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  • 1
    Online-Ressource
    Online-Ressource
    Saint Louis :Elsevier Science & Technology,
    Schlagwort(e): Antigens--Genetic aspects. ; Electronic books.
    Materialart: Online-Ressource
    Seiten: 1 online resource (461 pages)
    Ausgabe: 1st ed.
    ISBN: 9780080475882
    DDC: 571.9645
    Sprache: Englisch
    Anmerkung: Intro -- Contents -- Contributors -- Foreword -- Preface -- 1 Mechanisms of Antigenic Variation: an Overview -- Random 'unprogrammed' variation -- Programmed antigenic variation: general principles -- Recombinational mechanisms of antigenic variation -- In situe activation of surface antigen genes by altering the size of simple DNA repeats or by DNA modification -- Gene families controlled without detectable DNA alternations -- As a survival strategy, programmed antigenic variation is not as simple as it looks -- Unsolved problems and challenges -- 2 HIV Variation - a Question of Signal-to-Noise -- The HIV lentiviruses -- Mutation, recombination and fixation rates -- A touch of 'flu -- An inside look at HIV replication -- Tempo of HIV replication -- Gulliver and HIVland -- Rampant recombination -- If not by mutation, how does HIV persist? -- In vivo most viral variation is basically noise -- 3 Calicivirus -- Clinical, antigenic and genetic variability -- Antigenic structure of the capsid -- Virus evolution -- Conclusion -- 4 Influenza - the Chameleon Virus -- X-ray crystallography of influenza haemagglutinin -- Genetic variation of the haemagglutinin -- X-ray crystalography of influenza neuraminidase -- The biological properties of antibody to influenza HA -- Are T cells responses important in the immune response to influen za HA? -- The practical consequences of antigenic change in HA and NA: pandemics and epidemics -- The conflicting theories of the origin of pandemic influenza -- The 1918/19 great pandemic of influenza A and subsequent outbreaks in humans caused by influenza A/swine (H1N1) virus -- The 1957 'Asian' influenza pandemic -- The vanishing pandemic virus -- The 'Hong Kong' virus pandemic and the period 1968-2003 -- A curiosity and a warning: reappearance of a influenza A (H1N1) virus in 1977. , Nucleotide sequence analysis of the influenza HA gene from samples from the great 1918 pandemic -- Could the human infections in Hong Kong in 1997 with avian influenza A viruses warn of a new pandemic? -- Biological factors which drive antigenic drift of HA -- Would influenza vaccine viruses replicated in MDCK cells ratehr than eggs be more immunogenic? -- Conclusions -- 5 Rotavirus -- Virus classification and structure -- Antigens and epidemiological markers -- Pathogensis and immunity -- 6 Haemophilus i nfluenzae -- Capsule phase variation -- Phase variation mediated by simple nucleotide repeats -- Phase variation by modulation of transcription -- Phase variation mediated by tetranucleotide repeats -- Factors influencing the rate of phase variation -- 7 Phase Variation in Helicobacter Pylori l ipopolysaccaride -- H pylori LPS expresses blood group antigens -- Phase variation in H pylori LPS Lewis antigens -- Biological role of LPS phase variation -- Lewis antigen mimicry and immune evasion -- H pylori LPS phase variation and bacterial adhesion -- 8 Genetic Variation in Pathogenic Neisseria Species -- Genetic diversity and evolutionary adaptability of Neisseria species -- Rapid micro-environmental adaptation -- Molecular models for pilE variation -- Genetic variation via the illegitimate route -- Functional significance of genetic variation -- 9 Candida albicans -- The discovery of switching in C albicans -- The white-opaque transition -- The white-opaque transition affects the budding yeast cell morphology -- Antigenic chagnes in the white-opaque transition -- Switching involves differential gene expression -- A contextual framework for investigating the mechamisms of gene regulation during switching -- Phase-specific trans-acting factors -- Possible switching mechanisms -- Gross chromosomal rearrangements are not the basis of switching. , The deacetylases play a role in the suppression of switching -- Heat-induced mass conversion and a model for switching -- The role of C albicans switching in pathogenesis -- Switching in C glabrata -- Phase varation in the fungi: general lessons and summary -- 10 The MSG Gene Family and Antigenic Variation in the Fucus Pneumocystis carinii -- P carinii is one species in a large fungal genus -- P carinii and laboratory rats -- P carinii has a gene family that confers the potential for antigenic variation -- The MSG gene family is expressed in a way that could cause antigenic variation -- Translation and transport of MSG probably involves the UCS -- A protease family appears to have co-evolved with the MSG family -- A third gene family closely related to MSG -- Expression of a specific MSG is correlated with the presence of its cognate gene at the UCS locus -- MSG and antigenic variation -- On the possibility that the MSG gene family does not cause antigenic variation -- Conclusion -- 11 Trypanosome Antigenic Variation - a Heavy Investment in the Evasion of Immunity -- Biology of antigenic variation -- VSG genes and the genome -- DNA recombination as the main driver of antigenic variation -- Transcription control of metacyclic VSGS -- Secondary phenotypes associated with antigenic variation -- Conclusion -- 12 Antigenic Variation in Anaplasma marginale and Ehrlichia (Cowdria) ruminatium -- Phylogentic re-classification of A marginale and C ruminantium -- Disease pathogenesis -- Anaplasma marginale -- Ehrlichia (Cowdria) ruminantium -- Discussion and conclusion -- 13 Antigenic Variation and its Significance to Babesia -- The phenotype of antigenic variation in Babesia bovis -- Probable mechanism of antigenic variation in B bovis -- Association of antigenic variation with pathology -- Future directions. , 14 Antigenic Variation in Plasmodium falciparum and Other Plasmodium Species -- Antigenic variation of infected red blood cells -- Phenotypic/antigenic variation of merozoites -- Antigenic diversity, another way of increasing the repertoire of genes -- Conclusions -- 15 Antigenic Variation in Borrelia: Relapsing Fever and Lyme Borreliosis -- Ecology and epidemiology -- Clinical manifestations and pathology -- Morphology and physiology -- Phylogeny and genetics -- Pathogenesis -- Immunity -- Variable antigens -- Evolution of variable antigens -- Mechanisms of antigenic variation -- 16 Surface Antigenic Variation in Giardia lamblia -- Characteristics of antigenic variation in vitro -- Characteristics of variant-specific surface proteins -- Biology of variant-specific proteins -- Role of immune and biological selection -- Molecular mechanisms -- 17 Free-living and Parasitic Ciliates -- Paramecium variable surface antigens -- I-antigens in the context of infection and immunity -- 18 The Impact of Antigenic Variation on Pathogen Population Structure, Fitness and Dynamics -- Influence of antigenic variation on pathogen fitness -- Inter-strain competition and epidemiological constraints on diversity -- Control of antigenically variable pathogens -- Conclusions -- Appendix: model details -- Index.
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  • 2
    ISSN: 1365-2958
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Biologie , Medizin
    Notizen: The Plasmodium falciparum multigene var family codes for approximately 50 variant adhesive proteins expressed in a mutually exclusive manner at the surface of infected red blood cells (iRBCs). Switching expression of var genes can lead to fundamental changes in the adhesive and antigenic properties of iRBCs. For example, a specific phenotypic switch in adhesion from CD36 to chondroitin sulphate A (CSA) is associated with malaria pathogenesis in pregnant women. The factors and DNA elements that control the expression of a particular member of the var gene family during gestational malaria remains enigmatic. Here, we report that the subtelomeric FCR3 varCSA is expressed under the control of a unique DNA element of 1.8 kb, whereas the other members of the var multigene family are flanked by common regulatory elements. The 5′varCSA-type element is conserved as a single copy in laboratory strains and clinical isolates from Brazil and West Africa and contains two distinct repetitive elements of 150 bp and 60 bp respectively. The 5′varCSA-type sequence tags a var gene in the 3D7 genome that is homologous to the FCR3 varCSA gene. A recombinant DBLγ domain of this var gene showed specific binding to CSA. This subtelomeric varCSA gene is transcribed in the opposite sense when compared with the usual orientation of telomere-adjacent var genes. This unique arrangement might explain why the varCSA gene is relatively conserved in genetically distinct parasites despite being located in a highly recombinogenic chromosome compartment. The 5′ untranslated region (UTR) of the varCSA-type sequence is also transcribed in placental isolates that bind to CSA, illustrating an important role for the unique 5′varCSA-type sequence in the regulation of var genes involved in malaria pathogenesis in pregnant women. However, this promoter is not always found to be transcribing var genes selected for expression of products that bind to CSA in vitro. Our work identifies a sequence tag for the identification of varCSA genes in placental isolates for the first time.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    ISSN: 1365-2958
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Biologie , Medizin
    Notizen: The complications of malaria in pregnancy are caused by the massive sequestration of parasitized erythrocytes (PE) in the placenta. Placental isolates of Plasmodium falciparum are unusual in that they do not bind the primary microvasculature receptor CD36 but instead bind chondroitin sulphate A (CSA). Pregnant mothers develop antibodies that recognize placental variants worldwide, suggesting that a vaccine against malaria in pregnancy is possible. Some members of the Duffy binding-like γ (DBL-γ) domain of the large and diverse P. falciparum erythrocyte membrane protein-1 (PfEMP-1) family, when expressed on Chinese hamster ovary (CHO) cells, bind CSA. To characterize better the molecular requirements for DBL-γ adhesion to CSA, we determined the binding of various DBL-γ domains. Most DBL-γ did not bind CSA, and no conserved region was identified that strictly differentiated binders from non-binders. Structure–function analysis of the FCR3-CSA DBL-γ domain localized the minimal CSA binding region to a 67-residue fragment. This region was partially conserved among some binding sequences. Serum from a rabbit immunized with the minimal domain reacted with CSA-binding parasite lines, but not with non-CSA-adherent PE lines that adhered to CD36 and other receptors. The identification of a minimal binding region from a highly variable cytoadherent family may have application for a vaccine against malaria in pregnancy.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    ISSN: 1365-2958
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Biologie , Medizin
    Notizen: Protection against maternal malaria has been associated with the acquisition of a specific antibody response that prevents adhesion of Plasmodium falciparum-infected erythrocytes to the glycosaminoglycan chondroitin-4-sulphate (CSA), which is present in the placental intervillous space. These antibodies are directed against variant forms of the P. falciparum erythrocyte membrane protein 1 (PfEMP1) that mediate binding to CSA. We have generated insertional disruption mutants of the gene encoding the CSA-binding phenotype in the P. falciparum clone FCR3 (var CSA) to test the hypothesis that strategies targeting the parasite's determinant for this adhesive phenotype may prevent sequestration of infected erythrocytes in the placenta and hence the development of maternal malaria. The var CSA-disruption mutants were initially unable to adhere to CSA; however, they could recover the phenotype after repeated selection over CSA. We show that recovery of CSA binding is var CSA independent and mediated by the activation of a novel var variant. Importantly, the corresponding PfEMP1 protein reacts with a monoclonal antibody recognizing the DBL3γ domain of the var CSA gene product, indicating that the DBL3γ CSA-binding domains are conserved between these PfEMP1-binding variants. Our data support strategies exploring these conserved epitopes as vaccine candidates against maternal malaria.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] Persistent and recurrent infections by Plasmodium falciparum malaria parasites result from the ability of the parasite to undergo antigenic variation and evade host immune attack. P. falciparum parasites generate high levels of variability in gene families that comprise virulence ...
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] Fig. 1 Cloning of genomic DNA from P. falciparum in the expression vector pUK270. The vector pUK270 carries the lacZ and lac Y genes with six unique restriction sites and a frameshift mutation in the promoter proximal part of the lacZ gene. Introduction of DNA inserts into the Pstl site after dG/dC ...
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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