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1.
Nat Biomed Eng ; 6(10): 1180-1195, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-36229662

RESUMO

New antibiotics should ideally exhibit activity against drug-resistant bacteria, delay the development of bacterial resistance to them and be suitable for local delivery at desired sites of infection. Here, we report the rational design, via molecular-docking simulations, of a library of 17 candidate antibiotics against bone infection by wild-type and mutated bacterial targets. We screened this library for activity against multidrug-resistant clinical isolates and identified an antibiotic that exhibits potent activity against resistant strains and the formation of biofilms, decreases the chances of bacterial resistance and is compatible with local delivery via a bone-cement matrix. The antibiotic-loaded bone cement exhibited greater efficacy than currently used antibiotic-loaded bone cements against staphylococcal bone infections in rats. Potent and locally delivered antibiotic-eluting polymers may help address antimicrobial resistance.


Assuntos
Antibacterianos , Cimentos Ósseos , Ratos , Animais , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Biofilmes , Próteses e Implantes
2.
FEBS Lett ; 594(6): 1005-1020, 2020 03.
Artigo em Inglês | MEDLINE | ID: mdl-31724164

RESUMO

Topoisomerases, the ubiquitous enzymes involved in all DNA processes across the biological world, are targets for various anticancer and antimicrobial agents. In Entamoeba histolytica, the causative agent of amebiasis, we found one of seven unexplored putative topoisomerases to be highly upregulated during heat shock and oxidative stress, and also during the late hours of encystation. Further analysis revealed the upregulated enzyme to be a eukaryotic type IIA topoisomerase (TopoII) with demonstrable activity in vitro. This enzyme is localized to newly forming nuclei during encystation. Gene silencing of the TopoII reduces viability and encystation efficiency. Notable susceptibility of Entamoeba TopoII to prokaryotic topoisomerase inhibitors opens up the possibility for exploring this enzyme as a new antiamoebic target.


Assuntos
Amebicidas/farmacologia , DNA Topoisomerases Tipo II/metabolismo , Sistemas de Liberação de Medicamentos , Entamoeba histolytica/enzimologia , Resposta ao Choque Térmico , Estresse Oxidativo , Proteínas de Protozoários , Inibidores da Topoisomerase II/farmacologia , Proteínas de Protozoários/antagonistas & inibidores , Proteínas de Protozoários/metabolismo
3.
Mol Biochem Parasitol ; 220: 19-27, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29331577

RESUMO

Phosphorylation is an important post-translational modification of proteins and is involved in the regulation of a variety of cellular events. The proteome of Entamoeba invadens, the reptilian counterpart of Entamoeba histolytica consists of an overwhelming number of putative protein kinases, and some may have a role to play in Entamoeba encystation. In this study, we have identified a novel protein kinase named as EiCSpk (Entamoeba invadenscyst specific protein kinase) which expressed almost exclusively during encystation. It is an active Protein kinase C with a characteristic substrate phosphorylation and auto-phosphorylation property. Gene silencing study has unveiled its role as a regulator of chitin synthesis through transcriptional activation of the chitin synthesis pathway genes along with glycogen phosphorylases that are involved in the influx of glucose from glycogen breakdown for chitin synthesis.


Assuntos
Quitina/biossíntese , Entamoeba/enzimologia , Entamoeba/metabolismo , Proteína Quinase C/metabolismo , Vias Biossintéticas/genética , Entamoeba/genética , Inativação Gênica , Glicogênio Fosforilase/metabolismo , Proteína Quinase C/genética , Ativação Transcricional
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