year 10, Issue 6 (January - February 2017)                   Iran J Med Microbiol 2017, 10(6): 25-33 | Back to browse issues page

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Hashemi Karoui S Z, Kasra Kermanshahi R, Fatholahzadeh H, Gharavi S. Isolation and identification of resistant bacteria from dental clinic and evaluation of biofilm formation by them. Iran J Med Microbiol 2017; 10 (6) :25-33
URL: http://ijmm.ir/article-1-538-en.html
1- , s.hashemii@yahoo.com
Abstract:   (10208 Views)

Background and Aim: Surface bacterial contamination has been shown to be a potential source of cross-infection. The aim of this study was to identify resistant bacterial isolates in the dental clinic before and after disinfection and evaluation of biofilm formation by them.

Materials and Methods: Sampling was performed at a dental clinic in Isfahan, Iran, on 2014. Samples were obtained by using swab and settle plate method. In the firs method, sterile swabs were used to sample of dental instrument and unit chair surface before and after disinfection, then swabs were transferred to TSB media (60 tubes). In the second method, air monitoring was carried out by settling blood agar and nutrient agar plates at the certain distance from the patient for 1 hour (24 plates). Then these samples incubated aerobically for 2 days at 37°C. Isolates were identified to species level with morphological and biochemical features and 16S ribosomal RNA gene sequencing. In addition, the strength of biofilm formation by isolates was measured by using microtiter plate method.

Results: Most of these isolates were spore-forming Bacillus species and environmental Staphylococcus species. On the basis of the strength of biofilm formation, the most important identified bacteria were Staphylococcus xylosus and Bacillus safensis.

Conclusions: Bacteria that are able to form biofilm, can survive after disinfection of dental instruments and can enhance the risk of infection in dental practice by providing a surface for colonization of pathogens.

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Type of Study: Original Research Article | Subject: Nosocomial infections
Received: 2016/03/16 | Accepted: 2016/07/25 | ePublished: 2016/10/17

References
1. Andrews N, Brandon-Kelsch N. Current dental surface disinfection protocols and a review of the new one minute surface disinfectants CaviCide1 and CaviWipes1. Inside Dent Assist. 2013; 9(3):46-47 [Article]
2. Valian A, Shahbazi R, Farshidnia S, Tabatabaee F. Evaluation of the Bacterial Contamination of Dental Units in Restorative and Peridontics Departments of Dental School of ShahidBeheshti University of Medical Sciences. J Mash Dent Sch. 2014;37(4): 345-56. [In Persian] [Article]
3. Azari RM, Ghadjari A, MassoudiNejad MR, FaghihNasiree N. Airborne microbial contamination of dental units. Tanaffos. 2008;7(2):54-57. [Article]
4. Taheri J, BakianianVaziri P, Fallah F, NikKerdar N. Assessment of the efficacy of BIB forte in disinfection of dental instruments. J Dent Sch. 2010; 27 (4):179-186 [In Persian] [Article]
5. Ghosh S, Mallick SK. Microbial biofilm: contamination in dental chair unit. Ind Med Gaz. 2012; 145(10):383-387.
6. Motta RH, Ramacciato JC, Groppo FC, Pacheco Ade B, de Mattos-Filho TR. Environmental contamination before, during, and after dental treatment. Am J Dent. 2005;18(5):340-4. [PubMed]
7. Napoli C, Marcotrigiano V, Teresa Montagna M. Air sampling procedures to evaluate microbial contamination: a comparison between active and passive methods in operating theatres. BMC Public Health. 2012; 12:594. [PubMed]
8. Holt, J.G, Krieg, N.R. Bergey's Manual of Determinative Bacteriology. 9th ed .Philadelphia: The Williams & Wilkins Co, Baltimore; 2009. [Article]
9. Kasra-Kermanshahi R, Kazemi MJ, Taherzadeh M. Laboratory exercises in microbiology with safety precaution and culture specific and fastidious bacteria. 1st ed. Yazd: Islamic Azad university; 1389. p.254-255. [In Persian]
10. Cassat JE, Lee CY, Smeltzer MS. Investigation of Biofilm Formation in Clinical Isolates of Staphylococcus aureus. Methods Mol Biol. 2007; 391:127–144. [PubMed]
11. Aminnezhad S, Kasra-Kermanshahi R. Antibiofilm activity of cell-free supernatant from Lactobacillus casei in Pseudomonas aeruginosa. KAUMS Journal(FEYZ). 2014; 18 (1):30-37. [In Persian] [Article]
12. Stepanoic S, Vukoic D, Dakic I, Branislava S, Svabic-Vlahovic M. A modified microtiter-plate test for quantification of Staphylococcal biofilm formation. J Microbiol Methods. 2000; 40(2):175-179. [PubMed]
13. Klindworth A, Pruesse E, Schweer T, Peplies J, Quast C, Horn M, Oliver Glöckner F. Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucl.Acids Res(NAR). 2013; 41(1): e1. [PubMed]
14. Dordet-Frisoni E, Dorchies G, De Araujo C, Talon R, Leroy S. Genomic diversity in Staphylococcus xylosus. Appl Environ Microbiol. 2007; 73(22):7199–7209. [Article]
15. Azih A, Enabulele I. Species distribution and virulence factors of coagulase negative Staphylococci isolated from clinical samples from the University of benin teaching hospital. JNSR. 2013; 3(9):38-43. [Article]
16. Al-Mathkhury HJF, Flaih MT, Al-Ghrairy Z KA. Pathological study on Staphylococcus xylosus isolated from patients with urinary tract infection. JNUS. 2008; 11(2):123-130. [Article]
17. Laborda PR, Fonseca FSA, Angolini CFF, Oliveira VM, Souza AP, Marsaioli AJ. Genome sequence of Bacillus safensis CFA06, isolated from biodegraded petroleum in Brazil. GenomeA. 2014; 2 (4). [PubMed]
18. Vela J, Hildebrandt K, Metcalfe A, Rempel H, BittmanSh, Topp E, et al. Characterization of Staphylococcus xylosus isolated from broiler chicken barn bioaerosol. PSJ. 2012; 91(12):3003-3012. [PubMed]
19. Jain K, Parida Sh, Mangwani N, R Dash H, Das S. Isolation and characterization of biofilm-forming bacteria and associated extracellular polymeric substances from oral cavity. Ann Microbiol. 2013; 63(4):1553-1562. [Article]

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