Background: The emergence of carbapenem-resistant Escherichia coli has become a major public health concern due to the production of carbapenemase enzymes, particularly metallo-β-lactamases (MBLs). These enzymes confer resistance to a broad spectrum of β-lactam antibiotics, limiting therapeutic options and contributing to increased morbidity and mortality. Early detection of MBL-producing isolates is essential for effective antimicrobial stewardship and infection control.
Aim: To detect carbapenemase-producing Escherichia coli isolates using the Modified Carba NP Test and to determine the prevalence of MBL-producing strains among clinical samples.
Materials and Methods: This prospective observational hospital-based study was conducted in the Department of Microbiology, Muzaffarnagar Medical College and Hospital, over a period of 11 months from April 2025 to February 2026. A total of 100 clinical samples, including urine, blood, sputum, pus, and pleural fluid specimens, were processed. Isolation and identification of E. coli were performed using standard microbiological techniques. Antibiotic susceptibility testing was carried out by the Kirby–Bauer disc diffusion method according to CLSI guidelines. Carbapenem-resistant isolates were further screened for carbapenemase production using the Modified Carba NP Test.
Results: Out of 100 clinical isolates processed, 50 E. coli isolates demonstrated resistance to carbapenem antibiotics. Among these carbapenem-resistant isolates, 28 (56%) were confirmed as metallo-β-lactamase producers by the Modified Carba NP Test. Urine samples constituted the highest proportion of specimens (34.1%), followed by pus (20.6%), sputum (19.5%), blood (17.6%), and pleural fluid (8.2%). The MBL-producing isolates exhibited multidrug-resistant patterns, significantly limiting available treatment options.
Conclusion: The study revealed a considerable prevalence of MBL-producing carbapenem-resistant E. coli among clinical isolates. The Modified Carba NP Test proved to be a useful and reliable phenotypic method for the rapid detection of carbapenemase-producing strains. Routine screening, continuous surveillance, and strict antibiotic stewardship practices are essential to control the spread of these highly resistant pathogens and improve patient outcomes
Metallo beta-lactamases (MBLs) are a group of enzymes produced by certain Gram-negative bacteria that confer resistance to a wide range of beta-lactam antibiotics, including carbapenems. These enzymes require zinc ions for their activity and are capable of hydrolysing many clinically important antibiotics, making infections difficult to treat. The emergence and spread of MBL-producing organisms such as Escherichia coli represent a serious threat to public health and hospital infection control. Early detection and surveillance of MBL-producing strains are therefore essential to guide appropriate antibiotic therapy and limit their dissemination.
AIM AND OBJECTIVES
MATERIALS AND METHODS
RESULTS
Out of the total 100 bacterial isolates obtained, a 50 isolates (E.Coli) showed resistance to carbapenem antibiotics. Among these resistant isolates, 28 were confirmed as MBL producers through Modified Carba NP testing. These strains exhibited multidrug resistance patterns, limiting treatment options.
Figure:1
Figure: 02
MODIFIED CARBA NP TEST
Fig 3: Age and gender wise distribution of patients
Fig 4: Distribution of Samples
Majority of the Samples was Urine(34.1%) followed by Pus (20.6%), and least number was pleural fluid (8.2%) followed by Blood (17.6%).
Figure 5: RESISTANCE SHOWING TO MEROPENEM, IMIPENEM,IRTAPENEM
|
Sample Type |
Number |
Percentage |
|
Urine |
34 |
34.1% |
|
Pus |
21 |
20.6% |
|
Sputum |
20 |
19.5% |
|
Blood |
18 |
17.6% |
|
Pleural Fluid |
8 |
8.2% |
DISCUSSION
The Modified Carba NP Test is a rapid, economical, and reliable phenotypic method for detecting carbapenemase-producing E. coli. A high prevalence of MBL-producing isolates was observed in the present study, highlighting the need for routine screening, antimicrobial stewardship, and infection control measures.
The study was conducted at a single center with a relatively small sample size. Molecular characterization of carbapenemase genes was not performed.
REFERENCE