ABSTRACT
Autophagy is a highly conserved intracellular degradation and energy-recycling mechanism that contributes to the maintenance of cellular homeostasis. Extensive researches over the past decades have defined the role of autophagy innate immune cells. In this review, we describe the current state of knowledge regarding the role of autophagy in neutrophil biology and a picture of molecular mechanism underlying autophagy in neutrophils. Neutrophils are professional phagocytes that comprise the first line of defense against pathogen. Autophagy machineries are highly conserved in neutrophils. Autophagy is not only involved in generalized function of neutrophils such as differentiation in bone marrow but also plays crucial role effector functions of neutrophils such as granule formation, degranulation, neutrophil extracellular traps release, cytokine production, bactericidal activity and controlling inflammation. This review outlines the current understanding of autophagy in neutrophils and provides insight towards identification of novel therapeutics targeting autophagy in neutrophils.
Subject(s)
Autophagy , Biology , Bone Marrow , Extracellular Traps , Homeostasis , Inflammation , Neutrophils , PhagocytesABSTRACT
ABSTRACT Spathulenol was isolated from an extract of Azorella compacta Phil., Apiaceae, by various chromatographic method; identification of the chemical structure was confirmed by comparing its spectroscopic data with those reported in the literature. The anti-Mycobacterium tuberculosis activity of spathulenol was evaluated on MDR, pre-XDR, and XDR clinical isolates of M. tuberculosis, as well as on the reference susceptible strain H37Rv and its cytotoxic activity was evaluated on the Vero Cell Line. The anti-M. tuberculosis activity of spathulenol was twice as potent against the MDR, pre-XDR, and XDR clinical isolates (6.25 µg/ml) than on the susceptible H37Rv strain (12.5 µg/ml). Additionally, the anti-M. tuberculosis activity shown by spathulenol was established as bactericidal on drug-resistant and susceptible strains of M. tuberculosis. Finally, cytotoxic activity on the Vero cell line (CC50 = 95.7 µg/ml) indicated that spathulenol is a selective anti-M. tuberculosis compound, with a selective index of 15.31 against drug-resistant clinical isolates of M. tuberculosis.
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Infectious diseases are the health disorders that are caused by infection causing organisms which use human body for surviving, reproducing and colonizing. These organisms are known as pathogens. Gradually increasing microbial resistance has made it more complicated. Therefore, everyone wants to explore remedies from natural source. Rasa sindoora is a Kupipakva Rasayana which is very popular and is widely used in therapeutics. In vitro evaluation of its bactericidal activity against the strains of some bacteria those are responsible for disease was carried out in microbiology laboratory, SBLD Ayurved Vishwabharti. Agar well diffusion method and disc diffusion methods was followed to assess the bactericidal activity like bacteria Salmonella Sp., Staphylococcus aureus subsp. aureus, Pseudomonas aeruginosa, and Escherichia coli and the zone of inhibition were calculated. Staphylococcus aureus subsp.aureus and Escherichia coli show maximum zone of inhibition result. All the bacteria were found susceptible against samples of Rasa sindoora with different concentration. When Rasa sindoora concentration will be increasing the gradually microbial concentration will be decreasing. After calculation of minimum inhibitory concentration E.Coli Show Maximum susceptibility against Rasa sindoora on concentration of 0.50 mg/ml and Pseudomonas aeruginosa show minimum inhabitation against Rasa sindoora on concentration of 0.50 mg/ml.
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Objective: To evaluate the bactericidal activity of an antiseptic gel for hygiene and disinfection of the hands by rubbing. Methods: The dilution-neutralization method was used according to Colombian Technical Standard NTC, 2009, 12, 16 in Instituto Colombiano de Normas Técnicas y Certificación (ICONTEC), 5 strains, over 6 different types and with 6 replicas per time were exposed to the antiseptic gel, using Letheen Broth as a neutralizer substance. Results: A 99% of reduction was obtained with Staphylococcus aureus 6538, Enterococos hirae 10541, Pseudomonas aeruginosa 15442 and Klebsiella sp, within the first 30 s of exposure to the gel and within the first 60 s of exposure using the Escherichia coli 19538. All strains used coming from American Type Culture Collection (ATCC). Conclusion: It was confirmed that the product is effective. In presence of a neutralizer substance, the microorganisms were not inhibit, so the growing reduction occurs due to the action of the product.
ABSTRACT
Intrdoduction: in the area of ââhealth, ozone has many therapeutic properties. Several pathologies can be treated with ozone therapy, such as infectious, acute and chronic diseases caused by viruses, bacteria, fungi and parasites, autoimmune diseases, diseases with chronic ischemia, lung diseases, neuropathies, dermatological diseases, dental caries, among others. Objective: to evaluate the effect of ozone applied in vitro in the following strains: Escherichia coli CCCD E003, Salmonella enterica subsp. enterica serovar Typhi CCCD S009, Staphylococcus aureus CCCD S003, Pseudomonas aeruginosa CCCD P013, Streptococcus mutans ATCC 25175 and Enterococcus faecalis ATCC 18211. For this purpose use was made of different cell concentrations and different times of exposure to ozone. Methods: we used concentrations of 1 x 102, 1 x 103, 1 x 10 4, 1 x 105, 1 x 106, 1 x 107, 1 x 108 and 1 x 109 CFU/mL of NaCl (0.5 percent w/v) exposed to ozone for different time intervals (30, 60, 90, 120, 150, 180, 210, 240, 270, 300, 330, 360, 390, 420, 450, 480, 510 and 540 s). Bacterial viability was determined by CFU and the colorimetric method with 2,3,5-Triphenyltetrazolium Chloride. Results: it was found that the species S. aureus, E. coli, S. typhi, S. mutans and E. faecalis were sensitive to ozone, showing a decrease of 45-80 percent of viable cells after 30 s of ozone exposure relative to the initial population, whereas P. aeruginosa was reduced 25 percent compared to the initial population. The viability of bacteria exposed to ozone was dependent on the cell concentration and time exposure. Conclusions: ozone had a bactericidal effect on the bacteria used in this study and that this effect was proportional to the concentration of bacterial cells and the time of exposure to O3. The results show significant efficacy of ozone to control populations of pathogenic bacteria, providing relevant information for its use in different areas, but always taking into account the microorganism involved(AU)
Introducción: el ozono tiene muchas aplicaciones terapéuticas en la esfera de la salud. Algunas patologías pueden tratarse con ozonoterapia, entre ellas enfermedades infecciosas, agudas y crónicas causadas por virus, bacterias, hongos o parásitos, enfermedades autoinmunitarias, enfermedades con isquemia crónica, enfermedades pulmonares, neuropatías, enfermedades dermatológicas y caries dentales, entre otras. Objetivo: evaluar el efecto del ozono aplicado in vitro sobre las siguientes cepas: Escherichia coli CCCD E003, Salmonella enterica subesp. enterica serovar Typhi CCCD S009, Staphylococcus aureus CCCD S003, Pseudomonas aeruginosa CCCD P013, Streptococcus mutans ATCC 25175 y Enterococcus faecalis ATCC 18211. Con este propósito se utilizaron diferentes concentraciones celulares y diferentes tiempos de exposición al ozono. Métodos: utilizamos concentraciones de 1 x 102, 1 x 103, 1 x 104, 1 x 105, 1 x 106, 1 x 107, 1 x 108 y 1 x 109 UFC/mL de NaCl (0,5 por ciento m/v) expuestas a ozono durante diferentes intervalos de tiempo (30, 60, 90, 120, 150, 180, 210, 240, 270, 300, 330, 360, 390, 420, 450, 480, 510 y 540 s). La viabilidad bacteriana se determinó mediante UFC y el método colorimétrico con cloruro de 2,3,5-trifeniltetrazolio. Resultados: se observó que las especies S. aureus, E. coli, S. typhi, S. mutans y E. faecalis eran sensibles al ozono, mostrando una disminución de 45-80 por ciento de las células viables luego de una exposición de 30 s al ozono en comparación con la población inicial, mientras que la especie P. aeruginosa se redujo en un 25 por ciento en comparación con la población inicial. La viabilidad de las bacterias expuestas al ozono dependió tanto de la concentración celular como del tiempo de exposición. Conclusiones: el ozono mostró tener un efecto bactericida sobre las bacterias utilizadas en el estudio, y ese efecto fue proporcional tanto a la concentración de las células bacterianas como al tiempo de exposición al O3. Los resultados demuestran la significativa eficacia del ozono para controlar poblaciones de bacterias patógenas, y ofrecen información relevante con vistas a su uso en diferentes áreas, pero siempre teniendo en cuenta el microorganismo en cuestión(AU)
Subject(s)
Humans , Ozone/therapeutic use , Bacteria/drug effects , In Vitro Techniques/methods , Anti-Bacterial AgentsABSTRACT
Fungal perylenequinones have photodynamic activity and are promising photosensitizers for photodynamic therapy (PDT). Here, we investigated the bactericidal and antitumor activities of phleichrome from the fungal perylenequinone family in vitro. Photodynamic bactericidal activity of phleichrome was analyzed by agar-well diffusion method under dark and illuminated conditions. The photodynamic antitumor activity of phleichrome was analyzed in MCF-7, HeLa, SW480, and HepG2 human cancer cell lines using in vitro cytotoxicity assays. Photodynamic bactericidal activities against Gram-negative and Gram-positive bacteria were species-specific. Antitumor activity against all tumor cell lines increased under the illuminated condition. Depending on the results of the analyses, Phleichrome has potential for further drug development related to its antibacterial and antitumor activities.
Subject(s)
Humans , Cell Line , Cell Line, Tumor , Cladosporium , Diffusion , Fungi , Gram-Positive Bacteria , In Vitro Techniques , Methods , Photochemotherapy , Photosensitizing AgentsABSTRACT
Objective To evaluate the feasibility of using neutrophil bactericidal activity assay for analyzing the anti-bactericidal ability of hypervirulent Klebsiella pneumoniae ( hvKP) strains that harbored the virulence genes of rmpA and rmpA2 and were positive for string test .Methods A total of 150 non-duplicate blood-borne Klebsiella pneumoniae strains were collected from Zhejiang Province from January 2016 to July 2017.PCR was performed to detect carbapenem resistance genes (blaKPC, blaNDM, blaIMP-1, blaIMP-2), cap-sule genotypes (K1, K2, K5, K20, K54 and K57) and virulence genes (rmpA, rmpA2, iucA and iroN). Klebsiella pneumoniae strains that were positive for string test and harbored rmpA and rmpA2 genes were iden-tified as hvKP strains, while classic Klebsiella pneumoniae (cKP) strains were negative for string test, rmpA or rmpA2 gene.Neutrophil bactericidal activity assay was performed to analyze the virulence of Klebsiella pneumoniae strains and the survival rate was determined by using the following equation: the number of colony-forming units ( CFUs) in experimental group divided by the number of CFUs in control group .Re-sults Of the 150 Klebsiella pneumoniae strains, 43.3％ (65/150) harbored the rmpA2 gene and among them, strains positive for genes of rmpA, iroN and blaKPC and K2 respectively accounted for 73.8％, 80.0％, 75.4％and 40.0％.Twenty-four (36.9％) rmpA2 gene-positive strains showed positive result of string test.The survival rates of hvKP and cKP groups were respectively 0.866±0.056 and 0.368±0.058 and the difference between them was statistically significant (P<0.001).Conclusion Most of the hvKP strains that carry rmpA and rmpA2 genes and are positive for string test in Zhejiang Province survive the neu-trophil treatment , which indicates that the neutrophil bactericidal activity assay is an effective and simple method for identifying the virulence of Klebsiella pneumoniae.
ABSTRACT
RESUMO Este trabalho teve por objetivo avaliar o efeito bactericida in vitro de dezesseis óleos essenciais sobre Escherichia coli enterotoxigênica (ETEC). Dentre os óleos essenciais estudados, três foram extraídos in situ por arraste a vapor e treze foram adquiridos comercialmente. Todos os óleos foram analisados por CG-EM e CG-DIC. A atividade bactericida foi avaliada pelo método de microdiluição utilizando-se caldo triptona de soja e microplacas de poliestireno de 96 poços, com posterior plaqueamento das culturas em ágar triptona de soja. Os óleos essenciais de Cinnamomum cassia e de Thymus vulgaris apresentaram concentração mínima bactericida (CMB) de 0,12% e 0,25%, respectivamente. Já os óleos comerciais de Syzygium aromaticum e Origanum vulgare apresentaram ambos CMB de 0,50% e os óleos extraídos in situ de Cymbopogon citratus e Origanum vulgare apresentaram ambos CMB de 1,00%. Os dezesseis óleos essenciais apresentaram composição química qualitativa e quantitativa distintas. As análises químicas dos óleos essenciais de Cinnamomum cassia e de Thymus vulgaris tiveram a presença majoritária de E-cinamaldeído (84,52%) e timol (50,89%). Conclui-se que os óleos de C. cassia e T. vulgaris foram os mais eficazes na inibição do crescimento in vitro dessa bactéria, a qual possui diferentes níveis de sensibilidade dependendo da composição química do óleo.
ABSTRACT This study aimed to evaluate the bactericidal effect in vitro of sixteen essential oils on enterotoxigenic Escherichia coli (ETEC). Among the essential oils, three were extracted in situ by steam distillation and thirteen were purchased commercially. All oils were analyzed by GC-MS and GC-FID. The bactericidal activity was evaluated by the microdilution method using tryptone soy broth, and 96-well polystyrene microplates with subsequent plating of the cultures in tryptone soy agar. Cinnamomum cassia and Thymus vulgaris essential oils showed minimal bactericidal concentration (MBC) 0.12% and 0.25%, respectively. Both commercial oils of Syzygium aromaticum and Origanum vulgare showed MBC of 0.50% and the oils extracted in situ Origanum vulgare and Cymbopogon citratus showed both MBC of 1.00%. The sixteen essential oils pointed out distinct qualitative and quantitative chemical composition. Chemical analysis of Cinnamomum cassia and Thymus vulgaris oils had the predominant presence of E-cinnamaldehyde (84.52% ± 0.07%) and thymol (50.89% ± 0.31%). In conclusion, T. vulgaris and C. cassia oils were the most effective in inhibiting in vitro growth of this bacterium, which has different sensitivity levels depending on the chemical composition of the oil.
Subject(s)
Oils, Volatile/analysis , Chemistry , Enterotoxigenic Escherichia coli/classification , Chromatography, Gas/methods , Cinnamomum zeylanicum , Thymus Plant/classificationABSTRACT
Peroxiredoxin-3 (Prdx3) is a mitochondrial protein of the thioredoxin family of antioxidant peroxidases and is the principal peroxidase responsible for metabolizing mitochondrial hydrogen peroxide. Recent reports have shown that mitochondrial reactive oxygen species (mROS) contribute to macrophage-mediated bactericidal activity in response to Toll-like receptors. Herein, we investigated the functional effect of Prdx3 in bactericidal activity. The mitochondrial localization of Prdx3 in HEK293T cells was confirmed by cell fractionation and confocal microscopy analyses. To investigate the functional role of Prdx3 in bactericidal activity, Prdx3-knockdown (Prdx3(KD)) THP-1 cells were generated. The mROS levels in Prdx3(KD) THP-1 cells were significantly higher than those in control THP-1 cells. Moreover, the mROS levels were markedly increased in response to lipopolysaccharide. Notably, the Salmonella enterica serovar Typhimurium infection assay revealed that the Prdx3(KD) THP-1 cells were significantly resistant to S. Typhimurium infection, as compared with control THP-1 cells. Taken together, these results indicate that Prdx3 is functionally important in bactericidal activity through the regulation of mROS.
Subject(s)
Humans , Cell Fractionation , Hydrogen Peroxide , Lipopolysaccharides , Microscopy, Confocal , Mitochondrial Proteins , Peroxidase , Peroxidases , Reactive Oxygen Species , Salmonella enterica , Serogroup , Thioredoxins , Toll-Like ReceptorsABSTRACT
The intracellular bacteria Piscirickettsia salmonis is the most prevalent pathogen in the Chilean salmon industry, responsible for 50 percent of losses in recent years. So far, there are no effective treatments to control infections by this pathogen due to the emergence of antibiotics resistance. Therefore, it is extremely important to conduct research to find successful antibacterial therapies. In this paper, we evaluated the in vitro bactericidal activity of flavonoids and aromatic geranyl derivatives isolated from the resinous exudate of species Heliotropium filifolium, H. sinuatum y H. huascoense. The results showed that the compounds Filifolinone, Naringenine and 3-O- methylgalangine cause different percentage of mortality of bacteria and therefore they are good candidates to continue its evaluation in vitro and in vivo.
La bacteria intracelular Piscirickettsia salmonis es el patógeno de mayor incidencia en la industria salmonera chilena siendo responsable de un 50 por ciento de las pérdidas en los últimos años. Hasta ahora no hay tratamientos efectivos para este patógeno que permitan controlar las infecciones provocadas por él debido a la aparición de resistencia a antibióticos. Por lo tanto, resulta de gran importancia investigar para encontrar terapias antibacterianas efectivas. En este trabajo nosotros evaluamos la actividad bactericida in vitro de flavonoides y derivados aromáticos geranilados aislados desde el exudado resinoso de las especies vegetales Heliotropium filifolium, H. sinuatum y H. huascoense. Los resultados mostraron que los compuestos Filifolinona, Naringenina y 3-O-metilgalangina provocan diferentes porcentajes de mortalidad de la bacteria y, por lo tanto, son candidatos para seguir siendo evaluados tanto in vitro como in vivo.
Subject(s)
Anti-Bacterial Agents/pharmacology , Heliotropium/chemistry , Piscirickettsia , Plant Extracts/pharmacology , Salmon , Flavonoids/pharmacologyABSTRACT
Snake venom galactoside-binding lectins (SVgalLs) comprise a class of toxins capable of recognizing and interacting with terminal galactoside residues of glycans. In the past 35 years, since the first report on the purification of thrombolectin from Bothrops atrox snake venom, several SVgalLs from Viperidae and Elapidae snake families have been described, as has progressive improvement in the investigation of structural/functional aspects of these lectins. Moreover, the advances of techniques applied in protein-carbohydrate recognition have provided important approaches in order to screen for possible biological targets. The present review describes the efforts over the past 35 years to elucidate SVgalLs, highlighting their structure and carbohydrate recognition function involved in envenomation pathophysiology and potential biomedical applications.(AU)
Subject(s)
Animals , Snake Venoms , Biological Products , Viperidae , Bothrops , Research Report , Lectins , GalactosidesABSTRACT
Snake venom galactoside-binding lectins (SVgalLs) comprise a class of toxins capable of recognizing and interacting with terminal galactoside residues of glycans. In the past 35 years, since the first report on the purification of thrombolectin from Bothrops atrox snake venom, several SVgalLs from Viperidae and Elapidae snake families have been described, as has progressive improvement in the investigation of structural/functional aspects of these lectins. Moreover, the advances of techniques applied in protein-carbohydrate recognition have provided important approaches in order to screen for possible biological targets. The present review describes the efforts over the past 35 years to elucidate SVgalLs, highlighting their structure and carbohydrate recognition function involved in envenomation pathophysiology and potential biomedical applications.
Subject(s)
Animals , Animals, Poisonous , Bothrops , Galactosides , Lectins , Crotalid Venoms/therapeutic useABSTRACT
OBJECTIVE:To study the bactericidal activity of thymopentin and its derived peptides. METHODS:Agar plate count was adopted to determine the bactericidal activity of thymopentin [arginine(R)-lysine(K)-aspartic acid(D)-valine(V)-tyro-sine(Y),RKDVY],its derived peptide 1 [RKN(agedoite,N)VY] and derived peptide 2(RKKVY)to Gram negative bacterial (Proteusbacillus vulgaris,Escherichia coli) and Gram positive bacterial (Staphylococcus aureus,Enterococcus faecium). There were 15.625-1 000 μg/ml for peptides,102 CFU for bacteria. RESULTS:Three pentapeptides possessed bactericidal activity against Gram negative bacteria. The activities of RKKVY and RKNVY were stronger than RKDVY(P0.05). They also possessed bactericidal activity against Gram positive bacteria,and the activity from strong to weak was RKKVY>RKNVY>RKDVY(P<0.01). CONCLUSIONS:Thymopentin and its derived peptides possess bactericidal activity against Gram negative and positive bacteria,with dose-effect relationship.
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Resumen El mercurio es un contaminante xenobiótico encontrado frecuentemente en ecosistemas naturales, representando un aspecto relevante en salud pública y ambiental debido a los niveles encontrados en fuentes de agua en correlación con la bioacumulación en organismos vivos. El objetivo fue evaluar los efectos inmunotoxicológicos e histopatológicos de la exposición a concentraciones subletales de Cloruro de Mercurio (HgCl2) en cachama blanca (Piaractus brachypomus). Se utilizaron alevinos de cachama blanca, con un peso de 10 ± 2,1 g, distribuidos en acuarios con aireación constante, sin filtro. El periodo experimental fue de 18 días, utilizando 4 concentraciones basadas en la décima parte de la CL50 descrita para cachama, así como un grupo control. Se realizaron seis muestreos (días 1, 2, 4, 7, 12 y 18) en los cuales se tomaron muestras de sangre para la evaluación de la explosión respiratoria y la capacidad bactericida del plasma. Se calculó el índice hepatosomático y se tomaron muestras para procesamiento histopatológico. Se evidenció una elevación del nivel de explosión respiratoria (estrés oxidativo) en animales expuestos a HgCl2 de una manera dependiente de la concentración, siendo más marcado este efecto al día 12 de exposición. No se encontraron diferencias significativas en los valores de índice hepatosomático (IHS). En la actividad bactericida del plasma se halló una actividad menor en animales expuestos a HgCl2. En el análisis histopatológico se encontraron cambios como hiperplasia, aneurismas y sinequias en branquias; inclusiones hialinas en hígado y centros melanomacrófagos en riñón. Los alevinos de cachama blanca expuestos a dosis subletales de HgCl2, muestran un incremento significativo en la explosión respiratoria (estrés oxidativo), así como cambios en la actividad bactericida del plasma, además de cambios anatomopatológicos a nivel branquial, hepático y renal.
Mercury is a xenobiotic contaminant often found in natural ecosystems. It is relevant for public and environmental health because of the existing correlation between its content in water sources and mercury bioaccumulation in living organisms. This work assessed the immune and histopathological effects of exposure to sublethal concentrations of mercury chloride (HgCl2) in Pacu (Piaractus brachypomus). Pacu fingerlings weighing 10 ± 2.1 g were distributed in constantly aerated tanks with no filter. The experimental period was 18 days. A negative control group and four Hg levels were used based on the tenth of LC50 for Pacu. Six blood samples were taken on days 1, 2, 4, 7, 12 and 18 to measure respiratory burst and bactericidal activity of the plasma. The hepatosomatic index was calculated and samples were taken for histopathological examination. Increased respiratory burst (oxidative stress) was observed in animals exposed to HgCl2 in a concentration-dependent manner. This effect was more pronounced at day 12 of exposure. Hepatosomatic index (HSI) values showed no significant differences. Animals exposed to HgCl2 showed low bactericidal activity of plasma. Histopathological changes such as hyperplasia, aneurysms and synechiae were found in gills, while hyaline inclusions were observed in liver and melanomacrophage centers in kidney. Pacu fingerlings exposed to sublethal doses of HgCl2 had a significant increase in oxidative stress and changes in plasma bactericidal activity in addition to pathological changes in the gills, hepatic and renal tissues.
O mercúrio é um contaminante xenobiótico encontrado frequentemente nos ecossistemas naturais, o qual representa um aspecto muito importante na saúde pública e ambiental devido aos níveis encontrados nas fontes de agua, as quais além, tem correlação com a bioacumulação em organismos vivos. O objetivo desta pesquisa foi avaliar os efeitos imunotoxicológicos e histopatológicos da exposição a concentrações subletais de Cloreto de Mercúrio (HgCl2) em Pirapitinga branca (Piaractus brachypomus). Utilizaram-se alevinos de Pirapitinga branca com um peso médio de 10 ± 2,1 g, distribuídos em aquários com tanques de aireação constante sem filtro. O período experimental foi de 18 dias, utilizando quatro concentrações baseadas na decima parte da CL50 descrita para Pirapitinga branca assim como no grupo controle. Realizaram-se seis amostragens (dias 1, 2, 4, 7, 12 e 18) nos quais tomaram-se amostras de sangue para a avaliação da explosão respiratória e a capacidade bactericida do plasma. Calculou-se o índice hepatosomático e pegaram-se amostras para processamento histopatológico. Evidenciou-se uma elevação do nível de explosão respiratória (estresse oxidativo) em animais expostos ao HgCl2 de uma maneira dependente da concentração, sendo mais marcado este efeito ao dia 12 da exposição. Não se encontraram diferenças significativas nos valores do índice hepatosomático (IHS). Na atividade bactericida do plasma achou-se uma atividade menor em animais expostos ao HgCl2. Na análise histopatológica encontraram-se mudanças como hiperplasia, aneurisma e sinéquias em brânquias, inclusões hialinas no fígado e centros melanomacrófagos nos rins. Os alevinos de Pirapitinga branca expostos a doses sub-letais de HgCl2, amostraram um incremento significativo na explosão respiratória (estresse oxidativo) assim como mudanças na atividade bactericida do plasma, além de mudanças anatomopatológicas no nível branquial, hepático e renal.
ABSTRACT
Objective To dynamically analyze the antibodies with regard to in vitro serum bacteri-cidal activity and the quantity of IgG in healthy adults received one dose of immunization with ACYW 135 me-ningococcal polysaccharide vaccine .To investigate the term of protection with polysaccharide vaccine and the correlation between bactericidal titer and IgG concentration .Methods Twenty healthy adults were given one dose of immunization with quadrivalent meningococcal polysaccharide vaccine .Serum samples were col-lected before and after vaccination at specific time points .Test for serum bactericidal activity ( SBA ) and quantitative ELISA were performed to detect bactericidal titers and IgG concentrations in serum samples .Re-sults Certain levels of antibodies against capsular polysaccharides of serogroup A , C, Y and W135 strains had already existed prior to immunization .Moreover, bactericidal titers against serogroup A , Y and W135 strains except serogroup C strain were relatively high .Specific IgG concentrations and bactericidal titers for all serogroup stains were significantly increased on day 15 after vaccination (P0.05).However, a close correla-tion was demonstrated between GMTs and GMCs of serum samples (r>0.7, P<0.05).Conclusion The geometric mean titers ( GMTs) and geometric mean concentrations ( GMCs) of serum samples collected be-fore and after vaccination at different time points were reliable and consistent parameters for the evaluation of vaccine .The term of protection of quadivalent meningococcal polysaccharide vaccine was about 3 years upon a single dose of immunization .
ABSTRACT
Uno de los principales problemas que enfrenta la comunidad científica en la actualidad, es la aparición cada vez más frecuente de cepas bacterianas patógenas resistentes a los antibióticos y antimicrobianos actuales, porque dichos gérmenes tienen la capacidad, bajo determinadas circunstancias, de hacerse inmunes a tales agentes químicos; por tanto, es necesaria la búsqueda de nuevos agentes antibacterianos. Para este propósito, una buena fuente puede provenir de los insectos sociales, los cuales han desarrollado como estrategia de supervivencia la producción de agentes bactericidas para proteger sus colonias. Este trabajo se centró en determinar si ciertas hormigas que se adaptaron a los ámbitos urbanos, tienen esta actividad. Para ello, se capturaron hormigas de los géneros Crematogaster sp. y Solenopsis sp., que se sometieron a procesos de extracción por maceración, obteniéndose extractos etanólicos totales, muy poco hidrosolubles, los cuales se evaluaron a diferentes concentraciones sobre cepas de bacterias Gram negativas (Klebsiella pneumoniae y Pseudomona aeruginosa) y Gram positivas (Bacillus subtilis spizizenii y Staphylococcus aureus), encontrando actividad inhibitoria al crecimiento en diferentes grados sobre todas ellas, incluyendo una S. aureus resistente a los antibióticos Amoxicilina/Ac. Clavulánico, Ampicilina/Sulbactam y Ceftriazona/Oxacilina; por tanto, estas especies se pueden clasificar como promisorias en la búsqueda de nuevos agentes antimicrobianos.
One of the main problems faced today by the scientific community is the increasingly frequent occurrence of pathogenic bacterial strains resistant to current antibiotics and antimicrobial, because these germs are able, under certain circumstances, to be immune to such chemicals, it is therefore necessary to pursue the search for new agents. For this purpose, a good source can come from social insects, which have developed as a survival strategy, the production of bactericidal agents to protect their colonies. The purpose of this work was to determine if certain ants that have adapted to urban environments, have antibacterial activity and to what extent. For this purpose, ants of the genus Crematogaster sp. and sp. Solenopsis were captured and subjected to extraction process by maceration, yielding total ethanolic extracts, very little soluble, which were evaluated at different concentrations on Gram negative bacteria strains (Klebsiella pneumoniae and Pseudomona aeruginosa) and Gram positive (Bacillus subtilis spizizenii and Staphylococcus aureus), finding growth inhibitory activity at different degrees over all strains, including an S. aureus one resistant to antibiotics Amoxicillin/Clavulanate, Ampicillin/Sulbactam, Ceftriaxone and Oxacillin; therefore, these species can be classified as promising in the search for new antimicrobial agents.
ABSTRACT
Objective:To investigate the synergic antibacterial activity of garlic and tazma honey against standard and clinical pathogenic bacteria. Methods:Antimicrobial activity of tazma honey, garlic and mixture of them against pathogenic bacteria were determined. Chloramphenicol and water were used as positive and negative controls, respectively. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration of antimicrobial samples were determined using standard methods. Results: Inhibition zone of mixture of garlic and tazma honey against all tested pathogens was significantly (P≤0.05) greater than garlic and tazma honey alone. The diameter zone of inhibition ranged from (18±1) to (35±1) mm for mixture of garlic and tazma honey, (12±1) to (20±1) mm for tazma honey and (14±1) to (22±1) mm for garlic as compared with (10±1) to (30±1) mm for chloramphenicol. The combination of garlic and tazma honey (30-35 mm) was more significantly (P≤0.05) effective against Salmonella (NCTC 8385), Staphylococcus aureus (ATCC 25923), Lyesria moncytogenes (ATCC 19116) and Streptococcus pneumonia (ATCC 63). Results also showed considerable antimicrobial activity of garlic and tazma honey. MIC of mixture of garlic and tazma honey at 6.25%against total test bacteria was 88.9%. MIC of mixture of garlic and tazma honey at 6.25%against Gram positive and negative were 100%and 83.33%, respectively. The bactericidal activities of garlic, tazma honey, and mixture of garlic and tazma honey against all pathogenic bacteria at 6.25%concentration were 66.6%, 55.6%and 55.6%, respectively. Conclusions: This finding strongly supports the claim of the local community to use the combination of tazma honey and garlic for the treatment of different pathogenic bacterial infections. Therefore, garlic in combination with tazma honey can serve as an alternative natural antimicrobial drug for the treatment of pathogenic bacterial infections. Further in vivo study is recommended to come up with a comprehensive conclusion.
ABSTRACT
Salvia officinalis (L.), or common sage, is an aromatic herb that has been used in medicine and cooking since ancient times and has been investigated for the treatment of various diseases, especially infections and skin inflammation. We conducted phytochemical prospecting and quality control with hydroalcoholic extracts of dried sage, to identify active compounds in the plant. The aim was to assess antibacterial and antifungal activity against Staphylococcus aureus, Streptococcus agalactiae, Candida albicans and Candida tropicalis. Antimicrobial susceptibility was investigated in vitro by agar-overlay and well-diffusion techniques, in which disc and well were used. Salvia officinalis (L.) was not effective against Streptococcus agalactiae, Candida albicans or Candida tropicalis, but best results were observed for antibacterial activity against Staphylococcus aureus. Considering the results of the inhibition tests presented here, we suggest that cosmetic formulations containing Salvia officinalis (L.) could contribute to inhibitor of pathogens in the skin microbiota.
A Salvia officinalis (L.) é uma planta com uso difundido, utilizada no tratamento de diversas patologias, principalmente para infecções e inflamações cutâneas. Neste trabalho foi realizada prospecção fitoquímica e controle de qualidade com a planta seca e extrato hidroalcoólico para identificação dos compostos ativos da sálvia, tendo como finalidade comprovar sua atividade antibacteriana e antifúngica frente à Staphylococcus aureus, Streptococcus agalactiae Candida albicans e Candida tropicalis. Os métodos de escolha para avaliação in vitro foram ensaios de sensibilidade antimicrobiana por difusão em ágar com discos e cilindros. Dentre os ensaios realizados a sálvia não se mostrou efetiva para Streptococcus agalactiae, Candida albicans e Candida tropicalis, sendo o melhor resultado obtido com Staphylococcus aureus, em que se pode verificar-se atividade antibacteriana. Diante dos resultados obtidos, propôs-se uma formulação de sabonete líquido com extrato hidroalcoólico de Salvia officinalis (L.), para atuar na higiene da pele.
Subject(s)
Anti-Bacterial Agents , Hydroalcoholic Solution , Phytotherapy , Salvia officinalis , Skin Care , Plants, MedicinalABSTRACT
Antihistaminics are widely used for various indications during microbial infection. Hence, this paper investigates the antimicrobial activities of 10 antihistaminics belonging to both old and new generations using multiresistant Gram-positive and Gram-negative clinical isolates. The bacteriostatic activity of antihistaminics was investigated by determining their MIC both by broth and agar dilution techniques against 29 bacterial strains. Azelastine, cyproheptadine, mequitazine and promethazine were the most active among the tested drugs. Diphenhydramine and cetirizine possessed weaker activity whereas doxylamine, fexofenadine and loratadine were inactive even at the highest tested concentration (1 mg/ml). The MIC of meclozine could not be determined as it precipitated with the used culture media. The MBC values of antihistaminics were almost identical to the corresponding MIC values. The bactericidal activity of antihistaminics was also studied by the viable count technique in sterile saline solution. Evident killing effects were exerted by mequitazine, meclozine, azelastine and cyproheptadine. Moreover, the dynamics of bactericidal activity of azelastine were studied by the viable count technique in nutrient broth. This activity was found to be concentration-dependant. This effect was reduced on increasing the inoculum size while it was increased on raising the pH. The post-antimicrobial effect of 100 fg/ml azelastine was also determined and reached up to 3.36 h.
Subject(s)
Humans , Histamine H1 Antagonists/analysis , Histamine H1 Antagonists/pharmacology , Drug Resistance, Microbial , In Vitro Techniques , Culture Media/analysis , Culture Media/pharmacology , Methods , Methods , Therapeutic UsesABSTRACT
The phytochemical investigation on the aereal parts of Lychnophora pinaster Mart., Asteraceae, was carried to isolation of triterpenes. 3-O-Acetyl-lupeol (1), 3-O-acetyl-pseudotaraxasterol (2), and 3-O-acetyl-α-amyrin (3) were isolated from hexanic extract and 4,4-dimethyl-cholesta-22,24-dien-5-ol (4), α-amyrin (5), and lupeol (6) were isolated from hexanic/dichlorometanic extract of the leaves. Compounds Δ7-bauerenyl acetate (7), friedelin (8), stigmasterol (9), and sitosterol (10) were isolated from the hexanic/dichlorometanic extract of the stems. The steroids 9 and 10 were also isolated from the hexanic/dichlorometanic extract of the flowers. Triterpenes 1, 3, 4, and 7 are described for the first time in the genus Lychnophora. The apolar fractions of the leaf and stem extracts and some isolated triterpenes showed low trypanocidal activity. Moreover, apolar fractions of the leaf and stem extracts and 5 showed antibacterial action against Staphylococcus aureus.