Photodynamic therapy on mRNA levels in bacteria

Bruno Ricardo Barreto Pires1, Flavia de Paoli2, Andre Luiz Mencalha1

  • 1Departamento de Biofísica e Biometria, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Boulevard Vinte e Oito de Setembro, 87, fundos, Vila Isabel, Rio de Janeiro, 20551030, Brazil.

PubMed

Insights

Antimicrobial photodynamic therapy (aPDT) effectively inactivates bacteria. Quantitative reverse transcription polymerase chain reaction (RT-qPCR) can measure bacterial mRNA levels to understand aPDT resistance mechanisms and confirm its effectiveness against infections.

Area of Science:

  • Microbiology
  • Photochemistry
  • Molecular Biology

Background:

  • Antimicrobial photodynamic therapy (aPDT) uses photosensitizers and light to generate reactive oxygen species, inactivating bacteria.
  • While generally effective, potential bacterial resistance mechanisms like reactive oxygen species detoxification and photosensitizer efflux exist.
  • Measuring bacterial mRNA levels offers a way to investigate these resistance mechanisms.

Purpose of the Study:

  • To evaluate mRNA levels in bacteria treated with photodynamic therapy (PDT).
  • To assess the utility of quantitative reverse transcription polymerase chain reaction (RT-qPCR) in studying aPDT effects on bacteria.
  • To understand gene expression changes related to bacterial responses to aPDT.

Main Methods:

  • Literature search on MEDLINE/Pubmed for studies measuring mRNA levels in bacteria post-PDT.
  • Analysis of RT-qPCR data from bacterial cells exposed to aPDT.
  • Evaluation of gene expression related to various cellular functions.

Main Results:

  • RT-qPCR successfully measured mRNA levels in both Gram-positive and Gram-negative bacteria after aPDT.
  • The study demonstrated the feasibility of assessing gene expression changes in response to aPDT.
  • Data indicated aPDT's effectiveness in impacting bacterial gene expression.

Conclusions:

  • RT-qPCR is a valuable tool for investigating bacterial responses and potential resistance to aPDT.
  • Understanding mRNA level changes enhances the comprehension of aPDT's mechanisms of action.
  • This approach reinforces the efficacy of aPDT in combating bacterial infections.