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1.
Proc Natl Acad Sci U S A ; 118(28)2021 07 13.
Artículo en Inglés | MEDLINE | ID: mdl-34244425

RESUMEN

Virus infection causes major rearrangements in the subcellular architecture of eukaryotes, but its impact in prokaryotic cells was much less characterized. Here, we show that infection of the bacterium Bacillus subtilis by bacteriophage SPP1 leads to a hijacking of host replication proteins to assemble hybrid viral-bacterial replisomes for SPP1 genome replication. Their biosynthetic activity doubles the cell total DNA content within 15 min. Replisomes operate at several independent locations within a single viral DNA focus positioned asymmetrically in the cell. This large nucleoprotein complex is a self-contained compartment whose boundaries are delimited neither by a membrane nor by a protein cage. Later during infection, SPP1 procapsids localize at the periphery of the viral DNA compartment for genome packaging. The resulting DNA-filled capsids do not remain associated to the DNA transactions compartment. They bind to phage tails to build infectious particles that are stored in warehouse compartments spatially independent from the viral DNA. Free SPP1 structural proteins are recruited to the dynamic phage-induced compartments following an order that recapitulates the viral particle assembly pathway. These findings show that bacteriophages restructure the crowded host cytoplasm to confine at different cellular locations the sequential processes that are essential for their multiplication.


Asunto(s)
Bacillus subtilis/virología , Compartimento Celular , Virosis/patología , Bacillus subtilis/ultraestructura , Bacteriófagos/fisiología , Bacteriófagos/ultraestructura , Cápside/metabolismo , Replicación del ADN , ADN Viral/biosíntesis , ADN Polimerasa Dirigida por ADN , Interacciones Huésped-Patógeno , Complejos Multienzimáticos , Factores de Tiempo , Virión/metabolismo
2.
Viruses ; 10(12)2018 12 11.
Artículo en Inglés | MEDLINE | ID: mdl-30544981

RESUMEN

Bacillus subtilis bacteriophage SPP1 is a lytic siphovirus first described 50 years ago [1]. Its complete DNA sequence was reported in 1997 [2]. Here we present an updated annotation of the 44,016 bp SPP1 genome and its correlation to different steps of the viral multiplication process. Five early polycistronic transcriptional units encode phage DNA replication proteins and lysis functions together with less characterized, mostly non-essential, functions. Late transcription drives synthesis of proteins necessary for SPP1 viral particles assembly and for cell lysis, together with a short set of proteins of unknown function. The extensive genetic, biochemical and structural biology studies on the molecular mechanisms of SPP1 DNA replication and phage particle assembly rendered it a model system for tailed phages research. We propose SPP1 as the reference species for a new SPP1-like viruses genus of the Siphoviridae family.


Asunto(s)
Fagos de Bacillus/genética , Bacillus subtilis/virología , Genoma Viral , Replicación del ADN , ADN Viral/genética , Evolución Molecular , Genes Virales , Transcripción Genética , Ensamble de Virus/genética
3.
Virology ; 495: 79-91, 2016 08.
Artículo en Inglés | MEDLINE | ID: mdl-27179995

RESUMEN

Bacteriophages use most frequently a tail apparatus to create a channel across the entire bacterial cell envelope to transfer the viral genome to the host cell cytoplasm, initiating infection. Characterization of this critical step remains a major challenge due to the difficulty to monitor DNA entry in the bacterium and its requirements. In this work we developed a new method to study phage DNA entry that has the potential to be extended to many tailed phages. Its application to study genome delivery of bacteriophage SPP1 into Bacillus subtilis disclosed a key role of the host cell membrane potential in the DNA entry process. An energized B. subtilis membrane and a millimolar concentration of calcium ions are shown to be major requirements for SPP1 DNA entry following the irreversible binding of phage particles to the receptor YueB.


Asunto(s)
Bacillus subtilis/virología , Bacteriófagos/fisiología , ADN Viral , Técnicas de Transferencia de Gen , Transducción Genética , Bacillus subtilis/metabolismo , Calcio/metabolismo , Genoma Viral , Gramicidina/farmacología , Potenciales de la Membrana , Microscopía Fluorescente , Imagen Molecular , Internalización del Virus/efectos de los fármacos , Desencapsidación Viral
4.
Virology ; 422(2): 425-34, 2012 Jan 20.
Artículo en Inglés | MEDLINE | ID: mdl-22154073

RESUMEN

The mechanism of genome transfer from the virion to the host cytoplasm is critical to understand and control the beginning of viral infection. The initial steps of bacteriophage SPP1 infection of the Gram-positive bacterium Bacillus subtilis were monitored by following changes in permeability of the cytoplasmic membrane (CM). SPP1 leads to a distinctively faster CM depolarization than the one caused by podovirus ϕ29 or myovirus SP01 during B. subtilis infection. Depolarization requires interaction of SPP1 infective virion to its receptor protein YueB. The amplitude of depolarization depends on phage input and concentration of YueB at the cell surface. Sub-millimolar concentrations of Ca(2+) are necessary and sufficient for SPP1 reversible binding to the host envelope and thus to trigger depolarization while DNA delivery to the cytoplasm depends on millimolar concentrations of this divalent cation. A model describing the early events of bacteriophage SPP1 infection is presented.


Asunto(s)
Fagos de Bacillus/fisiología , Bacillus subtilis/virología , Internalización del Virus , Calcio/metabolismo , Cloruro de Calcio , Membrana Celular/fisiología , Genoma Viral , Potenciales de la Membrana , Microscopía Fluorescente , Permeabilidad , Acoplamiento Viral
5.
J Bacteriol ; 193(18): 4893-903, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21705600

RESUMEN

Entry into the host bacterial cell is one of the least understood steps in the life cycle of bacteriophages. The different envelopes of Gram-negative and Gram-positive bacteria, with a fluid outer membrane and exposing a thick peptidoglycan wall to the environment respectively, impose distinct challenges for bacteriophage binding and (re)distribution on the bacterial surface. Here, infection of the Gram-positive rod-shaped bacterium Bacillus subtilis by bacteriophage SPP1 was monitored in space and time. We found that SPP1 reversible adsorption occurs preferentially at the cell poles. This initial binding facilitates irreversible adsorption to the SPP1 phage receptor protein YueB, which is encoded by a putative type VII secretion system gene cluster. YueB was found to concentrate at the cell poles and to display a punctate peripheral distribution along the sidewalls of B. subtilis cells. The kinetics of SPP1 DNA entry and replication were visualized during infection. Most of the infecting phages DNA entered and initiated replication near the cell poles. Altogether, our results reveal that the preferentially polar topology of SPP1 receptors on the surface of the host cell determines the site of phage DNA entry and subsequent replication, which occurs in discrete foci.


Asunto(s)
Fagos de Bacillus/fisiología , Bacillus subtilis/virología , Internalización del Virus , Proteínas Bacterianas/metabolismo , ADN Viral/metabolismo , Unión Proteica , Receptores Virales/metabolismo , Acoplamiento Viral , Replicación Viral
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