Screening a mushroom extract library for activity against Acinetobacter baumannii and Burkholderia cepacia and the identification of a compound with anti-Burkholderia activity 英文参考文献.docVIP
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Screening a mushroom extract library for activity against Acinetobacter baumannii and Burkholderia cepacia and the identification of a compound with anti-Burkholderia activity 英文参考文献
Schwanetal.AnnalsofClinicalMicrobiologyandAntimicrobials2010,9:4
/content/9/1/4
RESEARCH
OpenAccess
Screeningamushroomextractlibraryforactivity
againstAcinetobacterbaumanniiandBurkholderia
cepaciaandtheidentificationofacompound
withanti-Burkholderiaactivity
WilliamRSchwan1*,CraigDunek1,2,MichaelGebhardt1,KathleenEngelbrecht1,TiffanyKlett1,AaronMonte2,
JosephToce2,MarcRott1,ThomasJVolk3,JohnJLiPuma4,Xue-TingLiu2,RonaldMcKelvey2
Abstract
Background:AcinetobacterbaumanniiandspecieswithintheBurkholderiacepaciacomplex(BCC)aresignificant
opportunisticbacterialpathogensofhumans.Thesespeciesexhibitahighdegreeofantibioticresistance,and
someclinicalisolatesareresistanttoallcurrentlyavailableantimicrobialdrugsusedfortreatment.Thus,newdrugs
areneededtotreatinfectionsbythesespecies.MushroomscouldbeapotentialsourcefornewdrugstotreatA.
baumanniiandBCCinfections.
Methods:Theaimofthisstudywastoscreenalibraryofcrudeextractsfrom330wildmushroomsbydisk
diffusionassaysforantibacterialactivityagainstA.baumanniiandBurkholderiacepaciainthehopeofidentifyinga
novelnaturaldrugthatcouldbeusedtotreatinfectionscausedbythesespecies.Oncepositivehitswere
identified,theextractsweresubjectedtobioassay-guidedseparationstoisolateandidentifytheactivedrug
molecules.MICswereperformedtogaugetheinvitroactivityofthepurifiedcompounds.
Results:Onlythreecrudeextracts(0.9%)hadactivityagainstA.baumanniiandB.cepacia.Compoundsfromtwoof
theseextractshadMICsgreaterthan128μg/ml,andfurtheranalyseswerenotperformed.Fromthethirdextract,
preparedfromLeucopaxillusalbissimus,2-aminoquinoline(2-AQ)wasisolated.Thiscompoundexhibitedamodest
MICinvitroagainststrainsfromninedifferentBCCspecies,includingmulti-drugresistantclinicalisolates(MIC=8-
64μg/ml),andaweakMIC(128μg/ml)againstAbaumannii.TheIC50 againstamurinemonocytelinewas1.5mg/
ml.
Conclusion:Thesmallnumberofpositivehitsinthisstudysuggeststhatfindinganewdrugfrommushroomsto
treatGram-negativebacterialinfectionsmaybedifficult.Although2-AQwasidentifiedinonemushroom,andi
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