Leishmaniases are tropical zoonotic diseases, caused by kinetoplastid parasites from the genus Leishmania. New World (NW) species are related to sylvatic cycles although urbanization processes have been reported in some South American Countries such as Colombia. Currently, few studies show the relative distribution of Leishmania species related to cutaneous Leishmaniasis (CL) in South America due to the lack of accurate surveillance and public health systems. Herein, we conducted a systematic estimation of the Leishmania species causing CL in Colombia from 1980 to 2001 via molecular typing and isoenzymes. A total of 327 Leishmania isolates from humans, sandflies and reservoirs were typed as L. panamensis 61.3% (201), L. braziliensis 27.1% (88), L. lainsoni 0.6% (2), L. guyanensis 0.9% (3), L. infantum chagasi 4% (12), L. equatoriensis 0.6% (2), L. mexicana 2.1% (8), L. amazonensis 2.8% (9) and L. colombiensis 0.6% (2). This is the first report of two new Leishmania species circulating in Colombia and suggests the need to convince the Colombian government about the need to deploy and standardize tools for the species identification to provide adequate management to individuals suffering this pathology.
Leishmaniases include a spectrum of diseases caused by the flagellate protozoan Leishmania, an obligate intracellular protozoan parasite that infects humans and other mammals1. The clinical manifestations of the disease include cutaneous leishmaniasis (skin ulcers), mucocutaneous leishmaniasis and visceral leishmaniasis (lethal spleen/liver inflammation); the parasite is transmitted to humans by the bite of infected sandflies (Psychodidae family)2. Leishmaniases are prevalent in 98 countries with an incidence of 1.3 million of new cases each year, although only half is reported. The visceral form causes 300,000 cases (90% in Bangladesh, Brazil, Ethiopia, India, Nepal, South Sudan and Sudan) and one million belong to the cutaneous (mostly in Afghanistan, Algeria, Brazil, Colombia, Iran, Pakistan, Peru, Saudi Arabia, Syria and Tunisia) or mucocutaneous forms (especially in Brazil, Peru and Bolivia)1. The genus Leishmania includes more than 20 species and is divided into 3 subgenera, according to the development site of the parasite in the sandfly: Leishmania (Leishmania), Leishmania (Viannia) and Leishmania (Sauroleishmania). Species and subspecies grouped in complexes are under constant review and debate with recent descriptions of new cryptic species3,4. The difficult classification of multiple species and subspecies of Leishmania depends on several aspects and species identification is needed to provide adequate treatment for infected patients: i) Biological: development in the sandfly, growth in culture media and development in vertebrate hosts5 ii) Biochemical: isoenzyme patterns, sequencing of multiple loci (multilocus enzyme typing)-current “gold standard”5,6 iii) Immunological: parasitic analysis with monoclonal antibodies7; iv) Phylogenetical: multilocus sequence typing and DNA sequencing of single/multiple loci8.
Cutaneous leishmaniasis (CL) is the most common form of leishmaniasis and causes ulcers on the exposed parts of the body, leaving scars for life. About 95% of CL cases occur in the Americas, the Mediterranean, the Middle East and Central Asia. More than two thirds of new cases of CL occur in six countries: Afghanistan, Algeria, Brazil, Colombia, Iran and Syria. An estimated of 0.7 million to 1.3 million new cases occur worldwide annually1,2,9. Although leishmaniasis is estimated to cause the greatest burden of disease among single infectious disease, it is ignored in discussions on priorities for tropical disease control10. This is due to its complex epidemiology and ecology, lack of simple and easy tools to apply for case management and limited current incidence data11,12. Also, the variations of etiologic agents causing a number of different pathologies complicate the treatment, management and control of this tropical disease.
Colombia is one of the three countries with the highest number (seven species) of Leishmania parasites affecting humans13,14. About 99.3% of all cases are CL, 0.4% mucocutaneous leishmaniasis (MCL) and 0.3% visceral leishmaniasis (VL)15. The disease prevails in much of the country, moving from sylvatic to domestic cycles16. Cutaneous leishmaniasis outbreaks caused by L. braziliensis, L. panamensis and L. guyanensis are associated with intra and peridomiciliary transmission, which have been reported since 198417. However, most studies in the country do not report the species involved and likewise have never assessed the genetic variability of the species circulating in the country.
From 1990 to 1999, 58897 cases were recorded in Colombia, 96.35% of CL, 2.65% of MCL and 1% of VL. Epidemiological data does not include species identification and to date, data on parasite species distribution on a country scale is scarce. The aim of this study was to assess Leishmania distribution in Colombia based on parasite isolates from patients with CL, mammals and sandfly vectors collected in different geographical regions of Colombia and recruited in the National Leishmaniasis surveillance program from 1980 to 2001, using techniques unavailable at the time data were collected. The cytochrome b gene was sequenced in order to establish the circulating species, determine the genetic diversity and assessing its potential use in relation to the gold standard markers as MLEE.
Materials and Methods
Intensive sampling was conducted during 21 years as part of the epidemiological surveillance of CL conducted by the National Health Institute in Colombia. Isolates from humans, sandflies and mammals from 22 departments in Colombia (Antioquia, Bolivar, Boyaca, Caldas, Caqueta, Casanare, Choco, Cordoba, Cundinamarca, Guainia, Guajira, Guaviare, Huila, Magdalena, Meta, Norte de Santander, Putumayo, Risaralda, Santander, Sucre, Tolima and Vichada) with high, medium and low endemicity were obtained. Sandflies (Lutzomyia longipalpis, Pintomyia spinicrassa and Psathyromyia shannoni) and mammals (Canis lupus familiaris, Didelphis marsupialis and Akodon sp.) were captured in domestic (within dwellings), peridomestic (near dwellings) and sylvatic (more than 250 meters from dwellings) localities. To perform mammal sampling, technicians previously trained by veterinarians took the punch biopsy; sampled species were not endangered or protected. In the case of domestic animals, the owners provided oral informed consent to allow the sampling. Animals were anesthetized and a punch biopsy was collected. In all cases, animals were released and manipulated following the international guiding principles for biomedical research involving animals, as issued by the Council for International Organizations of Medical Sciences. The methods were carried out in accordance with the above mentioned approved guidelines. All experimental protocols were approved by the ethics and technical scientific committee of National Institute of Health in Bogotá, Colombia.
Leishmania parasites were isolated from human patients performing methods that were carried out in accordance with the approved guidelines by the ethics and technical scientific committee of National Institute of Health in Bogotá, Colombia (All experimental protocols were approved by this institute´s committee). Written informed consent was obtained from all subjects.
Leishmania Cytb barcoding and comparison with MLEE
We obtained 327 isolates (311 from humans, 6 from mammalian reservoirs and 10 from sandflies). Punch biopsies were triturated in sterile Ten Broeck homogenizers containing phosphate buffered saline (PBS), gentamicin (40 ug/ml) and 5-fluorocytosine (500 μg/mL). The resultant tissue suspension was inoculated directly into 2 tubes of NNN medium. The methods used for processing sand flies for parasite isolation were as reported elsewhere18. DNA was extracted from 200–μL aliquots of the exponential phase cultures using a QIAamp DNA Isolation Kit. The DNA quality and concentration were measured at 260 nm and stored at −20 °C.
The isolates included in this study were previously typed by Multilocus Enzyme Electrophoresis using distinct enzymes such as Lactate dehydrogenase (1.11.27), Malate dehydrogenase (126.96.36.199), Malic enzyme (188.8.131.52), Isocitrate dehydrogenase (184.108.40.206), Phosphogluconate dehydrogenase (220.127.116.11), Glucose-6-phosphate dehydrogenase (18.104.22.168), Glutathion reductase (e22.214.171.124), Glutamate-oxaloacetransaminase (126.96.36.199), Glutamate-pyruvate transaminase (188.8.131.52), Hexokinase (184.108.40.206) 6-Phosphofructokinase (220.127.116.11), Phosphoglucomutase (18.104.22.168), Acid phosphatase (22.214.171.124), Peptidase D (126.96.36.199), Fumarate hydratase (188.8.131.52), Mannose phosphate isomerase (184.108.40.206) and Glucose phosphate isomerase (220.127.116.11) following the specifications and reference strains reported elsewhere19. Additionally, the partial region of the cytochrome b gene (marker encoded on maxicircles) was amplified by PCR in a total volume of 50 uL containing 1X of Buffer, 100 mM of dNTPs, 50 pM of each primer, 5U of Taq Polymerase (Invitrogen) and 10 ng of DNA. The PCR products were digested with EXOSAP (Affymetrix, USA) and sequenced by the dideoxy-terminal method in an automated capillary sequencer (AB3730, Applied Biosystems) by both strands in Macrogen (Korea). The sequences were submitted to BLASTn for similarity search with Leishmania sequences deposited on the databases. Since Cytb marker is not able to discriminate L. braziliensis from L. peruviana species, those isolates typed as L. braziliensis were subsequently typed by direct sequencing of HSP70 as recommended elsewhere20,21.
Phylogenetic reconstruction and diversity analyses
The resulting sequences were edited in MEGA 5.0 and aligned using ClustalW 1.8 with reference sequences from L. donovani donovani (AB095957), L. donovani infantum (AB095958), L. donovani chagasi (AB095959), L. tropica (AB095960), L. major (AB095961), L. aethiopica (AB095962), L. mexicana mexicana (AB095963), L. amazonensis (AB095964), L. garnhami (AB095965), L. braziliensis (AB095966), L. panamensis (AB095968), L. guyanensis (AB095969), L. equatoriensis (AB434687), L. pifanoi (EF579907), L. lainsoni (AB433280), L. colombiensis (KF302738) and L. peruviana (AB433282) retrieved from GeneBank as suggested by different studies22,23. A maximum composite likelihood (MCL) analysis using a Tamura-3 parameter was run in RaxML Phylogeny.fr platform. To evaluate the robustness of the nodes in the resulting phylogenetic tree, 1000 bootstrap replicates were performed.
In addition to ML analyses, a Nexus matrix was constructed for haplotype network analysis in Network 2.0 using a median-joining model based on 1000 iterations with default parameters. The purpose of this analysis was to determine the diverse number of mitochondrial alleles across the population and determine the biological and geographical distribution of the alleles depicted for four species (L. panamensis, L. braziliensis, L. amazonensis and L. infantum chagasi). Lastly, sequence genetic diversity was estimated for Cytb gene fragment by species set. π and θ nucleotide diversity indexes and haplotype diversity were calculated in DNAsp v.5.0.
Spatial, temporal and ecological distribution patterns
To address the spatial distribution of Leishmania parasites isolated, a georeferenced database was constructed. Data on human isolates belong to the health center where patients were diagnosed and location of insects and mammals belong to the capture locality. To assess temporal variation, the database was divided in four ranks and distribution maps for each time-set were built. Although this temporal variation does not reflect parasite dispersal, it does reunite all epidemiological information available in the country and allow us to describe potential distribution during the time of the study. For those parasite species with seven or more collection data points, ecological analyses were performed. Using ArcGIS10.3 we extracted values of Ecoregions24 and Colombian Ecosystems25 in order to describe parasite distribution by Ecosystems and land´s use coverage. Additionally, using vector species potential distribution maps, published by Ferro and collaborators in 2015, we described phlebotominae of medical importance in Colombia spatially associated to parasite occurrences.
Leishmania Cytb barcoding and comparison with MLEE
A total of 327 Leishmania isolates were typed by means of Cytb barcoding and MLEE profiles. Edited sequences were submitted to Blastn search for sequence and hit similarity to conduct the Cytb barcoding, in general the sequences showed an average identity of 98% with the reported Genbank sequences. Overall, the concordance between MLEE and Cytb was high (Kappa Cohen Index 0.833 p < 0.05), a total of 19 (5.8%) isolates showed incongruences as follows: MLEE did not identify four isolates (Identity uncertain) that Cytb barcoding reported as L. colombiensis (2 isolates) and L. equatoriensis (2 isolates); two isolates were typed as L. guyanensis by MLEE and typed as L. lainsoni by Cytb. MLEE classified 2 isolates as L. mexicana that Cytb typed as L. amazonensis. Lastly, there were 11 strains that showed a hybrid profile L. panamensis/L. braziliensis by MLEE and typed as L. panamensis by Cytb.
These incongruences were further confirmed by sequencing of HSP70 gene fragment where the Blastn hits showed concordance with the Cytb barcoding findings. Based on the final consensus of Cytb and HSP70 typing (Incongruent isolates and further typing of L. braziliensis isolates), the frequency of Leishmania species detected were as (Table S1): L. panamensis 61.3% (201), L. braziliensis 27.1% (88), L. lainsoni 0.6% (2), L. guyanensis 0.9% (3), L. infantum chagasi 4% (12), L. equatoriensis 0.6% (2), L. mexicana 2.1% (8), L. amazonensis 2.8% (9) and L. colombiensis 0.6% (2). The sequences were aligned and robust phylogenetic reconstruction was conducted observing concordance with the genetic clustering reported by other groups using Cytb marker and the independent barcoding of the samples. The ML unrooted tree showed high support bootstrap for the species identified across our dataset (Fig. 1).
Phylogenetic reconstruction and diversity analyses
In total, the Cytb gene showed 82 polymorphic sites for all the species studied with a total of 87 mutations. The genetic diversity by species was measured showing that L. panamensis presented the highest genetic diversity followed by L. infantum chagasi and L. braziliensis based on the haplotype diversity index. Leishmania guyanensis, L. amazonensis and L. colombiensis showed moderate levels of haplotype diversity index. Lastly, L. lainsoni showed a tailored degree of haplotype diversity (Hd = 1) and L. mexicana and L. equatoriensis showed absence of haplotypic diversity (Hd = 0) (Table 1). When π and θ were observed, the pattern maintained as the observed with the haplotypic diversity index. In particular, L. lainsoni showed high values along these genetic diversity indexes.
Haplotype networks were constructed to determine the mitochondrial alleles distributed according to geography and host (human, sandfly, mammalian reservoir). These analyses were only conducted in L. panamensis, L. braziliensis, L. infantum chagasi and L. amazonensis isolates because were the most prevalent species across our study. We divided the department based on eco-geographical regions and observed that all four species alleles are circulating in the Andean region. L. panamensis was the most diverse species with one dense haplotype harboring alleles from Andean and Orinoquia region, a second haplotype harboring alleles from Andean and Pacific regions and a third haplotype harboring alleles from Orinoquia and Amazon region. The rest of the haplotypes were considered independent based on the geographical subdivisions. The genetic connectivity was illustrated and each geographical region is clustered with the exception of the Orinoquia region haplotypes that showed two genetic backgrounds (Andean region and Amazon region) (Fig. 2A). For L. braziliensis, there was one unique haplotype harboring different geographical regions alleles (Atlantic, Orinoquia and Andean regions); the rest of haplotypes were unique based on the geographical region. Curiously, Amazon region alleles are shared with the Andean and Atlantic regions (Fig. 2B). L. infantum chagasi showed three haplotypes with independent alleles from the Andean and Amazon regions and in the case of L. amazonensis three haplotypes with alleles from the Orinoquia, Andean and Atlantic regions (Fig. 2C,D). Network analyses were also conducted and colored based on the hosts; this analysis is limited due to the high number of isolates obtained from humans and the low number from sandflies and mammalian reservoirs. However, in all the cases (L. panamensis, L. braziliensis, L. infantum chagasi and L. amazonensis), it was possible to determine that alleles from the three hosts are shared confirming the maintenance of the transmission in the areas (Fig. 2).
Spatial, temporal and ecological distribution patterns
The most widespread species in Colombia was L. panamensis, 201 isolates in 109 localities distributed across 19 departments (Fig. 3); its distribution ranges from lowlands to highlands in the Andean region. Similar patterns of geographical distribution were found for Leishmania braziliensis, isolated in 63 localities from 17 departments while L. amazonensis was isolated in nine localities widely distributed in five departments and L. infantum chagasi in nine localities in six departments. Three departments showed the highest abundance of the isolates (Antioquia, Cundinamarca and Santander). Interestingly, Antioquia contributed the highest number of CL and ML cases and only five departments contributed 52% of CL cases from 1990 to 1999. Poorly known species with few records were detected during the sampling: L. lainsoni (2 isolates), obtained from humans in Antioquia and Putumayo and L. equatoriensis (2 isolates) from humans in Antioquia.
In general, sampling was performed successively in all the departments during the time of the study, except for Bolivar, Magdalena and Sucre that were sampled once. From 1980 to 1986 six parasite species were detected in the country, mainly distributed in the Magdalena River Valley with most localities positive for L. panamensis in eight Departments. From 1986 to 1990 L. braziliensis was recorded in the Amazonia and Orinoquia regions while L. panamensis was detected in the north and west. In 1988 L. colombiensis was isolated from P. shannoni. From 1991 to 1995 L. braziliensis and L. panamensis were reported in new localities, with L. panamensis being found almost in every region of the country except the Amazonia and L. braziliensis reaching the northern corner of Colombia in La Guajira. From 1996 to 2001, L. lainsoni was isolated for the first time in two spatially separated localities, Putumayo, in the south in 1997 and Antioquia in the north in 2001. L. panamensis was found in two new departments, Caquetá and Vichada in 1996 while L. braziliensis appeared for the first time in Cordoba in 1997 (Fig. 4).
Most collection localities (51%) belonged to Montane Forest coverage followed by moist forest (25%) and dry forest (16%); however, regarding land use coverages, 92% of the collection records were distributed in transformed ecosystems. It is important to note that collection data points did not belong to actual transmission sites thus further analyses could not be performed. Vector species present in all parasite isolation sites were Psychodopygus panamensis, P. shannoni and Lutzomyia gomezi. Isolation sites for Leishmania amazonensis furthermore coincided with Nyssomyia yuilli yuilli, L. braziliensis with Pintomyia ovallesi, and L. mexicana with Nyssomyia antunesi. Additionally, L. infantum chagasi, as expected for their proven association, was isolated in Lu. longipalpis distribution areas.
Despite the high number of cases annually occurring in Colombia and the relevance of parasite species identification in the establishment of adequate management for Leishmaniases in Colombia, the surveillance systems have not developed an active and accurate strategy to control this pathology, as happens for many other neglected tropical diseases in Latin America. This premise is observed in the lack of updated studies regarding the epidemiology of the infection. Few studies have highlighted the over-representation of L. panamensis, L. guyanensis and L. braziliensis in humans, sandflies and mammalian reservoirs in Colombia17,26 and a retrospective study conducted in seven departments, detected the presence of L. panamensis (74,45%), L. braziliensis (15,33%), L. guyanensis (0,73%), L. mexicana complex (3,65%) and Leishmania mexicana (5,11%) in 137 isolates14. The technique employed in those studies was MLEE, but direct sequencing of genetic markers was never performed so far. Herein, we conducted the first retrospective study in Colombia (including 22 departments) using Cytb barcoding, finding the existence of nine species associated with CL (Figs 1 and 3).
Genetic barcoding using Cytb or other genetic marker has been useful for Leishmania species identification. The WHO suggests MLEE as the ‘gold standard’, but this method is time consuming limiting its potential as a gold standard27. Recently, the use of PCR-RFLP directed to Heat Shock Protein genes has shown a reasonable potential for species typing28. Also, the use of HRM (High Resolution Melting) platforms has proven to be useful for this purpose29. However, all these methods present some drawbacks that gene sequencing can solve. Some authors have shown how useful the Cytb barcoding could be in clinical samples and isolates due to its high sensitivity, specificity and be an uniparental informative22,30,31. In our case, the direct sequencing of Cytb allowed the discrimination of nine Leishmania species, just in the case of L. braziliensis we had to submit the samples to confirmation by HSP70 sequencing due to the equal identity percentage of L. braziliensis and L. peruviana in GenBank. Nevertheless, the congruence between Cytb barcoding and MLEE profiling was high (KI = 0.833 p < 0.05), the incorrect assignment was observed for L. colombiensis, L. equatoriensis, L. mexicana and L. lainsoni, this must have occurred due to the inability of MLEE to discriminate closely related species within the Viannia subgenus. Also, another explanation could be the likely existence of interspecies hybrids but we would need to conduct phylogenetic analyses with several molecular markers to prove this hypothesis. One vestige of this premise is that Corredor et al., in 1980 reported a low percentage of isolates with ‘uncertain identity’ by MLEE means, which could have been the species herein reported. Our results show the high potential in the use of Cytb for species barcoding as has been demonstrated in Argentina where a high concordance was also observed23. However, it is well known that parasite isolation is not always successful and the distribution may have been biased because the analyses were only performed on isolates. New studies using clinical samples, insect vectors and samples from reservoirs are required to have an unbiased picture of the true distribution of Leishmania species in the country.
One of the advantages about using gene sequencing is the understanding of the intra-specific genetic diversity of Leishmania species. Our attempt was to describe the species circulating in the country but we could also determine its genetic diversity based on one single gene marker (Table 1; Fig. 2). All of the studies reported in Colombia have just shown the species distribution but never its diversity. In Brazil and Argentina a series of study using Multilocus Sequence Typing have been published but mainly focused on L. braziliensis32,33. MLST approaches have been conducted in Old World species as L. donovani, L. infantum chagasi, L. tropica, and L. major but not systematically in New World Leishmania species8,34,35,36. Our data supports interesting findings regarding a high genetic diversity displayed by L. panamensis (Hd = 0.123; S = 80). An important point to address is the high frequency of mutations in a conserved marker (Cytb) due to its uniparental inheritance status, therefore if examining single copy housekeeping genes the diversity may be greater than expected. In the haplotype network is observed that most of the isolates cluster in one dense haplotype (Fig. 2A). We just mentioned the case of L. panamensis due to the absence of MLST studies within this species but when examining L. braziliensis we observed a similar pattern (Hd = 0.390; S = 5). In the case of the haplotype network retrieved from L. braziliensis strains, two clear and dense haplotypes are tailored, one mainly disperse in the Andean region and the second across the Orinoquia and Atlantic region. This could provide insights about parasite genotype dispersal but future studies using high-resolution markers are required to fulfill these statements. This clearly suggests the need to apply MLST markers within L. panamensis and L. braziliensis in Colombia in order to understand the transmission dynamics and the plausible events of clonality and recombination across our dataset as discussed by different authors37,38.
Isolates from sandflies and mammals resulted according to previously published results and contributes new evidence of vector-parasite associations in Colombia. Pintomyia spinicrassa is a proven vector of L. braziliensis in Colombia and Venezuela and was found infected with that parasite in one collection site in 198539,40. Psathyromyia shannoni is a suspected vector of L. braziliensis in Bolivia and was found infected with Leishmania spp. parasites in Colombia40. Our study provides new findings of L. colombiensis and L. braziliensis isolated from three individuals of this vector species in Santander. Interestingly, Lu. longipalpis was found infected with three parasite species (L. infantum chagasi, L. braziliensis and L. panamensis) in the same collection site in 1998 and 1992 suggesting vector permissivity. This vector species is suspected vector of L. braziliensis, L. amazonensis and L. mexicana in Brazil41,42.
Leishmania equatoriensis was originally reported in Choloepus hoffmani and Sciurus granatensis from Ecuador43 but not reported in humans so far. In this study we detected the parasite in two human isolates in 1995 from different localities in Antioquia where the highest number of CL cases is reported and six Leishmania species are known to occur (Fig. 3). This data need to be treated cautiously because a recent report argues about the true status of L. equatoriensis and L. hertigi as Leishmania species3. Leishmania lainsoni was also detected form two isolates; the geographical distribution of this species includes Brazil, Peru and Bolivia and has been isolated from humans, sandflies and mammalian reservoirs44,45. Recent descriptions incriminate Nyssomyia umbratilis as the vector and a different range of mammals such as Agouti paca, Cebus paella and Mesocricetus auratus as reservoirs for this species44,46. Likewise, frequent mixed infections with L. braziliensis in humans with CL are reported in Peru and Bolivia. In Colombia, the sandfly N. umbratilis is present but probably remained undetected due to the low resolution of the methods employed in the past40.
Overall, we observed that L. panamensis and L. braziliensis are the most frequent species associated with CL in Colombia as previously reported14,26. Mucosal leishmaniasis (MCL) is also present in the country but we were not able to disregard if this clinical manifestation was present after isolation and patient follow-up. We also observed that L. mexicana, L. amazonensis, L. guyanensis and L. infantum chagasi are incriminated with CL (Fig. 1). Curiously, the autochthonous species L. colombiensis also reported in Venezuela and Panama was not detected in humans but detected in the sandfly P. shannoni. Laboratory studies indicate that at least three species of Leishmania parasites: L. mexicana, L. panamensis and L. infantum chagasi can develop in P. shannoni47, which is known to feed on mammals, including humans and has been reported to transmit visceral leishmaniasis in dogs, hamsters and other mammals. This would be the first report of natural infection in P. shannoni since previous reports show Lutzomyia hartmanni and Lutzomyia gomezi as vectors of this species48,49,50.
Regarding mammal species infected with Leishmania parasites, few studies on reservoir species have been conducted in Colombia51,52. This study revealed the presence of L. panamensis and L. amazonensis infecting dogs in two localities in the inter-Andean valleys. Dogs can get infected with the same parasite species and show lesions similar to humans, but their role as reservoirs is discussed and they are preferentially considered accidental hosts53,54. In our study, parasites were also isolated from synanthropic mammals such as Didelphis marsupialis infected with L. infantum chagasi and the rodent Akodon infected with L. braziliensis. Didelphis marsupialis is a known reservoir of L. infantum chagasi in Colombia55 and according to Brandao-Filho and collaborators, who found one Akodon arviculoides infected with L. braziliensis in Brazil, opposums and rodents constitute L. braziliensis reservoirs in Colombia and the Brazilian Amazonia56.
When the geographical distribution of Leishmania species was depicted, we did not detect a geographical clustering of the species as suggested by some authors in Colombia, but a broad distribution that seemed to increase during the time of the study14. We found that L. panamensis is broadly distributed in the country but L. braziliensis was more widespread (Fig. 3). Although distribution of Leishmania in an ecological context is variable and parasite dispersal includes migration of sandflies and reservoirs, parasite successive adaptations to new vector species and blood sources (Man/domestic animals), the broad pattern observed in this study could suggest that human migration can be highly affecting parasite species dispersal57,58. The constant human displacement in Colombia due to violence and political instability could be favoring the wider distribution of the different species. Recently, migration of L. guyanensis from the Amazonia forest, with new vector-parasite associations, was detected in two different habitats: the Andean valleys located above 1000 meters in the municipality of Chaparral (Tolima) and Sucre in the Colombian Caribbean coast14. The understanding of the ecology of leishmaniasis has to be proven from a continental level. It is interesting to observe the species distribution of Leishmania in neighbor countries as Ecuador, Peru and Venezuela. In Ecuador, L. panamensis, L. guyanensis, L. braziliensis, L. mexicana, L. amazonensis and L. equatoriensis have been described. In Peru, there exist reports of L. peruviana, L. lainsoni, L. amazonensis, L. guyanensis and L. braziliensis. Lastly, in Venezuela reports of L. braziliensis, L. colombiensis, L. venezualensis, L. amazonensis, L. panamensis, L. garnhami, L. infantum chagasi and L. guyanensis2. This broad geographical view supports our findings of new species circulating in Colombia, due to likely migrations of humans, insect vector or reservoirs from neighbor countries59.
In conclusion, we were able to discriminate nine Leishmania species isolated from cases of CL in Colombia from 1980 to 2001. Herein, we reported two new species circulating in the country and confirm the predominance of L. panamensis and L. braziliensis as the agents of CL in the country. We also showed the potential of the use of Cytb barcoding for species assignment and the need to pursue MLST studies to untangle the genetic diversity of an unknown species as L. panamensis and to contribute further information about L. braziliensis. These results are of paramount importance for the epidemiological surveillance of CL in the country and highlight the need to convince the Colombian government about the need to deploy and standardize tools for the species identification to provide adequate management to individuals suffering this pathology.
How to cite this article: Ramírez, J. D. et al. Taxonomy, diversity, temporal and geographical distribution of Cutaneous Leishmaniasis in Colombia: A retrospective study. Sci. Rep. 6, 28266; doi: 10.1038/srep28266 (2016).
World Health Assembly The World Health Assembly Resolution (WHA60.13) on the “Control of leishmaniasis”. Geneva, Switzerland. 5 p. (2007).
Alvar, J. et al. WHO Leishmaniasis Control Team: Leishmaniasis worldwide and global estimates of its incidence. PLoS. One. 7, e35671 (2012).
Marcili, A. et al. Phylogenetic relationships of Leishmania species based on trypanosomatid barcode (SSU rDNA) and gGAPDH genes: Taxonomic revision of Leishmania (L.) infantum chagasi in South America. Infect. Genet. Evol. 25, 44–51 (2014).
Schönian, G., Kuhls, K. & Mauricio, I. Molecular approaches for a better understanding of the epidemiology and population genetics of Leishmania. Parasitol 138, 405–425 (2011).
Schönian, G., Mauricio, I. & Cupolillo, E. Is it time to revise the nomenclature of Leishmania? Trends Parasitol. 26, 466–469 (2010).
Rioux, A. et al. Taxonomy of Leishmania. Use of isoenzymes. Suggestions for a new classification. Ann Parasitol Hum Comp. 65, 111–125 (1990).
Grimaldi, G. Jr. & McMahon-Pratt, D. Monoclonal Antibodies for the Identification of New World Leishmania Species. Mem. Inst. Oswaldo. Cruz. 91, 37–42 (1996).
Lukes, J. et al. Evolutionary and geographical history of the Leishmania donovani complex with a revision of current taxonomy. Proc. Natl. Acad. Sci. 29, 9375–8930 (2007).
Reithinger, R. et al. Cutaneous leishmaniasis. Lancet. Infect. Dis. 7, 581–596 (2007).
Hotez, P., Bundy, D. & Beegle, K. Helminth infections: Soil-Transmitted Infections and Schistosomiasis. The International Bank for Reconstruction and Development/The World Bank 1, 123–28 (2006).
Alvar, J., Yactayo, S. & Bern, C. Leishmaniasis and poverty. Trends Parasitol. 22, 552–557 (2006).
Bern, C., Maguire, J. & Alvar, J. Complexities of assessing the disease burden attributable to leishmaniasis. PLoS. Negl. Trop. Dis. 2, e313 (2008).
Corredor, A. et al. Epidemiology of visceral leishmaniasis in Colombia. Am. J. Trop. Med. Hyg. 40, 480–86 (1989).
Ovalle, C., Porras, L., Rey, M., Ríos, M. & Camargo, Y. Distribución geográfica de especies de Leishmania aisladas de pacientes consultantes al Instituto Nacional de Dermatología Federico Lleras Acosta,E.S.E., 1995–2005. Biomédica 26, 145–151 (2006).
Weigle, M. et al. Cutaneous leishmaniasis in Subtropical Ecuador: popular perceptions, knowledge and treatment. Bull PAHO 28, 142–55 (1993).
Ferro, C. et al. Spatial Distribution of Sand Fly Vectors and Eco-Epidemiology of Cutaneous Leishmaniasis Transmission in Colombia. PLoS One doi: 10.1371/journal.pone.0139391 (2015).
Valderrama, C. et al. Environmental risk factors for the incidence of American cutaneous leishmaniasis in a sub-Andean Zone of Colombia (Chaparral, Tolima). Am. J. Trop. Med. Hyg. 82, 243–250 (2010).
Young, D. et al. Isolations of Leishmania braziliensis (Kinetoplastida: Trypanosomatidae) from cryopreserved Colombian sand flies (Diptera: Psychodidae). J. Med. Entomol. 24, 587–589 (1987).
Corredor, A. et al. Distribution and etiology of leishmaniasis in Colombia. Am. J. Trop. Med. Hyg. 42, 206–214 (1990).
Montalvo, A., Fraga, J. & Hassan, S. Direct Leishmania species typing in Old World clinical samples: Evaluation of 3 sensitive methods based on the heat-shock protein 70 gene. Diagn. Micr. Infec. Dis. 80, 35–39 (2014).
Van der Auwera, G. et al. Heat-shock protein 70 gene sequencing for Leishmania species typing in European tropical infectious disease clinics. Euro Surveill. 18, 205–43 (2014).
Foulet, F. et al. Detection and identification of Leishmania species from clinical specimens by using a real-time PCR assay and sequencing of the cytochrome B gene. J Clin Mic. 45, 2110–2115 (2007).
Marco, J. et al. Are cytochrome b gene sequencing and polymorphism-specific polymerase chain reaction as reliable as multilocus enzyme electrophoresis for identifying Leishmania spp. from Argentina? Am. J. Trop. Med. Hyg. 75, 256–260 (2006).
Olson, D. et al. Terrestrial ecoregions of the world: a new map of life on Earth. Bioscience 51, 933–938 (2001).
Etter, A. Mapa general de ecosistemas de Colombia. En: Chaves, M. E., Arango, M., editores. Informe Nacional sobre el Estado de la Biodiversidad en Colombia. Tomo I. Diversidad Biológica. Instituto de Investigación de Recursos Biológicos Alexander von Humboldt, PNUMA, Bogotá: Ministerio del Medio Ambiente. 1–150 (1998).
Saravia, N. et al. Heterogeneity, geographic distribution and pathogenicity of serodemes of Leishmania Viannia in Colombia. Am. J. Trop. Med. Hyg. 66, 738–744 (2002).
Hernández, C. & Ramírez, J. Molecular diagnosis of vector-borne parasitic diseases. Air Water Borne Diseases. 2, 1 (2012).
Van der Auwera, G. & Dujardin, J. Species typing in dermal leishmaniasis. Clin. Microbiol. 28, 265–294 (2015).
Hernández, C. et al. dentification of Six New World Leishmania species through the implementation of a High-Resolution Melting (HRM) genotyping assay. Parasit. Vector. 7, 501 (2014).
Myint, C. K., Asato, Y., Yamamoto, Y. et al. Polymorphisms of cytochrome b gene in Leishmania parasites and their relation to types of cutaneous leishmaniasis lesions in Pakistan. Journal of Dermatology, 35, 76–85 (2008).
Asato, Y. et al. Phylogenic analysis of the genus Leishmania by cytochrome b gene sequencing Exp. Parasitol. 121, 352–361 (2009).
Boité, M., Mauricio, I., Miles, M. & Cupolillo, E. New Insights on Taxonomy, Phylogeny and Population Genetics of Leishmania (Viannia) Parasites Based on Multilocus Sequence Analysis. PLoS. Negl. Trop. Dis. 6, e1888 (2012).
Marlow, M., Boité, M., Ferreira, G., Steindel, M. & Cupolillo, E. Multilocus sequence analysis for Leishmania braziliensis outbreak investigation. PLoS. Negl. Trop. Dis. 13, e2695 (2014).
Zemanova, E. et al. The Leishmania donovani complex: genotypes of five metabolic enzymes (ICD, ME, MPI, G6PDH and FH), new targets for multilocus sequence typing. Int. J. Parasitol. 37, 149–60 (2007).
Mauricio, I. et al. Towards multilocus sequence typing of the Leishmania donovani complex: resolving genotypes and haplotypes for five polymorphic metabolic enzymes (ASAT, GPI, NH1, NH2, PGD). Int. J. Parasitol. 36, 757–769 (2006).
Gelanew, T. et al. Inference of population structure of Leishmania donovani strains isolated from different Ethiopian visceral leishmaniasis endemic areas. PLoS. Negl. Trop. Dis. 4, e889 (2010).
Rougeron, V., De Meeûs, T. & Bañuls, A. A primer for Leishmania population genetic studies. Trends Parasitol. 31, 52–59 (2015).
Ramírez, J. D. & Llewellyn, M. Reproductive clonality in protozoan pathogens – truth or artefact? Mol. Ecol. 23, 4195–4202 (2014).
Feliciangeli, M. Vectors of leishmaniasis in Venezuela. Parasitol. 33, 229–236 (1991).
Young, D. & Duncan, M. Guide to the identification and geographic distribution of Lutzomyia sand flies in Mexico, the West Indies, Central and South America (Diptera: Psychodidae). Associated Publishers, Gainesville (Florida) (United States of America) 1, 881 (1994).
Savani, E. et al. The finding of Lutzomyia almerioi and Lutzomyia longipalpis naturally infected by Leishmania spp in a cutaneous and canine visceral leishmaniases focus in Serra da Bodoquena, Brazil. Vet. Parasitol. 160, 18–24 (2009).
Lopez, Y. et al. Sandfly Lutzomyia longipalpis in a cutaneous leishmaniasis focus in central Colombia. Mem. Inst. Oswaldo. Cruz. 91, 415–419 (1996).
Grimaldi, G. & Tesh, R. Leishmaniases of the New World: current concepts and implications for future research. Clin. Microbiol. Rev. 6, 230–50 (1993).
Corrêa, J. et al. Axenic promastigote forms of Leishmania (Viannia) lainsoni as an alternative source for Leishmania antigen production. J. Parasitol. 91, 551–556 (2005).
Eresh, S., de Bruijn, M., Mendoza-Leon, J. & Barker, D. Leishmania (Viannia) lainsoni occupies a unique niche within the subgenus Viannia. Trans. R. Soc. Trop. Med. Hyg. 89, 231–236 (1995).
Silveira, F. et al. Cutaneous leishmaniasis in Amazonia: isolation of Leishmania (Viannia) lainsoni from the rodent Agouti paca (Rodentia: dasyproctidae), in the state of Para, Brazil. Rev. Inst. Med. Trop. Sao Paulo. 33, 18–22 (1991).
Ferro, C., Cardenas, E., Corredor, D., Morales, A. & Munsterman, L. Life Cycle and Fecundity Analysis of Lutzomyia shannoni (Dyar) (Diptera: Psychodidae). Mem, Inst. Oswaldo Cruz. 93, 195–199 (1998).
Kreutzer, D. et al. Characterization of Leishmania colombiensis sp. n. (Kinetoplastida: Trypanosomatidae), a new parasite infecting humans, animals and phlebotomine sand flies in Colombia and Panama. Am. J. Trop. Med. Hyg. 44, 662–675 (1991).
Dutari, L. & Loaiza, J. American cutaneous leishmaniasis in Panama: a historical review of entomological studies on anthropophilic Lutzomyia sand fly species. Parasit. Vectors 7, 218 (2014).
Rodriguez-Bonfante, C., Bonfante-Garrido, R., Grimaldi, G., Momen, Jr. H. & Cupolillo, E. Genotypically distinct Leishmania colombiensis isolates from Venezuela cause both cutaneous and visceral leishmaniasis in humans. Infect. Genet. Evol. 3, 119–124 (2003).
Travi, B., Arteaga, L., Leon, A. & Adler, G. Susceptibility of spiny rats (Proechimys semispinosus) to Leishmania (Viannia) panamensis and Leishmania (Leishmania) chagasi. Mem. Inst. Oswaldo. Cruz. 97, 887–892 (2002).
Alexander, B., Lozano, C., Barker, D., McCann, S. & Adler, G. Detection of Leishmania (Viannia) braziliensis complex in wild mammals from Colombian coffee plantations by PCR and DNA hybridization. Acta Trop. 69, 41–50 (1998).
Vélez, I., Carrillo, L., López, L., Rodríguez, E. & Robledo, S. An epidemic outbreak of canine cutaneous leishmaniasis in Colombia caused by Leishmania braziliensis and Leishmania panamensis. Am. J. Trop. Med. Hyg. 86, 807–811 (2012).
Santaella, J. et al. Leishmania (Viannia) infection in the domestic dog in Chaparral, Colombia. Am. J. Trop. Med. Hyg. 84, 674–680 (2011).
Travi, B. et al. Didelphis marsupialis, an important reservoir of Trypanosoma (Schizotrypanum) cruzi and Leishmania (Leishmania) chagasi in Colombia. Am. J. Trop. Med. Hyg. 50, 557–65 (1994).
Brandão-Filho, S. et al. Wild and synanthropic hosts of Leishmania (Viannia) braziliensis in the endemic cutaneous leishmaniasis locality of Amaraji, Pernambuco State, Brazil. Trans. R. Soc. Trop. Med. Hyg. 97, 291–296 (2003).
Dujardin, J. et al. Cryptic speciation in Lutzomyia (Nyssomyia) trapidoi (Fairchild & Hertig) (Diptera:Psychodidae) detected by Multilocus Enzyme Electrophoresis. Am. J. Trop. Med. Hyg. 54, 42–45 (1996).
Davies, C. et al. Spraying houses in the Peruvian Andes with lambda-cyhalothrin protects residents against cutaneous leishmaniasis. Trans. R. Soc. Trop. Med. Hyg. 94, 631–636 (2000).
Lainson, R. & Shaw, J. In Biology of the Kinetoplastida. (ed. Lumsden, W. & Evans, D. ) Ch. 9, 678–699. (London Academic Press, 1979).
We thank the Departamento Administrativo de Ciencia, Tecnología e Innovación ‘COLCIENCIAS’ for funding the Project “Fortalecimiento de la capacidad diagnóstica, de investigación y de vigilancia de enfermedades transmisibles emergentes y reemergentes en Colombia” grant number 757–13.
The authors declare no competing financial interests.
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Ramírez, J., Hernández, C., León, C. et al. Taxonomy, diversity, temporal and geographical distribution of Cutaneous Leishmaniasis in Colombia: A retrospective study. Sci Rep 6, 28266 (2016). https://doi.org/10.1038/srep28266
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