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This investigation aimed to identify the bioremediation potential of Mn2+-resistant bacterial strains cultured from the Surya Kund hot spring, Yamunotri, Uttarakhand. In this study, eight heavy metal-resistant isolates belonging to two phyla, i.e., Firmicutes and Proteobacteria, were investigated for their Mn2+biosorption potential. The metal tolerance potential of all the thermophilic bacterial strains was determined by MIC. Bioremediation assay of these metal-resistant strains was performed for Mn2+ through the live and dead biomass of the bacterial cell. The evaluation of the bioremediation rate of metal ions through bacteria was done by AAS. All the selected bacterial strains were evaluated with effective biosorption rates for Mn2+. Acinetobacter sp. LSN-10 (YII-1) has been showing the highest potential for the removal of Mn2+ in both live (41.202%) and dead biomass (64.721%) conditions. The bioremediation rate of dead biomass was observed quite higher in comparison to bioremediation through live bacterial cells in the maximum number of isolates. This study may provide a new eco-friendly and cost-effective approach to dealing with metal toxicity. However, further investigation is needed to identify the most effective applications and potential limitations of this method. [ABSTRACT FROM AUTHOR]

Background: Staphylococcus haemolyticus is a clinically significant Coagulase Negative Staphylococci (CoNS) accountable for various infections and is often multi-drug resistant along with resistance to linezolid. Aim and Objectives: This study was carried out to detect the presence of cfr and optrA gene in clinical isolates of linezolid resistant S. haemolyticus in a tertiary care hospital. Material and Methods: A total of 227 clinical isolates of S. haemolyticus recovered from various clinical samples were tested to determine susceptibility to linezolid by phenotypic method. Further, the presence of cfr & optrA gene was looked for, in clinical isolates of S. haemolyticus. Results: S. haemolyticus was isolated predominantly from inpatient department mainly from blood culture (85%). Linezolid resistance was confirmed in 9.2% isolates of S. haemolyticus phenotypically and they were also methicillin resistant. On genotypic characterization, cfr gene could be detected in 7.04% the isolates. However, all the isolates were negative for optrA gene. Conclusion: Emergence of resistance to linezolid in S. haemolyticus was reported for the first time. The presence of cfr gene is the most common mechanism of resistance to linezolid. Correct identification of these isolates and adherence to strict infection control protocols will help in better clinical outcomes. [ABSTRACT FROM AUTHOR]