Figures
Abstract
Background
Triatoma dimidiata, currently the major Central American vector of Trypanosoma cruzi, the parasite that causes Chagas disease, inhabits caves throughout the region. This research investigates the possibility that cave dwelling T. dimidiata might transmit the parasite to humans and links the blood meal sources of cave vectors to cultural practices that differ among locations.
Methodology/Principal Findings
We determined the blood meal sources of twenty-four T. dimidiata collected from two locations in Guatemala and one in Belize where human interactions with the caves differ. Blood meal sources were determined by cloning and sequencing PCR products amplified from DNA extracted from the vector abdomen using primers specific for the vertebrate 12S mitochondrial gene. The blood meal sources were inferred by ≥99% identity with published sequences. We found 70% of cave-collected T. dimidiata positive for human DNA. The vectors had fed on 10 additional vertebrates with a variety of relationships to humans, including companion animal (dog), food animals (pig, sheep/goat), wild animals (duck, two bat, two opossum species) and commensal animals (mouse, rat). Vectors from all locations fed on humans and commensal animals. The blood meal sources differ among locations, as well as the likelihood of feeding on dog and food animals. Vectors from one location were tested for T. cruzi infection, and 30% (3/10) tested positive, including two positive for human blood meals.
Conclusions/Significance
Cave dwelling Chagas disease vectors feed on humans and commensal animals as well as dog, food animals and wild animals. Blood meal sources were related to human uses of the caves. We caution that just as T. dimidiata in caves may pose an epidemiological risk, there may be other situations where risk is thought to be minimal, but is not.
Author Summary
Caves have enduring appeal to humans, and their lure in Central America includes tourism, religious ceremonies and shelter. The major Chagas disease vector in this region, Triatoma dimidiata, inhabits caves throughout its range. We challenge the assumption that cave-dwelling vectors are not important for human transmission by determining blood meal sources of vectors collected in caves from three locations that differ in the activities of humans at the caves, and link the results to cultural practices that differ among locations. Seventy percent of cave-collected vectors were positive for human DNA, and fed on 10 additional vertebrates with relationships to humans varying from companion animal (dog), food animals (pig, sheep/goat), wild animals (duck, bat, opossum) to commensal animals (mouse, rat). Feeding sources relate to human activities that vary among locations, for example, human and food animals were the main sources in Cahabón caves, located within deforested areas that are now agricultural fields and houses. We tested vectors from one location for infection with the Chagas disease parasite and found 30% (3 of 10) infected, including two of the three vectors from this location that had evidence of human blood. Humans should be aware of potential consequences of visiting and sleeping in caves.
Citation: Stevens L, Monroy MC, Rodas AG, Dorn PL (2014) Hunting, Swimming, and Worshiping: Human Cultural Practices Illuminate the Blood Meal Sources of Cave Dwelling Chagas Vectors (Triatoma dimidiata) in Guatemala and Belize. PLoS Negl Trop Dis 8(9): e3047. https://doi.org/10.1371/journal.pntd.0003047
Editor: Eric Dumonteil, Universidad Autónoma de Yucatán, Mexico
Received: October 2, 2013; Accepted: June 16, 2014; Published: September 11, 2014
Copyright: © 2014 Stevens et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study received financial support from NeTropica (www.netropica.org), National Institutes of Health (USA) Grant 1R15 A1079672-01A (http://www.nih.gov), and NSF grant BCS-1216193 as part of the joint NSF-NIH-USDA Ecology and Evolution of Infectious Diseases program (http://www.nsf.gov). Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the funding agencies. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Humans have been attracted to caves for much of our history for purposes as varied as religious ceremonies to simply shelter. In Guatemala people use caves for several cultural practices including religious ceremonies, tourism, and shelter [1]. In the department of Petén in northern Guatemala, caves are often used by hunters for sleeping and shelter from rain, especially in the rainy season. Also in northern Guatemala, caves in the department of Alta Verapaz are sacred places and sometimes the site of Mayan religious ceremonies; tourists also visit some caves. The religious ceremonies occur seasonally and are associated with periodic pilgrimages. In Belize, the Rio Frio caves in the Cayo District are a popular tourist attraction and workers are known to sleep in the caves to guard against vandalism. Although bat guano is harvested in many Latin American countries and the United States, our study did not include locations where this occurs.
The parasite that causes Chagas disease, Trypanosoma cruzi, is transmitted by blood feeding triatomine insects [2]. These vectors are generally wide-ranging feeders and what they feed on is an important aspect of epidemiological risk; for example, human blood meals may mean increased risk of transmission to humans [3].
The species Triatoma dimidiata is currently the major vector of Chagas disease in Central America [4]. Some vector populations are found entirely in sylvan ecotopes, including caves; whereas others are nearly entirely domesticated and some move between ecotopes [5]–[9]. It is generally thought that sylvan vectors are not important for human transmission; however, few data are available to support this assumption. It is important to know if they are feeding on humans to help prevent transmission and to target control.
Because Chagas disease is the most economically important parasitic disease in Latin America with 8–10 million persons infected [10], we decided to investigate the potential role of cave dwelling T. dimidiata in transmission of T. cruzi to humans. To investigate the possibility that cave-dwelling, sylvatic, T. dimidiata contribute to the human transmission cycle, we determined the blood meal sources of T. dimidiata collected from caves in three regions of Central America where T. dimidiata is the main vector.
We tested the hypothesis that T. dimidiata collected from caves would not contain human DNA, and thus are not likely to be involved in transmission of T. cruzi to humans. In addition, we discuss the relationship between human cultural interactions with the cave and the blood meal sources found at each location.
Methods
Sampling locations and collection
Adult males and females were collected from inside caves in the departments of Petén and Alta Verapaz in Guatemala and Cayo district in Belize (Table 1). All the vectors had characters typical of the cave dwelling morph of T. dimidiata and are easily distinguished from those found in nearby houses and peridomestic areas by their longer, larger heads and reduced eyes and ocelli, as well as darker color for the adults and nymphs that are lighter in color [5], [11]. Wearing protective gear, five or six professionals from Laboratorio de Entomología Aplicada y Parasitología (LENAP), Universidad de San Carlos de Guatemala (USAC) collected the vectors. These personnel are trained in the safe handling of infectious agents and were experienced in searching for vectors. Personnel searched the walls, ceiling (when possible), and floor of the cave for 25 min, four times at each geographic location, with a 5–10 min. break between searches. Repeated searches are important because it takes vectors some time to emerge from hiding spots, presumably attracted by CO exhaled by the searchers. Triatomine nymphs in these caves are pale colored compared to nearby non-cave vectors, and have been observed to emerge from hiding in cracks and crevices of the cave walls and ceiling within a half hour following humans entering the cave. Adults are darker in color and easy to see in the caves because of the contrast with the limestone walls. Vectors were identified as T. dimidiata sensu lato based on published taxonomic keys [11].
The human cultural practices in the caves differ among locations. Near the municipality of San Luis, Petén, insect vectors were collected from a small cave located on a privately owned cattle farm. This particular cave was selected because the owner of the farm requested a survey to find the origin of vectors found in their home. Access to the cave is restricted and only local hunters and farm workers know of the cave; however, feral dogs from the nearby village may enter the cave in the rainy season. In Petén, hunting is a traditional weekend entertainment and caves are frequently used as overnight shelters. In this region, caves are not used for religious purposes and although hunters and their dogs may sleep and seek shelter in the caves, domesticated animals other than dogs are not brought to caves. There are no houses near the cave, it is surrounded by pasture areas for cattle.
In Alta Verapaz, caves near Lanquín and Cahabón were examined. Grutas de Lanquín, a complex of caves known to be infested with T. dimidiata [12] was chosen because the main cave is a tourist attraction and is used for Mayan religious ceremonies. The Lanquín River runs through the center of the cave. Thousands of bats inhabiting the cave provide a popular daily tourist attraction as they leave en masse at twilight. Ceremonial stone altars within the cave are still used by local residents for Mayan religious ceremonies that are performed at night. Candles and offerings to the gods are found inside the cave. There are several cave entrances but municipality guards control access. Human houses are located nearby.
Santa Maria cave, in the municipality of Cahabón, maintains the tradition of seasonal pilgrimages organized by descendants of the Maya. Travelers leave offerings to the gods in the cave, including sacrificial animals, pottery, candles, liquor, plant resins, and tamales. There are houses near the one main entrance to the cave, but these houses do not have domestic animals in captivity, and access to the cave is not controlled.
The caves at Rio Frio, Belize are a popular tourist attraction with several entrances to a wide open sandy area with the river flowing through the cave being a popular place for bathing. The ceiling is too high to search in this location, thus the walls are the main source of the vectors collected. Guards often sleep in these caves to protect against vandalism but there are no houses near the cave.
DNA extraction, PCR amplification, cloning and sequencing
DNA was extracted from T. dimidiata abdomens as described previously [13], except we used the E.Z.N.A. Genomic DNA Isolation kit (Omega Bio-Tek, Norcross, GA). The T. cruzi infection status was determined for the vectors from Lanquin, Alta Verapaz using the TCZ primers following previously described methods [14], prior to starting the cloning procedure. Unfortunately, all of the extracted DNA from Rio Frio and San Luis Peten was used in the cloning assay and therefore we were unable to assess the T. cruzi infection status for the vectors from these locations. However a previous study found 25% T. cruzi prevalence in Peten [15].
The assay to identify blood meal sources was developed and previously reported by us [16]. Because the extractions of DNA from the insect abdomens potentially contain a mixture of blood meal DNA from multiple vertebrates, as well as insect DNA and parasite DNA (if infected), the initial PCR used primers specific for the mitochondrial 12S ribosomal RNA gene of vertebrates [17]. After confirming the PCR products were the expected size (∼215 bp), they were cloned using the pGEM-T Easy Vector System (Promega, Madison, WI, USA). Using the same 12S primers, cloning was verified by PCR, followed by sequencing in one direction with BigDye v3.1 (Applied Biosystems, Foster City, CA, USA) and analysis using an ABI PRISM 3730xl (Beckman Coulter, Fullerton, CA, USA). Sequence files were trimmed to 140 bp, edited using Sequencher v4.10 (Gene Codes Corporation, Ann Arbor, MI, USA) and taxonomic identification of the sequences was determined with a BLAST search using ≥99% identity as the criterion for a match.
Statistical methods
To determine if feeding on the different blood meal sources varied among the three locations or between sexes, we used one way analysis of variance (ANOVA) for each taxa (humans, dogs, food animals, animals commensal with humans and wild animals). All statistical analyses were done using the JMP statistical package (JMP Version 10 [SAS Institute Inc., Cary, NC]).
Results
Human was the most common blood meal source in all three locations (Table 2, Figure 1), with over half the vectors from each cave feeding on human (Table 2: Petén = 8 of 9 vectors, Alta Verapaz = 7 of 10, and Cayo = 4 of 7). In Alta Verapaz, pig was equally abundant to human (both at 70%). Data on T. cruzi infection show that in Alta Verapaz, two of the three vectors that had human blood meals sources also had the parasite (Table 3).
Vectors were scored as presence/absence for each ecological source. Data are percent of vertebrate host DNA by ecological source cloned from the abdomen of vectors from each location.
Overall we detected blood meals from eleven different taxa in the 24 vectors from the three locations, including duck and two species each of opossum and bat (Table 2). We examined a total of 218 sequences with 162 (74%) providing information on a blood meal source. On average, 9.04 clones were sequenced per vector, 7.11 sequences per vector were interpretable as a blood meal source, and individual vectors contained 2–3 blood meal sources ( = 2.63, range 1–5). Using this small region of the 12S gene and the criteria of ≥99% match to a published vertebrate sequence, were able to determine the species for nine of the eleven taxa (human, dog, pig, mouse, rat, duck and the two bat species). We could not distinguish between goat and/or sheep, these two Bovids in the Subfamily Caprinae have identical 12S sequences for the regions examined. Similarly, we were only able to determine the subfamily for the two different opossum sequences (Didelphinae: Didelphis sp. or Philander opossum)
The non-human hosts fall into four groups that relate to human cultural interactions with caves: companion animal (dog), food animals (goat/sheep and pig), human commensal species (mouse and rat) and wild species (mallard duck and the two species each of bat and opossum). The mouse and rat species, Mus musculus and Rattus norvegicus, are human commensals and likely occur at these locations because of human activities. Humans and commensal animals were blood meal sources at all three locations (Figure 1). Food animals were not a blood meal source in Petén, likewise wild animals were not a blood meal source in Alta Verapaz and there was no evidence of feeding on dogs in Cayo.
Feeding on dog (F = 3.57; d. f. 2, 23; P<0.05), food animals (F = 5.56; d. f. 2, 23; P<0.02) and sylvatic animals (F = 4.68; d. f. 2, 23; P<0.03) were significantly different among locations. Feeding on humans (F = 0.64; d. f. 2, 23; P>0.05) and commensal animals (F = 0.23; d. f. 2, 23; P>0.05) did not vary among locations. There were no significant differences between males and females in the detection of human (F = 1.14; d. f. = 1, 22; P>0.05), dog (F = 0.05; d. f. = 1, 22; P>0.05), food animal (F = 0.22; d. f. = 1, 22; P>0.05), commensal animal (F = 0.001; d. f. = 1, 22; P>0.05), or sylvatic animal (F = 0.03; d. f. = 1, 22; P>0.05) blood meal sources.
The number of vectors feeding on bats was small, one each from Petén and Cayo and the bats were different genera. In contrast opossum are a more common blood meal source (43%, 3 of 7 vectors examined from both Cayo and Petén, including one vector from Cayo that had feed on both types of opossums). None of the vectors from Alta Verapaz had fed on opossum.
Discussion
Our results indicate that cave dwelling, sylvatic T. dimidiata can contribute to the human transmission cycle. The evidence is that human was the most commonly found blood meal in T. dimidiata collected from caves. At the one location where we have T. cruzi infection data, we found 3 of 10 (30%) of vectors infected, and 2 of these 3 (2 of the 10 or 20% of vectors from that location) also had evidence of human blood. Human blood was found in >50% of all vectors in seven caves from three different locations. However, humans were not more common than the other blood meal sources combined. Of the total blood meals identified 27% at San Luis were from human (6 of 14 blood meal sources (43%), at Alta Verapaz 7 of 30 (23%), and at Rio Frio 4 of 19 (21%).
Further evidence of association with humans included substantial numbers of blood sources from the companion animal dog, domesticated food animals, and animals commensal with humans. Evidence of frequent human-bug contact was observed in the three different types of caves each with different ecological conditions and uses by humans. These results suggest a risk of transmission of T. cruzi to humans entering caves, however further study measuring the rates of T. cruzi infection in insects from all locations would clarify the transmission risk.
The high proportion of bugs that had evidence of human blood meals is surprising, given that caves are considered a sylvatic ecotope, and sylvatic vectors are generally thought not to be important in human transmission. Our results add weight to recent studies challenging this assumption. For example, in sylvan environments in Arizona and California, 38% of Triatoma rubida and Triatoma protracta had human blood sources [16], in Triatoma infestans in Bolivia 27% of blood meals detected were human [18]. However, a study of Triatoma gerstaeckeri, Triatoma indictiva, Triatoma sanguisuga and T. protracta in Texas found little evidence of feeding on humans [19]. Ecological factors including human encroachment into natural areas have been associated with emerging diseases worldwide [20].
The bugs from Santa Isabel Cave in Péten, a privately owned cattle farm with remnant forest patches, showed the highest incidence of human blood consumption (43%, Figure 1). We have anecdotal evidence from the owner of the farm that hunters and farm workers use the relatively cool cave for overnight sleeping or daytime resting, especially during the heat of the dry season. In addition, at the entrance of the cave we have found a clean wild animal skull, a common artifact at contemporary Maya hunting shrines [21], and machetes and plastic water bottles have been found inside the cave (M. C. Monroy, personal observation). Wild and human commensal animals were the next most preferred blood sources (29% and 21%, respectively). It is surprising that dog blood meals are rare (only 7%), since dogs usually accompany the hunters, but perhaps the dogs are eating bugs that come close [22]. Vectors from caves on this cattle farm had fed on the common vampire bat but interestingly had not fed on cattle, suggesting they do not leave the caves.
Humans and food animals are the main blood meal sources for T. dimidiata (both 30%) in the caves of Lanquín and Cahabón in Alta Verapaz, located within heavily deforested areas and surrounded by agricultural fields and houses (Figure 1). Frequent entry of human into the caves for tourism and religious ceremonies could explain the high proportion of blood meals from humans as these caves are popular destinations for tourists and Mayan religious ceremonies. The people performing the rituals may stay overnight in the caves; however, tourists are not likely to stay overnight in the caves, but rather camp near the caves (M. C. Monroy, personal communication or personal observation). Chickens, pigs, goats, and other food animals are free ranging in this area, which could explain high food animal blood sources (30%) in the bugs. The human companion animal dog (22%) and human commensal animals (17%) are the next most frequently found sources, and no wild animal blood sources were found in the bugs from these caves, demonstrating the strong association of humans and bugs in this area. Deforestation removes sylvan animal habitat and therefore sylvan blood sources. Anthropogenic change is known to alter blood meal sources [23].
Bugs found in Rio Frio, Cayo, Belize cave had fed mostly on human and human commensal animals (29% each, Figure 1). The cave is relatively small, has wide openings at both ends and is surrounded by forest. The high association with humans can be explained as the cave is a popular tourist attraction, frequented by swimmers, with guards often sleeping in the cave at night to protect against vandalism. Food animals and wild animals are the next most frequent blood source (21% each) which suggests it is a transit and resting place for wild and feral animals. For example, wild pigs have been reported in this area (http://www.belizeanway.com/destination-cayo). The bat fed upon in Cayo was most likely hairy-legged myotis (100% match to Myotis keaysi) but possibly elegant myotis (99% match to Myotis elegans) [24]. There was no evidence of dog blood meals in vectors collected in Rio Frio. The only nearby settlement is a British military base, and since the Belize military supervises the entrance to the cave it may be more restricted to hunters and their dogs.
Of the eleven taxa detected in the blood meals, about one-third were wild (five species total, duck, two opossum and two bat) and about one-third (7 of 24) of the vectors had fed on sylvatic animals. Due to land use practices, none of the vectors from Alta Verapaz had evidence of feeding on wild animals. The other locations showed similar wild animal blood sources: opossum was the most common (43% in both). In contrast, the number of vectors feeding on bats was small, one each from each locality (14%).
Although the vectors included in this study were all collected within caves, it is not known which of the blood meals we identified were actually obtained in the caves as it is possible the vectors could leave the caves to feed. However, our results are consistent with these vectors spending most or all of their lives in the caves. In Petén, although there is abundant cattle surrounding the caves, cattle blood was not found in the bugs. In addition several reports establish that T. dimidiata in caves in Central America differs morphologically from those found outside the caves suggesting they are different populations that do not intermingle [5], [25]. The bugs included in this study are the cave morphology. Therefore our results suggest the human-bug contact occurs when humans enter the cave. This may not be true everywhere as some T. dimidiata collected in houses in Colombia may be migrants from caves [5], [26] and in some localities T. dimidiata blood sources show evidence of migration between ecotopes [27]. Although a large number of different taxa (11) were detected in the abdomens of the 24 T. dimidiata this is likely a minimal estimate of blood sources as older blood meals may have been too degraded for detection [28].
Caves at all three locations had evidence of Chagas disease vectors feeding on humans and human commensal animals; as well as some combination of dogs, domesticated food animals and wild animals. The variation of blood meal sources among caves is understandable in the context of human uses of the caves at the three locations. We caution that human encroachment into natural areas may expose individuals to unanticipated risks of disease transmission.
Acknowledgments
Marinela Menes, Mariele Pellercer, Elisabeth Solorzano, Barbara Moguel, Carmen Lucia Yurrita, Eunice Enriquez and Maruricio Garcia assisted with the lab and field work in Guatemala and Belize. Nick de la Rúa, David Lucero, Sylvia Stevens-Goodnight and Katherine Sullivan assisted with the lab work in Vermont.
Author Contributions
Conceived and designed the experiments: LS MCM AGR PLD. Performed the experiments: LS MCM AGR PLD. Analyzed the data: LS MCM PLD. Contributed reagents/materials/analysis tools: LS MCM AGR PLD. Wrote the paper: LS MCM AGR PLD.
References
- 1. Brown LA (2005) Planting the bones: Hunting ceremonialism at contemporary and nineteenth-century shrines in the Guatemalan Highlands. Latin American Antiquity 16: 131–146.
- 2. Stevens L, Dorn PL, Klotz J, Schmidt J, Lucero D, et al. (2011) Kissing Bugs. The Vectors of Chagas. Advances in Parasitology 75: 169–192.
- 3. Gourbiere S, Dorn P, Tripet F, Dumonteil E (2012) Genetics and evolution of triatomines: from phylogeny to vector control. Heredity (Edinb) 108: 190–202.
- 4.
Monroy C, Castro X, Bustamante DM, Pineda S, Rodas A, et al., editors (2011) An ecosystem approach for the prevention of Chagas disease in Rural Guatemala. New York, NY, USA/International develomment Research Centre, Ottawa, Canada: Springer.
- 5. Bustamante DM, Monroy C, Menes M, Rodas A, Salazar-Schettino PM, et al. (2004) Metric variation among geographic populations of the Chagas vector Triatoma dimidiata (Hemiptera: Reduviidae: Triatominae) and related species. J Med Entomol 41: 296–301.
- 6. Calderon CI, Dorn PL, Melgar S, Chavez JJ, Rodas A, et al. (2004) A preliminary assessment of genetic differentiation of Triatoma dimidiata (Hemiptera: Reduviidae) in Guatemala by random amplification of polymorphic DNA-polymerase chain reaction. J Med Entomol 41: 882–887.
- 7. Calderon Fernandez G, Juarez MP, Ramsey J, Salazar Schettino PM, Monroy MC, et al. (2005) Cuticular hydrocarbon variability among Triatoma dimidiata (Hemiptera: Reduviidae) populations from Mexico and Guatemala. J Med Entomol 42: 780–788.
- 8. Calderon-Fernandez GM, Girotti JR, Juarez MP (2011) Cuticular hydrocarbons of Triatoma dimidiata (Hemiptera: Reduviidae): intraspecific variation and chemotaxonomy. Journal of medical entomology 48: 262–271.
- 9. Catala S, Sachetto C, Moreno M, Rosales R, Salazar-Schetrino PM, et al. (2005) Antennal phenotype of Triatoma dimidiata populations and its relationship with species of phyllosoma and protracta complexes. Journal of medical entomology 42: 719–725.
- 10. Rassi AJ, Rassi A, Marin-Neto J (2010) Chagas disease. Lancet 375: 1388–1402.
- 11. Lent H, Wygodzinsky PW (1979) Revision of the Triatominae (Hemiptera, Reduviidae), and their significance as vectors of Chagas' disease. Bull Am Mus Nat Hist 163: 127–520.
- 12. Dorn PL, Calderon C, Melgar S, Moguel B, Solorzano E, et al. (2009) Two distinct Triatoma dimidiata (Latreille, 1811) taxa are found in sympatry in Guatemala and Mexico. PLoS Negl Trop Dis 3: e393.
- 13. Pizarro JC, Stevens L (2008) A new method for forensic DNA analysis of the blood meal in Chagas disease vectors demonstrated using Triatoma infestans from Chuquisaca, Bolivia. PLoS ONE 3: e3585.
- 14. Pizarro JC, Lucero DE, Stevens L (2007) PCR reveals significantly higher rates of Trypanosoma cruzi infection than microscopy in the Chagas vector, Triatoma infestans: High rates found in Chuquisaca, Bolivia. Bmc Infectious Diseases 7: 66.
- 15. Monroy MC, Bustamante DM, Rodas AG, Enriquez ME, Rosales RG (2003) Habitats, dispersion and invasion of sylvatic Triatoma dimidiata (Hemiptera: Reduviidae: Triatominae) in Peten, Guatemala. J Med Entomol 40: 800–806.
- 16. Stevens L, Dorn P, Hobson J, de la Rua N, Lucero D, et al. (2012) Evidence of human and other vertebrate bloodmeals and Trypanosoma cruzi infection in Chagas disease vectors from the United States. Emerging Infectious Diseases 18: 646–649.
- 17. Kitano T, Umetsu K, Tian W, Osawa M (2007) Two universal primer sets for species identification among vertebrates. Int J Legal Med 121: 423–427.
- 18. Buitrago NL, Bosseno MF, Waleckx E, Bremond P, Vidaurre P, et al. (2013) Risk of transmission of Trypanosoma cruzi by wild Triatoma infestans (Hemiptera: Reduviidae) in Bolivia supported by the detection of human blood meals. Infect Genet Evol 19C: 141–144.
- 19. Kjos SA, Marcet PL, Yabsley MJ, Kitron U, Snowden KF, et al. (2013) Identification of Bloodmeal Sources and Trypanosoma cruzi Infection in Triatomine Bugs (Hemiptera: Reduviidae) from Residential Settings in Texas, the United States. Journal of Medical Entomology 50: 1126–1139.
- 20. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, et al. (2008) Global trends in emerging infectious diseases. Nature 451: 990–993.
- 21.
Brown LA (2010) Communal and Personal Hunting Shrines Around Lake Atitlan, Guatemala. In: Golden C, Houston S, Skidmore J, editors. Maya Archaeology. San Francisco: Precolumbia Mesoweb Press. pp. 36–59.
- 22. Roque AL, Xavier SC, Gerhardt M, Silva MF, Lima VS, et al. (2013) Trypanosoma cruzi among wild and domestic mammals in different areas of the Abaetetuba municipality (Para State, Brazil), an endemic Chagas disease transmission area. Vet Parasitol 193: 71–77.
- 23. Gottdenker NL, Calzada JE, Saldana A, Carroll CR (2011) Association of anthropogenic land use change and increased abundance of the Chagas disease vector Rhodnius pallescens in a rural landscape of Panama. Am J Trop Med Hyg 84: 70–77.
- 24. Hernåndez-Meza B, Domínguez-Castellanos Y, Ortega J (2005) Myotis keaysi. Mammalian Species Number 785: 1–3.
- 25. Garcia M, Menes M, Dorn PL, Monroy C, Richards B, et al. (2013) Reproductive isolation revealed in preliminary crossbreeding experiments using field collected Triatoma dimidiata (Hemiptera: Reduviidae) from three ITS-2 defined groups. Acta Trop 128: 714–718.
- 26. Gomez-Palacio A, Triana O, Jaramillo ON, Dotson EM, Marcet PL (2013) Eco-geographical differentiation among Colombian populations of the Chagas disease vector Triatoma dimidiata (Hemiptera: Reduviidae). Infect Genet Evol 20: 352–361.
- 27. Torres-Montero J, Lopez-Monteon A, Dumonteil E, Ramos-Ligonio A (2012) House infestation dynamics and feeding sources of Triatoma dimidiata in central Veracruz, Mexico. Am J Trop Med Hyg 86: 677–682.
- 28. Pizarro JC, Lucero D, Stevens L (2007) A method for the identification of guinea pig blood meal in the Chagas disease vector, Triatoma infestans. Kinetoplastid Biol Dis 6: 1.