Abstract:
Trypanosoma cruzi the causative agent of Chagas disease has a vast collection of surface antigen genes
classified into families. These families are mucins, transialidases and MASPS which constitute half of the
parasites genome. The members of these families are characterized by conserved sequence regions at their 5'
and 3' ends that do encode a signal peptide and GPI anchor sequence. Their central regions constitute
hypervariable regions some of which are marked with repeat sequences. A simple PCR technique that would
form the basis to a pilot study for capturing the intragenomic diversity of the T.cruzi surface antigen genes is
needed as a step towards more advanced techniques.Degenerate primers for targeting mucins, trans-sialidase
and MASP genes were designed from conserved nucleotide sequences at the 5' and 3' regions of the genes and
used in highly stringent PCR reactions to amplify a whole library of surface antigen genes. Purified PCR
products were cloned into pGEM-T Easy vectors sequenced by Sanger methodology. Generated sequences
were aligned against surface antigen gene sequences from the CL-Brener genome accessed through tritrypDB
database. Sequence analysis of the nucleotide sequence from PCR products were phylogenetically analysed to
determine their diversity. Degenerate mucin primers were able to produce PCR products from genomic DNA of
T. cruzi from all DTUs some of which were confirmed to mucins. The generated sequences were diverse from
each other with half of the sequences showing similarities to a cosmid C71. A non-surface antigen gene,
histone deacetylase, was also discovered and found to share similarity with 7 of the generated sequences.
Exploration of traditional southern, western and northern blots to microarray and next generation sequencing
techniques for study of parasite surface antigen are recommended.
