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.

Highlights

  • Besnoitia darlingi, B. neotomofelis and B. oryctofelisi are closely related coccidian parasites, for which cats have been established as definitive hosts (Dubey et al, 2003a; Dubey and Yabsley, 2010; Smith and Frenkel, 1977, 1984)

  • In-silico analysis revealed that probe Bb11-12, initially established to detect B. besnoiti DNA, was specific for Besnoitia spp. of ungulates, and matched the Internal Transcribed Spacer-1 (ITS-1) sequences of further Besnoitia species

  • DNA samples of parasites that were expected to be recognized by BdanjoRT1) and on the other hand DNA samples of Besnoitia spp. of ungulates (B. besnoiti, B. tarandi, B. bennetti) as well as DNA of related protozoan parasites N. caninum, H. heydorni, T. gondii, H. hammondi, Cystoisospora spp., S. cruzi, C. parvum and G. duodenalis and T. foetus

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Summary

Introduction

B. neotomofelis and B. oryctofelisi are closely related coccidian parasites, for which cats have been established as definitive hosts (Dubey et al, 2003a; Dubey and Yabsley, 2010; Smith and Frenkel, 1977, 1984). Whereas B. darlingi uses opossums (Didelphis virginiana) as intermediate hosts, B. neotomofelis and B. oryctofelisi have been described in the Southern Plains woodrat (Neotoma micropus) in the USA and in domestic rabbits from Argentina, respectively (Dubey and Yabsley, 2010; Smith and Frenkel, 1984; Venturini et al, 2002). Another closely related Besnoitia species, B. jellisoni, was initially described in the USA, with the white-footed deer mouse (Peromyscus maniculatus) and three species of kangaroo rats (Dipodomys species) as intermediate hosts (Ernst et al, 1968; Frenkel, 1953).

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