A facile method of ultrasound-assisted noncovalent functionalization of multiwalled carbon nanotubes (MWCNT) with fatty amide of castor oil and use of the same as a reactive component in the in situ polymerization of hyperbranched poly(ester amide) (HBPEA) via an A 2 + B 2 + A′A 2 approach is reported. The reaction entails anchoring of the amide groups to MWCNT to maximize the reaction with the diacids, resulting in formation of the nanocomposite. Fourier transform infrared analyses validated the anchorage of esteramide groups to the nanotubes. Intercalation and formation of dense polymer layers on the isotropically dispersed nanotubes (with mean coherency coefficient of 0.229) were evident from transmission electron microscopy. The changes in biophysico attributes were reflected in their selective efficacy against the Gram-positive bacteria with an enhanced cytotoxicity (death rate increase of Staphylococcus aureus by 137.5% and Bacillus subtilis by 107.6%) and significant decrease in the sheet resistance by 3 orders of magnitude (from 10 7 to 10 4 Ω sq −1 ) as compared to the pristine HBPEA at low loading of 1 wt % MWCNT. The multifunctional nanocomposites maintained the acceptable mechanical performance, and kinetics evaluation of activation energy revealed enhanced thermal stability over pristine HBPEA; the nanocomposites can be envisaged for MWCNT-based bionano applications, particularly in the field of advanced textiles.

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In this review, we highlight the variations of gut resistome studies, which may preclude comparisons and translational interpretations. Of 22 included studies, a range of 12 to 2000 antibiotic resistance (AR) genes were profiled. Overall, studies defined a healthy gut resistome as subjects who had not taken antibiotics in the last three to 12 months prior to sampling. In studies with de novo assembly, AR genes were identified based on variable nucleotide or amino acid sequence similarities. Different marker genes were used for defining resistance to a given antibiotic class. Validation of phenotypic resistance in the laboratory is frequently lacking. Cryptic resistance, collateral sensitivity and the interaction with repressors or promotors were not investigated. International consensus is needed for selecting marker genes to define resistance to a given antibiotic class in addition to uniformity in phenotypic validation and bioinformatics pipelines.

Curcumin is the principal curcuminoid obtained from the plant Curcuma longa and has been extensively studied for its biological and chemical properties. Curcumin displays a vast range of pharmacological properties, including antimicrobial, anti-inflammatory, antioxidant, and antitumor activity. Specifically, curcumin has been linked to the improvement of the outcome of tuberculosis. There are many reviews on the pharmacological effects of curcumin; however, reviews of the antitubercular activity are comparatively scarcer. In this review, we attempt to discuss the different aspects of the research on the antitubercular activity of curcumin. These include antimycobacterial activity, modulation of the host immune response, and enhancement of BCG vaccine efficacy. Recent advances in the antimycobacterial activity of curcumin synthetic derivatives, the role of computer aided drug design in identifying curcumin targets, the hepatoprotective role of curcumin, and the dosage and toxicology of curcumin will be discussed. While growing evidence supports the use of curcumin and its derivatives for tuberculosis therapy, further preclinical and clinical investigations are of pivotal importance before recommending the use of curcumin formulations in public health.

In this study, antimycobacterial activity of a set of synthesized chalcone derivatives against Mycobacterium tuberculosis H37Rv was investigated by quantitative structure-activity relationship (QSAR) analysis using density functional theory (DFT) and molecular mechanics (MM+)-based descriptors in both gas and solvent phases. The best molecular descriptors identified were hardness, E HOMO , MR A-4 and MR B-4¢ that contributed to the antimycobacterial activity of the chalcones as independent factors. The correlation of these four descriptors with their antimycobacterial activity increases with the inclusion of solvent medium, indicating their importance in studying biological activity. QSAR models revealed that in gas phase, lower values of E HOMO , MR A-4 and MR B-4¢ increase the antimycobacterial activity of the chalcone molecules. However, in solvent phase, lower values of E HOMO and MR B-4¢ and higher values of MR A-4 increase their activity.

Many CRISPR/Cas platforms have been established for the detection of SARS-CoV-2. But the detection platform of the variants of SARS-CoV-2 is scarce because its specificity is very challenging to achieve for those with only one or a few nucleotide(s) differences. Here, we report for the first time that chimeric crRNA could be critical in enhancing the specificity of CRISPR-Cas12a detecting of N501Y, which is shared by Alpha, Beta, Gamma, and Mu variants of SARS-CoV-2 without compromising its sensitivity. This strategy could also be applied to detect other SARS-CoV-2 variants that differ only one or a few nucleotide(s) differences.