Ja. Dediego et al., RELATIONSHIPS BETWEEN HISTOPATHOLOGICAL FINDINGS AND PHYLOGENETIC DIVERGENCE IN TRYPANOSOMA-CRUZI, TM & IH. Tropical medicine & international health, 3(3), 1998, pp. 222-233
Problems have been raised by natural genetic diversity of Trypanosoma
cruzi, the causal agent of Chagas' disease, and other protozoa in term
s of both basic and applied science. T. cruzi manifests a great divers
ity of medical and biological properties which could be the origin of
clinical variability in the disease. Me propose possible correlations
between genetic distances, or phylogenetic divergence, and histopathol
ogical data. To ascertain this aspect, 15 cloned stocks pertaining to
three major clones or genotypes (19, 20 and 39) were compared. Sets of
24 mice infected with each stock were studied for histopathological l
esions. Brain, heart, lung, liver, spleen, urinary bladder, bone marro
w colon, kidney and skeletal muscle were extracted from each mouse. Qu
alitative and quantitative differences showed at histopathological exa
mination. An important encephalic softening was found in brains of mos
t mice infected by genotype 20, corresponding to areas of inflammation
and liquified necrosis. Other inflammatory tissue lesions in the hist
ological sections of the three genotypes were similar. Skeletal muscle
tropism was higher than cardiac tropism in all the studied genotypes.
All three genotypes shared parasite presence in skeletal muscle. Diff
erences related to cardiac tropism were important: in genotype 19, 50%
of studied stocks presented pseudocysts; 20% in genotype 20 and 83% i
n genotype 39. Parasite presence in other tissues was scanty: in brain
only in genotype 20 and in spleen and liver only in genotype 39. We f
ound important histopathogenicity differences among the three studied
genotypes, but they do not support the hypothesis of zymodeme pathogen
ic specificity due to the great diversity among stocks within each gen
otype.