ABSTRACT
Slot-scanning technology is nowadays a valid solution for the follow-up of chronic musculoskeletal disorders on children and adolescent patients, but there is no commercial software designed for simulating this X-ray beam geometry. PC Program for X-ray Monte Carlo (PCXMC) is a widespread Monte Carlo software developed for dose computation in projection radiography. In this study, experimental measurements were performed to evaluate its applicability in examinations with a slit-beam device. Physical phantoms corresponding to an adult and a 5-y-old child with calibrated thermoluminescent dosemeters were used for experiments. Different simulation approaches were investigated. Differences between measured and calculated organ doses ranged from -95 to 67% and were statistically significant for almost all organs. For both patients, PCXMC underestimated the effective dose of about 25%. This study suggests that PCXMC is not suited for organ dose evaluation in examinations with slot-scanning devices. It is still a useful tool for effective dose estimation when a proper correction factor is applied.
Subject(s)
Software , Thermoluminescent Dosimetry , Adult , Child , Adolescent , Humans , Radiation Dosage , Monte Carlo Method , Computer Simulation , Phantoms, Imaging , RadiometrySubject(s)
Antibodies, Bacterial/blood , Chlamydia Infections/veterinary , Chlamydia/immunology , Fluorescent Antibody Technique/veterinary , Neutralization Tests/veterinary , Swine Diseases/immunology , Abortion, Veterinary/microbiology , Animals , Chlamydia/isolation & purification , Chlamydia Infections/immunology , Conjunctivitis, Bacterial/veterinary , Humans , Italy , Swine , Swine Diseases/microbiologyABSTRACT
Feral pigeons (Columba livia domestica), which thrive in most European towns and cities, are commonly infected with the zoonotic bacterium Chlamydophila psittaci, the agent of psittacosis (also known as ornithosis) in humans. A number of surveys carried out over the last thirty years across Europe have detected high seropositivity values and high percentages of infection in feral pigeon populations. Overall, when considering data from 11 European countries, seropositivity values to C. psittaci in the sampled populations ranged from 19.4% to 95.6%. In most surveys, the complement fixation test was used, and antibodies were detected in 19.4-66.3% of the samples, with a median of 46.1%. Indirect immunofluorescence and ELISA tests were employed less frequently, but led to the detection of higher percentages of seropositivity (23.7-67.7% and 35.9-95.6%, respectively). Attempts to grow C. psittaci in cell culture or embryonated chicken eggs were successful in 2-42.3% and 0-57.1% of samples, respectively, antigen detection methods were positive in 2.3-40% of samples, while conventional PCR and real-time PCR using different genomic targets detected the organism in 3.4-50% of samples. Twenty-five C. psittaci isolates from pigeons were typed as ompA genotype B (n=14), E (n=10) and E/B (n=1). The huge increase of feral pigeon populations in Europe is a major cause of concern for the detrimental effect of pigeon droppings on environmental hygiene, in addition to the extensive damage due to the fouling of buildings and monuments. The most important pathogenic organism transmissible from feral pigeons to humans is C. psittaci, with 101 cases of disease reported in the literature. Exposure to C. psittaci-contaminated dust, direct contact with pigeons through handling and, to a lesser extent, through pigeon feeding have been identified as hazardous exposures in more than half of the human cases, while loose or transient contacts with feral pigeons have been mentioned in about 40% of the cases. Education initiatives as to the communication of a health risk resulting from contact with pigeons and pigeon excreta should primarily be targeted at individuals who may be exposed to C. psittaci-contaminated dust, such as demolition/construction workers. Recommendations to this category of workers include wearing protective clothes with hoods, boots, gloves and air filter face masks when removing pigeon faeces from roofs, garrets and buildings, especially if working indoors. Monitoring for C. psittaci infections in these workers over time should also be considered. Children should be warned not to handle sick or dead pigeons, and immunocompromised individuals should be advised to carefully limit their contact to feral pigeons. Culling of pigeons by shooting or poisoning is both unethical and ineffective as the place of the killed birds in the population is quickly filled by new juveniles or immigrating birds from neighbouring areas. Pigeon-deterring systems, such as nets and plastic or metal spikes applied to buildings and monuments will prevent their fouling, and the administration of contraceptive drugs may allow size regulation of the pigeon populations. Nevertheless, the measure that will ultimately lead to permanent reduction and will establish healthy sustainable populations is the restriction of indiscriminate feeding by pigeon lovers. The erection of dovecotes and artificial breeding facilities should be considered for providing shelter and a balanced diet to the birds, as well as a chance of interaction for pigeon lovers in a hygienically controlled environment.
Subject(s)
Bird Diseases/microbiology , Chlamydia Infections/veterinary , Columbidae , Public Health , Animals , Animals, Wild , Bird Diseases/epidemiology , Chlamydia Infections/epidemiology , Europe/epidemiologyABSTRACT
The hard tick Ixodes ricinus (Ixodidae) is the sole animal thus far shown to harbour an intra-mitochondrial bacterium, which has recently been named Midichloria mitochondrii. The objectives of this work were (i) to screen ixodid ticks for Midichloria-related bacteria and (ii) to determine whether these bacteria exploit the intra-mitochondrial niche in other tick species. Our main goal was to discover further models of this peculiar form of symbiosis. We have thus performed a PCR screening for Midichloria-related bacteria in samples of ixodid ticks collected in Italy, North America and Iceland. A total of 7 newly examined species from 5 genera were found positive for bacteria closely related to M. mitochondrii. Samples of the tick species Rhipicephalus bursa, found positive in the PCR screening, were analysed with transmission electron microscopy, which revealed the presence of bacteria both in the cytoplasm and in the mitochondria of the oocytes. There is thus evidence that bacteria invade mitochondria in at least 2 tick species. Phylogenetic analysis on the bacterial 16S rRNA gene sequences generated from positive specimens revealed that the bacteria form a monophyletic group within the order Rickettsiales. The phylogeny of Midichloria symbionts and related bacteria does not appear completely congruent with the phylogeny of the hosts.
Subject(s)
Alphaproteobacteria/isolation & purification , Ixodes/microbiology , Mitochondria/microbiology , Alphaproteobacteria/genetics , Alphaproteobacteria/ultrastructure , Animals , Base Sequence , DNA, Bacterial/genetics , DNA, Mitochondrial/genetics , Microscopy, Electron, Transmission , Phylogeny , Polymerase Chain Reaction , RNA, Ribosomal/genetics , RNA, Ribosomal, 16S/genetics , Sequence Alignment , SymbiosisSubject(s)
Anti-Bacterial Agents/therapeutic use , Chlamydophila psittaci/drug effects , Doxycycline/therapeutic use , Lymphoma, B-Cell, Marginal Zone/drug therapy , Orbital Neoplasms/drug therapy , Psittacosis/drug therapy , Aged , Aged, 80 and over , Chlamydophila psittaci/isolation & purification , Chlamydophila psittaci/pathogenicity , Female , Humans , Lymphoma, B-Cell, Marginal Zone/complications , Lymphoma, B-Cell, Marginal Zone/microbiology , Lymphoma, B-Cell, Marginal Zone/pathology , Male , Middle Aged , Orbital Neoplasms/complications , Orbital Neoplasms/microbiology , Orbital Neoplasms/pathology , Psittacosis/complications , Remission Induction , Subcutaneous TissueSubject(s)
Chlamydia Infections/veterinary , Chlamydia/isolation & purification , Swine Diseases/epidemiology , Animals , Antibodies, Bacterial/analysis , Chlamydia/immunology , Chlamydia Infections/epidemiology , Fluorescence Polarization Immunoassay/veterinary , Italy/epidemiology , Seroepidemiologic Studies , Swine , Swine Diseases/blood , Swine Diseases/etiologySubject(s)
Antibodies, Bacterial/blood , Chlamydophila Infections/veterinary , Chlamydophila/immunology , Complement Fixation Tests/veterinary , Goat Diseases/diagnosis , Sheep Diseases/diagnosis , Animals , Chlamydophila Infections/diagnosis , Complement Fixation Tests/methods , Goat Diseases/microbiology , Goats , Reproducibility of Results , Sensitivity and Specificity , Sheep , Sheep Diseases/microbiologyABSTRACT
In Italy Neospora caninum has been reported in cattle, in buffaloes and in dogs. No data are available about the infection in sheep and goats. In this paper, the authors report the detection of protozoan cysts, identified as N. caninum by PCR, in the brain of an aborted goat foetus.
Subject(s)
Aborted Fetus/parasitology , Abortion, Veterinary/parasitology , Coccidiosis/veterinary , Goat Diseases/parasitology , Neospora/isolation & purification , Animals , Brain/parasitology , Coccidiosis/parasitology , DNA, Protozoan/chemistry , DNA, Protozoan/genetics , Female , Goats , Neospora/genetics , Polymerase Chain Reaction/veterinary , Pregnancy , RNA, Ribosomal, 18S/chemistry , RNA, Ribosomal, 18S/geneticsSubject(s)
Antibodies, Protozoan/blood , Coccidiosis/veterinary , Dog Diseases/epidemiology , Neospora/immunology , Animals , Cattle , Coccidiosis/epidemiology , Coccidiosis/immunology , Cross-Sectional Studies , Dog Diseases/immunology , Dog Diseases/parasitology , Dogs , Food Contamination , Logistic Models , Multivariate Analysis , Risk Factors , Seroepidemiologic Studies , Surveys and QuestionnairesABSTRACT
Two healthy buffaloes (Bubalus bubalis) in a herd which had not been vaccinated against infectious bovine rhinotracheitis (IBR), were selected for their seropositivity for anti-bovine herpesvirus type 1 (BoHV-1) glycoprotein E antibodies, and injected intramuscularly daily with dexamethasone for five consecutive days (day 1 to day 5) to reactivate any latent herpesvirus. Blood samples and nasal and vaginal swabs were collected daily from day 5 to day 15 from each buffalo for virological examination. All the vaginal swabs and blood samples were negative, but 13 of the 22 nasal swabs were positive; a cytopathic effect was observed in primary cultures of bovine fetal lung cells, and the viral isolates were identified as a herpesvirus by PCR. The viral strains were characterised by the sequence analysis of the genes coding for glycoproteins D and B, and the gene sequences were then used for phylogenetic analysis. The isolates from both buffaloes appeared identical at the level of the two genes, and were more closely related to bovine herpesvirus type 5 than to BoHV-1.
Subject(s)
Herpesvirus 1, Bovine/genetics , Herpesvirus 1, Bovine/immunology , Infectious Bovine Rhinotracheitis/immunology , Infectious Bovine Rhinotracheitis/prevention & control , Viral Vaccines/immunology , Amino Acid Sequence , Animals , Antibodies, Viral/analysis , Buffaloes , Cattle , DNA, Viral/analysis , Dexamethasone/pharmacology , Herpesvirus 1, Bovine/isolation & purification , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction/veterinaryABSTRACT
An outbreak of reovirus infection with high mortality in two groups of recently imported psittacine birds is reported. The disease in the two species involved, African grey parrots (Psittacus erithacus erithacus) and Australian king parrots (Alisterus scapularis), had differences in clinical presentation and gross lesions. Reovirus particles were observed by electron microscopy and ultrastructural examination of tissues, and two viruses were isolated in cell culture, one from each bird species. Both isolates were studied by cross-neutralization with antisera against reference avian reoviruses isolated from chickens and parrots, and were found to have the greatest similarity to viruses isolated from a budgerigar and a southern screamer.
ABSTRACT
The small-subunit (SSU) rDNA of the Neospora sp. NC-PV1 strain isolated in Italy from cattle has been sequenced and compared to the other five N. caninum strains SSU rDNA sequences deposited in the data bases. The NC-PV1 strain sequence is identical to three published sequences. Minor differences, respectively four nucleotide bases and one nucleotide base, have been found when comparing the NC-PV1 sequence with two other available sequences of N. caninum. According to these results, the Neospora sp. NC-PV1 strain is assigned to the species N. caninum.
Subject(s)
Neospora/genetics , RNA, Protozoan/genetics , RNA, Ribosomal/genetics , Animals , Cattle , Chlorocebus aethiops , Italy , Neospora/classification , Nucleic Acid Amplification Techniques , Sequence Analysis, DNA/methods , Vero CellsABSTRACT
A fatal pneumonia due to Legionella pneumophila was diagnosed in a young calf reared in a dairy herd located in northern Italy. Clinical symptoms consisted of watery diarrhea, hyperthermia, anorexia, and severe dyspnea. The pathological and histological findings were very similar to those observed in human legionellosis. Legionella pneumophila serogroup 1 (SG1) and SG10 were isolated from the calfs lung, and L. pneumophila SG1 was isolated from the calfs liver. L. pneumophila SG1 was also demonstrated in the lung tissue by immunofluorescence and immunohistochemical examinations. Nine of 10 L. pneumophila SG1 isolates belonged to the Olda subtype, and 1 belonged to the Camperdown subtype. A very low prevalence of antibodies to Legionella was detected in cows and calves reared in the same herd. Cultures of aqueous sediment of an old electric water heater which supplied hot water for the feeding of the calves yielded L. pneumophila SG1. Four of the colonies tested belonged to the Olda subtype. Ten clinical and four environmental isolates were examined for the presence of plasmids. Nine of them were also examined by pulsed-field gel electrophoresis assay, and the same patterns were found for L. pneumophila SG1 Olda strains isolated from the calf and from the electric heater. This is the first report of a documented case of a naturally occurring Legionella pneumonia in an animal. Cattle probably act as accidental hosts for legionellae, much the same as humans.
Subject(s)
Cattle Diseases/microbiology , Legionella pneumophila/isolation & purification , Legionnaires' Disease/veterinary , Animals , Cattle , Cattle Diseases/epidemiology , Cattle Diseases/pathology , DNA, Bacterial/analysis , Electrophoresis, Gel, Pulsed-Field , Equipment Contamination , Fatal Outcome , Fluorescent Antibody Technique, Indirect , Immunohistochemistry , Legionella pneumophila/classification , Legionnaires' Disease/epidemiology , Legionnaires' Disease/microbiology , Legionnaires' Disease/pathology , Liver/microbiology , Lung/microbiology , Lung/pathology , Plasmids/analysis , Water MicrobiologyABSTRACT
The authors describe an outbreak of Pacheco's Parrot Disease (PPD) which occurred in Italy in recently imported psittacine birds and was caused by Psittacid Herpesvirus type 2 (PsiHV2). The authors stress the different susceptibility to the disease in the species involved. This outbreak showed the failure of the vaccine prophylaxis that had been administered to the birds with ordinary commercial preparations containing Psittacid Herpesvirus type 1. The authors emphasize the necessity of producing a vaccine containing inactivated viruses of all known serotypes.
Subject(s)
Bird Diseases/epidemiology , Disease Outbreaks/veterinary , Herpesviridae Infections/veterinary , Herpesviridae/isolation & purification , Psittaciformes , Animals , Antibodies, Viral/analysis , Antibodies, Viral/immunology , Bird Diseases/etiology , Bird Diseases/virology , Herpesviridae/classification , Herpesviridae/immunology , Herpesviridae Infections/epidemiology , Herpesviridae Infections/prevention & control , Italy/epidemiology , Liver/pathology , Liver/virology , Muscle, Skeletal/pathology , Muscle, Skeletal/virology , Spleen/pathology , Spleen/virology , Viral Vaccines/immunology , Viral Vaccines/standards , Viral Vaccines/therapeutic useSubject(s)
Antibiotic Prophylaxis , Bacteria/isolation & purification , Bacterial Translocation , Cefotaxime/therapeutic use , Colon/transplantation , Gentamicins/therapeutic use , Intestinal Mucosa/transplantation , Intestine, Small/transplantation , Transplantation, Homologous , Animals , Bacterial Translocation/drug effects , Colon/microbiology , Female , Immunosuppression Therapy , Intestinal Mucosa/microbiology , Intestine, Small/microbiology , Organ Specificity , Swine , Tacrolimus/therapeutic useABSTRACT
In order to clarify the supposed involvement of urban pigeons (Columba livia livia) in the epidemiology of Lyme disease, the presence of antibodies against Borrelia burgdorferi and Borrelia anserina in pigeons' sera, collected in 12 areas of northern and central Italy, was evaluated. This evaluation was carried out using a classic immunofluorescence assay (IFA), a surface immunofluorescence assay (SIFA) and a standard Western Blot (WB) assay. A total of 104 out of 3,186 (3.26%) serum samples were positive for both spirochetes when tested by IFA, with titres ranging from 1/40 to 1/1280. All positive specimens showed the same or a higher reactivity against B. anserina than against B. burgdorferi. Of the IFA positive samples, 30 were tested by WB and SIFA to evaluate further the specificity of the antibody response, i.e. to try to clarify against which spirochete the antibodies were raised. The presence of antibodies against the 23 kDa protein exclusive to B. anserina, and against epitopes which are not surface-exposed and which are common to B. anserina and B. burgdorferi, was assessed by WB and SIFA. No serological evidence that B. burgdorferi can infect pigeons was found.