In previous studies we have identified and characterized an 80-kDa Try
panosoma cruzi urinary antigen (UAg) eliminated during acute infection
. Polyclonal antibodies raised against this antigen revealed by wester
n blotting and immunoprecipitation analyses showed the existence of an
other antigenic component of 50-55 kDa in the UAg preparation, The ant
iserum was also used for screening of a T. cruzi expression library. S
equencing of inserts from selected cDNA clones showed high homology wi
th the 3' end of the T. cruzi beta-tubulin gene sequence encoding for
the C-terminus of the protein. The presence of T. cruzi tubulin in the
UAg was confirmed by immunoprecipitation of a 50-55-kDa protein from
I-125-labeled UAg with monoclonal antibodies (MAbs) to human alpha/bet
a-tubulin. Interestingly, MAbs recognized radiolabeled T. cruzi tubuli
n eliminated in the urine of infected mice 24 hr postinoculation of [S
-35]methionine-labeled viable trypomastigotes. Tubulin found in the ur
ine proved to be of T. cruzi origin because this protein could not be
identified in urinary specimens from uninfected animals or mice acutel
y infected with Leishmania infantum or Toxoplasma gondii We conclude t
hat tubulin is one of the parasite antigens eliminated in the urine of
T. cruzi-infected hosts. This finding may be used to develop a noninv
asive procedure for early diagnosis of Chagas' disease.