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Sensitive, quantitative detection of Besnoitia darlingi and related parasites in intermediate hosts and to assess felids as definitive hosts for known and as-yet undescribed related parasite species.
- Source :
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International journal for parasitology. Parasites and wildlife [Int J Parasitol Parasites Wildl] 2020 Jan 24; Vol. 11, pp. 114-119. Date of Electronic Publication: 2020 Jan 24 (Print Publication: 2020). - Publication Year :
- 2020
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Abstract
- Besnoitia darlingi, B. neotomofelis and B. oryctofelisi are closely related coccidian parasites with cats as definitive hosts. While B. darlingi uses opossums as intermediate hosts, B. neotomofelis and B. oryctofelisi have been described in Southern Plains woodrats ( Neotoma micropus ) from the USA and in domestic rabbits from Argentina, respectively. A comparison of the Internal Transcribed Spacer-1 (ITS-1) region of the ribosomal DNA (rDNA) of these Besnoitia spp. showed only a few differences. The present study aimed at developing a real-time PCR to detect B. darlingi, B. neotomofelis and B. oryctofelisi in tissues of intermediate and in faeces of definitive hosts in order to support studies of these organisms' epidemiology and pathogenesis. The established PCR was based on primer regions distinct from the ITS-1 sequences of ungulate Besnoitia spp. and made use of a Besnoitia universal probe. To monitor inhibition, a heterologous internal control was established based on the enhanced green fluorescent protein gene. The real-time PCR reacted with B. darlingi , B. neotomofelis and B. oryctofelisi, while the novel PCR did not recognize ungulate Besnoitia spp. ( B. besnoiti, B. bennetti, B. tarandi ). DNA of Apicomplexa ascribed to other Besnoitia-related genera, including other gut parasites of cats ( Cryptosporidium parvum , Giardia duodenalis , Tritrichomonas foetus ), was not recognized. The real-time PCR had an analytic sensitivity of less than 1 tachyzoite per reaction. In feline faeces spiked with B. darlingi oocysts, the limit of detection was a DNA amount equivalent to 1 oocyst per PCR reaction. In B. darlingi infected ɣ-interferon knock-out mice, the lung was identified as the predilection organ. In conclusion, this real-time PCR should advance further studies on these parasites and may inspire research on related species, not only in the Americas, but also in other parts of the world.<br />Competing Interests: The study described is original and is not under consideration by any other journal. All authors approved the final manuscript and its submission. The authors declare that they have no conflict of interest.<br /> (© 2020 The Author(s).)
Details
- Language :
- English
- ISSN :
- 2213-2244
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- International journal for parasitology. Parasites and wildlife
- Publication Type :
- Academic Journal
- Accession number :
- 32042587
- Full Text :
- https://doi.org/10.1016/j.ijppaw.2020.01.011