Population dynamics and intra-litter transmission patterns of Isospora suis in suckling piglets under on-farm conditions.

The aim of this study was to investigate the intra-litter infection dynamics of Isospora suis under natural conditions, and to study any association between parasite transmission and the contamination level of the farrowing pen by applying different interventions in order to reduce the transmission of I. suis infection within the litter. The study was divided in 2 trials including in total 22 litters (254 piglets). The first trial included 4 litters (where standard procedures practiced routinely on the farm piglets were applied) and the piglets were followed coprologically from farrowing until 2 weeks after weaning. The sows of those litters were also examined at various intervals before and after farrowing. The second trial included the application of 3 different management procedures: (A) standard farm hygiene and management procedures, (B) standard farm hygiene and management procedures+the first piglets found to excrete I. suis oocysts in each pen were removed from the pen, and (C) reduced cleaning. Each procedure was studied in 2 litters. This was replicated 3 times to yield a total of 18 litters. The results suggested that (i) the sow does not play an important role in transmission of I. suis in the farrowing pen; (ii) in natural infections, both the age of the piglet age at onset of oocyst excretion and the oocyst excretion patterns may vary considerably; (iii) the course of oocyst excretion or development of diarrhoea is related to the time of initial infection and (iii) piglets, which are heavy at birth, are more prone to acquire I. suis infection. Moreover, it was demonstrated that cleaning could be an effective means of restricting the spread of the parasite within the litter and thus the development of diarrhoea.

Isospora plectrophenaxia n. sp (Apicomplexa: Eimeriidae), a new coccidian parasite found in Snow Bunting (Plectrophenax nivalis) nestlings on Spitsbergen.

Faecal samples were collected from four 8 days old snow bunting nestlings from one nest in Ny-Alesund, Spitsbergen, in summer 2006. After sporulation, samples were examined for coccidian parasites using flotation centrifuging. We found isosporan oocysts in three birds, intensity of infection varied between individuals from 35 to 6,000 oocysts per defecation. All oocysts belonged to one species, which is described here as a new species. The spherical or subspherical oocysts (Fig. 1) have a brownish, smooth, relatively thin (about 1.1 microm) bilayered wall. Average size of sporulated oocysts was 26.2 +/- 0.13 x 23.6 +/- 0.16 microm (24.1-28.4 x 21.5-26.9; n = 10) with a shape index (length/width) of 1.11 +/- 0.01 (1.01-1.29). The sporulated oocysts have no micropyle or residuum but enclose one large (3.3 x 2.8 microm) ring-formed polar granule. The sporocysts are ovoidal, slightly pointed at the end opposite the Stieda body, 18.2 +/- 0.06 x 9.9 +/- 0.03 microm (17.1-19.0 x 9.0-10.8; n = 14), shape index 1.85 +/- 0.008 (1.70-1.99). The Stieda body has a prominent knob-like cap and a well-visible round substieda body. Sporocysts contain compact sporocyst residuum composed of small, uniform granules and sporozoits with usually three large refractile bodies and a smaller nucleus. The prepatent period is less than 8 days. This is the first description of an avian isosporan parasite that succeeds transmission while in the High Arctic.

Atoxoplasmosis in tanagers.

Atoxoplasma spp. (extraintestinal Isospora spp.) are coccidian parasites that infect a variety of passerine species. Atoxoplasmosis has been difficult to diagnose using buffy coat and organ impression smear examinations or histopathologic examination of tissues at necropsy. The prevalence of this parasite was studied in the tanager collection of a zoological park after the death of several tanagers from confirmed and suspected infections. A polymerase chain reaction assay was used to test blood, feces, or tissue samples (or all) from 88 individuals representing 18 species. Twenty-three of 60 (38.3%) blood samples from clinically healthy birds tested positive for Atoxoplasma, and one of six fecal samples was positive. Nineteen of 32 (59.4%) tissue samples from deceased tanagers tested positive. A total of 57 other institutions were also queried regarding the presence of Atoxoplasma. The high number of Atoxoplasma-positive clinically healthy birds suggests that the parasite is prevalent subclinically within tanager collections, with young birds and stressed adults being the most likely to develop clinical disease. Thorough disinfection of enclosures, consideration of enclosure designs, and preventing fecal contamination of food and water are important methods of decreasing transmission. Selective breeding programs and regular screening of breeding pairs may be recommended to decrease transmission to susceptible offspring. Care should also be taken when housing tanagers in mixed species or in outdoor enclosures because the transmission risks between species have not been well established.