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Snapshot of resistance and virulence features in ESCAPE strains frequently isolated from surgical wound infections in a Romanian hospital Cover

Snapshot of resistance and virulence features in ESCAPE strains frequently isolated from surgical wound infections in a Romanian hospital

Open Access
|May 2022

References

  1. 1. Sattar F, Sattar Z, Zaman M, Akbar S. Frequency of Post-operative Surgical Site Infections in a Tertiary Care Hospital in Abbottabad, Pakistan. Cureus. 2019;11(3):e4243. DOI: 10.7759/cureus.424310.7759/cureus.4243651661231131166
  2. 2. Călina D, Docea AO, Rosu L, Zlatian O, Rosu AF, Anghelina F, et. al. Antimicrobial resistance development following surgical site infections. Mol Med Rep. 2017;15(2):681-688. DOI: 10.3892/mmr.2016.603410.3892/mmr.2016.6034536485727959419
  3. 3. Mezemir R, Seid A, Gishu T, Demas T, Gize A. Prevalence and root causes of surgical site infections at an academic trauma and burn center in Ethiopia: a cross-sectional study. Patient Saf Surg. 2020;14(3):46. DOI: 10.1186/s13037-019-0229-x10.1186/s13037-019-0229-x694578831921353
  4. 4. Menz BD, Charani E, Gordon DL, Leather AJM, Moonesinghe SR, Phillips CJ. Surgical Antibiotic Prophylaxis in an Era of Antibiotic Resistance: Common Resistant Bacteria and Wider Considerations for Practice. Infect Drug Resist. 2021;7;14:5235-5252. DOI: 10.2147/IDR.S31978010.2147/IDR.S319780866588734908856
  5. 5. Bediako-Bowan AAA, Kurtzhals JAL, Mølbak K, Labi AK, Owusu E, Newman MJ. High rates of multi-drug resistant gram-negative organisms associated with surgical site infections in a teaching hospital in Ghana. BMC Infect Dis. 2020;20:890. DOI: 10.1186/s12879-020-05631-110.1186/s12879-020-05631-1768998233238903
  6. 6 Berceanu Văduva D, Moldovan R, Dumitraşcu V, Muntean D, Bădiţoiu L, Licker M, et. al. [Incidence and sensitivity to antibiotics of germs isolated from surgical wound infections]. Bacteriol Virusol Parazitol Epidemiol. 2003;48(2-3):123-9. [Romanian].
  7. 7. Iskandar K, Sartelli M, Tabbal M, Ansaloni L, Baiocchi GL, Catena F, et. al. Highlighting the gaps in quantifying the economic burden of surgical site infections associated with antimicrobial-resistant bacteria. World J Emerg Surg. 2019;14:50. DOI: 10.1186/s13017-019-0266-x10.1186/s13017-019-0266-x686873531832084
  8. 8. Dhar Y, Han Y. Current developments in biofilm treatments: Wound and implant infections. Eng Regen. 2020;1:64-75. DOI: 10.1016/j.engreg.2020.07.00310.1016/j.engreg.2020.07.003
  9. 9. Barlean MC, Balcos C, Bobu LI, Cretu CI, Platon AL, Stupu A, et. al. Microbiological Evaluation of Surgical Site Infections in the Clinic of Oral and Maxillofacial Surgery of the Sf.Spiridon Clinical Hospital in Iasi, Romania. Rev. Chim.[internet]. 2019;70(11):4077-4082. DOI: 10.37358/RC.19.11.770510.37358/RC.19.11.7705
  10. 10. Mihai MM, Preda M, Lungu I, Gestal MC, Popa MI, Holban AM. Nanocoatings for Chronic Wound Repair-Modulation of Microbial Colonization and Bio-film Formation. Int J Mol Sci. 2018;19(4):1179. DOI: 10.3390/ijms1904117910.3390/ijms19041179597935329649179
  11. 11. Mihai MM, Holban AM, Giurcăneanu C, Popa LG, Buzea M, Filipov M,et. al. Identification and phenotypic characterization of the most frequent bacterial etiologies in chronic skin ulcers. Rom J Morphol Embryol. 2014;55(4):1401-8.
  12. 12. Gheorghe I, Tatu AL, Lupu I, Thamer O, Cotar AI, Pircalabioru GG, et. al. Molecular characterization of virulence and resistance features in Staphylococcus aureus clinical strains isolated from cutaneous lesions in patients with drug adverse reactions. Rom Biotech Lett. 2017;22(1):12321-7.
  13. 13. Czobor I, Gheorghe I, Banu O, Velican A, Lazăr V, Mihăescu G, et. al. ESBL genes in Multi Drug Resistant Gram negative strains isolated in a one year survey from an Intensive Care Unit in Bucharest, Romania. Rom Biotech Lett. 2014;19(4):9553-60.
  14. 14. Potron A, Poirel L, Bussy F, Nordmann P. Occurrence of the carbapenem-hydrolyzing β-lactamase gene bla-OXA-48 in the environment in Morocco. Antimicrob Agents Chemother. 2011;55(11):5413-4. DOI: 10.1128/AAC.05120-1110.1128/AAC.05120-11319504521876064
  15. 15. Handal R, Qunibi L, Sahouri I, Juhari M, Dawodi R, Marzouqa H, et al. Characterization of carbapenem-resistant Acinetobacter baumannii strains isolated from hospitalized patients in Palestine. Int J Microbiol. 2017;2017: 8012104. DOI: 10.1155/2017/801210410.1155/2017/8012104554950128814955
  16. 16. Cattoir V, Poirel L, Rotimi V, Soussy CJ, Nordmann P. Multiplex PCR for detection of plasmid-mediated quinolone resistance qnr genes in ESBL-producing enterobacterial isolates. J Antimicrob Chemother. 2007;60(2):394-7. DOI: 10.1093/jac/dkm20410.1093/jac/dkm20417561500
  17. 17. Martineau F, Picard FJ, Lansac N, Ménard C, Roy PH, Ouellette M, et al. Correlation between the Resistance Genotype Determined by Multiplex PCR Assays and the Antibiotic Susceptibility Patterns of Staphylococcus aureus and Staphylococcus epidermidis. Antimicrob Agents Chemother. 2000;44(2):231-8. DOI: 10.1128/AAC.44.2.231-238.200010.1128/AAC.44.2.231-238.20008966310639342
  18. 18. Strommenger B, Kettlitz C, Werner G, Witte W. Multiplex PCR assay for simultaneous detection of nine clinically relevant antibiotic resistance genes in Staphylococcus aureus. J Clin Microbiol. 2003;41(9):4089-94. DOI: 10.1128/JCM.41.9.4089-4094.200310.1128/JCM.41.9.4089-4094.200319380812958230
  19. 19. Zhang K, McClure JA, Elsayed S, Louie T, Conly JM. Novel multiplex PCR assay for characterization and concomitant subtyping of staphylococcal cassette chromosome mec types I to V in methicillin-resistant Staphylococcus aureus. J Clin Microbiol. 2005;43(10):5026-33. DOI: 10.1128/JCM.43.10.5026-5033.200510.1128/JCM.43.10.5026-5033.2005124847116207957
  20. 20. Milheiriço C, Oliveira DC, de Lencastre H. Update to the multiplex PCR strategy for assignment of mec element types in Staphylococcus aureus. Antimicrob Agents Chemother. 2007;51(9):3374-7. DOI: 10.1128/AAC.00275-0710.1128/AAC.00275-07204319817576837
  21. 21. Coffey BM, Anderson GG. Biofilm formation in the 96-well microtiter plate. Methods Mol Biol. 2014;1149:631-41. DOI: 10.1007/978-1-4939-0473-0_4810.1007/978-1-4939-0473-0_4824818938
  22. 22. Holban AM, Cotar AI, Chifiriuc MC, Bleotu C, Banu O, Lazar V. Variation of virulence profiles in some Staphylococcus aureus and Pseudomonas aeruginosa stains isolated from different clinical patients. Afr J Microbiol Res. 2013;7(27):3453-60.
  23. 23. Bleotu C, Chifiriuc M, Dracea O, Iordache C, Delcaru C, Lazar V. In vitro modulation of adherence and invasion ability of enteroinvasive Escherichia coli by different viruses. Int J Appl Biol Pharm Technol. 2010;1(3):1359-63.
  24. 24. Mihai MM, Holban AM, Giurcăneanu C, Popa LG, Buzea M, Filipov M, et. al. Identification and phenotypic characterization of the most frequent bacterial etiologies in chronic skin ulcers. Rom J Morphol Embryol. 2014;55(4):1401-8.
  25. 25. Magiorakos AP, Srinivasan A, Carey R, Carmeli Y, Falagas M, Giske C, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268-81. DOI: 10.1111/j.1469-0691.2011.03570.x10.1111/j.1469-0691.2011.03570.x21793988
  26. 26. Sadik O, Ditu LM, Gheorghe I, Holban AM, Curutiu C, Parcalabioru GG, et al. Phenotypic and genotypic evaluation of adherence and biofilm development in Candida albicans respiratory tract isolates from hospitalized patients. Rev Romana Med Lab. 2019;27(1):73-83. DOI: 10.2478/rrlm-2019-000710.2478/rrlm-2019-0007
  27. 27. Li X, Sun L, Zhang P, Wang Y. Novel Approaches to Combat Medical Device-Associated BioFilms. Coatings. 2021; 11:294. DOI: 10.3390/coatings1103029410.3390/coatings11030294
  28. 28. Gonçalves TG, Timm CD. Bioflm production by coagulase-negative Staphylococcus: a review. Arq. Inst. Biol. 2020. 87:1-9,e1382018. DOI: 10.1590/1808-165700138201810.1590/1808-1657001382018
  29. 29. Roy S, Santra S, Das A, Dixith S, Sinha M, Ghatak S, et al. Staphylococcus aureus Biofilm Infection Compromises Wound Healing by Causing Deficiencies in Granulation Tissue Collagen. Ann Surg. 2020; 271(6):1174-85. DOI: 10.1097/SLA.000000000000305310.1097/SLA.0000000000003053706584030614873
  30. 30. Bjarnsholt T, Ciofu O, Molin S, Givskov M, Høiby N. Applying insights from biofilm biology to drug development-can a new approach be developed? Nat Rev Drug Discov. 2013;12(10):791-808. DOI: 10.1038/nrd400010.1038/nrd400024080700
  31. 31. Sun L, Chen Y, Wang D, Wang H, Wu D, Shi K, et al. Surgical site infections caused by highly virulent methicillin-resistant Staphylococcus aureus sequence type 398, China. Emerg Inf Dis. 2019;25(1):157. DOI: 10.3201/eid2501.17186210.3201/eid2501.171862630260930561317
  32. 32. Duman Y, Sevimli R. Investigation of the presence of pantone-valentine leukocidin in Staphylococcus aureus strains isolated from orthopedic surgical site infections. Mikrobiyol bul. 2018;52(4):340-7. DOI: 10.5578/mb.6732810.5578/mb.6732830522420
  33. 33 Agyepong N, Govinden U, Owusu-Ofori A, Essack SY. Multidrug-resistant Gram-negative bacterial infections in a teaching hospital in Ghana. Antimicro Res Infect Control. 2018;7(1):37. DOI: 10.1186/s13756-018-0324-210.1186/s13756-018-0324-2584514429541448
  34. 34. Pochhammer J, Kramer A, Schaeffer M. [Enterococci and surgical site infections : Causal agent or harmless commensals?] Chirurg. 2017;88(5):377-84. [German]. DOI: 10.1007/s00104-017-0388-110.1007/s00104-017-0388-128233041
  35. 35. Kamble E, Pardesi K. Antibiotic Tolerance in Biofilm and Stationary-Phase Planktonic Cells of Staphylococcus aureus. Microb Drug Res. 2020; 27(1):3-12. DOI: 10.1089/mdr.2019.042510.1089/mdr.2019.042532013708
  36. 36. Hadjieva NS, Philipova I, Petrov M, Velinova V, Dicheva V. Surgical site infections in “Queen Joanna-ISUL” University Hospital - etiological structure and antibiotic resistance, a part of INICC project, Int J Infect Dis. 2012;16(S1):E372. DOI: 10.1016/j.ijid.2012.05.47510.1016/j.ijid.2012.05.475
  37. 37. Salmanov AG, Dyndar OA, Vdovychenko YP, Nykoniuk TR, Maidanny IVK, Chorna OO, et.al. Surgical Site Infections and Antimicrobial Resistance in Kyiv City Hospitals, Ukraine. Wiad Lek. 2019;72(5 cz 1):760-764. DOI: 10.36740/WLek20190510710.36740/WLek201905107
DOI: https://doi.org/10.2478/rrlm-2022-0014 | Journal eISSN: 2284-5623 | Journal ISSN: 1841-6624
Language: English
Page range: 215 - 226
Submitted on: May 6, 2021
Accepted on: Mar 12, 2022
Published on: May 9, 2022
Published by: Romanian Association of Laboratory Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2022 Sajjad Mohsin I Rayyif, Wathek N. Alwan, Hamzah B. Mohammed, Ilda Czobor Barbu, Alina M. Holban, Irina Gheorghe, Otilia Banu, Omar S. Shalal, Mariana C. Chifiriuc, Grigore Mihaescu, published by Romanian Association of Laboratory Medicine
This work is licensed under the Creative Commons Attribution 4.0 License.