 Research
 Open Access
 Published:
Endemicity response timelines for Plasmodium falciparum elimination
Malaria Journal volume 8, Article number: 87 (2009)
Abstract
Background
The scaling up of malaria control and renewed calls for malaria eradication have raised interest in defining timelines for changes in malaria endemicity.
Methods
The epidemiological theory for the decline in the Plasmodium falciparum parasite rate (Pf PR, the prevalence of infection) following intervention was critically reviewed and where necessary extended to consider superinfection, heterogeneous biting, and aging infections. Timelines for malaria control and elimination under different levels of intervention were then established using a wide range of candidate mathematical models. Analysis focused on the timelines from baseline to 1% and from 1% through the final stages of elimination.
Results
The RossMacdonald model, which ignores superinfection, was used for planning during the Global Malaria Eradication Programme (GMEP). In models that consider superinfection, Pf PR takes two to three years longer to reach 1% starting from a hyperendemic baseline, consistent with one of the few largescale malaria control trials conducted in an African population with hyperendemic malaria. The time to elimination depends fundamentally upon the extent to which malaria transmission is interrupted and the size of the human population modelled. When the Pf PR drops below 1%, almost all models predict similar and proportional declines in Pf PR in consecutive years from 1% through to elimination and that the waiting time to reduce Pf PR from 10% to 1% and from 1% to 0.1% are approximately equal, but the decay rate can increase over time if infections senesce.
Conclusion
The theory described herein provides simple "rules of thumb" and likely time horizons for the impact of interventions for control and elimination. Starting from a hyperendemic baseline, the GMEP planning timelines, which were based on the RossMacdonald model with completely interrupted transmission, were inappropriate for setting endemicity timelines and they represent the most optimistic scenario for places with lower endemicity. Basic timelines from Pf PR of 1% through elimination depend on population size and lowlevel transmission. These models provide a theoretical basis that can be further tailored to specific control and elimination scenarios.
Background
The Roll Back Malaria Partnership (RBM) recently called for universal coverage with vector control and effective drugs by 2010 [1], and major international agencies are realigning their shortterm goals and activities to achieve the longterm goal of global malaria eradication [2–4]. Many countries are now contemplating malaria elimination, so there is a need to define plausible timelines for planning. Much of the previous experience in setting malaria elimination timelines comes from the Global Malaria Eradication Programme (GMEP), which was launched in 1955 and implemented in four phases called planning, attack, consolidation, and maintenance [5, 6]. The attack phase was based on three to four years of indoor spraying with residual insecticides to completely interrupt transmission; success was judged by several criteria, one of which was that by the end of spraying, the Plasmodium falciparum parasite rate (Pf PR, the prevalence of malaria infection) was reduced to less than 1% of the precontrol baseline [7]. The GMEP prioritized this short duration attack phase to reduce the opportunity for the evolution of insecticide resistance in Anopheles vectors. During the GMEP, expected Pf PR declines within the attack phase were based on the RossMacdonald model [7].
The end of a successful GMEP attack phase marked the beginning of a new control phase, called consolidation, defined in part by new requirements for monitoring and evaluation; when Pf PR drops below 1%, parasite surveys become an inefficient way of sampling malaria and measuring progress [8]. The focus of malaria control programmes during consolidation shifted to developing health and surveillance systems, identifying and eliminating residual transmission foci and preparing countries for malaria free status certification [9]. While the GMEP established welldefined timelines for the attack phase, timelines for the consolidation phase were not outlined [8].
By 1964, several GMEP control initiatives outside of Africa had successfully reduced Pf PR below 1% after three to four years of spraying [7], which provided some validation for the GMEP model and timelines, but there were fewer successes in Africa [10]. Before GMEP, there had been a polarizing debate among malaria experts about the feasibility of malaria control and elimination in hyperendemic Africa [11], which is defined by Pf PR in children aged 2–10 greater than 50% [12]. In Kenya and Tanzania, the PareTaveta Malaria Scheme was launched in 1955 to help address many points of contention [11]. The indoor residual spraying campaign in Pare and Taveta lasted for three and a half years during which the Pf PR remained high initially, but then fell from above 60% to around 5% in older children [13, 14] (Figure 1). The results of the insecticide spraying when evaluated using traditional criteria were not thought to have demonstrated complete interruption of transmission [7]. Direct estimates suggested the basic reproductive number for malaria [15] had been reduced to below one [13], however, and that the decay rates were consistent with a reproductive number under control of 0.7 [7].
A result of intense exposure to malaria in populations with hyperendemic malaria, such as those in PareTaveta, is that new infections accumulate on top of uncleared infections: a phenomenon called "superinfection" [16]. These complex infections are comprised of multiple founding parasite genotypes from multiple infectious bites, and the number of distinct founding parasite genotypes is called the multiplicity of infection (MOI). Theory [16–19] and empirical studies [20] have suggested that infections with high MOI take longer to clear. The RossMacDonald model used by the GMEP assumed that infections were simple (the MOI was at most one) and, therefore, may have set inappropriate timelines for changing endemicity from a hyperendemic baseline.
Superinfection had been discussed and modelled before the GMEP [16, 21], and several additional models have been developed since [18, 22, 23]. These alternative models had not been used to reevaluate response timelines to intervention in areas where superinfection would have been common, such as PareTaveta. It is clear that the same theory can be also be used for predicting the results of scaling up of malaria interventions today [1].
In this study, the theoretical basis for estimating endemicity responses following intensive control across the malaria transmission spectrum is critically reviewed and extended. A range of simple mathematical models of malaria transmission and parasite clearance were investigated, to describe likely timelines for the changing Pf PR in hyperendemic areas from baseline to 1%. The theory is further extended to establishing basic expectations about the timelines for the consolidation phase, the likely timelines for the changes in Pf PR from 1% to elimination.
Methods
The timelines for changing Pf PR following malaria control without mass drug administration are determined by the waiting times to clear untreated human infections. The RossMacdonald model, on which GMEP planning was based, was used as a starting point for analysis. To evaluate whether the RossMacdonald forms a good basis for planning across the endemicity spectrum and during all phases of malaria control and elimination, changes in Pf PR were simulated and compared using several other models of malaria infections. These models are described briefly in the following sections. A more detailed mathematical description of the models is found in Additional File 1.
Clearance rates
The waiting time to clear a simple infection is an important parameter in these models. Estimates of the waiting time to clear an infection come from several different sources. One important source was data from the malaria therapy of neurosyphilis patients, which estimated an average duration of 220 days [24]. The 200day waiting time was also consistent with an older study in Puerto Rico [25], and with recent studies that compared models and estimated waiting time to clear infections of 150 days in northern Ghana [26].
In these analyses, the expected changes in Pf PR were examined under the assumption that the average duration of an infection is 200 days. This value was fixed by the empirical evidence outlined above and numerous studies conducted during the GMEP, where transmission was considered by many criteria to be completely interrupted and the documented declines in Pf PR were broadly consistent with an average duration of infection and maximum rate of decline of about 200 days [7].
RossMacdonald
The RossMacdonald model assumed that people were either infected or not, and that once infected, infections would clear at a constant percapita rate, r. The assumption applied regardless of how long a person had already been infected or whether the person had acquired multiple infections. The model thus implies that the waiting time to lose an infection is exponentially distributed with a mean waiting time of 1/r days. During the GMEP, r was assumed to be 0.5% per day, which implied an average waiting time to clear of 200 days. Figure 1 shows a diagram of the human infection dynamics in the RossMacdonald model.
Queuing models
A challenge to the RossMacdonald model is that it does not consider the time to clear malaria when superinfection occurs. A simple formula to describe the waiting time to clear complex infections while transmission continues was derived during the Garki Project [17], but the formula converges rapidly to the RossMacdonald model if vectorcontrol measures reduce transmission (Additional File 1).
To describe the timelines for changing MOI when transmission is interrupted, it is necessary to track changes in the full distribution of MOI. Superinfection and dynamic changes in Pf PR were, therefore, simulated using a family of queuing models [18]. Queuing models were extended here to consider other biological scenarios, including finite or infinite "strains," and infections that cleared independently, or with competition that would increase clearance rates of parasite types, or with facilitation that would slow down clearance rates of parasite types (Figure 2). The queuing model was further extended to include heterogeneous biting; a queuing model described the dynamics of MOI in each human population stratum, defined by their relative rate of exposure.
Stochasticity
The RossMacdonald model and the queuing models are deterministic: nothing happens by chance. Deterministic models are good approximations when the law of large numbers applies. In the approach to malaria elimination, however, as the number of people who are infected becomes small, it is no longer sensible to ignore chance. During the consolidation phase, there must be a point when the emphasis begins to shift from the proportion of a population that is infected to the number infected. Pf PR defines the basis for switching malaria control phases, in part because of the impractically large sample sizes required to use changes in Pf PR as a measure of progress. When Pf PR is 1%, the number of people who remain infected is proportional to the population size. A Pf PR of 1% means, for example, that one person is infected in a population of 100 people, but that ten thousand people would be infected in a population of a million. Starting from a Pf PR of 1%, the waiting time to elimination is, therefore, longer in larger populations because there are more people who remain infected. To consider stochasticity and the effect of population size on the time to elimination, stochastic analogues of the RossMacdonald model and the queuing models were also developed and the changes in Pf PR were simulated in populations of various sizes.
Stagestructured models
The RossMacdonald model and the queuing models consider the waiting time to clear an infection without regard to the age of the infection. In the RossMacdonald model, for example, a person who has been infected for just one week and a person who has already been infected for 200 days are equally likely to remain infected for 200 more days. This may not be realistic if clearance rates change with the age of the infection. Stagestructured models are a useful way to model infections that clear faster or slower as they age [27], but it is computationally difficult to model stagestructure and superinfection deterministically (Additional File 1). Aging infections were modelled in stochastic models with superinfection, under the assumption that infections clear independently. An extreme version of this model was tested here in which infections progressed through n equal "stages," and were cleared from the last stage. This is called senescence because infection rates increase as infections age [27].
R_{0} and vector dynamics
Mosquito infection dynamics and the force of infection were simulated in a minimal mosquito model (Additional File 1). In all these models, the intensity of transmission by mosquitoes in the absence of control was determined by the basic reproductive number, R_{0}. The intensity of transmission under control was determined by the controlled basic reproductive number, R_{ C }. The two terms are directly analogous in every way but one; whereas R_{0} is only defined in an environment that lacks control, R_{ C }describes potential transmission in a population with some level of control. In the simulations, R_{0} sets the baseline, which determines the Pf PR at the start of a simulation. In models with superinfection, R_{0} also sets the equilibrium distribution of MOI. R_{ C }determines the rate of decline in Pf PR and the waiting time to elimination from that baseline. Transmission would be interrupted eventually if malaria elimination were the endpoint in the absence of imported malaria (R_{ C }< 1), but it would be completely and immediately interrupted if R_{ C }= 0.
Results
The results focus on the Pf PR timelines and decay rates when the endpoint was elimination. The Pf PR over time was simulated numerically in all these models and compared plotting the Pf PR over time. Another useful way of comparing models was to plot the decay rates versus Pf PR (Figure 3). The daily decay rate is the logarithm of the daily change in Pf PR, and over any interval, the decay rate is the logarithm of the change in Pf PR divided by the length of the interval.
PfPR from baseline to 1%
In all the queuing models, the waiting time to clear malaria increases with MOI; it is the sum of waiting times to clear a simple infection (1/r) plus the time to progressively decrement MOI. With independent clearance, for example, the expected waiting time to clear an infection with m types was therefore 1/r + 1/2r + 1/3r + ... + 1/mr. Queuing models with competition, independent clearance, or facilitation each made quantitatively different predictions about the decline of Pf PR from baseline to 1% (Figure 3a). Some model identifiability problems were obvious. A model with four strains and facilitation was very similar to a model with infinite strains and independent clearance, for example, and a model with infinite strains and competition was similar to a model with two strains and independent clearance. As a general rule, models with a large number of strains or facilitation had longer timelines, while models with a small number of strains or competition had shorter timelines.
The queuing models predicted different rates and patterns of decline than the RossMacdonald model (Figure 3a, b, c). In the RossMacdonald model, the decay rate in Pf PR was initially faster than in models with superinfection, but the Pf PR decay rate subsequently declined. In queuing models in hyperendemic areas, the decay rate was initially slow as MOI declined, but after average MOI had declined to approximately one, Pf PR decay rates then followed the same pattern as the RossMacdonald model. The initial rate of decline was related to the initial distribution of MOI. Each one of the queuing models made a different prediction about the distribution of MOI in relation to baseline Pf PR, and heterogeneous biting strongly influenced this relationship (Figure 3d). When biting was more aggregated on a few individuals, the average MOI at a given level of endemicity was higher, and the initial rate of decline was slower (Figure 3e). The average MOI increased with Pf PR, but it remained close to one until malaria was hyperendemic, when it began to increase sharply (Figure 3f). The transition from an area with predominantly simple infections to one with predominantly complex infections was related to the degree of heterogeneous biting; for the same Pf PR, higher R_{0} and higher MOI were correlated. The queuing models did not differ substantially from the RossMacdonald model at low endemicity when MOI is typically close to one, which is consistent with the GMEP experience outside Africa [7]. Because of the slow initial rate of decline, the waiting time to reach a Pf PR of 1%, starting from a hyperendemic baseline, was two to three years longer than the RossMacdonald model.
The initial rate of decline differed substantially among the models, and it was also affected by the degree of biting heterogeneity, but it was not affected by R_{ C }. Holding all else but R_{ C }equal, the differences in Pf PR over time were not apparent until Pf PR had fallen (Figure 3f). In other words, the model determined the initial rate of decline, but R_{ C }determined the asymptotic rate of decline. In models that ignored the age of the infection, when R_{ C }= 0, the fastest decay rate possible was r. In other words, the GMEP planning timelines, which used the RossMacdonald model with completely interrupted transmission, described the most optimistic timelines for changes in Pf PR from baseline to 1%.
Table 1 reports the waiting time to reach a Pf PR of 1% in the infinite queuing model with heterogeneous biting. This model provides a good empirical fit to data describing the entomological inoculation rate and Pf PR in African children [28], and it also has other empirical support [29]. The values are shown for Pf PR baselines ranging from 5% up to 80%, and for a range of R_{ C }values. Also shown are the waiting times to reach Pf PR of 1% for R_{ C }= 1.05, when the endpoint Pf PR is 0.7%.
From 1% to elimination
After Pf PR falls below 1%, the decay rate of Pf PR in all the models, except for those with senescing infections, was approximately r(R_{ C }1) because superinfection is rare at very low endemicity (Figure 3, bottom). In the deterministic RossMacdonald model, declines in Pf PR from 1% through to elimination are approximated by the formula (SI):
With a 200 day waiting time to clear infections, as the GMEP model assumed, completely interrupted transmission would result in an 84% proportional reduction in Pf PR each year. Compared with completely interrupted transmission, Pf PR declines half as fast at R_{ C }= 0.5, and a fourth as fast at R_{ C }= 0.75. The model predicts that the ratio of Pf PR in consecutive years remains constant through elimination; the waiting time to reduce Pf PR from 10% to 1% is approximately the same as the waiting time to reduce Pf PR from 1% to 0.1%, or from 1,000 infected individuals to 100.
The expected waiting time to elimination, T_{ E }, can be approximated using Eq. 1 as the time when only one person in the population is infected, or in a population of size H, when Pf PR is less than 1/H:
The larger H, therefore, the longer it takes to achieve elimination. In a population of 1,000 humans with completely interrupted transmission (i.e. R_{ C }= 0), It would take 2.5 years to eliminate malaria from a population of 1,000 people, but 5 years from a population of 100,000. The waiting times also depend on R_{ C }. Compared with completely interrupted transmission, the time to elimination takes twice as long if R_{ C }= 0.5 and four times as long if R_{ C }= 0.75. Sample values are shown in Table 2.
The waiting time to elimination was simulated in the stochastic analogue of the models starting from a Pf PR of 1%; using R_{ C }as an index of ongoing transmission, all of the queuing models produced similar results, including those with heterogeneous biting (see Additional File 1). As the number of people who were infected becomes small (<1,000), stochasticity introduces noticeable fluctuation in the Pf PR and this affects the time to elimination.
The average proportional reductions in Pf PR from the ensemble of simulations tracked the deterministic models, but there was noticeable variability when populations became small. The waiting times to elimination were, therefore, extremely variable. Similar results were predicted by all of the models, except those with senescent infections, which produced much shorter and less variable waiting times to elimination when transmission was completely interrupted (Figure 4). Again, there were model identifiability issues; a model with senescence and R_{ C }= 0.5 was similar to a model with no senescence and completely interrupted transmission (Figure 3b). Without senescent infections, the sharpest annual decline in Pf PR that would be expected is 84%, but for models with senescent infections, the Pf PR decay rate would steadily increase and much faster declines are possible.
The PareTaveta malaria scheme
Because of model identifiability issues and some uncertainty about the underlying biology of P. falciparum transmission, it is impossible to make strong conclusions about whether malaria transmission had been interrupted in PareTaveta based upon only the initial decay rate in Pf PR. Other evidence suggested that transmission had not been interrupted, especially malaria infections in infants who had never travelled outside the sprayed area [13, 14].
The initial decay rates in Pare and Taveta, where malaria was hyperendemic at the baseline, were slow initially and then increased, consistent with models of superinfection (Figure 5). Exponential decay models also provide a good statistical fit to the data, but the rate is difficult to interpret as a measure of ongoing transmission in the context of a malaria transmission model [30]. One model of interest is the queuing model with heterogeneous biting and independent clearance, which provides a good fit to estimates of the entomological inoculation rate and Pf PR, and the parameter estimates from the model fitting were consistent with direct observations [28]. Because of the low number of data points, however, there is not sufficient statistical power to test the models with any degree of confidence. Nevertheless, superinfection does occur in hyperendemic areas, and the models provide a better visual fit to the observed patterns [29].
Discussion
The RossMacdonald model was used during the GMEP for planning endemicity response timelines during the attack phase, when Pf PR was reduced from the precontrol baseline to 1%. A comparison of several different models suggests that the RossMacdonald model remains useful today in planning for the responses to massive scalingup of malaria control, but with two important caveats; the GMEP timelines represent the most optimistic scenario in areas where superinfection is uncommon, and in hyperendemic areas where superinfection is common, the GMEP timelines are unrealistically fast. Queuing models suggest that, because of superinfection, the initial decay rates are very slow in hyperendemic areas. As Pf PR declines and MOI approaches one, after two to three years of intensive control, the decay rates will resemble places that started from a lower baseline. This pattern was consistent with the response to malaria control observed in PareTaveta. Reasonable "attack" phases to bring Pf PR to below 1% could last two to three years longer than the GMEP timelines. During the GMEP, the three to four year response timelines were inadequate for hyperendemic Africa, including PareTaveta. Also of note is that interventions during the Garki Project lasted only 18 months [31].
These models also generate useful timelines for the consolidation phase. Many studies have suggested that R_{ C }< 1 represents a threshold for elimination, but this analysis suggests that the timelines for control and elimination are extremely long unless R_{ C }is reduced substantially below one. High levels of control must also be sustained for several years after Pf PR falls below 1%. The waiting time to fall from 10% to 1% is the same as the waiting time to fall from 1% to 0.1% or from 1,000 infected individuals to 100 infected individuals. After reducing Pf PR below 1%, therefore, the waiting time to complete elimination can be longer than the waiting time to reach 1%, depending on the population size and the degree to which malaria transmission is interrupted.
An important recommendation is that malaria control planning timelines for consolidation after Pf PR drops below 1% should be based on the number of people who are infected, not the Pf PR. Large populations must wait longer than small populations to achieve elimination because when Pf PR is 1%, more people remain infected in the larger population. After reaching a low endemicity of 1%, the waiting time to elimination ranges from 2.5 additional years in a population of a thousand humans to 6.3 additional years in a population of a million, assuming transmission is completely and immediately interrupted. When there is some low level transmission, populations of a million people can reasonably expect to wait a decade or more until the endemic reservoir of parasites has cleared.
These timelines are largely based on models that ignore the age of malaria infections. If infections do "senesce" such that older infections clear faster than new ones, the time to elimination would be much shorter. There has been some mixed evidence for senescence [29, 32], but Pf PR decay rates that are broadly consistent with nonsenescing infections were found often during GMEP experiences [7]. In the documentation of successful attacks during the GMEP, decay rates were found that were faster than the predicted 84% maximum decline, but only when programmes used drugs, or when Pf PR was very low and sampling error was an important concern [7]. The GMEP studies were also generally of short duration (three to four years), so that senescence might not have become apparent in the data. When there is some ongoing lowlevel transmission on the way to elimination, infections in the population will be a mix of young and old infections, and senescence may not be important or apparent. Because of uncertainty about senescence, however, projections based on the RossMacdonald model should be considered a worstcase scenario for the consolidation phase, because shorter elimination timelines can be expected if infections senesce.
There is some uncertainty about the waiting time to clear an infection, and the timelines described here would change if the duration of an infection were actually closer to 150 or 250 days. This analysis has focused instead on comparing models, and it demonstrated that the same patterns could arise from differences in either r, in R_{ C }, or in the model. A basis exists for predicting R_{0} based on Pf PR and Pf EIR [28, 33], and there is also a basis for predicting R_{ C }in relation to usage of insecticide treated nets [34, 35], so it is possible to develop a predictive theory for malaria control endpoints and timelines. Regardless of the uncertainty, most models give broadly similar results when transmission intensity is reduced below the threshold for elimination, but not completely interrupted (i.e. when R_{ c }< 1).
One way to resolve the identifiability issues is to design studies that concurrently estimate r, Pf PR, MOI, and R_{ C }. The analysis thus suggests that a fieldestimate of MOI could be an important complement to Pf PR. After fixing Pf PR, biting heterogeneity, R_{0}, and the time to reach Pf PR of 1% all increase with MOI. A gap currently exists, however, between the notion of MOI in these models and MOI in studies.
MOI in the models is based on the notion of a parasite "brood," the number of founding parasite genotypes. Superinfection can also arise if a person is simultaneously bitten by many infectious mosquitoes [36], or if a bite transmits several parasite genotypes. The problems of defining broods and relating these to empirical estimates of MOI are complicated by parasite populations that are highly genetically polymorphic and infections that are highly variable – parasite population densities and frequencies can fluctuate by several orders of magnitude over short periods of time. Similar counting problems arise in ecology, where there has been a longstanding interest in estimating species diversity [37]. Ecologist measure diversity in two ways: richness is the total number of different entities present, and evenness is the probability that any two random individuals would have the same type. Sequencing methods that sample random parasites tend to measure evenness, not richness, because they resample common types. Sequencing methods that identify genetic polymorphisms can't infer the genotypes of individual parasites, which sets an upper limit on the ability to estimate MOI. MOI in the models is based on the notion of richness, so the relevance of existing MOI estimates not clear. If MOI could be developed as a standardized and interpretable fieldmeasure of transmission, it would represent a highly useful complement to Pf PR as a basis for setting timelines.
Timelines for elimination can be advanced with antimalarial drugs. Mass drug administration can rapidly reduce the number of infected people and advance the timelines for elimination, but the expense and risks may not be justified since the declines would happen regardless. The use of drugs to cure malaria infections can prevent ongoing transmission, reduce R_{ C }and speed up elimination; other models suggest that using drugs for treating clinical malaria controls transmission better in low endemicity settings [27]. Active case detection to find, treat and cure nearby asymptomatic infections can speed up progress towards elimination. Prompt treatment of a high fraction of clinical malaria, casebased investigations, and active case detection become increasingly important for reducing ongoing transmission from imported malaria in the end phases of consolidation and after malaria has been eliminated [38], so implementing such policies during the consolidation phase provides an opportunity to train and build capacity.
This modelling framework was designed to establish basic expectations and a template that can be tailored to local situations. Planning for malaria elimination must also consider the risk of imported malaria and ongoing transmission from imported cases. This is of great concern during elimination campaigns, and it would continue to be a concern after achieving elimination, but it is a separate issue from the initial goal of eliminating the endemic reservoir. Other important considerations are natural fluctuations in mosquito population densities, changes in the coverage levels or effectiveness of various interventions, and the spatial structure of populations. These factors would lead to quantitative changes and increased variability in the expected waiting times to elimination, but so long as there is not a temporal trend in these factors, the basic expectations established here would still be useful. Given the large number of factors and possible permutations of those factors, it would be impractical to consider every scenario prospectively. Expansion of the basic models may be best done in case studies, which can consider these other factors in countryspecific malaria elimination plans.
Several models were used to evaluate decay rates in Pf PR in response to malaria control; the analysis demonstrates that many different plausible models produce very similar patterns. The timelines described here can help to establish reasonable planning horizons for countries that are contemplating elimination. A substantial body of further work is required to investigate the most locally appropriate and effective suite of interventions needed to affect that goal. This modelling framework, when combined with contemporary global maps of P. falciparum prevalence [39] and summaries of existing intervention coverage [40], provides a basis for setting plausible timelines for changing malaria endemicity in Africa and this is the subject of ongoing work.
Abbreviations
 (GMEP):

Global Malaria Eradication Programme
 (Pf PR) Plasmodiumfalciparum:

parasite rate
 (MOI):

multiplicity of infection
 (R_{0}):

basic reproductive number
 (R_{ C }):

basic reproductive number under control.
References
 1.
RBMP: The global malaria action plan for a malaria free world. 2008, Geneva, Switzerland: Roll Back Malaria Partnership, World Health Organization
 2.
Greenwood B, Fidock D, Kyle D, Kappe S, Alonso P, Collins F, Duffy P: Malaria: progress, perils, and prospects for eradication. J Clin Invest. 2008, 118 (4): 12661276. 10.1172/JCI33996.
 3.
Feachem R, Sabot O: A new global malaria eradication strategy. Lancet. 2008, 371 (9624): 16331635. 10.1016/S01406736(08)604249.
 4.
Roberts L, Enserink M: Malaria. Did they really say ... eradication?. Science. 2007, 318 (5856): 15441545. 10.1126/science.318.5856.1544.
 5.
Pampana EJ: A textbook of malaria eradication. 1969, London: Oxford University Press
 6.
Yekutiel P: The Global Malaria Eradication Campaign. Eradication of infectious diseases: a critical study. Edited by: A KM. 1980, Basel, Switzerland: Karger, 3: 3488.
 7.
Macdonald G, Göeckel GW: The malaria parasite rate and interruption of transmission. Bull World Health Organ. 1964, 31: 365377.
 8.
Hay SI, Smith DL, Snow RW: Measuring malaria endemicity from intense to interrupted transmission. Lancet Infect Dis. 2008, 8 (6): 369378. 10.1016/S14733099(08)700690.
 9.
W.H.O.: Malaria elimination: a field manual for low and moderate endemic countries. 2007, Geneva, Switzerland: World Health Organization
 10.
Kouznetsov RL: Malaria control by application of indoor spraying of residual insecticides in tropical Africa and its impact on community health. Trop Doct. 1977, 7 (2): 8191.
 11.
Dobson MJ, Malowany M, Snow RW: Malaria control in East Africa: the Kampala Conference and the PareTaveta Scheme: a meeting of common and high ground. Parassitologia. 2000, 42 (1–2): 149166.
 12.
Metselaar D, van Thiel PH: Classification of Malaria. Tropical and Geographical Medicine. 1959, 11: 157161.
 13.
Draper CC, Smith A: Malaria in the Pare area of Tanganyika. Part II. Effects of three years' spraying of huts with dieldrin. Trans R Soc Trop Med Hyg. 1960, 54: 342357. 10.1016/00359203(60)901152.
 14.
Smith A, Draper CC: Malaria in the Taveta area of Kenya and Tanganyika. Part II. Results after three and a half years' treatment of huts with dieldrin. East African Medical Journal. 1959, 36: 629643.
 15.
Macdonald G: Epidemiological basis of malaria control. Bull World Health Organ. 1956, 15 (3–5): 613626.
 16.
Macdonald G: The analysis of infection rates in diseases in which superinfection occurs. Trop Dis Bull. 1950, 47 (10): 907915.
 17.
Dietz K, Molineaux L, Thomas A: A malaria model tested in the African savannah. Bull World Health Organ. 1974, 50 (3–4): 347357.
 18.
Bailey NTJ: The biomathematics of malaria. 1982, Oxford: Oxford University Press
 19.
Fine PEM: Superinfection – a problem in formulating a problem. Tropical Diseases Builletin. 1975, 75 (6): 475488.
 20.
Smith T, Felger I, FraserHurt N, Beck HP: Effect of insecticidetreated bed nets on the dynamics of multiple Plasmodium falciparum infections. Trans R Soc Trop Med Hyg. 1999, 93 (Suppl 1): 5357. 10.1016/S00359203(99)903280.
 21.
Walton GA: On the control of malaria in Freetown, Sierra Leone. I. Plasmodium falciparum and Anopheles gambiae in relation to malaria occurring in infants. Ann Trop Med Parasitol. 1947, 41 (34): 380407.
 22.
Dietz K: Densitydependence in parasite transmission dynamics. Parasitol Today. 1988, 4 (4): 9197. 10.1016/01694758(88)900348.
 23.
Dietz K: Mathematical models for transmission and control of malaria. Principles and Practice of Malaria. Edited by: Wernsdorfer W, McGregor I. 1988, Edinburgh, UK: Churchill Livingstone, 10911133.
 24.
Eyles DE, Young MD: The duration of untreated or inadequately treated Plasmodium falciparum infections in the human host. Journal of the National Malaria Society. 1951, 10: 327336.
 25.
Earle WC, Pérez M, del Río J, Arzola C: Observations on the course of naturally acquired malaria in Puerto Rico. The Puerto Rico Journal of Public Health and Tropical Medicine. 1939, 14: 391406.
 26.
Sama W, OwusuAgyei S, Felger I, Vounatsou P, Smith T: An immigrationdeath model to estimate the duration of malaria infection when detectability of the parasite is imperfect. Stat Med. 2005, 24 (21): 32693288. 10.1002/sim.2189.
 27.
Okell LC, Drakeley CJ, Bousema T, Whitty CJ, Ghani AC: Modelling the impact of artemisinin combination therapy and longacting treatments on malaria transmission intensity. PLoS Med. 2008, 5 (11): e22610.1371/journal.pmed.0050226. discussion e226
 28.
Smith DL, Dushoff J, Snow RW, Hay SI: The entomological inoculation rate and Plasmodium falciparum infection in African children. Nature. 2005, 438 (7067): 492495. 10.1038/nature04024.
 29.
Sama W, OwusuAgyei S, Felger I, Dietz K, Smith T: Age and seasonal variation in the transition rates and detectability of Plasmodium falciparum malaria. Parasitology. 2006, 132 (Pt 1): 1321.
 30.
Sama W, Killeen G, Smith T: Estimating the duration of Plasmodium falciparum infection from trials of indoor residual spraying. Am J Trop Med Hyg. 2004, 70 (6): 625634.
 31.
Molineaux L, Gramiccia G: The Garki Project. 1980, Geneva: World Health Organization
 32.
Sama W, Dietz K, Smith T: Distribution of survival times of deliberate Plasmodium falciparum infections in tertiary syphilis patients. Trans R Soc Trop Med Hyg. 2006, 100 (9): 811816. 10.1016/j.trstmh.2005.11.001.
 33.
Smith DL, McKenzie FE, Snow RW, Hay SI: Revisiting the basic reproductive number for malaria and its implications for malaria control. PLoS Biol. 2007, 5 (3): e4210.1371/journal.pbio.0050042.
 34.
Le Menach A, Takala S, McKenzie FE, Perisse A, Harris A, Flahault A, Smith DL: An elaborated feeding cycle model for reductions in vectorial capacity of nightbiting mosquitoes by insecticidetreated nets. Malar J. 2007, 6: 1010.1186/14752875610.
 35.
Killeen GF, Smith TA: Exploring the contributions of bed nets, cattle, insecticides and excitorepellency to malaria control: a deterministic model of mosquito hostseeking behaviour and mortality. Trans R Soc Trop Med Hyg. 2007, 101 (9): 867880. 10.1016/j.trstmh.2007.04.022.
 36.
Smith TA: Estimation of heterogeneity in malaria transmission by stochastic modelling of apparent deviations from mass action kinetics. Malar J. 2008, 7: 1210.1186/14752875712.
 37.
Hurlbert SH: The Nonconcept of Species Diversity: A Critique and Alternative Parameters. Ecology. 1971, 52 (4): 577586. 10.2307/1934145.
 38.
W.H.O.: Expert Committee on Malaria, Sixth Report. World Health Organization Technical Report Series. 1957, Geneva, Switzerland: World Health Organization, 123:
 39.
Hay SI, Guerra CA, Gething PW, Patil AP, Tatem AJ, Noor AM, Kabaria CW, Manh BH, Elyazar IR, Brooker S, Smith DL, Moyeed RA, Snow RW: World malaria map: Plasmodium falciparum endemicity in 2007. PLoS Medicine. 2009, 6: e1000048
 40.
Noor AM, Mutheu JJ, Tatem AJ, Hay SI, Snow RW: Insecticidetreated net coverage in Africa: mapping progress in 2000–07. Lancet. 2009, 373 (9657): 5867. 10.1016/S01406736(08)615962.
Acknowledgements
Thanks to Eili Klein, F. Ellis McKenzie, Abdisalan M. Noor, Robert W. Snow and Andrew J. Tatem for comments on the manuscript. The R code used to generate all of the figures is freely available upon request. DLS is supported by a grant from the Bill & Melinda Gates Foundation (#49446) and funding from the RAPIDD program of the Science & Technology Directorate, Department of Homeland Security, and the Fogarty International Center, National Institutes of Health. SIH is funded by a Senior Research Fellowship from the Wellcome Trust (#079091). The authors acknowledge the support of the Emerging Pathogens Institute, University of Florida. This work also forms part of the output of the Malaria Atlas Project (MAP, http://www.map.ox.ac.uk), principally funded by the Wellcome Trust, UK.
Author information
Additional information
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
DLS wrote the first draft of the manuscript and outlined the models. SIH contributed to the refining of the models and the writing of the manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Received
Accepted
Published
DOI
Keywords
 Malaria
 Malaria Control
 Mass Drug Administration
 Malaria Elimination
 Entomological Inoculation Rate
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate. Please note that comments may be removed without notice if they are flagged by another user or do not comply with our community guidelines.