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1.
J Microbiol Methods ; 104: 79-81, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-24978592

RESUMEN

A simple method for preparing agar plates is presented, which allows an efficient transfer of Ureaplasma colonies to nitrocellulose membranes for subsequent immunological detection. This simple and reproducible procedure was used to demonstrate antigenic variation in the phase-variable mba-locus of Ureaplasma parvum serovar 3.


Asunto(s)
Immunoblotting/métodos , Ureaplasma/química , Variación Antigénica , Proteínas Bacterianas/análisis , Proteínas Bacterianas/inmunología , Immunoblotting/instrumentación , Ureaplasma/crecimiento & desarrollo , Ureaplasma/inmunología
2.
FEMS Microbiol Lett ; 292(2): 187-93, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19220471

RESUMEN

Ureaplasma urealyticum and Ureaplasma parvum are commensals and pathogens of the human urogenital tract and of newborn infants. There are four distinct U. parvum serovars and 10 distinct U. urealyticum serovars. Both species possess a distinct immunodominant variable surface protein, the multiple banded antigen (MBA), which shows size variability among isolates as a result of changes in the number of C-terminal repeating units. Adjacent to the MBA gene (UU375) lies UU376, which was annotated as 'Ureaplasma-specific conserved hypothetical gene'. In four different strains of U. parvum serovar 3, we demonstrated expression of UU376 by Western blot analysis and phase variation between UU376, here designated Upvmp376 (Ureaplasma phase-variable membrane protein 376), and MBA after application of selective pressure with hyperimmune antisera directed against either protein. By Southern blot analysis, we found that the switch between MBA and Upvmp376 expression is associated with a DNA inversion event in which the nonrepetitive region of the MBA gene and its putative promoter region are opposed to either the repetitive region of MBA or UU376. We propose that in U. parvum serovar 3, and presumably in all U. parvum and U. urealyticum, an inversion event at specific sites effects an alternate ON/OFF switching of the genes UU375 and UU376.


Asunto(s)
Variación Antigénica , Antígenos Bacterianos/biosíntesis , Proteínas de la Membrana/biosíntesis , Ureaplasma/inmunología , Antígenos Bacterianos/inmunología , Southern Blotting , ADN Bacteriano/química , ADN Bacteriano/genética , Orden Génico , Humanos , Recién Nacido , Proteínas de la Membrana/inmunología , Modelos Biológicos , Datos de Secuencia Molecular , Recombinación Genética , Análisis de Secuencia de ADN , Ureaplasma/fisiología
3.
Expert Opin Drug Deliv ; 3(1): 11-22, 2006 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-16370937

RESUMEN

Although there are powerful drugs against infectious diseases and cancer on the market, delivery systems are needed to decrease serious toxic and noncurative side effects. In order to enhance compliance, several delivery systems such as polymeric micro- and nanoparticles, liposomal systems and erythrocyte ghosts have been developed. Bacterial ghosts representing novel advanced delivery and targeting vehicles suitable for the delivery of hydrophobic or water-soluble drugs, are the main focus of this review. They are useful nonliving carriers, as they can carry different active substances in more than one cellular location separately and simultaneously. Bacterial ghosts combine excellent natural or engineered adhesion properties with versatile carrier functions for drugs, proteins and DNA plasmids or DNA minicircles. The simplicity of both bacterial ghost production and packaging of drugs and/or DNA makes them particularly suitable for the use as a delivery system. Further advantages of bacterial ghost delivery vehicles include high bioavailability and a long shelf life without the need of cold-chain storage due to the possibility to freeze-dry the material.


Asunto(s)
Portadores de Fármacos , Bacterias Gramnegativas , Animales , Bacteriófago phi X 174 , Membrana Celular , ADN/administración & dosificación , Humanos , Preparaciones Farmacéuticas/administración & dosificación , Vacunas/administración & dosificación
4.
Curr Opin Biotechnol ; 15(6): 530-7, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15560979

RESUMEN

Despite the exponential rate of discovery of new antigens and DNA vaccines resulting from modern molecular biology and proteomics, the lack of effective delivery technology is a major limiting factor in their application. The bacterial ghost system represents a platform technology for antigen, nucleic acid and drug delivery. Bacterial ghosts have significant advantages over other engineered biological delivery particles, owing to their intrinsic cellular and tissue tropic abilities, ease of production and the fact that they can be stored and processed without the need for refrigeration. These particles have found both veterinary and medical applications for the vaccination and treatment of tumors and various infectious diseases.


Asunto(s)
Antígenos/administración & dosificación , Bacterias , Sistemas de Liberación de Medicamentos , Ácidos Nucleicos/administración & dosificación , Preparaciones Farmacéuticas/administración & dosificación , Animales , Humanos
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