• This record comes from PubMed

Isolation of Enterococcus faecalis pathogenic genes isolated from oral infection by the effect of ionic liquids based on amino acid and its expression by real-time PCR

. 2022 Oct ; 67 (5) : 777-784. [epub] 20220519

Language English Country United States Media print-electronic

Document type Journal Article

Links

PubMed 35588041
DOI 10.1007/s12223-022-00972-7
PII: 10.1007/s12223-022-00972-7
Knihovny.cz E-resources

Enterococcus faecalis is an important factor in nosocomial infections. The aim of this study was the isolation of the pathogenic genes of Enterococcus faecalis in mouth infection and the study of the expression of these genes by real-time PCR. In this study, 60 isolates of E. faecalis were isolated from oral infections. The presence and frequency of cyl, hyl, and esp genes and their expression by ionic liquid were evaluated using real-time PCR. MIC was determined by broth dilution method and biofilm production was measured, then biofilm inhibition ability and cytotoxicity test were performed by MTT method. The esp, cyl, and hyl genes were observed in 10, 11, and 2 isolates, respectively. cyl gene with the highest frequency of expression in the treated group was reduced by 1.14% under the influence of ionic liquid with methionine base. The results of MIC and Sub MIC concentrations were obtained with the effect of ionic liquid including 125 and 225 µg/mL, respectively. Amino-acid-based ionic liquids can also reduce biofilm production at sub-MIC concentrations (P < 0.05), and changes in cytotoxicity at different concentrations and over time are significant (P-value < 0.001). E. faecalis strains are genetically diverse and this indicates the polyclonal prevalence of strains in clinical specimens. Combination treatment of ionic liquid with common antimicrobial drugs has good antibacterial effects against Enterococcus species, and ionic liquid with a minimum dose can be a good alternative to single-drug treatment of Enterococcus infections.

See more in PubMed

Aas JA, Paster BJ, Stokes LN, Olsen I, Dewhirst FE (2005) Defining the normal bacterial flora of the oral cavity. J Clin Microbiol 43:5721–5732. https://doi.org/10.1128/JCM.43.11.5721-5732.2005 PubMed DOI PMC

Andersson DI, Balaban NQ, Baquero F, Courvalin P, Glaser P, Gophna U, Kishony R, Molin S, Tønjum T (2020) Antibiotic resistance: turning evolutionary principles into clinical reality. FEMS Microbiol Rev 44:171–188. https://doi.org/10.1093/femsre/fuaa001 PubMed DOI

Bakis E, van den Bruinhorst A, Pison L, Palazzo I, Chang T, Kjellberg M, Welton T (2021) Mixing divalent ionic liquids: effects of charge and side-chains. Phys Chem Chem Phys 8:4624–4635.  https://doi.org/10.1039/D1CP00208B

Biendo M, Adjide C, Castelain S, Belmekki M, Rousseau F, Slama M, Ganry O, Schmit J, Eb F (2010) Molecular characterization of glycopeptide-resistant enterococci from hospitals of the picardy region (France). Int J Microbiol 2010:150464. https://doi.org/10.1155/2010/150464 PubMed DOI PMC

Chomicz L, Szubińska D, Piekarczyk J, Wojtowicz A, Piekarczyk B, Starościak B, Fiedor P (2004) Occurrence of oral subclinical infections in insulin treated diabetics. Wiad Parazytol 50:177–180 PubMed

de Sousa ESO, Pinheiro SB, Cortez ACA, Cruz KS, de Souza ÉS, Melhem MdSC, Frickmann H, de Souza JVB (2021) Modifications of antifungal sensibility testing as suggested by CLSI document M27–A4: proposal for using different culture medium and buffer. Diagn Microbiol Infect Dis 101:115488. https://doi.org/10.1016/j.diagmicrobio.2021.115488 PubMed DOI

Duman AN, Ozturk I, Tunçel A, Ocakoglu K, Colak SG, Hoşgör-Limoncu M, Yurt F (2019) Synthesis of new water-soluble ionic liquids and their antibacterial profile against gram-positive and gram-negative bacteria. Heliyon 5:e02607. https://doi.org/10.1016/j.heliyon.2019.e02607 PubMed DOI PMC

Ferraz R, Teixeira V, Rodrigues D, Fernandes R, Prudêncio C, Noronha JP, Petrovski Ž, Branco LC (2014) Antibacterial activity of ionic liquids based on ampicillin against resistant bacteria. RSC Adv 4:4301–4307. https://doi.org/10.1039/C3RA44286A DOI

Ghasemi A, Moniri R, Khorshidi A, Musavi GA (2009) The survey of virulence factors of Enterococcus faecalis isolated from urine samples. Iranian J Med Microbiol 2:53–58

Gindri IM, Siddiqui DA, Bhardwaj P, Rodriguez LC, Palmer KL, Frizzo CP, Martins MA, Rodrigues DC (2014) Dicationic imidazolium-based ionic liquids: a new strategy for non-toxic and antimicrobial materials. RSC Adv 4:62594–62602. https://doi.org/10.1039/C4RA09906K DOI

Jans C, Meile L, Lacroix C, Stevens MJ (2015) Genomics, evolution, and molecular epidemiology of the Streptococcus bovis/Streptococcus equinus complex (SBSEC). Infect Genet Evol 33:419–436. https://doi.org/10.1016/j.meegid.2014.09.017 PubMed DOI

Komiyama EY, Lepesqueur LSS, Yassuda CG, Samaranayake LP, Parahitiyawa NB, Balducci I, Koga-Ito CY (2016) Enterococcus species in the oral cavity: prevalence, virulence factors and antimicrobial susceptibility. PLoS ONE 11:e0163001. https://doi.org/10.1371/journal.pone.0163001 PubMed DOI PMC

Leavis H, Top J, Shankar N, Borgen K, Bonten M, van Embden J, Willems RJ (2004) A novel putative enterococcal pathogenicity island linked to the esp virulence gene of Enterococcus faecium and associated with epidemicity. J Bacteriol 186:672–682. https://doi.org/10.1128/JB.186.3.672-682.2004 PubMed DOI PMC

Lewis CM, Zervos M (1990) Clinical manifestations of enterococcal infection. Eur J Clin Microbiol Infect Dis 9:111–117. https://doi.org/10.1007/BF01963635 PubMed DOI

Mundy LM, Sahm DF, Gilmore M (2000) Relationships between enterococcal virulence and antimicrobial resistance. Clin Microbiol Rev 4:513–522. https://doi.org/10.1128/CMR.13.4.513 DOI

Najar Peerayeh S, Eslami M, Memariani M, Siadat SD (2013) High prevalence of blaCTX-M-1 group extended-spectrum β-lactamase genes in Escherichia coli isolates from Tehran. Jundishapur J Microbiol 6:7. https://doi.org/10.5812/jjm.6863 DOI

Najar Peerayeh S, Rostami E, Eslami M, Ahangarzadeh Rezaee M (2016) High frequency of extended-spectrum β-lactamase-producing Klebsiella pneumoniae and Escherichia coli isolates from male patients’ Urine. Arch Clin Infect Dis 11:2

Nezhad SK, Zenouz AT, Aghazadeh M, Kafil HS (2017) Strong antimicrobial activity of Hypericum perforatum L. against oral isolates of Lactobacillus spp. Cell Mol Biol 63:58–62. https://doi.org/10.14715/cmb/2017.63.11.11

O’Driscoll T, Crank CW (2015) Vancomycin-resistant enterococcal infections: epidemiology, clinical manifestations, and optimal management. Infect Drug Resist 8:217. https://doi.org/10.2147/IDR.S54125 PubMed DOI PMC

Pillay S, Zishiri OT, Adeleke MA (2018) Prevalence of virulence genes in Enterococcus species isolated from companion animals and livestock. Onderstepoort J Vet Res 85:1–8. https://hdl.handle.net/10520/EJC-fbdbae617

Pournaras S, Tsakris A, Palepou M-F, Papa A, Douboyas J, Antoniadis A, Woodford N (2000) Pheromone responses and high-level aminoglycoside resistance of conjugative plasmids of Enterococcus faecalis from Greece. J Antimicrob Chemother 46:1013–1016. https://doi.org/10.1093/jac/46.6.1013 PubMed DOI

Rasko DA, Sperandio V (2010) Anti-virulence strategies to combat bacteria-mediated disease. Nat Rev Drug Discov 9:117–128. https://doi.org/10.1038/nrd3013 PubMed DOI

Sava IG, Heikens E, Huebner J (2010) Pathogenesis and immunity in enterococcal infections. Clin Microbiol Infect 6:533–540. https://doi.org/10.1111/j.1469-0691.2010.03213.x DOI

Seno Y, Kariyama R, Mitsuhata R, Monden K, Kumon H (2005) Clinical implications of biofilm formation by Enterococcus faecalis in the urinary tract. Acta Med. Okayama 59:79–87. https://doi.org/10.18926/AMO/31979

Shahi F, Hamidi H, Khoshnood S, Mehdipour G, Dezfouli AA, Sheikh AF (2020) Virulence determinants and biofilm formation in clinical isolates of Enterococcus: a cross-sectional study. J Acute Dis 9:27. https://doi.org/10.4103/2221-6189.276079 DOI

Shafiei M, Ghasemian A, Eslami M, Nojoomi F, Rajabi-Vardanjani H (2019) Risk factors and control strategies for silicotuberculosis as an occupational disease. New Microbes New Infect 27:75–77. https://doi.org/10.1016/j.nmni.2018.11.002 PubMed DOI

Tanideh N, Ghafari V, Ebrahimi R, Habibagahi R, Koohi-Hosseinabadi O, Iraji A (2020) Effects of Calendula officinalis and Hypericum perforatum on antioxidant, anti-inflammatory, and histopathology indices of induced periodontitis in male rats. J Dent 21:314. https://doi.org/10.30476/DENTJODS.2020.83660.1056

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...