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Memórias do Instituto Oswaldo Cruz
Fundação Oswaldo Cruz, Fiocruz
ISSN: 1678-8060 EISSN: 1678-8060
Vol. 95, Num. s1, 2000, pp. 89-93
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Untitled Document
Mem. Inst. Oswaldo
Cruz vol.95 s.1 Rio de Janeiro 2000 pp. 89-93
Paleoparasitology
and the Antiquity of Human Host-parasite Relationships
Adauto Araújo+,
Luiz Fernando Ferreira
Escola Nacional de Saúde Pública-Fiocruz,
Rua Leopoldo Bulhões 1480, 21041-210 Rio de Janeiro, RJ, Brasil
+Corresponding
author. Fax: +55-21-598.2610. E-mail: adauto@ensp.fiocruz.br
Received 7 August 2000
Accepted 4 September 2000
Code Number: OC00164
Paleoparasitology may be
developed as a new tool to parasite evolution studies. DNA sequences dated thousand
years ago, recovered from archaeological material, means the possibility to
study parasite-host relationship coevolution through time. Together with tracing
parasite-host dispersion throughout the continents, paleoparasitology points
to the interesting field of evolution at the molecular level. In this paper
a brief history of paleoparasitology is traced, pointing to the new perspectives
opened by the recent techniques introduced.
Key words: paleoparasitology
- coprolites - mummies - parasitism - infectious diseases
Paleoparasitology appeared
as a new branch of parasitology when the first parasite eggs were recovered
from archaeological material. In the beginning of the century, the development
of a technique to rehydrate desiccated tissues allowed the finding of Schistosoma
haematobium eggs in infected kidneys of Egyptian mummies dated of 3,200
years old (Ruffer 1910).
What is known now as the pioneer
period of paleoparasitology can be characterized mainly by the findings of parasites
in fecal material recovered from archaeological sites. Although organic remains
may be found in a variety of environments, preservation seems to be best in
moist anaerobic environments or desiccating environments. Latrines readly provide
for the former conditions while caves and rock-shelters in arid regions provide
for the later (Reinhard et al. 1988).
Coprolites are desiccated
or mineralized feces and especial techniques were developed to search parasites
in their contents. To rehydrate desiccated coprolites, a trissodium phosphate
solution is used (Callen & Cameron 1960), and for fossilized coprolites,
modified polen analysis techniques are used (Reinhard et al. 1985, Ferreira
et al. 1993, Duarte et al. 1999).
Coprolites can be recovered
from archaeological layers or cesspits, and directly from mummified bodies.
They are the main source for parasite remains. Desiccation, and sometimes mineralization,
results in excelent preservation of parasite larvae and eggs, whereas protozoan
cysts are rarely found (Ferreira et al. 1992). Helminth species that normally
hatch out of their eggs and leave feces are trapped by drying, providing records
of hookworm (Araújo et al. 1981, Ferreira et al. 1987) and Strongyloides
infection in ancient human (Reinhard et al. 1987) and animal (Araújo et
al. 1989) populations.
With the cooperation among
archaeologists and paleoparasitologists, pictures of parasite infections have
been traced from ancient times to present days (Araújo et al. 1981, Horne 1985,
Nozais 1985).
From the pioneer period, when
the reporting of a parasite in archaeological materials deserved attention for
the finding itself, sometimes as a curiosity, emerged interpretations and hypothesis
for the presence of a given parasite in a determined place and time. Cockburn
(1967) was the first to call attention for the potentiality of parasite studies
in coprolites, and Ferreira et al. (1979) named paleoparasitology this new field
of science.
Paleoparasitology advances
by interpreting findings and making inferences about the impact of parasitic
diseases among prehistoric populations. Hunter-gatherers were found to be less
infected by helminths, whereas agricultural groups showed comparatively higher
prevalences of intestinal parasites in archaeological sites in the United States
(Reinhard 1992). Food habits of prehistoric inhabitants in the Chilean desert
were discussed by Ferrreira et al. (1984) by the finding of Diphyllobothrium
pacificum eggs, a sea lion parasite, in human coprolites dated of 6,000
years before present (B.P.).
Heirloom parasites are well
exemplified by Enterobius vermicularis studies. This helminth infection
was recorded in Norht America dated up to 10,000 years B.P. (Moore et al. 1969)
through colonial times (Reinhard et al. 1997). E. vermicularis infection
was found in cold climates, in Greenland, dated 1400 A.D. (Anno Domini) (Hausen
1986), and in the South American Pacific coast from 4,000 to 2,000 years B.P.
(Pizzi & Schenone 1954, Araújo et al. 1985). Its absence in Brazilian archaeological
material remains to be explained. Human-parasite coevolutionary studies based
on paleoparasitological finds were performed showing the antiquity of parasite-host
relationships, and tracing the origin and dispersion of the infection in prehistorical
times (Confalonieri et al. 1991, Araújo & Ferreira 1995, Hugot et al. 1999).
The finding of human hookworm
and whipworm eggs in pre-Columbian America (Allison et al. 1974, Ferreira et
al. 1980,1983, Araújo et al. 1981) raised an interesting debate (Hawdon &
Johnston 1996, Ferreira & Araújo 1996). Both are geohelminths, with an obligatory
passage in the soil. They can only maintain their biological cycle to infect
a new host if environmental conditions are suitable.
Hookworm eggs were found in
human coprolites in South American archaeological sites radiocarbon dated as
old as 7,200 years (Ferreira et al. 1987). Trichuris trichiura eggs were
found in the Andean region and in the other side of the continent, in Brazilian
Northeast, dated 2,000 years B.P. (Ferreira et al. 1989). In both cases, eggs
were recovered from intestinal contents of South American mummies (Pizzi &
Schenone 1954, Allison et al. 1974, Ferreira et al. 1983).
Prehistoric migrations crossing
the Bering Land Bridge would not be responsible for the introduction of hookworm
and whipworm infection during the first steps to the peopling of the Americas.
Cold climate and nearly frozen conditions of the soil would have impaired larvae
and eggs to evolve and be transmissible to a new host. Prehistoric transpacific
contacts of Asian groups with South American Indians, proposed by archaeologists
(Rivet 1926, Meggers & Evans 1966) based on cultural similarities may now
be established also by a biological indicator. Dating the first Americans is
under an intense debate and the recent archaeological findings in South America
(Guidon & Delibrias 1986, Guidon & Arnaud 1991) turned the peopling
of the New World a story to be rewritten (Gruhn 2000). Paleoparasitology, especially
focused as an interdisciplinary science, certainly is contributing to this issue
(Araújo & Ferreira 1996, 1997), together with paleogenetics (Ribeiro et
al. 1996, Bonatto & Salzano 1997, Callegari-Jacques & Salzano 1999).
Paleoparasitological findings
in the Old World revealed infections recorded in peat bog mummies (Fischer 1980,
Jones 1986, Jones & Nicholson 1988, Hill 1990) and latrine soils (Szidat
1944, Taylor 1955, Pike 1967, 1968, 1975, Herrmann 1986, Reinhard et al. 1988).
Interesting results were obtained by soil analysis and intestinal contents of
mummified bodies by the French paleoparasito-logical team (Bouchet & Paicheler
1995, Bouchet et al. 1996, 1999).
Classical paleoparasitology
based on coprolite rehydration and microscopic analysis after parasite concentration
techniques is still contributing to the knowledge of parasitc disease past distribution
throughout ancient times. But new techniques point to new perspectives, more
sensible and capable to detect parasite traces in archaeological remains to
the level of DNA fragments. Molecular paleoparasitology constitutes a powerful
tool to the research of parasitic diseases in the past.
During the last ten years
infectious diseases started to be diagnosed using technologies based on nucleic
acid. Ancient DNA (aDNA) are nucleic acids recovered from archaeological material
or museum specimens. In a broader sense it can be applied to any nucleic acid
recovered after death when the autolysis process was started (Herrmann &
Hummel 1994). aDNA was amplified from human bones and mummified tissues (Horay
et al. 1989, Hagelberg et al. 1989, 1991, Hänni et al. 1990, Hagelberg &
Clegg 1991, Pääbo 1993) and perspectives and limits were discussed with the
new technology (Brown & Brown 1992). The polymerase chain reaction (PCR)
was then incorporated in paleoparasitological analysis and adapted to detect
parasite DNA fragments (Araújo et al. 1998).
The amplification of Borrelia
burgodorferi DNA isolated from 13 of 1,036 mite museum samples in the United
States (Persing et al. 1990), and the positive PCR for Leishmania amazonensis
in taxidermized rodents sampled from museum specimens (Cantarino et al. 1998)
showed the potentiality of this technique for the diagnosis of parasitic infections
in preserved museum collections. PCR was used to study Mycobacterium tuberculosis
infection in mediaeval skeletons in Europe (Spigelman & Lemma 1993), in
a Peruvian pre-columbian mummy (Salo et al. 1994), and in Chilean prehistoric
skeletons (Arriaza et al. 1995).
Chagas disease is an excelent
example for the development of this technique applied to the diagnosis of a
parasitic infection in prehistorical times.
The first histological microscopic
examination of suspected amastigote nests in mummified tissues were discussed
(Rothhammer 1985, Rothhammer et al. 1985), but later confirmed in a Peruvian
mummy (Fornaciari et al. 1992).
Mummies are a scarce remain
of ancient cultures, but bones can be found more abundantly. The search for
Trypanosoma cruzi DNA fragments started with experimental approachs to
test techniques in laboratory desiccated infected mice (Bastos et al. 1995)
and then applied to the diagnosis of Chagas disease in mummified tissues of
South American mummies (Guhl et al. 1997, 1999, Ferreira et al. 2000).
The focus is now directed
to attempts to isolate T. cruzi DNA from bones and skeletons as they
may be representative samples of prehistoric populations in an epidemiological
sense (Guhl et al. 2000). Moreover, they are in most of the cases the only available
material for analysis. One or two mummies or a handfull of bones found to be
positive for some infection may indicate a infectious disease in a population,
but rather a paleoepidemio-logical approach. What is possible now with the molecular
paleoparasitology is the possibility of investigating significative samples
of a skeleton population where traces of a parasite were not visible to a microscopic
level.
This is really a new branch
of science: the perspective of recovering a genome of a parasite that infected
a human being living more than 10,000 years ago, and the comparisons that may
be made with present lineages are opening possibilities to study the genome
evolution through time. Origin, dispersion, virulence, and pathogenicity will
certainly be more clearly understood under molecular paleoparasitological approaches.
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