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Spatio-temporal patterns of distribution of West Nile virus vectors in eastern Piedmont Region, Italy
Parasites & Vectors volume 4, Article number: 230 (2011)
West Nile Virus (WNV) transmission in Italy was first reported in 1998 as an equine outbreak near the swamps of Padule di Fucecchio, Tuscany. No other cases were identified during the following decade until 2008, when horse and human outbreaks were reported in Emilia Romagna, North Italy. Since then, WNV outbreaks have occurred annually, spreading from their initial northern foci throughout the country. Following the outbreak in 1998 the Italian public health authority defined a surveillance plan to detect WNV circulation in birds, horses and mosquitoes. By applying spatial statistical analysis (spatial point pattern analysis) and models (Bayesian GLMM models) to a longitudinal dataset on the abundance of the three putative WNV vectors [Ochlerotatus caspius (Pallas 1771), Culex pipiens (Linnaeus 1758) and Culex modestus (Ficalbi 1890)] in eastern Piedmont, we quantified their abundance and distribution in space and time and generated prediction maps outlining the areas with the highest vector productivity and potential for WNV introduction and amplification.
The highest abundance and significant spatial clusters of Oc. caspius and Cx. modestus were in proximity to rice fields, and for Cx. pipiens, in proximity to highly populated urban areas. The GLMM model showed the importance of weather conditions and environmental factors in predicting mosquito abundance. Distance from the preferential breeding sites and elevation were negatively associated with the number of collected mosquitoes. The Normalized Difference Vegetation Index (NDVI) was positively correlated with mosquito abundance in rice fields (Oc. caspius and Cx. modestus). Based on the best models, we developed prediction maps for the year 2010 outlining the areas where high abundance of vectors could favour the introduction and amplification of WNV.
Our findings provide useful information for surveillance activities aiming to identify locations where the potential for WNV introduction and local transmission are highest. Such information can be used by vector control offices to stratify control interventions in areas prone to the invasion of WNV and other mosquito-transmitted pathogens.
West Nile virus (WNV) is a mosquito-borne virus (family Flaviviridae) and a neuropathogen for humans, horses, and birds . The virus is indigenous to the Old World, and is maintained in a bird-mosquito transmission cycle primarily involving Culex spp. mosquitoes. Humans, horses and other mammals are dead-end hosts for the virus . Neurological human manifestations (< 1% of all cases) are associated with severe morbidity and can be fatal . Early reports of WNV human infections date from the late 1930's in Africa . However, a dramatic expansion of the virus was registered in recent decades, with infections reported in Asia, Europe, and, since 1999, in the New World [5, 6]. Early reports of human and equine WNV infection in Europe date from 1964 in the Camargue region, France . Since then the virus has spread throughout Europe, showing an erratic temporal and spatial pattern .
Understanding the interrelated ecology of vectors, suitable habitats, and preferential hosts is paramount to predict the emergence and amplification of WNV infection . Multiple European mosquito species are considered competent vectors of WNV: Culex pipiens (Linnaeus 1758), Culex theileri (Theobald 1903), Culex modestus (Ficalbi 1890), Culex univittatus (Theobald 1901), Ochlerotatus caspius (Pallas 1771), and Anopheles maculipennis s.l. (Meighen 1818) . However, only the first three species appear to play an important role as putative vectors in European countries [7, 9, 10]. In the Volgograd region, Russia, Cx. pipiens was involved in WNV transmission in urban areas, and Cx. modestus in periurban areas . In France, Cx. modestus and Oc. caspius are considered the main vectors in wetland areas, and Cx. pipiens in urban and periurban areas . In Portugal, the presence of Cx. pipiens, An. maculipennis s.l., and Cx. theileri in wetland areas was associated with two human WNV cases .
In Italy, the first WNV cases were recorded in 1998 in a wetland area in the central Tuscany Region (an outbreak involving 14 horses) . After the 1998 outbreak, Italian public health authorities initiated a national surveillance plan aiming to quantify vector abundance, perform targeted vector control in highly infested areas and detect the circulation of WNV. In 1999, Cx. pipiens, Cx. impudicus (Ficalbi 1890), Oc. caspius and An. maculipennis s.l. mosquito pools from Tuscany were tested for the presence of WNV infection with negative results . WNV was assumed to be absent in Italy until 2007, when high antibody titers were reported in sentinel birds in the northern Region of Trentino-Alto Adige . In 2008, the largest WNV outbreak --involving 794 horses (from 251 farms) and 9 human infections-- occurred in eight provinces in the northern Regions of Emilia Romagna, Veneto, and Lombardy [10, 17, 18]. Most cases were located near natural and artificial water sources such as the Po river delta, an area that provides favourable habitats for local and migratory birds . Three pools of Cx. pipiens and four of Oc. caspius from traps located in the outbreak area were positive for WNV, representing the first isolation of the virus from Italian mosquitoes . WNV transmission continued in 2009, when another outbreak (involving 18 humans and 221 horses, resulting in 4 and 9 fatalities, respectively) occurred in the same area and expanded to the central Italian Regions of Tuscany and Lazio [5, 20, 21]. In 2010, new equine cases were reported at the end of the summer in the Italian territory: 46 in Sicily, 16 in Molise, 3 in Veneto, and 1 in Emilia Romagna (5 fatal in total) , and 13 WNV positive mosquito pools were found in Emilia Romagna and in Veneto Regions . In the same year a jay (Garrulus glandarius), a magpie (Pica pica) in Emilia Romagna, and sentinels birds in Puglia and Molise (southern Italy) tested positive for WNV . WNV appears to have expanded its range and colonized new areas throughout the country , underlining the need for detailed studies determining the suitability of areas not yet invaded for potential establishment of WNV.
In this study we evaluated the effects of environmental (e.g., landscape and weather) determinants on the spatial distribution of Oc. caspius, Cx. pipiens and Cx. modestus. By applying rigorous statistical analysis of longitudinal (2000-2006) CO2-baited trap collection data for each of the three putative WNV vectors in the eastern Piedmont Region, Italy, we: (a) described their abundance and spatial distribution, and (b) predicted their geographic distribution based on environmental and ecological data. Our predicted vector distribution maps allowed us to identify areas with high potential risk of WNV introduction and amplification.
Our study area covered a territory of 987 km2 in the eastern Piedmont Region (population: 120.593 habitants, centroid: 45.07° N, 8.39° E), North-western Italy (Figure 1). The unique topography and landscape characteristics of this territory are of particular interest for the study of the distribution of potential WNV vectors due to the presence of suitable habitats for migratory birds and abundant larval breeding sites for local mosquito species. The territory (political subdivision equivalent to a US County) is divided evenly between hills (mean elevation 268 m) and plains where the landscape is dominated by mixed agricultural patches (72.2%, mostly in the north-eastern plans), rice fields (14.2%, mostly in northern plans), deciduous tree forests (8.6%, mostly on southern hills), urban environments (3.1%, highly populated cities are located in the plains), and the Po river with its tributaries (1.9%, North) (Figure 1). Cold winters and hot-warm summers (0.4°C and 24.0°C average daily temperature, respectively) and abundant spring and autumn rainfall (~600 mm/yr) are characteristic of the region (Agenzia Regionale per la Protezione dell'Ambiente del Piemonte, ARPA ).
Mosquito surveillance and control
The mosquito population surveillance in the Piedmont programme started in 1997 by Istituto per le Piante da Legno e l'Ambiente (IPLA). Surveillance is constituted by an array of 36 mosquito sampling locations distributed at a minimum distance of 5 km from each other following a random pattern (Figure 1). Trap placement was based on habitat features suitable for mosquito development: near rice fields, woodlands, and at the periphery of urban areas. In each sampling location, weekly overnight adult mosquito collections were performed using CDC CO2-baited traps from May to October (the period when mosquitoes are active). After collection, all adult mosquitoes were sexed, counted and identified using proper keys .
Different strategies (ongoing since 1998) were implemented in the study area to reduce mosquito abundance. Starting in the spring, breeding sites were treated with larvicides such as Bacillus thuringiensis var. israelensis (Bti), Temephos and Diflubenzuron. Bti has no toxic effect on other animals and plants , but its field performance is greatly influenced by the presence of organic matter or of solids in the water . Highly polluted breeding sites were treated with Themephos, an organophosphate authorized in EU until 2006, and Diflubenzuron, a benzamide inhibiting the production of chitin. Rice fields, the most important breeding sites of the main nuisance species in the area, were treated in a belt of 23.000 hectares around the main cities by performing space sprays of Bti water suspensions with aircrafts. Since 2007, and in order to cut down the cost of aerial applications, rice growers took charge of treating their rice seeds with Diflubenzuron just before seeding.
Data management and processing
All geographic data were merged in a Geographic Information System (GIS) based on GRASS system  and projected from geographic to planar units (UTM zone 32, datum WGS84). Spatial data used to generate mosquito suitability maps included land surface temperature (LST), Normalized Difference Vegetation Index (NDVI), rainfall, elevation, and land-use. LST and NDVI were derived from the Moderate Resolution Imaging Spectroradiometer (MODIS) satellite (National Aeronautics and Space Administration, NASA ).
Daily rainfall records for the period 2000-2006 and for 2010 (the year used to create the mosquito prediction maps) for each sample location were derived from a map interpolation (1 km pixel size) generated using the data collected by five ground level weather stations managed by the regional agency of meteorology (ARPA ) and spaced ~10 km apart .
LST data consisted of spatially continuous 8-day averages at a spatial resolution of 1 km, and NDVI was based on 16-day averages at a resolution of 250 m. All MODIS images were corrected geometrically using ground control points (GCP) of known coordinates and edited to eliminate atmospheric disturbance allowing comparison among different periods . Elevation data (in meters above sea level, m.a.s.l.) were obtained from the Shuttle Radar Topography Mission dataset (90 m pixel size ), and land-use was acquired as raster image from the European Environment Agency (100 m pixel size ). We generated raster maps depicting the distance of every pixel in the study area to the nearest urban areas, rice fields, and woodlands by applying the straight line distance interpolation function in GRASS . This function calculates the measured Euclidean distance from every point in the study area to the nearest landscape feature, and represents it as a raster file with spatial resolution of 1 km.
We applied the Ripley's K-function ()  to assess whether the distribution of traps within the study area differed from a random distribution. Significance was evaluated by comparing the observed values with the expected values under the complete spatial randomness assumption based on 999 Monte Carlo permutations . The spatial patterns of Oc. caspius, Cx. pipiens and Cx. modestus abundance per trap were quantified by the Getis local statistic . To identify spatial patterns in mosquito abundance we grouped and analyzed the data for three study seasons: Spring (1st May - 21st June), Early summer (22nd June - 15th August) and Late Summer (16th August - 15th September). Mosquito abundance was estimated as the median number of mosquitoes per week per study season.
The association between the abundance of each mosquito species and selected environmental and ecological factors was analyzed using a spatially explicit generalized linear mixed model (GLMM). Briefly, the GLMM is an extension of a classic generalized linear model that accounts for correlated data structures (e.g. clustered or longitudinal data) by including random cluster and/or subject effects . The correlated spatial effect in the model was added by considering the geographic position of each sampling location as a structured spatial random effect. The spatial random effect was modelled as a Gaussian Markov random Field  using a nearest neighbour structure to define the spatial relationship between sampling locations . We fitted the data using a zero-inflated negative binomial distribution (ZINB) to account for the overdispersion observed in the distribution of the median number of mosquitoes per trap. We used a Bayesian approach based on the Integrated Nested Laplace Approximation (INLA)  to fit our GLMM models. The choice of this method was based on its time and analytical efficiency in approximating to the posterior marginal probabilities in comparison to classic MCMC approaches .
A subset of 30 trap locations with weekly entomologic and environmental information for the period 2000-2006 was used to build the GLMM models (i.e., training dataset), whereas the remaining 6 trap locations were used to test the performance of the models (i.e., test dataset). The period 2000-2006 was chosen because: a) was the time with the highest spatial coverage of CO2baited-traps; b) vector control actions in the study region were minimum; and c) from 2007 to 2010 control interventions increased in intensity and quality, potentially impacting our ability to predict the abundance and spatial distribution of each mosquito species.
By selecting environmental and ecological parameters deemed as the most influential in predicting the abundance and spatial distribution of each mosquito species, we outlined the following full model (full code in Additional file 1: Table 2A):
Where y represented the abundance of each species (i.e., Oc. caspius, Cx. pipiens, Cx. modestus) at the sampling locations. RAIN (rainfall) represented the cumulative rainfall 10-17 days prior to trapping, this lagged variable was chosen to take into account the cumulative effect of rain on mosquito productivity and abundance. TWEEK represented the average LST for each sampling location during the 8-15 days prior to trapping. This time lag aimed to capture potential impacts of temperature on mosquito population dynamics (by covering the conditions experienced by the earlier stages of larval development). Given the known seasonal pattern in mosquito abundance, we introduced seasonality (SIN) as a sinusoidal curve with a phase of 1 year. The SIN value was set to have a peak in the first week of August (when abundance of most mosquito species in the study area presents peaks). Elevation (in m.a.s.l) of each sampling location (ELEV) was selected to account for topographic (altitudinal) differences across the study area. Since the study area is in an agricultural zone, and the environmental changes during the year could be influenced by human agricultural activities, we used NDVI as a surrogate for environmental (i.e., vegetation) change over time. The potential effects of environmental features on mosquito collections were tested by estimating the distance (in km) of each sampling location to urban areas (DISTU), rice fields (DISTR), and woodlands (DISTW). We included in the models the area covered by rice fields (in Km2) located nearest to each sampling location (RICEA). We also included the interaction between the environmental factors potentially affecting mosquito development: temperature and rainfall (TWEEK * RAIN), NDVI and rainfall (NDVI * RAIN), and temperature and NDVI (TWEEK * NDVI). We considered each sampling location (RNDtrap) as an unstructured spatial random effect. The RNDtrap represented the difference between each trap which was not possible to account with the chosen regressor, but which can affect the number of collected mosquitoes. We used a spatially structured random effect modelled with a GMRF with a Gaussian distribution (SRNDtrap) to represent the effect of the spatial position of each trap location . As the trap location did not vary across years ELEV, DISTUR, DISTR, DISTW, and RICEA remained as constant values in the model. The TWEEK, RAIN, and NDVI were not constant due to their seasonal variation during the study period. The treatment was not included in the models because all the sampling locations were inside the treated area and so the various control strategies did not have a significant differential effect. We built and tested 169 GLMM models formulated in according with the ecological characteristics of each mosquito species.
The best model (among all tested models) was chosen using the Deviance Information Criterion (DIC) [34, 37]. DIC is one of the most commonly used Bayesian selection criteria to select models based on the need to compromise between goodness of fit and model complexity. This index is useful to confront mixed effect models with fixed and random effects because it estimates the effective number of parameters included in the model . DIC is obtained by the sum of the posterior mean of deviance and the number of effective parameters used in the model . Low DIC values are indicative of models showing the best trade off between model fit and complexity, and presenting a good performance predicting unobserved quantities [38, 39]. The Logarithmic Score (LS) was used to test the internal cross-validation of the model and its predictive performance, to calculate the cross-validation one observation is excluded from each step of the validation process and the remaining observations are used to perform the predictive distribution . The negative logarithm of predictive distribution is the LS of a given model. The model with the smallest LS has the highest predictive power . Models showing the lowest DIC were considered to best explain the data, and hence selected to predict the abundance of each mosquito species. In case of models with a difference in DIC less than 5 units the one with the smaller LS was chosen
Vector suitability map
We computed a highly detailed distribution map (500 meter pixel size) of the abundance of Oc. caspius, Cx. pipiens and Cx. modestus using the best GLMMs for all three species. The model parameters (i.e., β) from each significant variable were multiplied by the respective rasterized variable to generate a continuous representation of mosquito abundance. The maps were developed to predict the abundance of the three species in August 2010, when they show their peak of high abundance. The year 2010 was selected for the predictions because we were interested in assessing the abundance and spatial distribution of vectors when WNV was known to circulate in Italy, and because these maps could be used to design vector control interventions for 2011.
All analyses were performed using R software . GLMM models were fitted using the INLA package . All the GIS operations and spatial analyses were performed with GRASS GIS software .
A total of 1, 223, 974 female mosquitoes belonging to eleven species were trapped from 2000 to 2006 (Table 1), employing a total trapping effort of 6, 200 trap-nights. The most commonly trapped species were Oc. caspius (61.8%), Cx. pipiens (21.2%) and Cx. modestus (16.3%). All the three species investigated showed a seasonal activity pattern, with abundance peaking in mid-summer (July-August, Figure 2). Monthly Oc. caspius adult collections were higher in 2003 (median (Md) = 3, 270, interquartile range (IQR) = 1, 625-4, 420) and 2006 (Md = 3, 522; IQR = 1, 933-5, 516) and lower in 2004 (Md = 596, IQR = 1, 134-1, 598). The highest numbers of Cx. pipiens per month were obtained in 2000 with a median (Md = 1, 592; IQR = 621-2, 271) whereas the lowest numbers were obtained in 2003 (Md = 179.5; IQR = 74-402). The minimum number of monthly collected Cx. modestus was in 2001 (Md = 36; IQR = 5-273) and increased during 2005 (Md = 266, IQR = 82-816) and 2006 (Md = 343, IQR = 158-1, 105).
All species showed the highest abundance (weekly median) in the northern extreme of the study area, within an area composed by rice fields, highly populated urban areas and the Po river (Figure 3). Oc. caspius extended its spatial distribution during the early summer (22nd June - 15th August), showing high abundance also at higher elevations (Figure 3). Cx. modestus adults were practically absent during the spring (1st May - 21st June) when all sample locations had a Md = 0 (IQR = 0-3) (Figure 3).
Temperature trends fluctuated during the 7-year study period (supplementary Figure 1-A). The warmest year was 2003 (mean = 23°C; CI 95% = 21.6-24.3°C) and the coldest was 2002 (mean = 20.5°C; CI 95% = 20-22.7°C), when most rainfall was also occurred. The driest year was 2003 (122 mm) and the wettest 2002 (512 mm) (Additional file 1: Figure 1-A).
The seasonal spatial patterns of mosquito distribution showed evidence of clustering (Gi*(d) < 3.71, P < 0.05) for the three species tested (Figure 4). Hot- spots of high Oc. caspius abundance were recorded in spring and early summer near rice fields in the north-western part of the study area. During late summer, spatial clustering shifted towards the north-east, also near rice fields (Figure 4). Cx. pipiens hot-spots were, for all seasons, located in the highly urbanized parts of the study area (i.e., near Casale Monferrato, pop: 36, 095 habitants). This species was the only one that also had cold-spot clusters, which were present in early and late summer in the more rural and hilly parts in the south-west of the study area. The hot-spots of Cx. modestus abundance occurred with low intensity (1-2 years) only during summer. They were concentrated near rice fields located mostly in the north-eastern part of the study area (Figure 4). K-function analysis confirmed that the observed clustering patterns were not the result of heterogeneous spatial distribution of traps within the study area, as traps were randomly distributed (|L(d)| < d for all 0 < d < 10 Km; P > 0.05; data not shown).
The DIC and LS of the top three models for Oc. caspius, Cx. pipiens and Cx. modestus are shown in supplementary Table 1-A. The difference in DIC of the top three models for each mosquito species was above 10 units: these differences allow selection of a unique best model for each species. Such models had an LS value closer to zero compared to the other models tested, indicating a high power in predicting the data (Additional file 1: Table 1-A). The parameters estimated for the best GLMM model for each of the three mosquito species tested are summarized in Table 2. The spatial structured random effects were not present in the best model chosen. Oc. caspius weekly abundance was significantly and positively associated with the average temperature during the week prior to trapping, cumulative amount of rain during the 10 days prior to trapping, the seasonal fixed effect term (SIN), and the bi-weekly NDVI values around a trap (Table 2). Distance to rice fields and elevation, although not statistically significant, had a major influence in determining the best GLMM model for Oc. caspius. Cx. pipiens weekly abundance was significantly and positively associated to the cumulative rain during the 10 days prior to trapping, the average temperature during the week prior to trapping, and the seasonal fixed effect term (SIN); and negatively associated with the elevation (in m.a.s.l) of each trapping location (Table 2). The inclusion of distance of each trapping location to the nearest urban center was not significant, but had influence in determining the best GLMM model for Cx. pipiens (Table 2). The best model of Cx. modestus included as significant and positively associated parameters the average temperature during the week prior to trapping, the NDVI and seasonal fixed effect (Table 2). The two negatively associated environmental features were the distance from each trap location to the nearest rice field (non-significant) and the elevation (significant). The best models for the three species showed high predictive power (root mean square error, RMSE, 149.2 ± 129.4, for Oc. caspius, 75.3 ± 34.2 for Cx. pipiens, and 90.4 ± 18.6 for Cx. Modestus), capturing the seasonality (Additional file 1: Figure 3-A, 4-A, 5-A) and spatial distribution (Figure 5) of each species. Residuals plots (Additional file 1: Figure 2-A, 3-A, 4-A, and 5-A) suggest that the best models tended to underestimate the number of collected individuals during the period of peak abundance. The best model of Cx. modestus was the only one that overestimated the number of captured adults during the beginning of the sampling season (Additional file 1: Figure 2-A, and 5-A).
Vector suitability map
The best GLMM models for Oc. caspius, Cx. pipiens and Cx. modestus were used to generate a vector suitability prediction map for the first week of August 2010 (close to the seasonal peak of abundance of each species) (Figure 5). The high abundance of Oc. caspius was predicted to occur in close proximity to rice fields present in the northern part of the study area. The predicted distribution of Cx. pipiens showed that this species was abundant near the urban areas located in the eastern part of the study area, where the majority of urban centers are located. Cx. modestus was predicted to be more abundant in areas where the landscape is dominated by mixed agricultural patches (42%) and rice fields (27%) (North-East and part in the South). The high abundance areas, for all the species, were concentrated within the Po River basin, where rice fields, abundant vegetation and large urban centres may provide unique opportunities of WNV introduction, amplification and transmission. The models accurately predicted the location of traps with high and low vector abundances in August 2010 (Figure 5), validating the ability of GLMM models to predict spatial and temporal patterns of vector abundance in the region.
The impacts of spatially heterogeneous environmental and ecological factors on mosquito population dynamics are complex and poorly understood for many species. Particularly for zoonotic mosquito-borne diseases, understanding the inter-relationships between vectors, hosts, and their environment can provide valuable information for identifying conditions suitable for pathogen introduction, amplification, and transmission. By analyzing a highly detailed longitudinal dataset of the abundance and spatial distribution of the three putative WNV vectors in the eastern Piedmont Region of Italy (i.e., Oc. caspius, Cx. pipiens, and Cx. modestus) we identified a set of environmental and ecological conditions that are favourable for their development, predicted their spatial occurrence, and identified potential areas that, due to their environmental conditions, would be suitable for the introduction and amplification of WNV. The Piedmont Region is located between two European regions where outbreaks of WNV occur annually: Camargue, France, (to the East) and Emilia Romagna, Italy (to the West), increasing the relevance of our findings for the understanding of WNV transmission dynamics in southern Europe.
The three mosquito species varied in degree of heterogeneity of their spatial distribution throughout the study region. Most of the Oc. caspius hot-spots occurred near rice fields, where the abundance of larval development habitats and avian hosts allow for very large mosquitoes population [42–44]. Mark-release-recapture experiments have shown that rice fields are not only important breeding habitats for Oc. caspius but also serve as major sources of dispersing adults, which were found to be passively dispersed by wind to distances of up to 10 km from their release point . Moreover, the temporal trend in spatial clustering showed differences between hot-spots across seasons: whereas the spring clusters occurred near rice fields located in the North, summer clusters occurred in the North-East, in close proximity to the largest city in the study region (Casale Monferrato). Interestingly, late summer/early fall was the period when most WNV equine cases were reported in Northern Italy . Therefore, clustering of Oc. caspius near urban environments during late summer may bring humans into higher risk of exposure to potentially infective mosquito bites.
In the Camargue Region, France, wetlands and rice fields were important hot-spots for the transmission of WNV due to their high vector productivity (particularly Oc. caspius, Cx. pipiens and Cx. modestus) and the occurrence of large equine WNV outbreaks and human cases near by [45, 46]. The capacity of Oc. caspius to feed interchangeably on birds and mammals makes this species a potential bridge vector for WNV and for other zoonotic arboviruses in proximity to rice fields [12, 47]. Moreover, rice fields in the Mediterranean Region are also an important habitat for residential and migratory birds , and may represent one of the main entry doors of WNV into Europe.
Oc. caspius, Cx. pipiens, and Cx. modestus may play a key role as enzootic vectors of WNV in eastern Piedmont because they feed both on mammals and birds, but with different preference [11, 47, 49]. Although laboratory experiments showed a low vector competence of Oc. caspius for WNV , infected pools of this species have been found recently in Israel and in Italy [10, 50], increasing the interest in investigating its role as a potential WNV vector. Given that natural populations of this species can reach very high numbers (being the most important nuisance mosquito species in northern Italy), their potential role as amplifying vectors in eastern Piedmont cannot be ruled out.
Cx. pipiens was significantly clustered in the most urbanized areas of the region, the main habitat for this species . This species is the most important WNV vector in USA and one of the main vectors in Europe  where it comprises two forms Cx. pipiens pipiens, and Cx. pipiens molestus . These two sub-species may play a different role in the spill-over of WNV from birds to humans. Cx. pipiens pipiens is strictly ornitophilic and feeds only rarely on humans, whereas Cx. pipiens molestus is more anthropophilic and may play role as a bridge vector of WNV [52, 53]. In contrast, in the United States Cx. pipiens pipiens feeds both on human and birds and is considered the main bridge vector of WNV Central US [52, 54].
Several studies have shown the importance of migratory birds from the Sub-Saharan region as introducers of WNV into Europe [55–58], a plausible mechanism to explain the occurrence of multiple WNV outbreaks in Northern Italy. Genetic analysis of WNV isolates obtained from field collected mosquitoes during the 2008 outbreak showed, in northern Italy, a high degree (98.8%) of similarity with a virus isolate obtained from an earlier outbreak of 1998 [10, 59]. Serological investigations of residential birds in the area of the 2008 outbreak showed high levels of WNV seroprevalence near the sites with high level of mosquito infection [10, 17]. These two findings suggest that enzootic WNV transmission in Northern Italy may involve another mechanism (in addition to the contribution of migratory birds) for the recrudescence of WNV transmission.
The suitability maps predicted that the highest number of mosquito adults for all three species will be found in the plains where the rice fields and the main city are located. The predictions indicated that the hot-spots coincide with locations where the highest number of mosquitoes was collected. These findings indicate that the three mosquito species are abundant in the plain, underlining the importance of control program in that area. The map also showed that the Po River, one of the most important breeding habitats for local and migratory birds , is predicted to have the highest vector abundance. The results of this study can be used to improve the surveillance and control of WNV vectors. The IPLA Institute, responsible for the vector control interventions in eastern Piedmont, coupled the model developed in this study with weather forecasting in order to define priority areas and targeted actions to reduce vector abundance and prevent WNV establishment and amplification. A similar surveillance system based on model-derived predictions derived from environmental and climatic variable is currently used to predict the abundance of Cx. tarsalis, one of the main vectors of WNV in California . One of the limitations of this study has been the lack of information on WNV circulation in birds and mosquitoes. Future studies will attempt to incorporate information about the composition of the bird population in the area, and the role of different bird species and the landscapes they utilize in the potential establishment of WNV in eastern Piedmont.
The distribution of three putative vectors of WNV within an area of Northern Piedmont, Italy, was spatially heterogeneous and was accurately predicted after accounting for the contribution of environmental and climatic factors. The vector suitability maps derived from our study can help inform surveillance and control programmes about the location of areas that, due to their environmental suitability, could potentially become points of entry of WNV into the region. The development of carefully validated vector suitability maps can also help inform public health officers about the entomologic potential for the introduction of other vector-borne diseases of current or future global significance.
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This research was supported by the ISI (Institute for Scientific Interchange) Foundation of Torino, Italy (Lagrange Fellowship awarded to DB), the Ministero dell'Università e della Ricerca Scientifica e Tecnologica (award to MG), and Emory University (UK, Department of Environmental Studies). This work was partially funded by Ricerca Sanitaria Finalizzata 2008 - Regione Piemonte (award LBertolotti). Mosquito surveillance and control have been possible by the contribution of Regione Piemonte, Provincia di Alessandria, and the municipalities of the Casale Monferrato Agreement for Mosquito Control. Special thanks to the field technicians that collected, counted, and identified more than one million of mosquitoes. Thanks also to Prof. Alessandro Mannelli, Dr. Stefano Guazzetti e Dr. Luis Fernando Chavez for comments and suggestions on earlier versions of this manuscript. UK and GVP acknowledge the support of the Research and Policy for Infectious Disease Dynamics (RAPIDD) program of the Science and Technology Directorate, U.S. Department of Homeland Security, and the Fogarty International Center, National Institutes of Health.
The authors declare that they have no competing interests.
All authors participated in the conceptualization of the study. DB built the GIS system and analyzed the data. DB and GVP drafted the manuscript. AM and LBalbo coordinated the mosquito collections. UK and GVP provided statistical advice. All authors participated in the revision of the manuscript and approved the submitted version.
Electronic supplementary material
Additional file 1: Weather conditions and model evaluation parameters. File contains: table with the parameters used in model selection process, plots showing the weather conditions for the period 2000-2006, model residuals, and model performance. (PDF 871 KB)
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Bisanzio, D., Giacobini, M., Bertolotti, L. et al. Spatio-temporal patterns of distribution of West Nile virus vectors in eastern Piedmont Region, Italy. Parasites Vectors 4, 230 (2011). https://doi.org/10.1186/1756-3305-4-230
- Normalize Difference Vegetation Index
- West Nile Virus
- Rice Field
- Land Surface Temperature
- Mosquito Species