Search PubMed⌕ Search

Biomedical subjects

R Ducatelle

Publications and source records attributed to R Ducatelle.

At least 163 records · Page 9Linked to original sources

Immunoperoxidase study of Aujeszky's disease in pigs.

Viral antigen was detected by an immunoperoxidase technique in histological sections from pigs with Aujeszky's disease. The antigen was found mainly in association with focal necrosis in the cerebellum, tonsils, oral and nasal mucosa, salivary glands, lungs, liver, kidneys, pancreas, spleen and adrenal glands. Cells at the margin of the necrotic foci especially were strongly positive. Viral antigen was also demonstrated in the cerebral cortex and in the brain stem. Two types of intranuclear inclusion bodies were found to contain viral antigen and one type also contained viral nucleic acids. Inflammatory cells usually contained no viral antigen. The possible significance of some of these infected tissues in the excretion of the virus is discussed.

Animals↗

Replication of porcine enteric adenoviruses in vivo.

The replication of an enteropathogenic porcine adenovirus in the intestinal epithelial cells of naturally and experimentally piglets has been studied by transmission electron microscopy (TEM) and by immunoperoxidase (Ip) staining of paraffin sections. Three types of intranuclear inclusion bodies were observed. Viral particles appeared to be assembled from electron dense crescents which seemed to originate from type II intranuclear inclusion bodies. Virus accumulated in the nucleus of infected cells. It formed paracrystalline arrays in the electron dense centre of the nucleus but was dispersed in the peripheral electron translucent zone. Virus was released from the cells after rupture of the nuclear and plasma membranes. The results are compared with published data on the replication of adenoviruses in cell cultures.

Adenoviridae↗

Baby pig diarrhea caused by coccidiosis.

An outbreak of coccidiosis on two Belgian farms is described. Diarrhea started in piglets at 9 or 10 days of life. Zero to three pigs died per litter. The morbidity rate varied from 70 to 90 per cent. Histological examination of the intestines revealed shortening of villi and different stages of the life cycle of coccidia were seen in the enterocytes. Virological examination was negative for corona-, corona-like, and rotavirus. A haemolytic E. coli strain was isolated in one case. As for treatment, good results were obtained by the adding of 1 kg amproleum pre-mix per ton sow feed. Scouring pigs were treated orally with 2 cc of an amprol solution once a day. The diarrhea stopped one day after treatment.

Animals↗

Adenovirus enteritis in pigs.

Experimental transmissions were done with adenovirus strain 6618 in hysterectomy-produced colostrum-deprived pigs. After an incubation period of 3 to 4 days, all inoculated animals had diarrhea. Histopathologically, many intranuclear inclusion bodies were present on short villi of the terminal parts of jejunum and ileum. With electron microscopy, the inclusion bodies were observed to contain numerous adenovirus particles. Immunoperoxidase-positive cells were seen on short villi of the terminal parts of jejunum and ileum. Adenovirus particles also were detected by negative staining of intestinal contents. In 1 pig (naturally occurring infection), adenovirus enteritis was studied by the aforementioned techniques. Similar intestinal lesions as described in the experimental pigs were observed.

Adenoviridae Infections↗

Coronavirus infection in a litter of pups.

An outbreak of a coronavirus infection in a litter of 10-week-old poodle pups from a commercial kennel is described. Coronavirus-like particles were demonstrated by electron microscopy in the intestinal contents and in the colonic mucosa. Treponemas and campylobacters were excreted in great numbers in the faeces. The gastrointestinal disturbances were complicated by hepatic and renal degeneration and severe bronchopneumonia.

Animals↗

Lucigenin- and luminol-enhanced chemiluminescence in turkey monocytes.

Monocytes from 10 week-old specific pathogen-free turkeys were isolated from peripheral blood by density centrifugation and assayed for their oxidative activity by means of a luminometer. Chemiluminescence (CL) properties after stimulation with different soluble and particulate stimuli were compared in lucigenin- and luminol-enhanced assays. A distinct response could be measured with 12-phorbol 13-myristate acetate (PMA) and Zymosan A, but only a weak signal was obtained with calcium ionophore A23187. No oxidative activity could be induced with N-formyl-methionyl-phenylalanine. Peak maxima for both lucigenin- and luminol-enhanced CL were ranked: PMA > Zymosan A > calcium ionophore. The velocity of the lucigenin- and luminol-enhanced responses induced by calcium ionophore were of similar magnitude, but the lucigenin-enhanced responses of Zymosan A and PMA-stimulated monocytes were respectively about 5 and 10 times higher than those obtained in luminol-enhanced assays. No peroxidase activity could be detected in the purified turkey monocytes. As luminol-enhanced CL primarily results from the peroxidase activity, this lack of myeloperoxidase may explain the observed lower responses to the different stimuli, in the presence of a luminol. In contrast, lucigenin-enhanced CL is not related to peroxidase activity, but is a selective probe of oxidase activity. Irrespective of the myeloperoxidase deficiency, different soluble and particulate stimuli induced a significant and reproducible CL response in turkey monocytes, in the presence of both chemiluminigenic probes, lucigenin and luminol. The possibility of measuring the phagocyte oxygenation activity of turkey monocytes represents a useful tool for the study of monocyte mediated host defence in the turkey.

Acridines↗

The inflammatory response in the mouse stomach to Helicobacter bizzozeronii, Helicobacter salomonis and two Helicobacter felis Strains.

The inflammatory response in the mouse stomach was evaluated as a means of distinguishing different non-pylori Helicobacter (H.) strains in terms of virulence. Mice of four strains (BALB/c, SJL, C57BL/6 and CFW) were infected intragastrically with four bacterial strains (H. felis ATCC 49179 and CCUG 37471, H. bizzozeronii and H. salomonis). The animals were killed for gastric examination at 3, 9 or 16 weeks post-inoculation. H. salomonis could not be detected by the polymerase chain reaction, but the other three organisms were detected in all stomach samples at all timepoints. SJL mice consistently showed particularly severe gastric inflammation regardless of bacterial strain. Lymphocytes and occasionally neutrophils were seen in submucosa and lamina propria mucosae. BALB/c mice showed the least severe inflammatory changes. H. bizzozeronii differed from the two H. felis strains in producing less striking pathological changes in mice. Of the two H. felis strains, ATCC 49179 produced the more severe inflammatory changes in SJL mice.

Animals↗

Keratin pattern in hyperkeratotic and ulcerated gastric pars oesophagea in pigs.

Ulceration of the gastric pars oesophagea is a serious problem in the pig industry, and in spite of numerous studies the underlying mechanisms of the development of such ulcers remains largely unknown. The present study was designed first to test the hypothesis that the epithelium of the pars oesophagea of affected pigs would be more susceptible to the irritating action of acidic gastric content owing to a change in the pattern of expression of keratin, and second to look for a member of the keratin family that could be a suitable indicator of early lesions. Samples were collected from the gastric pars oesophagea of slaughter pigs with and without grossly visible mucosal changes, and the keratin patterns of normal and hyperkeratotic and ulcerated epithelium were compared immunohistochemically. The keratin pairs K 4/K 13, and K 5/K 14 were present in both normal and affected epithelia, and had a similar pattern of expression in both conditions. K 4 and K 13 were expressed in all the suprabasal layers, and K 5 and K 14 were expressed only in the basal and epibasal cells. Immunological reactivity with the monoclonal antibodies LL020 and LHK6-markers for hyperproliferative conditions-was present in the suprabasal layers of the epithelium of the hyperkeratotic and the ulcerated pars oesophagea but not in the normal epithelium. These results indicate that K 6 is expressed in association with the mucosal changes. The pattern of the intermediate filaments of keratin suggests that in basic to gastric ulcers in pigs there is an epithelial proliferation leading to visible hyperkeratosis.

Animals↗

Oxygen radicals and nitric oxide production by turkey respiratory macrophages.

The influence of different induction protocols on the recovery of elicited turkey respiratory macrophages (RM), and on their oxygenation activity and nitric oxide (NO) production was examined. RM were induced in three week old specific pathogen free turkeys with Sephadex G-50, Thioglycollate broth, and an emulsion of incomplete Freund's adjuvant (IFA), supplemented either with Mycoplasma hyorhinis grown in Modified Channock broth (IFA-M. hyorhinis) or with Modified Channock broth (IFA-Broth). The RM were recovered by lavage of the lungs and air sacs and were purified by centrifugation through a Percoll suspension. Their oxygenation activity was evaluated in luminol-enhanced chemiluminescence assays, following stimulation with Zymosan A. The NO production was evaluated by incubating the RM with lipopolysaccharide (LPS) from Salmonella enteritidis for 24 or 48 hours. The number of recovered RM was slightly, but not significantly lower for Sephadex G-50 and IFA-Broth than for Thioglycollate broth and IFA-M. hyorhinis. RM elicited with Sephadex G-50 and IFA-Broth showed a significantly higher oxidative burst response to Zymosan A, compared to the Thioglycollate and IFA-M. hyorhinis elicited RM. Although all elicited RM showed a high NO production upon stimulation with LPS, no significant differences were seen in the NO production of the RM obtained following the different induction treatments. Our results point out that care should be taken when applying elicited RM for in vitro assays, as distinct levels of oxygenation activity were obtained using different induction protocols.

Animals↗

Uterine oestrogen and progesterone receptor expression in experimental pyometra in the bitch.

Pyometra was induced in five bitches by the intraluminal inoculation of a ligated uterine horn in metoestrus with an Escherichia coli suspension, the other horn serving as an uninoculated control. Histologically, the inoculated horns resembled those with naturally occurring pyometra, while the uninoculated horns had an inactive appearance instead of the normal metoestrus appearance. Immunohistochemically, the expression of sex hormone receptors in the inoculated horns corresponded with that in natural cases of pyometra. In the uninoculated horns, virtually no expression of sex hormone receptors was observed, in contrast to such expression in normal metoestrus. Bacteria-associated ovario-uterine interactions may have been responsible for the hyperplastic (inoculated horn) and inactive (uninoculated horn) uterine changes observed in this experiment.

Animals↗

Interactions of Salmonella enterica subsp. enterica serovar Muenchen with intestinal explants of the turtle Trachemys scripta scripta.

Salmonella infections in reptiles, in contrast to those in birds and mammals, are limited to the intestinal tract. In this study, interactions of a strain of Salmonella enterica subsp. enterica serovar Muenchen (SEEM) with intestinal explants of the turtle Trachemys scripta scripta were examined by scanning electron microscopy (SEM). Adhesion and invasion in the chelonian intestinal explants at 30 degrees C and 37 degrees C were evaluated quantitatively. For purposes of comparison, the invasive capacity of SEEM in the continuous avian epithelial cell line DIV-1 at 30 degrees C and 37 degrees C was determined. Small numbers of M-like cells were found in the ileum of the turtles. The bacteria adhered mainly to the mucus of the intestinal explants. Only small numbers of salmonellae were associated with epithelial cells. Higher numbers of bacteria adhered at 30 degrees C than at 37 degrees C. Epithelial damage, embedding of bacteria in the epithelial surface and a ruffling-like process were noted only at 37 degrees C. Minimal numbers of salmonellae invaded the explants at 30 degrees C and 37 degrees C. Invasion of DIV-1 cells was greater at 37 degrees C than at 30 degrees C. The study suggested that the intestinal mucous layer provides an important site of colonization for salmonellae in the chelonian host and protects the underlying epithelial cells.

Animal Diseases↗

Reovirus serology in broiler parents and their progeny and its correlation with performance.

An intensive vertically integrated monitoring program for broiler breeders and their offspring was set up in a Belgian poultry integration between 1993 and 1997. Serology for anti-reovirus antibodies was performed by enzyme-linked immunosorbent assay on blood samples taken from the broiler parents throughout rearing and production and also on blood samples taken at day-old and at slaughter from the broilers. Furthermore, production parameters of the birds were registered. All data were used two by two in a simple correlation study to calculate the degree to which these variables were linearly correlated. The reovirus antibody pattern indicated frequent field infections breaking through vaccinal immunity in the broiler parents. Under the epidemiologic conditions of this study, high antibody titers in the parents or in the broilers at day-old were significantly correlated with poor feed conversion, increased mortality, increased slaughterhouse condemnation, and low production score in the broilers. These correlations strongly support the view that reovirus infections can be economically important under European conditions of broiler production. Improvement of reovirus vaccines or the vaccination scheme in broiler parents or both may lead to better production results in the broiler offspring.

Animal Husbandry↗