Evolution of carbapenem resistance in Klebsiella pneumoniae at Sahloul University Hospital
PDF (Français (France))

Keywords

Antibiotic Resistance
Klebsiella pneumoniae
carbapenemase
epidemiology

Categories

How to Cite

Dga, S., Azouzi, F., Ghali, H., Boughattas, S., Tilouche, L., Ketata, S. ., Ben Lamine, Y. ., Laatiri, H. ., & Trabelsi, A. . (2026). Evolution of carbapenem resistance in Klebsiella pneumoniae at Sahloul University Hospital. Revue Tunisienne De BIOLOGIE CLINIQUE, 33(2). Retrieved from https://rtbc.org.tn/ojs/index.php/rtbc/article/view/344

Abstract

Introduction : The emergence of carbapenem-resistant K. pneumoniae (CRKP) strains has become a critical public health issue. Our aim was to investigate the phenotypic characteristics and antibiotic resistance of CRKP strains.  

Materials and Methods :  It’s a descriptive retrospective study including CRKP strains isolated at the Microbiology laboratory of Sahloul Hospital between 2017 and 2021. Bacterial identification was performed using conventional methods and the Vitek2 system. Antibiotic susceptibility testing followed CA-SFM/EUCAST guidelines. Carbapenemase detection was performed using the Rosco phenotypic combined  disc test.

Results : A total of 335 CRKP strains were isolated, showing an overall increasing trend (p=0,03). Strains were mainly isolated from urine samples (45.4%), followed by blood cultures (18.5%). The general postoperative ward was the most affected (13.7%). Temporal distribution revealed a peak incidence during the hot and humid season (August-September). All strains were resistant to amoxicillin-clavulanic acid and piperacillin-tazobactam. Resistance rates to cefotaxime, ciprofloxacin, and gentamicin were 97%, 94.8%, and 71%, respectively. The lowest resistance rates were observed for fosfomycin (39.8%, n=99/249) and colistin (17.3%, n=13/75). Phenotypic study of carbapenem resistance showed co-dominance of OXA-48-producing strains (35%) and MBL-producing strains (35%).  

Conclusion: The spread of CRKP and the emergence of metallo-β-lactamase-producing strains at Sahloul University Hospital require the implementation of reliable control strategies to limit their transmission.

PDF (Français (France))

References

Références :

Bush K, Bradford PA. β-Lactams and β-Lactamase Inhibitors: An Overview. Cold Spring Harb Perspect Med. 2016;6(8):a025247.

Hawkey PM. The growing burden of antimicrobial resistance. J Antimicrob Chemother. 2008;62 Suppl 1:i1-9.

HCSP. Prévention de la transmission croisée des « Bactéries Hautement Résistantes aux antibiotiques émergentes » (BHRe) [Internet]. Rapport de l’HCSP. Paris: Haut Conseil de la Santé Publique; 2013 juill [cité 27 sept 2024]. Disponible sur: https://www.hcsp.fr/explore.cgi/avisrapportsdomaine?clefr=372

Patel G, Bonomo RA. “Stormy waters ahead”: global emergence of carbapenemases. Front Microbiol. 2013;4:48.

Xu L, Sun X, Ma X. Systematic review and meta-analysis of mortality of patients infected with carbapenem-resistant Klebsiella pneumoniae. Ann Clin Microbiol Antimicrob. 2017;16(1):18.

Pitout JDD, Nordmann P, Poirel L. Carbapenemase-Producing Klebsiella pneumoniae, a Key Pathogen Set for Global Nosocomial Dominance. Antimicrobial Agents and Chemotherapy. 2015;59(10):5873‑84.

L’Antibiorésistance en Tunisie (LART). Données de 2011 K. pneumoniae [Internet]. 2011 [cité 25 avr 2025]. Disponible sur: https://www.infectiologie.org.tn/pdf_ppt_docs/resistance/1544641973.pdf

L’Antibiorésistance en Tunisie (LART). Données de 2021 K. pneumoniae [Internet]. 2021 [cité 25 avr 2025]. Disponible sur: https://www.infectiologie.org.tn/pdf_ppt_docs/resistance/1714732452.pdf

ROSCO. Eurobio Scientific. [cité 10 avr 2024]. Les règles d’interprétation du test KPC, MBL AND OXA-48 Confirm KIT de ROSCO®. Disponible sur: https://rosco-diagnostica.com/wp-content/uploads/98006-98010-98015-Print-Insert20191-2023-ny-adresse.pdf

Abdeta A, Bitew A, Fentaw S, Tsige E, Assefa D, Lejisa T, et al. Phenotypic characterization of carbapenem non-susceptible gram-negative bacilli isolated from clinical specimens. PLOS ONE. 2021;16(12):e0256556.

Lin X chen, Li C li, Zhang S yang, Yang X feng, Jiang M. The Global and Regional Prevalence of Hospital-Acquired Carbapenem-Resistant Klebsiella pneumoniae Infection: A Systematic Review and Meta-analysis. Open Forum Infectious Diseases. 2024;11(2):ofad649.

Messaoudi A, Mansour W, Jaidane N, Chaouch C, Boujaâfar N, Bouallègue O. Epidemiology of resistance and phenotypic characterization of carbapenem resistance mechanisms in Klebsiella pneumoniae isolates at Sahloul University Hospital-Sousse, Tunisia. Afr Health Sci. 2019;19(2):2008‑20.

Modi C, Singh S, Pandya Y, Patel C, Patel R. Prevalence of Carbapenem Resistant Enterobacteriaceae in a Tertiary Care Hospital of Gujarat, India. Journal of Clinical and Diagnostic Research. 2021;15.

Antimicrobial resistance surveillance in Europe 2022 - 2020 data [Internet]. 2022 [cité 28 sept 2024]. Disponible sur: https://www.ecdc.europa.eu/en/publications-data/antimicrobial-resistance-surveillance-europe-2022-2020-data

Chatterjee N, Nirwan PK, Srivastava S, Rati R, Sharma L, Sharma P, et al. Trends in carbapenem resistance in Pre-COVID and COVID times in a tertiary care hospital in North India. Ann Clin Microbiol Antimicrob. 2023;22:1.

Ocampo DP, Echeverri-Toro LM, Jiménez JN, Salazar L, Vargas C, Roncancio G, et al. Device-Associated Infections in COVID-19 Patients: Frequency of Resistant Bacteria, Predictors and Mortality in Medellín, Colombia. Microorganisms. 2024;12(4):640.

Zhou F, Yu T, Du R, Fan G, Liu Y, Liu Z, et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. The Lancet. 2020;395(10229):1054‑62.

Adams BG, Marrie TJ. Hand carriage of aerobic Gram-negative rods by health care personnel. J Hyg (Lond). 1982;89(1):23‑31.

Roux J, Nekkab N, Colomb-Cotinat M, Astagneau P, Crépey P. Time-series modelling for the quantification of seasonality and forecasting antibiotic-resistant episodes: application to carbapenemase-producing Enterobacteriaceae episodes in France over 2010–20. Journal of Antimicrobial Chemotherapy. 2021;76(1):226‑32.

Cascio GL, Soldani F, Mazzariol A, Lleo MM. The high incidence of carbapenem-resistant Klebsiella pneumoniae in urine from elderly hospital patients may facilitate the spread of resistant strains to the community. Microb Drug Resist. 2014;20(1):67‑72.

Hsu JY, Chuang YC, Wang JT, Chen YC, Hsieh SM. Healthcare-associated carbapenem-resistant Klebsiella pneumoniae bloodstream infections: Risk factors, mortality, and antimicrobial susceptibility, 2017-2019. J Formos Med Assoc. 2021;120(11):1994‑2002.

Thomsen J, Abdulrazzaq NM, Everett DB, Menezes GA, Senok A, Ayoub Moubareck C. Carbapenem resistant Enterobacterales in the United Arab Emirates: a retrospective analysis from 2010 to 2021. Front Public Health. 2023;11:1244482.

Jafari Z, Harati AA, Haeili M, Kardan-Yamchi J, Jafari S, Jabalameli F, et al. Molecular Epidemiology and Drug Resistance Pattern of Carbapenem-Resistant Klebsiella pneumoniae Isolates from Iran. Microb Drug Resist. 2019;25(3):336‑43.

Huang Y, Rana AP, Wenzler E, Ozer EA, Krapp F, Bulitta JB, et al. Aminoglycoside-resistance gene signatures are predictive of aminoglycoside MICs for carbapenem-resistant Klebsiella pneumoniae. Journal of Antimicrobial Chemotherapy. 2022;77(2):356‑63.

Monaco M, Giani T, Raffone M, Arena F, Garcia-Fernandez A, Pollini S, et al. Colistin resistance superimposed to endemic carbapenem-resistant Klebsiella pneumoniae: a rapidly evolving problem in Italy, November 2013 to April 2014. Euro Surveill. 2014;19(42):20939.

Bonomo RA, Burd EM, Conly J, Limbago BM, Poirel L, Segre JA, et al. Carbapenemase-Producing Organisms: A Global Scourge. Clin Infect Dis. 2018;66(8):1290‑7.

Mairi A, Pantel A, Sotto A, Lavigne JP, Touati A. OXA-48-like carbapenemases producing Enterobacteriaceae in different niches. Eur J Clin Microbiol Infect Dis.2018;37(4):587‑604.

Ben Helal R, Dziri R, Chedly M, Klibi N, Barguellil F, El Asli MS, et al. Occurrence and Characterization of Carbapenemase-Producing Enterobacteriaceae in a Tunisian Hospital. Microb Drug Resist. 2018;24(9):1361‑7.

Mansour W, Haenni M, Saras E, Grami R, Mani Y, Ben Haj Khalifa A, et al. Outbreak of colistin-resistant carbapenemase-producing Klebsiella pneumoniae in Tunisia. J Glob Antimicrob Resist. 2017;10:88‑94.

Ktari S, Mnif B, Louati F, Rekik S, Mezghani S, Mahjoubi F, et al. Spread of Klebsiella pneumoniae isolates producing OXA-48 β-lactamase in a Tunisian university hospital. Journal of Antimicrobial Chemotherapy. 2011;66(7):1644‑6.

Yong D, Toleman MA, Giske CG, Cho HS, Sundman K, Lee K, et al. Characterization of a new metallo-beta-lactamase gene, bla(NDM-1), and a novel erythromycin esterase gene carried on a unique genetic structure in Klebsiella pneumoniae sequence type 14 from India. Antimicrob Agents Chemother. 2009;53(12):5046‑54.

Bush K, Bradford PA. Epidemiology of β-Lactamase-Producing Pathogens. Clin Microbiol Rev. 2020;33(2):e00047-19.

Dos Santos S, Diene SM, Benouda A, Zerouali K, Ghaith DM, El-Mahdy RH, et al. Carbapenem- and colistin-resistant Enterobacterales in intensive care unit patients in Mediterranean countries, 2019. Front Microbiol. 2024;15:1370553.

Ben Nasr A, Decré D, Compain F, Genel N, Barguellil F, Arlet G. Emergence of NDM-1 in Association with OXA-48 in Klebsiella pneumoniae from Tunisia. Antimicrobial Agents and Chemotherapy. 2013;57(8):4089‑90.

Dziri O, Alonso CA, Dziri R, Gharsa H, Maraoub A, Torres C, et al. Metallo-β-lactamases and class D carbapenemases in south-east Tunisia: Implication of mobile genetic elements in their dissemination. Int J Antimicrob Agents. 2018;52(6):871‑7.

Ben Sallem R, Laribi B, Arfaoui A, Ben Khelifa Melki S, Ouzari HI, Ben Slama K, et al. Co‐occurrence of genes encoding carbapenemase, ESBL, pAmpC and non‐β‐Lactam resistance among Klebsiella pneumonia and E. coli clinical isolates in Tunisia. Letters in Applied Microbiology. 2022;74(5):729‑40.

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2026 Samar Dga, Farah Azouzi, Hela Ghali, Samah Boughattas, Lamia Tilouche, Soumaya Ketata, Yomna Ben Lamine, Houyem Laatiri, Abdelhalim Trabelsi

Downloads

Download data is not yet available.