Streptococcus agalactiae (group B streptococci (GBS)) is an important infections agent in newborns associated with maternal vaginal colonization. Intrapartum antibiotic prophylaxis in GBS-colonized pregnant women has led to a significant reduction in the incidence of early neonatal infection in various geographic regions. However, this strategy may lead to resistance selecting among GBS, indicating the need for new alternatives to prevent bacterial transmission and even to treat GBS infections. This study reported for the first time the effect of eugenol on GBS isolated from colonized women, alone and in combination with silver nanoparticles produced by Fusarium oxysporum (AgNPbio). Eugenol showed a bactericidal effect against planktonic cells of all GBS strains, and this effect appeared to be time-dependent as judged by the time-kill curves and viability analysis. Combination of eugenol with AgNPbio resulted in a strong synergistic activity, significantly reducing the minimum inhibitory concentration values of both compounds. Scanning and transmission electron microscopy revealed fragmented cells and changes in bacterial morphology after incubation with eugenol. In addition, eugenol inhibited the viability of sessile cells during biofilm formation and in mature biofilms. These results indicate the potential of eugenol as an alternative for controlling GBS infections.
Trichophyton rubrum and Trichophyton mentagrophytes complex, or Trichophyton spp. are the main etiologic agents of dermatophytosis, whose treatment is limited by the high cost of antifungal treatments, their various side effects, and the emergence of resistance amongst these species. This study evaluated the in vitro antidermatophytic activity of 23 crude extracts from nine plant species of semiarid vegetation (caatinga) found in Brazil. The extracts were tested at concentrations ranging from 1.95 to 1,000.0 mg/mL by broth microdilution assay against the reference strains T. rubrum ATCC 28189 and T. mentagrophytesATCC 11481, and 33 clinical isolates of dermatophytes. All plants showed a fungicidal effect against both fungal species, with MIC/MFC values of the active extracts ranging from 15.6 to 250.0 µg/mL. Selected extracts of Eugenia uniflora (AcE), Libidibia ferrea (AE), and Persea americana (AcE) also exhibited a fungicidal effect against all clinical isolates of T. rubrum and T. mentagrophytes complex. This is the first report of the antifungal activity of Schinus terebinthifolius, Piptadenia colubrina, Parapiptadenia rigida, Mimosa ophthalmocentra, and Persea americana against both dermatophyte species.
These results indicate the potential of copaiba oil, alone or in combination with AgNPbio, for the development of new alternative strategies for controlling GBS infections.
<p class="MsoNormal" style="text-align: justify;"><em></em></p><!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <w:Zoom>0</w:Zoom> <w:TrackMoves /> <w:TrackFormatting /> <w:HyphenationZone>21</w:HyphenationZone> <w:PunctuationKerning /> <w:ValidateAgainstSchemas /> <w:SaveIfXMLInvalid>false</w:SaveIfXMLInvalid> <w:IgnoreMixedContent>false</w:IgnoreMixedContent> <w:AlwaysShowPlaceholderText>false</w:AlwaysShowPlaceholderText> <w:DoNotPromoteQF /> <w:LidThemeOther>PT-BR</w:LidThemeOther> <w:LidThemeAsian>X-NONE</w:LidThemeAsian> <w:LidThemeComplexScript>X-NONE</w:LidThemeComplexScript> <w:Compatibility> <w:BreakWrappedTables /> <w:SnapToGridInCell /> <w:WrapTextWithPunct /> <w:UseAsianBreakRules /> <w:DontGrowAutofit /> <w:SplitPgBreakAndParaMark /> <w:DontVertAlignCellWithSp /> <w:DontBreakConstrainedForcedTables /> <w:DontVertAlignInTxbx /> <w:Word11KerningPairs /> <w:CachedColBalance /> </w:Compatibility> <w:BrowserLevel>MicrosoftInternetExplorer4</w:BrowserLevel> <m:mathPr> <m:mathFont m:val="Cambria Math" /> <m:brkBin m:val="before" /> <m:brkBinSub m:val=" " /> <m:smallFrac m:val="off" /> <m:dispDef /> <m:lMargin m:val="0" /> <m:rMargin m:val="0" /> <m:defJc m:val="centerGroup" /> <m:wrapIndent m:val="1440" /> <m:intLim m:val="subSup" /> <m:naryLim m:val="undOvr" /> </m:mathPr></w:WordDocument> </xml><![endif]--> <p class="MsoNormal" style="margin-bottom: .0001pt; text-align: justify; line-height: normal; mso-layout-grid-align: none; text-autospace: none;"><strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Bold;">Objetivo: </span></strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">Descrever o conhecimento atual dos principais mecanismos de resistência aos β-lactâmicos e glicopeptídeos apresentados por </span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">Staphylococcus aureus</span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">. </span><strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Bold;">Metodologia: </span></strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">Foram selecionados artigos de pesquisa originais e de revisão disponíveis nas bases de dados PubMed, Portal Periódicos CAPES e SCIELO. Os seguintes descritores foram utilizados: methicillin-resistant </span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">Staphylococcus aureus </span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">(MRSA), MRSA infection, vancomycin-intermediate </span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">S. aureus </span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">(VISA), heterogeneous-VISA (hVISA), staphylococcal </span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">cassete </span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">chromosome </span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">mec </span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">(SCC</span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">mec</span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">). A seleção dos artigos foi baseada em dois critérios: 1) publicação entre os anos 2000 e 2014 (até a data de submissão); 2) artigos cujos autores contribuíram com descobertas relevantes sobre os temas, independente do ano de publicação. </span><strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Bold;">Resultados: </span></strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">As consultas realizadas nos bancos de dados resultaram em 268 artigos, dos quais 59 foram utilizados para escrita dessa revisão. </span><strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Bold;">Conclusão: </span></strong><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">As comunidades, médica e científica, são constantemente desafiadas com a emergência de bactérias resistentes aos antimicrobianos. MRSA continua sendo um grande problema de saúde pública no mundo todo. Resistência aos glicopeptídeos (vancomicina e teicoplanina), uma das últimas escolhas para o tratamento intravenoso de infecções causadas por cepas de MRSA também tem sido descrita. A partir deste novo cenário, observou-se o surgimento de VRSA (</span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">vancomycin-resistant S. aureus</span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">), VISA (</span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">vancomycin-intermediate S. aureus</span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">) e hVISA (</span><em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri-Italic;">heterogeneous</span></em><span style="font-size: 8.0pt; mso-bidi-font-family: Calibri;">-VISA). Esses dados indicam a necessidade urgente de adoção de métodos mais sensíveis e rigorosos para detecção dessas cepas no laboratório de microbiologia clínica. 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