Optimization of Loop-Mediated Isothermal Amplification (LAMP) for the Rapid Detection of Nosocomial Pathogens on Environmental Surfaces

Contamination of environmental surfaces by nosocomial pathogens like <i>Pseudomonas aeruginosa</i> (<i>P. aeruginosa</i>), <i>Staphylococcus aureus</i> (<i>S. aureus</i>), and <i>Enterococcus</i> spp. poses significant health risks worldwide. However, gold-standard detection methods are too time-consuming and labor-intensive. This study aimed to optimize loop-mediated isothermal amplification (LAMP) as a rapid, innovative, and cost-effective approach, comparing its effectiveness with the gold-standard cultural method. Sterile surfaces (24 cm<sup>2</sup>) were contaminated in duplicate with different concentrations of <i>P. aeruginosa</i>, <i>S. aureus</i>, and <i>Enterococcus faecalis (E. faecalis)</i> reference stains. For each pair of contaminated surfaces, one was analyzed using the agar contact plate method (UNI EN 17141:2021), while the other was analyzed using LAMP, following three different pre-incubation times (three, six, and nine hours). The sensitivity and accuracy of LAMP for <i>P. aeruginosa</i> improved with longer incubation times, reaching a value of 1.00 at nine hours, while the specificity and positive predictive value (PPV) remained at 1.00 regardless of the incubation time. For <i>S. aureus</i>, LAMP achieved a sensitivity, specificity, accuracy, PPV, and negative predictive value (NPV) of 1.00 across all incubation times. Finally, for <i>E. faecalis</i>, sensitivity increased from 0.57 at three hours to 1.00 at six and nine hours, with a high specificity, accuracy, PPV, and NPV from six hours onwards. These findings showed that LAMP can be used as a rapid and reliable alternative to gold-standard methods for detecting pathogens on surfaces. The high sensitivity and specificity achieved, especially at six and nine hours of pre-incubation, suggested its use for real-time monitoring in healthcare settings. Further research in real-world environments is needed to confirm these findings.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-06-20
DOI
https://doi.org/10.3390/ijms26135933
Citations
1
Primary Topic
Biosensors and Analytical Detection
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article
Field-Weighted Citation Impact
0.67
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article

Optimization of Loop-Mediated Isothermal Amplification (LAMP) for the Rapid Detection of Nosocomial Pathogens on Environmental Surfaces

Sandra Cristino, Federica Marino, Carlo Derelitto, Luna Girolamini et al.
1 citations
International Journal of Molecular Sciences
Biosensors and Analytical Detection
0.67
article

Optimization of Loop-Mediated Isothermal Amplification (LAMP) for the Rapid Detection of Nosocomial Pathogens on Environmental Surfaces

Sandra Cristino, Federica Marino, Carlo Derelitto, Luna Girolamini, Laura Caligaris, Letizia Bellucci
article en
1 citations

Abstract

Contamination of environmental surfaces by nosocomial pathogens like <i>Pseudomonas aeruginosa</i> (<i>P. aeruginosa</i>), <i>Staphylococcus aureus</i> (<i>S. aureus</i>), and <i>Enterococcus</i> spp. poses significant health risks worldwide. However, gold-standard detection methods are too time-consuming and labor-intensive. This study aimed to optimize loop-mediated isothermal amplification (LAMP) as a rapid, innovative, and cost-effective approach, comparing its effectiveness with the gold-standard cultural method. Sterile surfaces (24 cm<sup>2</sup>) were contaminated in duplicate with different concentrations of <i>P. aeruginosa</i>, <i>S. aureus</i>, and <i>Enterococcus faecalis (E. faecalis)</i> reference stains. For each pair of contaminated surfaces, one was analyzed using the agar contact plate method (UNI EN 17141:2021), while the other was analyzed using LAMP, following three different pre-incubation times (three, six, and nine hours). The sensitivity and accuracy of LAMP for <i>P. aeruginosa</i> improved with longer incubation times, reaching a value of 1.00 at nine hours, while the specificity and positive predictive value (PPV) remained at 1.00 regardless of the incubation time. For <i>S. aureus</i>, LAMP achieved a sensitivity, specificity, accuracy, PPV, and negative predictive value (NPV) of 1.00 across all incubation times. Finally, for <i>E. faecalis</i>, sensitivity increased from 0.57 at three hours to 1.00 at six and nine hours, with a high specificity, accuracy, PPV, and NPV from six hours onwards. These findings showed that LAMP can be used as a rapid and reliable alternative to gold-standard methods for detecting pathogens on surfaces. The high sensitivity and specificity achieved, especially at six and nine hours of pre-incubation, suggested its use for real-time monitoring in healthcare settings. Further research in real-world environments is needed to confirm these findings.

International Journal of Molecular SciencesVol. 26(13)
University of Bologna (IT)
Openalex Percentile: Top 30%
Biosensors and Analytical Detection
0.67
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