Abstract

The most important restriction for the detection in water samples is the low concentration of Giardia intestinalis cysts, additional difficulty is the presence of PCR inhibitors. We have carried out trials in order to assess the sensitivity of semi-nested PCR and TaqMan real time PCR on the basis of DNA extracted from G. intestinalis cysts coming from spiked environmental and distilled water samples, filtrated with the use of Filta-Max® equipment (1623 Method). Removal of inhibitors was carried out with addition of BSA in different concentrations. During the filtration and concentration of water samples, losses of cysts have been recorded. Moreover, addition of BSA to the PCR and real time PCR mix increases the sensitivity of reaction. The optimal concentration of BSA for semi-nested PCR was 15 and 20 ng/μl, whereas for real time PCR 5 ng/μl.

Highlights

  • We evaluated the efficiencies of different DNA extraction methods (Adamska et al, 2010)

  • We have carried out trials to assess the sensitivity of semi-nested PCR and TaqMan real time PCR on the basis of DNA extracted from G. intestinalis cysts providing from spiked environmental and distilled water samples

  • The intensity of signal obtained with semi-nested PCR was similar for isolates received from filtration of spiked distilled and lake water, whereas intensity was higher when isolates were directly received from G. intestinalis cysts in PBS

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Summary

Introduction

We have carried out trials to assess the sensitivity of semi-nested PCR and TaqMan real time PCR on the basis of DNA extracted from G. intestinalis cysts providing from spiked environmental and distilled water samples. SEMI-NESTED PCR AND TAQMAN REAL TIME PCR The intensity of signal obtained with semi-nested PCR was similar for isolates received from filtration of spiked distilled and lake water, whereas intensity was higher when isolates were directly received from G. intestinalis cysts in PBS.

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