Abstract

The widespread irrational use of antibiotics in recent years has resulted in an increase in the detection of multi-resistant bacterial strains, particularly methicillin-resistant Staphylococcus aureus (MRSA). The use of natural derivatives such as flavonoids is postulated as one of the most promising avenues to solve this emerging public health problem. The objective of the present study is to characterize the antimicrobial activity of icariin, a flavonoid compound isolated from a variety of plants of the Epimedium genus, against human and animal clinical MRSA isolates. Our study found that icariin alone did not have any antimicrobial effect on S. aureus or MRSA clinical isolates. However, icariin enhanced the effect of amoxycillin-clavulanate or ampicillin, whereas no effect was seen when used in combination with vancomycin. Specifically, co-incubation of S. aureus with amoxycillin-clavulanate plus icariin resulted in an increased proportion of dead cells, suggesting that this flavonoid potentially increases antimicrobial activity when used in combination with the beta-lactam antibiotic amoxycillin-clavulanate. Furthermore, we demonstrate that co-incubation of S. aureus with AmoxyClav plus icariin resulted in increased membrane disruption and growth inhibition. This study demonstrates the potential utility of icariin in permitting lower antibiotic therapeutic doses in alignment with strategies to reduce the spread of antibiotic resistance. Further research is required to determine the optimum concentration of icariin and to define clinically relevant combinations of flavonoid and antibiotic.

Highlights

  • The widespread irrational use of antibiotics has resulted in recent years in an increase in the detection of multi-resistant bacterial strains in clinical settings all over the world

  • Our study found that the combination of icariin 1% (w/v) with AmoxyClav increased the effectiveness of the activity of the antibiotic by approximately 12% against human and animal clinical methicillin-resistant Staphylococcus aureus (MRSA) isolates

  • Antibiotic sensitivity increased by up to 27% in mecA+ isolates while we observed a decrease in sensitivity of up to 12% in mecC+ strains, suggesting that these genotypic differences may play a role in determining the effectiveness of icariin-specific enhancement in the treatment of MRSA clinical isolates

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Summary

Introduction

The widespread irrational use of antibiotics has resulted in recent years in an increase in the detection of multi-resistant bacterial strains in clinical settings all over the world. Staphylococcus spp. infections have become a pressing problem in clinical practice [1,2] due primarily to the elevated resistance to new and commonly prescribed antibiotics, leading to a shortfall of therapeutic arsenal to combat these infections. This is postulated to arise due to selective pressure imposed by therapeutic misuse and abuse of antibiotics [3]. Icnernetgraartdisotno iotsfp0o.t0e1nt%ialiannhtiimbiictreodbiathl perogpreorwtietsh, CoofnePy.eaectnale.sduespcritboed40th%at, thereb gtehsetiunsge oaf idcaorisien-adte0p.0e8n%d(ewn/tv)rienlhaitbioitns sthheipgro[2w2th]. oWf Paronpgioneitbaactle.ripuumbalcinsehseindvtihtrosuep aromat foton7y0l%s ,iwnhCile-3a csounbcsetnittruattieodn oicf a0.r0i1in% dinehribivitaedtivtheesgmrowaythroefpPr. eacsneenstupa tnoo4v0%el, tchlearsesbyof antiasguegngtesst(imngetahdicoislel-idne-preesnidsetnatnrteSla.taiounrsehuisp; [M22R].SWAa)n[6g]e. tTahl.espeusbulibshsetadntcheossewaerorme sahticown to b thsaugelefanoltnlsoy(slmsteeintrhiCcic-is3lilitsneu-broesfstiiptsuteatnenditcSiic.lalairunirin-eubdsi;neMrdivRianStgAiv)pe[sr6om].taTeyhineres2eparseu(sPbesnBttaPna2cnaeos;vwreeelsrcpelaosshnsosowifbnalnetotif-boMirnRdthStAeo antimi rethseisatlalonscteeriocfsiMteRofSpAen),icriellsinu-lbtiinndginignparonteiinnh2iab(iPtiBoPn2ao;frecseplolnwsiabllel fsoyrnththeeasnitsim[6ic]r.obial resistance of MRSA), resulting in an inhibition of cell wall synthesis [6]

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