The Sylvatic Cycle of Trypanosoma
cruzi: a Still Unsolved Puzzle
Suppl. I: 203-204
Ana Maria Jansen/+,
Ana Paula Santos de Pinho, Cristiane Varella Lisboa, Elisa Cupolillo*, Regina Helena
Mangia**, Octavio Fernandes**
Departmento de Protozoologia
*Departmento de Imunologia ** Departamento de Medicina Tropical,
Instituto Oswaldo Cruz, Av. Brasil 4365, 21045-900 Rio de Janeiro, RJ, Brasil
Key words: Trypanosoma cruzi -
sylvatic cycle

Despite its clonal structure
(Miles & Cibulskis 1986, Tibayrenc & Ayala 1986) Trypanosoma cruzi presents
an extreme variability and the seminal studies described the pleomorphism of this
tripanosomatid. The slender blood forms have been taken for immature forms or male gametes
and the large blood forms, as mature forms or female gametes (Chagas 1909, Brumpt 1912).
Since then, all attempts made to correlate biological, biochemical and morphological
parameters of the parasite with the course of the experimental infection or with the
different aspects of Chagas disease, has led to controversial results. Nevertheless, the
study of enzyme electrophoresis profiles defined three major subpopulations (zymodemes) in
Brazil, associated to domestic (ZII) or sylvatic transmission cycle (ZI and ZIII) (Barrett
et al. 1980). More recently molecular markers separated two distinct and major
phylogenetically lineages in T. cruzi also associated to the domiciliar
transmission cycle (lineage 1), and to the sylvatic transmission cycle (lineage 2) (Souto
et al.1995, Zingales et al. 1997, Fernandes et al. 1998).
However, what is the so-called
"T. cruzi sylvatic transmission cycle"? It is well known that naturally
infected mammals and bugs can be found in almost any sylvatic ecotope, but very little is
known about the kinetics of the transmission of T. cruzi among its vertebrate and
invertebrate hosts in the natural environment. The performed surveys reflect a cross
sectional analysis of the enzooty, and do not consider the peculiarities of the
interaction of the parasite with a given host. The studies of the interaction of T.
cruzi with marsupials, considered to be the most important and probably the most
ancient reservoirs, has yielded a series of new data on the biology and ecology of this
flagellate. This is exemplified by the cycle undertaken by the parasite in the lumen of
the scent glands of Didelphis marsupialis, where the protozoan multiplies as
epimastigotes and differentiates into metacyclic forms (Deane et al. 1984). The
extracellular multiplication cycle of T. cruzi in the scent glands of the opossum D.
marsupialis evidences that, besides being a reservoir host, this species can also be a
vector of T. cruzi. Another peculiarity of the interaction of T. cruzi with
marsupials, is the effective control of the infection by D. marsupialis and Philander
opossum. Moreover, D. marsupialis are able to rapidly control and even
eliminate infections with T. cruzi Y strain, while maintaining other strains
indefinitely without any significant tissue lesion (Deane et al. 1984). P. opossum, on
the contrary, maintains both types of strains (Pinho et al. 1993).
Studying the circulation of T.
cruzi among triatomine vectors, P. opossum and D. marsupialis
captured in a same area of the Atlantic Coastal Rainforest we observed that 50% of the
marsupials and bugs, were naturally infected. The biological, biochemical and molecular
characterization of the T. cruzi isolates defined two groups, associated mainly to P.
opossum or D. marsupialis. The collected bugs (Rhodnius prolixus) were
most probably involved with the transmission of the parasite among D. marsupialis, since
their T. cruzi isolates displayed similar biological, biochemical and molecular
characteristics. Furthermore although P. opossum and D. marsupialis occupy the same
sylvan habitat exclusively D. marsupialis frequents and even colonize human
dwellings and therefore was considered as a link between the sylvan and domestic
transmission cycles but it was observed that only P. opossum harbored T. cruzi
lineage 1 parasites. The presence of lineage 1 in D. marsupialis is rare (Zingales
et al. 1998, Fernandes et al. 1999). These findings and our previous observations that in
experimental conditions P. opossum do not select subpopulations of T. cruzi,
contrary to D. marsupialis, strongly suggested two independent transmission cycles
occurring between these two marsupial species that live sympatrically. Furthermore suggest
an explanation to the absence oh human infection in the studied area.
Going further in our observations
we decided to study, in another area of the Atlantic Coastal Rainforest, a greater range
of hosts: sloths, rodents, marsupials and golden lion tamarins (Leonto-pithecus
rosalia), an endangered primate species included in a conservation program. There, we
observed a completely distinct enzootic picture since L. rosalia was the most
infected species, (52%) in comparison to the marsupials (5.3 %) and rodents (18%). All L.
rosalia isolates were typed as belonging to lineage 1. On the other hand, all isolates
derived from the other mammals including one sloth isolate, were typed as belonging to
lineage 2. The only bug found in that area, a Triatoma vitticeps, was infected with
flagellates which were in lineage 1 (Lisboa et al. 1996). Our observations suggest that
dispersion of T. cruzi in the sylvatic environment can occur through simultaneous
distinct and independent tansmission cycles which are ruled by still unknown factors, not
including e.g. forest strata, since golden lion tamarins and sloths are both arboreal
animals. Moreover, the sylvatic transmission cycle is much more complex than assumed up to
now. Therefore, no generalization or prediction should be made in an enzootical study of
parasites and each ecotope should be considered as a unique system by every program which
include managing of the sylvatic environment. Several pathogenic trypanosomatids of
mammals infect a broad range of vertebrate and invertebrate hosts circulating therefore
among dozens of different species of insects and mammals in distinct ecotopes.
Consequently, the outbreaks of the diseases are drive by diverse factors such as the
presence of carriers, wildlife reservoirs, concentration of infected animals and vectors,
husbandry practices which are strongly affected by the environmental conditions and should
be taken into account.
Among trypanosomatids, T.
cruzi has one of the broadest mammal host ranges, being able to parasitize the most
varied tissues, thereby colonizing almost every niche available. This versatility ensures
that many unorthodox niches such as the opossum scent glands and cartilage (Deane et al.
1984, Lagrange et al. 1992). This aspect, together with the capability of maintaining
distinct transmission cycles between sympatric hosts, gives an undoubted advantage to this
eclectic parasite characterizing T. cruzi as one of the most successful organisms
to adopt the parasitic way of life.

REFERENCES

+ Corresponding
author. Fax: +55-21- 598.4323. E-mail: jansen@gene.dbbm.fiocruz.br
Received 9 June 1999
Acceped 9 August 1999