Duplex quantitative real-time PCR assay for the detection and discrimination of the eggs of Toxocara canis and Toxocara cati (Nematoda, Ascaridoidea) in soil and fecal samples

<p>Abstract</p> <p>Background</p> <p>Toxocarosis is a zoonotic disease caused by <it>Toxocara canis</it> (<it>T. canis</it>) and/or <it>Toxocara cati</it> (<it>T. cati</it>)<it>,</it> two worldwide distributed roundworms which are parasites of canids and felids, respectively. Infections of humans occur through ingestion of embryonated eggs of <it>T. canis</it> or <it>T. cati</it>, when playing with soils contaminated with dogs or cats feces. Accordingly, the assessment of potential contamination of these areas with these roundworms eggs is paramount.</p> <p>Methods</p> <p>A duplex quantitative real-time PCR (2qPCR) targeting the ribosomal RNA gene internal transcribed spacer (ITS2) has been developed and used for rapid and specific identification of <it>T. canis</it> and <it>T. cati</it> eggs in fecal and soil samples. The assay was set up on DNA samples extracted from 53 adult worms including <it>T. canis</it>, <it>T. cati</it>, <it>T. leonina</it>, <it>Ascaris suum</it> (<it>A. suum</it>) and <it>Parascaris equorum</it> (<it>P. equorum</it>). The assay was used to assess the presence of <it>T. cati</it> eggs in several samples, including 12 clean soil samples spiked with eggs of either <it>T. cati</it> or <it>A. suum</it>, 10 actual soil samples randomly collected from playgrounds in Brussels, and fecal samples from cats, dogs, and other animals. 2qPCR results on dogs and cats fecal samples were compared with results from microscopic examination.</p> <p>Results</p> <p>2qPCR assay allowed specific detection of <it>T. canis</it> and <it>T. cati</it>, whether adult worms, eggs spiked in soil or fecal samples. The 2qPCR limit of detection (LOD) in spiked soil samples was 2 eggs per g of soil for a turnaround time of 3 hours. A perfect concordance was observed between 2qPCR assay and microscopic examination on dogs and cats feces.</p> <p>Conclusion</p> <p>The newly developed 2qPCR assay can be useful for high throughput prospective or retrospective detection of <it>T.canis</it> and/or <it>T. cati</it> eggs in fecal samples as well as in soil samples from playgrounds, parks and sandpits.</p

Optimized DNA-based identification of Toxocara spp. eggs in soil and sand samples.

Toxocara canis and Toxocara cati are globally distributed roundworms and causative agents of human toxocariasis, via ingestion of Toxocara eggs. Control of Toxocara infections is constrained by a lack of sensitive methods for screening of animal faeces and environmental samples potentially contaminated by Toxocara eggs. In this work, a pre-analytical method for efficient extraction of DNA from Toxocara eggs in environmental samples was set up using our previously validated T. canis- and T. cati-specific quantitative real-time polymerase chain reaction (qPCR). For this purpose, the influence of different methods for egg lysis, DNA extraction and purification for removal of PCR inhibitors were assessed on environmental samples. To select the best egg disruption method, six protocols were compared on pure T. canis egg suspensions, including enzymatic lysis and thermal or mechanical disruption. Based on the selected best method, an analytical workflow was set up to compare two DNA extraction methods (FastDNA™ SPIN Kit for Soil versus DNeasy PowerMax Soil Kit) with an optional dilution and/or clean-up (Agencourt AMPure) step. This workflow was evaluated on 10-g soil and 10-g sand samples spiked with egg suspensions of T. canis (tenfold dilutions of 10 eggs in triplicate). The capacity of the different methods, used alone or in combination, to increase the ratio of positive tests was assessed. The resulting optimal workflow for processing spiked soil samples was then tested on environmental soil samples and compared with the conventional flotation-centrifugation and microscopic examination of Toxocara eggs. The most effective DNA extraction method for Toxocara eggs in soil samples consisted in the combination of mechanical lysis of eggs using beads, followed by DNA extraction with the DNeasy PowerMax Soil Kit, and completed with an additional DNA clean-up step with AMPure beads and a sample DNA dilution (1:10). This workflow exhibited a limit of detection of 4 and 46 T. canis eggs in 10-g sand and 10-g soil samples, respectively. The pre-analytical flow process developed here combined with qPCR represents an improved, potentially automatable, and cost-effective method for the surveillance of Toxocara contamination in the environment