Characterizing carbapenemase production in Enterobacterales through combined disk test and genetic profiling

INTRODUCTION

Antimicrobial resistance (AMR) represents a well-documented global threat, significantly undermining the efficacy of commonly used antibiotics. This resistance leads not only to increased mortality rates but also escalates overall healthcare costs due to prolonged illness and the need for more complex treatments.^[1] The decline in the development of new antibiotics, coupled with the growing ineffectiveness of existing ones, portends a grim scenario where health-care systems could revert to conditions reminiscent of the pre-antibiotic era.^[2]

The World Health Organization has highlighted the critical urgency of addressing AMR, particularly within the Enterobacterales order, which includes bacteria that are increasingly resistant to carbapenems, a class of last-resort antibiotics.^[3] The Centers for Disease Control and Prevention has identified carbapenem-resistant Enterobacterales (CRE) – such as Klebsiella species, Escherichia coli, and Enterobacter species– as significant emerging threats to global health.^[4]

In the past decade, the misuse and overuse of carbapenems have precipitated an alarming rise in resistance among bacterial pathogens, especially those within the Enterobacterales family.^[5] This escalating trend presents a formidable challenge to global public health.^[6] The genes responsible for carbapenemase production, which confer resistance to carbapenems, are often located on mobile genetic elements such as plasmids and transposons.^[7] The presence of these genes on mobile elements facilitates their rapid transfer between bacteria through horizontal gene transfer mechanisms, thereby accelerating the spread of carbapenem resistance within bacterial communities.^[8]

This study was conducted to identify the most prevalent genes responsible for carbapenemase production. By pinpointing these genes, we aim to implement effective infection control measures and enhance antimicrobial stewardship practices to combat the spread of carbapenem-resistant pathogens.

MATERIALS AND METHODS

RESULTS

Among the 445 Enterobacterales isolates, 104 (23.4%) were identified as CRE. Klebsiella pneumoniae was the most commonly isolated CRE, constituting 62 (59.6%) of the total CRE organisms. E. coli accounted for 40 (38.5%), while Enterobacter species made up 2 (1.9%) of the CRE isolates.

The majority of CRE isolates (42.3%) were obtained from pus samples (44 out of 104), followed by urine samples and tracheal aspirates, each contributing 21.2% (22 out of 104). Blood samples accounted for 9.6% (10 out of 104), and pleural fluid samples made up 5.8% (6 out of 104). A significant proportion of CRE isolates (69%) were from patients admitted to intensive care units (72 out of 104), while 26.9% were from wards (28 out of 104), and 3.8% were from outpatient departments (four out of 104).

The phenotypic detection of carbapenemase production was performed using combined disk testing of meropenem with various carbapenemase inhibitors. The type of carbapenemase produced was identified based on the inhibition pattern observed. Synergy with meropenem combined with EDTA indicated the production of metallo-beta-lactamase [Figure 1].

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Figure 1:

Synergy has been seen with Meropenem + Ethylenediaminetetraacetic acid disk on a combined disk test showing the production of metallobetalactamase.

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Out of the 104 meropenem-resistant isolates tested, 77.9% (81 of 104) showed synergy with the meropenem + EDTA disk, indicating the production of metallo-beta-lactamase (class B carbapenemase). Only 1.9% (2 of 104) showed synergy with CLX, suggestive of AmpC beta-lactamase hyperproduction with porin loss. The remaining 20.2% showed no synergy with any of the drugs, indicating the potential presence of OXA-like enzymes (class D carbapenemase) or non-carbapenemase mechanisms responsible for resistance, such as extended-spectrum beta-lactamase (ESBL) with porin loss. No isolates showed synergy with the meropenem + PBA disk; thus, no class A carbapenemase was detected [Table 1].

The concordance, also known as the percentage of agreement, is the percentage of chance that an identical sample analyzed by two different methodologies will yield the same result. The concordance of combined disk testing with a molecular test in the detection of metallo-beta-lactamase was found to be 91.3% in this study, and in the detection of OXA-like enzymes, production alone was found to be 95.1%. The combined disk test could not detect the presence of OXA-like enzyme production in combination with other carbapenemase production.

Molecular testing revealed that the presence of both NDM and OXA-48 genes was the main mechanism responsible for carbapenemase production among CRE isolates. Specifically, 41 (39.4%) isolates carried both NDM and OXA-48, followed by 20 (19.2%) isolates with NDM alone. OXA-48 alone was present in 17 (16.3%) isolates, and OXA-23 alone was detected in 10 (9.6%) isolates. Overall, NDM was the most commonly detected gene, found in 72 out of 104 CRE isolates (69.2%), followed by OXA-48 in 63 out of 104 (60.6%) isolates. Some CRE isolates showed the presence of more than one gene, and no carbapenemase gene was detected in 3 (2.9%) isolates, suggesting other mechanisms of carbapenem resistance [Table 2].

The most common resistance gene combination in carbapenem-resistant K. pneumoniae, the predominant isolate, was NDM and OXA-48 in 31 (29.8%) isolates, followed by NDM alone in 9 (8.7%), OXA-48 alone, and OXA-23 alone in 8 (7.7%) isolates each. In carbapenem-resistant E. coli, the most common gene was NDM alone in 11 (10.6%) isolates, followed by the combination of NDM and OXA-48 in 9 (8.7%) isolates, and OXA-48 alone in 8 (7.7%) isolates. Among the carbapenem-resistant Enterobacter species, 1 isolate had a combination of NDM and OXA-48, and 1 had the OXA-48 gene alone [Table 3].

DISCUSSION

This study aimed to detect carbapenemase production in Enterobacterales through phenotypic methods and molecular characterization, with the objective of identifying the most prevalent genes responsible for carbapenemase production. Given the rising prevalence of CRE globally, understanding the predominant genes responsible for carbapenemase production in specific regions is crucial. Such knowledge assists healthcare professionals in selecting optimal empirical treatments for infections caused by CRE.^[11,12]

The prevalence of CRE in our study was notably high at 23.4%. This finding is consistent with studies conducted in various regions of India, which report similarly high prevalence rates: 29% in Gujarat,^[13] 27.18% in Bengaluru,^[14] and 29.4% in Bhubaneswar.^[15] These consistent findings across different parts of the country highlight the widespread issue of CRE and underscore the urgent need for robust infection control measures and antibiotic stewardship programs nationwide.

In our study, K. pneumoniae was the most commonly isolated CRE, accounting for 59.6% of the total CRE organisms, followed by E. coli at 38.5%. This is in alignment with most other studies,^[13,14] which also identified K. pneumoniae as the predominant species, followed by E. coli. Although some studies have reported high carbapenem resistance rates in Enterobacter species.^[16] Our findings indicated that Enterobacter species were relatively uncommon. The consistent identification of K. pneumoniae as the most prevalent CRE across various studies, including ours, underscores its significant role in CRE infections.

Phenotypic detection of carbapenemase production using inhibitor-based combination disk testing revealed that 77.9% of the isolates produced metallo-beta-lactamase, while 1.9% exhibited AmpC carbapenemase activity. The remaining 20.2% of isolates did not show inhibition by any of the combination disks used in the test, suggesting the presence of OXA-such as enzymes or non-carbapenemase mechanisms such as ESBL with porin loss. Notably, no isolates showed synergy with PBA, indicating the absence of class A carbapenemase genes [Table 1].

Our findings are consistent with other studies. For instance, one study found metallo-beta-lactamase production in 56% of isolates and K. pneumoniae carbapenemase (KPC) production in 18%.^[17] Another study reported metallo-beta-lactamase production in 59.09% and KPC production in 13.63% of isolates.^[18] These findings, in conjunction with ours, highlight the critical need for comprehensive surveillance and molecular diagnostics to inform targeted treatment strategies for CRE infections.

The main mechanism responsible for carbapenemase production among the CRE isolates in our study was the presence of NDM and OXA-48 together. A significant proportion (39.4%) of the isolates exhibited both NDM and OXA-48, followed by 19.2% with NDM alone and 16.3% with OXA-48 alone. Overall, NDM was the most frequently detected gene, present in 69.2% of the CRE isolates, followed closely by OXA-48 in 60.6%. These findings are consistent with other studies, although the prevalence of specific carbapenemase genes can vary regionally.^{[14,16,19-21]} This variability underscores the importance of localized surveillance and tailored treatment strategies to manage CRE infections effectively. The differences in carbapenemase types suggest the need for region-specific antimicrobial policies and diagnostic approaches to ensure appropriate and effective therapeutic interventions [Table 2].

The concordance of the combined disk test with the molecular test in the detection of metallo-beta-lactamase was 91.3% in this study, and in the detection of OXA-like enzymes, production alone was 95.1%. Thus, a combined disk test is a good alternative for the detection of carbapenemase where molecular tests are not available.

No variability was seen in the organism-wise characterization of carbapenemase genes [Table 3]. In other studies also, the same genes were identified in all CRE isolates.^[14,16,20] This shows that these genes have become widespread amongst Enterobacterales. These genes, through their capability of horizontal transfer, can spread both inter-species and intra-species. Therefore, surveillance of these genes is a must to monitor both their spread and the effectiveness of control measures.

This study has several limitations. Conducted in a single center with a relatively small sample size, the findings may lack generalizability. The phenotypic method used could not detect certain carbapenemases, such as OXA-48. In addition, the molecular methods employed did not identify non-carbapenemase mechanisms of resistance. Furthermore, the study did not examine risk factors and outcomes, which are crucial for a comprehensive understanding of CRE infections. Further research is required to know the outcomes in organisms according to their molecular pattern.

The landscape of CRE indeed varies significantly across regions, influencing treatment choices.^[22] The treatment of CRE infections depends on the infection site, the isolated pathogen, and the resistance profile.^[1] Preventing the spread of these organisms is as important as their prompt detection and treatment. This necessitates strict infection control practices, including standard and transmission-based precautions. Robust antimicrobial stewardship practices are also crucial in preventing the overuse and misuse of antibiotics, which are major risk factors for the emergence of resistant strains.^[23,24]

CONCLUSIONS

Our study identified metallo-beta-lactamases (NDM) as the predominant type of carbapenemase gene among the Enterobacterales isolates, with the coproduction of NDM and OXA-48 enzymes being the most common mechanism of resistance. OXA-48 enzymes, which were the second most frequently produced, often exhibit weaker activity and can be easily missed by standard detection methods.

Given the increasing prevalence of CRE, there is an urgent need for the development and implementation of newer point-of-care diagnostic tests. Prompt and accurate identification of these resistant organisms will enable timely and appropriate treatment interventions and the effective implementation of infection control measures to curb the spread of these pathogens.