Print version ISSN 0036-4665
Rev. Inst. Med. trop. S. Paulo vol.51 no.3 São Paulo May/June 2009
Helmintos animais em vestígios arqueológicos humanos: revisão de zoonoses no passado
Luciana SiantoI; Marcia ChameI; Cassius S.P. SilvaI; Marcelo L.C. GonçalvesII; Karl ReinhardIII; Martin FugassaIV; Adauto AraújoI
IFundação Oswaldo Cruz, Escola Nacional de Saúde Pública Sérgio Arouca, Rua Leopoldo Bulhões 1480, 21041-210 Rio de Janeiro, RJ, Brasil
IIUniversidade de Fortaleza, Av. Washington Soares 1321, Edson Queiroz, 60811-341 Fortaleza, CE, Brasil
IIIUniversity of Nebraska, Lincoln, NE 68588, USA
IVCONICET, Universidad Nacional de Mar del Plata, Diagonal J. B. Alberdi 2695 - (7600)- Mar del Plata, Argentina
The authors present a review of records of intestinal parasitic helminths from animals in human archaeological remains, reported since the emergence of paleopathological studies. The objective was to relate paleoparasitological findings to geographic, biotic, and abiotic factors from the environment in which the prehistoric populations lived, and understand some aspects related to the process of human dispersion and biological and cultural evolution. Modification of eating habits and the incorporation of new cultural practices are analyzed from the perspective of zoonoses from prehistory to the present day, especially in Brazilian indigenous populations. Three tables identifying the helminths, their natural hosts, dates, and sites of archaeological findings complete this review. In conclusion, various zoonoses known today have occurred since antiquity, and these data, combined with studies on the emergence and reemergence of diseases, could make possible to compose scenarios for the future.
Keywords: Coprolites; Paleoparasitology; Helminthiasis; Zoonoses; Ancient diseases.
São revistos os registros de ocorrência de helmintos intestinais parasitos de animais em vestígios arqueológicos humanos, relatados desde o surgimento dos estudos paleopatológicos. Busca-se relacionar os achados em paleoparasitologia com fatores geográficos, bióticos e abióticos do ambiente em que as populações pré-históricas viviam, e com aspectos do processo de dispersão e evolução biológica e cultural humana. A modificação de hábitos alimentares e a incorporação de novas práticas culturais são analisadas sob o ponto de vista das zoonoses desde a pré-história até a atualidade, em especial em populações indígenas brasileiras. Três tabelas identificando os helmintos, seus hospedeiros naturais, datações e local dos achados arqueológicos complementam esta revisão. Conclui-se que várias zoonoses conhecidas hoje ocorrem desde a antiguidade e que estes dados, combinados a estudos de emergência e reemergência de doenças, podem auxiliar a compor cenários para o futuro.
Parasites of animals may infect humans, and in some cases cause disease. On the other hand, false parasitism is also observed in individuals after eating infected animals with parasite species that are not able to infect humans. Therefore, the eggs pass with feces without causing infection, as recorded in indigenous groups29. In examining archaeological material one has to separate coprolites of human origin from others of animal origin. However, parasitism is a dynamic process, and changes may occur.
The finding of Echinostoma sp. in a mummified body from the pre-Colombian period in Minas Gerais State, Brazil119 can be used as an indication of modifications in the parasite fauna in human groups over time. These modifications reflect possible variations in eating habits among prehistoric human groups, since hunter-gatherers ingested wild animals, thus becoming potential hosts for new parasites over the course of their evolutionary history54.
Cases of animal parasites infecting humans were described in Europe, especially in the Neolithic and Medieval periods71, and in Patagonia in the pre-contact period45. Evidence of the ingestion of small animals, consumed whole or in pieces, without cooking, described by REINHARD103 in human coprolites, increased the interest in the investigations of animals used for food and as possible transmitters of parasites to humans.
The possibilities for the occurrence of parasitic helminths from wild animals in prehistoric human populations are wide and variable according to the local fauna and different habits and cultures around the world. The absence of many of these species today reflects the change in these parameters, especially since agriculture and domestication32,54.
Thus, the interest in studying eating habits in past times and the interaction with intermediate, definitive, and paratenic hosts motivated a review of findings of helminths in archaeological material, situating them in time and space, as well as associating them with the living habits of ancient human groups.
The study of parasites in archaeological material has developed extensively in recent decades40. Since its emergence nearly a century ago, paleoparasitology has contributed empirical data on the presence of infections and clinical disease conditions among populations that have already disappeared from the Old and New Worlds. This science provides data on the evolution of parasites and their hosts, in addition to helping understand the occupation of territories and retracing migratory paths of prehistoric populations2,4.
Paleoparasitological findings feature not only specific human parasites, inherited from ancestors, but also those acquired over the course of hominid dispersion and biological and cultural evolution3. Therefore, in paleoparasitology it is very important to know whether the coprolite is of human or other animal origin. Thus, the final diagnosis is based on evidences pointing to a true infection by a parasite or a false parasitism. A zoonosis may have occurred, i.e., a parasite of an animal may also have infected humans, and the paleoparasitologist has to deal with this possibility.
Rudolph Virchow coined the term zoonosis in 1855. Since then, other authors have attempted to define zoonoses and identify their causes, propelled by the early age of bacteriology that furnished data concerning their etiological agents and modes of transmission73. In the 1950s, the World Health Organization (WHO) issued its definition of zoonosis. The official concept (1959), adopted to this day, defines zoonosis as any disease or infection that is naturally transmissible from vertebrate animals to humans73,88 and vice-versa. This transmission is possible since parasites can occur in hosts over the course of the evolutionary process, that is, there is a parasite specificity that restricts infections, but the latter can occur by evolutionary adaptation in new host species9,54.
These various possibilities can include an accidental encounter between parasites and new hosts. Such encounters can generate new intraspecific relations (either successful or unsuccessful) and intermediate relations91. This fact can be exemplified by the sporadic finding of animal helminth eggs in human feces, merely meaning human consumption of some animal infected with the parasite and that the eggs passed through the human digestive tract together with the ingested food, without establishing a relationship and without even causing any damage to his health38.
REINHARD102 also refers to false parasitism, a relationship in which the parasite's lack of specificity with the individual that consumed it prevents the parasite from completing its biological cycle, developing, or multiplying inside this host; a large quantity of eggs in the feces would indicate true infection. The amount of eggs found in coprolites can vary according to the fragment of the sample used, the taphonomic processes involved, the diversity of parasites in an individual40,102, environmental factors63, and interaction between parasites that occupy the same habitat and that can express themselves in inter and intra-specific cooperation and/or competition6,12. COIMBRA Jr. & MELLO29 report the consumption of raw rodent liver by indigenous peoples, in whom Capillaria eggs are eliminated for days, but without infection occurring.
When an animal parasite manages to establish itself in the human body, a true infection occurs, thus a zoonosis, whether or not the parasite succeeds in completing its life cycle. For example, human infection with larvae of Ancylostoma caninum or Toxocara canis, both canine parasites, cause infection and clinical manifestations, but the parasites do not complete their life cycle in the human host105. Another example is Trichinella spiralis infection. Humans become infected when they eat raw or undercooked meat of infected animals, especially pigs. There are ancient records of T. spiralis infection in Egypt from 3,220 years BP30 (Before Present), Spain in the 19th century 19 AD13 (Anno Domini), and Alaska from 440 ±70 BP138. Currently, in addition to T. spirallis, eight other species of the genus have been recorded in humans99. Echinococcus granulosus also fails to complete its cycle in humans but has been found in archaeological remains in the USA79,89,132, Europe11,21,100,130,131, and Middle East5,137.
In this review we searched only for records of intestinal helminths. The article by GONÇALVES et al.52 guided the research. We conducted a search in electronic databases (PubMed, Isi Web of Science, Scopus, Scirus, and Scielo) up to January 2008 and a search in indexing journals. The attempt was to verify all the existing records on paleoparasitology and related sciences that in some way had recorded the occurrence of animal intestinal parasitic helminths in human archaeological remains. We excluded findings of uncertain origin, but false parasitism was considered.
This review is expected to expand the knowledge on the occurrence of animal parasites in humans from an evolutionary perspective, from prehistoric periods, correlating them to the various regions of the world, chronology, and different habits between populations, thus contributing to the studies conducted today among special populations, like indigenous groups in Brazil.
Principal Zoonoses of the Old World (except East and Southeast Asia)
As shown in Table 1, the majority of findings of animal parasites in human archaeological material from the Old World are concentrated in Europe, where numerous latrines provide material for paleoparasitological analyses of practically the entire continent18.
The first published studies containing zoonotic helminths were by SZIDAT124, who found Diphyllobothrium latum eggs in material from Austria dated 1,500 years BP, followed by findings of Dicrocoelium sp. in material from England dated 1,100 AD125. In Germany, JANSEN & OVER68 found D. latum, Taenia sp., and Fasciola hepatica eggs dated 100 BC - 500 AD. The paleoparasitological findings since then have always shown the presence of zoonotic parasites transmitted mainly by consumption of and/or contact with domesticated animals. The domestication of animals and plants favored an increase in the occurrence of parasitosis among human populations, as exemplified in specific regions. The increase in food production obtained through agriculture favored the agglomeration of individuals and consequently the occurrence of specific human parasites, transmitted by direct contact with environments and/or contaminated foods. In addition, the agricultural surplus was stored in deposits, increasing the potential risk of infection by contamination of the grain or other foodstuffs and by attracting animals like rodents7,31,87, the natural hosts of various zoonoses affecting humans92.
With domestication, humans kept animals close to them for consumption, like cattle, goats, and pigs, as well as companion animals like dogs and cats. ROCHA et al.112 and FERNANDES et al.37, studying material from Medieval European latrines, showed that specific human parasites like Ascaris lumbricoides and Trichuris trichiura, and animal parasites like Ascaris suum and Trichuris suis, that infect swine, appeared in association with each other, thus proving the close relationship between man and these animals, already demonstrated by archaeological records. This constant contact with animals facilitated the transmission of parasites, including zoonotic ones, that were previously acquired sporadically, like Taenia sp., Capillaria sp., and Fasciola sp., causing an increase in the number of animal parasite infections in human populations8,15,16,18,19,34,35,36,37,61,62,67,68,71,86,110.
Still, little or nothing is known about the parasites that affected Old World populations before the domestication of plants and animals, since most parasite findings in archaeological material date to after the introduction of agriculture as a means of subsistence. The oldest records of animal parasites in human archaeological remains are from the African continent and Middle East, already in agricultural societies, where eggs from the genera Diphyllobothrium, Dicrocoelium, Taenia, and Fasciola were found in material dating close to 10,000 BP in Israel, South Africa, and Egypt33,61,81.
In Europe, the oldest records date to 4,500 year old Fasciola hepatica eggs found in human and cattle coprolites in Germany34, and 3,900 - 2,900 BP, with Dicrocoelium sp., Fasciola hepatica, Opistorchiformes, Diphyllobothrium sp., Taenia sp., and Dioctophyma renale eggs found in archaeological material belonging to lacustrine communities in the Swiss and French Alps35,36,71. Although these findings are from communities that dominated farming techniques, they belong to the period in which the Pfn-Horgen transition occurred in the Neolithic (3,900 - 2,500 BC), when climate changes affected the production of cultivated grains, leading to subsistence crises. The population was thus forced to turn to the consumption of wild vegetables, and also hunting and fishing, often consuming raw items35,36,71.
East and Southeast Asia
In Asia, especially in Japan, findings are related mainly to parasites acquired through the consumption of raw fish, a cultural tradition that dates to prehistoric times, popularized with the emergence of sushi in the 4th century AD65 (Table 2). Clonorchis sinensis, Paragonimus sp., Metagonimus yokogawai, and Diphyllobothrium sp. eggs have been found in fecal material from Japanese archaeological sites dated from 2,300 BP to the 12th century 12 AD78. Unlike Japan, in China, where foods are traditionally cooked before eating, C. sinensis, Schistosoma japonicum, and T. solium eggs have been found in archaeological remains dated from 2,300 BP to 2,100 BP27,72,129,136. In Korea, C. sinensis eggs have been found in human remains dated to 668 - 935 AD and 1,411 ± 42 AD58,117. A mummy from 1,650 - 1750 AD was also found with Metagonimus yokogawai and Gymnophalloides seoi eggs118.
Currently, the main zoonotic helminths in the Asian population are still related to the consumption of raw fish and other seafood25.
Agriculture was not adopted at the same in the New World as in the Old World. Various prehistoric populations either continued their hunting-gathering habits - despite knowledge of farming techniques adopted by other groups in the same region - or used them jointly32,103.
PICKERSGILL97 reports four independent areas in which vestiges of agricultural development in the Americas by pre-Colombian groups can be observed: Southeast North America, Mesoamerica, the Andes region, and tropical lowlands in South America, with the cultivation of corn (Zea mays), beans (Phaseolus vulgaris), potatoes (Solanum tuberosum), manioc (Manihot esculenta), squash (Cucurbita spp.), and peanuts (Arachis hypogaea), among others, by pre-Colombian groups74,97,101,102,122.
However, the domestication of animals shows major differences in comparison to the process that occurred in the Old World22. DIAMOND31 explains this difference by local geography and climate, since the majority of large herbivores were located in Eurasia, while the Americas had few large species with chances of domestication, especially after the great extinctions of mammals in the Late Pleistocene.
Importantly, however, is that the great herds of Old World herbivores are migratory or occupy large areas, requiring continuous shifting of human populations to follow this resource, through areas that are sometimes inhospitable or used by other human groups, a phenomenon known as transhumance139. From this perspective, the investment in domestication brings advantageous results70. However, in the Americas, despite the existence of medium and large social herbivores like the Rocky Mountain Bighorn sheep (Ovis canadensis), American bison (Bison bison), moose (Alces alces), and others in North America51, there is no evidence that these species were domesticated, although they were hunted for food.
The domestication of animals in the New World occurred mainly in the Andean region and Mexico, where native groups domesticated ducks (Cairina moschata), turkeys (Meleagris gallopavo), guinea pigs (Cavia porcellus), and llamas (Lama glama), from which they obtained milk and meat, and alpaca (L. pacos), used mainly for wool22,123. Dogs were also raised for food in Mexico133, but domestication of the dog did not occur on this continent. Dogs (already domesticated) came in the company of prehistoric humans when they arrived on the American continent some 14,000 years ago115.
For most native groups in the South American lowlands, animals were not domesticated for food. In Brazil, for example, various indigenous groups kept wild animals either as pets or for plucking feathers in the case of birds101. Although there is no abundance of large herbivores in groups, like those that exist in Eurasia, North America, and Africa, some, like peccaries (Tayassu pecari and Pecari tajacu) and tapirs (Tapirus anta) could have been domesticated. However, since the browsing and grazing areas for these species are relatively small, they are not migratory. Other species such as wild pigs and capybaras live in large herds80,127 and thus provide permanently available food, in addition to the abundant supply of fish in many South American lowland regions81.
Unlike the Old World, in the New World there are samples of coprolites available from both hunting-and-gathering and farming populations, thus allowing to expand the knowledge on the possible consequences of the domestication of animals and especially of plants as alternative food sources in prehistoric populations, although in different scenarios and situations.
North and Central America
In North America, animal parasite findings in human coprolites are concentrated in the USA42,43,44,55,56,57,58,59,84. REINHARD102 reviews the occurrence of parasites in the United States according to the geographic areas where they were found. The author showed that most of the findings are situated in the southern part of North America and Mexico, with Acanthocephala and Hymenolepididae eggs, among others. A peculiar case is the finding of eggs from Moniliformis clarki, an acanthocephalan transmitted by consuming insects, a common eating habit among North American indigenous peoples. For a long time Acanthocephala findings were attributed to false parasitism. However, the frequency of these findings in prehistoric material from the Americas in association with cultural customs favoring infection suggests that these parasites really infected these populations. However, this frequency may only reflect the preference or abundance of the available supply of insects for eating.
Data obtained by REINHARD102, principally among the ancestral Pueblo of the United States (the ancient Anasazi), show that as occurred with Old World populations, the incidence of specific human parasites increased with the introduction of agriculture. Another episode that increased the occurrence of parasites in these populations occurred during an apparent ecological collapse which, similar to one that occurred in Europe71, led the inhabitants of the last occupation of the Antelope House in Arizona to consume wild plants like cacti to replace the lack of cultivated crops. This strategy was also apparently adopted during dry seasons, when wild plants and also dogs, rabbits, whole rodents, lizards, and other animals were consumed103.
In addition to the findings cited above, BOUCHET et al17,20 found eggs from genus Diphyllobothrium in samples from Alaska.
In South America, a zoonosis that is known to have occurred in a prehistoric population and that still exists in current-day populations in Peru and Chile is the presence of Diphyllobothrium pacificum. Swiss parasitologist Jean BAER10, called to Peru to study parasites found in persons with an intestinal clinical condition, identified the species D. pacificum in the patients, a parasite of sea lions whose larvae contaminate saltwater fish and shellfish. The presence of this parasite in the population is explained by the consumption of a traditional dish by the Pacific coastal populations, cebiche, made with raw sea fish. BAER raised the hypothesis that the prehistoric populations also had this parasitosis, a fact confirmed years later when D. pacificum eggs were found in Chilean coprolites 4,000 years old by FERREIRA et al.39, who commented on the coincidence in the findings. Other researchers also confirmed the presence of this parasite in prehistoric populations on the Pacific coast23,93,106,108.
In Brazil there are only three records of animal helminths in human coprolites. The first was by ARAÚJO et al.1, who found Trichostrongylus sp. eggs associated with T. trichiura eggs in a mummified body from the colonial period. GONÇALVES et al.52 found Acanthocephala eggs in material dated 4,905 - 1,325 BP in Minas Gerais. But perhaps the most significant finding of a zoonosis in archaeological material in Brazil came from a paleoparasitological review of coprolite samples from a naturally mummified body in the State of Minas Gerais, Southeast Brazil, dated 600 - 1,200 BP, which allowed the correct identification of Echinostoma sp. eggs and the certainty of this parasite's occurrence in humans119Echinostomiasis is an endemic zoonosis in Asia, that can produce debilitating symptoms in infected individuals41,53. Humans become infected by the ingestion of Echinostoma spp. larvae present in raw mollusks, fish, or amphibians, the parasite's intermediate hosts111. This is the first record of Echinostoma sp. in humans in Brazil, and the finding enriched the data on the circulation of other zoonotic parasites in ancient populations.
Echinostoma sp., Paragonimus sp., Diphyllobothrium sp., Diphyllobothrium pacificum, Capillaria spp., Trichostrongylus sp., and Acanthocephala are the zoonotic helminths that have already been found in South American populations (Table 3). We only considered findings that dated up to close to contact with Europeans, since they are what we can positively classify as pre-Colombian. Thus, the current study excluded the findings by HORNE & TUCK66 and FUGASSA45, of Taenia sp. eggs in 17th-century material from Canada and 19th-century material from Argentina, since they are related respectively to the introduction of swine and beef cattle on the American continent after discovery.
Currently, zoonoses caused by helminths have important impacts on human development around the world49,77,92. Recent publications have classified the majority of emerging or reemerging pathogens as zoonotic88,126,135.
Nevertheless, records are rare on the occurrence of zoonoses among current native populations in Brazil. This is curious, since many Brazilian indigenous groups have maintained their traditional eating habits and continue to hunt and consume wild animals as their principal source of protein81,85. Many game animals are natural hosts of parasites, including helminths46,64,109.
The explanation for this gap may lay in the fact that after contact with Brazilian national society, many indigenous communities have undergone social, economic, and environmental changes. Such changes have influenced the epidemiological profile of these groups, which have obtained easy access to antihelminthic drugs through indigenous health agents120, often administered without any control. In addition, geographical restrictions imposed by territorial demarcation and transformation of semi-nomadic into sedentary behavior in the majority of the South American indigenous groups have contributed to fixing large groups, resulting in villages with high population densities and precarious sanitation, facilitating the transmission of specific human parasites that compete with those of animal origin28,29,134.
Such data are provided by the publications by VIEIRA128 and SILVA120, both on intestinal parasitosis in Brazilian indigenous populations. In the literature review by VIEIRA128 covering indigenous groups from throughout Brazil, Hymenolepis sp., Taenia sp., and Capillaria sp. were the only zoonotic helminths cited.
SILVA120 conducted an extensive coprological analysis of the Suruí population, an indigenous tribe in the State of Rondônia in the Brazilian Amazon. Stool specimens were analyzed in two laboratories and were positive for the tapeworm Hymenolepis diminuta in 21/541 (3.9%) samples, and for Capillaria sp. in 28/541 samples (5.2%) of the specimens in this same set. A middle-aged woman's stool test showed eggs from Dipylidium caninum, a tapeworm rarely found in humans. D. caninum is a parasite of domestic and wild canids and felines that infects humans through the ingestion of an infected arthropod92. D. caninum and Hymenolepis diminuta have still not been found in paleoparasitological analyses. Hymenolepis spp. eggs were found in samples from the USA and Sudan61,107, although the species were not identified and may be H. nana, specific to humans.
Many Brazilian indigenous groups consider viscera from animal, especially liver, a delicacy. The liver is consumed raw, and thus the presence of Capillaria sp. eggs in the feces of native Brazilian populations is not uncommon24,29,50,113,114. Capillaria sp. eggs have also been found in paleoparasitological analyses in Europe7,37, but not in Brazil.
DISCUSSION AND CONCLUSION
Although in this review we adopted the World Health Organization's definition of zoonosis, we did not consider A. lumbricoides a zoonotic helminth as the WHO does. The A. lumbricoides cycle is direct and independent of another animal, and its origin is by the phylogenetic route, that is, descending from a common ancestor of humans and primates3,4. Parasites originating from the ecological route can be classified in two categories: (1) those that originated from other species and underwent modification over the course of the evolutionary process and became species-specific to humans (meaning that they differ from the original species) and (2) zoonoses. An example of the first category is the human immunodeficiency virus (HIV). MARX et al.76 argue that AIDS is not a zoonosis, since the virus underwent modifications from the original version to infect humans, which goes against the concept of zoonosis as a disease naturally shared by animals and humans. Among the helminths, a good example is H. nana. According to the Pan-American Health Organization, some parasitologists classify the species that infects humans as H. nana var. nana and the species that infects rodents as H. nana var. fraterna, on grounds that there is a parasite host-specificity, justified by the lack of evidence of H. nana transmission from rodents to humans92.
The parasitism phenomenon consists of dynamic relations within a natural evolutionary process as old as life itself38. An animal parasite that does not infect humans may begin to do so if pressure, genetic potentiality and plasticity allow it. The pressures for such an alteration can come from the environment itself, especially if the original hosts become scarce and thus its survival comes to depend on the incorporation of new hosts into its cycle12,95. A zoonosis occurs when these conditions appear. But if the alteration is so great that the parasite becomes totally specific to the new host9,90, the outcome could be similar to HIV infection76. This may be taken as a general rule, as probably different responses occur from virus to other parasite organisms.
During human history, populations have faced different environmental conditions with biological and cultural adaptations. Scarcity of food and other resources necessary for survival, and also climatic and environmental changes have facilitated contact between humans and parasites, from animal origin or even not known to science, as evidenced by the work of LE BAILLY71, FUGASSA45, and REINHARD103 in prehistoric populations of Europe, Argentina, and North America, respectively.
McMICHAEL80 argues that the historical transitions experienced by our prehistoric ancestors when they climbed down out of the trees onto the savannahs, incorporated meat into their diet, and more recently since the emergence of Homo sapiens, the development of agriculture, and the conquest of new territories and civilizations favored the emergence of (and exposure to) infectious agents of animal origin. ARMELAGOS et al.7 analyzed the epidemiological transitions experienced by humankind and concluded that we are undergoing a new transition, in which parasitic infections that were common 10,000 years ago, at the time of the first transition (with the development of techniques for cultivation of plants and domestication of animals), are now reemerging with the possibility of causing major economic impacts. The agricultural frontier's encroachment on natural areas and parasites' resistance to conventional treatments can explain this reemergence.
Paleoparasitological findings are important clues for knowledge on human adaptive progress since prehistory, in addition to revealing eating habits of extinct populations and the domestication of animals. The current study shows that various zoonoses known today have occurred since prehistoric times. The knowledge of which parasites circulated in the past and their geographic distribution helps understand whether a zoonosis is emerging or reemerging77.
Thus, the fact that D. caninum, Capillaria sp., and other parasites have not been found in human archaeological material in South America does not mean that they did not exist or that these infections did not occur.
We recently identified genus Spirometra (Cestoda) in feline coprolites from the Serra da Capivara National Park in Piauí State, Brazil (unpublished data). This parasite is the causative agent of sparganosis in humans, and one cannot ignore the possibility of this and other parasites circulating in the local human population. Few authors conduct studies with archaeological material of animal origin. This may represent a loss of information, since the parasite's presence in the local fauna, associated with environmental and socio-cultural factors like diet and type of dwellings, may indicate transmission routes for the parasites to human populations.
To the extent that more sensitive diagnostic techniques become available, more parasitic infections from the past are detected, and new paleoparasitological findings are recorded around the world. Additional studies on zoonotic infections from the past will expand the knowledge on biological and sociological aspects of the health-disease process and the co-evolution between parasites and animal and human hosts.
In addition, the identification of zoonoses that affected ancestral peoples, understanding their mechanisms of transmission and the factors affecting this dynamic (whether biogeographic, ecological, cultural, historical, or social), can help development of forecasting models to control parasitic diseases soon after their emergence or even to prevent them before they become public health problems.
Geographic, biotic, and abiotic factors from the environment in which prehistoric populations lived (biocenosis) and their cultural characteristics can trace models for the predictability and transmission of the parasite fauna in these groups, as done by MARTINSON et al.75 and REINHARD104, and are based on models grounded in the theory of natural foci94,96,121. These studies are especially applicable to zoonoses, since biocenosis in natural ecosystems is well defined121, but they can also be applied to human-specific parasites.
Recent advances correlating the processes of fragmentation and isolation of natural areas to genetic loss, the interruption of gene flow between species, and the introduction of invasive exotic species in the wild fauna26,69 can help compose prehistoric scenarios that favored the occurrence of animal parasites in humans, as well as drawing scenarios for the future.
Funding: CNPq, FAPERJ, CAPES
1. ARAÚJO, A.; CONFALONIERI, U. & FERREIRA, L.F. - Encontro de ovos de Trichostrongylidae e Trichuris trichiura em corpo mumificado do período colonial brasileiro. Rev. Cent. Cienc. biol. Saúde, 1: 11-16, 1984. [ Links ]
2. ARAÚJO, A. & FERREIRA, L.F. - Parasitismo, doença parasitária e paleoparasitologia. In: COURA, J.R., org. Dinâmica das doenças infecciosas e parasitárias. Rio de Janeiro, Guanabara Koogan, 2005. p. 7-18. [ Links ]
3. ARAÚJO, A.; JANSEN A.M.; BOUCHET, F.; REINHARD, K. & FERREIRA, L.F. - Parasitism, the diversity of life, and paleoparasitology. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 5-11, 2003. [ Links ]
4. ARAÚJO, A.; REINHARD, K.; FERREIRA, L.F. & GARDNER, S.L. - Parasites as probes for prehistoric human migrations? Trends Parasit., 24: 112-115, 2008. [ Links ]
5. ARIELI, R., 1998 apud HANSON, C.L. - Annotated bibliography. Paleopathol. Newsl., 105: 13, 1999. [ Links ]
6. ANDERSON, R.M. & MAY, R.M. - Population biology of infectious diseases. Berlin, Springer-Verlag, 1982. (Life sciences research report, 25). [ Links ]
7. ARMELAGOS, G.J.; BROWN, P.J. & TURNER, B. - Evolutionary, historical and political economic perspectives on health and disease. Soc. Sci. Med., 61: 755-765, 2005. [ Links ]
8. ASPÖCK, H.; BARTH, F.E.; FLAMM, H. & PICHER, O., 1974 apud ASPÖCK, H.; AUER, H. & PICHER, O. - Parasites and parasitic diseases in prehistoric human populations in Central Europe. Helminthologia, 36: 139-145, 1999. [ Links ]
9. ÁVILA-PIRES, F.D. - Zoonoses: hospedeiros e reservatórios. Cadern. Saúde públ. (Rio de J.), 5: 82-97, 1989. [ Links ]
10. BAER, J.G. - Diphyllobothrium pacificum, a tapeworm from sea lions endemic in man along the coastal area of Peru. J. Fish. Res. Board Canada, 26: 717-723, 1969. [ Links ]
11. BAUD, C.A. & KRAMAR, C., 1991 apud REINHARD, K.J. - Parasitology as an interpretative tool in archaeology. Amer. Antiq., 57: 231-245, 1991. [ Links ]
12. BEGON, M.; TOWNSEND, C.R. & HARPER, J.L. - Ecology: from individuals to ecosystems. 4. ed. Malden, Blackwell, 2006. [ Links ]
13. BELLARD, F.G. & CORTÉS, A. - Trichinosis in the mummy of a young girl (Toledo, Spain). In: Papers on Paleopathology, 8th European Meeting, Cambridge, 1990. p. 11, [ Links ]
14. BOUCHET, F. - Apport de la parasitologie sur les chantiers archéologiques - l'exemple de la ville de Paris. Mem. Group. Archaeol. Seine-et-Marne, 1: 55-61, 1993. [ Links ]
15. BOUCHET, F. - Recovery of helminth eggs from archaeological excavations of the Grand Louvre (Paris, France). J. Parasit., 81: 785-787, 1995. [ Links ]
16. BOUCHET, F.; BENTRAD, S. & PAICHELER, J.C. - Enquête épidémiologique sur les helminthiases à la cour de Louis XIV. Med. Sci., 14: 463-466, 1998. [ Links ]
17. BOUCHET, F.; LEFÈVRE, C.; WEST, D. & CORBETT, D. - First paleo-parasitological analysis of a midden in the Aleutian Island (Alaska): results and limits. J. Parasit., 85: 369-372, 1999. [ Links ]
18. BOUCHET, F.; HARTER, S. & LE BAILLY, M. - The state of the art of paleoparasitological research in the Old World. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 95-101, 2003. [ Links ]
19. BOUCHET, F.; PETREQUIN, P.; PAICHELER, J.C. & DOMMELIER-SPEJO, S. - Première approche paléoparasitologique du site néolithique de Chalain (Jura, France). Bull. Soc. Path. éxot., 88: 265-268, 1995. [ Links ]
20. BOUCHET, F.; WEST, D.; LEFÈVRE, C. & CORBETT, D. - Identification of parasitoses in a child burial from Adak Island (Central Aleutian Islands, Alaska). C. R. Acad. Sci. (Paris), 324: 123-127, 2001. [ Links ]
21. BROTHWELL, D.R., 1978 apud JONES, A.K.G. - Human parasite remains: prospects for a quantitative approach. In: HALL, A.R. & KENWARD, H.K., ed. Environmental archaeology in the urban context. England, The Council for British Archaeology, 1982. p. 66-70. (Research Report no. 43). [ Links ]
22. BROTHWELL, D. & BROTHWELL, P. - A alimentação na antiguidade. Lisboa, Editorial Verbo, 1971. [ Links ]
23. CALLEN, E.O. & CAMERON, T.W.M. - A prehistoric diet revealed in coprolites. New Sci., 8: 35-40, 1960. [ Links ]
24. CARME, B.; MOTARD, A.; BAU, P. et al. - Intestinal parasitoses among Wayampi Indians from French Guiana. Parasite, 9: 167-174, 2002. [ Links ]
25. CHAI, J.Y.; DARWIN-MURRELL, K. & LYMBERY, A.J. - Fish-borne parasitic zoonoses: status and issues. Int. J. Parasit., 35: 1233-1254, 2005. [ Links ]
26. CHAME, M.; BATOULI-SANTOS, A.L. & BRANDÃO, M.L. - As migrações humanas e animais e a introdução de parasitas exóticos invasores que afetam a saúde humana no Brasil. FUMDHAMentos, 7: 47-62, 2008. [ Links ]
27. CHENG, T.O. - Glimpses of the past from the recently unearthed ancient corpses in China. Ann. intern. Med., 101: 714-715, 1984. [ Links ]
28. COIMBRA Jr., C.E.A.; FLOWERS, N.; SALZANO, F. & SANTOS, R. - The Xavánte in transition - health, ecology, and bioanthropology in Central Brazil. Ann Arbor, University of Michigan Press, 2002. [ Links ]
29. COIMBRA Jr., C.E.A. & MELLO, D.A. - Enteroparasitas e Capillaria sp. entre o grupo Suruí, Parque Indígena Aripuanã, Rondônia. Mem. Inst. Oswaldo Cruz, 76: 299-302, 1981. [ Links ]
30. DE BONI, U.; LENCZNER, M.M. & SCOTT, J.W. - Autopsy of an Egyptian mummy (Nakht-ROM I). 6. Trichinella spiralis cysts. Canad. med. Ass. J., 117: 461-476, 1977. [ Links ]
31. DIAMOND, J. - Evolution, consequences and future of plant and animal domestication. Nature, 418: 700-707, 2002. [ Links ]
32. DIAMOND, J. - Armas, germes e aço: os destinos das sociedades humanas. 4. ed. Rio de Janeiro, Record, 2003. [ Links ]
33. DITTMAR, K. & STEYN, M. - Paleoparasitological analysis of coprolites from K2, an Iron Age archaeological site in South Africa: the first finding of Dicrocoelium sp. eggs. J. Parasit., 90: 171-173, 2004. [ Links ]
34. DITTMAR, K. & TEEGEN, W.R. - The presence of Fasciola hepatica (liver-fluke) in humans and cattle from a 4500 year old archaeological site in the Saale-Unstrut-Valley, Germany. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 141-145, 2003. [ Links ]
35. DOMMELIER-ESPEJO, S. - Contribuition à l'étude paléoparasitologique des sites néolithiques en environnement lacustre dans les domaines Jurassien et Péri-alpin. Reims, 2001. (Thesis - Université de Reims). [ Links ]
36. DOMMELIER, S.; BENTRAD, S.; PAICHELER, J.C.; PETREQUIN, P. & BOUCHET, F. - Parasitoses liées à l' alimentation chez les populations néolithiques du lac de Chalain (Jura, France). Anthropozoologica, 27: 41-49, 1998. [ Links ]
37. FERNANDES, A.; FERREIRA, L.F.; GONCALVES, M.L.C. et al. - Intestinal parasite analysis in organic sediments collected from a 16th-century Belgian archaeological site. Cadern. Saúde públ. (Rio de J.), 21: 329-332, 2005. [ Links ]
38. FERREIRA, L.F. - O fenômeno parasitismo. Rev. Soc. bras. Med. trop., 4: 261-277, 1973. [ Links ]
39. FERREIRA, L.F.; ARAÚJO, A.; CONFALONIERI, U. & NUÑEZ, L. - The finding of Diphyllobothrium pacificum in human coprolites (4100-1950 BC) from Northern Chile. Mem. Inst. Oswaldo Cruz, 79: 175-180, 1984. [ Links ]
40. FERREIRA, L.F.; REINHARD, K.J. & ARAÚJO, A. - Paleoparasitologia. Rio de Janeiro, Editora Fiocruz, 2008. [ Links ]
41. FRIED, B.; GRACZYK, T.K. & TAMANG, L. - Food-borne intestinal trematodiasis in humans. Parasit. Res., 93: 159-170, 2004. [ Links ]
42. FRY, G. - Preliminary analysis of the Hogup Cave coprolites. In: AIKENS, C.M., ed., Un. Utah Anthropol. Papers., 93, Salt Lake City, University of Utah Press, 1970. p. 247-250. [ Links ]
43. FRY, G.F. - Analysis of prehistoric coprolites from Utah. In: JENNINGS, J.D. & SWEENEY, L.S., ed., Un. Utah Anthropol. Papers, 97, Salt Lake City, University of Utah Press, 1977. [ Links ]
44. FRY, G.F. & HALL, H.J. - Parasitological examination of prehistoric human coprolites from Utah. Proc. Utah Acad. Sci. Art Lett., 46: 102-105, 1969. [ Links ]
45. FUGASSA, M.H. - Enteroparasitosis en poblaciones cazadoras-recolectoras de Patagônia Austral. Mar Del Plata, 2006. (Tesis Doctoral - Universidad Nacional de Mar Del Plata). [ Links ]
46. FUGASSA, M.H.; ARAÚJO, A.; SARDELLA, N. & DENEGRI, G.M. - New paleoparasitological finding in caves from Patagonia, Argentina. Paleopathol. Newsl., 137: 17-21, 2007. [ Links ]
47. FUGASSA, M.H. & BARBERENA, R. - Cuevas y zoonosis antiguas: paleoparasitología del sitio Orejas de Burro 1 (Santa Cruz, Argentina). Magallania, 34(2): 57-62, 2006. [ Links ]
48. FUTUYMA, D.J. - Evolutionary Biology. Sunderland, Sianauer Associates, 1986. [ Links ]
49. GAJADHAR, A.A. & ALLEN, J.R. - Factors contributing to the public health and economic importance of water-borne zoonotic parasites. Vet. Parasit., 126: 3-14, 2004. [ Links ]
50. GALVÃO, V.A. - Estudos sobre Capillaria hepatica: uma avaliação do seu papel patogênico para o homem. Mem. Inst. Oswaldo Cruz, 76: 415-433, 1981. [ Links ]
51. GEIST, V. - On Pleistocene bighorn sheep: some problems of adaptation, and relevance to today's American megafauna. Wildl. Soc. Bull., 13: 351-359, 1985. [ Links ]
52. GONÇALVES, M.L.C.; ARAÚJO, A. & FERREIRA, L.F. - Human intestinal parasites in the past: new findings and a review. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 103-118, 2003. [ Links ]
53. GRACZYK, T.K. & FRIED, B. - Echinostomiasis: a common but forgotten food-borne disease. Amer. J. trop. Med. Hyg., 58: 501-504, 1998. [ Links ]
54. GREENBLATT, C. & SPIGELMAN, M. - Emerging pathogens: archaeology, ecology and evolution of infectious disease. New York, Oxford University Press, 2003. [ Links ]
55. GUMMERMAN, G.J.; WESTFALL, D. & WEED, C.S., 1972 apud REINHARD, K.J. - Archaeoparasitology in North America. Amer. J. phys. Anthropol., 82: 145-163, 1990. [ Links ]
56. HALL, H.J. - Untitled notes. Paleopath. Newsl., 13: 9, 1976. [ Links ]
57. HALL, H.J., 1972 apud REINHARD, K. J. - Archaeoparasitology in North America. Amer. J. phys. Anthropol., 82: 145-163, 1990. [ Links ]
58. HALL, H.J., 1972 apud WILKE, P.J. & HALL, H.J. - Analysis of ancient feces: a discussion and annotated bibliography. Archaeol. Res. Facility. Berkeley, Department of Anthropology, University of California, 1975. [ Links ]
59. HALL, H.J., 1977 apud REINHARD, K.J. - Archaeoparasitology in North America. Amer. J. phys. Anthropol., 82: 145-163, 1990. [ Links ]
60. HAN, E.T.; GUK, S.M.; KIM, J.L. et al. - Detection of parasite eggs from archaeological excavations in the Republic of Korea. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 103-118, 2003. [ Links ]
61. HARTER, S. - Implication de la Paléoparasitologie dans l'étude des populations anciennes de la vallée du Nil et du Proche-Orient: études de cas. Reims, 2003. (PhD dissertation - Université de Reims Champagne-Ardenne). [ Links ]
62. HERRMANN, B. - Parasitologisch-Epidemiologische Auswertungen Mittelalterlicher Kloaken. Z. Archäol. Mittelalters, 13: 131-161, 1985. [ Links ]
63. HOAGLAND, K.E. & SCHAD, G.A. - Necator americanus and Ancylostoma duodenale: life history parameters and epidemiological implications of two sympatric species. Exp. Parasit., 44: 36-49, 1978. [ Links ]
64. HOBERG, E.P. - Phylogeny and historical reconstruction: host-parasite systems as keystones in biogeography and ecology. In: REAKA-KUDLA, M.L.; WILSON, D.E. & WILSON, E.O., ed. Biodiversity II, understanding and protecting our biological resources. Washington, Joseph Henry Press, 1997. p. 243-262. [ Links ]
65. HORIBE, Y., 2003 apud DE SILVA, D. & YAMAO, M. - A yen for sushi: an analysis of demographic and behavioural patterns of sushi consumption in Japan. J. Foodservice, 17: 63-76, 2006. [ Links ]
66. HORNE, P.D. & TUCK, J.A. - Archaeoparasitology at a 17th century colonial site in Newfoundland. J. Parasit., 82: 512-515, 1996. [ Links ]
67. JANSEN, J. & BOERSEMA, J.H. - Helminth eggs from the latrines of the Olofskapel Gatehouse, Amsterdam. Paleopathol. Newsl., 2: ab7-ab8, 1972. [ Links ]
68. JANSEN Jr., J. & OVER, H.J. - Het voorkomen van parasieten in terpmateriaal uit Noordwest Duitsland. Tijdschr. Diergeneesk., 87: 1377-1379, 1962. [ Links ]
69. KEESING, F.; HOLT, R.D. & OSTFELD, R.S. - Effects of species diversity on disease risk. Ecol. Lett., 9: 485-498, 2006. [ Links ]
70. KORMONDY, E.J. & BROWN, D.E. - Ecologia humana. São Paulo, Atheneu, 2002. [ Links ]
71. LE BAILLY, M. - Evolution de la relation hôte/parasite dans les systémes lacustres nord alpins au Néolithique (3900-2900 BC), et nouvelles données dans la délection des paléoantigénes de Protozoa. Reims, 2005. (PhD dissertation - Université de Reims Champagne-Ardenne). [ Links ]
72. LIANGBIAO, C. & TAO, H. - Scanning electron microscopic view of parasites worm ova in an ancient corpse. Acta Acad. Sinicae, 3: 64-65, 1981. [ Links ]
73. MANTOVANI, A.; LASAGNA, E. & SENIGALLIESI, A. - Considerazioni sull'evoluzione del concetto di zoonosi. Ann. Igiene, 16: 407-418, 2004. [ Links ]
74. MARTIN, G. - Pré-história do Nordeste do Brasil. 2. ed. Recife, Editora Universitária UFPE, 1997. [ Links ]
75. MARTINSON, E.; REINHARD, K.J.; BUIKSTRA, J.E. & DITTMAR, K. - Pathoecology of Chiribaya parasitism. Mem. Inst. Oswaldo Cruz, 98(suppl.1): 195-205, 2003. [ Links ]
76. MARX, P.A.; APETREI, C. & DRUCKER, E. - AIDS as a zoonosis? Confusion over the origin of the virus and the origin of the epidemics. J. med. Primatol., 33: 220-226, 2004. [ Links ]
77. MAS-COMA, S.; BARGUES, M.D. & VALERO, M.A. - Fascioliasis and other plantborne trematode zoonoses. Int. J. Parasit., 35: 1255-1278, 2005. [ Links ]
78. MATSUI, A.; KANEHARA, M. & KANEHARA, M. - Palaeoparasitology in Japan: discovery of toilet features. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 127-136, 2003. [ Links ]
79. McCLARY, A., 1972 apud WILKE, P.J. & HALL, H.J. - Analysis of ancient feces: a discussion and annotated bibliography. Berkeley, Archaeological Research Facility, Department of Anthropology, University of California, 1975. [ Links ]
80. McMICHAEL, A.J. - Environmental and social influences on emerging infectious diseases: past, present and future. Phil. Trans. roy. Soc. Lond. B, 359: 1049-1058, 2004. [ Links ]
81. MELATTI, J.C. - Índios do Brasil. 7. ed. Brasília, Edunb; Hucitec, 1993. [ Links ]
82. MICHALSKI, F. & PERES, C.A. - Disturbance-mediated mammal persistence and abundance-area relationship in Amazonian forest fragments. Conserv. Biol., 21: 1626-1640, 2007. [ Links ]
83. MITCHELL, P.D. & STERN, E. - Parasitic intestinal helminth ova from the latrines of the 13th century crusader hospital of St John in Acre, Israel. In: Paleopathology Association 13th Biennial European Members Meeting, Chieti, 2000. p. 21-22. [ Links ]
84. MOORE, J.G.; FRY, G.F. & ENGLERT Jr., E. - Thorny-headed worm infection in North American prehistoric man. Science, 163: 1324-1325, 1969. [ Links ]
85. MORÁN, E. F. - A ecologia humana das populações da Amazônia. Petrópolis, Vozes, 1990. [ Links ]
86. NANSEN, P. & JØRGENSEN, R.J. - Fund af parasitæg i arkæologisk materiale fra det vikingetidige Ribe. Nord. Vet-Med., 29: 263-266, 1977. [ Links ]
87. NOZAIS, J.P. - The origin and dispersion of human parasitic diseases in the Old World (Africa, Europe and Madagascar). Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 13-19, 2003. [ Links ]
89. ORTNER, D.J. & PUTSCHAR, W.G.J., 1981 apud REINHARD, K.J. - Archaeoparasitology in North America. Amer. J. phys. Anthropol., 82: 145-163, 1990. [ Links ]
90. OSTFELD, R.S. & HOLT, R.D. - Are predators good for your health? Evaluating evidence for top-down regulation of zoonotic disease reservoirs. Front. Ecol. Environ., 2: 13-20, 2004. [ Links ]
91. OSTFELD, R.S. & KEESING, F. - The function of biodiversity in the ecology of vector-borne zoonotic disease. Canad. J. Zool., 78: 2061-2078, 2000. [ Links ]
92. PAHO (Pan American Health Organization). ACHA, P.N. - Zoonoses and communicable diseases common to man and animals: parasitoses. 3. ed. Washington, PAHO, 2003. [ Links ]
93. PATRUCCO, R.; TELLO, R. & BONAVIA, D. - Parasitological studies of coprolites of pre-Hispanic Peruvian populations. Curr. Anthropol., 24: 393-394, 1983. [ Links ]
94. PAVLOVSKY, E.N. (s/d) apud SILVA, L.J. - O conceito de espaço na epidemiologia das doenças infecciosas. Cadern. Saúde públ. (Rio de J.), 13: 585-593, 1997. [ Links ]
95. PEARCE-DUVET, J.M.C. - The origin of human pathogens: evaluating the role of agriculture and domestic animals in the evolution of human disease. Biol. Rev., 81: 369-382, 2006. [ Links ]
96. PESSOA, S.B. & MARTINS, A.V. - Parasitologia médica. 10. ed. Rio de Janeiro, Guanabara Koogan, 1978. [ Links ]
97. PICKERSGILL, B. - Domestication of plants in the Americas: insights from Mendelian and molecular genetics. Ann. Bot. (London), 100: 925-940, 2007. [ Links ]
98. PIKE, A.W. & BIDDLE, M. - Parasite eggs in Medieval Winchester. Antiquity, 40: 293-296, 1966. [ Links ]
99. POZIO, E. - World distribution of Trichinella spp. infections in animals and humans. Vet. Parasit., 149(1-2): 3-21, 2007. [ Links ]
100. PRINCE, J.L., 1975 apud WELLS, C. & DALLAS, C. - Romano-British pathology. Antiquity, 50: 53-55, 1976. [ Links ]
101. PROUS, A. - Arqueologia brasileira. Brasília, Editora Universidade de Brasília, 1992. [ Links ]
102. REINHARD, K.J. - Archaeoparasitology in North America. Amer. J. phys. Anthropol., 82: 145-163, 1990. [ Links ]
103. REINHARD, K.J. - A coprological view of Ancestral Pueblo Cannibalism: debate over a single fecal fossil offers a cautionary tale of the interplay between science and culture. Amer. Sci., 94: 254-261, 2006. [ Links ]
104. REINHARD, K. - Pathoecology of two ancestral Pueblo Villages. In: REITZ, E.J.; SCUDDER, S.J. & SCARRY, C.M., ed. Case studies in environmental Archaeology. 2. ed. New York, Springer, 2008. p. 191-209. [ Links ]
105. REINHARD, K.J. & AUFDERHEIDE, A.C. - Diphyllobothriasis in pre-Columbian Chile and Peru: adaptive radiation of a helminth species to native American populations. In: Papers on Paleopathology, 8th European Members Meeting. Cambrigde, 1990. p.18. [ Links ]
106. REINHARD, K.J. & BARNUM, S.V., 1991 apud REINHARD, K.J. - Parasitology as an interpretative tool in archaeology. Amer. Antiq., 57: 231-245, 1992. [ Links ]
107. REINHARD, K.J.; HEVLY, R.H. & ANDERSON, G.A. - Helminth remains from prehistoric Indian coprolites on the Colorado Plateau. J. Parasit., 73: 630-639, 1987. [ Links ]
108. REINHARD, K.J. & URBAN, O. - Diagnosing ancient diphilobothriasis from Chinchorro mummies. Mem. Inst. Oswaldo Cruz, 98(suppl. 1): 191-193, 2003. [ Links ]
109. REY, L. - Parasitologia. 4. ed. Rio de Janeiro, Guanabara Koogan, 2008. [ Links ]
110. REYMAN, T.A.; ZIMMERMAN, M.R. & LEWIN, P.K. - Autopsy of an Egyptian mummy (Nakht-ROM I). 5. Histopathologic investigation. Canad. med. Ass. J., 117: 461-476, 1977. [ Links ]
111. ROBERTS, L.S. & JANOVY Jr., J. - Foundations of Parasitology. 6. ed. Boston, McGraw-Hill, 2000. [ Links ]
112. ROCHA, G.C.; HARTER-LAILHEUGUE, S.; LE BAILLY, M. et al. - Paleoparasitological remains revealed by seven historic contexts from "Place d'Armes", Namur, Belgium. Mem. Inst. Oswaldo Cruz, 101(suppl. 2): 43-52, 2006. [ Links ]
113. SANTOS, R.V.; COIMBRA Jr., C.E.A.; FLOWERS, N.M. & SILVA, J.P. - Intestinal parasitism in the Xavánte Indians, Central Brazil. Rev. Inst. Med. trop. S. Paulo, 37: 145-148, 1995. [ Links ]
114. SANTOS, R.V.; COIMBRA Jr., C.E.A. & OTT, A.M.T. - Estudos epidemiológicos entre os grupos indígenas de Rondônia. III. Parasitoses intestinais nas populações dos vales dos rios Guaporé e Mamoré. Cadern. Saúde públ. (Rio de J.), 1: 467-477, 1985. [ Links ]
115. SAVOLAINEN, P.; ZHANG, Y.; LUO, J.; LUNDEBERG, J. & LEITNER, T. - Genetic evidence for an East Asian origin of domestic dogs. Science, 298(5598): 1610-1613, 2002. [ Links ]
116. SCHIA, E., 1979 apud JONES, A.K.G. - Human parasite remains: prospects for a quantitative approach. In: HALL, A.R. & KENWARD, H.K., ed. Environmental Archaeology in the urban context. The Council for British Archaeology, 1982. p. 66-70. (Research Report no. 43) [ Links ]
117. SEO, M.; SHIN, D.H.; GUK, S.M. et al. - Paleoparasitological report on the stool from a medieval child mummy in Yangju, Korea. J. Parasit., 93: 589-592, 2007. [ Links ]
118. SEO, M.; SHIN, D.H.; GUK, S.M. et al. - Gymnophalloides seoi eggs from the stool of a 17th century female mummy found in Hadong, Republic of Korea. J. Parasit., 94: 467-472, 2008. [ Links ]
119. SIANTO, L.; REINHARD, K.J.; CHAME, M. et al. - The finding of Echinostoma (Trematoda: Digenea) and hookworm eggs in Coprolites collected from a Brazilian mummified body dated 600-1,200 years Before Present. J. Parasit., 91: 972-975, 2005. [ Links ]
120. SILVA, C.S.P. - Parasitoses intestinais entre os Índios Suruí, Região Amazônica, Brasil. Rio de Janeiro, 2006. (Master's Thesis - Fundação Oswaldo Cruz). [ Links ]
121. SILVA, L.J. - O conceito de espaço na epidemiologia das doenças infecciosas. Cadern. Saúde públ. (Rio de J.), 13: 85-93, 1997. [ Links ]
122. SMITH, B.D. - The initial domestication of Cucurbita pepo in the Americas 10,000 years ago. Science, 276: 932-934, 1997. [ Links ]
123. STAHL, P.W. - Pre-Columbian Andean animal domesticates at the edge of empire. World Archaeol., 34: 470-483, 2003. [ Links ]
124. SZIDAT, L. - Über die Erhaltungsfähigkeit von Helmintheneiern in Vor- und Frühgeschichtlichen Moorleichen. Z. Parasitenkd., 13: 265-274, 1944. [ Links ]
125. TAYLOR, E.L. - Parasitic helminths in medieval remains. Vet. Rec., 67: 218-228, 1955. [ Links ]
126. TAYLOR, L.H.; LATHAM, S.M. & WOOLHOUSE, M.E. - Risk factors for human disease emergence. Philos. Trans. roy. Soc. Lond. B. Biol. Sci., 356: 983-989, 2001. [ Links ]
127. TIEPOLO, L.M. & TOMAS, W.M. - Ordem Artidactyla. In: REIS, N.R.; PERACHI, A.L.; PEDRO, W.A. & LIMA, I.P., ed. Mamíferos do Brasil. Londrina, Edifurb, 2006. p. 283-304. [ Links ]
128. VIEIRA, G.O. - Enteroparasitoses em populações indígenas no Brasil: um estudo meta-analítico qualitativo de produção científica. Rio de Janeiro, 2003. (Master's thesis - Fundação Oswaldo Cruz). [ Links ]
129. WEI, O. - Internal organs of a 2100-year-old female corpse. Lancet, 2(7839): 1198, 1973. [ Links ]
130. WEISS, D.L. & MOLLER-CHRISTENSEN, V., 1971 apud WELLS, C. & DALLAS, C. - Romano-British pathology. Antiquity, 50: 53-55, 1976. [ Links ]
131. WELLS, C. & DALLAS, C. - Romano-British pathology. Antiquity, 50: 53-55, 1976. [ Links ]
132. WILLIAMS, J.A. - Evidence of hydatic cyst disease in a Plains Woodland Burial. Plains Anthropol., 30: 25-28, 1985. [ Links ]
133. WING, E.S. & BROWN, A.B. - Paleonutrition: method and theory in prehistoric foodways. New York, Academic Press, 1979. [ Links ]
134. WIRSING, R.L. - The health of traditional societies and the effects of acculturation. Curr. Anthropol., 26: 303-322, 1985. [ Links ]
135. WOOLHOUSE, M.E.J. & GOWTAGE-SEQUERIA, S. - Host range and emerging and reemerging pathogens. Emerg. infect. Dis., 11: 1842-1847, 2005. [ Links ]
136. YANG, W.; WEI, D.X.; SONG, G. & TENG, R. - Parasitologische Untersuchung einer alten Leiche aus der Chu-Dynastie der Streitenden Reiche aus dem Mazhuan-Grab Nr. 1, Kreis Jiangling, Provinz Hubei. Acta Acad. Med. Wuhan, 4: 23-27, 1984. [ Links ]
137. ZIAS, J. & MUMCUOGLU, K.Y. - Case reports on paleopathology: calcified hydatid cysts. Paleopathol. Newsl., 73: 7-8, 1991. [ Links ]
138. ZIMMERMAN, M.R. & AUFDERHEIDE, C. - The frozen family of Utqiagvik: the autopsy findings. Artic. Anthropol., 21: 53-64, 1984. [ Links ]
139. ZOBL, D. - Die Transhumanz (Wanderschafthaltung) der europaischen Mittelmeerlander im Mittelalter in historischer, geographischer und volkskundlicher Sicht. Berliner Geographische Studien, 10, 1982. [ Links ]
Fundação Oswaldo Cruz, Escola Nacional de Saúde Pública Sérgio Arouca
Rua Leopoldo Bulhões 1480
21041-210 Rio de Janeiro, RJ, Brazil
Received: 17 November 2008
Accepted: 7 April 2009