Coxiella burnetii, the causative agent of Q fever, is widely present in dairy products around the world. It has been isolated from unpasteurised milk and cheese and can survive for extended periods of time under typical storage conditions for these products. Although consumption of contaminated dairy products has been suggested as a potential route for transmission, it remains controversial. Given the high prevalence of C. burnetii in dairy products, we sought to examine the feasibility of transmitting the major sequence types (ST16, ST8 and ST20) of C. burnetii circulating in the United States. We delivered three strains of C. burnetii, comprising each sequence type, directly into the stomachs of immunocompetent BALB/c mice via oral gavage (OG) and assessed them for clinical symptoms, serological response and bacterial dissemination. We found that mice receiving C. burnetii by OG had notable splenomegaly only after infection with ST16. A robust immune response and persistence in the stomach and mesenteric lymph nodes were observed in mice receiving ST16 and ST20 by OG, and dissemination of C. burnetii to peripheral tissues was observed in all OG infected mice. These findings support the oral route as a mode of transmission for C. burnetii.

In the present study gut type was described and intestinal indices (i.e. mean gut length, relative gut length and Zihler's index) were estimated and compared for 58 fish species from the North Aegean Sea. A strong relationship between gut length (GL) and total length (TL) (significant relationships (P < 0.05) for 52 species) was found, whereas the hypothesis of the allometric growth of GL with TL was confirmed for 27 out of the 52 species. For the same TL, GL differs for species with different feeding habits (in omnivores > carnivores), as previously reported. Finally, for the same TL, GL also differs for species with different habitats (reef-associated > pelagic > benthopelagic > demersal) and gut types (Z-shaped with multiple loops > looped Z-shaped > Z-shaped >straight > convoluted > short with spiral valve).

For the first time the development of the alimentary tract of Levinseniella brachysoma metacercaria (Trematoda: Microphallidae) obtained experimentally from Gammarus oceanicus has been described. The foregut primordium in 16-day-old metacercariae is represented by a syncytial cylindrical cord, resulting from the fusion of embryonic cells. Non-fused parts of the plasma membranes of adjacent cells are revealed as gap cavities within the cord. Later (30th day post infection) the lumen of the foregut is formed as a result of both partial vacuolization of the cytoplasm and by a broadening of the gap cavities, resulting from a thinning of the cytoplasmic spaces between them. Besides the usual organelles, the foregut of the mature metacercaria (42nd day p.i.) contains dense secretory granules in the apical cytoplasm region and numerous microtubules in basal areas. The cellular gastrodermis is formed later than the foregut syncytium (on day 30 p.i.); its large cells contain well-developed Golgi complexes, RER and mitochondria. A noteable inclusion of the gastrodermal cells of mature metacercariae are spherical granules of moderate electron density measuring up to 3 μm in diameter. On the basis of an analysis of the ultrastructural data the possible functioning of the metacercarial alimentary tract is discussed.

To clarify the nature of M cells, the detailed ultrastructural characteristics and lectin-binding properties of M cells were investigated in follicle-associated epithelium (FAE) of chicken caecal tonsils. M cells presented various outlines from columnar to dome shaped. Their polymorphism was dependent on the number of harboured intraepithelial migrating cells. The lighter and larger nuclei of M cells were situated at more apical levels in the epithelial lining compared with those of neighbouring microvillous epithelial cells. The microvilli, which were significantly shorter and thicker than those of adjacent microvillous epithelial cells, were sparsely distributed or completely absent on the apical surfaces of M cells. In general, the apical cytoplasm of M cells without microvilli protruded slightly into the intestinal lumen. Numerous small vesicles were often contained in the apical cytoplasm. The numerous small invaginations of the apical and lateral cell surfaces suggested active transportation of luminal substances. No canaliculi existed in the apical cytoplasm of M cells whereas they were often detected in the neighbouring microvillous epithelial cells. A noteworthy finding was the frequent detection of multivesicular bodies in the apical cytoplasm of M cells. These multivesicular bodies suggest some degradation of ingested luminal substances during transcytoplasmic transportation. WGA and 4 other lectins strongly reacted with all epithelial cells except for M cells, this negativity suggesting a means of detecting M cells in chicken caecal tonsils. Three lectins, DSL, ConA and Jacalin, reacted weakly with the glycocalyx on M cells. The positive reactivity might allow chicken M cells to be utilised for specific antigen delivery into the mucosal immune system in some parenteral vaccinations.