RESUMO
Highly pathogenic (HP) avian influenza viruses (AIV) present an ongoing threat to the world poultry industry. In order to develop new AIV control strategies it is necessary to understand the underlying mechanism of viral infection at mucosal respiratory sites. Chicken and duck tracheal epithelial cells systems (TEC) were developed to study early host responses to AIV infection on TEC. Infection of 2 week-old chickens and ducks with the highly pathogenic AIV H5N1 Ck/Hong Kong/220/97 and Egret/Hong Kong/757.2/02 viruses together with TEC early responses to infection suggest the induction of differential innate immune responses. Growth curves indicated that although chicken and ducks TEC supported viral replication and re-infection, the capacity of the two viruses to replicate was not equal. A 42K probes chicken microarray system used to characterize differences in gene expression between chicken tracheal epithelial cells infected with these two highly pathogenic AIV identified expression of virus-specific molecular markers. The existence of dissimilar patterns of host gene expression as early as six hours post infection suggests that the differential growth characteristics of the two highly pathogenic AIV in tracheal epithelial cells is preceded by distinct host responses.
Assuntos
Genes Precoces , Virus da Influenza A Subtipo H5N1/patogenicidade , Traqueia/imunologia , Animais , Galinhas , Patos , Células Epiteliais/imunologia , Células Epiteliais/virologia , Perfilação da Expressão Gênica , Análise de Sequência com Séries de Oligonucleotídeos , Traqueia/virologiaRESUMO
Until recently, most vaccines against avian influenza were based on oil-emulsified inactivated low- or high-pathogenicity viruses. Now, recombinant fowl pox and avian paramyxovirus type 1 vaccines with avian influenza H5 gene inserts (+ or - N1 gene insert) are available and licensed. New technologies might overcome existing limitations to make available vaccines that can be grown in tissue culture systems for more rapid production; provide optimized protection, as a result of closer genetic relations to field viruses; allow mass administration by aerosol, in drinking-water or in ovo; and allow easier strategies for identifying infected birds within vaccinated populations (DIVA). The technologies include avian influenza viruses with partial gene deletions, avian influenza-Newcastle disease virus chimeras, vectored vaccines such as adenoviruses and Marek's disease virus, and subunit vaccines. These new methods should be licensed only after their purity, safety, efficacy and potency against avian influenza viruses have been demonstrated, and, for live vectored vaccines, restriction of viral transmission to unvaccinated birds. Use of vaccines in countries affected by highly pathogenic avian influenza will not only protect poultry but will provide additional safety for consumers. Experimental studies have shown that birds vaccinated against avian influenza have no virus in meat and minimal amounts in eggs after HPAI virus challenge, and that replication and shedding from their respiratory and alimentary tracts is greatly reduced.
Assuntos
Ovos/virologia , Virus da Influenza A Subtipo H5N1/imunologia , Vacinas contra Influenza/efeitos adversos , Influenza Aviária/prevenção & controle , Carne/virologia , Animais , Ovos/normas , Virus da Influenza A Subtipo H5N1/isolamento & purificação , Vacinas contra Influenza/administração & dosagem , Carne/normas , Aves Domésticas , Vacinação/efeitos adversos , Vacinação/normas , Vacinação/veterináriaRESUMO
Vaccines have played an important role in the control of diseases of livestock and poultry, including Transboundary Diseases. In the future, vaccines will play a greater role in controlling these diseases. Historically, inactivated whole viruses in various adjuvant systems have been used and will continue to be used in the near future. For the future, emerging technologies will allow targeted use of only the protective antigens of the pathogen and will provide the opportunity for differentiating between vaccinated and field-exposed animals. Furthermore, the expression of cytokines by vaccines will afford earlier or greater enhancement of protection than can be achieved by the protective response elicited by the antigenic epitopes of the pathogen alone. Avian influenza (AI) is a good case for studying future trends in vaccine design and use. Inactivated AI virus (AIV) vaccines will continue as the primary vaccines used over the next 10 years. These vaccines will use homologous haemagglutinin sub-types, either from the use of field strains or the generation of new strains through the use of infectious clones produced in the laboratory. The latter will allow creation of high growth reassortants, which will provide consistent high yields of antigen and result in potent vaccines. New viral and bacterial vectors with inserts of AIV haemagglutinin gene will be developed and potentially used in the field. Such new vectors will include herpesvirus-turkey, infectious laryngotracheitis virus, adenoviruses, various types of paramyxoviruses and Salmonella sp. In addition, there is a theoretical possibility of gene-deleted mutants that would allow the use of live AIV vaccines, but the application of such vaccines has inherent dangers for gene reassortment with field viruses in the generation of disease-causing strains. Subunit haemagglutinin protein and DNA haemagglutinin gene vaccines are possible, but with current technologies, the cost is prohibitive. In the future, effective AI vaccines must prevent clinical signs and death, increase resistance of the host to infection, decrease the rate of replication and shedding of a challenge or field virus and provide uniform protection following single immunization. Mass application technologies of new virus or bacterial vector systems will provide economic incentives for adoption over current labour-intensive manual individual bird injection methods used with today's AI vaccines.
Assuntos
Controle de Doenças Transmissíveis/métodos , Vacinas contra Influenza/imunologia , Influenza Aviária/prevenção & controle , Vacinação/veterinária , Animais , Biotecnologia , Vírus da Influenza A/genética , Vírus da Influenza A/imunologia , Vírus da Influenza A/patogenicidade , Vacinas contra Influenza/genética , Influenza Aviária/imunologia , Aves Domésticas , Vacinação/métodos , Vacinação/normas , Vacinas de Produtos Inativados/genética , Vacinas de Produtos Inativados/imunologia , Vacinas ViraisRESUMO
Exudative diathesis, a condition caused by a selenium (Se)/vitamin E deficiency, was studied in chicks. Trios of chicks that showed clinical signs of exudative diathesis were matched for severity. One was injected subcutaneously with 0.5 mL distilled water, and the other two received 15 microg of Se in 0.5 mL distilled water. A chick fed a diet with supplemental Se also received 0.5 mL distilled water. Blood was collected from three chicks 2 d after injection, and from the other chick, 6 d after injection. After blood was collected, pectoral muscle and bone marrow were collected. Deficient chicks showed varying degrees of necrosis in pectoral muscle, whereas recovering chicks had extensive fibrosis in pectoral muscle. An analysis of blood showed differences in CO2, glucose, Se, glutathione peroxidase, alanine aminotransferase, aspartate aminotransferase, and creatine kinase. Heterophils and monocytes were increased in deficient chicks; lymphocytes, basophils, and hemoglobin decreased. After 6 d of recovery, all of the changes noted above were correcting toward normal. Eosinophils, in contrast, were unaffected by a deficiency, but increased in recovering chicks. It is hypothesized that cytokines associated with the inflammatory response accentuate the clinical signs of exudative diathesis.
Assuntos
Deficiências Nutricionais/sangue , Fêmur/patologia , Selênio/deficiência , Deficiência de Vitamina E/sangue , Animais , Medula Óssea/patologia , Galinhas , Testes de Química Clínica , Deficiências Nutricionais/patologia , Contagem de Leucócitos , Necrose , Deficiência de Vitamina E/patologiaRESUMO
An immunohistochemistry technique was developed using fixed tissues to study the presence and location of transmissible gastroenteritis virus (TGEV) antigens in situ. Experimentally infected gnotobiotic and conventional pigs as well as pigs with natural TGEV infection were examined. The staining technique was based on detection of the major structural protein of TGEV, the nucleocapsid, by using a pool of 3 monoclonal antibodies. Formalin and periodate-lysine-paraformaldehyde (PLP)-fixed intestinal tissues from a gnotobiotic pig inoculated with virulent TGEV were used to determine optimal antibody concentrations and incubation times. The intestinal tissues remained in their respective fixatives for 6 months, and serial sections were removed at sequential times and embedded in paraffin blocks. PLP and 10% neutral buffered formalin were acceptable fixatives and preserved TGEV nucleocapsid antigenicity for up to 6 months. Formalin, in comparison with PLP as a fixative, was better for preserving original tissue morphology and provided better antigen detection. Conventional crossbred pigs were inoculated with virulent TGEV, and animals were euthanized on various postexposure days. Intestinal tissues were positive for TGEV nucleocapsid antigens on postexposure days 2, 4, and 8. The immunohistochemistry technique detected TGEV antigen in stored paraffin-embedded tissues from 14 naturally infected pigs previously confirmed as positive for TGEV using a direct immunofluorescence assay on intestinal mucosal smears, whereas 9 naturally infected pigs confirmed negative for TGEV antigen by the same immunofluorescence assay showed no staining consistent with the presence of TGEV antigen. Immunohistochemistry provides a method to detect TGEV and possibly other closely related coronaviruses such as porcine respiratory coronavirus in situ. A diagnostic test using the same fixed tissues processed for histopathology provides veterinary practitioners an alternative to delivering live pigs or refrigerated fresh intestinal samples containing infectious virus to a diagnostic laboratory. Investigators can utilize this technique to retrospectively screen fixed tissues for TGEV antigen.
Assuntos
Antígenos Virais/análise , Gastroenterite Suína Transmissível/patologia , Mucosa Intestinal/patologia , Vírus da Gastroenterite Transmissível/isolamento & purificação , Animais , Diarreia/veterinária , Diarreia/virologia , Duodeno/patologia , Duodeno/virologia , Feminino , Técnica Direta de Fluorescência para Anticorpo , Formaldeído , Técnicas Histológicas , Íleo/patologia , Íleo/virologia , Técnicas Imunoenzimáticas , Imuno-Histoquímica/métodos , Mucosa Intestinal/virologia , Jejuno/patologia , Jejuno/virologia , Parafina , SuínosRESUMO
Chicken polyclonal antibodies were prepared against a synthetic peptide corresponding to the first 36 N-terminal amino acids of parathyroid hormone-related protein (PTHrP) by immunizing laying hens. Significant increases of antibodies to PTHrP were first detected after the second immunization. Production of anti-PTHrP egg yolk antibodies peaked 1-2 weeks after the second through sixth immunizations and declined over a period of 2-4 weeks. Polyclonal IgG (IgY) to PTHrP was purified from the egg yolks with high levels of PTHrP specific binding. The anti-PTHrP IgG was used to develop a radioimmunoassay for PTHrP that was able to detect 100 pg PTHrP ml-1 (23 pM) in conditioned cell culture medium. The anti-PTHrP IgG was bound to a solid phase and utilized to immunopurify iodinated [Tyr36]-PTHrP (1-36). Anti-PTHrP IgG inhibited the in vitro biologic activity of PTHrP as demonstrated by the inhibition of adenylate cyclase stimulation in a rat osteoblast-like cell line (ROS 17/2.8). The anti PTHrP IgG was immunopurified and utilized for immunohistochemical localization of PTHrP in canine skin. Chickens were advantageous in producing large amounts of high affinity, neutralizing antibodies to a highly conserved mammalian protein such as PTHrP. The antibodies will be useful to investigate the function and metabolism of PTHrP in vivo and in vitro.
Assuntos
Galinhas/imunologia , Imunoglobulina G/biossíntese , Proteína Relacionada ao Hormônio Paratireóideo , Fragmentos de Peptídeos/imunologia , Proteínas/imunologia , Animais , Linhagem Celular , Células Cultivadas , Cromatografia de Afinidade , Gema de Ovo/imunologia , Técnicas Imunoenzimáticas , Imunoglobulina G/isolamento & purificação , Radioimunoensaio , Pele/químicaRESUMO
Tissue tropism properties of A/chicken/Alabama/75 (H4N8) were examined after intravenous inoculation of 5-week-old specific-pathogen-free chickens. From 14 clinically normal chickens euthanatized on days 1-20 postinoculation, the frequencies of virus recovery were highest for cloacal swabs (86%), bursal swabs (64%), and kidney tissues (64%) and lowest for tracheal swabs (14%), thymus tissues (14%), bone-marrow swabs (7%), and brain tissues (0%). Evidence that the high frequency of virus recovery from kidney tissues was associated with virus replication in the kidney tissues was provided by high virus titers, ranging up to 10(9.5) mean embryo infectious dose per gram of kidney tissue, and by identification of intranuclear and intracytoplasmic type A influenza nucleoprotein in kidney cells using immunohistochemistry. Virus-recovery and virus titer results from three chickens that died on days 4 and 5 postinoculation paralleled the results from the clinically normal chickens. These findings indicate that A/chicken/Alabama/75 has nephrotropic properties similar to nephrotropic properties previously reported for waterfowl-origin type A influenza viruses and provide evidence that kidney lesions could be manifestations of systemic influenza infections in commercial laying chickens.
Assuntos
Galinhas/microbiologia , Vírus da Influenza A/isolamento & purificação , Influenza Aviária/patologia , Rim/microbiologia , Doenças das Aves Domésticas/microbiologia , Proteínas de Ligação a RNA , Animais , Influenza Aviária/microbiologia , Injeções Intravenosas/veterinária , Rim/patologia , Proteínas do Nucleocapsídeo , Nucleoproteínas/análise , Doenças das Aves Domésticas/patologia , Proteínas do Core Viral/análiseRESUMO
Necrotizing typhlocolitis was diagnosed in 13 juvenile common rheas (Rhea americana) from three separate of geographically isolated Ohio flocks, with mortality ranging from 25% to 80%. At postmortem examination, a diphtheritic membrane covered ulcerated cecal mucosa. Histologically, cecal sections showed necrosis and granulomatous-to-suppurative inflammation that extended into the submucosa and often surrounded large eosinophilic colonies of bacteria. Warthin-Starry staining showed these colonies to be composed of entangled spirochetes that invaded the submucosa and frequently were present transmurally. Similar organisms were identified by Warthin-Starry staining in the cecum of a juvenile rhea from a fourth flock that histologically had mild lymphocytic typhlitis. Scanning and transmission electron microscopy demonstrated the presence of a spirochete in the ceca. Anaerobic culture yielded a gram-negative, beta-hemolytic spirochete. Coccidia, histomonads, and Salmonella spp. were consistently absent.
Assuntos
Doenças das Aves/microbiologia , Doenças do Ceco/veterinária , Colite/veterinária , Infecções por Spirochaetales/veterinária , Spirochaetales/isolamento & purificação , Animais , Doenças das Aves/patologia , Aves , Doenças do Ceco/microbiologia , Doenças do Ceco/patologia , Ceco/microbiologia , Ceco/patologia , Colite/microbiologia , Colite/patologia , Colo/microbiologia , Colo/patologia , Feminino , Inflamação , Fígado/patologia , Masculino , Microscopia Eletrônica , Microscopia Eletrônica de Varredura , Necrose , Spirochaetales/ultraestrutura , Infecções por Spirochaetales/microbiologia , Infecções por Spirochaetales/patologia , Baço/patologiaRESUMO
Transmural lymphocytic enteritis was diagnosed in thirteen Nashville warblers (Vermivora ruficapilla) during an epornitic with high mortality. In the intestinal lesions, asexual stages of coccidia were present within lymphocytes and asexual and sexual stages of coccidia were present within intestinal villar epithelium. Ultrastructurally, the infiltrating lymphocytes resembled granular ("intraepithelial") lymphocytes, a cell known to be important in the life cycle of some avian coccidia. Gross and histopathologic features of this enteritis resemble intestinal changes described for Isospora/Atoxoplasma spp. in other passeriformes and lymphoproliferative disease in gold-finches.
Assuntos
Doenças das Aves/etiologia , Coccidiose/veterinária , Enterite/veterinária , Enteropatias Parasitárias/veterinária , Linfócitos/patologia , Animais , Animais de Zoológico , Doenças das Aves/mortalidade , Doenças das Aves/patologia , Aves , Coccídios/ultraestrutura , Coccidiose/complicações , Coccidiose/mortalidade , Coccidiose/patologia , Duodeno/parasitologia , Duodeno/patologia , Duodeno/ultraestrutura , Enterite/etiologia , Enterite/mortalidade , Enterite/patologia , Enteropatias Parasitárias/complicações , Enteropatias Parasitárias/mortalidade , Enteropatias Parasitárias/patologia , Jejuno/parasitologia , Jejuno/patologia , Jejuno/ultraestrutura , Linfócitos/parasitologia , Linfócitos/ultraestrutura , Microscopia EletrônicaRESUMO
Intravenous inoculation of chickens with a waterfowl-origin type A influenza virus resulted in high titers of virus in kidney tissues and viral nucleoprotein in renal tubular epithelial cells and in intestinal mucosal epithelial cells. Virus titers in kidneys of four of eight clinically normal chickens sampled on days 3 and 5 postinoculation (PI), one dead chicken on day 3 PI, and one dead chicken on day 7 PI exceeded 10(6) mean embryo infectious dose per gram of tissue. Using immunofluorescent and immunoperoxidase staining, viral nucleoprotein was identified in the cytoplasm and nucleus of tubular epithelial cells in kidneys and in nucleus of mucosal epithelial cells lining villi in the lower small intestine. Based on the low intravenous pathogenicity index for this virus (0.3) along with the high virus titers in kidney tissues and localization of viral antigen in kidney important site for replication of avian influenza (AI) virus of low pathogenicity. Recovery of type A influenza viruses from cloacal swabs could result from viral replication in kidneys as well as in the lower intestine and/or the bursa of Fabricius.
Assuntos
Galinhas/microbiologia , Vírus da Influenza A/fisiologia , Influenza Aviária/microbiologia , Intestino Delgado/microbiologia , Rim/microbiologia , Animais , Imunofluorescência , Técnicas Imunoenzimáticas , Imuno-Histoquímica , Replicação ViralRESUMO
Ultrastructural findings in a feline ventral abdominal vascular tumour showed lack of basal lamina, few micropinocytotic vesicles and intercellular junctions and a discontinuous endothelial cell layer. A splenic cyst had a continuous basal lamina, numerous micropinocytotic vesicles and intercellular junctions and a continuous endothelial cell layer. These findings were compatible with diagnosis of lymphangiosarcoma (ventral abdomen and metastases) and haemangiosarcoma (splenic cyst).
Assuntos
Doenças do Gato/patologia , Hemangiossarcoma/veterinária , Linfangiossarcoma/veterinária , Animais , Gatos , Hemangiossarcoma/patologia , Hemangiossarcoma/ultraestrutura , Linfangiossarcoma/patologia , Linfangiossarcoma/ultraestrutura , MasculinoRESUMO
The intermediate filament desmin was present in three canine botryoid rhabdomyosarcomas. The use of desmin as a diagnostic tool may, as in these tumours in man, be of value in the classification of canine sarcomas where the origin of the tumour is not always apparent from routine histological sections.
Assuntos
Desmina , Doenças do Cão/diagnóstico , Rabdomiossarcoma/veterinária , Neoplasias da Bexiga Urinária/veterinária , Animais , Cães , Feminino , Imuno-Histoquímica , Masculino , Rabdomiossarcoma/diagnóstico , Rabdomiossarcoma/ultraestrutura , Neoplasias da Bexiga Urinária/diagnóstico , Neoplasias da Bexiga Urinária/ultraestruturaRESUMO
A poorly differentiated cutaneous lymphosarcoma with delayed multicentric anatomical distribution was diagnosed in a dog. The neoplasm had cells with chromosome numbers of 58 or 67 and the former cells lacked the subtelocentric marker chromosome seen in cells of canine transmissible venereal tumour with 58 chromosomes.
Assuntos
Aberrações Cromossômicas , Transtornos Cromossômicos , Doenças do Cão/genética , Linfoma não Hodgkin/veterinária , Neoplasias Cutâneas/veterinária , Animais , Doenças do Cão/patologia , Cães , Feminino , Cariotipagem , Linfoma não Hodgkin/genética , Linfoma não Hodgkin/patologia , Neoplasias Cutâneas/genética , Neoplasias Cutâneas/patologiaRESUMO
An incidental central nervous system tumor was found in a broiler breeder. The cellular mass was histologically similar to the normal pineal gland, but it was characterized by a decreased ratio of follicular/parafollicular cells, a relative increase in mitoses, a size three times greater than a normal pineal gland, and growth and expansion into adjacent cerebellar tissue. These characteristics warranted a diagnosis of pinealoma rather than pineal gland hyperplasia.