Colorimetric bacteria sensing of Pseudomonas aeruginosa using gold nanoparticle probes

• Published in: Journal of Genetic Engineering and Biotechnology 2023-12, Vol.21 (1), p.72-10, Article 72
• Main Authors: Mousivand, Zahra, Haddadi, Fatemeh, Kamaladini, Hossein
• Format: Article
• Language: English
• Subjects: Bacteria; Care and treatment; Colorimetric assay; Colorimetry; Deoxyribonucleic acid; Design; DNA; DNA probes; Genes; Gold; Gold nanoparticle probes; Health aspects; Hybridization; Infection; Infections; Methods; Microorganisms; Mortality; Multiplex PCR; Multiplexing; Nanoparticles; Nosocomial infection; Nucleic acids; Oligonucleotides; Pathogens; Polymerase chain reaction; Pseudomonas aeruginosa; rRNA 16S
• ISSN: 1687-157X; 2090-5920
• DOI: 10.1186/s43141-023-00527-4

Background Due to the advantages of molecular methods over biochemical methods, the use of molecular methods for diagnosing nosocomial infections such as Pseudomonas can be an appropriate and rapid way to choose the right diagnosis and treatment of infection and prevent further complications caused by the infection. The present article provides a description of the development of a nanoparticle-based detection technique for sensitive and specific deoxyribonucleic acid-based diagnostic of Pseudomonas aeruginosa. Specific thiolated oligonucleotide probes for one of the hypervariable regions of the 16S rDNA gene were designed and applied for colorimetric detection of the bacteria. Results The results of gold nanoprobe-nucleic sequence amplification indicated the probe attached to gold nanoparticles in the presence of the target deoxyribonucleic acid. It caused aggregation of gold nanoparticles in the form of connected networks resulting in color change and indicating the presence of the target molecule in the sample, which could be observed by the naked eye. In addition, the wavelength of gold nanoparticles changed from 524 to 558 nm. Multiplex polymerase chain reactions were performed using four specific genes of Pseudomonas aeruginosa (oprL, oprI, toxA, and 16S rDNA). The sensitivity and specificity of the two techniques were assessed. According to the observations, the specificity of both techniques was 100%, and the sensitivity was 0.5 ng/[mu]L and 0.01 ng/[mu]L of genomic deoxyribonucleic acid for multiplex polymerase chain reaction and colorimetric assay, respectively. Conclusions The sensitivity of colorimetric detection was about 50 times higher than the polymerase chain reaction using the 16SrDNA gene. The results of our study proved to be highly specific with potential use for early detection of Pseudomonas aeruginosa.