Lethal photosensitization of Porphyromonas gingivalis by their endogenous porphyrins under anaerobic conditions: An in vitro study

Photodiagnosis and Photodynamic Therapy

Volumn 10, Issue 4, 2013, Pages 677-682

  Hope, Christopher K ^a   Hindley, Jonathan A ^a   Khan, Zeeshan ^a   de Josselin de Jong, Elbert ^a,b   Higham, Susan M ^a  

^a UNIVERSITY OF LIVERPOOL   (United Kingdom)

^b Inspektor Research Systems bv   (Netherlands)

Author keywords

Lethal photosensitization; Light; Photodynamic therapy; Porphyromonas gingivalis; Protoporphyrin IX

Indexed keywords

PORPHYRIN;

ARTICLE; CONTROLLED STUDY; CULTURE MEDIUM; CYTOTOXICITY; IN VITRO STUDY; LIGHT; NONHUMAN; OPTICAL DENSITY; PHOTOSENSITIVITY; PHOTOSENSITIZATION; PORPHYROMONAS GINGIVALIS; PRIORITY JOURNAL;

PORPHYROMONAS GINGIVALIS;

LETHAL PHOTOSENSITIZATION; LIGHT; PHOTODYNAMIC THERAPY; PORPHYROMONAS GINGIVALIS; PROTOPORPHYRIN IX;

ANAEROBIOSIS; APOPTOSIS; DOSE-RESPONSE RELATIONSHIP, RADIATION; LIGHT; OXYGEN; PHOTOSENSITIZING AGENTS; PORPHYRINS; PORPHYROMONAS GINGIVALIS; RADIATION DOSAGE;

EID: 84888022259     PISSN: 15721000     EISSN: 18731597     Source Type: Journal    
DOI: 10.1016/j.pdpdt.2013.08.006     Document Type: Article

References (42)

1. Ochsner M. Photophysical and photobiological processes in the photodynamic therapy of tumours. Journal of photochemistry and photobiology B, Biology 1997, 39:1-18.
2. 2. Journal of the American Chemical Society 2003, 125:12803-12809.
3. Grossweiner L.I., Patel A.S., Grossweiner J.B. Type I and type II mechanisms in the photosensitized lysis of phosphatidylcholine liposomes by hematoporphyrin. Photochemistry and Photobiology 1982, 36:159-167.
4. Bertoloni G., Lauro F.M., Cortella G., Merchat M. Photosensitizing activity of hematoporphyrin on Staphylococcus aureus cells. Biochimica et Biophysica Acta 2000, 1475:169-174.
5. Chen T.S., Zeng S.Q., Zhou W., Luo Q.M. A quantitative theory model of a photobleaching mechanism. Chinese Physics Letters 2003, 20:1940-1943.
6. Copper M.P., Tan I.B., Ruevekamp M.C., Stewart F.A. Photodynamic therapy in the treatment of multiple primary tumours in the head and neck, located to the oral cavity and oropharynx. Clinical Otolaryngology 2007, 32:185-189.
7. Aghahosseini F., Arbabi-Kalati F., Fashtami L.A., Fateh M., Djavid G.E. Treatment of oral lichen planus with photodynamic therapy mediated methylene blue: a case report. Medicina Oral Patologia Oral y Cirugia Bucal 2006, 11:E126-E129.
8. Tschen E.H., Wong D.S., Pariser D.M., Dunlap F.E., Houlihan A., Ferdon M.B. Photodynamic therapy using aminolaevulinic acid for patients with nonhyperkeratotic actinic keratoses of the face and scalp: phase IV multicentre clinical trial with 12-month follow up. British Journal of Dermatology 2006, 155:1262-1269.
9. Wainwright M., Stanforth A., Jones R., Loughran C., Meegan K. Photoantimicrobials as a potential local approach to geriatric UTIs. Letters in Applied Microbiology 2010, 50:486-492.
10. Hamblin M.R., O'Donnell D.A., Murthy N., Contag C.H., Hasan T. Rapid control of wound infections by targeted photodynamic therapy monitored by in vivo bioluminescence imaging. Photochemistry and Photobiology 2002, 75:51-57.
11. Wilson M., Burns T., Pratten J. Killing of Streptococcus sanguis in biofilms using a light-activated antimicrobial agent. Journal of Antimicrobial Chemotherapy 1996, 37:377-381.
12. Komerik N., Nakanishi H., MacRobert A.J., Henderson B., Speight P., Wilson M. In vivo killing of Porphyromonas gingivalis by toluidine blue-mediated photosensitization in an animal model. Antimicrobial Agents and Chemotherapy 2003, 47:932-940.
13. Smalley J.W., Silver J., Marsh P.J., Birss A.J. The periodontopathogen Porphyromonas gingivalis binds iron protoporphyrin IX in the mu-oxo dimeric form: an oxidative buffer and possible pathogenic mechanism. Biochemical Journal 1998, 331:681-685.
14. Smalley J.W., Silver J., Birss A.J., Withnall R., Titler P.J. The haem pigment of the oral anaerobes Prevotella nigrescens and Prevotella intermedia is composed of iron(III) protoporphyrin IX in the monomeric form. Microbiology 2003, 149:1711-1718.
15. Zenkevich E., Sagun E., Knyukshto V., Shulga A., Mironov A., Efremova O., et al. Photophysical and photochemical properties of potential porphyrin and chlorin photosensitizers for PDT. Journal of Photochemistry and Photobiology B-Biology 1996, 33:171-180.
16. Bradshaw D.J., Marsh P.D., Watson G.K., Allison C. Oral anaerobes cannot survive oxygen stress without interacting with facultative/aerobic species as a microbial community. Letters in Applied Microbiology 1997, 25:385-387.
17. Hajishengallis G., Liang S., Payne M.A., Hashim A., Jotwani R., Eskan M.A., et al. Low-abundance biofilm species orchestrates inflammatory periodontal disease through the commensal microbiota and complement. Cell Host and Microbe 2011, 10:497-506.
18. Hope C.K., de Josselin de Jong E., Field M.R., Valappil S.P., Higham S.M. Photobleaching of red fluorescence in oral biofilms. Journal of Periodontal Research 2011, 46:228-234.
19. Tong-Sheng C.S.-Q., Wei Z., Qing-Ming Z. A quantitative theory model of a photobleaching mechanism. Chinese Physics Letters 2003, 20:1940-1943.
20. Andley U.P., Lewis R.M., Reddan J.R., Kochevar I.E. Action spectrum for cytotoxicity in the UVA-wavelength and UVB-wavelength region in cultured lens epithelial-cells. Investigative Ophthalmology and Visual Science 1994, 35:367-373.
21. Frankenberg L., Brugna M., Hederstedt L. Enterococcus faecalis heme-dependent catalase. Journal of Bacteriology 2002, 184:6351-6356.
22. Henry C.A., Dyer B., Wagner M., Judy M., Matthews J.L. Phototoxicity of argon laser irradiation on biofilms of Porphyromonas and Prevotella species. Journal of Photochemistry and Photobiology B 1996, 34:123-128.
23. Maclean M., MacGregor S.J., Anderson J.G., Woolsey G. Inactivation of bacterial pathogens following exposure to light from a 405-nm light-emitting diode array. Applied and Environmental Microbiology 2009, 75:1932-1937.
24. Kotoku Y., Kato J., Akashi G., Hirai Y., Ishihara K. Bactericidal effect of a 405-nm diode laser on Porphyromonas gingivalis. Laser Physics Letters 2009, 6:388-392.
25. Soukos N.S., Som S., Abernethy A.D., Ruggiero K., Dunham J., Lee C., et al. Phototargeting oral black-pigmented bacteria. Antimicrobial Agents and Chemotherapy 2005, 49:1391-1396.
26. Feuerstein O., Ginsburg I., Dayan E., Veler D., Weiss E.I. Mechanism of visible light phototoxicity on Porphyromonas gingivalis and Fusobacterium nucleatum. Photochemistry and Photobiology 2005, 81:1186-1189.
27. Chen W., Honma K., Sharma A., Kuramitsu H.K. A universal stress protein of Porphyromonas gingivalis is involved in stress responses and biofilm formation. Fems Microbiology Letters 2006, 264:15-21.
28. Loe H., Silness J. Periodontal disease in pregnancy. I. Prevalence and severity. Acta Odontologica Scandinavica 1963, 21:533-551.
29. Henry C.A., Judy M., Dyer B., Wagner M., Matthews J.L. Sensitivity of Porphyromonas and Prevotella species in liquid media to argon laser. Photochemistry and Photobiology 1995, 61:410-413.
30. Fukui M., Yoshioka M., Satomura K., Nakanishi H., Nagayama M. Specific-wavelength visible light irradiation inhibits bacterial growth of Porphyromonas gingivalis. Journal of Periodontal Research 2008, 43:174-178.
31. Guffey J.S., Wilborn J. In vitro bactericidal effects of 405-nm and 470-nm blue light. Photomedicine and Laser Surgery 2006, 24:684-688.
32. Enwemeka C.S., Williams D., Hollosi S., Yens D., Enwemeka S.K. Visible 405nm SLD light photo-destroys methicillin-resistant Staphylococcus aureus (MRSA) in vitro. Lasers in Surgery and Medicine 2008, 40:734-737.
33. Murdoch L.E., Maclean M., MacGregor S.J., Anderson J.G. Inactivation of Campylobacter jejuni by exposure to high-intensity 405-nm visible light. Foodborne Pathogens and Disease 2010, 7:1211-1216.
34. Ashkenazi H., Malik Z., Harth Y., Nitzan Y. Eradication of Propionibacterium acnes by its endogenic porphyrins after illumination with high intensity blue light. Fems Immunology and Medical Microbiology 2003, 35:17-24.
35. Ganz R.A., Viveiros J., Ahmad A., Ahmadi A., Khalil A., Tolkoff M.J., et al. Helicobacter pylori in patients can be killed by visible light. Lasers in Surgery and Medicine 2005, 36:260-265.
36. Hanson E.K., Ballantyne J. A blue spectral shift of the hemoglobin soret band correlates with the age (time since deposition) of dried bloodstains. PLoS ONE 2010, 5:e12830-e12840.
37. Butler I.B., Schoonen M.A.A., Rickard D.T. Removal of dissolved-oxygen from water - a comparison of 4 common techniques. Talanta 1994, 41:211-215.
38. Izzo A.D., Walsh J.T. Light-induced modulation of Porphyromonas gingivalis growth, Journal of photochemistry and photobiology B. Biology 2004, 77:63-69.
39. Maclean M., Macgregor S.J., Anderson J.G., Woolsey G.A. The role of oxygen in the visible-light inactivation of Staphylococcus aureus. Journal of Photochemistry and Photobiology B, Biology 2008, 92:180-184.
40. Huang L., Xuan Y., Koide Y., Zhiyentayev T., Tanaka M., Hamblin M.R., et al. mechanisms of antimicrobial photodynamic therapy: an in vitro study on gram-negative and gram-positive bacteria. Lasers in Surgery and Medicine 2012, 44:490-499.
41. Bouillaguet S., Wataha J.C., Zapata O., Campo M., Lange N., Schrenzel J. Production of reactive oxygen species from photosensitizers activated with visible light sources available in dental offices. Photomedicine and Laser Surgery 2010, 28:519-525.
42. Mettraux G.R., Gusberti F.A., Graf H. Oxygen tension (pO2) in untreated human periodontal pockets. Journal of Periodontology 1984, 55:516-521.