The transmission potential of Rift Valley fever virus among livestock in the Netherlands: a modelling study
© Fischer et al.; licensee BioMed Central Ltd. 2013
Received: 15 August 2012
Accepted: 27 June 2013
Published: 22 July 2013
Rift Valley fever virus (RVFV) is a zoonotic vector-borne infection and causes a potentially severe disease. Many mammals are susceptible to infection including important livestock species. Although currently confined to Africa and the near-East, this disease causes concern in countries in temperate climates where both hosts and potential vectors are present, such as the Netherlands. Currently, an assessment of the probability of an outbreak occurring in this country is missing. To evaluate the transmission potential of RVFV, a mathematical model was developed and used to determine the initial growth and the Floquet ratio, which are indicators of the probability of an outbreak and of persistence in a periodic changing environment caused by seasonality. We show that several areas of the Netherlands have a high transmission potential and risk of persistence of the infection. Counter-intuitively, these are the sparsely populated livestock areas, due to the high vector-host ratios in these areas. Culex pipiens s.l. is found to be the main driver of the spread and persistence, because it is by far the most abundant mosquito. Our investigation underscores the importance to determine the vector competence of this mosquito species for RVFV and its host preference.
Rift Valley fever virus (RVFV; Bunyaviridae: Phlebovirus) was first isolated during an outbreak in the 1930’s in the Rift Valley of Kenya . Between 1930 and 1977 outbreaks of RVF were limited to sub-Saharan Africa . In 1977 the first documented outbreak north of the Sahara occurred in Egypt, and since that time RVFV has been found in Madagascar and smaller islands of the coast of mainland Africa . In 2000 the first outbreak occurred outside Africa on the Arabian Peninsula in Saudi Arabia and Yemen . The increasing known area of distribution and an outbreak out of Africa feeds the fear of an expansion of the area affected by RVF and especially into the direction of the Middle East and Europe .
Many mammalian species are susceptible to infection with RVFV, including livestock such as cattle, goat, sheep and camels [1, 4], but also wildlife such as giraffe and African buffalo [5, 6]. RVFV infection in susceptible livestock animals causes abortion in pregnant animals and high mortality rates of new-borns. In older animals, infection is generally mild or asymptomatic. Birds and reptiles are refractory, and important livestock species such as pigs , horses and other equines are resistant to the infection [4, 8]. Susceptibility of deer-species (either European, Asian or American) is unknown to date.
Humans can become infected with RVFV following contact with infected animals or animal products, and although less likely as a result of a mosquito bite. RVFV infection in humans is generally mild or unapparent, but occasional severe and potentially fatal complications occur [2, 4].
RVFV is a vector-borne infection primarily transmitted by mosquitoes of many different species. These include Culex pipiens sensu lato (L.) and Aedes vexans (Meigen), which are both present in the Netherlands . One African vector species, Aedes lineatopennis (Ludlow), has been found to transmit the virus to their eggs . Based on this knowledge, vectors of the genus Aedes are thought to transmit the virus to their eggs (vertical transmission) [8, 10]. Other genera are thought not to transmit the virus vertically. Mechanical transmission of the virus by other insects, such as stable flies, has been observed in experiments .
The infection has entered and established itself in regions previously free of RVFV . The presence of vectors and hosts does not automatically imply that an outbreak will occur after introduction. Other epidemiological, ecological and environmental factors, such as temperature, host species composition and habitat overlap, determine the probability of an outbreak. To assess the probability of an outbreak and persistence in a country in the temperate zone we have chosen the Netherlands as case. The Netherlands is a country with high and low density livestock areas and potentially competent vectors are present [13–15]. An outbreak of RVF in the Netherlands would lead to massive economic losses, and poses a risk for public health and animal welfare . Therefore the transmission potential of RVFV needs to be evaluated under the climatological and epidemiological characteristics of this country.
Previous models of Rift Valley fever epidemiology either reproduced a spatial epidemic using a network model , or incorporated detailed information on the different stages of the vector , or incorporated transmission to humans . These models have shown the importance of decreasing the vector life span to reduce the potential of a major outbreak. These models do not, however, include seasonality of vector populations or changing parameters values due to temperature fluctuations. These effects are of importance to determine risk of persistence in areas with clear temporal fluctuations, such as the Netherlands.
For our purpose, a new mathematical model was developed to study the probability of a RVFV outbreak, and the probability of persistence of the infection during consecutive years. First, we apply the model to create risk maps of the Netherlands showing high risk areas for a RVFV outbreak and for persistence of RVFV in livestock. For these maps we consider host species to be cattle, sheep and goats, and consider vector species to be Aedes vexans vexans and Culex pipiens sensu lato as vectors . Finally, we conducted an uncertainty analysis of the input parameters, which yielded knowledge about influential input parameters and data gaps, which can help focus future research and improve the accuracy of the model predictions.
Material and methods
The mathematical model: general overview
Parameters and their definitions
Average latent period of host
γ h * k
Mean infectious period of host
(γ h ) 2 * k
Variance infectious period of host
1/μ v Aedes (T) = a 0 - a 1 T
Longevity of Ae. vexans as function of temperature T
1/μ v Culex (T) = a 0 - a 1 T
Longevity of Cx. pipiens as function of temperature T
d v Culex
Increased mortality of infected Cx. pipiens
b(T) mosquitoes = b slope (T- b min )
Biting rate of mosquito species as function of temperature T
1/φ v Aedes (T) = 1/( φ max - φ slope T)
Extrinsic incubation period Ae. vexans as function of temperature T. The slope is equal for Ae. vexans and Cx. pipiens.
1/φ v Culex (T) = 1/( φ max - φ slope T)
Extrinsic incubation period Cx. pipiens as function of temperature T. The slope is equal for Ae. vexans and Cx. pipiens
Vertical transmission Ae. vexans
Host to Ae. vexans transmission probability
Host to Cx. pipiens transmission probability
Ae. vexans to host transmission probability
Cx. pipiens to host transmission probability
π Aedes, j
Relative preference of Ae. vexans for a host species j
π Culex, j
Relative preference of Cx. pipiens for a host species j
We assume constant host population sizes and no effect of temperature on host related parameters. In contrast, vector-related parameters are temperature dependent based on average daily (24 h) temperatures in The Netherlands between 1971–2000 . Furthermore, vector populations fluctuate during the vector season. The vector season is the period in which vectors are active between 21st of April and 23rd of October, given the temperature threshold for biting of 9.6 °C .
Activity and survival of mosquitoes during winter months and especially how that affects the virus, is poorly understood. Therefore, in our model we assume a period of stasis during winter, i.e. the number of susceptible and infected vectors and the number of susceptible, infected and recovered hosts at the beginning of the vector season is equal to the situation at the end of the previous vector season. This implies that the infection cannot die out during the winter in our model. The rationale behind this assumption is that, without an outbreak, the overwintering strategies of vectors and the virus cannot be determined for RVFV in temperate countries like the Netherlands in which an outbreak has never occurred. For instance, the bluetongue virus overwintered in the country unexpectedly, and it is not clear how . Virus had overwintered and the epidemic reactivated, when the conditions were favourable again . A similar pattern is possible for RVFV.
For convenience we assumed stasis of the host as well. To test the effect of stasis of the host we performed a sensitivity analysis, to evaluate its impact (see Additional file 1). We found that a reappearing epidemic after a stasis period, very quickly returns to the pattern of a continued epidemic (Additional file 1: Figure S3).
The main host species are domestic cattle, sheep and goat. Pigs and equines are resistant to natural infection. Rodents are not taken into account, because they are assumed to play a negligible role in the epidemiology . Also humans are assumed not to add to the epidemiology. Deer are not taken into account for the creation of risk maps, because it is unknown whether these animals are susceptible to RVFV.
The abundances of livestock hosts per 5 × 5 km grid in the Netherlands were acquired from a central database, which contains the registered number of livestock per holding in the Netherlands. The location of the animals was assumed to be the location of the farm address. This database is maintained by and opened to our use by “Dienst Regelingen” of the Ministry of Economic Affairs, Agriculture and Innovation (currently the Ministry of Economic Affairs) to determine cattle, goat and sheep density.
The Dutch vector species are part of a species complex: Ae. vexans vexans and Cx. pipiens s.l. Ae. vexans vexans is the European sub-species of Ae. vexans. The Arabian sub-species Ae. vexans arabiensis (Patton) was a major vector in the Saudi-Arabian and West-African outbreaks [24–26]. We assume that the Dutch Ae. vexans vexans has the same vector competence as Ae. vexans arabiensis. We will denote this species by Ae. vexans. The situation for Cx. pipiens s.l. is more complex. The main two sub-species Cx. pipiens sensu stricto and Cx. pipiens molestus differ in host-preference. Cx. pipiens s.s. is strictly ornithophilic and does not bite on mammals, while Cx. pipiens molestus is opportunistic and bites on both birds and mammals. The sub-species hybridize to form populations with intermediate preferences. For the Netherlands it is unknown which species or hybrids are present (pers. com. Dr E.J. Scholte). In this study we assume that Cx. pipiens s.l. is purely biting on mammals as a worst case assumption, and denote the species simply by Cx. pipiens.
The mathematical model: description
Host are categorized into four states: susceptible (S h ), latent (L h ), infectious (I h ) and recovered (R h ). Host are born susceptible, and will enter the latent state after infection. After the latent state animals become infectious and after clearance of the infection will become recovered. Animals remain in the recovered class until death .
Here, α ij is the transmission probability per bite from vector species i to host species j, which is multiplied by the probability of a vector of species i biting a host of species j. The probability of biting a host of species j is calculated by multiplication of the preference π ij for host j by vector species i with the number of hosts of species j (N h j ), divided by the sum of all preferences times host population sizes. The biting rate (number of bites per vector per day) is not affected by the number of hosts nor is the composition of hosts of influence on the biting rate of an individual vector. After infection hosts are in the latent class (L h ) with average length 1/ days. Thereafter, hosts have a gamma-distributed infectious period of on average k * days. From the infectious state the hosts enter the recovered state. The hosts remain in this state until they die. Hosts die at rate , and are replaced by birth of new susceptible animals.
Insect populations are highly variable during a year and therefore the vector population sizes are explicitly modelled. The vector population size N v i depends on the number of new adult vectors entering the population h i (t) and the mortality of vectors μ v i (t). For Cx. pipiens s.l. the mortality rate increases with a factor d i v if the vector is infected by RVFV .
Vectors have a latent state (in entomology called the extrinsic incubation period) in which they cannot infect hosts, and which is followed by an infectious state in which they can infect hosts. These infectious vectors remain infectious until death.
Here, β ij is the transmission probability per bite of susceptible vector of type i on an infectious host of type j, which is multiplied by the probability that a bitten host of species j is bitten by vector species i (equal to Equation 1) and the probability of biting the one infectious host is given by dividing by the host population size: .
Mosquitoes of the genus Aedes are thought to transmit the virus from adult to egg. We developed a simple model to mimic the influx and outflow of infected eggs for Ae. vexans. The rate at which one female produces eggs, is determined by the biting rate b i (t) and the batch size c i . The batch size c i is determined in the model such that the vector population size remains equal between years (but fluctuates within a year). A fraction ζ i of eggs of infectious vertical transmitting vectors will become infected. After hatching and passing through larval states, these eggs develop into infectious female vectors. Infected eggs form an extra infected state Y i (see Figure 1). The number of hatching eggs is equal to the influx of new female adults h i (t). This means that we only consider those eggs that will survive, and the larvae and pupae will subsequently survive until emerging as adults. The rate of producing eggs, c i b i (t), is, thus, the number of eggs laid by a female that will survive at least until becoming an adult female.
The biting rate b i (t), mortality rate and rate of transition from the extrinsic incubation period change with time t due to the temperature dependence of these parameters. The average 24 h temperature is described by a sine function (see Additional file 1: Figure S1). Hatching parameter h i (t) is the number of eggs hatching at a certain moment in time and was estimated such that the population size equalled the observed seasonal pattern (see Additional file 1).
Initial epidemic growth rate and floquet ratio, RT
RVFV is not present in the Netherlands, hence the country is in the so-called disease-free equilibrium. An equilibrium can either be stable, which means that after a disturbance, the system returns to the original state. In our situation, this means that after introduction of an infected vector or host, the transmission cycle is self-limiting, i.e. no new infections occur even if enough susceptible hosts are present, and returns to the situation without the infection. The other option is that the disease-free equilibrium is unstable, meaning that a disturbance (i.e. introduction of an infected vector or host) will cause a major outbreak, which is only limited by a depletion of hosts.
The stability of the disease-free equilibrium is often determined by the well-known basic reproduction number, R 0 . The basic reproduction number, R 0 , is defined as the expected number of secondary cases caused by one primary case in a totally susceptible population . However, the basic reproduction number R 0 is difficult to determine for a seasonal system and if done, simplifying assumptions have to be made which are not valid for our purposes . Therefore, we chose to use another method, the newly defined Floquet ratio, R T . The Floquet ratio, R T , is the expected number of cases caused by a primary case after one complete cycle of seasons .
We will investigate the stability of the disease-free equilibrium at two time scales. Firstly, the initial epidemic growth rate gives a measure for growth of the number of infected hosts and vectors at the moment of introduction. We will use the initial epidemic growth rate, r, which can be calculated for each moment in time (as opposed to R T which is only applicable to the whole cycle of seasons). The initial growth rate r is easily derived from the model equations that are used to calculate R T as well. The initial epidemic growth rate r can be calculated by describing the increase in the number infections by the transmission matrix T and the decrease (by death and recovery) by matrix D (see Additional file 1). If the real part of the largest eigenvalue of this matrix (T-D) in the disease-free equilibrium is larger than zero using the Routh-Hurwitz criteria , the disease-free equilibrium is unstable and a major outbreak can occur. The initial epidemic growth rate r will be transformed to e r , so that it has the same threshold property as the Floquet ratio R T (i.e. e r > 1).
Secondly, we will investigate the long term epidemic growth which is the average growth in number of infected hosts and vectors over multiple years. Therefore, we have to deal with annually recurring patterns (seasonality). The recently suggested Floquet ratio R T  uses Floquet theory in analysing the long term multi-annual stability of a dynamic system. Application of Floquet theory to the field of epidemiology has been proposed previously , but has not been used frequently by a lack of easy applicable methods  or by simplification requirements of the model . The algorithm for R T differentiates between the short term periodic changes and long term changes in numbers of infecteds . In this algorithm the matrix (T-D) is expanded into Fourier series, which are used to determine the Floquet ratio. If the Floquet ratio exceeds 1 the disease-free equilibrium is unstable, and the infection is expected to persist. The exact mathematics of the algorithm used to determine the Floquet ratio are published by Boender et al. .
Areas differ in host density and vector abundance, resulting in different risks of an outbreak and of persistence in each of these areas, which can be visualised by risk maps. We created the maps to show the risk in different areas in the Netherlands of initial spread and of persistence. Furthermore, we investigated which vector-species contributes most to the spread by also creating individual risk maps for Cx. pipiens and Ae. vexans.
Risk maps are created by overlaying input data combined by specific calculations. Vector abundance (Figure 2) is based on the geographic and climatological features of a grid cell . The host abundance for each grid cell are the cattle, sheep and goats located in that grid cell based on data of the Ministry of Economic Affairs, Agriculture & Innovation (Figure 2). The host and vector abundance and the estimates of the other parameter values are input for the model. The model includes aspects of vector biology, ecology, and virology.
Initial spread of RVFV is assessed at three moments during the vector season: 30 days after the start of the vector season (21st May), half way (23rd July), and 30 days before the end of the vector season (23rd September). Persistence of the infection is determined by the Floquet ratio, R T , which summarizes growth over multiple years.
Rather than presenting a binary map with areas above or below the threshold, we depict maps with the probability that the initial growth rate r or the Floquet ratio, R T , exceeds the threshold. This probability is based on the accuracy and certainty of the estimated parameters within biological plausible ranges (see Additional file 1).
In the uncertainty analysis, the model outcomes are calculated with different parameter values sampled by Latin Hypercube sampling  from their biological plausible interval. The range in outcomes reflects the magnitude of uncertainty introduced in the model outcome by the uncertainty in parameter estimates.
Twenty-five parameters were analysed in the uncertainty analysis. The 21 basic parameters of the RVF model, the ratio between Cx. pipiens and Ae. Vexans, the ratio between Cx. pipiens s.l. and Cx. pipiens molestus, the percentage of refractory hosts and the vector-host ratio. The vector-host ratio is varied in the uncertainty analysis by sampling from the vector-host ratios observed in the grids of 5 × 5 km areas. Additionally, the uncertainty in the estimation of mosquito abundance is taken into account by changing the estimated value by 10 fold (smaller or larger) using an extra parameter, with which the original vector-host ratio was thus multiplied.
The correlation between outcome of the model and each of the sampled parameter values is determined by the Kendall rank correlation coefficient (KRC) [34, 35]. KRC coefficients of −1 or 1 represent a perfect correlation of outcome with parameter, correlation of 0 means no correlation.
Characteristics (in number per 5 by 5 km area) of a sparsely (SPLA) and a densely (DPLA) populated livestock area in the Netherlands, and the resulting Floquet ratio R T
Sheep & goat
Floquet ratio R T
The mathematical model developed in this paper provides insight into the spatial risk (risk maps) and major uncertainties of the potential risk of a Rift Valley fever outbreak in the Netherlands.
Counter-intuitively, the areas at risk of RVFV are predominantly the sparsely populated livestock areas (SPLAs, Figure 6) in which vector-host ratios are high. No other sources than cattle, sheep and goats are assumed in the area, such as wildlife or birds, to be present for a blood meal of the mosquitoes, thus leading to these high vector-host ratios. This results in a high probability of an outbreak occurring, because an initial infected host is bitten by many vectors. Stochastic fade-out or depletion of susceptible hosts is in SPLAs very likely to occur within the vector-season. Spill-over to densely populated livestock areas (DPLAs) contributes to an increased national impact of an outbreak in an SPLA. However, spatial spread between areas was not taken into account here.
The negative relationship between livestock density and the probability of an outbreak occurring is well known from other mathematical models of vector-borne infections (e.g. ). Also, within the definition of the vector-capacity, i.e. the potential of a vector-population to transmit a disease, includes the vector-host ratio . This high sensitivity to the vector-host ratio was not observed in previous model studies of the potential of a major RVFV outbreak, because these studies did not include this parameter in their analyses [10, 17]. However, our results do confirm the importance of the vector-lifespan found in these studies. The sensitivity to transmission probabilities found by Gaff et al.  was not observed in our analyses, and might have been obscured by the high influence of the vector-host ratio. In the bluetongue epidemic in France it has also been observed that an increase in cattle density resulted in lower seropositivity , indicating that higher host densities decrease the transmission potential. Due to the absence of outbreaks in areas similar to the Netherlands it is impossible to directly determine the risk of an outbreak, therefore this risk needs to be determined from underlying mechanisms. Mathematical models are a good tool to systematically follow an inductive line of reasoning . In our model this meant that we needed to translate information from Africa to the situation in the Netherlands. Mortality rates of animals are likely to be much higher in naïve European herds than in African herds . However, the uncertainty analyses showed that this had little impact on our results. Also, other factors that might be influenced by difference in susceptibility between breeds, i.e. transmission probability and length of the infectious period, were not found to have a substantial impact on the results.
The model was applied to the Netherlands, but this country can represent other areas in the temperate zone of at least northwest Europe. Livestock densities in some areas of the Netherlands are very high, but in other areas they are low (Figure 2). Our results indicate that areas with similar livestock and environmental characteristics should be considered at risk of RVFV outbreaks. Application of the model to other areas is possible when population dynamics of vectors and vector abundances are known.
The overwintering strategies of viruses, such as RVFV, in vectors cannot be determined in temperate zone, as long as no outbreaks have occurred. For instance, the bluetongue virus serotype 8 (BTV-8) overwintered in the Netherlands, Belgium and Germany unexpectedly, and it is still not clear how. For BTV-8 we do know that little happens in winter, and very quickly after reappearance of the vectors, the epidemic reappeared. Cx. pipiens s.l. is the main driver of a RVF-outbreak and can overwinter in the adult stage  and thus, infectious vectors can immediately become active again during the favourable season. Obviously there is a gradual decline in vector activity with declining temperature, and a gradual increase with increasing temperature. We modelled this in the form of a very abrupt end of transmission and an abrupt reappearance (stasis during the vector-free season), which, given the right choice of this winter period, does hardly affect the results (see Additional file 1: Figure S4). If RVFV cannot overwinter, persistence in the temperate zone is not possible, and the calculations of persistence (R T ) are irrelevant. Based on the overwintering of BTV in Europe and the survival of RVFV during inter-epidemic periods in East-Africa, however, assuming survival during the winters is not unlikely.
Direct transmission of RVFV between mammals has been suggested , but never been experimentally proven to exist. Direct transmission increases the transmission rate locally (see Additional file 1: Figure S3), which could cause survival of the virus in absence of vectors (e.g. during the winter). Furthermore, direct transmission increases the outbreak potential such that densely populated livestock areas might be at risk of an outbreak.
Cx. pipiens contributes by far most to the spread and persistence of RVFV in the Netherlands (Figure 4), because it is by far the most common mosquito in the country. As a result, the uncertainty analysis of the model output shows that the results are strongly correlated with the estimated abundance of this vector population.
Here, Cx. pipiens is modelled as purely biting on mammals (livestock), and not on birds. The vector capacity for RVFV among livestock decreases if this mosquito takes blood meals from birds as well, which are not hosts for RVFV. Part of the population of Cx. pipiens might be ornithophilic (being Cx. pipiens s.s.) and the exact composition of the mosquito species complex in The Netherlands is still unknown (pers. com. E.J. Scholte). Populations from the south of France are known to be competent , but vector competence of the Cx. pipiens s.l. population in the Netherlands is unknown. Also when other animals, such as wildlife or rodents, are present in sparsely populated livestock areas, this may decrease the transmission potential substantially. Less than one refractory host per livestock animal (i.e. 0.65) is required to reduce the spread potential to values below the threshold. If refractory hosts are birds, it is likely that the value of 0.65 additional refractory host per livestock animal is exceeded and the threshold for spread is not reached. This will only occur, when vectors will be actually biting these refractory hosts. The model and thus the risk maps are in such a case an overestimation of the risk of a Rift Valley fever outbreak. Investigation into the vector properties of the major potential vector species for RVFV, Cx. pipiens s.l., is thus warranted.
Vertical transmission of the virus from adult Ae. vexans to eggs has almost no effect on an outbreak and even not on persistence of the infection in the Netherlands, because of the minor role of this vector species in the transmission (Figure 4). The existence and role of vertical transmission is subject to controversy. To our knowledge only one report  suggests the possibility of RVFV transmission via eggs in a related vector species, Ae. linneatopennis, which is not present in Europe. Studies that reproduce these findings under laboratory conditions are unknown .
Also unknown is the impact of the stable fly Stomoxys calcitrans (L.) which is highly efficient in transmitting the infection mechanically between hamsters in the laboratory . In contrast to mosquitoes, stable flies are less likely to disperse over large areas, as their preferred breeding sites consist of straw, hay and manure . Hence, stable flies do not have to leave a farm to find suitable breeding sites. The stable fly might act as an amplifying vector on a local farm if transmission between livestock hosts is as efficient as between hamsters: after introduction of a RVFV infection by a mosquito vector, the infection spreads very fast from animal to animal due to the presence of stable flies. Stable flies should be monitored during a RVFV epidemic to obtain valuable epidemiological data. However, whether these infected flies can be found during an entomological surveillance depends on the time between collection of vectors and virus detection, due to denaturation of the virus. The half life time of the virus in aerosols is only 6 h .
Another unknown actor is deer. Several deer species occur throughout Europe  and might play a role in the epidemiology of RVFV. Livestock in unaffected areas can get infected by migrating deer if these deer are infected. However, to our knowledge no deer species have been tested for RVFV competence and the preference of vectors for deer is unknown.
In summary, areas with a high vector to host ratio are most likely to experience an outbreak and persistence of the infection. The high vector-host ratio in the Netherlands is almost entirely due to the wide spread abundance of Cx. pipiens s.l. Our investigation underscores the importance to determine the vector competence and host preference of this mosquito species and others associated with cattle, sheep and goat.
EF is a theoretical biologist with a PhD in Health Sciences. GB has a PhD in Biophysics and his work focusses on spatial epidemiology of veterinary infections. AdK is a theoretical biologist with a PhD in applied mathematics and is working on veterinary infectious disease modelling. GN is a DVM with a PhD in Veterinary Epidemiology and her work focusses on control of animal diseases and veterinary epidemiology. HvR has a PhD in modelling of insect population dynamics and is involved since then in veterinary epidemiology. All authors are researchers at the Central Veterinary Institute, part of Wageningen UR, in the Netherlands and are involved in both commercial, academic and government policy supporting research.
Bluetongue virus (serotype 8)
Densely Populated Livestock Area
Extrinsic Incubation Period
(Dutch) ministery of economic affairs, Agriculture and Innovation
Kendal Rank Correlation
Latently infected class
Basic reproduction number
Rift Valley fever (Virus)
Sparsely Populated Livestock Area
This research was funded by the Ministry of Agriculture, Nature and Food Quality (LNV, now EL&I) in The Netherlands (project BO-08-010-022). The authors would like to thank W van Bortel and V Versteirt (ITG Antwerp) for mosquito observation data from Belgium, EJ Scholte and J Beeuwkes of the Center Monitoring Vectors for discussions about mosquito abundances and behaviour. R Moormann, J Kortekaas (CVI, Lelystad) and JW Zijlker (EL&I) for discussions about Rift Valley fever. We also want to thank two anonymous reviewers for their remarks, which have improved to manuscript.
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