Key result
Infection of C3H/He mice with T. cruzi clone X10/7 resulted in 94.3% mortality compared to 5.1% with clone X10/4, demonstrating constant pathogenicity despite long-term in vitro maintenance.
T. cruzi clones maintain constant pathogenicity in inbred mice despite long-term in vitro maintenance, providing a reproducible model for studying host-parasite interactions such as Chagas cardiomyopathy.
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Stable T. cruzi clones enable reproducible murine models; leaves open translation to human Chagas cardiomyopathy.
The reproducibility of infection of C3H/He mice with T. cruzi clones Sylvio-X10/4 and Sylvio-X10/7 maintained in the laboratory for 946 and 496 days respectively was assayed. Clone X10/7 from 15 different in vitro passages consistently induced an acute lethal infection (94.3% mortality) and constant survival time (Mean = 24.6 d.p.i.). Female mice survived significantly longer than males and mice older than 30 days at the time of infection survived significantly longer than younger mice. The mortality of mice infected with clone X10/4 from 23 different in vitro passages was lower (5.1%) and their survival longer (Mean = 42.7 d.p.i.) than mice infected with clone X10/7. High anti-T. cruzi IgG titres were detected in the plasma of all mice killed after 30 d.p.i. Histologically, the heart, skeletal muscles and/or large intestine contained intracellular parasites in 59% of the mice; parasites were found in mice of all groups tested. The hearts of all mice were comparably inflammed regardless of parasite passage number or duration of infection. These data demonstrate that the presentation and course of infection of inbred mice with two T. cruzi clones is not changed by either the duration or protocol used for in vitro maintenance; the reported loss or change in virulence of T. cruzi strains during long-term in vitro maintenance did not occur. Consequently, T. cruzi clones and inbred mice provide a dependable and reproducible means to study host-parasite interactions.
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Postan et al. (1986) studied Trypanosoma cruzi infection. T. cruzi clone Sylvio-X10/7 vs. T. cruzi clone Sylvio-X10/4 was evaluated on Mortality. Infection of C3H/He mice with T. cruzi clone X10/7 resulted in 94.3% mortality compared to 5.1% with clone X10/4, demonstrating constant pathogenicity despite long-term in vitro maintenance.
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