RESUMEN
Of the eight phylogenetic groups comprising the genus Streptococcus, Lancefield group C and G streptococci (GCS and GGS, resp.) occupy four of them, including the Pyogenic, Anginosus, and Mitis groups, and one Unnamed group so far. These organisms thrive as opportunistic commensals in both humans and animals but may also be associated with clinically serious infections, often resembling those due to their closest genetic relatives, the group A streptoccci (GAS). Advances in molecular genetics, taxonomic approaches and phylogenomic studies have led to the establishment of at least 12 species, several of which being subdivided into subspecies. This review summarizes these advances, citing 264 early and recent references. It focuses on the molecular structure and genetic regulation of clinically important proteins associated with the cell wall, cytoplasmic membrane and extracellular environment. The article also addresses the question of how, based on the current knowledge, basic research and translational medicine might proceed to further advance our understanding of these multifaceted organisms. Particular emphasis in this respect is placed on streptokinase as the protein determining the host specificity of infection and the Rsh-mediated stringent response with its potential for supporting bacterial survival under nutritional stress conditions.
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Filogenia , Streptococcus/clasificación , Streptococcus/genética , Factores de Virulencia/genética , Animales , Antígenos Bacterianos/clasificación , Antígenos Bacterianos/genética , Antígenos de Superficie/clasificación , Proteínas Bacterianas/clasificación , Proteínas Bacterianas/genética , Membrana Celular , Pared Celular , ADN Bacteriano , Exotoxinas/clasificación , Exotoxinas/genética , Genes Bacterianos , Especificidad del Huésped , Humanos , Infecciones Estreptocócicas/microbiología , Streptococcus/patogenicidad , Estreptoquinasa/genética , SimbiosisRESUMEN
BACKGROUND: E.coli ST131 is a globally disseminated clone of multi-drug resistant E. coli responsible for that vast majority of global extra-intestinal E. coli infections. Recent global genomic epidemiological studies have highlighted the highly clonal nature of this group of bacteria, however there appears to be inconsistency in some phenotypes associated with the clone, in particular capsule types as determined by K-antigen testing both biochemically and by PCR. RESULTS: We performed improved quality assemblies on ten ST131 genomes previously sequenced by our group and compared them to a new reference genome sequence JJ1886 to identify the capsule loci across the drug-resistant clone H30Rx. Our data shows considerable genetic diversity within the capsule locus of H30Rx clone strains which is mirrored by classical K antigen testing. The varying capsule locus types appear to be randomly distributed across the H30Rx phylogeny suggesting multiple recombination events at this locus, but that this capsule heterogeneity has little to no effect on virulence associated phenotypes in vitro. CONCLUSIONS: Our data provides a framework for determining the capsular genetics of E. coli ST131 and further beyond to ExPEC strains, and highlights how capsular mosaicism may be an important strategy in becoming a successful globally disseminated human pathogen.
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Escherichia coli/genética , Genoma Bacteriano , Antígenos Bacterianos/clasificación , Antígenos Bacterianos/genética , Antígenos de Superficie/clasificación , Antígenos de Superficie/genética , Cápsulas Bacterianas/genética , Hibridación Genómica Comparativa , Farmacorresistencia Bacteriana/genética , Escherichia coli/clasificación , Escherichia coli/patogenicidad , Sitios Genéticos , Mosaicismo , Fenotipo , Filogenia , Virulencia/genéticaRESUMEN
Group B protective surface protein (BPS) is expressed on the cell surface of some group B streptococcal (GBS) (Streptococcus agalactiae) strains and adds to the identification by capsular polysaccharide (CPS), and c or R proteins. We investigated the prevalence of BPS among GBS clinical isolates (303 invasive, 4122 colonizing) collected over 11 years in four American cities. Hot HCl cell extracts were tested by immunoprecipitation in agarose with rabbit antisera to BPS; the alpha (α) and beta (ß) components of c protein; R1, R3, and R4 species of R protein; and CPS serotypes Ia-VIII. BPS was found in 155 isolates (seven invasive, 148 colonizing). Of these, 87 were Ia, 37 II, 20 V; none were III. BPS was expressed usually with another protein: a species of R by 87 or a component of c by 39. The predominant CPS/protein profiles with BPS were Ia/R1,BPS and II/c(α + ß),BPS. Thus, along with CPS serotype and other surface proteins, BPS can be a valuable marker for precise strain characterization of unique GBS clinical isolates with complex surface protein profiles.
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Antígenos Bacterianos/análisis , Antígenos de Superficie/análisis , Infecciones Estreptocócicas/microbiología , Streptococcus agalactiae/química , Streptococcus agalactiae/aislamiento & purificación , Américas , Antígenos Bacterianos/clasificación , Antígenos de Superficie/clasificación , Portador Sano/microbiología , Ciudades , Humanos , Inmunoprecipitación , Meningitis Bacterianas/microbiología , Sepsis/microbiología , Streptococcus agalactiae/clasificaciónRESUMEN
Stem cells possess multipotent properties that allow them to differentiate into various cells, which may be potentially useful in tissue regeneration. Stem cell populations are reported to be present in various tissues of hematopoietic, neural and mesenchymal lineages, with the presence of stem cell populations in dental pulp tissue first described more than 10 years ago. The main components of dental pulp tissue are dental pulp cells, which are mesenchymal cells derived from the neural crest.(1,2) Some of these cells demonstrate high growth potential and possess multiple differentiation properties, and have been designated dental pulp stem cells (DPSCs). These cell populations are present not only in adult pulp tissue, but also in deciduous tooth pulp and apical papilla. DPSCs isolated by different methods, such as high growth potential, using various surface markers, and high efflux of a fluorescent nuclear stain (Hoechst 33342), all show multipotency, however their surface marker expression is somewhat different from each other. In vivo studies have revealed the possibility use of DPSCs in the regeneration of various tissue. DPSCs are of dental pulp origin, and dental pulp tissue is regenerated from DPSCs. Many researchers have focused on the dentine- and bone-forming properties of DPSCs, but their neuronal and muscular differentiation capacity suggests they may have a wider clinical application.
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Pulpa Dental/citología , Células Madre Hematopoyéticas/citología , Células Madre Mesenquimatosas/citología , Células Madre Pluripotentes/citología , Regeneración/fisiología , Animales , Antígenos de Superficie/clasificación , Antígenos de Superficie/metabolismo , Biomarcadores/metabolismo , Células Madre Hematopoyéticas/metabolismo , Humanos , Células Madre Mesenquimatosas/metabolismo , Ingeniería de TejidosRESUMEN
INTRODUCTION: Lately, several new stem cell sources and their effective isolation have been reported that claim to have potential for therapeutic applications. However, it is not yet clear which type of stem cell sources are most potent and best for targeted therapy. Lack of understanding of nature of these cells and their lineage-specific propensity might hinder their full potential. Therefore, understanding the gene expression profile that indicates their lineage-specific proclivity is fundamental to the development of successful cell-based therapies. METHODS: We compared proliferation rate, gene expression profile, and lineage-specific propensity of stem cells derived from human deciduous (SCD) and permanent teeth (DPSCs) over 5 passages. RESULTS: The proliferation rate of SCD was higher (cell number, 25 x 10(6) cells/mL; percent colony-forming units [CFUs], 151.67 +/- 10.5; percent cells in S/G2 phase, 12.4 +/- 1.48) than that of DPSCs (cell number, 21 x 10(6) cells/mL; percent CFUs, 133 +/- 17.62; percent cells in S/G2 phase, 10.4 +/- 1.18). It was observed that fold expression of several pluripotent markers such as OCT4, SOX2, NANOG, and REX1 were higher (>2) in SCD as compared with DPSCs. However, DPSCs showed higher expression of neuroectodermal markers PAX6, GBX2, and nestin (fold expression >100). Similarly, higher neurosphere formation and neuronal marker expression (NF, GFAP) were found in the differentiated DPSCs into neuron-like cells as compared with SCD. CONCLUSIONS: This study thus demonstrates that both SCD and DPSCs exhibit specific gene expression profile, with clear-cut inclination of DPSCs toward neuronal lineage.
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Diferenciación Celular/fisiología , Linaje de la Célula/fisiología , Pulpa Dental/citología , Células Madre/clasificación , Adulto , Células Madre Adultas/clasificación , Células Madre Adultas/citología , Células Madre Adultas/fisiología , Análisis de Varianza , Antígenos de Superficie/clasificación , Antígenos de Superficie/fisiología , Proliferación Celular , Niño , Preescolar , Dentición Permanente , Perfilación de la Expresión Génica , Humanos , Placa Neural/citología , Placa Neural/fisiología , Células Madre Pluripotentes/citología , Células Madre Pluripotentes/fisiología , Análisis de Componente Principal , ARN/análisis , Células Madre/citología , Células Madre/fisiología , Diente Primario , Adulto JovenRESUMEN
Oral squamous cell carcinoma (OSCC) is common in many Asian countries. The immunopathogenesis of OSCC is unclear. The authors analyzed the lymphocyte subtypes and surface activation markers in healthy Taiwanese people (n=130) and patients with OSCC (n=97)/oral leukoplakia (OL, n=28) using flow cytometry. Univariate analysis found an elevation in the percentage of CD56+ NK cells, CD4+/CD69+ T cells, CD19+/CD69+ B cells and CD56+/CD69+ NK cells in OSCC patients relative to healthy people. The CD19+ and CD19+/CD25+ lymphocyte subtypes decreased in OSCC patients. CD56+ NK cells increased in OL patients. CD56+/CD69+ NK cells were elevated in recurrent and advanced OSCC. Multivariate analysis revealed an increase in CD56+ NK and CD19+/CD69+ cells in OL patients relative to controls. CD19+ B cells declined during progression from OL to OSCC. Betel quid chewing, alcohol, smoking, tumour location and staging showed little effect on lymphocyte subtypes. These results suggest that alterations and activation of NK cells, T and B cells are important and associated with disease status in oral carcinogenesis.
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Antígenos CD/inmunología , Carcinoma de Células Escamosas/inmunología , Leucoplasia Bucal/inmunología , Subgrupos Linfocitarios/citología , Neoplasias de la Boca/inmunología , Adulto , Anciano , Anciano de 80 o más Años , Análisis de Varianza , Antígenos CD/clasificación , Antígenos CD/metabolismo , Antígenos de Superficie/clasificación , Antígenos de Superficie/inmunología , Antígenos de Superficie/metabolismo , Estudios de Casos y Controles , Femenino , Humanos , Modelos Logísticos , Subgrupos Linfocitarios/inmunología , Subgrupos Linfocitarios/metabolismo , Masculino , Persona de Mediana Edad , Lesiones Precancerosas/inmunología , Valores de Referencia , Taiwán , Adulto JovenRESUMEN
Research into late embryogenesis abundant (LEA) proteins has been ongoing for more than 20 years but, although there is a strong association of LEA proteins with abiotic stress tolerance particularly dehydration and cold stress, for most of that time, their function has been entirely obscure. After their initial discovery in plant seeds, three major groups (numbered 1, 2 and 3) of LEA proteins have been described in a range of different plants and plant tissues. Homologues of groups 1 and 3 proteins have also been found in bacteria and in certain invertebrates. In this review, we present some new data, survey the biochemistry, biophysics and bioinformatics of the LEA proteins and highlight several possible functions. These include roles as antioxidants and as membrane and protein stabilisers during water stress, either by direct interaction or by acting as molecular shields. Along with other hydrophilic proteins and compatible solutes, LEA proteins might also serve as "space fillers" to prevent cellular collapse at low water activities. This multifunctional capacity of the LEA proteins is probably attributable in part to their structural plasticity, as they are largely lacking in secondary structure in the fully hydrated state, but can become more folded during water stress and/or through association with membrane surfaces. The challenge now facing researchers investigating these enigmatic proteins is to make sense of the various in vitro defined functions in the living cell: Are the LEA proteins truly multi-talented, or are they still just misunderstood?
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Glicoproteínas de Membrana/fisiología , Proteínas de Plantas/fisiología , Secuencia de Aminoácidos , Animales , Antígenos de Superficie/clasificación , Antígenos de Superficie/fisiología , Proteínas Bacterianas/fisiología , Desecación , Desastres , Invertebrados , Glicoproteínas de Membrana/clasificación , Filogenia , Proteínas de Plantas/clasificación , Semillas/fisiología , Agua/metabolismoRESUMEN
We sequenced the genome of Rickettsia felis, a flea-associated obligate intracellular alpha-proteobacterium causing spotted fever in humans. Besides a circular chromosome of 1,485,148 bp, R. felis exhibits the first putative conjugative plasmid identified among obligate intracellular bacteria. This plasmid is found in a short (39,263 bp) and a long (62,829 bp) form. R. felis contrasts with previously sequenced Rickettsia in terms of many other features, including a number of transposases, several chromosomal toxin-antitoxin genes, many more spoT genes, and a very large number of ankyrin- and tetratricopeptide-motif-containing genes. Host-invasion-related genes for patatin and RickA were found. Several phenotypes predicted from genome analysis were experimentally tested: conjugative pili and mating were observed, as well as beta-lactamase activity, actin-polymerization-driven mobility, and hemolytic properties. Our study demonstrates that complete genome sequencing is the fastest approach to reveal phenotypic characters of recently cultured obligate intracellular bacteria.
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Genoma Bacteriano , Plásmidos/genética , Rickettsia felis/genética , Aclimatación , Antígenos de Superficie/análisis , Antígenos de Superficie/clasificación , Mapeo Cromosómico , ADN Bacteriano/genética , Genes Bacterianos , Genómica , Microscopía Electrónica de Transmisión , Datos de Secuencia Molecular , Sistemas de Lectura Abierta , Fenotipo , Plásmidos/aislamiento & purificación , Rickettsia felis/patogenicidad , Rickettsia felis/ultraestructura , Homología de Secuencia de Ácido NucleicoAsunto(s)
Antígenos de Superficie/inmunología , Interferón gamma/inmunología , Interleucinas/inmunología , Esclerosis Múltiple/inmunología , Factor de Necrosis Tumoral alfa/inmunología , Anticuerpos Antiidiotipos/inmunología , Antígenos de Superficie/clasificación , Apoptosis/inmunología , Autoantígenos/inmunología , Biomarcadores , Regulación hacia Abajo , Humanos , Inmunohistoquímica , Interleucinas/clasificación , Metaloproteinasas de la Matriz/metabolismo , Esclerosis Múltiple/metabolismo , Proteína Básica de Mielina/metabolismo , Óxido Nítrico/metabolismo , Especies Reactivas de Oxígeno/metabolismo , Ácido Úrico/metabolismoRESUMEN
Mucosal leishmaniasis (ML) generally shows progressive tissue destruction, not yet fully elucidated, associated with an intense inflammatory response. To contribute to the understanding of this process and of how treatment interferes with it, we studied several anatomopathological parameters, including those analyzed by immunohistochemistry, such as Leishmania antigens, cells participating in the immune response and cytokine expression. Biopsies were taken from 20 patients with ML before and after treatment. A mixed Th1 and Th2 pattern response occurred inside ML before treatment, persist after treatment. Nevertheless, this mixed response was smaller than in active lesions, with reduced but present numbers of cells expressing TNF-alpha, IFN-gamma and IL-4 and sustained numbers of cells expressing IL-10. We may conclude that specific treatment causes a reduction of inflammatory lesions and disappearance of amastigote forms of Leishmania although the factors related to the pathogenesis of the lesion, such as T CD4+ and T CD8+ lymphocytes and Leishmania antigens, persist in treated lesions. The maintenance of these inflammatory patterns may be due to a specific host-parasite relationship response, strongly indicating the need for continuous surveillance of LM patients at risk of reactivation, despite effective cicatrization after therapy.
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Leishmaniasis Mucocutánea/tratamiento farmacológico , Leishmaniasis Mucocutánea/inmunología , Adulto , Anciano , Animales , Anticuerpos Monoclonales , Antígenos de Superficie/análisis , Antígenos de Superficie/clasificación , Antiprotozoarios/uso terapéutico , Citocinas/análisis , Femenino , Interacciones Huésped-Parásitos , Humanos , Inmunohistoquímica , Inflamación/inmunología , Interferón gamma/análisis , Interleucina-10/análisis , Interleucina-4/análisis , Leishmaniasis Mucocutánea/patología , Masculino , Fenotipo , Resultado del Tratamiento , Factor de Necrosis Tumoral alfa/análisisRESUMEN
Granulocyte (neutrophil) antibodies can cause autoimmune neutropenia, drug-induced neutropenia, immune neutropenia after bone marrow transplantation, neonatal immune neutropenia, refractoriness to granulocyte transfusions as well as febrile and pulmonary transfusion reactions. In the last decade, considerable progress has been made in the characterization of the implicated antigens. In 1998, the Granulocyte Antigen Working Party of the ISBT introduced a new nomenclature for human neutrophil alloantigens (HNA), which is based on the antigens' glycoprotein location. In the HNA nomenclature the immunogenic (glyco-) proteins are indicated by arabic numbers followed by a letter of the alphabet which identify the (glyco-) proteins' polymorphisms, i.e. the specific antigens. Currently, seven HNA antigens are assigned to five systems. The HNA-1a, HNA-lb and HNA-1c antigens, the former NA1, NA2, and SH antigens, have been identified as polymorphic forms of the neutrophil Fc gamma receptor IIIb (CD16b) encoded by three alleles. Recently, we could elucidate the primary structure of the HNA-2a antigen, the former NB1. We could identify the HNA-2a-bearing glycoprotein as a novel member of the Ly-6/uPAR superfamily which has been clustered meanwhile as CD177. The HNA-3a antigen, the former 5b, is located on a 70-95 kDa glycoprotein. However, its molecular basis is still unknown. Finally, the HNA-4a and HNA-5a antigens, the former MART and OND, were found to be caused by single nucleotide mutations in the alphaM (CD11b) and alphaL (CD11a) subunits of the leucocyte adhesion molecules (beta2 integrins). The glycoproteins CD11b, CD16b, and CD177 have been found to be also frequent targets of autoantibodies - approximately 30% of neutrophil autoantibodies are directed against CD16b. Characterization of granulocyte antigens have expanded our diagnostic tools by the introduction of genotyping techniques and immunoassays for antibody identification. In addition, it allowed new insights in the pathophysiology of immune neutropenias and transfusion reactions. Ongoing studies will further improve the prevention and management of granulocyte antibody-mediated diseases.
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Granulocitos/inmunología , Isoantígenos/clasificación , Neutropenia/inmunología , Anticuerpos Anticitoplasma de Neutrófilos , Antígenos de Superficie/clasificación , Antígenos de Superficie/genética , Antígenos de Superficie/inmunología , Humanos , Isoantígenos/genética , Isoantígenos/inmunología , Neutropenia/etiología , Terminología como AsuntoRESUMEN
In this work a typing battery of sera was developed to test lymphocyte antigens in sheep. Eight antigens were detected in a Latxa sheep sample. The serological determination of these antigens is described. As some of the detected antigens segregated in close linkage with class II DRB1 SSCP patterns in two half-sib families, we can conclude that they are coded by genes located in the MHC. Gene frequencies were very similar in Latxa Mutur Gorria and Latxa Mutur Beltza, the two varieties of the Latxa breed. Although few animals were typed in the comparison with other typing sera, it seems that two of our sera clusters detect the same antigens as those detected by other research groups working in other breeds with their own typing batteries.
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Antígenos de Superficie/genética , Antígenos de Superficie/inmunología , Genes MHC Clase II/genética , Linfocitos/inmunología , Ovinos/genética , Ovinos/inmunología , Animales , Antígenos de Superficie/clasificación , Análisis por Conglomerados , Femenino , Amplificación de Genes , Frecuencia de los Genes , Genes MHC Clase II/inmunología , Sueros Inmunes/inmunología , Técnicas de Inmunoadsorción , Masculino , Linaje , Polimorfismo Conformacional Retorcido-Simple , Especificidad de la Especie , Terminología como AsuntoAsunto(s)
Antígenos de Superficie/clasificación , Antígenos de Grupos Sanguíneos/clasificación , Membrana Eritrocítica/inmunología , Isoantígenos/sangre , Sistema del Grupo Sanguíneo Rh-Hr/química , Terminología como Asunto , Sustitución de Aminoácidos , Antígenos de Superficie/genética , Antígenos de Grupos Sanguíneos/genética , Carbohidratos/sangre , Carbohidratos/inmunología , Epítopos/clasificación , Humanos , Sistema del Grupo Sanguíneo Rh-Hr/inmunologíaRESUMEN
This paper presents a review of the Trichinella antigens within the context of species variation. As with other parasites, Trichinella antigens can be classified according to their localisation as surface, excretory/secretory (ES) and somatic components. Surface antigens are mainly constituents of the outer cuticle although secretions from inner parts of the body wall as well as from the oesophagus can temporarily accumulate in the surface. ES antigens come mainly from the excretory granules of the stichosome, whereas somatic constitutive antigens come from the internal parts of the worms. ES products are considered very important from an immunological point of view as they are easily targeted by the immune system, whereas parasite death is required for exposure of somatic products. Some of the antigenic components have been characterised chemically. Phosphorylcholine is an important hapten that modulates the immune responses in Trichinella infections. Glycoproteins are the major components of surface and excretory/secretory products. A 43-kDa glycoprotein has been regarded as a good candidate for diagnosis and vaccination purposes. Recently some glycans have received special attention either as relevant epitopes or as parasite evasion strategies.
Asunto(s)
Antígenos Helmínticos/clasificación , Trichinella/inmunología , Animales , Variación Antigénica , Antígenos de Superficie/clasificación , Peso Molecular , Propiedades de SuperficieRESUMEN
BACKGROUND: Six serotypes of Porphyromonas gingivalis have recently been described. We sought to test the hypothesis that serotype specific carbohydrates from these strains are important antigens that elicit potent immune responses. METHODS: Serum concentrations of IgG reactive with P. gingivalis serotypes K1-K6 were determined for 28 adult (AP) and 28 generalized early-onset (G-EOP) periodontitis patients previously determined to be seropositive for a broken cell preparation of P. gingivalis. To confirm relationships suggested for K1, K2, and K6 in the analysis of initial data, the study population was increased to 133. RESULTS: Frequency of seropositivity for the 6 serotypes ranged from 26 to 54% of subjects. IgG concentrations ranged from 0 to 453 microg/ml with many subjects seropositive to more than one serotype. Concentrations for the subset of patients who was seropositive were high (mean responses ranged from 20 to 105 microg/ml for the 6 serotypes). Significant correlations between seropositivity to serotypes K1 and K5 as well as between K5 and K6 were found. CONCLUSIONS: We examined the relationship of diagnosis, race, gender, smoking, probing depth, attachment loss, and antibody reaction with the P. gingivalis serotypes by analysis of variance. Initial findings suggested potential relationships between diagnosis, smoking, race, gender, and antibody reactive with serotypes K1, K2, and K6. A significant relationship did exist between smoking and decreased antibody reactive with P. gingivalis serotype K2. No other relationships were substantiated. We also examined the IgG subclass distribution and found that responses were almost exclusively IgG2. These data support the concept that antibody responses to all 6 serotypes are common in both AP and G-EOP and that these K serotype carbohydrates elicit potent IgG2 responses.
Asunto(s)
Periodontitis Agresiva/microbiología , Anticuerpos Antibacterianos/inmunología , Periodontitis/microbiología , Porphyromonas gingivalis/clasificación , Adulto , Análisis de Varianza , Antígenos Bacterianos/clasificación , Antígenos Bacterianos/inmunología , Antígenos de Superficie/clasificación , Población Negra , Humanos , Inmunoglobulina G/clasificación , Inmunoglobulina G/inmunología , Persona de Mediana Edad , Pérdida de la Inserción Periodontal/patología , Bolsa Periodontal/patología , Polisacáridos Bacterianos/clasificación , Polisacáridos Bacterianos/inmunología , Porphyromonas gingivalis/inmunología , Serotipificación , Factores Sexuales , Fumar , Población BlancaRESUMEN
The ezrin-radixin-moesin (ERM) homolog EM10 is expressed by the larval stage of the parasite E. multilocularis and shows 46.9% overall identity in the primary structure with human ezrin. To determine whether EM10 has similar activities to ERM proteins, we investigated properties of the protein expressed in mammalian cells. In particular, we transiently expressed haemagglutinin-tagged (HA-tagged) versions of the full-length EM10 as well as the amino- and the carboxy-terminal halves of EM10 in HtTA-1 cells. In addition we stably transfected NIH-3T3 cells with untagged full-length EM10. The data demonstrate that EM10 polypeptides behave like their corresponding portions of radixin when transiently expressed in mammalian cells. The full-length and amino-terminal EM10 polypeptides were localized to cortical structures. Cells expressing the carboxy-terminal polypeptide of EM10 showed long actin-filled protrusions. Cells expressing full-length EM10 showed a reduction in endogenous moesin-staining at cortical structures. In stably transfected NIH-3T3 cells EM10 was not crisply localized but rather was diffuse throughout the cytoplasm. These cells showed a conspicuous loss of stress-fibers, a phenotype that was not seen in analogous experiments with ERM proteins. The results demonstrate both similarities and differences between the functional properties of EM10 and ERM proteins expressed in vertebrate cells.
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Antígenos Helmínticos/metabolismo , Antígenos de Superficie/metabolismo , Proteínas del Citoesqueleto , Echinococcus/metabolismo , Células 3T3 , Actinas/metabolismo , Animales , Antígenos Helmínticos/clasificación , Antígenos Helmínticos/inmunología , Antígenos de Superficie/clasificación , Antígenos de Superficie/inmunología , Proteínas Sanguíneas/metabolismo , Western Blotting , Células Cultivadas , Cartilla de ADN , Células HeLa , Humanos , Proteínas de la Membrana/metabolismo , Ratones , Proteínas de Microfilamentos/inmunología , Proteínas de Microfilamentos/metabolismo , Microscopía Fluorescente , Microvellosidades/metabolismo , Faloidina/metabolismo , Fosfoproteínas/metabolismo , Seudópodos/metabolismo , TransfecciónRESUMEN
The three antigenic variants of the K88 fimbrial adhesin (K88ab, K88ac, and K88ad) of enterotoxigenic Escherichia coli (ETEC) each exhibit unique specificity with regard to their hemagglutination characteristics. The variants are also unique in the specificity of their binding to the brush borders of enterocytes isolated from pigs with different genetic backgrounds. Diversity in enterocyte binding specificity suggests the existence of several K88 receptors, expressed individually or in various combinations on porcine enterocytes. Three candidate receptors have been identified that may explain the adhesion of K88 fimbrial variants to various porcine enterocytes. These receptors are an intestinal mucin-type sialoglycoprotein (IMTGP), an intestinal transferrin (GP74), and an intestinal neutral glycosphingolipid (IGLad). The IMTGP binds K88ab and K88ac, but not K88ad. The GP74 binds K88ab, but not K88ac or K88ad, and the IGLad binds K88ad, but not K88ab or K88ac. Each of the candidate receptors has been found in brush borders that are adhesive for the fimbriae that bind the respective receptor. They have not been found in brush borders that are not adhesive for those same fimbriae. The presence of IMTGP was highly correlated with susceptibility of neonatal gnotobiotic pigs to ETEC expressing K88ab or K88ac.
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Adhesinas de Escherichia coli/metabolismo , Antígenos Bacterianos , Antígenos de Superficie/metabolismo , Proteínas de Escherichia coli , Escherichia coli/metabolismo , Proteínas Fimbrias , Mucosa Intestinal/metabolismo , Receptores de Antígenos/metabolismo , Adhesinas de Escherichia coli/clasificación , Animales , Antígenos de Superficie/clasificación , Escherichia coli/inmunología , Intestinos/microbiología , Fenotipo , PorcinosRESUMEN
Previous reports have described six serotypes based on K antigens in Porphyromonas gingivalis strains. The purpose of the present study was to investigate the prevalence and distribution of these serotypes in 185 patients with P. gingivalis-associated periodontitis. Polyclonal rabbit antisera, raised against each of the different type strains, were used in double-immunodiffusion and immunoelectrophoresis assays. In addition, a subset of 76 strains was investigated for the presence of capsular structures by means of the India ink and Bruce White staining techniques. These strains were also tested for auto-aggregation in phosphate-buffered saline (PBS). All six K serotypes were present in the study sample. In total, 84 (45.4%) patients were colonized with a K-typeable P. gingivalis strain with a predominance of types K5 (12%) and K6 (23.2%). A correlation was found between arbitrary age categories and the prevalence of currently known K serotypes, which were found in 60% of patients aged 12 to 30 years, in 49% of patients aged 31 to 50, and in 25% of patients aged 51 to 70 years. In the subset of 76 P. gingivalis strains, 32 (42.1%) were K-typeable. Fifty-three strains (69.7%) showed microscopic evidence of encapsulation, suggesting the existence of K serotypes other than K1 to K6. Twenty-one strains (27.6%) auto-aggregated in PBS and were not K-typeable, nor did they show any evidence of encapsulation. It was concluded that the majority of clinical P. gingivalis isolates is encapsulated and that encapsulation is associated with the presence of a K antigen. Auto-aggregation seems to be associated with the absence of a capsular structure and, consequently, the absence of a K antigen.
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Cápsulas Bacterianas/aislamiento & purificación , Infecciones por Bacteroidaceae/microbiología , Periodontitis/microbiología , Porphyromonas gingivalis/aislamiento & purificación , Adolescente , Adulto , Anciano , Antígenos Bacterianos/análisis , Antígenos Bacterianos/clasificación , Antígenos de Superficie/análisis , Antígenos de Superficie/clasificación , Cápsulas Bacterianas/clasificación , Cápsulas Bacterianas/inmunología , Infecciones por Bacteroidaceae/epidemiología , Niño , Femenino , Encía/microbiología , Humanos , Inmunodifusión , Inmunoelectroforesis , Masculino , Persona de Mediana Edad , Periodontitis/epidemiología , Porphyromonas gingivalis/clasificación , Porphyromonas gingivalis/inmunología , Prevalencia , Estudios Seroepidemiológicos , SerotipificaciónRESUMEN
The present study was designed to immunolocalize CD44-v6 and -v5 isoforms in normal, dysplastic and malignant oral mucosa as well as in primary and metastatic oral squamous cell carcinomas. Routinely formalin-fixed and paraffin-embedded tissues of 100 oral carcinoma patients were immunohistochemically investigated following wet autoclave antigen retrieval. Both CD44-v6 and -v5 epitopes were uniformly strongly expressed on the cell surface of basal and intermedial epithelial cells of normal and dysplastic mucosa and in all primary and metastatic squamous cell carcinomas with the exception of end-differentiated keratinizing cells. Our results strongly suggest that CD44-v6 and -v5 isoform expression is not altered during development and progression of oral carcinomas. Thus, they seem to be irrelevant factors in the prediction of prognosis in this type of cancer.
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Antígenos de Neoplasias/genética , Carcinoma de Células Escamosas/patología , Receptores de Hialuranos/genética , Neoplasias de la Boca/patología , Antígenos de Neoplasias/clasificación , Antígenos de Superficie/clasificación , Antígenos de Superficie/genética , Carcinoma de Células Escamosas/inmunología , Carcinoma de Células Escamosas/secundario , Diferenciación Celular/genética , Progresión de la Enfermedad , Epitelio/inmunología , Epitelio/patología , Epítopos/clasificación , Epítopos/genética , Femenino , Fijadores , Predicción , Formaldehído , Regulación Neoplásica de la Expresión Génica , Humanos , Receptores de Hialuranos/clasificación , Inmunohistoquímica , Queratinocitos/inmunología , Queratinocitos/patología , Masculino , Persona de Mediana Edad , Mucosa Bucal/inmunología , Mucosa Bucal/patología , Neoplasias de la Boca/inmunología , Adhesión en Parafina , Pronóstico , Fijación del TejidoRESUMEN
Recently van Winkelhoff et al. (1) described 3 novel serotypes in virulent Porphyromonas gingivalis strains, which were based on different polysaccharide antigens. These antigens probably represent capsular structures and have been designated K1, K2 and K3. In the present study we report on 3 novel capsular serotypes, which are represented by P. gingivalis strains ATCC 49417, HG 1690 and HG 1691. The strains, isolated from patients with periodontitis, showed obvious encapsulation in wet India ink preparations. Thermostable antigens could be detected in the supernatant fractions of autoclaved cells. These antigens appeared to be negatively charged, sensitive to periodate degradation, and resistant to proteinase K treatment. On the basis of these characteristics we conclude that the antigens are probably extra-cellular polysaccharides representing a bacterial capsular structure. These K-antigens did not cross-react with K1, K2 or K3 immune-sera of P. gingivalis, with the exception of the K2 antiserum, which partially recognized K5- and K6-antigens. In contrast, K5 and K6 antisera did not react with the K2-antigen. After absorbtion of the K2 antiserum with cells of strains HG 1690 (K5) and HG 1691 (K6) cross-reactivity was no longer present. We propose these novel serotypes to be designated: K4 (ATCC 49417), K5 (HG 1960) and K6 (HG 1691).