Clinically immune hosts as a refuge for drug-sensitive malaria parasites
© Klein et al; licensee BioMed Central Ltd. 2008
Received: 28 January 2008
Accepted: 25 April 2008
Published: 25 April 2008
Mutations in Plasmodium falciparum that confer resistance to first-line antimalarial drugs have spread throughout the world from a few independent foci, all located in areas that were likely characterized by low or unstable malaria transmission. One of the striking differences between areas of low or unstable malaria transmission and hyperendemic areas is the difference in the size of the population of immune individuals. However, epidemiological models of malaria transmission have generally ignored the role of immune individuals in transmission, assuming that they do not affect the fitness of the parasite. This model reconsiders the role of immunity in the dynamics of malaria transmission and its impact on the evolution of antimalarial drug resistance under the assumption that immune individuals are infectious.
The model is constructed as a two-stage susceptible-infected-susceptible (SIS) model of malaria transmission that assumes that individuals build up clinical immunity over a period of years. This immunity reduces the frequency and severity of clinical symptoms, and thus their use of drugs. It also reduces an individual's level of infectiousness, but does not impact the likelihood of becoming infected.
Simulations found that with the introduction of resistance into a population, clinical immunity can significantly alter the fitness of the resistant parasite, and thereby impact the ability of the resistant parasite to spread from an initial host by reducing the effective reproductive number of the resistant parasite as transmission intensity increases. At high transmission levels, despite a higher basic reproductive number, R0, the effective reproductive number of the resistant parasite may fall below the reproductive number of the sensitive parasite.
These results suggest that high-levels of clinical immunity create a natural ecological refuge for drug-sensitive parasites. This provides an epidemiological rationale for historical patterns of resistance emergence and suggests that future outbreaks of resistance are more likely to occur in low- or unstable-transmission settings. This finding has implications for the design of drug policies and the formulation of malaria control strategies, especially those that lower malaria transmission intensity.
Malaria is the leading cause of death in children under five in sub-Saharan Africa . Prompt treatment with effective antimalarial drugs could prevent much of the morbidity and mortality associated with clinical malaria, but the evolution of resistance has diminished the therapeutic efficacy of two previous first-line antimalarials, chloroquine (CQ) and sulphadoxine-pyrimethamine (SP). Historically, it has been suggested that resistance to both CQ and SP emerged from a limited number of de novo selection events in areas of low or unstable transmission [2, 3]. Genetic evidence suggests that most CQ-resistant parasites in the world today are descended from one of four founder events [4, 5] that occurred in Southeast Asia, South America and Papua New Guinea, and then spread to other regions, including sub-Saharan Africa. Evidence also suggests that resistance to SP originated from only a few foci [6–8]. Several hypotheses about the de novo mutation rate and the selection pressure resistant parasites face and their relation to transmission intensity have been proposed to explain why CQ resistance originated in what is presumed to be low or unstable transmission areas outside of sub-Saharan Africa, including (a) a lower frequency of resistant alleles in higher transmission areas because of within-host competition ; (b) less drug treatment (per parasite) in higher transmission areas [2, 9, 10]; and (c) a lower frequency of selfing in higher transmission areas, which increases the probability that multilocus resistant genotypes will be broken up by the action of Mendelian segregation [9, 11, 12]. An additional explanation is that in high transmission areas, where immunity is better developed, mutant parasites are less likely to survive a host immune response [10, 13].
Although the evolution of resistant parasites within a single host is a significant risk factor for the emergence of resistance within a population, the effectiveness of an antimalarial drug is affected only if these resistant parasites spread, a process that is driven both by the overall rate of transmission and by the relative fitness of drug-resistant and drug-sensitive parasites. Parasite fitness is related to the population treatment rate and to the biological cost of resistance. Because of differences in vector ecology and biting preferences, transmission intensities vary from less than one infectious bite per decade to more than 1,000 per year , and the basic reproductive number (R0) can exceed 3,000 . Higher transmission intensity is associated with a higher level of clinical immunity to malaria – reduced frequency and severity of clinical symptoms in older children and adults – which results in a reduction in the need for antimalarial drugs [16–19]. Immunity to malaria has consequences for transmission as well; blood-stage immunity reduces asexual parasite and gametocyte densities in older children and adults , and transmission-blocking immunity can block development of the parasite in the mosquito . Importantly, despite significant reductions in clinical symptoms and infectiousness, older individuals still become infected and remain infectious to mosquitoes, albeit at relatively lower levels, even in holoendemic areas [22–24].
Even though immunity affects both the transmission dynamics and treatment rates, epidemiological models have generally assumed that immune individuals are not infectious to mosquitoes, and thus do not contribute to parasite fitness [20, 25–27]. Consequently, an epidemiological model for the spread of resistance found no difference in the ability of resistant parasites to spread at different transmission rates , or why resistance to CQ emerged outside of sub-Saharan Africa.
This paper reconsiders the role of immunity in the transmission dynamics of malaria and its effect on the evolution of antimalarial drug resistance under the assumption that immune individuals are infectious. Using a novel epidemiological model with two immune stages, nonimmune and clinically immune, the role of immunity in the emergence of resistance is reexamined based on quantitative effects associated with clinical immunity. Individuals in the clinically immune stage have lower transmission, lower incidence of clinical disease, and consequently a lower rate of drug treatment. Based on the defined relationship between transmission intensity, immunity, and clinical malaria, the model is used to explore the relationship between vector ecology, human epidemiology, and the ability of a resistant parasite to spread.
Individuals living in areas of endemic P. falciparum transmission develop immunity to malaria with age  and exposure [29, 30]; immunity is manifest as a decline in parasite densities (both trophozoites and gametocytes) in the blood , a lower probability of transmission from humans to mosquitoes [22, 23], and a decline in the frequency and severity of clinical malaria [16–19], though little decline in the probability of becoming infected [24, 31]. Thus, it is assumed that individuals develop a form of clinical immunity over time in which they are less likely to infect mosquitoes or manifest clinical symptoms but are no less likely to become infected.
The model is based on earlier models developed for the Garki Project , in which individuals acquire immunity after being infected for a period of time. However, the number of infected classes was simplified and the assumption that individuals develop full transmission-blocking immunity was relaxed. As with the Garki model, clinical immunity is incorporated as a second immune stage in a susceptible-infected-susceptible (SIS) model. Though, in this model clinically immune individuals remain infectious to mosquitoes and infect mosquitoes with lower probability; also, a smaller fraction of new infections progress to clinical malaria. Clinical episodes of malaria are important for the evolution of resistance because individuals who develop clinical symptoms are more likely to seek treatment; thus an increasing frequency of clinical episodes is associated with increasing drug pressure. Consequently, in this model clinically immune individuals represent a refuge for drug-sensitive pathogens because of lower treatment rates. The evolution of resistance is incorporated by assuming that individuals can be infected by either resistant or sensitive parasites.
It is assumed that both nonimmune and clinically immune individuals can be susceptible, infected with sensitive parasites, or infected with resistant parasites. The human population density in each state is denoted S i , I wi , I xi , where the subscripts w and x denote infections with drug-sensitive wild-type and resistant phenotypes, respectively, and the i subscript denotes the immune stage. The population size is normalized to one, and the population birthrate B is set equal to the per capita death rate of the human population, μ, so that the total population size stays constant.
Model notation follows Macdonald  and Smith and McKenzie ; m denotes the number of mosquitoes per human and a the human feeding rate (the number of bites on humans per mosquito per day). The instantaneous death rate is g (e-gis the probability of a mosquito surviving one day), and n is the number of days required for sporogony. Vectorial capacity (V), the number of infectious bites by a mosquito over its lifetime, is then given by the formula V = ma2e-gn/g.
The fraction P of bites on humans that infect a mosquito depends on the differing transmission intensities of the two-stages, c1 and c2, and the number of humans in each stage; thus P = c1(Iw 1+ Ix 1) + c2(Iw 2+ Ix 2). The sporozoite rate, or the fraction of infectious mosquitoes, is aPe-gn/(g + aP). The entomological inoculation rate (EIR), the number of infectious bites per person per day, is calculated as the product of the human biting rate (ma) and the sporozoite rate (aPe-gn/(g + aP)). The force of infection, or happenings rate (h), is b EIR, where b, the infectivity rate, measures the fraction of bites in humans that produce a patent infection. It follows that h=(bVP)/(1 + sP), where s = a/g is called the stability index, the number of bites on a human per vector per lifetime. The fraction of infections that are drug sensitive is F w = (c1Iw 1+ c2Iw 2)/P and the fraction that are drug resistant is F x = (c1Ix 1+ c2Ix 2)/P. Happenings rates for drug-sensitive and drug-resistant infections are h w = F w h and h x = F x h, respectively.
Immunity acquisition and parasite clearance
Clinical immunity is assumed to develop in infected individuals after ten years. Once individuals gain immunity, protection is retained through biting and is lost at a faster rate (γ) than it is gained (θ). The values are based on a significant number of age-prevalence studies suggesting that children acquire immunity after approximately five to 10 years [29, 30, 34], and additional studies that suggest a strong role of biting in maintaining immunity, and a loss of immunity that occurs after exposure to infection is eliminated . Because not all infections result in fever and other associated symptoms, it is assumed that clinical symptoms arise in infected individuals at a rate σ i and that a fraction f i are treated and cleared of parasites. Thus, existing infections are cleared by drugs at the rate ρ i = f i σ i . It is further assumed that a fraction of new infections ξ i in susceptible individuals develop clinical symptoms and are treated with drugs and cleared immediately prior to the development of gametocytes, thus precluding the possibility of transmission. In these individuals it is as if the infection never occurred.
Mutations conferring resistance to antimalarial drugs are likely to be disadvantageous to the parasite. For example, resistance to CQ in P. falciparum has been shown to have a fitness cost of approximately 25 percent in vitro  and 5 percent in vivo [37, 38]. Although a fitness cost could conceivably occur at any or all stages of the parasite life-cycle, where it is implemented in this model is not particularly important for the transmission dynamics (though it could be important in other models), so it is assumed that resistant infections are cleared at a faster rate and therefore transmit for a relatively shorter period. Thus, infections clear naturally at rate r w when an individual is infected with a drug-sensitive phenotype and r x for drug-resistant infections.
Baseline Parameter Values
Acquisition of clinical immunity
Loss of clinical immunity
Fraction of new infections that are treated and cleared
Rate clinical symptoms arise (σ i ) times Fraction treated (f i ) equals rate existing infections are cleared by drugs (ρ i )
σ1f1 = ρ1
0.025(0.2) = 1/200
σ2f2 = ρ2
0.01(0.2) = 1/500
Disease induced death rate
Human feeding rate
Mosquito death rate
Number of days required for sporogony
r w (fitness cost)
Because symptomatic individuals are more likely to use antimalarial drugs, the number of individuals experiencing a clinical episode affects the transmission dynamics by changing the drug pressure facing the parasite. Individuals that acquire clinical immunity, have reduced rates of clinical episodes [16–19], which reduces the rate of drug use. Though individuals will continue to receive antimalarial treatments throughout their lives, these treatments occur less frequently as immunity increases, and often can be unconnected to the peaks of parasitemia . This reduction in the treatment rate reduces the resistance selection pressure, providing a refuge for drug-sensitive parasites. In previous epidemiological models of transmission, these immune individuals were not assumed to have a significant qualitative effect on the dynamics of the system, because young children were assumed to dominate transmission events . However, clinically immune individuals are infectious and can significantly affect the dynamics of transmission when the distribution between sensitive and resistant infections is different in nonimmune and clinically immune individuals.
Previous models suggested that the parasite with the highest R0 would be the most fit and should predominate [27, 40]. That conclusion always holds when r x = r w , c1 = c2, and ρ1 = ρ2. However, differences in the drug treatment rates between clinically immune and nonimmune individuals can change the result, and it was found that resistant parasites may not spread even when they have the dominant R0. This can be explained by calculating the effective reproductive number of the resistant parasite, R x , where R x = R0,xd, and d is the fraction of the population that can be infected and will transmit the resistant infection. The effective reproductive number of the resistant parasite is
R x = (S1 + S2)((1 - f) R0,x 1+ fR0,x 2) (9)
where f is the fraction of the population that is clinically immune, and S1 and S2 are the proportion of the population that is susceptible and nonimmune, and susceptible and clinically immune, respectively.
Simulations of the model found a significant relationship between malaria immunity and the ability of resistant parasites to spread from an initial locus. Previous epidemiological models of malaria transmission assumed that immune individuals were not infectious; however, the best available evidence in malaria suggests that immune individuals remain infectious, though they transmit less efficiently to mosquitoes [22–24, 31] and the frequency and severity of clinical disease declines [16–19]. Because they remain infectious but asymptomatically infected, their relatively lower usage of antimalarials creates a natural refuge for sensitive parasites, similar to the way nontransgenic crops act as refugia for Bt-sensitive insects in agriculture . Increases in the transmission rate result in concomitant increases in the proportion of clinically immune individuals, which increases the size of the refuge and reduces the ability of the resistant parasite to spread. This suggests an epidemiological rationale for the more likely emergence of resistance in low- or unstable-transmission settings.
The presence of a refuge of clinically immune individuals alters the ecological landscape that resistant parasites face, and introduces a mechanism for the coexistence of resistant and sensitive parasites. Simple models of directly transmitted infections , and a previous model of malaria transmission , suggested there was a critical threshold level of treatment above which resistance would fix and below which it would not spread. However, in those models, there was either no immunity, or immune individuals were assumed to be noninfectious and were, therefore, irrelevant for transmission and selection for resistance. Clinical immunity changes the criteria for determining the critical threshold so that the fraction of clinical episodes that are treated, as well as the level of immunity in the community, which determines the fraction of new infections that result in a clinical episode, are both important. Therefore, in populations where immunity has developed, the resistant parasite faces a different fitness landscape; they may not be the most fit, despite having the highest R0, which can prevent the parasite from either fixing or spreading. This result also suggests that differential treatment levels of host-groups can create differential ecological niches allowing the resistant and sensitive parasites to coexist .
History of epidemiological models of malaria
There is a striking difference between the findings of this paper and a previously published epidemiological model of antimalarial resistance . To explain the differences, a brief history of malaria models is warranted. A quantitative approach to malaria epidemiology organized around the parasite life-cycle was first described mathematically by Ross , and later revised by Macdonald to consider mosquito mortality during sporogony [32, 44]. In the 1970s several major innovations in malaria modeling were first introduced and field-tested during a malaria control project in the Garki region of Nigeria . The mathematical model of control developed for the Garki project considered the clearance of infection in hosts that have been infected by more than one parasite brood [20, 45], and the development of blood-stage immunity and transmission-blocking immunity in the human host . Despite a model that assumed parasite infections were complex and evidence that gametocytes remain present throughout life, the Garki model made a simplifying assumption that new infections remained infectious for a short period of time. Thereafter, infections persisted until the person either cleared the infection or developed immunity. The Garki model called this a semi-immune state. In this semi-immune state, humans could become re-infected, but they were never infectious. Mathematical epidemiologists later noted that individuals who were infected but not infectious were epidemiologically irrelevant for transmission, and the Garki model was simplified into an SIRS compartment model in which the dynamics of infection in the semi-immune population were replaced by a recovered and immune state with immune boosting [25, 26]. The SIRS model was a familiar model to mathematical epidemiologists, and it has been the basis for many subsequent papers on malaria epidemiology, but the assumptions about immunity have been propagated and revised without much critical thought.
This paper is an attempt to demonstrate the importance of immunity in modeling the transmission dynamics of malaria with respect to the introduction of resistance. While the implications of the results are significant for drug policy, it is prudent to note that as with all models a number of simplifying assumptions have been made. In incorporating immunity, the process of immunity acquisition has been simplified so that individuals acquire immunity in a stepwise fashion after 10 years of continuous infection, and they lose immunity after two years of continuous non-infection. This is a simplification of the complicated process that is immunity. It ignores age effects, differences between immune individuals at older ages and younger ages, and faster acquisition of immunity, which may occur in areas of higher transmission  or after fewer challenges in low transmission areas . While this is a simplification, evidence suggests that it gives a representation of reality that is close enough to make qualitative observations [29, 30, 34, 35]. Despite the simplification of immunity, the basic model (without resistance) accords well with both field data and other models of transmission dynamics, and changes in these values did not change the qualitative results. Thus, the model, as formulated, likely captures the qualitative differences that exist between areas with different transmission levels, and is, hopefully, only the first step in more detailed modeling of the spread of antimalarial resistance which takes account of the importance of immunity.
The link between the transmission rate and the probability that de novo mutants can both arise and spread is a critical issue for developing strategies to mitigate resistance emergence. Though it is impossible to be certain, historical analysis of the evolution of resistance has suggested that it originated in low or unstable transmission areas [2, 3]. Quantitative population genetic models have supported this assertion, suggesting that there may be genetic reasons why resistance is less likely to evolve in high-transmission settings [3, 9, 11, 12], but individual models may not always explain population-level phenomena. Epidemiological models, which can take account of specific population characteristics, have been hampered by the assumption that immune individuals play no qualitative role in the dynamics of transmission. Consequently, an epidemiological model could not offer an explanation for why resistance emerged outside Africa . The model in this paper demonstrates that the existence of a refuge for drug-sensitive parasites in high-transmission areas can slow or prevent the evolution of resistance; this has enormous implications for the design of effective malaria control strategies.
Efforts to control malaria have been undermined by the emergence of resistance, which now exists to all known antimalarials except the artemisinin compounds. To help ensure a longer period of efficacy for artemisinin, the World Health Organization has proposed a global subsidy to comply with its mandate that all new artemisinin-based therapies be deployed as combinations . One concern with this strategy is that increased use in high-transmission areas may engender resistance at a faster rate. The results as determined by this model, mitigates that concern, showing that the existence of a refuge of immune individuals makes this outcome highly unlikely. However, in areas with low transmission intensity, the relative paucity of immune individuals increases the risk that resistance will emerge. Because the emergence of resistance to an antimalarial in any country threatens the viability of the drug in all countries , areas of relatively lower transmission should be a focus in controlling the emergence of resistance. As a corollary, eliminating malaria from areas of low transmission intensity may have the global benefit of prolonging the effective lifetime of antimalarial drugs.
Although areas of low transmission should implement strategies to reduce the likelihood of resistance, high-transmission areas are also a concern because transmission intensity is reduced through mass distribution of insecticide-treated bed nets. The analysis in this paper suggests that among-host selection for resistance increases as functional immunity wanes and the refuge for drug-sensitive parasites shrinks or disappears. Thus, implementation of transmission reduction strategies should also include improved surveillance for drug resistance with resources to deploy appropriate containment strategies to prevent the geographical dissemination of resistance.
The intention of this study was to evaluate the qualitative importance of immunity in the transmission dynamics of malaria and its role in the development of resistance. Epidemiological models of malaria transmission, which can synthesize various factors about how emergence and spread are linked to the composition of the population, can be useful tools in determining optimal drug treatment strategies to extend the effective life of newly introduced therapies; however, they must take account of immune individuals and the refuge they provide for sensitive parasites.
We are grateful to Peter Billingsley and Sunetra Gupta for their input on the design of the model as well as Karen I Barnes, Anders Bjorkman, Ian C Boulton, Karen P Day, Abdoulaye Djimde, Arjen M Dondorp, Ogobara Doumbo, Rose McGready, Malcolm Molyneux, Myaing M Nyunt, Christopher V Plowe, Ric N Price, Allan Schapira and Nicholas J White for their comments on the model at the Gordon Research Conference on Malaria. This research was supported by a grant from the Bill & Melinda Gates Foundation. Decisions concerning the study design; the collection, analysis, and interpretation of data; the writing of the manuscript; and the decision to submit the manuscript for publication, were made entirely by the authors with no input from the Bill & Melinda Gates Foundation.
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