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. Author manuscript; available in PMC: 2007 Apr 20.
Published in final edited form as: Parasitology. 2006 Jan;132(Pt 1):57–65. doi: 10.1017/S0031182005008772

Table 1.

PCR-based identification of Trypanosoma cruzi lineages in faeces and culture isolates from triatomine bugs: DNA targets, application, primer sets and amplicon expected sizes in base pairs

DNA Target Application Primer sets TCl TClla TCllb TCllc TClld TClle
I Spliced leader intergenic region Distinction of TCl from TClla, llc & TCllb, lld, lle TCC-TC1-TC2a 350 n/a 300 n/a 300 300
TCac-UTCCb 157 200 150 200 150 150
II 24S alpha rDNA Distinction between TClla & TCllc or between TClld & TCllb, lle D71-D76b 125 135 140 125 125+140 140
III 18S rDNA A10 fragment Distinction between TCllb & TClle V1-V2c 175 155 165 165 165 n/ac,d
P3-P6c n/a 657 n/a 657 657 657

I to III: Work flow for lineage identification. Boxed amplicon sizes denote the PCR findings of this survey.

n/a: no amplification.

b

Heminested PCR (Burgos et al. 2005).

d

Most TClle isolates from northwestern Argentina amplify a 165bp 18S rDNA fragment.