Detection of VIM-2-, IMP-1- and NDM-1-producing multidrug-resistant Pseudomonas aeruginosa in Malaysia

Siew Mun Liew1, Ganeswrei Rajasekaram2, Savithri D Puthucheary1

  • 1Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

Abstract

Insights

Three multidrug-resistant Pseudomonas aeruginosa strains producing carbapenem-resistant metallo-β-lactamases (MBLs) were identified in Malaysia. These strains harbored blaIMP-1, blaVIM-2, and blaNDM-1 genes, with blaIMP-1 and blaNDM-1 being novel findings in Malaysia.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genetics

Background:

  • Rising carbapenem resistance in Pseudomonas aeruginosa is a global health concern.
  • Metallo-β-lactamases (MBLs) are key enzymes conferring carbapenem resistance.
  • The prevalence of MBL-producing P. aeruginosa in Malaysia required investigation.

Purpose of the Study:

  • To investigate the isolation and characterization of MBL-producing P. aeruginosa clinical strains in Malaysia.
  • To identify the specific carbapenemase genes present in these resistant strains.
  • To determine the genetic relatedness of the identified MBL-producing isolates.

Main Methods:

  • Isolation and identification of 53 P. aeruginosa clinical strains from Malaysia.
  • Antimicrobial susceptibility testing and determination of Minimum Inhibitory Concentrations (MICs) for carbapenems.
  • Screening for MBL production using phenotypic tests (e.g., IMP-EDTA synergy test, MBL Etest) and genotypic confirmation via PCR for carbapenemase genes.
  • Multilocus Sequence Typing (MLST) for molecular typing of isolates.

Main Results:

  • Three out of 53 (5.7%) P. aeruginosa strains were identified as MBL producers.
  • All three MBL-producing strains exhibited multidrug resistance, with two being resistant to all tested antimicrobials.
  • Sequencing confirmed the presence of blaIMP-1, blaVIM-2, and blaNDM-1 genes in individual isolates.
  • MLST identified two sequence types: ST235 and ST308.

Conclusions:

  • The emergence of IMP-1 and NDM-1 producing P. aeruginosa in Malaysia is reported for the first time.
  • These findings highlight the increasing threat of carbapenem-resistant bacteria in the region.
  • The presence of these novel MBL genes may be linked to travel-associated transmission.

Related Concept Videos

Predicting Products: SN1 vs. SN202:27

Predicting Products: SN1 vs. SN2

Nucleophilic substitution reactions of alkyl halides can proceed via an SN1 or an SN2 mechanism. While in SN2 reactions, the nucleophile attacks the substrate simultaneously as the leaving group departs, in SN1 reactions, the substrate first dissociates to give the carbocation intermediate. Various factors such as the structure of the substrate, the strength of the nucleophile, and the nature of the solvent promote one mechanism over the other.
With increased substitution on the alkyl halide,...
17.4K
SN1 Reaction: Stereochemistry02:15

SN1 Reaction: Stereochemistry

This lesson provides an in-depth discussion of the stereochemical outcomes in an SN1 reaction.
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
10.5K
SN1 Reaction: Kinetics02:05

SN1 Reaction: Kinetics

In an SN2 reaction, the reaction rate depends on both the type of nucleophile and the substrate. A hindered tertiary alkyl halide is practically inert to the SN2 mechanism despite using a strong nucleophile.
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
9.7K
SN1 Reaction: Mechanism02:25

SN1 Reaction: Mechanism

Kinetic studies of ionization of a tertiary halide in a protic solvent suggest that only the substrate participates in the rate-determining step (slow step). The nucleophile is involved only after the slowest step. The SN1 reaction takes place in a multiple-step mechanism. 
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
14.5K
Acidity of 1-Alkynes02:42

Acidity of 1-Alkynes


The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
11.3K
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview01:26

1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview

Nitrous acid and nitric acids are two types of acids containing nitrogen, among which nitrous acid is weaker than nitric acid. Nitrous acid with a pKa value of 3.37 ionizes in water to give a nitrite ion and the hydronium ion.
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
4.0K