RESUMO
The emergence of lactic acid bacteria (LABs) resistant to existing antimicrobial drugs is a growing health crisis. To decrease the overuse of antibiotics, molecular diagnostic systems that can rapidly determine the presence of antibiotic resistance (AR) genes in LABs from yogurt samples are needed. This paper describes a fully integrated, miniaturized plastic chip and closed-tube detection chemistry that performs multiplex nucleic acid amplification. High-throughput identification of AR genes was achieved through this approach, and six AR genes were analyzed simultaneously in < 2 h. This time-to-result included the time required for the extraction of DNA. The detection limit of the chip was 103 CFU mL-1, which was consistent with that of tube LAMP. We detected and identified multiple DNAs, including streptomycin, tetracycline, and vancomycin resistance-associated genes, with complete concordance to the Kirby-Bauer disk diffusion method.Key Points⢠A miniaturized chip was presented, and multiplex nucleic acid amplification was performed.⢠The device can be integrated with LAMP for rapid detection of antibiotic resistance genes.⢠The approach had a high throughput of AR gene analysis in lactic acid bacteria.
Assuntos
Farmacorresistência Bacteriana/genética , Genes Bacterianos , Lactobacillales/genética , Microfluídica/métodos , Antibacterianos/farmacologia , Microbiologia de Alimentos , Lactobacillales/efeitos dos fármacos , Lactobacillales/isolamento & purificação , Testes de Sensibilidade Microbiana , Microfluídica/instrumentação , Técnicas de Amplificação de Ácido Nucleico , Polimetil Metacrilato , Sensibilidade e Especificidade , Iogurte/microbiologiaRESUMO
Since biofouling challenges negatively influence the marine and transportation industries, developing effective antifouling materials have attracted extensive concern. A tyrosine-based antifouling phenolic resin (TPP resin) was synthesized using tyrosine as a natural phenol source. TPP exhibited shell-like surface morphology with micro-ripples and excellent anti-adhesion properties against bacteria and diatom. The micro-ripples surface might be caused by the strong hydrogen bonding or ionic interaction among tyrosine units resulting in microphase separation during the curing process. Tyrosine content in TPP resin has a great influence on the surface properties, morphology and antifouling characteristics. The higher the tyrosine content, the higher is the surface hydrophilicity, the denser and more regular is the micro-ripples morphology, and the stronger is the antifouling performance. TPP-60 % exhibited the best antifouling performance. Combination of the surface hydrophilicity and regular micro-ripples surface morphology afford TPP excellent antifouling performance. TPP resins offer a broad prospect for developing phenolic resin in the antifouling field.
Assuntos
Incrustação Biológica , Incrustação Biológica/prevenção & controle , Formaldeído , Interações Hidrofóbicas e Hidrofílicas , Fenóis/farmacologia , Polímeros , Propriedades de Superfície , TirosinaRESUMO
ETHNOPHARMACOLOGICAL RELEVANCE: Enterovirus 71 (EV71) has a propensity to cause hand-foot-and-mouth disease (HFMD) epidemics associated with neurological sequelae. Unfortunately, no drugs are currently available for the clinical treatment of EV71 infections. Sophoridine (SRI) is one of the most abundant alkaloids in Sophora flavescens Aiton (Leguminosae), which has been used to treat fever, throat inflammation, cancer, and other diseases. MATERIALS AND METHODS: In this study, we found that SRI inhibits EV71 infection in Vero cells. To study the antiviral activity of SRI, Vero cells were divided into 3 treatment groups based on the timing of SRI dosing: prior to viral adsorption (Group A), during viral adsorption (Group B), and after viral adsorption (Group C). We further revealed the antiviral activity of SRI with the attachment assay and the penetration assay. For Group A, 50% viability of Vero cells was observed at a SRI concentration of 61.39⯵g/mL, whereas for Groups B, 50% viability was observed at SRI concentrations of 196.86⯵g/mL. Furthermore, 29.7% cell viability was observed even at a SRI concentration of 1000⯵g/mL in Groups C. The results show that SRI was highly effective against EV71 when Vero cells were pretreated with SRI for 2â¯h (Group A). Further researches indicate SRI was highly effective at inhibiting EV71 attachment when the SRI concentrations over 250⯵g/mL (Pâ¯<â¯0.001). CONCLUSIONS: We have shown that Vero cell viability increases when SRI is administered prior to viral adsorption. This suggests that SRI has the considerable potential as an antiviral for EV71 disease prevention.