Sensitive detection of nucleic acids by PNA hybridization directed co-localization of fluorescent beads

We have designed a pair of biotinylated peptide nucleic acid (PNA) probes targeting two sequences in 18S rRNA (from the parasite Trypanosoma brucei) at a distance of 191 nt (corresponding to maximum distance of ca. 60 nm) from each other. The PNA probes were individually bound to (strept)avidin-coated fluorescent beads, differing in size and color [green beads (1 microm) and red beads (5.9 microm)], thereby allowing distinct detection of each PNA probe by conventional fluorescence microscopy. These two PNA beads showed easily detectable co-localization when simultaneously hybridizing to a target nucleic acid. The assay detected the parasite 18S rRNA down to 1.6 fmol while there was no such co-localization visible with human 18S rRNA not containing the PNA targets. Furthermore, the assay showed positive detection with 1.6 ng of total RNA (corresponding to RNA from ca. 300 parasites). Upon further optimization this method may provide a new tool for a diagnosis of Human African Trypanosomiasis (HAT) and it may more generally have applications within diagnostics for (neglected) infectious diseases.

Jaar van publicatie:2011

Trefwoorden:Protozoal diseases, Sleeping sickness, Trypanosomiasis-African, Trypanosoma brucei gambiense, Trypanosoma brucei rhodesiense, Vectors, Tsetse flies, Glossina, Detection, Diagnosis, Development, Research, Nucleic acids, Hybridization, Peptide nucleic acid probes, Fluorescence microscopy, RNA, Laboratory techniques and procedures