INTRODUCTION
Leptospirosis is a re-emerging disease caused by pathogenic spirochetes of the genus Leptospira [Reference Bharti1–Reference Hartskeerl, Collares-Pereira and Ellis3], of which rodents are believed to be important carriers [Reference Perez4–Reference Cosson6]. According to the World Health Organization the global burden of leptospirosis is estimated at over one million severe human cases per year, with a growing number of countries reporting leptospirosis outbreaks [Reference Hartskeerl, Collares-Pereira and Ellis3, Reference Abela-Ridder, Sikkema and Hartskeerl7]. Leptospirosis can represent up to 20–40% of idiopathic febrile illness [Reference Ko8]. South-East Asia is a region of particularly high incidence with Thailand, Cambodia, Laos, Philippines and Vietnam considered as areas in which leptospirosis is endemic [Reference Ivanova5, Reference Laras9, Reference Berlioz-Arthaud10]. The disease shows seasonal peaks of incidence during the rainy season in this tropical region, where most outbreaks seem to be related to flooding events [Reference Thaipadungpanit11–Reference Amilasan13].
Human infection is related to normal daily activities associated with poor sanitation and climatic conditions [Reference Victoriano14]. Exposure to pathogenic leptospires occurs by direct contact with urine of infected animal reservoirs, or indirectly with water contaminated by urine of infected animals. Generally, these animals are rodents, but also include dogs or livestock, in which leptospires can persist without clinical signs [Reference Desvars, Cardinale and Michault15]. Rodents are repeatedly cited as the main reservoirs [Reference Ivanova5, Reference Cosson6, Reference Wangroongsar16–Reference Benacer20]. However, pathogenic bacteria can survive in water long enough (from a few days to several months) to become the source of human or animal contamination [Reference Trueba21]. For instance, Ganoza et al. [Reference Ganoza22] showed that the concentration and species of leptospires found in environmental surface water correlated with the risk of severe leptospirosis in humans.
In Thailand, the disease was recorded for the first time in 1942 [Reference Tangkanakul23]. While leptospirosis incidence remained low until the 1990s, the number of cases increased markedly in 1995 with 143 cases reported, and continued to increase to a peak of 14 285 reported cases in 2000 [Reference Tangkanakul23]. Seasonal peak incidence occurs in the wet season, from September to October, 1 month after the rainfall peak. The eastern and northern parts of Thailand are the most affected regions [Reference Wuthiekanun24].
In order to better understand leptospirosis infection, this study attempted to overview the evolution of human infection over the past decade with regard to the influence of the public health campaign introduced by the Thai government in 2006, and identify the environmental factors that correlate with the incidence of bacteria in rodents and the clinical incidence in humans. Hence, in 2006, heavy flooding in Nan province led the provincial authorities to greatly improve health prevention by conducting regular awareness campaigns (encouraging farmers to wear boots and controlling rodent populations) and prophylaxis by allowing large distribution of antibiotics during flooding events. We then investigated the potential effects of these campaigns on the relationships between environmental factors and leptospirosis incidence, by comparing the periods before and after 2006. We hypothesized that, before 2006, human incidence should be mainly explained by the population size of the villages according to the environmental source of infection of this disease, whereas due to the campaigns conducted after 2006, human incidence in villages should be independent of their population size.
By investigating the environmental factors that correlate with rodent infection, we also tested the role of rodents in leptospire transmission to humans. We hypothesized that if rodents are a potential source of leptospire infection to humans, a co-occurrence of infection in rodents and humans should be observed in the same environment (i.e. habitat in land use). By using a rodent screening survey, we were able to test this hypothesis for the period 2008–2009.
Our approach is at the interface between health geography and spatial epidemiology. For this, we used an extensive survey of Leptospira infection in rodents conducted in 2008 and 2009 together with the human incidence of the disease from 2003 to 2012 in two districts of Nan province, Thailand and a land-use cover implemented in a Geographic Information System [Reference Dupuy25, Reference Morand26].
MATERIALS AND METHODS
Ethical statement
Systematic field sampling was performed by joint Thai and French research institute teams. Traps were set within houses with the oral approval of the owner or tenant. Outdoors, traps were set with the agreement of the head of the village. None of the rodent species investigated are on the CITES list, nor the Red List (IUCN). Animals were treated in accordance with the guidelines of the American Society of Mammalogists, and European Union legislation (Directive 86/609/EEC). Each trapping campaign was approved by the national, regional and local health authorities. Human incidence cases were gathered by the district hospitals of Tha Wang Pha and Pua. Approval notices for trapping and investigation of rodents, and use of human incidence recordings were given by the Ethics Committee of Mahidol University, Bangkok, Thailand (no. 0517.1116/661).
Study location
Nan province is located in northern Thailand where prevalence of leptospirosis is high compared to other regions of the country [Reference Wuthiekanun24]. In this rural area, farmers are thought to be exposed to leptospirosis in rice fields with standing water. In 2006, Nan was affected by a flood event and 1400 cases were reported after the peak of the flooding. Following this event, the government decided to introduce a prevention campaign by encouraging farmers to wear boots and by controlling rodent populations. Because of the high prevalence there and the government's major concern regarding leptospirosis emergence, Nan represents an important location to study both the impacts of environmental factors and the efficiency of health prevention policy.
We restricted the screening of leptospires to rodents, although domesticated animals have been mentioned to be involved as reservoirs of leptospires. However, the two districts investigated showed low abundance of water buffaloes and cattle due to agricultural intensification both in mechanization and cropping, especially corn, that reduced the presence of cattle herds. Dogs were also believed to be reservoirs, but as they live mainly in settlements (i.e. South-East Asian village dogs) they were not considered as main reservoirs for the whole habitats such as forests and agricultural lands [Reference Kurilung27].
We used the data published on rodents in the two districts in 2008–2009 concerning 94 individual rodents [Reference Cosson6], which were obtained by a screening of 131 individual rodents trapped at the same period. We summarize below the methods used for rodent sampling, rodent identification and Leptospira identification, which were extensively developed in previous published studies [Reference Cosson6].
Rodent sampling
Rodents were trapped in Nan province, Thailand (19·15 N, 100·83 E) in 2008 and 2009, within the framework of the CERoPath project (www.ceropath.org). Thirty lines of 10 traps were placed during four nights in three different habitats: (1) forests and mature plantations; (2) non-flooded lands or fields (shrubby wastelands, young plantations, orchards), (3) rain-fed lowland paddy rice fields (cultivated floodplain) (according to [Reference Herbreteau28]). Villages and isolated houses, which correspond to a fourth habitat category (4), namely the human settlement, were sampled using cage-traps distributed to residents. We used locally made cage live-traps (about 40 × 12 × 12 cm). We sampled twice: once in the wet season and once in the dry season with 1200 night-traps per trapping session (2400 in total). In both seasons, trap lines were located at the same place (using a Global Positioning System receiver). (For more detailed description of the trapping protocols see [Reference Morand26, Reference Bordes29].)
Rodent identification
Rodent species were identified in the field using morphological criteria (see www.ceropath.org/references/rodent_field_guide). When morphological criteria did not allow distinguishing species of some genera, molecular techniques were also used. We used a mitochondrial gene for barcoding Mus species and some Rattus species [Reference Galan, Pagès and Cosson30]. Voucher specimens (skulls) are deposited at the Institut des Sciences de l'Evolution (Montpellier, France), rodent tissues (liver preserved in alcohol) are deposited at the Kasetsart University (Department of Veterinary Medicine, Bangkok, Thailand).
Leptospira infection in rodents
The screening of leptospires was performed on rodent kidneys. Real-time polymerase chain reaction (RT–PCR) targeting lipL32 and β-actin genes was performed on rodent kidney DNA, extracted with a Bio Basic EZ-10 96 Well Plate genomic DNA isolation kit and the Qiagen DNeasy® Blood & Tissue kit (Qiagen S.A.S., France). Following alignment of β-actin gene sequences of Asian rodents, β-actin primers (forward: 5′-CCA TGA AAC TAC ATT CAA TTC CA-3′; reverse: 5′-TTC TGC ATC CTG TCA GCA A-3′) and probe (5′-AGA CCT CTA TGC CAA CAC AGT GCT G-3′) were designed using the highly conserved fifth exon sequence along with the Probe Design software for Light Cycler LC480 (Roche, USA). β-actin was used as an internal control for RT-PCR. In order to identify the human pathogenic strains, the TaqMan lipL32 assay, which targets a gene encoding for a pathogen-specific outer membrane protein in Leptospira, was performed using primers (forward: 5′-AAG CAT TAC CGC TTG TGG TG-3′; reverse: 5′-GAA CTC CCA TTT CAG CGA TT-3′) and probe (5′-AAA GCC AGG ACA AGC GCC G-3′). The amplification was performed on a Light Cycler 480 thermocycler (Roche). A Ct < 40 for the lipL32 amplicons was considered positive for Leptospira. (For more detailed information see [Reference Cosson6].)
Conventional PCR assays targeting the rrs gene were performed on positive RT–PCR samples. All samples were also amplified for secY. The rrs and secY PCR products were sequenced at the Platform Genotyping of Pathogens and Public Health (Institut Pasteur, Paris, France). Leptospira species were identified by sequencing rrs genes and subsequent BLAST searches using the GenBank database. (For more detailed information see [Reference Cosson6].)
Land cover and environmental indices
Recent (2007–2008) high spatial resolution (2·5 m in panchromatic mode and 10 m in multispectral mode) SPOT 5 satellite images were acquired (CNES 2009, distributed by Astrium Services/Spot Image S.A., France). SPOT-Digital Elevation Model (DEM) with a spatial resolution of 20 m together with the SRTM (Shuttle Radar Topography Mission, http://srtm.usgs.gov/) DEM (90-m spatial resolution) were also acquired, allowing estimations of elevation and slope. The SPOT scene was classified into different land-cover types using an object-based approach (eCognition Developer software) [Reference Dupuy25]. Each scene was first segmented into objects, which were then classified using a supervised process based on three types of object properties: intrinsic characteristics (reflectance values, slope values, shape and texture), topological characteristics (relationships to neighbouring objects) and contextual characteristics (semantic relationships between objects). The schemes were merged into five main classes: forest, steep agricultural land (i.e. non-flooded agriculture), flat agricultural land (i.e. flooded, irrigated, paddy fields), water surface (ponds, lakes, rivers), and built-up surfaces (i.e. villages, cities). The land-cover map and the DEM were integrated into a Geographic Information System (GIS) in ArcGIS 10.0 software (ESRI, USA). Landscape metrics to assess actual fragmentation were extracted from the land-cover classifications using the Fragstats freeware (www.umass.edu/landeco/research/fragstats/fragstats.html) and included proportions of each land-cover type, patch density (i.e. density of the different land-cover types), and border density (i.e. density of the contour of all patches) [Reference Dupuy25]. (See more detailed information in [Reference Morand26].)
Human incidence
Data on leptospirosis incidence were obtained for each of 168 villages, for the years 2003–2012, from the district hospitals of Tha Wan Pha and Pua. Patients were clinically diagnosed in district hospitals, and only patients with severe symptoms were laboratory-confirmed for leptospirosis. The GPS localizations of villages were obtained in the field with the help of the Department of Agriculture Extension of both districts of Tha Wan Pha and Pua (Fig. 1). Sixty percent of villages have <35% of forest area 2 km around the village. Data on human incidence in both villages are given in Figure 2.
Simplified land use of Tha Wang Pha and Pua districts showing the villages with number of leptospirosis cases. (a) 2003–2012, (b) 2003–2006, (c) 2007–2012.
Values of leptospirosis incidence in the two districts of Tha Wang Pha and Pua from 2003 to 2012.
Statistical analyses
To analyse the infection of rodents, we modelled the probability of presence/absence of the Leptospira infection as a function of several environmental indices with a logistic regression [Generalized Linear Model (GLM) with logit function] using package lme4 implemented in R [31]. Cases in each logistic regression were infected or non-infected individual rodents. A first initial model (rodent model 1) included the explanatory variables related to distance between the place where each individual rodent were trapped and the main habitats: distance from forest (Dist Forest), distance from human settlement (Dist Settl), distance from agriculture on steep land (Dist Agri steep), distance from agriculture on flat land (Dist Agri flat). The second initial model (rodent model 2) included the environmental indices related to the habitat structure, and was calculated for a buffer of 100 m for each individual rodent trapped: cover of agriculture on steep land (%Agri steep), cover of agriculture on flat land (%Agri flat), cover of forest (%Forest), cover of human settlement (%Settl) and patch density. No interactions were added to the independent variables. Selection of the best model was done using a step-forward procedure based on Akaike's Information Criterion (AIC) for both initial models.
To analyse the leptospirosis incidence in humans, we modelled the number of leptospirosis infection by village as a function of population size and several environmental indices with a GLM with a negative binomial distribution using package lme4 implemented in R. The environmental indices related to the distance to water source (river), altitude and the habitat structure calculated for a buffer of 4 km diameter for each village (corresponding roughly to the agricultural lands of the villages): cover of agriculture on steep land (%Agri steep), cover of agriculture on flat land (%Agri flat), cover of forest (%Forest), cover of human settlement (%Settl), patch density,
We analysed the total number of incidence cases from 2003 to 2012 (human model 1), and separately the period 2003–2006 (human model 2) and the period 2007–2012 (human model 3) in order to test the effect of the public health policy of the Nan provincial administration, characterized by an improvement of prevention and campaign for leptospirosis infection and the provision of antibiotics as prophylaxis during flooding events. We analysed the period (2008–2009) (human model 4) in order to compare leptospirosis infection in humans and rodents. We tested the existence of potential spatial autocorrelation using the package mass implemented in R.
RESULTS
Rodent infection
The 225 individual trapped rodents from eight species were tested by PCR for infection by Leptospira (merged with the data published in [Reference Cosson6]). The percentage of trapping success is low, <5%, with more 5000 night-traps including lines and traps given to local people. Of these, 10 (4·4%) were found to be infected by Leptospira interrogans (Table 1). Bandicota indica was the most infected rodent, although the bacteria were found in Berylmys berdmorei, Berylmys bowersi and Rattus tanezumi.
Rodent species trapped and tested for Leptopsira infection in Tha Wang Pha and Pua districts of Nan province (Northern Thailand)
The best GLMs with logit function showed the importance of several environmental indices in explaining the presence of Leptospira in rodents (Table 1). An infection was likely observed in relation to forest habitat and human settlement (Table 2). Increase in habitat fragmentation, together with large patches of forest, appears to be positively associated with rodent infection (Table 3, Fig. 3).
Partial contribution of (a) distance to the forest, (b) forest cover (in %) and (c) habitat fragmentation (patch density) in explaining Leptospira infection in rodents from GLM (see selected rodent models in Table 3).
Comparison of models used to test the effect of several independent variables on individual rodent infection (GLM with logit function)
Models are ranked from the least to the most supported according to corrected Akaike's Information Criterion (AIC). Two initial models were tested: rodent model 1 included the following explanatory variables: slope (Slope), distance from forest (Dist Forest), distance from human settlement (Dist Settl), distance from agriculture on steep land (Dist Agri steep), distance from agriculture on flat land (Dist Agri flat). Rodent model 2 included the following explanatory variables: cover of agriculture on steep land (Agri steep), cover of agriculture on flat land (Agri flat), cover of forest (Forest), cover of human settlement (Settl), patch density (Patch).
Results of the best GLM (with logit link function) of Table 2 explaining the presence of Leptospira species in rodents as a function of habitat characteristics obtained from land cover layers
The initial rodent model 1 included the following explanatory variables: distance from forest (Dist Forest) and distance from human settlement (Dist Settl). The initial rodent model 2 included the following explanatory variables: cover of agriculture on steep (Agri steep), land cover of agriculture on flat land (Agri flat), cover of forest (Forest), cover of human settlement (Settl), patch density (Patch). Values of factors were obtained from the land covers. Explanatory variables were ranked according to their contribution to the model. [LR χ 2 = likelihood ratio χ 2 test for test of fit for explanatory variable; residual deviance with degrees of freedom (d.f.); global fit given by Wald test.]
Human incidence
The evolution of human incidence in Tha Wang Pha and Pua districts shows that before 2006 incidence was low. In 2006 we observed a sudden increase in incidence, related to flooding events in this area (Fig. 2). After 2006 and the beginning of a new public health policy, incidence became low again, but still higher than before. The best GLMs with negative binomial function showed that, for all years 2003–2012 (human model 1), villages with high leptospirosis incidence were situated close to a river in a non-patchy habitat, dominated by agricultural land on steep slopes, at low altitude (Tables 4 and 5). Population size was also a significant factor explaining human incidence. These results are visualized using partial contribution of village population size, partial contribution of distance to the river and partial contribution of patch density to human cases (Fig. 4a – c ). High human incidence was better related to a lower distance to the river than a lower habitat fragmentation (patch density).
Partial contribution of (a) population size, (b) distance to river and (c) habitat fragmentation (patch density) in explaining leptospirosis infection in Tha Wang Pha and Pua districts in 2003–2006 from GLM (selected human model 2 in Table 5). Partial contribution of (d) population size, (e) distance to river and (f) cover of agriculture in slope (in %) in explaining leptospirosis infection in Tha Wang Pha and Pua districts in 2007–2012 from GLM (selected human model 3 in Table 5).
Comparison of models used to test the effect of several independent variables on leptospirosis incidence in villages of Tha Wang Pha and Pua districts (Nan province, Thailand) using GLM with negative binomial function
Models are ranked from the least to the most supported according to corrected Akaike's Information Criterion (AIC). Four initial models were tested: human model 1 (2003–201); human model 2 (2003–2006); human model 3 (2007–20012); human model 4 (2008–2009). Each model included the following explanatory variables: population size (Pop), altitude (Alt), distance from river (Dist riv), cover of agriculture on steep land (Agri steep), cover of agriculture on flat land (Agri flat), cover of forest (Forest), cover of human settlement (Settl) and patch density (Patch).
Results of the best GLM (with negative binomial function) of Table 4 explaining the leptospirosis incidence in the villages of Tha Wang Pha and Pua districts (Nan province, Thailand) as a function of habitat characteristics obtained from land cover layers
Four initial models were tested: human model 1 (2003–2012); human model 2 (2003–2006); human model 3 (2007–20012); human model 4 (2008–2009). Each model included the following explanatory variables: population size (Pop), altitude (Alt), distance from river (Dist riv), cover of agriculture on steep land (Agri steep), cover of agriculture on flat land (Agri flat), cover of forest (Forest), cover of human settlement (Settl) and patch density (Patch). Explanatory variables were ranked according to their contribution to the model. [Theta and s.d. of the negative binomial distribution; LR χ 2 = likelihood ratio χ 2 test for test of fit for explanatory variable; residual deviance with degrees of freedom (d.f.); global fit given by Wald test.]
Separating the analyses before (human model 2) and after (human model 3) 2006 showed contrasting results (Tables 4 and 5). Human model 2 was similr to human model 1, with the influences of distance to river, altitude, population and agricultural land on steep slopes explaining human incidence (Tables 4 and 5). Partial contribution of distance to the river to human cases followed the same trend (Fig. 4). Human model 3 differed from human models 1 and 2 by showing the importance of forest cover in the vicinity of villages leading to high incidence of cases. Partial contribution of distance to the river and forest area to human cases illustrate those links (Fig. 4e , f ). Moreover, also retained in the best model (lower AIC value), population size appeared not to be statistically associated with human incidence after 2006 (Table 5, Fig. 4d ).
Human incidence during the rodent trapping session (2008–2009)
To compare environmental factors between rodent infection and human incidence, human model 4 analysed human incidence restricted to the rodent trapping session (2008–2009). The model showed no differences with the previous human models 2 and 3. Increased human cases were found associated with low habitat patchiness and close distance to the river, whereas rodents were likely infected in fragmented habitats comprising large patches of forest and low human settlement cover (Table 5).
Control for spatial autocorrelation
We detected a strong spatial autocorrelation for human leptospirosis incidence in 2003–2012 (Moran's I statistic, s.d. = 7·48, P < 0·0001), population size (Moran's I statistic, s.d. = 3·13, P = 0·0009), and for altitude of village (Moran's I statistics.d. = 14·53, P < 0·0001). These values suggested strong spatial correlation between all these variables. However, the residual values of the GLM model with the binomial distribution function explaining disease incidence in humans for human model 1 (2003–2012) (see above, Table 5) showed no spatial autocorrelation (Moran's I statistic, s.d. = 0·30, P = 0·38). Similar lack of spatial autocorrelation of residuals was observed for human models 2–4.
DISCUSSION
Rodent infection and habitat
The results presented here for the two districts of Nan province are similar to those obtained in the analyses performed on rodents from seven different sites in Thailand, Cambodia and Lao PDR [Reference Cosson6]. Similar to the study of Cosson et al. [Reference Cosson6], although restricted to these two districts of Nan province, we found that the rodents carrying Leptospira were those trapped in forests or in patchy environment mostly located on hills.
An analysis of agrarian systems was made in one village of Tha Wang Pha district (P. Belchi, unpublished data), which appears fairly representative of the villages affected by the 2006 outbreak and also of a rapid shift in crop cultivation. Maize and rice are the main crops cultivated. Rice is grown and consumed mostly locally, whereas maize is a cash crop that has increased significantly over the last 10 years fostered by a strong public sector investment in research and extension, maize production being promoted by the Ministry of Agriculture particularly for the production of input for livestock producers and feed millers [Reference Ekasingh, Thong-Ngam, Gulati and Dixon32]. Indeed, Northern Thailand has become the leading producer of corn in the country, with a contribution of 49% to the national production [Reference Ekasingh33]. The spread of this new culture has profoundly impacted the agricultural landscape. Maize is cultivated under rain-fed conditions on hill land where the soil surface devoted to cultivation is insufficiently watered, even during the rainy season, due to the steepness of the slope. Farmers recognized strong erosion problems associated with significant decline in soil fertility. They noted that the expansion of the cultivation of corn was associated with a significant increase in the number of rats on this agricultural land. A rodent outbreak was noticed in 2008, which particularly affected some cornfields.
Human incidence and habitat
Since the floods of 2006, the authorities have implememted regular awareness campaigns on prevention of leptospirosis (and measures of prophylaxis such as free antibiotic distribution). The results of the GLM analyses showed that, before and after 2006, the dynamics of leptospirosis seemed to change significantly. For example, during the flooding of 2011 there were threefold fewer cases than during the flooding of 2006. After 2006, the human infection appears more strongly linked to land use, obviously dependent on land management options. Based on the results from 2003 to 2006, the human incidence was correlated with a short distance to the river, which is in accord with the increase of cases during the flooding of 2006. After 2006, the correlated variables were more related to land use with no influence of human population size. This result confirms the significant and positive effects of the provincial public health on the incidence of the diseases in these two districts of Nan province.
The observation that population size did not further correlate with human incidence after 2006 suggests that public health campaigns have improved the knowledge, attitudes and practices of the population toward leptospirosis. Hence, a study based on individual interviews conducted in a village of Tha Wang Pha district in 2013 [Reference Della34], confirmed the population's awareness regarding leptospirosis infection and prevention. A better diagnosing and reporting of the disease may have occurred after 2006 with a population better informed about symptoms, and health officers more aware than before. The level of human incidence after 2006 is likely to be explained by risky behaviours and lack of prevention by infected people.
Humans and rodents were not infected in similar habitats
Although the dynamics of the disease has changed over the past decade, the rodent infection showed different environmental patterns than human infection when investigating the period 2008–2009. Leptospirosis in rats correlated with a significant proportion of forest in a patchy landscape principally situated on hills, whereas human infections occurred in villages in non-forested and non-patchy areas located in the vicinity of rivers. The water factor, i.e. distance to river or the potential of flooding, was investigated for human and rodent infection, but appeared related only to human infection. The water factor, as depicted as distance to river, seems to have a greater influence on human infection than on rodent infection.
These results challenge the role of rodents as carriers or reservoirs of Leptospira. Moreover, the overall decrease of livestock, either cattle or buffaloes, linked to the increase of agricultural intensification and productivity also questions their roles in the transmission of the disease.
Finally, the statistical observation that humans and rodents are infected in different habitats/environments, at least for the period investigated in this study, urges us to improve our knowledge on the microbial ecology of the bacteria. Indeed, few studies have investigated the requirements of the free-living bacteria in the soil or the role of the virulence factors in its survival and growth [Reference Ganoza22, Reference Picardeau35, Reference Aviat36]. Further studies should collect environmental samples in order to collect and grow environmental leptospires. Our study may help in targeting habitats for sampling.
Limits and implications of the study
One can question the choice of variables in relation to these different time scales as the human epidemiological data covered the years 2003–2012, while the variables concerning the rodent infection and land use were related to 2007–2008. In a context of rapidly changing land use as observed in Nan province, this may have potentially biased the analyses concerning the data prior to 2006 even if the land cover has been simplified in order to reduce the potential biases linked to land-use changes. During the period of the propagation of corn culture, farmers in Nan province encroached on the lands of forest reserves to the detriment of the forested areas resulting in rapid land-use changes and the deterioration of water catchments due to a massive use of pesticides to increase maize production (encouraged by the implementation of a governmental natural disaster risk insurance scheme for maize from 2007).
In order to limit the encroachment of agriculture in forested areas, the government implemented an agrarian reform, leading to the regulation of land by granting property titles, thus limiting the expansion of agricultural land into the forest [Reference Ekasingh, Thong-Ngam, Gulati and Dixon32].
Nowadays, agricultural parcels have little chance of returning to a forest plot in a context where the pressure on agricultural land is still strong. However, shifts to rubber plantations were also observed due to the provision of subsidies to local farmers of the province (from 2005) as an incentive to grow rubber. In addition, as stated by Suzuki [Reference Suzuki37], financial incentives such as REDD+ could benefit climate change mitigation and adaptation and at the same time, provide support for the communities to manage the forests sustainably. In ‘utilization forest’ zones where some activities such as farming are possible, it has been noted that community management could lead to natural regeneration and biodiversity similar to ‘conservation’ forests, where human activity is forbidden [Reference Kijtewachakul, Shivakoti and Webb38]. It might go alongside community watershed management and restoration. However, from 2007 the slight increase of forest land area (National Statistical Office of Thailand, 2013) could be explained by the existence and promotion of community forest management, an area of forest managed by the local community. Even though community forest management has been practised for more than 100 years by Thai people [Reference Salam39], it was not legally framed [Reference Lubanski40].
The overlapping systems of management of natural resources associated with water or forest community management, agricultural practices, dam projects, and flood management are leading to natural-resource and land-use changes. For instance, deforestation for agricultural purposes resulted in an increased run-off coefficient [Reference Pakoksung and Koontanakulvong41]. This dynamics of change should be studied further as it affects the risk of leptospirosis, particularly in a context of climate change. If the environment is influenced first by physical factors it is also a result of policies and regulations in various sectors such as forest conservation, water resource management, agricultural policies and rural property law. Ultimately, environmental changes are linked with political and economic choices which may contribute to the changes regarding the risk of leptospirosis [Reference Morand26].
ACKNOWLEDGEMENTS
This study was funded by the French ANR Biodiversity, grant ANR 07 BDIV 012 CERoPath project (‘Community Ecology of Rodents and their Pathogens in a changing environment’) (www.ceropath.org), and by the French ANR CP&ES, grant ANR 11 CPEL 002 BiodivHealthSEA project (‘Local impacts and perceptions of global changes: Biodiversity, health and zoonoses in Southeast Asia’) (www.biodivhealthsea.org). SPOT images and SPOT DEMs were obtained with financial support of the ISIS (‘Incitation à l'utilisation Scientifique des Images SPOT’) programme operated by the French Space Agency, CNES (Centre National d'Etudes Spatiales). The authors thank S. Dupuy, CIRAD, for image processing, and special thanks to all participants in the fieldwork for their great help. We also thank two anonymous reviewers for helpful comments.
DECLARATION OF INTEREST
None.
