hydrophobicity
در نشریات گروه پزشکی-
مقدمه
در حال حاضر، مقاومت به داروهای ضدقارچی شیمیایی مشکل بهداشتی بزرگی است؛ بنابراین، شناسایی مولکول های جدید ضدقارچی مانند فرآورده های طبیعی برای ایجاد راهبردهای جدید درمانی به منظور پیشگیری و حذف کاندیدیازیس ضروری است. اهداف این کار شامل مطالعه تاثیر آنتول روی رشد، آب گریزی سطح سلولی، میزان ارگوسترول و تشکیل بیوفیلم کاندیدا گلابراتای جداشده از دستگاه ادراری است.
مواد و روش هاروش انتشار دیسک (حساسیت به داروهای ضدقارچی شیمیایی)، روش میکرودایلوشن براث (حساسیت به آنتول)، سنجش کاهش MTT (تشکیل بیوفیلم)، تکنیک HPLC (میزان ارگوسترول) و اتصال به n- هگزادکان (آب گریزی سطح سلولی) برای تعیین تاثیر آنتول برابر جدایه های کاندیدا گلابراتا به کار گرفته شدند. تجزیه وتحلیل آماری داده ها با نرم افزار GraphPad Prism vol.9.0.0.121 و آزمون One-Way ANOVA و آزمون های دوتایی Tukey Test / Post-hoc ANOVA در سطح معنا دار 05/0 انجام گرفت.
یافته های پژوهش:
دامنه حداقل غلظت مهارکنندگی کاندیدا گلابراتا حدود 1250-5/312 میکروگرم در میلی لیتر برای آنتول بود (75/343±75/843 میکروگرم در میلی لیتر). درصدهای آبگریزی سطح سلولی به طور معناداری در گروه های تیمارشده با غلظت های MIC/2 (37/6±73/24 درصد) و MIC/4 (61/6±01/29 درصد) آنتول بودند؛ همچنین تغییرات درصدی در میزان ارگوسترول غشایی حدود 35/23، 46/46 و 92/73 درصد در غلظت های 125/0، 25/0 و 5/0 میکروگرم در میلی لیتر آنتول در مقایسه با گروه شاهد غیرتیمار بود.
بحث و نتیجه گیریاین نتایج اثربخشی آنتول برابر سلول های پلانکتونیک و بیوفیلمی جدایه های کاندیدا گلابراتا و تداخل با میزان ارگوسترول، آبگریزی سطح سلولی و تشکیل بیوفیلم را نشان دادند که بیان کننده توانایی بالقوه این ترکیب به عنوان یک ضدقارچ طبیعی است.
کلید واژگان: کاندیدا گلابراتا، آنتول، بیوفیلم، ارگوسترول، آبگریزی سطح سلولیIntroductionResistance to synthetic antifungal agents is a considerable health problem nowadays. Therefore, it is necessary to identify new antifungal molecules, such as natural products, to develop new therapeutic strategies to prevent and eradicate candidiasis. The aims of this work were to study the effect of anethole on growth, cell surface hydrophobicity, ergosterol content, and biofilm formation of Candida glabrata (C. glabrata) isolated from the urinary system.
Materials & MethodsThe disc diffusion method (susceptibility to synthetic antifungals), the broth micro-dilution method (susceptibility to anethole), the MTT reduction assay (biofilm formation), the HPLC technique (ergosterol content), and adherence to n-hexadecane (cell surface hydrophobicity; CSH) were employed to determine the effect of anethole against C. glabrata isolates. Statistical analysis of the data was performed using GraphPad Prism V.9, employing the one-way ANOVA test and pairwise comparisons using the Tukey test/post-hoc ANOVA at a significance level of 0.05.
ResultsThe range of MIC of C. glabrata was 1250-5000 µg/ml for anethole (3375±1375 µg/ml). The percentages of CSH were significantly in groups treated with MIC/2 (24.73±6.37%) and MIC/4 (29.01±6.61%) concentrations of anethole. Also, the percentage changes in membrane ergosterol were 23.35% at 0.125 µg/ml, 46.46% at 0.25 µg/ml, and 73.92% at 0.5 µg/ml of anethole, compared to the control that wasn't treated.
ConclusionThe results showed the effectiveness of anethole against planktonic and sessile cells of C. glabrata isolates and the interference with ergosterol content, CSH, and biofilm formation, reinforcing the potential of this natural compound as a natural antifungal.
Keywords: Candida Glabrata, Anethole, Biofilm, Ergosterol, Hydrophobicity -
Comparative Study of <i>Candida albicans</i> Strains from Clinical and Environmental Sources in IranBackground
Candida species are a leading cause of fungal infections worldwide. Candidiasis, the disease caused by Candida , represents a significant public health concern globally. Candida albicans is the most common causative agent, responsible for 50 - 90% of invasive candidiasis cases. Candida albicans employs various virulence factors to adhere to, invade host tissues, and cause disease.
ObjectivesThis study aimed to detect and compare the virulence factors of C. albicans , including hydrophobicity, biofilm formation, ergosterol content, and secretory enzymes, in clinical and environmental samples.
MethodsA total of 105 clinical and 165 environmental samples suspected of containing C. albicans were collected from Imam Khomeini Hospital in Ahvaz, Iran. The isolates were evaluated for five potential virulence factors: Ergosterol content, cell surface hydrophobicity (CSH), biofilm formation, protease activity, and phospholipase activity.
ResultsSixty C. albicans isolates were identified, consisting of 30 clinical and 30 environmental isolates. Biofilm production was observed in 100% of clinical isolates and 80% of environmental isolates (P < 0.001). Protease activity was detected in 66.6% of clinical isolates and 76.7% of environmental isolates (P = 0.008). Phospholipase activity was present in 60% of clinical isolates and 76.7% of environmental isolates (P = 0.262). Clinical isolates exhibited higher CSH (66.4 ± 9.8) compared to environmental isolates (47.7 ± 17.0) (P < 0.001). The ergosterol content was 1.2 ± 0.5 in clinical isolates and 1.1 ± 0.3 in environmental isolates.
ConclusionsBiofilm formation was a consistent characteristic of clinical isolates, while phospholipase and protease activity were more prevalent in environmental C. albicans isolates. The results suggest possible cross-contamination between patients and the environment, as the virulence factors of clinical and environmental isolates were similar.
Keywords: Candida Albicans, Hydrophobicity, Biofilms, Ergosterol, Phospholipases -
Background and Objectives
The term "probiotic," which is relatively novel and means "for life," is typically used to refer to bacteria that include positive effects on humans and animals. In this study, probiotic characteristics of Limosilactobacillus fermentum IMAU70160, isolated from local yogurt were investigated.
Materials and MethodsIn this study, molecular identification of a strain isolated from local yogurt was carried out by 16S rRNA gene analysis using 27FYM and 1492R universal primers. Probiotic potential of L. fermentum IMAU70160 was carried out.
ResultsStrain was resistant to low pH, bile salts and simulated gastrointestinal conditions. The strain cell surface hydrophobicity, auto-aggregation, co-aggregation, adhesion capacity, anti-adhesion effect, antioxidant activity and cholesterol removal ability were 44.49, 33.29, 20.11, 10.30, 19.16–42.40, 48.40 and 43.20%, respectively. Staphylococcus aureus and Escherichia coli were the most sensitive and the most resistant bacterial species to cell-free supernatant (CFS) of L. fermentum IMAU70160, respectively. The two aCFS and nCFS were capable of inhibiting growth of pathogens. In general, aCFS included a greater antimicrobial activity than that nCFS did. Similar results were observed in the modified double-layer method. It showed no hemolytic or DNase activity and was unable to generate biogenic amines. The strain was greatly sensitive to imipenem (22.10 mm), chloramphenicol (22.80 mm), nitrofurantoin (24.50 mm) and ciprofloxacin (28.20 mm) with inhibition zones.
ConclusionsFurther studies are needed to verify biological and functional characteristics of L. fermentum IMAU70160-loaded food products.
Keywords: Limosilactobacillus fermentum, Antioxidant activity, Caco-2 cells, Hydrophobicity -
Lactobacillus plantarum was the most common species in the microflora of artisanal Siahmazgi white brined cheese with 41.6% occurrence among the total isolated LAB. In this study, the attachment properties of 5 different L. plantarum strains isolated from Siahmazgi traditional cheese were evaluated by in vitro tests including auto and co-aggregation, hydrophobicity, and cell adhesion. A relatively high amount of auto-aggregation ranged from 58.21 to 73.99% was seen in selected isolates. Co-aggregation was highly variable from 1.46 to 49%, depending on the pathogenic bacteria and L. plantarum isolates. Hydrophobicity was also highly different in tested strains ranging from 6.58 to 73.3%. Two isolates showed great affinity about 73% to chloroform. All the isolates presented high adhesion to Caco-2 cell line up to about 90%. In conclusion, five L. plantarum isolates showed appropriate attachment properties and could be good candidates for further studying, including safety evaluation, that support their use as probiotics.Keywords: Adhesion, Auto, co-aggregation, Hydrophobicity, Lactobacillus plantarum, Siahmazgi cheese
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زمینه و هدفلاکتوباسیلوس سالیواریوس، باکتری پروبیوتیک شناخته شده ای است که از دستگاه گوارش انسان و حیوانات جدا می شود. هدف از این مطالعه، جداسازی لاکتوباسیلوس سالیواریوس از شیر خام گاومیش و شناسایی مولکولی و بررسی ویژگی های ضدمیکروبی آن در شرایط آزمایشگاهی است.مواد و روش کارتعداد 20 نمونه شیر خام گاومیش از دامداری های سنتی و صنعتی شهرستان ارومیه تهیه و پس از انتقال به آزمایشگاه، روی محیط MRS کشت داده شدند. در ادامه کلنی های مشکوک از نظر شکل و خصوصیات بیوشیمیایی انتخاب و به منظور تعیین گونه آنها از روش واکنش زنجیره ای پلی مراز و به دنبال آن چندشکلی طولی قطعه محدودشونده (PCR-RFLP) و تعیین توالی نوکلئوتیدی ژن 16S rRNA استفاده شد. اثرات ضدمیکروبی لاکتوباسیلوس سالیواریوس و مایع رویی آن بر علیه لیستریا منوسیتوژنز، سالمونلا تیفی موریوم، اشریشیا کلی و استافیلوکوکوس اورئوس به ترتیب به روش نقطه ای و دیسک بررسی شد. همچنین هیدروفوبیسیتی سطحی باکتری به روش اتصال باکتری به هیدروکربن گزیلن و تولئن ارزیابی شد.یافته هااز 60 جدایه مشکوک به دست آمده از شیر گاومیش، پس از تعیین توالی نوکلئوتیدی، تعداد 23 جدایه مختلف از باکتری های اسید لاکتیک شناسایی شد که فقط یک جدایه لاکتوباسیلوس سالیواریوس بود. جدایه لاکتوباسیلوس سالیواریوس اثر مهاری معنی داری در مقایسه با باکتری استاندارد، بر عوامل بیماری زای مطالعه شده داشت. بیشترین و کمترین اثر مهاری به ترتیب در استافیلوکوکوس اورئوس و سالمونلا تیفی موریوم مشاهده شد. هیدروفوبیستی باکتری نسبت به گزیلن 55/3 درصد و تولئن 55/6 درصد گزارش شد.نتیجه گیرینتایج این مطالعه نشان داد که شیوع جنس لاکتوباسیلوس در شیر گاومیش بسیار پایین است و لاکتوباسیلوس سالیواریوس جداشده از خصوصیات ضدمیکروبی منحصربه فردی در مقایسه با باکتری پروبیوتیک استاندارد برخوردار است.کلید واژگان: گاومیش، لاکتوباسیلوس سالیواریوس، قدرت ضدمیکروب، هیدروفوبیستی، تشخیص مولکولی، شیرBackground And AimsLactobacillus salivarius is a well-known probiotic bacterium, which is commonly isolated from gastro-intestinal tract of human and animals. The objectives of the present study were isolation, molecular detection and antimicrobial characterization of L. salivarius from buffalos raw milk.Materials And MethodsA total number of 20 buffalo milk samples were collected aseptically from traditional buffalo farms in Urmia city, Iran. Milk samples were cultured and incubated on MRS agar, then suspected colonies were primarily determined according to their appearance and biochemical characteristics. Bacteria species were confirmed by polymerase chain reaction accompanied by restriction fragment length polymorphism (PCR-RFLP) and nucleotide sequencing of 16s rRNA gene. Antimicrobial activity of L. salivarius against pathogenic bacteria including Listeria monocytogenesis, Escherichia coli, Salmonella typhimurium, and Staphylococcus aureus was examined using agar-spot and agar-disk diffusion methods. Cell surface hydrophobicity of L. salivarius was also investigated according to microbial adhesion to xylene and toluene hydrocarbons.ResultsFrom 60 suspected colonies which were selected according to phenotypic characteristics, 23 colonies were confirmed as lactic acid bacteria based on the molecular identification. Only one isolate belonged to L. salivarius. The antimicrobial activity results showed a significant growth inhibitory effect of L. salivarius on pathogenic bacteria comparing to standard bacteria. L. salivarius had the most inhibitory effect on S. aureus while it had the least inhibitory against S. typhimurium. The hydrophobicity of L. salivarius to xylene and toluene were 55.3% and 55.6% respectively.ConclusionsBased on the results, the frequency of the Lactobacillus genus s was very low in buffalo milk. In addition, isolated L. salivarius had strong antimicrobial activity against pathogenic bacteria.Keywords: Buffaloes, Lactobacillus salivarius, Antimicrobial Capacity, Hydrophobicity, Molecular Diagnostics, Milk
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Objective(s)This study was designed to determine the relationship of Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli isolates in multispecies biofilms and their individual phenotypic characters in biofilm consortia.Materials And MethodsThe subject isolates were recovered from different food samples and identified on the basis of growth on differential and selective media. Tube methods, Congo-red agar method, and scanning electron microscopy (SEM) were used to study biofilms phenotypes. The hydrophobicity of the strains was evaluated by the adhesion to apolar solvent.ResultsThe results showed that E. coli dominated the pre-biofilm stage. It has been observed that E. coli adopted biofilm life much before S. aureus and P. aeruginosa. However, after adopting biofilm lifestyle, slowly and gradually, P. aeruginosa dominated the consortia and dispersed other stakeholders. The subject isolates of P. aeruginosa produce cis-2-decanoic acid to disperse or inhibit S. aureus and E. coli biofilms. Gas-chromatography and mass spectrometry results showed that cis-2-decanoic was higher in the co-culture condition and increased at late log-phase or at stationary phase. Although majority of S. aureus were unable to compete with P. aeruginosa, however, a minor population competed, survived, and persisted in biofilm consortia as small colony variants. The survivors showed higher expression of sigB and sarA genes. P. aeruginosa showed comparatively higher hydrophobic surface properties.ConclusionComparative analysis showed that cell surface hydrophobicity, growth rate, and small colony variants (SCVs) are correlated in biofilm consortia of the P. aeruginosa, S. aureus, and E. coli.Keywords: Biofilms, Escherichia coli, Hydrophobicity, Pseudomonas aeruginosa, Small colony variants, Staphylococcus aureus
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