International Journal of Medical and Pharmaceutical Research
2026, Volume-7, Issue 3 : 2261-2264
Research Article
MODIFIED CARBA NP TEST FOR THE DETECTION OF CARBAPENEMASE PRODUCING ESCHERICHIA COLI SPECIES
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 ,
Received
March 8, 2026
Accepted
May 24, 2026
Published
June 7, 2026
Abstract

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

Keywords
INTRODUCTION

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

  • To detect the presence of Metallo beta-lactamase-producing E.Coli among clinical isolates.
  • To identify carbapenem-resistant isolates, performing  tests for MBL production, and analysing the prevalence of MBL-producing E.Coli in clinical samples.

 

MATERIALS AND METHODS

  • TYPE OF STUDY: Prospective Observational hospital based study
  • NUMBER OF SAMPLES BEING PROCESSED: 100 samples
  • PLACE AND DURATION OF STUDY: Department of Microbiology, Muzaffarnagar Medical College & Hospital over a period of 11 months from April 2025 to February 2026.
  • INCLUSION CRITERIA: Clinical samples such as urine, blood, sputum, and wound swabs were collected from patients in a Muzaffarnagar medical college.
  • EXCLUSION CRITERIA: Including all sample in Lab except stool sample.
  • SAMPLE PROCESSING: The isolates were cultured on appropriate media and identified using standard microbiological techniques. Antibiotic susceptibility testing was performed using the Kirby–Bauer disc diffusion method according to CLSI guidelines. Carbapenem-resistant isolates were further screened for MBL production using modified Carba NP test. The results were recorded and analysed to determine the prevalence of MBL-producing strains

 

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

Table 1. Distribution of Clinical Samples

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 study highlights the increasing occurrence of metallo-beta-lactamase-producing bacteria in clinical settings.
  • Early detection through routine screening methods is essential for effective infection control and appropriate antibiotic therapy.
  • Continuous monitoring and strict antibiotic stewardship programs are necessary to prevent the spread of these highly resistant pathogens.

 

CONCLUSION

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.

LIMITATIONS

The study was conducted at a single center with a relatively small sample size. Molecular characterization of carbapenemase genes was not performed.

 

REFERENCE

  1. Yong D, Toleman MA, Giske CG, Cho HS, Sundman K, Lee K, et al. Characterization of a new metallo-âlactamase gene, blaNDM-1, and a novel erythromycin esterase gene carried on a unique genetic structure in E. coli Sequence from India. Antimicrob Agents Chemother. 2009;53:5046-54.
  2. Behera B, Mathur P, Das A, Kapil A, Sharma V. An evaluation of four different phenotypic techniques for detection of metallo-â-lactamase producing E. Coli. Indian J Med Microbiol. 2008;26:233-7.
  3. Walsh TR, Toleman MA, Poirel L, Nordmann P. Metallo-ß-lactamases: the quiet before the storm? Clin Microbiol Rev. 2005;18:306-25.
  4. Peleg AY, Franklin C, Bell JM, Spelmann DW. Dissemination of the metallo-â lactamase gene bla IMP4 among gram-negative pathogens in a clinical setting in Australia. Clin Infect Dis. 2005;41:1549-56.
  5. Nordmann P, Poirel L. Emerging carbapenemases in gram-negative aerobes. Clin Microbial Infect. 2002;8:321-31.
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