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Aim of the study: In view of the frequent occurrence of immunosuppression in pigeons, which is a consequence of viral infections, studies with the use of a synthetic immunomodulator (methisoprinol) were undertaken to evaluate its impact on the course of an experimental infection with PPMV-1. The aim of the study was to determine the usefulness of methisoprinol for the treatment or prophylaxis of viral infections in pigeons. Materials and Methods: Three groups of 5-week-old pigeons, with 15 birds in each, were used in the experiment. Before the experiment, the birds were tested for the presence of antibodies specific to paramyxovirus, and their sensitivity to PPMV-1 infection was evaluated. The virus had been cultured earlier on SPF chicken embryos of 9-12 days. The pigeons from all three groups were infected intravenously with aparamyxovirus suspension (strain APMV-1/ pigeon/Poland/AR3/95 obtained from the Veterinary Institute in Puławy) at a concentration of LD50 10-7 in 0.1 ml at a dose of 0.1 ml/pigeon. The birds in the experimental groups (B1 and B2) were immunomodulated with methisoprinol administered at a dose of 200 mg/1 kg of body weight. The immunomodulator was administered by intramuscular injection for 3 successive days before (group B1) or three successive days after (group B2) the experimental infection. Pigeons in group K (used as a control) were given water by intramuscular injection for 3 days before and 3 days after infection. On days 4, 8, and 12 after infection, 5 birds from each group were euthanized, and sections of internal organs (lung, kidney, brain), as well as cloacal swabs, were collected to detect viral RNA by the RT-PCR method. Results and discussion: Symptoms were recorded from the first day after infection. Neurological symptoms occurred in birds from all groups: in 100% of pigeons from groups B1 and K, and in 80% of pigeons from group B2. Deaths of birds occurred from day 5 after infection in group B1. In the other groups, deaths were observed from day 6 after infection. The total mortality of the infected birds ranged from 70% (group B2) to 100% (groups B1 and K). The resolution of symptoms was observed from day 6 after infection in pigeons from group B2. During molecular examination, it was noted that the highest number of positive samples (presence of PPMV-1) on each day of the investigation was obtained from brain samples and cloacal swabs. The highest number of positive results in kidney samples was obtained from groups B1 and K on day 4 after infection. On the successive days of the investigation the percentage of positive samples increased to 100 in birds from all groups except group B2. Based On the basis of the results of the present study, it can be concluded that methisoprinol, used at a dose of 200 mg/kg of body weight after infection, has antiviral activity, manifested by a slower development of paramyxovirosis in pigeons infected intravenously with PPMV-1. Therefore, the administration of methisoprinol to naturally infected and diseased birds may be useful in the treatment of viral diseases.
The paper describes the immunological response in the matter of percentage of T cells (receptor CD5+) and subpopulations (Th with receptor CD4+, Tc/Ts with receptor CD8+, T with receptor CD25+) and B cells with receptor CD19+, as well as the percentage of apoptotic granulocytes and lymphocytes, in rabbits experimentally infected with the Hagenow strain of the RHD virus. The material chosen for the experiment is special, as among all strains of RHD virus, there are only two strains which carry the variable haemagglutination capacity of red cells. The results of the study show that the Hagenow strain gives an untypical picture of T and B lymphocytes, whereas the results in inducing apoptosis seems to corespond with previous data, confirming the inclusion of apoptosis from 4 h p.i. and the intensity of the phenomenon being higher in granulocytes.
Live Anisakis simplex third-stage larvae (L3) penetrate gastrointestinal mucosa after they are ingested in raw or undercooked seafood, thereafter causing gastrointestinal manifestations and allergic manifestations such as urticaria and anaphylaxis. These allergic reactions are mediated by specific IgE to L3 allergens, especially excretory-secretory (ES) allergens. Recent evidences suggest that only live larvae can cause allergic reactions, although cases attributable to ingestion of cooked, frozen seafood have been reported. Therefore the risk of Anisakis-associated hypersensitivity by ingestion of properly cooked and frozen fish remains controversial. No prior report describes the kinetics of antibody production in experimental animals after oral inoculation with dead L3. This study used ELISA to assess antibody production in rats inoculated orally with dead L3. Positive absorbance value in IgG, IgM, and IgE specific to ES antigen from L3 were found in rats inoculated with live L3 but not with dead L3 (frozen, heated, cut, or homogenized). At one week post re-inoculation with live or frozen L3 to the initially sensitized rats, the absorbance value of the specific IgM and IgE to ES antigen elevated quickly and highly in rats that had been re-inoculated with live L3, but they decreased slightly or did not change in rats inoculated with frozen L3. These results suggest that only ingestion of live L3 can produce the specific antibody and induce initial and secondary sensitizations to L3.
Metacercariae of Diplostomum spp. have been detected in the eyes (lens, humour and under retina) of many species of fish. Adult forms occure in the intestine of piscivorous birds, mostly Laridae. Eight young black-headed gulls, Larus ridibundus (L.) were infected with eye-flukes from the eyes of three-spined stickleback, Gasterosteus aculeatus (L.): five with flukes from the eye-lenses and three from the vitreous humour of eyes. After few days birds were euthanised with an ether overdose and the intestines were studied. In the intestine of experimentally infected birds were found adult stages of Diplostomum sp.
The aim of the study was to determine the influence of Yersinia enterocolitica (Y. enterocolitica) experimental infection on the carrying and shedding states of the microorganism by pregnant sows and on the bacteria occurrence in tissues of the infected animals and aborted or stillborn piglets. Twelve pregnant sows were divided into 4 groups and infected per os on 33 – group I (n=3), 54 – group II (n=3) and 89 – group III (n=3) day of pregnancy with the Y. enterocolitica strain isolated from the palatine tonsil of aborted swine fetus. The control group (n=3) remained uninfected. Rectal, oral and vaginal swabs from sows, placentas and the specimens of tissues from stillborn piglets were collected for bacteriological examination. Eight weeks after delivery, the sows were slaughtered and samples of internal organs were subjected to bacteriological examination. Pregnancy in all groups of sows took a normal course, and no cases of abortion were observed. Y. enterocolitica was isolated from oral, rectal and vaginal swabs of all infected sows. The number of stillborn piglets in the litters was highest in group III, where two macerated fetuses with putrefactive lesions were found. The bacteria were isolated from tissues of stillborn piglets in groups I and III, and only from placenta in group II. In rectal swabs of piglets in all groups, Y. enterocolitica was not isolated. The results of experimental infection of pregnant sows with Y. enterocolitica revealed that in animals infected in the last part of pregnancy, the microorganisms were isolated most frequently from vaginal, rectal and oral swabs of sows as well as from internal organ tissues of stillborn piglets.
Anisakis simplex stage 3 larvae found in herring were used to experimentally infect 155 sticklebacks and 6 nine-spined sticklebacks, caught in the Gdynia marina (Gulf of Gdańsk). The larvae were observed in the fish body cavity as early as 24 h after infection, only the sticklebacks being affected. Altogether, 50 live and 2 dead larvae were found in the stickleback body cavity. The infection prevalence and mean intensity were 13.6% and 2.4 larvae, respectively, from 1 to 8 larvae per fish being recorded. It is concluded that the stickleback may serve as a paratenic host for Anisakis simplex.
Histological studies of the brain, lungs, liver, kidneys, heart, and the spleen were carried out in mice previously infected with 6 pathogenic strains of free-living amoebae of the genus Acanthamoeba. The potential virulence of the strains studied was determined on the basis of re-isolation of the amoebae from the organs of the inoculated animals and by the extent of the histopathological changes inflicted. The most virulent was strain AD16, affecting all organs of the inoculated mice, while the least virulent was strain AD148 re-isolated from the brain of a single mouse. The extent of the changes in the brain depended upon the amoebae strain, while in the remaining organs it also depended upon the duration of the infection.
The aim of the present study was to evaluate the ability of Ornithobacterium rhinotracheale (ORT) to colonize chosen organs of chicks infected intratracheally (group A1), or intravenously (group A2), with the use of bacteriological methods and PCR. The bacteriological methods enabled to reisolate ORT bacteria from trachea and lungs of the birds from group A1 only on day 3 and 6 after infection. The PCR technique additionally detected the bacterial genetic material in these organs on the 9th day after infection, and gave positive results in the samples from air sacs until the 6th day of the experiment. In birds infected intravenously (A2) ORT was reisolated from liver on day 3 and from spleen on day 3 and 6 after infection, whereas the reisolation from the tibiotarsal joint occurred during the entire experimental period. PCR enabled to detect the bacterial DNA in the liver, spleen and lungs of chickens until the 9th day after infection and in case of tibiotarsal joint during the whole time of the study.
The presence of turkey Coronavirus (TCoV) was monitored in meat-type turkey flocks in Poland between 2008 and 2009. Clinical samples (10 individual faecal swabs/flock) from turkeys, aged from 7 d to 19 weeks, from 136 flocks were collected from different regions of the country. TCoV detection was accomplished by molecular techniques. The prevalence of Coronavirus in 7.3% of tested flocks was found. To investigate the virus shedding and its presence in the intestines, liver, kidneys, and bursa of Fabricius of infected SPF turkeys and contact chickens, the quantitative real time reverse transcription-polymerase chain reaction was applied. The presence of virus in turkey swabs from 5 to 14 d post infection and also in intestines and bursa of Fabricius was detected. Surprisingly, contact chickens revealed to be sensitive to TCoV infection.
Serological tests applied in poultry flocks can be a valuable tool in assessing health of hens. One obstacle in making this assessment is that results of serological tests in a given flock are not always correlated with results of bacteriological tests. The aim of this study was to determine dependencies between the level of antibodies in egg yolk and the contamination of egg contents (whites and yolks) with Salmonella Enteritidis bacilli. Infected birds were also treated with selected antibiotics. It was determined that Salmonella Enteritidis was not found in experimentally infected laying hens until day 12 post-inoculation. The results of the study also suggest the existence of relation between the level of anti-Salmonella antibodies in egg yolks and the frequency of isolation of Salmonella from eggs. It was also found that the lowest level of yolk antibodies was found in the group of birds treated with enrofloxacin.
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