Main Article Content

Abstract

Initially identified as a low-virulence opportunistic bacterium, Serratia marcescens has emerged as a significant pathogen, particularly in high-risk settings. Increasing reports of multidrug-resistant (MDR) and carbapenem-resistant (CR) isolates emphasise its role in healthcare-associated infections. Outbreaks have been documented, often linked to invasive devices, contaminated solutions, and lapses in infection prevention and control (IPC). While data from Southeast Asia remains limited, evidence suggests an upward trend. This narrative review summarises developments in S.marcescens resistance and therapeutic options. A PRISMA-informed search was conducted in ScienceDirect, PubMed and Google Scholar for English-language articles published between 2019 and 2025. Eligible studies included original research, surveillance reports, and case reports. Data were synthesised qualitatively. Published literature describes a global rise in resistant isolates. S.marcescens demonstrates intrinsic resistance to colistin, ampicillin, and first-generation cephalosporins, while also harbouring inducible AmpC β-lactamase. Acquisition of extended-spectrum β-lactamases (ESBLs) and carbapenemases further limits therapeutic options. Ceftazidime-avibactam (CZA) alone or in combination with aztreonam demonstrates efficacy against KPC-producing strains and metallo-β-lactamase producers. Cefiderocol, despite limited availability, has shown promising activity. In conclusion, the rising resistance of S.marcescens underscores the need for strengthened microbiological surveillance and antimicrobial stewardship. Future research should prioritise local resistance mechanisms and the optimisation of therapeutic strategies.

Keywords

Serratia marcescens Antimicrobial Resistance Carbapenem-resistant Therapeutic Options

Article Details

References

  1. Al-Kadmy IMS, Al-Saryi NA, Salman IMA, Garallah ET, Aziz SN, Al-Jubori SS, et al. Multidrug-resistant Serratia marcescens: A growing threat in Iraqi intensive care units. Gene Reports. 2025;39:102197. https://doi.org/10.1016/j.genrep.2025.102197
  2. Boldeanu MV, Mihăescu G, Popescu GA. Emerging role of Serratia marcescens in healthcare-associated infections: Epidemiology and clinical impact. Microorganisms. 2025;13(2):XXX–XXX.
  3. Chen W, Li Z, Zheng J, Wang D, Gao S, Zhou W, et al. A comprehensive analysis of the epidemiological and genomic characteristics of global Serratia marcescens. J Glob Antimicrob Resist. 2025;40:81–89. https://doi.org/10.1016/j.jgar.2024.11.013
  4. Cosimato I, Santella B, Rufolo S, Sabatini P, Galdiero M, Capunzo M, et al. Current epidemiological status and antibiotic resistance profile of Serratia marcescens. Antibiotics. 2024;13(4):323. https://doi.org/10.3390/antibiotics13040323
  5. Cruz TPPS, Azevedo FKSF, Pepato MA, Sousa ATHI, Rizzo PS, Souto FJD, et al. Outbreak of KPC-2-producing Serratia marcescens MDR in a tertiary hospital in the Midwest region, Brazil. Res Soc Dev. 2021;10(9):e45110918078. https://doi.org/10.33448/rsd-v10i9.18078
  6. Dyar OJ, Huttner B, Schouten J, Pulcini C. What is antimicrobial stewardship? Clin Microbiol Infect. 2017;23(11):793–798. https://doi.org/10.1016/j.cmi.2017.08.026
  7. Falcone M, Daikos GL, Tiseo G, Bassoulis D, Giordano C, Galfo V, et al. Efficacy of ceftazidime-avibactam plus aztreonam in patients with bloodstream infections caused by metallo-β-lactamase-producing Enterobacterales. Clin Infect Dis. 2020;72(11):1871–1878. https://doi.org/10.1093/cid/ciaa586
  8. Hu Y, Liu C, Shen H. Clinical characteristics and outcomes of Serratia marcescens infections in neonates: A multicenter analysis. Front Pediatr. 2025;13:XXXXX.
  9. Ismail BS, Toh HX, Seah JH, Tan KY, Lee LC, Tay YY, et al. Serratia marcescens outbreak at a neonatal intensive care unit in an acute care tertiary hospital in Singapore. J Hosp Infect. 2025;156:21–25. https://doi.org/10.1016/j.jhin.2024.10.002
  10. Ito A, Nishikawa T, Matsumoto S, Yoshizawa H, Sato T, Nakamura R, et al. Siderophore cephalosporin cefiderocol utilizes ferric iron transporters to penetrate Gram-negative bacteria. Antimicrob Agents Chemother. 2018;62(1):e01454-17. https://doi.org/10.1128/AAC.01454-17
  11. Overmeyer AJ, Prentice E, Brink A, Lennard K, Moodley C. The genomic characterization of carbapenem-resistant Serratia marcescens at a tertiary hospital in South Africa. JAC Antimicrob Resist. 2023;5(4):dlad089. https://doi.org/10.1093/jacamr/dlad089
  12. Papagianni M, Mylona E, Kostourou S, Kolokotroni C, Kounatidis D, Vallianou NG, et al. An outbreak of Serratia marcescens in a cardiothoracic surgery unit associated with an infected solution of pre-prepared syringes. Antibiotics. 2025;14(3):319. https://doi.org/10.3390/antibiotics14030319
  13. Papp-Wallace KM, Endimiani A, Taracila MA, Bonomo RA. Carbapenems: Past, present, and future. Antimicrob Agents Chemother. 2011;55(11):4943–4960. https://doi.org/10.1128/AAC.00296-11
  14. Ramirez MS, Tolmasky ME. Amikacin: Uses, resistance, and prospects for inhibition. Molecules. 2017;22(12):2267. https://doi.org/10.3390/molecules22122267
  15. Roberts JA, Abdul-Aziz MH, Davis JS, Dulhunty JM, Cotta MO, Myburgh J, et al. Continuous versus intermittent β-lactam infusion in severe sepsis: A meta-analysis. Lancet Infect Dis. 2014;14(7):681–691. https://doi.org/10.1016/S1473-3099(14)70788-3
  16. Ruan X, Gong Z, Zeng M, Zhong Z, Chen Y, Wei F, et al. Aztreonam acts as a synergist for ceftazidime-avibactam against carbapenem-resistant Enterobacteriaceae (CRE) of various carbapenemase phenotypes in Southwestern China. Infect Drug Resist. 2025;18:2243–2253. https://doi.org/10.2147/IDR.S523498
  17. Sannathimmappa MB, Nambiar V, Al Siyabi KHSH, Hussain AS, Shah YA, Marimuthu Y, et al. Antimicrobial resistance pattern, predisposing factors, and outcome of Serratia infection in patients treated at a secondary-care hospital in Oman: A 5-year retrospective study. Adv Biomed Res. 2024;13:101. https://doi.org/10.4103/abr.abr_381_23
  18. Shields RK, Nguyen MH, Chen L, Press EG, Kreiswirth BN, Clancy CJ. Ceftazidime-avibactam is superior to other treatment regimens against carbapenem-resistant Enterobacteriaceae. Antimicrob Agents Chemother. 2017;61(8):e00883-17. https://doi.org/10.1128/AAC.00883-17
  19. Taha R, Kader O, Shawky S, Rezk S. Ceftazidime-avibactam plus aztreonam synergistic combination tested against carbapenem-resistant Enterobacterales characterized phenotypically and genotypically: A glimmer of hope. Ann Clin Microbiol Antimicrob. 2023;22:21. https://doi.org/10.1186/s12941-023-00573-3
  20. Tamma PD, Aitken SL, Bonomo RA, Mathers AJ, van Duin D, Clancy CJ. Infectious Diseases Society of America guidance on treatment of AmpC β-lactamase–producing Enterobacterales. Clin Infect Dis. 2021;73(3):e106–e114. https://doi.org/10.1093/cid/ciaa1478
  21. Tavares-Carreon F, De Anda-Mora K, Rojas-Barrera IC, Andrade A. Serratia marcescens antibiotic resistance mechanisms of an opportunistic pathogen: A literature review. PeerJ. 2023;11:e14399. https://doi.org/10.7717/peerj.14399
  22. Tootla HD, Copelyn J, Botha A, Brink AJ, Eley B. Using ceftazidime-avibactam for persistent carbapenem-resistant Serratia marcescens infection highlights antimicrobial stewardship challenges. S Afr Med J. 2021;111(8):729–731. https://doi.org/10.7196/SAMJ.2021.v111i8.15762
  23. Wang Y, Wang J, Wang R, Cai Y. Resistance to ceftazidime-avibactam and underlying mechanisms. J Glob Antimicrob Resist. 2022;28:130–139. https://doi.org/10.1016/j.jgar.2021.12.019
  24. Yamano Y. In vitro activity of cefiderocol against a broad range of clinically important Gram-negative bacteria. Clin Infect Dis. 2019;69(Suppl 7):S544–S551. https://doi.org/10.1093/cid/ciz827
  25. Zhu H, Li F, Cao X, Zhang Y, Liu C, Chen Y, et al. Epidemiology, resistance profiles, and risk factors of multidrug- and carbapenem-resistant Serratia marcescens infections: A retrospective study of 242 cases. BMC Infect Dis. 2025;25(1):1105. https://doi.org/10.1186/s12879-025-11569-z