Evaluation of loop-mediated isothermal amplification assays for rapid detection of blaKPC producing Serratia spp. in

Xinwei Liu1, Dayang Zou2, Chunxia Wang1

  • 1Department of Clinical Laboratory, Henan Province Hospital of Traditional Chinese Medicine, Zhengzhou, Henan 450002, P.R. China.

Insights

A new loop-mediated isothermal amplification (LAMP) assay rapidly detects carbapenem-resistant Serratia spp. producing blaKPC. This sensitive and economical method offers a feasible alternative for clinical settings.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Clinical Diagnostics

Background:

  • Carbapenem-resistant Serratia spp. are a growing global health threat.
  • The spread of blaKPC carbapenemase contributes to this resistance.
  • Limited effective therapies necessitate rapid and sensitive pathogen detection.

Purpose of the Study:

  • To develop a rapid and sensitive loop-mediated isothermal amplification (LAMP) assay.
  • To detect Serratia spp. carrying the blaKPC gene in pure cultures and clinical samples.
  • To evaluate the LAMP assay's performance against conventional methods.

Main Methods:

  • Development of a LAMP assay using specific primers for Serratia spp. and blaKPC.
  • Detection of amplification via calcein indicator and real-time turbidity.
  • Comparison of LAMP with conventional PCR and real-time PCR kits.
  • Assessment of sensitivity, specificity, and feasibility in clinical specimens.

Main Results:

  • The LAMP assay successfully amplified target DNA at 65°C for 60 minutes.
  • Detection limits reached 3.92 pg/µl DNA, demonstrating 10-fold higher sensitivity than conventional PCR.
  • The assay showed high specificity and was less affected by clinical specimen matrices.
  • LAMP proved more sensitive, easier to master, and feasible than culture and real-time PCR.

Conclusions:

  • A rapid, sensitive, and economical LAMP assay for detecting blaKPC-producing Serratia spp. was successfully developed.
  • The LAMP assay is a feasible and advantageous diagnostic tool for clinical settings.
  • This method aids in the timely identification of critical carbapenem-resistant pathogens.