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. Author manuscript; available in PMC: 2010 Sep 1.
Published in final edited form as: Am J Trop Med Hyg. 2009 Sep;81(3):390–395.

TABLE 1.

Serologic analysis of dogs naturally or experimentally infected with T. cruzi

Weeks post-infection

T. cruzi infection Week 0 Week 1 Week 2 Week 3 Week 4 Week 10
IHA
    Natural (A) + + + + + +
    Zump (B) + + + +
    Sylvio (C) + + + ND
    None (D)
ELISA—OD450nm ± SD
    Natural (A) 1.85 ± 0.07 1.81 ± 0.03 1.88 ± 0.05 1.89 ± 0.02 1.88 ± 0.02 1.92 ± 0.05
    Zump (B) 0.11 ± 0.03 0.14 ± 0.01 0.16 ± 0.05 0.25 ± 0.04 0.38 ± 0.07 1.05 ± 0.61
    Sylvio (C) 0.09 ± 0.03 0.18 ± 0.03 0.16 ± 0.04 0.28 ± 0.04 0.53 ± 0.2 ND
    None (D) 0.13 ± 0.01 0.13 ± 0.02 0.17 ± 0.03 0.13 ± 0.003 0.14 ± 0.02 0.15 ± 0.01
    Cut-off (CV) 0.23 (0.21–0.26) 0.23 (0.28–0.25) 0.27 (0.25–0.30) 0.23 (0.28–0.25) 0.24 (0.22–0.27) 0.25 (0.22–0.27)

Sera samples were collected from dogs with natural T. cruzi infection (Group A) and dogs that were experimentally infected with Zumpahuacan (Zump, Group B) or Sylvio-X10 (Sylvio, Group C) isolates of T. cruzi at 1, 2, 3, 4, and 10 weeks post-infection. Normal, uninfected dogs (none, Group D) were used as controls. The sera level of anti-T. cruzi antibodies was determined by IHA and ELISA. IHA: +, positive at least at a 1/8 serum dilution; −, negative. The + and − represent mean of triplicate observations from four dogs in each group. ELISA: cut-off = average of negative controls +0.1 (±10%). Absorbance (OD450nm) ± SD values are representative of mean of triplicate observations per dog, four dogs per group, with variation coefficient subtracted at 10% level.

CV = coefficient of variation; ND = not determined because dogs died, and no samples were available.