) are associated with lower larval presence, building quality is associated with lower larval presence (less accumulation on sheet metal and uncovered tanks), higher maintenance, access to potable waterAbsence of manicured vegetation in deprived areas creates favourable microclimate for mosquitoesAedes aegyptiHouse Index, Container Index, Breteau Index (BI)Good
Fuentes-Vallejo M et al.
2015
Colombia
[39]
High housing density in deprived areas increased vector density and lower land care and poor building quality Favourable elements are unplanned urbanisation (coincides with proximity to waterways), low and close buildings (favourable microclimate), irregularly shaped yards (water stagnation), unmaintained common areas, lack of drainageProximity to waterways is associated with poor urban quality and poor drainage but also with alluvial features that promote water accumulationAedes aegyptiPupae per person index (PPI), Breteau Index (BI)Good
The socio-demographic factors associated with a higher vector density primarily included overcrowded housing and a low socioeconomic status, recognised in nearly all analysed studies as key elements impacting vector density through various causal pathways. A notable exception was observed in one study [28], which a linked higher vector presence to high socioeconomic status in a specific urban context, particularly due to private green areas.
The urban–architectural factors associated with a higher vector density primarily concerned informal and unplanned urbanisation [37,39], a reduced drainage capacity for surface and rainwater [34,36,39], the use of substandard materials in degraded urban contexts [41], reduced building height, urban heat islands, and waste accumulation on streets or specific locations, such as tyres, which due to their shape facilitate widespread water stagnation in poorly managed contexts. Specific architectural factors included the use of materials like corrugated metal roofs, favouring rainwater accumulation in contexts lacking effective drainage systems, and exposed porous materials, such as uncovered hollow bricks, which can trap stagnant water, creating breeding grounds for vectors. In Indian contexts, uncovered water tanks on rooftops, especially in highly informal urban areas with limited piped water access, played a prominent role.
Beyond high temperatures and humidity, the natural factors associated with higher vector density included the poor management of riverside areas and neglected green spaces. Specific factors included water pH and bacterial presence, although these are likely correlational rather than causal [31]. Bacterial proliferation often characterises stagnant water accumulations, even in uncovered or poorly managed drinking water reservoirs, sometimes associated with other invasive animal species.
All studies were rated as “good” [28,29,30,31,32,33,34,36,37,38,39,40,41], with the exception of one which was “fair” [35].

4. Discussion

The literature review highlights several points of interest regarding the available evidence, potential research directions, and general assessments of the existing literature. All the results, following the adopted evaluation model, are presented in Table 1.
The identification of socio-demographic, architectural, and environmental factors influencing vector density offers valuable guidance for targeted and context-specific vector control strategies. Overcrowding and a low socioeconomic status consistently correlate with an increased vector presence, underscoring the need to integrate social equity into public health interventions. Architectural features—such as poor drainage, informal construction, and materials that promote water stagnation—highlight the critical intersection between urban design and vector ecology. Additionally, context-dependent findings, such as a higher vector density in affluent areas with private green spaces, emphasise the complexity of urban ecosystems. These insights support the development of multidisciplinary approaches combining urban planning, environmental management, and public health to effectively mitigate arbovirus transmission in diverse urban settings [28,29,30,31,32,33,34,35,36,37,38,39,40,41].
The first significant observation is the absence of studies specific to high-income countries. This represents a limitation in the generalisability of the results but also highlights a lack of interest in urban contexts in regions such as Europe and North America. Nevertheless, as presented in the introduction, early outbreaks of vector-borne diseases have already been observed in these regions, albeit limited in time and space, primarily due to habitat modifications driven by climate change and increased transcontinental connectivity. A prominent biomedical report addressing climate change impacts [16] emphasises that such diseases require greater global attention. Unfortunately, it is not possible to compare measurements obtained using different methodologies, which represents a significant limitation. All the methods used and analysed are validated and reflect a necessary differentiation in measurement capacity, as this is strongly influenced by contextual characteristics, as well as by the type of vector and the location where it is being investigated [42].
Moreover, there is little focus in the literature on systematically studying contextual characteristics as specific exposure variables, combining robust entomological assessments of anthropogenic habitats with contextual characteristics.
Such studies could provide concrete evidence to guide public policies in urban and architectural planning. The reviewed studies suggest potential research directions, while also highlighting a lack of awareness about the necessity to integrate biomedical knowledge with expertise from other fields, particularly urban planning, and combine qualitative and quantitative methodologies. This interdisciplinary approach is further explored at the conclusion of the discussion.
Socioeconomic factors emerge as critical determinants of vector density, although causality is clearly mediated by urban and architectural factors. While this conclusion is influenced by the selection of study contexts—where low-income urban areas often feature extensive formal neighbourhoods alongside informal settlements or slums [43]—it is still possible to identify recurring general aspects. Socioeconomic factors are literally “the causes of the causes” [44], as lower socioeconomic populations are more likely to live in degraded urban contexts, often without drainage systems for rainwater or proper sewage management [45]. In this sense, we highlight that patterns of inequality in the distribution of vectors within the same city—depending on the socioeconomic status of neighbourhoods—are also observed in diverse urban contexts.
In these neighbourhoods, buildings are often constructed in a disorderly fashion, lacking planned spaces for green infrastructure, thus favouring water collection in urban interstices, exacerbating heat islands, and creating ideal conditions for vector proliferation [46]. These contexts are further characterised by substandard infrastructure, necessitating the use of uncovered water tanks for potable water storage. Building materials, often recycled debris such as hollow bricks and corrugated sheets improperly installed, facilitate water accumulation in crevices, creating breeding grounds for vectors. Waste accumulation on streets and the lack of proper waste disposal also contribute to additional vector habitats. In this sense, cisterns and used car tires are both well-known and notorious due to the volume of water they can hold, as well as the protection they offer from evaporation and UV exposure, promoting vector proliferation [47].
Architectural, urban, and economic variables have a major impact on the transmission of arboviral infections [48]. Economic disparities between countries and regions influence socioeconomic conditions, which impact healthcare access, infrastructure, and mosquito control strategies [49]. Additionally, because highly crowded places, inadequate waste management, and a lack of natural space can all act as vector breeding grounds, urban design is crucial. Indoor ventilation, water storage, and mosquito exposure are all impacted by architectural design, which is frequently tailored to the temperature and terrain [50]. Additionally, by emphasising regional vulnerabilities and intervention goals, the inclusion of a geographical classification and an economic country–city framework in disease transmission analysis improves comprehension [51].
It is evident that urban–architectural and socio-demographic factors (including overcrowding, often confused with population density but representing its opposite in terms of social stratification and the spread of infectious diseases [52]) are intrinsically linked. None of the reviewed studies delves deeply into this causal relationship, suggesting potential further research avenues.
In this regard, it is essential to leverage additional knowledge and practices already employed in other fields of epidemiology and urban studies, through the targeted use of GISs (Geographical Information Systems) integrated with reliable data sources, both social and health-related. GIS-driven studies are, therefore, highly desirable and relatively feasible, particularly in high-income settings. These could especially benefit from population-specific record-linkage methodologies, enabling a thorough investigation of the phenomenon while accounting for population mobility within urban contexts.
The integration of geospatial modelling and geoinformation systems (GISs) offers a transformative potential in the surveillance and control of vector-borne diseases in urban settings. By enabling the visualisation and analysis of spatial patterns of vector density in relation to socioeconomic, architectural, and environmental factors, GIS-driven approaches can support evidence-based decision-making. Advanced techniques such as spatial interpolation, hotspot analysis, and predictive modelling can identify high-risk areas, optimising resource allocation for targeted interventions. Furthermore, coupling GISs with machine learning algorithms and real-time environmental monitoring (e.g., weather and humidity sensors) could enhance the predictive accuracy of vector proliferation models. This geospatially informed approach aligns with the global shift towards data-driven urban health strategies, providing a critical toolset for addressing the complexities of vector-borne diseases in rapidly urbanising regions [53,54].
From the perspective of natural factors, it becomes clear that vector density is not merely linked to the presence of green or blue spaces but rather to their management. Parks, private green areas, and riverbanks favour vector density when neglected. Moreover, the loss of biodiversity appears to disrupt natural balances that regulate vector proliferation, especially in wetlands where predator species may control vector populations [55,56].

5. Limitations and Conclusions

This study suggests that more multidisciplinary research is required to assess environmental management and sustainable urban design strategies for the prevention of arbovirosis. In order to achieve the global Sustainable Development Goals (SDGs), especially Goal 3 (Good Health and Well-Being), Goal 11 (Sustainable Cities and Communities), and Goal 13 (Climate Action), it is highly recommended that integrated and sustainable urban policies be developed that concurrently address the urban, socioeconomic, and behavioural determinants of vector proliferation [57]. Using important international strategic documents like the WHO’s Global Vector Control Response (2017–2030), the Lancet Countdown on Health and Climate Change, and reports from the EU’s Climate Change and Health (CCM) program, longitudinal and interventional studies would be helpful in evaluating the effect of sustainable urban interventions on the spread of vector-borne diseases [58,59,60].
In light of climate change, the European Climate Risk Assessment (EUCRA) also emphasises the growing threats to public health posed by vector-borne illnesses. The expansion of vectors like Aedes mosquitoes is being facilitated by rising temperatures and changing precipitation patterns, which could raise the danger of arbovirus transmission in previously non-endemic locations [61].
This study has certain limitations. The primary challenge lies in the significant heterogeneity of the studies analysed, which complicated the data extraction and discussion. This heterogeneity is reflected in the diverse methodologies, both qualitative and quantitative, employed by the reviewed studies. As a result, it was not feasible to perform a robust quantitative synthesis, necessitating a predominantly qualitative evaluation, which may introduce subjective interpretation biases. Additionally, the lack of standardised methodologies for vector density assessment represents another limitation. Although the indices used are valid within their specific contexts, the absence of a uniform approach restricts direct comparisons across results. Owing to the heterogeneity of the findings across the included studies, conducting a quantitative meta-analysis or performing a statistical synthesis was not feasible. Certainly, there may also be issues of article selection related to publication bias, as grey literature was not taken into account.
Most of the studies adopted a cross-sectional design, providing a static snapshot of associations between the analysed factors and vector density. Longitudinal studies are needed to better understand the temporal and causal dynamics, especially in rapidly changing contexts. Another limitation is the lack of generalisability of the findings to high-income urban contexts, as most studies focus on urban settings with a high informality, which are characteristic of specific global areas.
This review clearly shows that vector density results from complex interactions between socioeconomic, urban, and environmental factors. However, the findings strongly emphasise that deficiencies in urban planning, particularly in informal settlements, amplify public health risks. These results underscore the importance of urban regeneration policies that integrate solutions to improve water drainage, promote high-quality building materials, and reduce vector habitats through sustainable waste and water infrastructure management. Urban planning is not merely a technical tool but a necessity for public health [62].
Another significant limitation was that it was not possible to evaluate the standardisation of Global Urban Health in the countries reported in the literature, despite the differences in the health budgets of the various countries, due to the absence of information on this.
The evidence collected calls for a future research agenda that is interdisciplinary, global, and action-oriented. Prospective studies are needed to assess the impact of integrated and context-specific interventions. Additionally, governments must adopt a proactive approach by investing in resilient infrastructure and developing urban planning strategies that address the health risks associated with climate change. Only by doing so will it be possible to systematically and sustainably tackle the challenges posed by vector-borne diseases in urban settings.
The implementation of comprehensive, evidence-based policies by policymakers is crucial in reducing the development of arboviral infections in urban environments. Addressing the socioeconomic disparities that increase exposure to vector habitats should be a top priority, especially in underprivileged areas with limited housing and poor infrastructure. To avoid water build-up and eradicate breeding grounds, urban development regulations must guarantee the installation of efficient drainage systems, controlled building techniques, and the preservation of green areas. By making investments in geospatial technology, such as spatial analysis, GIS mapping, and predictive modelling, surveillance can be greatly improved and focused, resource-efficient interventions made possible. Furthermore, sustaining urban natural spaces and biodiversity are crucial elements of long-term vector control. In high-income nations, where global mobility and climate change are promoting the formation of new danger zones, policymakers must also broaden their research and monitoring frameworks. Building resilient urban health systems that can address the changing problems of vector-borne diseases requires a multisectoral, forward-looking approach.

Author Contributions

Conceptualisation, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; methodology, L.C., M.S., L.P. and C.D.P.; software, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; validation, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; formal analysis, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; investigation, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; resources, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; data curation, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; writing—original draft preparation, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; writing—review and editing, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G.; visualisation, L.C. and M.S.; supervision, L.P. and C.D.P.; project administration, L.C., M.S., L.P., C.D.P., M.A.D. and S.D.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

All data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. United Nations. World Urbanization Prospects: The 2014 Revision, Highlights (ST/ESA/SER.A/352); United Nations: New York, NY, USA, 2014. [Google Scholar]
  2. Lenzi, A. Why urbanisation and health? Acta Biomed. 2019, 90, 181–183. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  3. Harpham, T. Urban health in developing countries:what do we know and where do we go? Health Place 2009, 15, 107–116. [Google Scholar] [CrossRef] [PubMed]
  4. Kolimenakis, A.; Heinz, S.; Wilson, M.L.; Winkler, V.; Yakob, L.; Michaelakis, A.; Papachristos, D.; Richardson, C.; Horstick, O. The role of urbanisation in the spread of Aedes mosquitoes and the diseases they transmit—A systematic review. PLOS Negl. Trop. Dis. 2021, 15, e0009631. [Google Scholar] [CrossRef] [PubMed]
  5. Liao, J.; Tu, W.; Chiu, M.; Kuo, M.; Cheng, H.; Chan, C.; Dai, S. Joint influence of architectural and spatiotemporal factors on the presence of Aedes aegypti in urban environments. Pest Manag. Sci. 2023, 79, 4367–4375. [Google Scholar] [CrossRef]
  6. World Health Organization (WHO); UNICEF; UNDP; World Bank. Special Programme for Research and Training in Tropical Diseases; Global Vector Control Response 2017–2030; World Health Organization: Geneva, Switzerland, 2017. [Google Scholar]
  7. Bellini, R.; Michaelakis, A.; Petrić, D.; Schaffner, F.; Alten, B.; Angelini, P.; Aranda, C.; Becker, N.; Carrieri, M.; Di Luca, M.; et al. Practical management plan for invasive mosquito species in Europe: I. Asian tiger mosquito (Aedes albopictus). Travel Med. Infect. Dis. 2020, 35, 101691. [Google Scholar] [CrossRef] [PubMed]
  8. Soto, S.M. Human migration and infectious diseases. Clin. Microbiol. Infect. 2009, 15 (Suppl. 1), 26–28. [Google Scholar] [CrossRef] [PubMed]
  9. Vora, N. Impact of anthropogenic environmental alterations on vector-borne diseases. Medscape J. Med. 2008, 10, 238. [Google Scholar] [PubMed]
  10. Whiteman, A.; Loaiza, J.R.; Yee, D.A.; Poh, K.C.; Watkins, A.S.; Lucas, K.J.; Rapp, T.J.; Kline, L.; Ahmed, A.; Chen, S.; et al. Do socioeconomic factors drive Aedes mosquito vectors and their arboviral diseases? A systematic review of dengue, chikungunya, yellow fever, and Zika Virus. One Health 2020, 11, 100188. [Google Scholar] [CrossRef]
  11. Little, E.; Biehler, D.; Leisnham, P.T.; Jordan, R.; Wilson, S.; LaDeau, S.L. Socio-Ecological Mechanisms Supporting High Densities of Aedes albopictus (Diptera: Culicidae) in Baltimore, MD. J. Med. Entomol. 2017, 54, 1183–1192. [Google Scholar] [CrossRef]
  12. Yitbarek, S.; Chen, K.; Celestin, M.; McCary, M. Urban mosquito distributions are modulated by socioeconomic status and environmental traits in the USA. Ecol. Appl. A Publ. Ecol. Soc. America 2023, 33, e2869. [Google Scholar] [CrossRef]
  13. Jones, R.; Kulkarni, M.A.; Davidson, T.M.; Radam-Lac Research Team; Talbot, B. Arbovirus vectors of epidemiological concern in the Americas: A scoping review of entomological studies on Zika, dengue and chikungunya virus vectors. PLoS ONE 2020, 15, e0220753. [Google Scholar] [CrossRef] [PubMed]
  14. Evans, M.V.; Hintz, C.W.; Jones, L.; Shiau, J.; Solano, N.; Drake, J.M.; Murdock, C.C. Microclimate and Larval Habitat Density Predict Adult Aedes albopictus Abundance in Urban Areas. Am. J. Trop. Med. Hyg. 2019, 101, 362–370. [Google Scholar] [CrossRef] [PubMed]
  15. Grimm, N.B.; Faeth, S.H.; Golubiewski, N.E.; Redman, C.L.; Wu, J.; Bai, X.; Briggs, J.M. Global change and the ecology of cities. Science 2008, 319, 756–760. [Google Scholar] [CrossRef] [PubMed]
  16. Romanello, M.; Di Napoli, C.; Drummond, P.; Green, C.; Kennard, H.; Lampard, P.; Scamman, D.; Arnell, N.; Ayeb-Karlsson, S.; Ford, L.B.; et al. The 2022 report of the Lancet Countdown on health and climate change: Health at the mercy of fossil fuels. Lancet 2022, 400, 1619–1654, Erratum in Lancet 2022, 400, 1680. Erratum in Lancet 2022, 400, 1766. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  17. Zardini, A.; Menegale, F.; Gobbi, A.; Manica, M.; Guzzetta, G.; D’Andrea, V.; Marziano, V.; Trentini, F.; Montarsi, F.; Caputo, B.; et al. Estimating the potential risk of transmission of arboviruses in the Americas and Europe: A modelling study. Lancet Planet. Health 2024, 8, e30–e40. [Google Scholar] [CrossRef]
  18. Caputo, A.; Garavelli, P.L. Climate, environment and transmission of malaria. Infez. Med. 2016, 24, 93–104. [Google Scholar] [PubMed]
  19. Leung, X.Y.; Islam, R.M.; Adhami, M.; Ilic, D.; McDonald, L.; Palawaththa, S.; Diug, B.; Munshi, S.U.; Karim, N. A systematic review of dengue outbreak prediction models: Current scenario and future directions. PLOS Negl. Trop. Dis. 2023, 17, e0010631. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  20. Liu, Y.; Lillepold, K.; Semenza, J.C.; Tozan, Y.; Quam, M.B.; Rocklöv, J. Reviewing estimates of the basic reproduction number for dengue, Zika and chikungunya across global climate zones. Environ. Res. 2020, 182, 109114. [Google Scholar] [CrossRef]
  21. Marinho, R.d.S.S.; Duro, R.L.S.; Mota, M.T.d.O.; Hunter, J.; Diaz, R.S.; Kawakubo, F.S.; Komninakis, S.V. Environmental Changes and the Impact on the Human Infections by Dengue, Chikungunya and Zika Viruses in Northern Brazil, 2010–2019. Int. J. Environ. Res. Public Health 2022, 19, 12665. [Google Scholar] [CrossRef]
  22. Osman, S.; Preet, R. Dengue, chikungunya and Zika in GeoSentinel surveillance of international travellers: A literature review from 1995 to 2020. J. Travel Med. 2020, 27, taaa222. [Google Scholar] [CrossRef]
  23. Paull, S.H.; Song, S.; McClure, K.M.; Sackett, L.C.; Kilpatrick, A.M.; Johnson, P.T. From super-spreaders to disease hotspots: Linking transmission acrosshosts and space. Front. Ecol. Environ. 2012, 10, 75–82. [Google Scholar] [CrossRef] [PubMed]
  24. Acevedo, M.A.; Prosper, O.; Lopiano, K.; Ruktanonchai, N.; Caughlin, T.T.; Martcheva, M.; Osenberg, C.W.; Smith, D.L. Spatial heterogeneity, host movement and mosquito-borne disease transmission. PLoS ONE 2015, 10, e0127552. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  25. Vazquez-Prokopec, G.M.; Morrison, A.C.; Paz-Soldan, V.; Stoddard, S.T.; Koval, W.; Waller, L.A.; Perkins, T.A.; Lloyd, A.L.; Astete, H.; Elder, J.; et al. Inapparent infections shape the transmission heterogeneity of dengue. PNAS Nexus 2023, 2, pgad024. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  26. Page, M.J.; Moher, D.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. PRISMA 2020 explanation and elaboration: Updated guidance and exemplars for reporting systematic reviews. BMJ 2021, 372, n160. [Google Scholar] [CrossRef]
  27. Palmieri, V.; Colamesta, V.; La Torre, G. Evaluation of methodological quality of studies. Senses Sci. 2016, 3, 235–241. [Google Scholar] [CrossRef]
  28. Liu, Q.; Liu, X.; Cirendunzhu; Woodward, A.; Pengcuociren; Bai, L.; Baimaciwang; Sang, S.; Dazhen; Wan, F.; et al. Mosquitoes established in Lhasa city, Tibet, China. Parasites Vectors 2013, 6, 224. [Google Scholar] [CrossRef]
  29. Wu, S.; Ren, H.; Chen, W.; Li, T. Neglected urban villages in current vector surveillance system: Evidences in Guangzhou, China. Int. J. Environ. Res. Public Health 2020, 17, 2. [Google Scholar] [CrossRef]
  30. Santos, J.P.C.; Honório, N.A.; Barcellos, C.; Nobre, A.A. A perspective on inhabited urban space: Land use and occupation, heat islands, and precarious urbanization as determinants of territorial receptivity to dengue in the city of Rio de Janeiro. Int. J. Environ. Res. Public Health 2020, 17, 6537. [Google Scholar] [CrossRef]
  31. French, M.A.; Barker, S.F.; Taruc, R.R.; Ansariadi, A.; Duffy, G.A.; Saifuddaolah, M.; Agussalim, A.Z.; Awaluddin, F.; Zainal, Z.; Wardani, J.; et al. A planetary health model for reducing exposure to faecal contamination in urban informal settlements: Baseline findings from Makassar, Indonesia. Environ. Int. 2021, 155, 106679. [Google Scholar] [CrossRef]
  32. Kigozi, S.P.; Pindolia, D.K.; Smith, D.L.; Arinaitwe, E.; Katureebe, A.; Kilama, M.; Nankabirwa, J.; Lindsay, S.W.; Staedke, S.G.; Dorsey, G.; et al. Associations between urbaniity and malaria at local scales in Uganda. Malar. J. 2015, 14, 374. [Google Scholar] [CrossRef]
  33. Wai, K.T.; Arunachalam, N.; Tana, S.; Espino, F.; Kittayapong, P.; Abeyewickreme, W.; Hapangama, D.; Tyagi, B.K.; Htun, P.T.; Koyadun, S.; et al. Estimating dengue vector abundance in the wet and dry season: Implications for targeted vector control in urban and peri-urban Asia. Ann. Trop. Med. Parasitol. 2012, 106, 436–445. [Google Scholar] [CrossRef] [PubMed]
  34. Kang, S.Y.; Battle, K.E.; Gibson, H.S.; Cooper, L.V.; Maxwell, K.; Kamya, M.; Lindsay, S.W.; Dorsey, G.; Greenhouse, B.; Rodriguez-Barraquer, I.; et al. Heterogeneous exposure and hotspots for malaria vectors at three study sites in Uganda. Gates Open Res. 2018, 2, 32. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  35. Xavier, A.; Bonfim, C.; Júnior, W.B.; Bezerra, G.; Oliveira, C.; Uchikawa, R.; da Silva, F.; Aguiar-Santos, A.; Medeiros, Z. Influence of social and environmental factors for Culex quinquefasciatus distribution in Northeastern Brazil: A risk index. Int. J. Environ. Health Res. 2022, 33, 1580–1590. [Google Scholar] [CrossRef] [PubMed]
  36. Francisco, M.E.; Carvajal, T.M.; Ryo, M.; Nukazawa, K.; Amalin, D.M.; Watanabe, K. Dengue disease dynamics are modulated by the combined influences of precipitation and landscape: A machine learning approach. Sci. Total. Environ. 2021, 792, 148406. [Google Scholar] [CrossRef]
  37. Gómez-Vargas, W.; Ríos-Tapias, P.A.; Marin-Velásquez, K.; Giraldo-Gallo, E.; Segura-Cardona, A.; Arboleda, M. Density of Aedes aegypti and dengue virus transmission risk in two municipalities of Northwestern Antioquia, Colombia. PLoS ONE 2024, 19, e0295317. [Google Scholar] [CrossRef]
  38. Telle, O.; Nikolay, B.; Kumar, V.; Benkimoun, S.; Pal, R.; Nagpal, B.; Paul, R.E. Social and environmental risk factors for dengue in Delhi city: A retrospective study. PLOS Negl. Trop. Dis. 2021, 15, e0009024. [Google Scholar] [CrossRef]
  39. Fuentes-Vallejo, M.; Higuera-Mendieta, D.R.; García-Betancourt, T.; Alcalá-Espinosa, L.A.; García-Sánchez, D.; Munévar-Cagigas, D.A.; Brochero, H.L.; González-Uribe, C.; Quintero, J. Territorial analysis of Aedes aegypti distribution in two Colombian cities: A chorematic and ecosystem approach. Cad. Saúde Pública 2015, 31, 517–530. [Google Scholar] [CrossRef]
  40. Ferdousi, F.; Yoshimatsu, S.; Ma, E.; Sohel, N.; Wagatsuma, Y. Identification of essential containers for Aedes larval breeding to control dengue in Dhaka, Bangladesh. Trop. Med. Health 2015, 43, 253–264. [Google Scholar] [CrossRef]
  41. Romeo-Aznar, V.; Paul, R.; Telle, O.; Pascual, M. Mosquito-borne transmission in urban landscapes: The missing link between vector abundance and human density. Proc. R. Soc. B Biol. Sci. 2018, 285, 20180826. [Google Scholar] [CrossRef]
  42. Bowman, L.R.; Runge-Ranzinger, S.; McCall, P.J. Assessing the relationship between vector indices and dengue transmission: A systematic review of the evidence. PLOS Negl. Trop. Dis. 2014, 8, e2848. [Google Scholar] [CrossRef]
  43. Kamalipour, H. Informal urban design: Forms of informal settlement. In Research Handbook on Urban Design; Edward Elgar Publishing: Cheltenham, UK, 2024. [Google Scholar] [CrossRef]
  44. Braveman, P.; Gottlieb, L. The Social Determinants of Health: It’s Time to Consider the Causes of the Causes. Public Health Rep. 2014, 129 (Suppl. 2), 19–31. [Google Scholar] [CrossRef] [PubMed]
  45. Sanya, T.; Lewis, C.A.; Mogola, I. Guidelines for Water-Sensitive Informal Settlement Upgrading in the Global South. In The Palgrave Encyclopedia of Urban and Regional Futures; Brears, R.C., Ed.; Palgrave Macmillan: Cham, Germany, 2022. [Google Scholar] [CrossRef]
  46. Wang, J.; Kuffer, M.; Sliuzas, R.; Kohli, D. The exposure of slums to high temperature: Morphology-based local scale thermal patterns. Sci. Total Environ. 2019, 650, 1805–1817. [Google Scholar] [CrossRef] [PubMed]
  47. Abdulai, A.; Owusu-Asenso, C.M.; Haizel, C.; Mensah, S.K.E.; Sraku, I.K.; Halou, D.; Doe, R.T.; Mohammed, A.R.; Akuamoah-Boateng, Y.; Forson, A.O.; et al. The Role of Car Tyres in the Ecology of Aedes aegypti Mosquitoes in Ghana. Curr. Res. Parasitol. Vector-Borne Dis. 2024, 5, 100176. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  48. Gibb, R.; Colón-González, F.J.; Lan, P.T.; Huong, P.T.; Nam, V.S.; Duoc, V.T.; Hung, D.T.; Dong, N.T.; Chien, V.C.; Trang, L.T.T.; et al. Interactions between climate change, urban infrastructure and mobility are driving dengue emergence in Vietnam. Nat. Commun. 2023, 14, 8179. [Google Scholar] [CrossRef]
  49. Power, G.M.; Vaughan, A.M.; Qiao, L.; Clemente, N.S.; Pescarini, J.M.; Paixão, E.S.; Lobkowicz, L.; Raja, A.I.; Souza, A.P.; Barreto, M.L.; et al. Socioeconomic risk markers of arthropod-borne virus (arbovirus) infections: A systematic literature review and meta-analysis. BMJ Glob. Health 2022, 7, e007735. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  50. Kagaba Amina, G.; Kampala International University IX. Socio-Economic Determinants and Malaria Risk: Assessing the Impact of Poverty, Housing Conditions, and Healthcare Accessibility in High-Incidence Regions. Newport Int. J. Res. Med. Sci. 2024, 5, 120–124. [Google Scholar]
  51. Tsiotas, D.; Dialesiotis, S.; Christopoulou, O. Examining the relationship between regional economic resilience and epidemiologic spread of COVID-19: Evidence from Greece. Environ. Dev. Sustain. 2023, 27, 8433–8469. [Google Scholar] [CrossRef]
  52. Herath, S.; Mansour, A.; Bentley, R. Urban density, household overcrowding and the spread of COVID-19 in Australian cities. Health Place 2024, 89, 103298. [Google Scholar] [CrossRef]
  53. Alrasheed, H.; Alballa, N.; Al-Turaiki, I.; Almutlaq, F.; Alabduljabbar, R. City Transmission Networks: Unraveling Disease Spread Dynamics. ISPRS Int. J. Geo-Inf. 2024, 13, 283. [Google Scholar] [CrossRef]
  54. Román-Pérez, S.; Aguirre-Gómez, R.; Hernández-Ávila, J.E.; Íñiguez-Rojas, L.B.; Santos-Luna, R.; Correa-Morales, F. Identification of Risk Areas of Dengue Transmission in Culiacan, Mexico. ISPRS Int. J. Geo-Inf. 2023, 12, 221. [Google Scholar] [CrossRef]
  55. Chaves, L.S.M.; Bergo, E.S.; Conn, J.E.; Laporta, G.Z.; Prist, P.R.; Sallum, M.A.M. Anthropogenic landscape decreases mosquito biodiversity and drives malaria vector proliferation in the Amazon rainforest. PLoS ONE 2021, 16, e0245087. [Google Scholar] [CrossRef] [PubMed]
  56. Perrin, A.; Glaizot, O.; Christe, P. Worldwide impacts of landscape anthropization on mosquito abundance and diversity: A meta-analysis. Glob. Change Biol. 2022, 28, 6857–6871. [Google Scholar] [CrossRef] [PubMed]
  57. Transforming Our World: The 2030 Agenda for Sustainable Development. Available online: https://sdgs.un.org/2030agenda (accessed on 21 February 2025).
  58. World Health Organization; UNICEF. “Global Vector Control Response 2017–2030.” Global Vector Control Response 2017–2030. 2017. Available online: https://www.who.int/publications/i/item/9789241512978 (accessed on 21 February 2025).
  59. Di Napoli, C.; McGushin, A.; Romanello, M.; Ayeb-Karlsson, S.; Cai, W.; Chambers, J.; Dasgupta, S.; Escobar, L.E.; Kelman, I.; Kjellstrom, T.; et al. Tracking the impacts of climate change on human health via indicators: Lessons from the Lancet Countdown. BMC Public Health 2022, 22, 663. [Google Scholar] [CrossRef]
  60. Programme for the Environment and Climate Action (LIFE). Available online: https://commission.europa.eu/funding-tenders/find-funding/eu-funding-programmes/programme-environment-and-climate-action-life_en (accessed on 21 February 2025).
  61. European Environment Agency. European Climate Risk Assessment; Publications Office of the European Union: Luxembourg, 2024. [Google Scholar] [CrossRef]
  62. Capolongo, S.; Rebecchi, A.; Dettori, M.; Appolloni, L.; Azara, A.; Buffoli, M.; Capasso, L.; Casuccio, A.; Conti, G.O.; D’amico, A.; et al. Healthy Design and Urban Planning Strategies, Actions, and Policy to Achieve Salutogenic Cities. Int. J. Environ. Res. Public Health 2018, 15, 2698. [Google Scholar] [CrossRef]
Figure 1. PRISMA flowchart for search strategy.
Figure 1. PRISMA flowchart for search strategy.
Sustainability 17 04077 g001
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Cofone, L.; Sabato, M.; Di Paolo, C.; Di Giovanni, S.; Donato, M.A.; Paglione, L. Urban, Architectural, and Socioeconomic Factors Contributing to the Concentration of Potential Arbovirus Vectors and Arbovirosis in Urban Environments from a One Health Perspective: A Systematic Review. Sustainability 2025, 17, 4077. https://doi.org/10.3390/su17094077

AMA Style

Cofone L, Sabato M, Di Paolo C, Di Giovanni S, Donato MA, Paglione L. Urban, Architectural, and Socioeconomic Factors Contributing to the Concentration of Potential Arbovirus Vectors and Arbovirosis in Urban Environments from a One Health Perspective: A Systematic Review. Sustainability. 2025; 17(9):4077. https://doi.org/10.3390/su17094077

Chicago/Turabian Style

Cofone, Luigi, Marise Sabato, Carolina Di Paolo, Stefano Di Giovanni, Maria Assunta Donato, and Lorenzo Paglione. 2025. "Urban, Architectural, and Socioeconomic Factors Contributing to the Concentration of Potential Arbovirus Vectors and Arbovirosis in Urban Environments from a One Health Perspective: A Systematic Review" Sustainability 17, no. 9: 4077. https://doi.org/10.3390/su17094077

APA Style

Cofone, L., Sabato, M., Di Paolo, C., Di Giovanni, S., Donato, M. A., & Paglione, L. (2025). Urban, Architectural, and Socioeconomic Factors Contributing to the Concentration of Potential Arbovirus Vectors and Arbovirosis in Urban Environments from a One Health Perspective: A Systematic Review. Sustainability, 17(9), 4077. https://doi.org/10.3390/su17094077

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop