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1.
Viruses ; 14(2)2022 01 21.
Artículo en Inglés | MEDLINE | ID: mdl-35215798

RESUMEN

The interaction of phages with abiotic environmental surfaces is usually an understudied field of phage ecology. In this study, we investigated the virucidal potential of different metal salts, metal and ceramic powders doped with Ag and Cu ions, and newly fabricated ceramic and metal surfaces against Phi6 bacteriophage. The new materials were fabricated by spark plasma sintering (SPS) and/or selective laser melting (SLM) techniques and had different surface free energies and infiltration features. We show that inactivation of Phi6 in solutions with Ag and Cu ions can be as effective as inactivation by pH, temperature, or UV. Adding powder to Ag and Cu ion solutions decreased their virucidal effect. The newly fabricated ceramic and metal surfaces showed very good virucidal activity. In particular, 45%TiO2 + 5%Ag + 45%ZrO2 + 5%Cu, in addition to virus adhesion, showed virucidal and infiltration properties. The results indicate that more than 99.99% of viruses deposited on the new ceramic surface were inactivated or irreversibly attached to it.


Asunto(s)
Bacteriófago phi 6/efectos de los fármacos , Cobre/farmacología , Plata/farmacología , Bacteriófago phi 6/crecimiento & desarrollo , Bacteriófago phi 6/fisiología , Cerámica/química , Cobre/química , Concentración de Iones de Hidrógeno , Polvos/química , Plata/química , Propiedades de Superficie , Temperatura
2.
Int J Mol Sci ; 22(24)2021 Dec 14.
Artículo en Inglés | MEDLINE | ID: mdl-34948232

RESUMEN

Low density polyethylene (LDPE) films covered with active coatings containing mixtures of rosemary, raspberry, and pomegranate CO2 extracts were found to be active against selected bacterial strains that may extend the shelf life of food products. The coatings also offer antiviral activity, due to their influence on the activity of Φ6 bacteriophage, selected as a surrogate for SARS-CoV-2 particles. The mixture of these extracts could be incorporated into a polymer matrix to obtain a foil with antibacterial and antiviral properties. The initial goal of this work was to obtain active LDPE films containing a mixture of CO2 extracts of the aforementioned plants, incorporated into an LDPE matrix via an extrusion process. The second aim of this study was to demonstrate the antibacterial properties of the active films against Gram-positive and Gram-negative bacteria, and to determine the antiviral effect of the modified material on Φ6 bacteriophage. In addition, an analysis was made on the influence of the active mixture on the polymer physicochemical features, e.g., mechanical and thermal properties, as well as its color and transparency. The results of this research indicated that the LDPE film containing a mixture of raspberry, rosemary, and pomegranate CO2 extracts incorporated into an LDPE matrix inhibited the growth of Staphylococcus aureus. This film was also found to be active against Bacillus subtilis. This modified film did not inhibit the growth of Escherichia coli and Pseudomonas syringae cells; however, their number decreased significantly. The LDPE active film was also found to be active against Φ6 particles, meaning that the film had antiviral properties. The incorporation of the mixture of CO2 extracts into the polymer matrix affected its mechanical properties. It was observed that parameters describing mechanical properties decreased, although did not affect the transition of LDPE significantly. Additionally, the modified film exhibited barrier properties towards UV radiation. Modified PE/CO2 extracts films could be applied as a functional food packaging material with antibacterial and antiviral properties.


Asunto(s)
Embalaje de Alimentos/métodos , Extractos Vegetales/farmacología , Polietileno/química , Antibacterianos/química , Antibacterianos/farmacología , Antivirales/química , Antivirales/farmacología , Bacteriófago phi 6/efectos de los fármacos , Biopelículas , Quitosano/química , Bacterias Gramnegativas/efectos de los fármacos , Bacterias Grampositivas/efectos de los fármacos , Humanos , Extractos Vegetales/química , Polietileno/farmacología , Polímeros/química , Granada (Fruta) , Rosmarinus/química , Rubus , SARS-CoV-2/efectos de los fármacos
3.
Int J Mol Sci ; 22(23)2021 Nov 24.
Artículo en Inglés | MEDLINE | ID: mdl-34884521

RESUMEN

The Coronavirus Disease (COVID-19) pandemic is demanding the rapid action of the authorities and scientific community in order to find new antimicrobial solutions that could inactivate the pathogen SARS-CoV-2 that causes this disease. Gram-positive bacteria contribute to severe pneumonia associated with COVID-19, and their resistance to antibiotics is exponentially increasing. In this regard, non-woven fabrics are currently used for the fabrication of infection prevention clothing such as face masks, caps, scrubs, shirts, trousers, disposable gowns, overalls, hoods, aprons and shoe covers as protective tools against viral and bacterial infections. However, these non-woven fabrics are made of materials that do not exhibit intrinsic antimicrobial activity. Thus, we have here developed non-woven fabrics with antimicrobial coatings of cranberry extracts capable of inactivating enveloped viruses such as SARS-CoV-2 and the bacteriophage phi 6 (about 99% of viral inactivation in 1 min of viral contact), and two multidrug-resistant bacteria: the methicillin-resistant Staphylococcus aureus and the methicillin-resistant Staphylococcus epidermidis. The morphology, thermal and mechanical properties of the produced filters were characterized by optical and electron microscopy, differential scanning calorimetry, thermogravimetry and dynamic mechanical thermal analysis. The non-toxicity of these advanced technologies was ensured using a Caenorhabditis elegans in vivo model. These results open up a new prevention path using natural and biodegradable compounds for the fabrication of infection prevention clothing in the current COVID-19 pandemic and microbial resistant era.


Asunto(s)
Farmacorresistencia Bacteriana Múltiple/efectos de los fármacos , Extractos Vegetales/farmacología , SARS-CoV-2/efectos de los fármacos , Textiles , Vaccinium macrocarpon/química , Animales , Antibacterianos , Antiinfecciosos , Bacteriófago phi 6/efectos de los fármacos , COVID-19/prevención & control , Caenorhabditis elegans/efectos de los fármacos , Humanos , Staphylococcus aureus Resistente a Meticilina , Staphylococcus aureus/efectos de los fármacos , Staphylococcus epidermidis/efectos de los fármacos
4.
J Phys Chem Lett ; 12(39): 9557-9563, 2021 Oct 07.
Artículo en Inglés | MEDLINE | ID: mdl-34581569

RESUMEN

Lipid-enveloped viruses, such as Ebola, influenza, or coronaviruses, are a major threat to human health. Ethanol is an efficient disinfectant that is widely used to inactivate these viruses and prevent their transmission. However, the interactions between ethanol and enveloped viruses leading to their inactivation are not yet fully understood. This study demonstrates the link between ethanol-induced viral inactivation and the nanostructural and chemical transformations of the model virus Phi6, an 85 nm diameter lipid-enveloped bacterial virus that is commonly used as surrogate for human pathogenic viruses. The virus morphology was investigated using small-angle X-ray scattering and dynamic light scattering and was related to its infectivity. The Phi6's surface chemistry was characterized by cryogenic X-ray photoelectron spectroscopy, and the modifications in protein structure were assessed by circular dichroism and fluorescence spectroscopy. Ethanol-triggered structural modifications were found in the lipid envelope, detaching from the protein capsid and forming coexisting nanostructures.


Asunto(s)
Bacteriófago phi 6/química , Etanol/farmacología , Inactivación de Virus/efectos de los fármacos , Bacteriófago phi 6/efectos de los fármacos , Bacteriófago phi 6/ultraestructura , Proteínas de la Cápside/química , Proteínas de la Cápside/metabolismo , Dicroismo Circular , Dispersión Dinámica de Luz , Etanol/química , Microscopía Electrónica de Transmisión , Espectroscopía de Fotoelectrones , Dispersión del Ángulo Pequeño , Difracción de Rayos X
5.
Int J Mol Sci ; 22(17)2021 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-34502431

RESUMEN

Transparent materials used for facial protection equipment provide protection against microbial infections caused by viruses and bacteria, including multidrug-resistant strains. However, transparent materials used for this type of application are made of materials that do not possess antimicrobial activity. They just avoid direct contact between the person and the biological agent. Therefore, healthy people can become infected through contact of the contaminated material surfaces and this equipment constitute an increasing source of infectious biological waste. Furthermore, infected people can transmit microbial infections easily because the protective equipment do not inactivate the microbial load generated while breathing, sneezing or coughing. In this regard, the goal of this work consisted of fabricating a transparent face shield with intrinsic antimicrobial activity that could provide extra-protection against infectious agents and reduce the generation of infectious waste. Thus, a single-use transparent antimicrobial face shield composed of polyethylene terephthalate and an antimicrobial coating of benzalkonium chloride has been developed for the next generation of facial protective equipment. The antimicrobial coating was analyzed by atomic force microscopy and field emission scanning electron microscopy with elemental analysis. This is the first facial transparent protective material capable of inactivating enveloped viruses such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in less than one minute of contact, and the methicillin-resistant Staphylococcus aureus and Staphylococcus epidermidis. Bacterial infections contribute to severe pneumonia associated with the SARS-CoV-2 infection, and their resistance to antibiotics is increasing. Our extra protective broad-spectrum antimicrobial composite material could also be applied for the fabrication of other facial protective tools such as such as goggles, helmets, plastic masks and space separation screens used for counters or vehicles. This low-cost technology would be very useful to combat the current pandemic and protect health care workers from multidrug-resistant infections in developed and underdeveloped countries.


Asunto(s)
Antiinfecciosos/farmacología , Farmacorresistencia Bacteriana Múltiple/efectos de los fármacos , Equipo de Protección Personal , Antiinfecciosos/química , Bacteriófago phi 6/efectos de los fármacos , Compuestos de Benzalconio/química , Compuestos de Benzalconio/farmacología , COVID-19/patología , COVID-19/virología , Pruebas Antimicrobianas de Difusión por Disco , Humanos , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , Tereftalatos Polietilenos/química , SARS-CoV-2/efectos de los fármacos , SARS-CoV-2/aislamiento & purificación , Staphylococcus epidermidis/efectos de los fármacos
6.
PLoS One ; 12(2): e0172734, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28231311

RESUMEN

To prevent Ebola transmission, frequent handwashing is recommended in Ebola Treatment Units and communities. However, little is known about which handwashing protocol is most efficacious. We evaluated six handwashing protocols (soap and water, alcohol-based hand sanitizer (ABHS), and 0.05% sodium dichloroisocyanurate, high-test hypochlorite, and stabilized and non-stabilized sodium hypochlorite solutions) for 1) efficacy of handwashing on the removal and inactivation of non-pathogenic model organisms and, 2) persistence of organisms in rinse water. Model organisms E. coli and bacteriophage Phi6 were used to evaluate handwashing with and without organic load added to simulate bodily fluids. Hands were inoculated with test organisms, washed, and rinsed using a glove juice method to retrieve remaining organisms. Impact was estimated by comparing the log reduction in organisms after handwashing to the log reduction without handwashing. Rinse water was collected to test for persistence of organisms. Handwashing resulted in a 1.94-3.01 log reduction in E. coli concentration without, and 2.18-3.34 with, soil load; and a 2.44-3.06 log reduction in Phi6 without, and 2.71-3.69 with, soil load. HTH performed most consistently well, with significantly greater log reductions than other handwashing protocols in three models. However, the magnitude of handwashing efficacy differences was small, suggesting protocols are similarly efficacious. Rinse water demonstrated a 0.28-4.77 log reduction in remaining E. coli without, and 0.21-4.49 with, soil load and a 1.26-2.02 log reduction in Phi6 without, and 1.30-2.20 with, soil load. Chlorine resulted in significantly less persistence of E. coli in both conditions and Phi6 without soil load in rinse water (p<0.001). Thus, chlorine-based methods may offer a benefit of reducing persistence in rinse water. We recommend responders use the most practical handwashing method to ensure hand hygiene in Ebola contexts, considering the potential benefit of chlorine-based methods in rinse water persistence.


Asunto(s)
Bacteriófago phi 6/efectos de los fármacos , Cloro , Brotes de Enfermedades/prevención & control , Escherichia coli/efectos de los fármacos , Desinfección de las Manos/métodos , Desinfectantes para las Manos , Jabones , Adolescente , Bacteriófago phi 6/aislamiento & purificación , Escherichia coli/aislamiento & purificación , Femenino , Fiebre Hemorrágica Ebola , Humanos , Masculino , Microbiología del Agua , Adulto Joven
7.
Artículo en Inglés | MEDLINE | ID: mdl-20183493

RESUMEN

Two bacteriophages, phi6 and phi8, were investigated as potential surrogates for H5N1 highly pathogenic avian influenza virus in persistence and chlorine inactivation studies in water. In the persistence studies, phi6 and phi8 remained infectious at least as long as the H5N1 viruses at both 17 and 28 degrees C in fresh water, but results varied in salinated water. The bacteriophage phi6 also exhibited a slightly higher chlorine resistance than that of the H5N1 viruses. Based upon these findings, the bacteriophages may have potential for use as surrogates in persistence and inactivation studies in fresh water.


Asunto(s)
Bacteriófago phi 6/efectos de los fármacos , Cloro/toxicidad , Subtipo H5N1 del Virus de la Influenza A , Inactivación de Virus/efectos de los fármacos , Microbiología del Agua , Bacteriófago phi 6/fisiología , Salinidad , Temperatura
8.
J Cell Biol ; 147(3): 671-82, 1999 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-10545509

RESUMEN

Studies on the virus-cell interactions have proven valuable in elucidating vital cellular processes. Interestingly, certain virus-host membrane interactions found in eukaryotic systems seem also to operate in prokaryotes (Bamford, D.H., M. Romantschuk, and P. J. Somerharju, 1987. EMBO (Eur. Mol. Biol. Organ.) J. 6:1467-1473; Romantschuk, M., V.M. Olkkonen, and D.H. Bamford. 1988. EMBO (Eur. Mol. Biol. Organ.) J. 7:1821-1829). straight phi6 is an enveloped double-stranded RNA virus infecting a gram-negative bacterium. The viral entry is initiated by fusion between the virus membrane and host outer membrane, followed by delivery of the viral nucleocapsid (RNA polymerase complex covered with a protein shell) into the host cytosol via an endocytic-like route. In this study, we analyze the interaction of the nucleocapsid with the host plasma membrane and demonstrate a novel approach for dissecting the early events of the nucleocapsid entry process. The initial binding of the nucleocapsid to the plasma membrane is independent of membrane voltage (DeltaPsi) and the K(+) and H(+) gradients. However, the following internalization is dependent on plasma membrane voltage (DeltaPsi), but does not require a high ATP level or K(+) and H(+) gradients. Moreover, the nucleocapsid shell protein, P8, is the viral component mediating the membrane-nucleocapsid interaction.


Asunto(s)
Bacteriófago phi 6/metabolismo , Membrana Celular/fisiología , Endocitosis , Nucleocápside/metabolismo , Pseudomonas/virología , Adenosina Trifosfato/metabolismo , Adsorción/efectos de los fármacos , Bacteriófago phi 6/efectos de los fármacos , Bacteriófago phi 6/inmunología , Bacteriófago phi 6/ultraestructura , Membrana Celular/efectos de los fármacos , Membrana Celular/ultraestructura , Transporte de Electrón/efectos de los fármacos , Endocitosis/efectos de los fármacos , Concentración de Iones de Hidrógeno , Potenciales de la Membrana/efectos de los fármacos , Microscopía Electrónica , Pruebas de Neutralización , Nucleocápside/efectos de los fármacos , Nucleocápside/inmunología , Nucleocápside/ultraestructura , Potasio/antagonistas & inhibidores , Potasio/metabolismo , Inhibidores de la Bomba de Protones , Bombas de Protones/metabolismo , Fuerza Protón-Motriz/efectos de los fármacos , Pseudomonas/citología , Pseudomonas/metabolismo , Pseudomonas/ultraestructura , Esferoplastos/citología , Esferoplastos/metabolismo , Esferoplastos/ultraestructura , Esferoplastos/virología , Temperatura , Factores de Tiempo , Desacopladores/farmacología , Proteínas Virales/inmunología , Proteínas Virales/metabolismo
9.
J Virol ; 69(5): 2926-31, 1995 May.
Artículo en Inglés | MEDLINE | ID: mdl-7707518

RESUMEN

Bacteriophage phi 6 has a genome of three segments of double-stranded RNA enclosed in a procapsid composed of four different proteins. The preformed procapsid is capable of packaging plus-strand transcripts of the genomic segments in an in vitro reaction. The packaging of the three segments shows a strong order of dependence in that segment S packages alone, but segment M requires S and and segment L requires S and M for efficient packaging. Packaging of individual segments is dependent on unique packaging sequences of about 200 nucleotides near the 5' ends of the segments. Deletions that invade these regions destroy packaging competence for the particular segment and for the dependent segments as well. In the presence of 2 mM phosphate and at magnesium ion concentrations above 4 mM, packaging becomes progressively more independent and ultimately nonspecific with respect to phi 6 sequences.


Asunto(s)
Bacteriófago phi 6/crecimiento & desarrollo , Bacteriófago phi 6/genética , Genoma Viral , Bacteriófago phi 6/efectos de los fármacos , Cápside/genética , ADN Complementario/genética , Escherichia coli/virología , Magnesio/farmacología , Plásmidos/genética , ARN Viral/genética , Mapeo Restrictivo , Eliminación de Secuencia
10.
Antimicrob Agents Chemother ; 39(4): 921-3, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7785996

RESUMEN

This study was designed to evaluate the independent effects of various test methods on the activities of antiviral chemical germicides. The activities of germicides against MS2 and phi 6 bacteriophages in a new porcine tissue carrier model were compared to those obtained by four other methods (suspension, glass carrier, tile carrier, and fingerpad tissue carrier tests). After a 1-min contact followed by neutralization (and elution off the carriers), the residual virus in the treated samples was quantified and the amount was compared with that in the saline controls. Antiviral activity was highly dependent on the test method for both viruses and was always greatest in suspension tests and lowest in tissue carrier tests. Results obtained for hydrophilic MS2 with the porcine tissue carrier were comparable to those from fingerpads, but lipophilic phi 6 was subject to spontaneous inactivation on human skin and proved unsuitable for fingerpad testing. These data indicate that the activities of germicides in tests with nonbiological substrates may overestimate antiviral antiseptic activity on skin surfaces. Products intended for use as antiviral antiseptics or hand-washing agents should be evaluated in a tissue carrier system. The porcine tissue carrier model provides a safe, inexpensive, accurate, and reproducible method for testing the activities of antiseptics.


Asunto(s)
Antiinfecciosos Locales/farmacología , Antivirales/farmacología , Desinfectantes/farmacología , Animales , Bacteriófago phi 6/efectos de los fármacos , Humanos , Levivirus/efectos de los fármacos , Porcinos
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