Ograniczanie wyników

Czasopisma help
Autorzy help
Lata help
Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 123

Liczba wyników na stronie
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 7 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników

Wyniki wyszukiwania

help Sortuj według:

help Ogranicz wyniki do:
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 7 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
Marek’s disease (MD) is a lymphoproliferative disease of poultry caused by a cell-associated herpesvirus called Marek’s disease virus (MDV). The disease has a significant economic impact on the poultry industry. MD is the first oncogenic disease controlled by vaccination. Live vaccines are administered either to one-day old chicks or to 18-day old embryos. However, although MD vaccines target MDV replication in the cytolic phase and prevent lymphoma development, they do not prevent infection and replication of pathogenic strains of MDV. One of the important problems is an evolution toward greater virulence and the emergence of vvMDV and vv+MDV strains. The development of novel vaccines is necessary. DNA vaccines based on entire viral genomes cloned as bacterial artificial chromosomes (BAC) are considered. The genetic incorporation into recombinant vaccines of genes for immunomodulatory stimuli or vaccines from deletion mutants prepared from virulent MDV strains lacking vIL8 and gene meq are also under consideration.
The study describes construction of five recombinant very virulent (vv) and very virulent plus (vv+) strains lacking meq and viral telomerase (vTR). Deletion of both copies of meq and vTR was achieved by Red E/T recombination in GS1783 E. coli cells. The constructed bacterial artificial chromosome (BAC) clones reconstituted in chicken embryo fibroblasts were examined by immunofluorescence assay to compare the features of recombinant strains with wild-type viruses. The results demonstrated that recombinant BAC strains caused slightly reduced cytophatic effect and decreased level of the fluorescence obtained from the monoclonal antibody in comparison to the parental viruses. Generation of recombinant BAC clones may provide more detailed information on the function of Marek's disease virus oncogenes and the potential use of recombinants for the preparation of the new vaccine against Marek's disease.
DNA microarrays is a method used for the determination of gene expression level, detection of single nucleotide polymorphism (SNP) and quantification of the exact number of viral gene copies per one cell. The technique has a broad application in studies on tumorous diseases of humans and animals. Microarrays are also applied in studies of drug influence on the cell metabolism and the molecular silencing of genes. The main advantage of DNA and protein microarrays is the possibility to analyse a number of complex cellular processes in progress of a tumoral disease during a single run of analysis. In the case of a tumorous disease the microarray technique makes it possible to quickly identify the main genes responsible for the oncogenesis and to determine the type of the disease. In spite of a high costs of microarray production as well as the need to synthesize probes and substrates for specific analyses, microarrays become increasingly popular in numerous research laboratories.
The characteristics of the avian influenza viruses (AIV) have been presented, including their classification, structure and variability mechanisms. Depending on their pathogenicity they were divided into highly pathogenic (HP) and low pathogenic (LP) pathotypes. The definition of avian influenza according to the directive of the European Union was cited, indicating, among others, that HP strains emerge exclusively from H5 and H7 subtypes. The change takes place in poultry and not in wild birds. The outbreak of HPAI H5N1 in South East Asia at the end of 2003, which spread during subsequent years to Asia, Europe and Africa, has put an increased focus on wild, migratory birds that participated each in year seasonal flights. The cited literature indicates that these birds, representing a very large number of species, are carriers of LPAI strains, not being pathogenic for poultry and man. However, if these birds, particularly ducks, survive infection with highly pathogenic avian influenza strains they are able to fly for long distances, while simultaneously being carriers of HPAI H5N1. In such cases they may spread the pathogenic virus intercontinentally. Because of the difficulties in identification of carriership of avian influenza viruses in migrating birds, their role in spreading HPAI H5N1 is not fully clear and needs further investigation. According to the present point of view the probability of causing avian influenza in poultry in connection with migratory birds ranges from low to high with a high degree of uncertainly. The risk of infection of poultry kept in free-range conditions is high with a medium uncertainty of infection and disease.
The aim of the study was to develop RT-PCR and Nested-PCR methods for the detection and identification of the West Nile virus in wild birds. The method was based on West Nile Virus genome non-coding region 3'NCR. All the samples were examined with NRT-PCR and also with a commercial West Nile Virus Kit Prodesse™. There was no positive case of West Nile virus infection in the examined samples. All control samples were positive in both methods. The NRT-PCR method proved to be quick and reliable for the testing of wild birds' tissue samples for WNV.
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 7 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.