Abstract
This article provides an overview of three research projects which designed and implemented innovative interventions for Chagas disease vector control in Bolivia, Guatemala and Mexico. The research initiative was based on sound principles of community-based ecosystem management (ecohealth), integrated vector management, and interdisciplinary analysis. The initial situational analysis achieved a better understanding of ecological, biological and social determinants of domestic infestation. The key factors identified included: housing quality; type of peridomestic habitats; presence and abundance of domestic dogs, chickens and synanthropic rodents; proximity to public lights; location in the periphery of the village. In Bolivia, plastering of mud walls with appropriate local materials and regular cleaning of beds and of clothes next to the walls, substantially decreased domestic infestation and abundance of the insect vector Triatoma infestans. The Guatemalan project revealed close links between house infestation by rodents and Triatoma dimidiata, and vector infection with Trypanosoma cruzi. A novel community-operated rodent control program significantly reduced rodent infestation and bug infection. In Mexico, large-scale implementation of window screens translated into promising reductions in domestic infestation. A multi-pronged approach including community mobilisation and empowerment, intersectoral cooperation and adhesion to integrated vector management principles may be the key to sustainable vector and disease control in the affected regions.
Keywords: Chagas disease, Community, Eco-bio-social research, Ecohealth, Integrated vector management, Vector-borne diseases
Introduction
With 8–12 million infected people, Chagas disease ranks among the most important infectious diseases in the Americas in terms of disability-adjusted life-years.1,2 The disease is caused by the protozoan Trypanosoma cruzi which infects at least 150 mammalian species and is mainly transmitted by blood-sucking triatomine bugs.3 Chagas disease has strong links to rural poverty, poor quality housing, subsistence economies, and marginalized populations.2 Increased international migration from Latin America to high-income countries has expanded the distribution of human Chagas disease to the global scale through transfusional and vertical transmission.
Of the approximately 140 species of triatomine bugs identified, only a handful has adapted to live in houses and blood-feed on humans and domestic animals.3 These vector species are the most successful in terms of abundance and parasite transmission, and are the main targets of vector control programs: Triatoma infestans in the southern cone countries; Rhodnius prolixus in the northern section of South America and formerly in several countries of Central America; Panstrongylus megistus in Brazil; Triatoma dimidiata in Central America, southern Mexico, Colombia and Ecuador. However, a much longer list of sylvatic triatomine species may also infest peridomestic structures and eventually establish domestic colonies, contact humans and transmit T. cruzi. These species are hard to control by classical strategies and include Triatoma brasiliensis in northeastern Brazil;4 Rhodnius pallescens in Central America;5 and Rhodnius ecuadoriensis in Ecuador and northern Peru,6 among others. Yet another group of triatomine species may be in the process of adapting to domestic habitats, pushed by large-scale changes in land use.
In the absence of vaccines, the primary prevention of human T. cruzi infection has relied almost exclusively on residual insecticide spraying campaigns conducted by vertically-structured vector control programs starting in the late 1940s. The only two drugs available for treatment since the early 1970s were until recently restricted to the acute or recent stage of infection.7 A series of intergovernmental initiatives created in the 1990s coordinated vector control efforts at regional levels and substantially reduced house infestation indices and disease incidence in several countries of South and Central America.3,8 Progress was uneven, and what was effective in some areas (e.g. Brazil, Uruguay and Chile) had lower impact elsewhere, such as in the case of T. infestans in the Gran Chaco region of Argentina, Bolivia and Paraguay.9,10 For R. prolixus in South America,11,12 T. dimidiata in Central America and Mexico,8 and T. brasiliensis,4 the goal of vector elimination is not feasible and control programs have to grapple with the recurrent nature of house invasion and recolonisation, vector surveillance and insecticide treatment.
Centralized vertical control programs are ill-equipped to deal with these recurrent tasks, especially in resource-constrained rural areas with low-density, dispersed human populations that are difficult to access, resulting in high operating costs. Furthermore, the operational capacity of most Chagas disease vector control programs has been seriously compromised by the health care reforms (decentralization) started in the early 1980s,9 in a context of unstable developing economies and sociopolitical situations. This problem was further compounded with the low political priority assigned to Chagas disease by many of the affected countries. In the absence of permanent vector suppression, the question of how to sustain the open-ended vector surveillance phase still is unresolved.
Failure to achieve the stated program goals of vector elimination led to 1) the search for more sustainable, integrated control strategies that address ecological and social determinants of parasite transmission; 2) more emphasis on participatory frameworks and intersectoral cooperation (to ensure sustainability); 3) the application of integrated vector management (IVM) principles (virtually absent in Chagas disease vector control).13 Rural housing programs and other environmental management measures14 were rarely considered part of an integrated Chagas disease control strategy and reliance on insecticides has stayed approximately the same since they first came into use more than 60 years ago.
Building upon a multi-country research initiative for targeted dengue vector interventions in Asia,15 in 2007 the Special Programme for Research and Training in Tropical Diseases (TDR/WHO) and the Ecosystem and Human Health Program of Canada's International Development Research Centre (IDRC) launched a research and capacity building partnership named ‘Innovative community-based ecosystem management interventions for improved dengue and Chagas disease prevention in Latin America.’ This initiative aimed to improve dengue and Chagas disease vector control through innovative interventions based on sound principles of community-based ecosystem management (ecohealth),16 IVM13 and interdisciplinary analysis. The initiative's goals were to achieve a better understanding of ecological, biological and social (eco-bio-social) determinants of vector abundance and parasite transmission,15,17 and to develop, implement and evaluate intersectoral, community-centred interventions directed at reducing transmission risks.
Here we provide an overview of the three research projects on Chagas disease vector control interventions whose results are published in this issue.18–20 We briefly review the characteristics of study sites and methods, describe the main results obtained before implementing carefully designed control interventions and assess the initial impacts of these interventions in search of common patterns. This cross-site comparison is intended to bring together the main outcomes of the three projects and their repercussions for Chagas disease vector control beyond the specificities of each site and vector species implicated.
Methods
Study area and design
The studies were carried out in rural areas of Bolivia, Guatemala and Mexico with clearly established threats of transmission of T. cruzi in domestic and peridomestic habitats (Table 1). Although the three projects did not constitute a multi-site study, they shared the same general scope in overall study design and methods.18–22
Table 1.
Reference | Research sites (village/municipality; department; country) | Baseline study design and sample size | Risk factors for house infestationa | Additional findings |
---|---|---|---|---|
Dumonteil et al. 201321 | Bokoba, Teya and Sudzal; Yucatan; Mexico. | Simple random survey of 20% of all houses; 346 houses in the three villages. | Most important factors: Number of dogs Keeping chickens in a coop Proximity to the periphery of the village Cleaning of peridomestic areas Storage of firewood indoors Moderately important factors: Peridomestic rock piles Proximity to public lights |
Baseline house infestation: Sudzal: 14.3% (10/70) Bokoba: 8.5% (9/106) Teya: 20.5% (27/132) Mean: 14.9% (46/308) Very limited house colonization; extensive transient infestation. Storage of firewood and cleaning of peridomicile associated inversely with house infestation. |
Bustamante et al. 201422 | Comapa and Zapotitlán municipalities; Jutiapa; Guatemala. | Two-stage cluster sampling including 32 villages and 472 houses. | Most important factors: Number of dogs Rodent infestation Condition of interior wall plaster Dirt floor Tiled roofing Coffee tree |
Baseline house infestation: Timed searches: 25.4% (120/472) Householders' bug collections: 30.2% (144/477) Houses infested with ≥1 infected bug: 30.8% (40/130) House infestation by rodents: 59.8% (149/249) |
Lardeux et al. 201518 | Eje Pampa and Lagar Pampa; Cochabamba; Bolivia. Palmarito and La Brecha; Santa Cruz de la Sierra; Bolivia. |
Complete enumeration of all listed houses: two villages with 80 and 87 houses (Chaco region); two villages with 123 and 95 houses (Valleys region). | Statistically significant factors in the Chaco region: Cracked walls Chickens nesting indoors Presence of beds in the room Poor roof condition Statistically significant factors in the Valleys region: Bags stored hanging on walls |
Baseline domestic infestation: Chaco region: 95% (76/80) and 92% (76/83) Valleys region: 28% (13/47) and 35% (15/43) Houses with ≥1 bug-infested bed: Chaco region: 43.9% (141/321) and 46.8% (110/235) Valleys region: 1% (1/74) and 3% (1/38) |
a Domestic infestation assessed by householders' bug collections over a one-year period (Mexico); timed manual searches in domestic and peridomestic habitats and householders' bug collections (Guatemala); manual searches in domestic and peridomestic habitats (Bolivia).
Local stakeholders, including health departments, participated in the projects from their onset. All projects included a baseline situational analysis (phase I) with common objectives: 1) To assess three key ecosystem dimensions affecting the presence and abundance of Chagas disease vectors in human dwellings and their interactions: vector biology/ecology and related environmental factors; the social, cultural, economic and community context; vector control program organisation and functioning; 2) To analyse the relative importance of eco-bio-social factors associated with different levels of vector presence and abundance; 3) Based on the situational analysis, to identify and design specific interventions appropriate to the domestic and peridomestic environments through a community-based, participatory process. Consideration of the specificities of each study site and triatomine species led to a range of interventions and their combinations. Phase II included three objectives: 1) to implement and monitor the designed interventions; 2) to evaluate their effectiveness; 3) to recommend community-centred intersectoral ecosystem intervention approaches.
Design of interventions and impact assessment
The research teams used the outcomes of the situational analysis to design specific intervention packages tailored to each system through a participatory process involving multiple stakeholders and the affected communities (Table 2). Their cultural practices, concerns or priorities were considered in the design and implementation of the interventions. An explicit goal was to achieve community empowerment. The costs of interventions were partially or fully covered by the projects.18–20
Table 2.
Reference | Research sites (village/ municipality; department; country) | Interventions |
Midterm or endpoint results | ||
---|---|---|---|---|---|
Village | Intervention type | Number of houses intervened | |||
Waleckx et al. 201520 | Bokoba, Teya and Sudzal; Yucatan; Mexico. | Teya | Window screens | 702 houses | Screen cost per house: US$35. Moderate to strong participation of local communities and stakeholders. Significant midterm reduction of indoor versus outdoor house infestation when window screens were present. High potential for sustainable reductions in human-vector contact rates, including triatomines and mosquitoes. |
Sudzal | Window screens Education about cleaning of chicken coops (poultry husbandry). |
416 houses | |||
Bokoba | Control | 570 houses | |||
De Urioste-Stone et al. 201519 | Comapa municipality; Jutiapa; Guatemala. | Nine intervened and nine control villages. | Full-coverage insecticide spraying including tiled roofs and all walls. Participatory education on Chagas disease, risk factors and training in rodent control. Organic waste management combined with productive activities. |
18 villages and 429 houses | Effects on domestic infestation: Pre-intervention: Treatment (n=194): 19.3% ±10.2%; Control (n=199): 19.0%±9.0% Post-intervention: Treatment (n=194): 7.9%±7.0%; Control (n=199): 5.9%±5.8% Endpoint effects: no statistically significant differences between treatment and control. Reduced relative odds of early-stage bug infection in treated versus control villages. Effects on Rattus rattus and Mus musculus infestation: Post-intervention rat infestation significantly reduced: Treatment: 8.4% (16/190) Control: 15.6% (30/192) Post-intervention mouse infestation not significantly reduced: Treatment: 33.2% (63/190) Control: 39.6% (76/192) Sustainability closely related to stakeholders' cooperation. |
Lardeux et al. 201518 | Eje Pampa and Lagar Pampa; Cochabamba; Bolivia. Palmarito and La Brecha; Santa Cruz de la Sierra; Bolivia. |
Intervention villages: Eje Pampa and Palmarito Control villages: Lagar Pampa and La Brecha |
Wall coating with a standardized mud mixture. House cleaning including beds and objects on walls. Removal of animals from houses, especially poultry. |
Eje Pampa: 42 houses. Pamarito: 75 houses. |
Midterm effects on domestic bug abundance and prevalence of domestic infestation: Chaco region: both outcome measures were significantly lower in the treated village. Valleys region: similar decreasing trends in all indices of house infestation, no significant differences detected. Limited sustainability because Chagas disease is not perceived as a health risk. |
In Guatemala, the intervention package was based on the PRECEDE-PROCEED model for situational analysis, implementation and intervention evaluation.19,22 The package integrated the following: 1) educational workshops; 2) improved insecticide spraying procedures with full coverage of tiled roofs and walls; 3) participatory training workshops and implementation of rodent control activities; 4) multisectoral training in organic waste management and productive household activities; 5) a participant-based reflective process.19
In Bolivia, the intervention package included low-cost housing improvement techniques and community participation in two intervention versus two control villages.18 The goals were to eliminate refuges for bugs in the walls through plastering the surface with appropriate local materials; to promote house cleaning activities directed at beds and objects next to the walls; to remove chickens and dogs from human sleeping quarters, over a 6-month period.18 To promote community participation the research team used a multi-pronged strategy based on interpersonal communication, community mobilization, lobbying at community and regional levels, and supported advertising.
In Yucatan (Mexico), the research team conducted a series of meetings with multiple stakeholders to review the main findings of phase I,21 proposed the installation of window screens as a barrier against triatomine bugs in two intervention communities, and implemented the interventions in more than 800 houses.20 Education workshops addressing management and cleaning of chicken coops were also implemented in one of the villages.
The main outcomes measured included the degrees of acceptance, support and community participation throughout the intervention process. Control and intervention groups were compared in terms of domestic infestation indices at baseline, in a midterm evaluation and at the end point. Measurement of knowledge, attitudes and practices regarding Chagas disease, risk factors and related issues were conducted at set time points. The impacts of interventions were assessed initially within six months of finishing their implementation,18–20 and end-point assessments were planned for late 2014.
Results
Cross-site findings
Pre-intervention domestic infestation levels combined with bug infection prevalence suggested substantial risks of domestic transmission of T. cruzi in the three study sites (Table 1). Despite the fact that official insecticide spraying operations had been conducted in the Bolivian and Guatemalan study areas a few years before, baseline house infestation levels were comparable with active vector-borne transmission as indicated by vector, dog or rodent infection rates with T. cruzi. Vector control programs in Mexico traditionally have not conducted systematic insecticide sprays in response to the domestic catch of T. dimidiata or any other triatomine bug. The status of transmission was rather uncertain in Yucatan, where the house-invading bugs were infected with T. cruzi, domestic colonization was transient and the rates of vector-human contact apparently were more sporadic than in the other study sites. Unpublished data collected locally indicated that the seroprevalence of human T. cruzi infection in Bolivia was an order of magnitude higher than in Yucatan.
The three projects used multivariate statistical methods to identify the key factors explaining variations in domestic infestation.18,21,22 These factors were related to housing quality, characteristics of peridomestic habitats, availability of domestic animal hosts and location effects (Table 1). Housing quality attributes included the occurrence of cracked walls, earthen floors, tiled roofing (only in the Guatemalan study), bags and objects on the walls (for storage purposes). Relevant aspects of peridomestic habitats included the presence of chicken coops or nests, rock piles and coffee trees. Host availability included the presence and abundance of domestic dogs, chickens and rodents. Proximity to public lights and location in the periphery of the village suggested that house invasion by T. dimidiata in Yucatan originated from surrounding sylvatic habitats which initially dispersed towards public light sources.
The implementation time for interventions varied from 9 months in Bolivia and Guatemala to 12 months in Mexico. Midterm assessments of intervention effects indicated sizable reductions in domestic infestation and bug abundance in Yucatan and Bolivia, and reductions of rat infestations, human- and rodent-vector contact and domestic bug infection in Guatemala (Table 2).18–20
Discussion
The research projects covered two different model systems of house infestation by triatomine bugs: one in which there is stable domestic and peridomestic colonization (T. infestans in Bolivia and T. dimidiata in Guatemala),18,19,22 and one in which house invasion is seasonal and domestic colonization appears to be transient with occasional human-vector contact (T. dimidiata in Yucatan, Mexico).20,21 Baseline domestic infestation levels ranged from 14.9% (46/308) in the Mexican Yucatan region to 95% (76/80) in the Bolivian Chaco region, as determined by different methods, and in most cases are expected to underestimate the actual infestation.23 House infestations in Bolivia and Guatemala (as determined by timed manual searches) implied that there were established vector colonies in domestic and peridomestic habitats, whereas ‘domestic infestation’ in Yucatan actually represented transient infestations or house invasions detected by householders and notified to the local health post. Householders' bug collections are appropriate for continued domestic vector surveillance and corroborated that in Yucatan, house invasion was seasonal and stable across years.21
The three study locations were rural and differed in house density, infrastructure, degree of remoteness, resource constraints and history of insecticide spraying. Housing quality in Yucatan was substantially better (owing to extensive housing development plans during recent decades) than in Bolivia and Guatemala, households were much less isolated and poverty levels were apparently lower. For example, Teya in Yucatan had street signs and public lights. Conversely, rural villages in Bolivia were very poor, especially in the Chaco region. The Bolivian and Guatemalan studies produced strong evidence of vector-borne transmission of T. cruzi in domestic habitats, despite the fact that both areas had been sprayed with pyrethroid insecticides several times over the previous years and no local pyrethroid resistance was detected. In contrast, transmission threats were seasonally recurrent in Yucatan. Current routine operations against T. dimidiata in Central America rely on indoor (domestic) residual spraying with insecticides whereas full-coverage of domestic and peridomestic sites is recommended for T. infestans.
The initial situational analysis provided a deeper understanding of the study systems, guided the design and successful implementation of control interventions in community-centred efforts and gained support from several stakeholders. The key factors explaining variations in domestic bug infestation across study sites may be grouped according to housing quality, availability of animal hosts and location effects. Housing quality affected the availability of refuges for bugs in human sleeping quarters (i.e. cracked walls, earthen floors, tiled roofing, bags and clothes hanging on walls) and in peridomestic habitats (chicken coops or nests, rock piles and coffee trees).18,21,22 These results confirm previous findings that housing design and construction materials combined with their degree of maintenance affect the susceptibility of a house to bug invasion and subsequent development of domestic bug colonies.24–28 More specifically, the surface structure of indoor walls and the occurrence of thatched roofs were significant predictors of domestic infestation and abundance for the four major domestic vectors of T. cruzi elsewhere.11,25,26,29–32
However, the specificities of how housing quality affects domestic infestation vary between settings and triatomine bug species. Earthen floors are highly important for T. dimidiata which displays singular camouflage behaviour with dirt, unlike other triatomines.33 In the past, however, the predicted effects of earthen floors were not always supported by multivariate analyses of relatively large numbers of houses.31,34 Using a multi-model inference frame and an extensive database, the Guatemalan study documented that earthen floors and wall plaster condition were of high relative importance for domestic infestation.22 The Bolivian project emphasized the role of bags, objects on the walls and beds as important refuges for T. infestans.18 Beds were also a prime bug habitat in the Argentine Chaco:25 bugs from beds have immediate access to a human blood meal and are frequently infected with T. cruzi. Regular cleaning of beds and removing objects and clothes from the walls were therefore predicted to substantially decrease domestic infestation and bug abundance in the Bolivian study sites. The midterm assessment of intervention effects demonstrated substantial impacts on both outcome measures overall and in the specific bug habitats, especially in the Chaco region of Bolivia.18
Following a pilot trial showing that window screens greatly reduced house invasion by T. dimidiata in Yucatan,35 the large-scale situational analysis corroborated these results and provided another entry point for intervention.21 The intervention package addressed the concerns of the affected communities and stakeholders and gained their full support. It was successfully implemented at a village-wide scale and showed promising reductions in domestic infestation by T. dimidiata.20 The planned end-point assessment will take into account seasonal effects on house invasion and provide concluding evidence on intervention impacts.
The three studies highlighted the relevance of peridomestic structures as breeding or resting sites and sources of the triatomines that invade human sleeping quarters despite the fact that the study settings were notably different. Chicken coops or nests27 and poorly-built goat or pig corrals36 with many refuges and hosts were productive sources of T. infestans and other triatomines in the Argentine Chaco before and after residual insecticide spraying. These habitats provide better conditions and resources for the triatomine bugs than sylvatic habitats where the local hosts may not be available throughout the year. Improvement of goat corrals37 and other peridomestic structures38 may therefore reduce local infestations and contribute both to integrated vector control and enhanced livestock or poultry production, because high-density triatomine colonies also cause significant blood loss and anaemia. Implementing these environmental management measures indispensably requires the participation of householders and rural development agencies.
The Yucatan project suggests that regular clean-up of peridomestic areas may have mixed effects on domestic infestation by T. dimidiata depending on other unidentified factors.21,35 Cleaning peridomiciles may both reduce peridomestic bug habitats and (peri)domestic infestation, as observed in Costa Rica,38 but it may also facilitate the invasion of domestic premises by sylvatic triatomines that are no longer deflected by suitable peridomestic sites. In line with these findings, elsewhere in Guatemala the plastering of walls combined with insecticide spraying modified substantially the relative abundance of domestic and peridomestic T. dimidiata compared with insecticide spraying alone: reduction in the abundance of domestic refuges was followed by a decrease in the abundance of domestic bugs and an increase of peridomestic bugs.28 These results highlight the need for integrated environmental management of domestic and peridomestic habitats.
Host availability includes the presence or abundance of domestic and synanthropic hosts as blood meal sources. The key roles of chickens and dogs in the domestic ecology of Chagas disease vectors have been corroborated across multiple settings and triatomine species.18,21,22,25,27 Blood meal identification tests also demonstrated that chickens, dogs and humans are major hosts of domestic and peridomestic T. dimidiata and T. infestans in the study areas and elsewhere.22,39,40 The frequent practice of keeping chickens indoors for protection in rural areas with a subsistence economy notoriously resists change,18 and so does the habit of letting domestic dogs wander freely and share domestic premises with house-dwellers in poverty-stricken regions. These challenges still need to be addressed effectively.
The additional contribution of house mice and rats to domestic bug infection with T. cruzi, combined with the strong association between T. dimidiata and rodent infestations, are novel findings with clear implications for the design of innovative, integrated vector control strategies. Although synanthropic rodents were infected by T. cruzi in various settings,41,42 their role as (peri)domestic reservoir hosts and the effects of rodent control measures on bug infestation and parasite transmission had not been assessed. The Guatemalan project corroborated large house infestation rates with rodents,31 and revealed strong links between rats and mice in walls and tiled roofs, infestation with T. dimidiata and T. cruzi infection.22 These results paved the way for a novel community-based rodent control program that received immediate acceptance and was fully implemented by the affected communities. The endpoint assessment showed significant reductions in rodent infestation or abundance and in the prevalence of T. cruzi infection among early-stage nymphs.19 It remains to be seen whether reducing the abundance of rodents will decrease house infestation with T. dimidiata and bug infection over time, and how this may impact on human-vector contact rates. If rodent numbers have an additive effect on bug population growth and infection, as domestic dogs do in northern Argentina,43 the risk of bug infection is predicted to decline with effective rodent control, as the impact assessment suggests. However, the direct effects of reducing the abundance of rodents on domestic bug infestation may not be obvious in the presence of several other domestic hosts (humans, dogs and chickens) to which the bugs may shift. Furthermore, sylvatic T. dimidiata may still invade the premises and confound the relationship between domestic bug infestation or infection and rodents.
Spatial risk factors for domestic infestation by T. dimidiata were identified in Yucatan, where proximity to the periphery of the village apparently favoured house invasion from the surrounding sylvatic habitats.21 These results are consistent with other risk factor analyses of (peri)domestic infestation by Triatoma pallidipennis and R. prolixus, which showed that the spatial characteristics of residences or their distance to specific vegetation harbouring bug colonies need to be considered more closely.12,44
Other risk factors usually associated with domestic triatomine infestations were found to be relatively not as important as in many other studies, including the number of people resident in the household27,32,45 and household insecticide use.25,27 Because of the close links between domestic triatomines and humans as main blood meal sources,40,46 the absence of statistically significant effects of household size on domestic infestation needs to be interpreted with caution.
Future efforts to identify relevant risk factors for house infestation may take advantage of current results and explore further avenues. Measuring the impact of control interventions on additional response variables (i.e. host-vector contact and vector blood-feeding rates;46,47 combined measures of bug abundance and infection at well-defined habitats; domestic host infection10) is needed to translate reductions in house infestation into transmission risks and human infection. Improved estimates of local bug abundance (rather than presence/absence estimates) are needed for assessing habitat suitability and transmission risks. Knowledge on the key sources of triatomine bugs in domestic, peridomestic and sylvatic habitats and their relative habitat suitability may be used for targeted vector control and risk stratification,48 as with R. prolixus and Attalea butyracea palm trees in Venezuela.12 The combined use of site-specific timed manual searches and bug sensing devices for continuous monitoring of infestations may give valuable information on the different demographic processes involved in house (re)infestation. The frequent finding of peridomestic colonies of T. dimidiata49 suggests that IVM (including modification of key peridomestic habitats combined with carefully administered peridomestic insecticide sprays) may be justified in areas with recurrent domestic infestation and transmission risks. More investigations including the social determinants of health, house infestation and domestic transmission of T. cruzi are needed.50
Community-based vector control interventions with an emphasis on sustainability demand additional follow-up time and efforts for a full appraisal. Some crucial questions include: How can sustainability be evaluated and how long is needed to do so? How feasible is it that the communities will continue with the interventions on their own and that such interventions will be incorporated into local control programmes? Window screens also addressed a major local concern (mosquito nuisance) and may also help prevent dengue in Yucatan,51 whereas rodent reduction was welcome in Guatemala because of its effects on food production and storage. These collateral benefits52 may be crucial for the sustainability of community-based control interventions against Chagas disease vectors.
Conclusions
The three projects identified quasi-stable determinants of domestic infestation that most likely underlie the recurrent nature of house recolonisation by triatomine bugs. Improving the quality of rural housing and living conditions results in healthier homes with direct repercussions on community health beyond Chagas disease. Partnering with stakeholders working on other diseases or disciplines may help address problems that have similar causes. A multi-pronged approach including community mobilisation and empowerment, intersectoral cooperation and adhesion to IVM principles may be the key to sustainable vector and disease control in the affected regions.
Acknowledgments
Authors' contributions: REG and ZEY conceived, wrote and revised the article. Both authors read and approved the final manuscript. REG is guarantor of the paper.
Acknowledgements: The authors are grateful to Pamela M. Pennington (Universidad del Valle de Guatemala, Guatemala), Eric Dumonteil (Universidad de Yucatán, Mérida, Mexico) and Fréderic Lardeux (Institut de Recherche pour le Développement, France), Principal Investigators of the participating research projects and authors of the single-site articles presented in this special issue, for providing access to unpublished materials and helpful discussions.
Funding: This investigation received financial support from the UNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases (TDR) with the aid of a grant from the International Development Research Centre (IDRC), Ottawa, Canada.
Competing interests: None declared.
Ethical approval: Not required.
References
- 1.Lee BY, Bacon KM, Bottazzi ME, Hotez PJ. Global economic burden of Chagas disease: a computational simulation model. Lancet Infect Dis. 2013;13:342–8. doi: 10.1016/S1473-3099(13)70002-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Hotez PJ, Bottazzi ME, Franco-Paredes C, et al. The neglected tropical diseases of Latin America and the Caribbean: a review of disease burden and distribution and a roadmap for control and elimination. PLoS Negl Trop Dis. 2008;2:e300. doi: 10.1371/journal.pntd.0000300. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.WHO. Geneva: World Health Organization; 2002. Control de la Enfermedad de Chagas. Comité de expertos de la OMS en control de la Enfermedad de Chagas [in Spanish]. Serie de Informes Técnicos 905. [Google Scholar]
- 4.Diotaiuti L, Faria Filho OF, Carneiro FC, et al. Operational aspects of Triatoma brasiliensis control [in Portuguese] Cad Saude Publica. 2000;16:61–7. [PubMed] [Google Scholar]
- 5.Gottdenker NL, Chaves LF, Calzada JE, et al. Host life history strategy, species diversity, and habitat influence Trypanosoma cruzi vector infection in changing landscapes. PLoS Negl Trop Dis. 2012;6:e1884. doi: 10.1371/journal.pntd.0001884. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Grijalva MJ, Terán D, Dangles O. Dynamics of sylvatic Chagas disease vectors in coastal Ecuador is driven by changes in land cover. PLoS Negl Trop Dis. 2014;8:e2960. doi: 10.1371/journal.pntd.0002960. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Viotti R, Alarcón de Noya B, Araujo-Jorge T, et al. Towards a paradigm shift in the treatment of chronic Chagas disease. Antimicrob Agents Chemother. 2014;58:635–9. doi: 10.1128/AAC.01662-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Yamagata Y, Nakagawa J. Control of Chagas disease. Adv Parasitol. 2006;61:129–65. doi: 10.1016/S0065-308X(05)61004-4. [DOI] [PubMed] [Google Scholar]
- 9.Gürtler RE. Sustainability of vector control strategies in the Gran Chaco Region: current challenges and possible approaches. Mem Inst Oswaldo Cruz. 2009;104:52–9. doi: 10.1590/s0074-02762009000900009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Gürtler RE, Kitron U, Cecere MC, et al. Sustainable vector control and management of Chagas disease in the Gran Chaco, Argentina. Proc Natl Acad Sci USA. 2007;104:16194–9. doi: 10.1073/pnas.0700863104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Campbell-Lendrum D, Angulo VM, Esteban L, et al. House-level risk factors for triatomine infestation in Colombia. Int J Epidemiol. 2007;36:866–72. doi: 10.1093/ije/dym065. [DOI] [PubMed] [Google Scholar]
- 12.Sanchez-Martin MJ, Feliciangeli MD, Campbell-Lendrum D, Davies CR. Could the Chagas disease elimination programme in Venezuela be compromised by reinvasion of houses by sylvatic Rhodnius prolixus bug populations? Trop Med Int Health. 2006;11:1585–93. doi: 10.1111/j.1365-3156.2006.01717.x. [DOI] [PubMed] [Google Scholar]
- 13.WHO. Handbook for integrated vector management. Geneva: World Health Organization; 2012. [Google Scholar]
- 14.Ault SK. Environmental management: a re-emerging vector control strategy. Am J Trop Med Hyg. 1994;50:35–49. doi: 10.4269/ajtmh.1994.50.35. [DOI] [PubMed] [Google Scholar]
- 15.Sommerfeld J, Kroeger A. Eco-bio-social research on dengue in Asia: a multicountry study on ecosystem and community-based approaches for the control of dengue vectors in urban and peri-urban Asia. Pathog Glob Health. 2012;106:428–35. doi: 10.1179/2047773212Y.0000000055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Charron DF. New York: Springer; 2012. Ecohealth research in practice. Innovative applications of an ecosystem approach to health; pp. 1–282. [Google Scholar]
- 17.Arunachalam N, Tana S, Espino F, et al. Eco-bio-social determinants of dengue vector breeding: a multi-country study in urban and periurban Asia. Bull World Health Organ. 2010;88:173–84. doi: 10.2471/BLT.09.067892. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Lardeux F, Depickère S, Aliaga C, et al. Experimental control of Triatoma infestans in poor rural villages of Bolivia through community participation. Trans R Soc Trop Med Hyg. 2015;109:150–8. doi: 10.1093/trstmh/tru205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.De Urioste-Stone SM, Pennington PM, Pellecer E, et al. Development of a community-based intervention for the control of Chagas disease based on peridomestic animal management: an eco-bio-social perspective. Trans R Soc Trop Med Hyg. 2015;109:159–67. doi: 10.1093/trstmh/tru202. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Waleckx E, Camara-Mejia J, Ramirez-Sierra MJ, et al. An innovative ecohealth intervention for Chagas disease vector control in Yucatan, Mexico. Trans R Soc Trop Med Hyg. 2015;109:143–9. doi: 10.1093/trstmh/tru200. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Dumonteil E, Nouvellet P, Rosecrans K, et al. Eco-bio-social determinants for house infestation by nondomiciliated Triatoma dimidiata in the Yucatan peninsula, Mexico. PLoS Negl Trop Dis. 2013;7:e2466. doi: 10.1371/journal.pntd.0002466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Bustamante DM, de Urioste-Stone SM, Cruz JG, Pennington PM. Ecological, social and biological risk factors for continued Trypanosoma cruzi transmission by Triatoma dimidiata in Guatemala. PLoS One. 2014;9:e104599. doi: 10.1371/journal.pone.0104599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Abad-Franch F, Vega M, Rolón M, et al. Community participation in Chagas disease vector surveillance: systematic review. PLoS Negl Trop Dis. 2011;5:e1207. doi: 10.1371/journal.pntd.0001207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Schofield CJ, Briceño-León R, Kolstrupp N, et al. The role of house design in limiting vector-borne disease. In: Curtis CF, editor. Appropriate technology in vector control. Boca Raton, FL, USA: CRC Press; 1990. pp. 187–212. [Google Scholar]
- 25.Cecere MC, Gürtler RE, Chuit R, Cohen JE. Factors limiting the domestic density of Triatoma infestans in north-west Argentina: a longitudinal study. Bull World Health Organ. 1998;76:373–84. [PMC free article] [PubMed] [Google Scholar]
- 26.Cecere MC, Gürtler RE, Canale DM, et al. Effects of partial housing improvement and insecticide spraying on the reinfestation dynamics of Triatoma infestans in rural northwestern Argentina. Acta Trop. 2002;84:101–16. doi: 10.1016/s0001-706x(02)00183-3. [DOI] [PubMed] [Google Scholar]
- 27.Gurevitz JM, Ceballos LA, Gaspe MS, et al. Factors affecting infestation by Triatoma infestans in a rural area of the humid Chaco in Argentina: a multi-model inference approach. PLoS Negl Trop Dis. 2011;5:e1365. doi: 10.1371/journal.pntd.0001349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Monroy C, Bustamante DM, Pineda S, et al. House improvements and community participation in the control of Triatoma dimidiata re-infestation in Jutiapa, Guatemala. Cad Saude Publica. 2009;25:S168–78. doi: 10.1590/s0102-311x2009001300016. [DOI] [PubMed] [Google Scholar]
- 29.Mott KE, Muniz TM, Lehman JS, Jr, et al. House construction, triatomine distribution, and household distribution of seroreactivity to Trypanosoma cruzi in a rural community in northeast Brazil. Am J Trop Med Hyg. 1978;27:1116–22. doi: 10.4269/ajtmh.1978.27.1116. [DOI] [PubMed] [Google Scholar]
- 30.Rojas de Arias A, Ferro EA, Ferreira ME, Simancas LC. Chagas disease vector control through different intervention modalities in endemic localities of Paraguay. Bull World Health Organ. 1999;77:331–9. [PMC free article] [PubMed] [Google Scholar]
- 31.Bustamante DM, Monroy C, Pineda S, et al. Risk factors for intradomiciliary infestation by the Chagas disease vector Triatoma dimidiata in Jutiapa, Guatemala. Cad Saude Publica. 2009;25:S83–92. doi: 10.1590/s0102-311x2009001300008. [DOI] [PubMed] [Google Scholar]
- 32.Andrade AL, Zicker F, De Oliveira RM, et al. Evaluation of risk factors for house infestation by Triatoma infestans in Brazil. Am J Trop Med Hyg. 1995;53:443–7. doi: 10.4269/ajtmh.1995.53.443. [DOI] [PubMed] [Google Scholar]
- 33.Zeledón R, Vargas LG. The role of dirt floors and of firewood in rural dwellings in the epidemiology of Chagas' disease in Costa Rica. Am J Trop Med Hyg. 1984;33:232–5. doi: 10.4269/ajtmh.1984.33.232. [DOI] [PubMed] [Google Scholar]
- 34.Starr MD, Rojas JC, Zeledón R, et al. Chagas' disease: risk factors for house infestation by Triatoma dimidiata, the major vector of Trypanosoma cruzi in Costa Rica. Am J Epidemiol. 1991;133:740–7. doi: 10.1093/oxfordjournals.aje.a115949. [DOI] [PubMed] [Google Scholar]
- 35.Ferral J, Chavez-Nuñez L, Euan-Garcia M, et al. Comparative field trial of alternative vector control strategies for non-domiciliated Triatoma dimidiata. Am J Trop Med Hyg. 2010;82:60–6. doi: 10.4269/ajtmh.2010.09-0380. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Gürtler RE, Canale DM, Spillmann C, et al. Effectiveness of residual spraying of peridomestic ecotopes with deltamethrin and permethrin on Triatoma infestans in rural western Argentina: a district-wide randomized trial. Bull World Health Organ. 2004;82:196–205. [PMC free article] [PubMed] [Google Scholar]
- 37.Gorla DE, Abrahan LB, Hernández ML, et al. New structures for goat corrals to control peridomestic populations of Triatoma infestans (Hemiptera: Reduviidae) in the Gran Chaco of Argentina. Mem Inst Oswaldo Cruz. 2013;108:352–8. doi: 10.1590/S0074-02762013000300014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Zeledón R, Rojas JC, Urbina A, et al. Ecological control of Triatoma dimidiata (Latreille, 1811): five years after a Costa Rican pilot project. Mem Inst Oswaldo Cruz. 2008;103:619–21. doi: 10.1590/s0074-02762008000600020. [DOI] [PubMed] [Google Scholar]
- 39.Pellecer MJ, Dorn PL, Bustamante DM, et al. Vector blood meals are an early indicator of the effectiveness of the Ecohealth approach in halting Chagas transmission in Guatemala. Am J Trop Med Hyg. 2013;88:638–44. doi: 10.4269/ajtmh.12-0458. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Rabinovich JE, Kitron UD, Obed Y, et al. Ecological patterns of blood-feeding by kissing-bugs (Hemiptera: Reduviidae: Triatominae) Mem Inst Oswaldo Cruz. 2011;106:479–94. doi: 10.1590/s0074-02762011000400016. [DOI] [PubMed] [Google Scholar]
- 41.Barrett TV, Hoff R, Mott KE, et al. An outbreak of acute Chagas's disease in the São Francisco Valley region of Bahia, Brazil: triatomine vectors and animal reservoirs of Trypanosoma cruzi. Trans R Soc Trop Med Hyg. 1979;73:703–9. doi: 10.1016/0035-9203(79)90025-7. [DOI] [PubMed] [Google Scholar]
- 42.Zeledón R, Solano G, Burstin L, Swartzwelder JC. Epidemiological pattern of Chagas' disease in an endemic area of Costa Rica. Am J Trop Med Hyg. 1975;24:214–25. doi: 10.4269/ajtmh.1975.24.214. [DOI] [PubMed] [Google Scholar]
- 43.Cohen JE, Gürtler RE. Modeling household transmission of American Trypanosomiasis. Science. 2001;293:694–8. doi: 10.1126/science.1060638. [DOI] [PubMed] [Google Scholar]
- 44.Cohen JM, Wilson ML, Cruz-Celis A, et al. Infestation by Triatoma pallidipennis (Hemiptera: Reduviidae: Triatominae) is associated with housing characteristics in rural Mexico. J Med Entomol. 2006;43:1252–60. doi: 10.1603/0022-2585(2006)43[1252:ibtphr]2.0.co;2. [DOI] [PubMed] [Google Scholar]
- 45.Levy MZ, Bowman NM, Kawai V, et al. Periurban Trypanosoma cruzi-infected Triatoma infestans, Arequipa, Peru. Emerg Infect Dis. 2006;12:1345–52. doi: 10.3201/eid1209.051662. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Gürtler RE, Cecere MC, Vazquez-Prokopec GM, et al. Domestic animal hosts strongly influence human-feeding rates of the Chagas disease vector Triatoma infestans in Argentina. PLoS Negl Trop Dis. 2014;8:e2894. doi: 10.1371/journal.pntd.0002894. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Monteon V, Alducin C, Hernandez J, et al. High frequency of human blood in Triatoma dimidiata captured inside dwellings in a rural community in the Yucatan peninsula, Mexico, but low antibody seroprevalence and electrocardiographic findings compatible with Chagas disease in humans. Am J Trop Med Hyg. 2013;88:566–71. doi: 10.4269/ajtmh.12-0583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Gürtler RE, Cecere MC, Fernández MP, et al. Key source habitats and potential dispersal of Triatoma infestans populations in Northwestern Argentina: Implications for vector control. PLoS Negl Trop Dis. 2014;8:e3238. doi: 10.1371/journal.pntd.0003238. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Reyes-Novelo E, Ruiz-Piña H, Escobedo-Ortegón J, et al. Triatoma dimidiata (Latreille) abundance and infection with Trypanosoma cruzi in a rural community of Yucatan, Mexico. Neotrop Entomol. 2013;42:317–24. doi: 10.1007/s13744-013-0120-x. [DOI] [PubMed] [Google Scholar]
- 50.WHO. A conceptual framework for action on the social determinants of health. Geneva: World Health Organization; 2010. [Google Scholar]
- 51.Rosecrans K, Cruz-Martin G, King A, Dumonteil E. Opportunities for improved Chagas disease vector control based on knowledge, attitudes and practices of communities in the Yucatan peninsula, Mexico. PLoS Negl Trop Dis. 2013;8:e2763. doi: 10.1371/journal.pntd.0002763. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Ehrenberg JP, Ault SK. Neglected diseases of neglected populations: thinking to reshape the determinants of health in Latin America and the Caribbean. BMC Public Health. 2005;5:119. doi: 10.1186/1471-2458-5-119. [DOI] [PMC free article] [PubMed] [Google Scholar]