The development of antimicrobial resistance is part of natural evolutionary process among microorganisms, delivering beneficial traits in bacteria that protect the cell from the effects of specific antibiotics, thus conferring a survival advantage. However, the increased use, and misuse, of antimicrobials promotes the accelerated spread of resistance mechanisms, leading to the development of multi and pan-resistant bacteria that are untreatable with the antibiotics currently in use1. The detection, correct diagnosis and treatment and surveillance of antimicrobial resistant organisms is key to fighting this growing global issue.
One mechanism of drug resistance—carbapenem resistance among Gram negative bacteria—has become significantly more prevalent since the 1990s2. Carbapenems (e.g. Meropenem, Imipenem, Ertapenem, Doripenem) are broad-spectrum β-lactam antibiotics traditionally used as drugs of last resort targeting healthcare-associated and severe community-acquired infections. The increasing prevalence of extended-spectrum β-lactamases (ESBL’s), enzymes conferring resistance to β-lactam antibiotics by breaking/hydrolysis of their structure, among Escherichia coli and Klebsiella pneumoniae in 1980s-1990s contributed to increased consumption of Carbapenems, which in turn prompted the evolution of various mechanisms of carbapenem resistance3:
The prevalence of different carbapenem resistance mechanisms varies geographically with Klebsiella pneumoniae carbapenemases (KPC) being the most prevalent in the Americas and parts of Europe, metallo-β-lactamases (eg. NDM, VIM, IMP) most prevalent in Asia and OXA-48-like resistance being highest around the Mediterranean area and the Middle East 4, 7, 8. Of particular concern is the spread of KPC producing Klebsiella pneumoniae which is one of the most common types of carbapenem resistant Gram negative bacteria9. K. pneumoniae is a major cause of hospital-acquired infections such as pneumonia, bloodstream infections and UTI, and KPC infections are currently associated with mortality rates as high as 41%9, 10.
The international spread of KPC producing Enterobacterales is primarily due to clonal expansion of K. pneumoniae strains harbouring KPC coding genes (blaKPC) which are often located in a transposon or a plasmid enabling rapid dissemination of these genes among Enterobacterales 4, 5, 11. The level of carbapenem resistance, measured as minimum inhibitory concentration (MIC) value, has been discovered to be linked to blaKPC gene copy number 4.
As the fight to control multi-drug resistant organisms continues, it is of upmost importance to ensure antimicrobial susceptibility testing (AST) solutions can recognize different resistance patterns through antibiograms in order to guide effective patient treatment. The accuracy and reliability of a chosen AST system to detect antimicrobial resistance present in a clinical isolate should be evaluated through in vitro analysis using characterized microbial strains with known antibiotic susceptibility profiles, as part of routine Quality Control (QC) testing.
Guidelines by CLSI12 and EUCAST13 are continuing to evolve as more and more antimicrobial resistant QC strains are added into routine QC recommendations. Best practice QC is of particular relevance for those strains with plasmid mediated resistance (such as KPCs) that are prone to spontaneous plasmid loss due to over-passaging. By following best practice guidance on QC strain maintenance – avoiding over-passaging and maintaining optimal storage and growth conditions - laboratories can ensure proper handling of these strains12.
Thermo Scientific™ Culti-Loops™ include carbapenem resistant Klebsiella pneumoniae strains ATCC® BAA-2814™ and ATCC® BAA-1705™ . View the latest additions to the Thermo Scientific Culti-Loops portfolio here, to gain access to the full, ready-to-use QC strains according to recommendations by CLSI and EUCAST. All Culti-Loop™ strains are fully characterised, including those harbouring a variety of antimicrobial resistance patterns such as ESBL & Carbapenemase producing strains, Vancomycin-Resistant Enterococci (VRE) and Methicillin-Resistant Staphylococcus aureus (MRSA).
*KPC: Klebsiella pneumoniae carbapenemase-producing Enterobacterales; NDM: New Delhi metallo-β-lactamase; VIM: Verona integron-encoded metallo-β-lactamase; IMP: Imipenem-resistant Pseudomonas-type carbapenemase; OXA-48: carbapenem-hydrolysing oxacillinase-48; AmpC: ampicillinase C; SHV: sulfydryl variant; TEM: Temoneira; CTX-M: cefotaximase.