PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of procbThe Royal Society PublishingProceedings BAboutBrowse by SubjectAlertsFree Trial
 
Proc Biol Sci. 2017 December 20; 284(1869): 20171880.
Published online 2017 December 20. doi:  10.1098/rspb.2017.1880
PMCID: PMC5745407

Rabies elimination research: juxtaposing optimism, pragmatism and realism

Abstract

More than 100 years of research has now been conducted into the prevention, control and elimination of rabies with safe and highly efficacious vaccines developed for use in human and animal populations. Domestic dogs are a major reservoir for rabies, and although considerable advances have been made towards the elimination and control of canine rabies in many parts of the world, the disease continues to kill tens of thousands of people every year in Africa and Asia. Policy efforts are now being directed towards a global target of zero human deaths from dog-mediated rabies by 2030 and the global elimination of canine rabies. Here we demonstrate how research provides a cause for optimism as to the feasibility of these goals through strategies based around mass dog vaccination. We summarize some of the pragmatic insights generated from rabies epidemiology and dog ecology research that can improve the design of dog vaccination strategies in low- and middle-income countries and which should encourage implementation without further delay. We also highlight the need for realism in reaching the feasible, although technically more difficult and longer-term goal of global elimination of canine rabies. Finally, we discuss how research on rabies has broader relevance to the control and elimination of a suite of diseases of current concern to human and animal health, providing an exemplar of the value of a ‘One Health’ approach.

Keywords: rabies, elimination, dog vaccination, One Health, neglected tropical disease

1. Introduction

For thousands of years, people have lived in fear of rabies transmitted from domestic dogs, and more than half of the world's population still do so today. From the time of the first written reference to rabies in the 23rd century BC, the link between the bite of a mad dog and the risk of human death has been well recognized [1,2]. Although many mammalian hosts can be infected with the rabies virus, the domestic dog remains to this day by far the most important species causing human rabies deaths and tens of thousands of people die from canine-mediated rabies each year [3,4], mostly in Asia and Africa where the disease is maintained in domestic dog reservoirs.

In developing the first vaccines against rabies, Louis Pasteur recognized the potential for eliminating human rabies deaths, and considered that ‘to solve the problem of rabies would be a blessing for humanity’ [5]. The need for and feasibility of rabies elimination through interventions in the dog population has also been recognized for more than a century. Since the first large-scale implementation of canine vaccination in the 1920s, canine rabies has now been eliminated in several parts of the world, for example in island and peninsula states of Asia (e.g. Japan, Taiwan), in the USA, western Europe and across parts of Latin America [1,6,7].

In this review, we address the reasons why, despite the long history of rabies research and earlier successes in canine rabies elimination, new research has been needed to tackle the problem of rabies in low- and middle-income countries (LMICs) of Africa and Asia. We demonstrate how research has generated optimism about the feasibility of achieving global targets of zero human deaths from dog-mediated rabies, guided pragmatism in the design of dog vaccination strategies in LMICs, and instilled realism in the path towards global canine rabies elimination.

2. Shifting priorities in rabies research

While the first decades of rabies research focused on the problem in domestic dogs, the successful control of canine rabies in many of the world's richer countries shifted emphasis towards the growing problem of wildlife rabies. During World War II, the red fox (Vulpes vulpes) emerged as the main rabies reservoir in Europe, and the disease spread rapidly affecting most of western and southeastern Europe by the mid-1970s [8]. In response, rabies research efforts focused on development of oral rabies vaccines and vaccination strategies for wildlife (figure 1), with large-scale distribution of oral bait vaccines across western Europe in the 1980s and 1990s [8]. Over 25 years, oral vaccination of foxes has resulted in the elimination of the rabies virus from western Europe, with rapid progress being made towards elimination in eastern Europe [9].

Figure 1.
Number of journal articles published on rabies from 1960 to 2016 illustrating: (a) the shift in emphasis from oral vaccination of wildlife in the 1980s and 1990s to dog vaccination from 2000s; and (b) the increase in publications relating to canine rabies ...

Over this same time period, canine rabies was being brought under control in north America, and research efforts independently became directed to the emerging problem of wildlife rabies focusing on control of rabies in terrestrial carnivore reservoirs [10]. A further concern in north America related to bat-transmitted rabies [11], coinciding with a growing interest in bats as hosts of a wider range of Lyssaviruses, [12] and other emerging pathogens of global concern, such as SARS coronavirus, Ebola virus and MERS coronavirus.

It is not surprising that set against this backdrop, research into the control of canine rabies in LMICs received only limited attention during the latter part of the twentieth century (figure 1). However, this resulted in a deficit of data and understanding of the burden and scale of the disease in poorer parts of the world and limited interest in potential solutions, reinforcing a cycle of neglect [13].

3. Insights from studies on the global burden of canine rabies

It has always been known that dog bites are an important source of human rabies exposures worldwide, but reliable data have been lacking on the number of dog-mediated human rabies deaths [14], with the few hundred deaths officially reported in the African region [15] widely recognized to be a major underestimate.

An initial approach to estimating human rabies deaths in Africa used a probability decision tree model that incorporated data on the incidence of bite injuries from suspected rabid dogs and availability of post-exposure prophylaxis (PEP) [16]. This was first applied in Tanzania and then used to generate country- and regional-level estimates of human deaths across Africa and Asia [1721] and to assess the economic impacts of canine rabies [22]. Further refinements resulted in more detailed and comprehensive estimates of global disease burden by country [4]. These studies indicated that more than 99% of canine-mediated rabies deaths occurred in Africa and Asia, with a global estimate of 59 000 (95% confidence interval (CI) 25 000–159 000) deaths in 2010 [4]. Other approaches have been adopted by the Global Burden of Disease (GBD) collaborators, including a cause of death ensemble modelling approach, which have generated estimates ranging from 54 100 deaths (95% CI 32 400–103 400) in 1990, 26 400 (95% CI 15 200–45 200) in 2010, 23 500 (95% CI 17 300–28 600) in 2013, and 13 300 in 2016 (95% CI 7200–19 100) [3,23,24].

It is well recognized that these modelling approaches all have limitations, particularly in the degree of extrapolation from data that is of variable quality, from a limited geographical area or that has been generated indirectly [25]. For several neglected tropical diseases (NTDs), GBD figures are thought likely to represent an underestimate of current disease burden [26]. For rabies, there is no evidence that control measures have been implemented on a scale that would explain the dramatic recent decline in deaths indicated by the GBD estimates [23,24]. GBD estimates rely on vital registration and verbal autopsy data and these are very limited or absent in many of the countries where rabies and other NTDs are most prevalent [24]. Another critical issue is the appropriate modelling of pathways from infection to disease and death [26]. While the rabies probability tree study [4] was also limited by data quality and availability, this analysis incorporated detailed data from disease-specific research in rabies-endemic countries and was based on a well-defined series of steps from rabies exposure to death. We draw further confidence from comparison with estimates derived from empirical studies. For example, annual human rabies deaths in India were estimated at 20 565 through a multi-centre community survey conducted in 2003 [27], very similar to the figure of 20 847 deaths derived for India in 2010 through the probability tree approach [4].

The PEP data used in the probability tree model also provided important information for demonstrating the economic burden of canine rabies, indicating that $1.7 billion direct costs were incurred annually in providing PEP for 29 million dog-bite victims in canine-endemic countries [4] (figure 2). Regionally, the highest expenditure is seen in Asia ($1.4 billion annually) reflecting a continuing high demand for PEP in areas where canine rabies has not been brought under control, and contrasting with Latin America where, despite much lower annual expenditure on PEP ($129 million), the region is on the brink of eliminating canine-mediated human rabies as a result of relatively modest investments in mass dog vaccination ($61 million) [4]. These data contribute to a growing body of evidence that the most cost-effective preventive strategies are those underpinned by mass dog vaccination rather than reliance on PEP alone [2830].

Figure 2.
Schematic illustrating the impacts of canine rabies and role of domestic dogs in maintaining rabies transmission (shown by solid lines). Other host species (humans, livestock and wildlife) may be infected as a result of spillover transmission from dogs ...

Compiling data for the global burden study also highlighted PEP availability as a major determinant of human rabies deaths, with cases occurring disproportionately in impoverished rural communities. Detailed contact tracing studies reveal the extent to which people have struggled to obtain PEP and the consequences of the resulting delays [31,32], which invariably include intense anxiety as bite victims await an uncertain outcome and, in some cases, the development of a horrifying and fatal disease.

While human deaths and high PEP costs dominate in burden of disease studies, several other components of disease burden are also of concern, including livestock losses, which still remain poorly quantified but can have important impacts [22,33] and wildlife conservation, with canine rabies threatening several endangered wildlife populations including the Ethiopian wolf (Canis simensis) and African wild dog (Lycaon pictus) [34] (figure 2).

4. The feasibility of canine rabies elimination: a cause for optimism

A considerable body of research now exists to demonstrate the feasibility of canine rabies elimination. The basic reproductive number, R0, a key parameter used to understand the effectiveness of control interventions, is usually measured from the growth rates of epidemics. Applying this approach to canine rabies demonstrates that R0 is typically between 1 and 2 in populations that differ in density by an order of magnitude [3537]. Alternative approaches to estimating transmission are all consistent with this low value of R0 [29,36,38,39] suggesting that rabies should be easily controlled through mass dog vaccination and, conversely, that approaches based on reducing dog density are likely to be ineffective [40]. Theoretical and empirical research has demonstrated that rabies can be eliminated where 70% coverage is sustained [35,36]. By contrast, attempts to reduce dog population density through indiscriminate culling have consistently failed to control rabies outbreaks [41] and, in some cases, have increased disease spread through human-mediated dog movements [37]. Muzzling, restriction of dog movements, and selective removal or euthanasia of unowned dogs have historically been part of successful dog rabies control, including in the UK and USA [1,42], but these measures are distinguished from indiscriminate culling operations in being specifically targeted to reduce rabies transmission risk rather than to reduce dog population size or density.

The question of rabies reservoir dynamics has long been debated [6,4347], and is of major importance in sub-Saharan Africa where the abundance of wildlife has been seen as an obstacle for canine rabies control that would render elimination efforts futile [15]. However, despite the fact that rabies can infect all mammalian species, only a few hosts are capable of maintaining infection as reservoirs, with ecological and genetic factors both likely to be important determinants of rabies reservoirs [46,47]. While rabies virus variants are typically maintained by only a single mammalian host species, multiple variants may circulate in an area [47]. However, this need not be an insurmountable obstacle to canine rabies elimination, as shown by countries in Latin America and in the USA, where canine rabies has been brought under control or eliminated even though rabies variants circulate in wild mammal populations. The overlapping circulation of multiple variants does, however, introduce different surveillance requirements for verifying the elimination of the canine rabies variant.

Establishing the reservoir of multi host pathogens is not easy and typically requires integration of multiple lines of evidence [44,48]. In the Serengeti ecosystem, Tanzania, inference from both epidemiological and genetic data supports the idea of rabies being maintained in domestic dogs not wildlife, with occasional spillover from domestic dogs into wildlife resulting in short-lived chains of infection that are not sustained [4951]. The conclusion from these studies is that control of canine rabies should eliminate infection in dogs, wildlife and people. It is unclear the extent to which the Serengeti scenario is generalizable more globally, but currently there is no clear evidence that, in areas with domestic dog reservoirs, the canine rabies virus variants circulating in dogs are maintained independently in wildlife. In South Africa, a canine variant circulates in jackals in the Limpopo region [52], but it is still unknown whether this cycle will be sustained in the absence of canine rabies, which has now been well controlled in the area. If so, vaccination of jackals may be needed to achieve canine rabies elimination, but this is likely to be feasible given the demonstration of the safety, efficacy and feasibility of oral vaccination in jackals from earlier work in Zimbabwe and Israel [5356].

Demonstration of the operational feasibility of mass dog vaccination provides a further cause for optimism. Evidence now exists to show that, contrary to widely held perceptions, the vast majority of dogs in Africa have owners, dog accessibility is higher than often recognized, and achieving target levels of vaccination coverage is feasible [57,58]. In south and southeast Asia, the situation may be more challenging as a result of a larger population of less accessible community or ‘street’ dogs, but target levels of vaccination coverage have also been achieved in these communities where campaigns are well organized [37,59,60].

In summary, the last decade has seen a rapid expansion of research into canine rabies vaccination and canine rabies elimination (figure 1) generating optimism that canine rabies can be effectively controlled, and ultimately eliminated, through mass dog vaccination and that this is the underpinning strategy needed to reach the 2030 target for elimination of human deaths from canine-mediated rabies [61]. The health and economic benefits would be substantial [22] (figure 2).

5. Strategies for control and elimination of canine rabies: a case for pragmatism

While it is often recommended that a detailed understanding of dog ecology is needed for effective canine rabies control, the consistency of research findings generated over the past 30 years allows us to be confident in concluding that mass dog vaccination is feasible across a wide range of settings and campaigns can and should be initiated without delay. In some cases, more nuanced understanding may be required to improve coverage, but these insights can be often be gained through implementation of control measures and used to progressively improve the design and delivery of subsequent interventions. Key considerations include the nature and degree of community engagement, timing of campaigns, placement of vaccination stations and whether or not to charge owner fees [6264]. The costs of implementing campaigns free of charge may exceed those readily available to government veterinary services [65], but many approaches can still be explored to improve affordability, acceptability and cost-effectiveness [66].

While there is widespread agreement about the central importance of mass dog vaccination in canine rabies control and elimination, the role of dog population management remains the subject of debate [67]. There is a rich literature around fertility control for management of roaming dog and wildlife populations [68,69]. However, as rabies transmission varies little with dog density, reproductive control measures carried out with the aim of reducing dog density are not likely to be effective for rabies control. In theory, reducing population turnover (e.g. through improving life expectancy and/or reducing fecundity) could help sustain population immunity between campaigns and improve cost-effectiveness. However, there is little empirical evidence that dog population management tools have been able to achieve this [67]. Furthermore, even in populations with a high turnover, achieving a 70% coverage during annual campaigns has been sufficient to sustain population immunity above critical thresholds determined by R0 [70]. The relatively high cost of sterilization also means that strategies which combine vaccination and sterilization are less cost-effective in terms of achieving human health outcomes than strategies based on dog vaccination alone, even in populations with a large proportion of roaming dogs [39]. Improved dog population management is undoubtedly a desirable longer-term goal for animal health and welfare and may have important secondary benefits for rabies control, for example by enhancing community or political support [67]. However, a focus on mass dog vaccination currently remains the most pragmatic and cost-effective approach to canine rabies control and elimination.

The limited availability and quality of routine animal rabies surveillance data in LMICs [14] has been an obstacle to the application of the analytical approaches from which we have learned so much about wildlife rabies. ‘Gold standard’ surveillance data based on laboratory-confirmed diagnosis is hampered not only by limited laboratory infrastructure but also by the practical challenges of locating, sampling and submitting specimens [71]. However, pragmatic approaches to improving rabies surveillance have yielded rich insights. In addition to providing a foundation for burden of disease estimates, data on animal-bite injuries have been a used as a reliable indicator of canine rabies incidence, revealing new understanding of rabies metapopulation dynamics [50], as well as improving detection of animal rabies cases, the management of animal bites and the cost-effectiveness of PEP [36,72].

Pragmatic solutions are also being found to improve rabies diagnosis in settings with limited laboratory infrastructure, including techniques to support decentralized laboratory testing (e.g. direct rapid immunohistochemical test, dRIT) [7376] and field diagnosis (e.g. immunochromatographic tests) [7779]. These have great potential for empowering field staff to engage in rabies surveillance and respond more effectively to surveillance data, but standardization and quality control of field diagnostic kits still needs improvement [80]. Given the rapid advances in metagenomic sequencing methods [81], future approaches may include real-time genomic surveillance. However, even simple technologies such as mobile phones can serve as leapfrogging technology that can dramatically improve the extent and resolution of rabies surveillance data [82].

6. Instilling realism on the path to elimination

While operational research on dog vaccination provides grounds for optimism, awareness is growing about the challenges, complexities and time scales of moving from control to elimination (figure 3).

Figure 3.
Hypothetical timeline of rabies control and elimination highlighting policy targets and epidemiological milestones, illustrating relative rapid progress to zero human deaths but the need for sustained effort to reach elimination of canine rabies and sustained ...

Given the low R0 for rabies, deterministic models of transmission predict that rabies should be eliminated very rapidly [29,30,8385]. But, these dynamic models typically assume that dog vaccination campaigns consistently achieve high and uniform levels of coverage. By contrast, analyses of rabies surveillance and control data indicate that vaccination coverage implemented during campaigns is often patchy and that time to rabies elimination is prolonged [37,86,87]. Once assumptions about the implementation of vaccination campaigns are more realistic, and rabies is considered on a spatial landscape, predictions about the time scale to elimination are tempered [86].

The disparities between theory and practice demand approaches that capture realism. It may be argued that the feasibility and effectiveness of mass dog vaccination should have been self-evident given the successes in Latin America but the road to elimination has been accompanied by substantial challenges [88]. Progress in Latin America has required decades of investment in large-scale dog vaccination programmes and builds on effective regional coordination. Sustaining such coverage, particularly across large geographical areas, is difficult and requires an investment in rabies control that focuses on the dog population and is over and above levels seen to date in Africa and Asia [65]. Local leadership is also an important factor. For example, canine rabies in north America was primarily controlled at the municipal level through dog licensure. Legislation and by-laws relating to rabies control and dog vaccination exist in many canine rabies-endemic countries, but there is still a need for greater engagement of local authorities to ensure appropriate and sensitive enforcement of relevant legislation.

Empirical evidence from wildlife rabies elimination programmes show that once controlled to less than 10% of endemic incidence, the time required to eliminate rabies is as long again [9], a lesson that should be heeded for canine rabies. Once rabies has been reduced to low levels, the remaining foci by their nature are persistent and in ‘hard-to-reach’ communities, socially, economically and geographically, and new challenges come to the fore [89].

Increasingly the importance of metapopulations has been recognized for the persistence of rabies [38,50] and genomic signatures in rabies-endemic countries highlight the frequent human-mediated movement of dogs [9092]. The implications of this movement are evident when rabies invades previously uninfected areas [37], and without maintained vigilance, rabies can re-emerge rapidly if control measures are no longer implemented effectively [93]. The long-term implications of these incursions to the persistence of rabies are not yet fully understood but will, undoubtedly prolong elimination efforts, and highlight the need for coordinated control at scale and across international boundaries as well as realistic projections of the investment required to eliminate rabies [94].

7. Rabies research as a driver of policy change

Recent research has contributed pivotal evidence in making the case for rabies to be considered a priority NTD and, in 2012, rabies was included within the World Health Organization (WHO) Accelerated Roadmap for NTDs [95]. In 2016, the tripartite partnership (WHO, the World Organization for Animal Health (OIE), and the Food and Agriculture Organization of the United Nations (FAO), together with the Global Alliance for Rabies Control, declared a goal of zero human deaths from dog-mediated rabies by 2030 [61], underpinned by an investment case incorporating data on the human health and economic burden of canine rabies [4,22]. This purposely sets dog-mediated human rabies deaths as the first target, both because of its public health importance, but also its shorter-term feasibility (figure 3) through a combination of mass dog vaccination and improved PEP provision to under-served communities. The longer-term goal of disrupting transmission and eliminating canine rabies will require more time. Nonetheless, the example of Latin America demonstrates that it is within reach [88].

The control and elimination of canine rabies provides an exemplar of ‘One Health’ interventions, that is, interventions in animal populations that generate human health benefits. Although challenges remain in the operationalization of One Health [96], these approaches not only provide the most cost-effective strategy for preventing human rabies deaths but also offer a more equitable approach than relying only on interventions directed at humans only (i.e. PEP) [97]. Interventions that effectively reduce the force of infection from the animal reservoir convey benefits to all without regard to socioeconomic status. By contrast, under a strategy of reliance on PEP, the social, political and economic factors constraining access to healthcare are likely to prevail, with rabies deaths continuing to affect the most disadvantaged communities well beyond 2030.

It is perhaps understandable that the medical sector emphasizes prevention of human rabies through PEP. But this approach can lead to neglect of the problem at source—in the dogs—and impede progress towards large-scale mass dog vaccination programmes. This is true even in upper middle-income countries which have clear capability to implement mass dog vaccination but, without effective programmes, still suffer a high burden of human deaths and an escalation in PEP demand, with costs amounting to tens of millions of dollars every year [4].

8. Conclusion

Recent research on rabies has generated a strong body of evidence for the feasibility of elimination of canine rabies through mass vaccination of domestic dogs. Global momentum is now building towards implementation of large-scale programmes to achieve first, the elimination of human deaths mediated by canine rabies, and second, disruption of transmission within the dog population and the elimination of canine rabies entirely. However, time is short to reach these global targets [61] and there is no cause for further delay.

Supplementary Material

File S1:

Supplementary Material

Data on rabies publications:

Acknowledgements

The views expressed here have been developed through many years of collaborative research with colleagues working on rabies around the world, and with international organizations, including the World Health Organization, the World Organization for Animal Health, the Food and Agriculture Organization of the United Nations and the Global Alliance for Rabies Control. For S.C., this includes over 25 years of interactions with colleagues at the Institute of Zoology, London, the London School of Hygiene and Tropical Medicine, the University of Edinburgh and the University of Glasgow; and, for K.H., 15 years of interactions with colleagues at Princeton University and the University of Glasgow. We are very grateful to support from Tanzanian institutions, particularly the Tanzania Wildlife Research Institute, Tanzania National Parks, Ifakara Health Institute and Sokoine University of Agriculture as well as national and local governments. We thank many colleagues for support, stimulating research and debate, but particularly acknowledge Chris Dye, Dan Haydon, Tiziana Lembo, Jonathan Dushoff, Magai Kaare, Felix Lankester, Rudovick Kazwala, Darryn Knobel, Michelle Morters and Louise Taylor.

Data accessibility

Data relating to the number of published articles shown in figure 1 are provided in the electronic supplementary material.

Authors' contributions

S.C. and K.H. jointly conceived the article, drafted the manuscript and prepared the figures.

Competing interests

S.C. and K.H. have received support for rabies research and dog vaccination campaigns in the Serengeti ecosystem, Tanzania through donations of dog rabies vaccines from MSD Animal Health.

Funding

S.C.'s research on rabies was supported by the Agriculture and Food Research Council (now BBSRC), the DfID Animal Health Programme, the Wellcome Trust (through a Fellowship in Tropical Medicine and grant no. 071259) and the NIH/NSF Ecology of Infectious Diseases Program (NSF/DEB0225453). K.H. was supported by the NIH/NSF Ecology of Infectious Diseases Program (NSF/DEB0225453), UBS Optimus Foundation and the Wellcome Trust (082715/Z/07/Z and 095787/Z/11/Z). Opinions, findings, conclusions and recommendations are those of the authors and do not necessarily reflect the view of NIH or NSF.

References

1. Baer GM. 2007. The history of rabies. In Rabies, 2nd edn (eds Jackson AC, Wunner WH), pp. 1–22. London, UK: Elsevier.
2. Tarantola A. 2017. Four thousand years of concepts relating to rabies in animals and humans, its prevention and its cure. Trop. Med. Infect Dis. 2, 5 (doi:10.3390/tropicalmed2020005).
3. Lozano R, et al. 2012. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the global burden of disease study 2010. Lancet 380, 2095–2128. (doi:10.1016/S0140-6736(12)61728-0) [PubMed]
4. Hampson K, et al. 2015. Estimating the global burden of endemic canine rabies. PLoS Negl. Trop. Dis. 9, e0003709 (doi:10.1371/journal.pntd.0003709) [PMC free article] [PubMed]
5. Debre P. 1998. Louis Pasteur. Baltimore, MD: John Hopkins University Press.
6. Rupprecht CE, et al. 2008. Can rabies be eradicated? Dev. Biologicals (Basel) 131, 95–121. [PubMed]
7. Vigilato MA, Clavijo A, Knobl T, Tamayo Silva HM, Cosivi O, Schneider MC, Fernando Leanes L, Belotto AJ, Espinal MA 2013. Progress towards eliminating canine rabies: policies and perspectives from Latin America and the Caribbean. Phil. Trans. R. Soc. B 368, 20120143 (doi: 10.1098/rstb.2012.0143) [PMC free article] [PubMed]
8. King AA, Fooks AR, Aubert M, Wandeler AI 2004. Historical perspective of rabies in Europe and the Mediterranean basin. Paris, France: World Organization for Animal Health.
9. Freuling CM, Hampson K, Selhorst T, Schroder R, Meslin FX, Mettenleiter TC, Muller T 2013. The elimination of fox rabies from Europe: determinants of success and lessons for the future. Phil. Trans. R. Soc. B 368, 20120142 (doi:10.1098/rstb.2012.0142) [PMC free article] [PubMed]
10. Rosatte RC, Tinline RR, Johnston DH 2007. Rabies control in wild carnivores. In Rabies (eds Jackson AC, Wunner WH), pp. 595–634. London, UK: Elsevier.
11. Kuzmin IV, Rupprecht CE 2007. Bat rabies. In Rabies, 2nd edn (eds Jackson AC, Wunner WH), pp. 259–307. London, UK: Elsevier.
12. Kuzmin IV, Rupprecht CE 2015. Bat Lyssaviruses. In Bats and viruses: a New frontier of emerging infectious disease (eds L-F Wang, C Cowled), pp. 47–97. Hoboken, NJ: John Wiley & Sons, Inc.
13. Molyneux D, et al. 2011. Zoonoses and marginalised infectious diseases of poverty: where do we stand? Parasites Vectors 4, 106 (doi:10.1186/1756-3305-4-106) [PMC free article] [PubMed]
14. Nel LH. 2013. Discrepancies in data reporting for rabies, Africa. Emerg. Infect. Dis. 19, 529–533. (doi:10.3201/eid1904.120185) [PMC free article] [PubMed]
15. Lembo T, Hampson K, Kaare MT, Ernest E, Knobel D, Kazwala RR, Haydon DT, Cleaveland S 2010. The feasibility of canine rabies elimination in Africa: dispelling doubts with data. PLoS Negl. Trop. Dis. 4, e0000626 (doi:10.1371/journal.pntd.0000626) [PMC free article] [PubMed]
16. Cleaveland S, Fevre EM, Kaare M, Coleman PG 2002. Estimating human rabies mortality in the United Republic of Tanzania from dog bite injuries. Bull. World Health Org. 80, 304–310. [PubMed]
17. Knobel DL, Cleaveland S, Coleman PG, Fevre EM, Meltzer MI, Miranda MEG, Shaw A, Zinsstag J, Meslin FX 2005. Re-evaluating the burden of rabies in Africa and Asia. Bull. World Health Org. 83, 360–368. [PubMed]
18. Fèvre EM, Kaboyo RW, Persson V, Edelsten M, Coleman PG, Cleaveland S 2005. The epidemiology of animal bite injuries in Uganda and projections of the burden of rabies. Trop. Med. Int. Health 10, 790–798. (doi:10.1111/j.1365-3156.2005.01447.x) [PubMed]
19. Ly S, Buchy P, Heng NY, Ong S, Chhor N, Bourhy H, Vong S 2009. Rabies situation in Cambodia. PLoS Negl. Trop. Dis. 3, e511 (doi:10.1371/journal.pntd.0000511) [PMC free article] [PubMed]
20. Tenzin DNK, Gyeltshen T, Firestone S, Zangmo C, Dema C, Gyeltshen R, Ward MP 2011. Dog bites in humans and estimating human rabies mortality in rabies endemic areas of Bhutan. PLoS Negl. Trop. Dis. 5, e1391 (doi:10.1371/journal.pntd.0001391) [PMC free article] [PubMed]
21. Frey J, Mindekem R, Kessely H, Doumagoum Moto D, Naissengar S, Zinsstag J, Schelling E 2013. Survey of animal bite injuries and their management for an estimate of human rabies deaths in N'Djamena, Chad. Trop. Med. Int. Health 18, 1555–1562. (doi:10.1111/tmi.12202) [PubMed]
22. Shwiff S, Hampson K, Anderson A 2013. Potential economic benefits of eliminating canine rabies. Antiviral Res. 98, 352–356. (doi:10.1016/j.antiviral.2013.03.004) [PubMed]
23. GBD Study 2013 Collaborators. 2015. Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: a systematic analysis for the global burden of disease study 2013. Lancet 386, 743–800. (doi:10.1016/s0140-6736(15)60692-4) [PMC free article] [PubMed]
24. GBD. 2016. Disease and injury incidence and prevalence collaborators. 2017 Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: a systematic analysis for the global burden of disease study 2016. Lancet 390, 1211–1259. (doi:10.1016/s0140-6736(17)32154-2) [PMC free article] [PubMed]
25. Taylor LH, Hampson K, Fahrion A, Abela-Ridder B, Nel LH 2017. Difficulties in estimating the human burden of canine rabies. Acta Trop. 165, 133–140. (doi:10.1016/j.actatropica.2015.12.007) [PMC free article] [PubMed]
26. Herricks JR, et al. 2017. The global burden of disease study 2013: what does it mean for the NTDs? PLoS Negl. Trop. Dis. 11, e0005424 (doi:10.1371/journal.pntd.0005424) [PMC free article] [PubMed]
27. Sudarshan MK, et al. 2007. Assessing the burden of human rabies in India: results of a national multi-center epidemiological survey. Int. J. Infect. Dis. 11, 29–35. (doi:10.1016/j.ijid.2005.10.007) [PubMed]
28. Bögel K, Meslin FX 1990. Economics of human and canine rabies elimination: guidelines for program orientation. Bull. World Health Org. 68, 281–291. [PubMed]
29. Zinsstag J, Dürr S, Penny MA, Mindekem R, Roth F, Gonzalez SM, Naissengar S, Hattendorf J 2009. Transmission dynamics and economics of rabies control in dogs and humans in an African city. Proc. Natl Acad. Sci. USA 106, 14 996–15 001. (doi:10.1073/pnas.0904740106) [PubMed]
30. Fitzpatrick MC, Hampson K, Cleaveland S, Mzimbiri I, Lankester F, Lembo T, Meyers LA, Paltiel D, Galvani AP 2014. Cost-effectiveness of canine vaccination to prevent human rabies in rural Tanzania. Ann. Int. Med. 160, 91–100. (doi:10.7326/m13-0542) [PMC free article] [PubMed]
31. Hampson K, Dobson A, Kaare M, Dushoff J, Magoto M, Sindoya E, Cleaveland S 2008. Rabies exposures, post-exposure prophylaxis and deaths in a region of endemic canine rabies. PLoS Negl. Trop. Dis. 2, e0000339 (doi:10.1371/journal.pntd.0000339) [PMC free article] [PubMed]
32. Sambo M, Cleaveland S, Ferguson H, Lembo T, Simon C, Urassa H, Hampson K 2013. The burden of rabies in Tanzania and its impact on local communities. PLoS Negl. Trop. Dis. 7, e2510 (doi:10.1371/journal.pntd.0002510) [PMC free article] [PubMed]
33. Jibat T, Mourits MC, Hogeveen H 2016. Incidence and economic impact of rabies in the cattle population of Ethiopia. Prev. Vet. Med. 130, 67–76. (doi:10.1016/j.prevetmed.2016.06.005) [PubMed]
34. Woodroffe R, Cleaveland S, Courtenay O, Laurenson MK, Artois M 2004. Infectious disease. In Biology and conservation of wild canids (eds Macdonald DW, Sillero-Zubiri C), pp. 123–142. Oxford, UK: Oxford University Press.
35. Coleman PG, Dye C 1996. Immunization coverage required to prevent outbreaks of dog rabies. Vaccine 14, 185–186. (doi:10.1016/0264-410X(95)00197-9) [PubMed]
36. Hampson K, Dushoff J, Cleaveland S, Haydon DT, Kaare M, Packer C, Dobson A 2009. Transmission dynamics and prospects for the elimination of canine rabies. PLoS Biol. 7, 462–471. (doi:10.1371/journal.pbio.1000053) [PMC free article] [PubMed]
37. Townsend SE, et al. 2013. Designing programs for eliminating canine rabies from islands: Bali, Indonesia as a case study. PLoS Negl. Trop. Dis. 7, e0002372 (doi:10.1371/journal.pntd.0002372) [PMC free article] [PubMed]
38. Bourhy H, et al. 2016. Revealing the micro-scale signature of endemic zoonotic disease transmission in an African urban setting. PLoS Pathog. 12, e1005525 (doi:10.1371/journal.ppat.1005525) [PMC free article] [PubMed]
39. Fitzpatrick MC, Shah HA, Pandey A, Bilinski AM, Kakkar M, Clark AD, Townsend JP, Abbas SS, Galvani AP 2016. One health approach to cost-effective rabies control in India. Proc. Natl Acad. Sci. USA 113, 14 574–14 581. (doi:10.1073/pnas.1604975113) [PubMed]
40. Morters MK, Restif O, Hampson K, Cleaveland S, Wood JLN, Conlan AJK 2013. Evidence-based control of canine rabies: a critical review of population density reduction. J. Anim. Ecol. 82, 6–14. (doi:10.1111/j.1365-2656.2012.02033.x) [PMC free article] [PubMed]
41. Knobel D, Lembo T, Morters M, Townsend S, Cleaveland S, Hampson K 2013. Dog rabies and its control. In Rabies: scientific basis of the disease and its management (ed. Jackson AC, editor. ), p. xxiii, 707 Amsterdam, the Netherlands: Academic Press.
42. Pemberton N, Worboys M 2007. Mad dogs and Englishmen. Rabies in Britain, 1830–2000. London, UK: Palgrave MacMillan.
43. Wandeler AI, Nadin-Davis SA, Tinline RR, Rupprecht CE 1994. Rabies epidemiology: some ecological and evolutionary perspectives. Curr. Top. Microbiol. Immunol. 187, 297–324. (doi:10.1007/978-3-642-78490-3_16) [PubMed]
44. Haydon DT, Cleaveland S, Taylor LH, Laurenson MK 2002. Identifying reservoirs of infection: a conceptual and practical challenge. Emerg. Infect. Dis. 8, 1468–1473. (doi:10.3201/eid0812.010317) [PMC free article] [PubMed]
45. Bingham J. 2005. Canine rabies ecology in southern Africa. Emerg. Infect. Dis. 11, 1337–1342. (doi:10.3201/eid1109.050172) [PMC free article] [PubMed]
46. Hanlon CA, Niezgoda M, Rupprecht CE 2007. Rabies in terrestrial animals. In Rabies (eds Jackson AC, Wunner WH), pp. 201–258. London, UK: Elsevier.
47. Mollentze N, Biek R, Streicker DG 2014. The role of viral evolution in rabies host shifts and emergence. Curr. Opin. Virol. 8, 68–72. (doi:10.1016/j.coviro.2014.07.004) [PMC free article] [PubMed]
48. Viana M, Mancy R, Biek R, Cleaveland S, Cross PC, Lloyd-Smith JO, Haydon DT 2014. Assembling evidence for identifying reservoirs of infection. Trends Ecol. Evol. 29, 270–279. (doi:10.1016/j.tree.2014.03.002) [PMC free article] [PubMed]
49. Lembo T, et al. 2008. Exploring reservoir dynamics: a case study of rabies in the Serengeti ecosystem. J. Appl. Ecol. 45, 1246–1257. (doi:10.1111/j.1365-2664.2008.01468.x) [PMC free article] [PubMed]
50. Beyer HL, Hampson K, Lembo T, Cleaveland S, Kaare M, Haydon DT 2011. Metapopulation dynamics of rabies and the efficacy of vaccination. Proc. R. Soc. B 278, 2182–2190. (doi:10.1098/rspb.2010.2312) [PMC free article] [PubMed]
51. Fitzpatrick MC, Hampson K, Cleaveland S, Meyers LA, Townsend JP, Galvani AP 2012. Potential for rabies control through dog vaccination in wildlife-abundant communities of Tanzania. PLoS Negl. Trop. Dis. 6, e0001796 (doi:10.1371/journal.pntd.00017960) [PMC free article] [PubMed]
52. Zulu GC, Sabeta CT, Nel LH 2009. Molecular epidemiology of rabies: focus on domestic dogs (Canis familiaris) and black-backed jackals (Canis mesomelas) from northern South Africa. Virus Res. 140, 71–78. (doi:10.1016/j.virusres.2008.11.004) [PubMed]
53. Bingham J, Schumacher CL, Aubert MF, Hill FW, Aubert A 1997. Innocuity studies of SAG-2 oral rabies vaccine in various Zimbabwean wild non-target species. Vaccine 15, 937–943. (doi:10.1016/S0264-410X(97)00009-1) [PubMed]
54. Bingham J, Schumacher CL, Hill FW, Aubert A 1999. Efficacy of SAG-2 oral rabies vaccine in two species of jackal (Canis adustus and Canis mesomelas). Vaccine 17, 551–558. (doi:10.1016/S0264-410X(98)00233-3) [PubMed]
55. Mähl P, Cliquet F, Guiot AL, Niin E, Fournials E, Saint-Jean N, Aubert M, Rupprecht CE, Gueguen S 2014. Twenty year experience of the oral rabies vaccine SAG2 in wildlife: a global review. Vet. Res. 45, 77 (doi:10.1186/s13567-014-0077-8) [PMC free article] [PubMed]
56. Linhart SB, King R, Zamir S, Naveh U, Davidson M, Perl S 1997. Oral rabies vaccination of red foxes and golden jackals in Israel: preliminary bait evaluation. Rev. Sci. Tech. 16, 874–880. (doi:10.20506/rst.16.3.1076) [PubMed]
57. Davlin SL, Vonville HM 2012. Canine rabies vaccination and domestic dog population characteristics in the developing world: a systematic review. Vaccine 30, 3492–3502. (doi:10.1016/j.vaccine.2012.03.069) [PubMed]
58. Jibat T, Hogeveen H, Mourits MC 2015. Review on dog rabies vaccination coverage in Africa: a question of dog accessibility or cost recovery? PLoS Negl. Trop. Dis. 9, e0003447 (doi:10.1371/journal.pntd.0003447) [PMC free article] [PubMed]
59. Gibson AD, Ohal P, Shervell K, Handel IG, Bronsvoort BM, Mellanby RJ, Gamble L 2015. Vaccinate-assess-move method of mass canine rabies vaccination utilising mobile technology data collection in Ranchi, India. BMC Infect. Dis. 15, 589 (doi:10.1186/s12879-015-1320-2) [PMC free article] [PubMed]
60. Harischandra LPA, Gunesekera A, Janakan N, Gongal G, Abela-Ridder B 2016. Sri Lanka takes action towards a target of zero rabies deaths by 2020 WHO South East Asia. J. Public Health 5, 113–116. (doi:10.4103/2224-3151.206247) [PubMed]
61. WHO, OIE. 2016. Global elimination of dog-mediated human rabies: the time is now! In Report of the Rabies Global Conference, Geneva, Switzerland, 10–11 December 2015 Paris: World Health Organization and World Organisation for Animal Health.
62. Dürr S, Mindekem R, Kaninga Y, Doumagoum Moto D, Meltzer MI, Vounatsou P, Zinsstag J 2009. Effectiveness of dog rabies vaccination programmes: comparison of owner-charged and free vaccination campaigns. Epidemiol. Infect 137, 1558–1567. (doi:10.1017/s0950268809002386) [PubMed]
63. Bardosh K, Sambo M, Sikana L, Hampson K, Welburn SC 2014. Eliminating rabies in Tanzania? Local understandings and responses to mass dog vaccination in Kilombero and Ulanga districts. PLoS Negl. Trop. Dis. 8, e2935 (doi:10.1371/journal.pntd.0002935) [PMC free article] [PubMed]
64. Lechenne M, et al. 2016. Operational performance and analysis of two rabies vaccination campaigns in N'Djamena, Chad. Vaccine 34, 571–577. (doi:10.1016/j.vaccine.2015.11.033) [PubMed]
65. Wallace RM, Undurraga EA, Blanton JD, Cleaton J, Franka R 2017. Elimination of dog-mediated human rabies deaths by 2030: needs assessment and alternatives for progress based on dog vaccination. Front. Vet. Sci. 4, 9 (doi:10.3389/fvets.2017.00009) [PMC free article] [PubMed]
66. Fahrion AS, et al. 2017. The road to dog rabies control and elimination: what keeps us from moving faster? Front. Public Health 5, 103 (doi:10.3389/fpubh.2017.00103) [PMC free article] [PubMed]
67. Taylor LH, Wallace RM, Balaram D, Lindenmayer JM, Eckery DC, Mutonono-Watkiss B, Parravani E, Nel LH 2017. The role of dog population management in rabies elimination: a review of current approaches and future opportunities. Front Vet. Sci. 4, 109 (doi:10.3389/fvets.2017.00109) [PMC free article] [PubMed]
68. Garside D, Gebril A, Alsaadi M, Ferro VA 2014. Fertility control in wildlife: review of current status, including novel and future technologies. In Reproductive sciences in animal conservation. 753 (eds Holt W, Brown J, Comizolli P), pp. 467–488. New York, NY: Springer.
69. ICAM. 2007. Humane dog population management guidance. International Companion Animal Management Coalition. See http://www.icam-coalition.org/downloads/Humane_Dog_Population_Management_Guidance_English.pdf.
70. Conan A, Akerele O, Simpson G, Reininghaus B, van Rooyen J, Knobel D 2015. Population dynamics of owned, free-roaming dogs: implications for rabies control. PLoS Negl. Trop. Dis. 9, e0004177 (doi:10.1371/journal.pntd.0004177) [PMC free article] [PubMed]
71. Halliday J, et al. 2012. Bringing together emerging and endemic zoonoses surveillance: shared challenges and a common solution. Phil. Trans. R. Soc. B 367, 2872–2880. (doi:10.1098/rstb.2011.0362) [PMC free article] [PubMed]
72. Undurraga EA, Meltzer MI, Tran CH, Atkins CY, Etheart MD, Millien MF, Adrien P, Wallace RM 2017. Cost-effectiveness evaluation of a novel integrated bite case management program for the control of human rabies, Haiti 2014–2015. Am. J. Trop. Med. Hyg. 96, 1307–1317. (doi:10.4269/ajtmh.16-0785) [PMC free article] [PubMed]
73. Lembo T, Niezgoda M, Velasco-Villa A, Cleaveland S, Ernest E, Rupprecht CE 2006. Evaluation of a direct, rapid immunohistochemical test for rabies diagnosis. Emerg. Infect. Dis. 12, 310–313. (doi:10.3201/eid1202.050812) [PMC free article] [PubMed]
74. Dürr S, Naissengar S, Mindekem R, Diguimbye C, Niezgoda M, Kuzmin I, Rupprecht CE, Zinsstag J 2008. Rabies diagnosis for developing countries. PLoS Negl. Trop. Dis. 2, e206 (doi:10.1371/journal.pntd.0000206) [PMC free article] [PubMed]
75. Madhusudana SN, Subha S, Thankappan U, Ashwin YB 2012. Evaluation of a direct rapid immunohistochemical test (dRIT) for rapid diagnosis of rabies in animals and humans. Virol Sin. 27, 299–302. (doi:10.1007/s12250-012-3265-6) [PubMed]
76. Coetzer A, Sabeta CT, Markotter W, Rupprecht CE, Nel LH 2014. Comparison of biotinylated monoclonal and polyclonal antibodies in an evaluation of a direct rapid immunohistochemical test for the routine diagnosis of rabies in southern Africa. PLoS Negl. Trop. Dis. 8, e3189 (doi:10.1371/journal.pntd.0003189) [PMC free article] [PubMed]
77. Nishizono A, et al. 2008. A simple and rapid immunochromatographic test kit for rabies diagnosis. Microbiol. Immunol. 52, 243–249. (doi:10.1111/j.1348-0421.2008.00031.x) [PubMed]
78. Ahmed K, et al. 2012. Evaluation of a monoclonal antibody-based rapid immunochromatographic test for direct detection of rabies virus in the brain of humans and animals. Am. J. Trop. Med. Hyg. 86, 736–740. (doi:10.4269/ajtmh.2012.11-0332) [PMC free article] [PubMed]
79. Lechenne M, Naissengar K, Lepelletier A, Alfaroukh IO, Bourhy H, Zinsstag J, Dacheux L 2016. Validation of a rapid rabies diagnostic tool for field surveillance in developing countries. PLoS Negl. Trop. Dis. 10, e0005010 (doi:10.1371/journal.pntd.0005010) [PMC free article] [PubMed]
80. Eggerbauer E, de Benedictis P, Hoffmann B, Mettenleiter TC, Schlottau K, Ngoepe EC, Sabeta CT, Freuling CM, Muller T 2016. Evaluation of six commercially available rapid immunochromatographic tests for the diagnosis of rabies in brain material. PLoS Negl. Trop. Dis. 10, e0004776 (doi:10.1371/journal.pntd.0004776) [PMC free article] [PubMed]
81. Quick J, et al. 2016. Real-time, portable genome sequencing for Ebola surveillance. Nature 530, 228–232. (doi:10.1038/nature16996) [PMC free article] [PubMed]
82. Mtema Z, et al. 2016. Mobile phones as surveillance tools: implementing and evaluating a large-scale intersectoral surveillance system for rabies in Tanzania. PLoS Med. 13, e1002002 (doi:10.1371/journal.pmed.1002002) [PMC free article] [PubMed]
83. Kitala PM, McDermott JJ, Coleman PG, Dye C 2002. Comparison of vaccination strategies for the control of dog rabies in Machakos District, Kenya. Epidemiol. Infect. 129, 215–222. (doi:10.1017/S0950268802006957) [PubMed]
84. Bilinski AM, Fitzpatrick MC, Rupprecht CE, Paltiel AD, Galvani AP 2016. Optimal frequency of rabies vaccination campaigns in Sub-Saharan Africa. Proc. R. Soc. B 283, 20161211 (doi:10.1098/rspb.2016.1211) [PMC free article] [PubMed]
85. Zhang J, Jin Z, Sun GQ, Zhou T, Ruan S 2011. Analysis of rabies in China: transmission dynamics and control. PLoS ONE 6, e20891 (doi:10.1371/journal.pone.0020891) [PMC free article] [PubMed]
86. Ferguson EA, et al. 2015. Heterogeneity in the spread and control of infectious disease: consequences for the elimination of canine rabies. Sci. Rep. 5, Article number: 18232 (doi:10.1038/srep18232) [PMC free article] [PubMed]
87. Sambo M, et al. 2017. Comparing methods of assessing dog rabies vaccination coverage in rural and urban communities in Tanzania. Front Vet. Sci. 4, 33 (doi:10.3389/fvets.2017.00033) [PMC free article] [PubMed]
88. Del Rio Vilas VJ, Freire de Carvalho MJ, Vigilato MAN, Rocha F, Vokaty A, Pompei JA, Molina Flores B, Fenelon N, Cosivi O 2017. Tribulations of the last mile: sides from a regional program. Front. Vet. Sci. 4, 4 (doi:10.3389/fvets.2017.00004) [PMC free article] [PubMed]
89. Klepac P, Metcalf CJE, McLean AR, Hampson K 2013. Towards the endgame and beyond: complexities and challenges for the elimination of infectious diseases. Phil. Trans. R. Soc. B 368, 20120137 (doi:10.1098/rstb.2012.0137) [PMC free article] [PubMed]
90. Denduangboripant J, Wacharapluesadee S, Lumlertdacha B, Ruankaew N, Hoonsuwan W, Puanghat A, Hemachudha T 2005. Transmission dynamics of rabies virus in Thailand: implications for disease control. BMC Infect. Dis. 5, 52 (doi:10.1186/1471-2334-5-52) [PMC free article] [PubMed]
91. Talbi C, et al. 2010. Phylodynamics and human-mediated dispersal of a zoonotic virus. PLoS Pathog. 6, e1001166 (doi:10.1371/journal.ppat.1001166) [PMC free article] [PubMed]
92. Brunker K, et al. 2015. Elucidating the phylodynamics of endemic rabies virus in eastern Africa using whole genome sequencing. Virus Evol. 1, vev011 (doi:10.1093/ve/vev011) [PMC free article] [PubMed]
93. Castillo-Neyra R, et al. 2017. Barriers to dog rabies vaccination during an urban rabies outbreak: qualitative findings from Arequipa, Peru. PLoS Negl. Trop. Dis. 11, e0005460 (doi:10.1371/journal.pntd.0005460) [PMC free article] [PubMed]
94. Lankester F, Hampson K, Lembo T, Palmer G, Taylor L, Cleaveland S 2014. Infectious disease. Implementing Pasteur's vision for rabies elimination. Science 345, 1562–1564. (doi:10.1126/science.1256306) [PubMed]
95. World Health Organization. 2012. Accelerating work to overcome the global impact of neglected tropical diseases—a roadmap for implementation. See http://www.who.int/neglected_diseases/NTD_RoadMap_2012_Fullversion.pdf.
96. Lee K, Brumme ZL 2013. Operationalizing the one health approach: the global governance challenges. Health Policy Plan. 28, 778–785. (doi:10.1093/heapol/czs127) [PubMed]
97. Cleaveland S, et al. 2017. One Health contributions towards more effective and equitable approaches to health in low- and middle-income countries. Phil. Trans. R Soc. B 372, 20160168 (doi:10.1098/rstb.2016.0168) [PMC free article] [PubMed]

Articles from Proceedings of the Royal Society B: Biological Sciences are provided here courtesy of The Royal Society