TY - JOUR
T1 - The remarkable effect of potassium iodide in eosin and rose bengal photodynamic action against salmonella typhimurium and staphylococcus aureus
AU - Santos, Adriele R.
AU - Batista, Andréia F.P.
AU - Gomes, Ana T.P.C.
AU - Neves, Maria da Graça P.M.S.
AU - Faustino, Maria Amparo F.
AU - Almeida, Adelaide
AU - Hioka, Noboru
AU - Mikcha, Jane M.G.
N1 - Funding Information:
Acknowledgments: The authors would like to thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—CAPES. Thanks are due to the University of Aveiro and FCT/MEC for the financial support to QOPNA (FCT UID/QUI/00062/2019), CESAM (UID/AMB/50017/2019) research units and to the project PREVINE (FCT-PTDC/ASPPES/29576/2017), to FCT/MEC through national funds and the co-funding by the FEDER-Operational Thematic Program for Competitiveness and Internationalization-COMPETE 2020, within the PT2020 Partnership Agreement. Thanks are also due to the Portuguese NMR and Mass Networks.
Publisher Copyright:
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2019/12
Y1 - 2019/12
N2 - Antimicrobial photodynamic therapy (aPDT) has been shown as a promising technique to inactivate foodborne bacteria, without inducing the development of bacterial resistance. Knowing that addition of inorganic salts, such as potassium iodide (KI), can modulate the photodynamic action of the photosensitizer (PS), we report in this study the antimicrobial effect of eosin (EOS) and rose bengal (RB) combined with KI against Salmonella enterica serovar Typhimurium and Staphylococcus aureus. Additionally, the possible development of bacterial resistance after this combined aPDT protocol was evaluated. The combination of EOS or RB, at all tested concentrations, with KI at 100 mM, was able to efficiently inactivate S. Typhimurium and S. aureus. This combined approach allows a reduction in the PS concentration up to 1000 times, even against one of the most common foodborne pathogenics, S. Typhimurium, a gram-negative bacterium which is not so prone to inactivation with xanthene dyes when used alone. The photoinactivation of S. Typhimurium and S. aureus by both xanthenes with KI did not induce the development of resistance. The low price of the xanthene dyes, the non-toxic nature of KI, and the possibility of reducing the PS concentration show that this technology has potential to be easily transposed to the food industry.
AB - Antimicrobial photodynamic therapy (aPDT) has been shown as a promising technique to inactivate foodborne bacteria, without inducing the development of bacterial resistance. Knowing that addition of inorganic salts, such as potassium iodide (KI), can modulate the photodynamic action of the photosensitizer (PS), we report in this study the antimicrobial effect of eosin (EOS) and rose bengal (RB) combined with KI against Salmonella enterica serovar Typhimurium and Staphylococcus aureus. Additionally, the possible development of bacterial resistance after this combined aPDT protocol was evaluated. The combination of EOS or RB, at all tested concentrations, with KI at 100 mM, was able to efficiently inactivate S. Typhimurium and S. aureus. This combined approach allows a reduction in the PS concentration up to 1000 times, even against one of the most common foodborne pathogenics, S. Typhimurium, a gram-negative bacterium which is not so prone to inactivation with xanthene dyes when used alone. The photoinactivation of S. Typhimurium and S. aureus by both xanthenes with KI did not induce the development of resistance. The low price of the xanthene dyes, the non-toxic nature of KI, and the possibility of reducing the PS concentration show that this technology has potential to be easily transposed to the food industry.
KW - Antimicrobial resistance
KW - Inorganic salt
KW - Photodynamic inactivation
KW - Salmonella
KW - Xanthene derivatives
UR - http://www.scopus.com/inward/record.url?scp=85074597190&partnerID=8YFLogxK
U2 - 10.3390/antibiotics8040211
DO - 10.3390/antibiotics8040211
M3 - Article
C2 - 31694195
AN - SCOPUS:85074597190
SN - 2079-6382
VL - 8
JO - Antibiotics
JF - Antibiotics
IS - 4
M1 - 211
ER -