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Published Online:https://doi.org/10.2217/fmb-2022-0191

Cutibacterium acnes protects skin homeostasis. The species has three subspecies, and associations between C. acnes subsp. acnes and acne, C. acnes subsp. defendens and prostate cancer, and C. acnes subsp. elongatum and progressive macular hypomelanosis have recently been suggested. Different phylotypes/clonal complexes may cause prosthetic joint and other infections, and virulence factors such as fimbriae, biofilms, multidrug-resistance plasmids, porphyrin, Christie–Atkins–Munch–Petersen factors and cytotoxicity contribute to infections. Isolates are subtyped by multiplex PCR or multi- or single-locus sequence typing; however, these methods could be better synchronized. Resistance of acneic strains to macrolides (25.0–73.0%), clindamycin (10.0–59.0%) and tetracyclines (up to 37.0%) is worrisome, but susceptibility testing is now facilitated by European Committee on Antimicrobial Susceptibility Testing disk diffusion breakpoints. New therapeutic approaches include sarecycline, antimicrobial peptides and bacteriophages.

What is this summary about?

Cutibacterium acnes is necessary for skin health. However, different subspecies and types may be associated with different diseases. At present, the species has three known subspecies and six known major phylotypes.

What were the results?

Acne results from a disturbance of the skin bacteria. It has often been linked to C. acnes, whereas associations of other subspecies with prostate cancer, skin disease and various infections have been observed. Strain typing can be performed with different techniques; however, methods should be better synchronized. Resistance of isolates from acne to antibiotics is high. Antibiotic susceptibility testing is necessary and is being facilitated. New treatments with newer antibiotics, antimicrobial peptides and phages are promising.

What do the results mean?

C. acnes has three subspecies and numerous types that can support skin health or be linked to different diseases. New associations between different subspecies and prostate cancer, skin disease and infections have been studied. C. acnes resistance to antibiotics is frequent; however, susceptibility testing has already been simplified.

Tweetable abstract

Cutibacterium acnes subspecies may be linked to #acne, #sarcoidosis, prostate #cancer and other #diseases. Outcomes depend on subtypes, virulence factors and microbial equilibrium.

Papers of special note have been highlighted as: • of interest; •• of considerable interest

References

  • 1. Scholz CFP, Kilian M. The natural history of cutaneous propionibacteria, and reclassification of selected species within the genus Propionibacterium to the proposed novel genera Acidipropionibacterium gen. nov., Cutibacterium gen. nov. and Pseudopropionibacterium gen. nov. Int. J. Syst. Evol. Microbiol. 66(11), 4422–4432 (2016).
  • 2. Dekio I, McDowell A, Sakamoto M, Tomida S, Ohkuma M. Proposal of new combination, Cutibacterium acnes subsp. elongatum comb. nov., and emended descriptions of the genus Cutibacterium, Cutibacterium acnes subsp. acnes and Cutibacterium acnes subsp. defendens. Int. J. Syst. Evol. Microbiol. 69(4), 1087–1092 (2019).
  • 3. Dagnelie MA, Khammari A, Dréno B, Corvec S. Cutibacterium acnes molecular typing: time to standardize the method. Clin. Microbiol. Infect. 24(11), 1149–1155 (2018). •• Suggests a suitable algorithm for Cutibacterium acnes molecular typing according to the degree of phylogeny identification needed.
  • 4. Liew-Littorin C, Brüggemann H, Davidsson S, Nilsdotter-Augustinsson Å, Hellmark B, Söderquist B. Clonal diversity of Cutibacterium acnes (formerly Propionibacterium acnes) in prosthetic joint infections. Anaerobe 59, 54–60 (2019).
  • 5. Dréno B, Pécastaings S, Corvec S, Veraldi S, Khammari A, Roques C. Cutibacterium acnes (Propionibacterium acnes) and acne vulgaris: a brief look at the latest updates. J. Eur. Acad. Dermatol. Venereol. 32(Suppl. 2), 5–14 (2018).
  • 6. Rozas M, Hart de Ruijter A, Fabrega MJ et al. From dysbiosis to healthy skin: major contributions of Cutibacterium acnes to skin homeostasis. Microorganisms 9(3), 628 (2021).
  • 7. Fischer K, Tschismarov R, Pilz A et al. Cutibacterium acnes infection induces type I interferon synthesis through the cGAS-STING pathway. Front. Immunol. 11, 571334 (2020).
  • 8. Flowers L, Grice EA. The skin microbiota: balancing risk and reward. Cell Host Microbe 28(2), 190–200 (2020).
  • 9. Brüggemann H, Al-Zeer MA. Bacterial signatures and their inflammatory potentials associated with prostate cancer. APMIS 128(2), 80–91 (2020). •• Discusses current data on prevalence, detection methods and probable association of bacterial species, including C. acnes, with prostate cancer.
  • 10. Nakase K, Koizumi J, Midorikawa R et al. Cutibacterium acnes phylogenetic type IC and II isolated from patients with non-acne diseases exhibit high-level biofilm formation. Int. J. Med. Microbiol. 311(7), 151538 (2021). • Reveals the clinical importance of high biofilm-producing C. acnes strains.
  • 11. Spittaels KJ, Ongena R, Zouboulis CC, Crabbé A, Coenye T. Cutibacterium acnes phylotype I and II strains interact differently with human skin cells. Front. Cell. Infect. Microbiol. 10, 575164 (2020).
  • 12. Spittaels KJ, van Uytfanghe K, Zouboulis CC, Stove C, Crabbé A, Coenye T. Porphyrins produced by acneic Cutibacterium acnes strains activate the inflammasome by inducing K+ leakage. iScience 24(6), 102575 (2021).
  • 13. Mayslich C, Grange PA, Dupin N. Cutibacterium acnes as an opportunistic pathogen: an update of its virulence-associated factors. Microorganisms 9(2), 303 (2021). •• Comprehensive review of numerous C. acnes virulence factors and their properties.
  • 14. Corvec S, Dagnelie MA, Khammari A, Dréno B. Taxonomy and phylogeny of Cutibacterium (formerly Propionibacterium) acnes in inflammatory skin diseases. Ann. Dermatol. Venereol. 146(1), 26–30 (2019).
  • 15. Dekio I, Asahina A, Shah HN. Unravelling the eco-specificity and pathophysiological properties of Cutibacterium species in the light of recent taxonomic changes. Anaerobe 71, 102411 (2021). • Discusses new data about Cutibacterium species, including C. acnes, Cutibacterium avidum, Cutibacterium modestum and Cutibacterium namnetense.
  • 16. Galobardes B, Davey Smith G, Jeffreys M, Kinra S, McCarron P. Acne in adolescence and cause-specific mortality: lower coronary heart disease but higher prostate cancer mortality: the Glasgow Alumni Cohort Study. Am. J. Epidemiol. 161(12), 1094–1101 (2005).
  • 17. Boisrenoult P. Cutibacterium acnes prosthetic joint infection: diagnosis and treatment. Orthop. Traumatol. Surg. Res. 104(1S), S19–S24 (2018).
  • 18. Sutcliffe S, Giovannucci E, Isaacs WB, Willett WC, Platz EA. Acne and risk of prostate cancer. Int. J. Cancer 121(12), 2688–2692 (2007).
  • 19. Ugge H, Udumyan R, Carlsson J et al. Acne in late adolescence and risk of prostate cancer. Int. J. Cancer 142(8), 1580–1585 (2018). •• Statistically proves the relationship between acne in puberty and risk of prostate cancer death in adulthood.
  • 20. Greydanus DE, Azmeh R, Cabral MD, Dickson CA, Patel DR. Acne in the first three decades of life: an update of a disorder with profound implications for all decades of life. Dis. Mon. 67(4), 101103 (2021).
  • 21. Tomida S, Nguyen L, Chiu BH et al. Pan-genome and comparative genome analyses of Propionibacterium acnes reveal its genomic diversity in the healthy and diseased human skin microbiome. mBio 4(3), e00003-13 (2013).
  • 22. Drent M, Crouser ED, Grunewald J. Challenges of sarcoidosis and its management. N. Engl. J. Med. 385(11), 1018–1032 (2021).
  • 23. Talreja J, Talwar H, Bauerfeld C et al. HIF-1α regulates IL-1β and IL-17 in sarcoidosis. Elife 8, e44519 (2019).
  • 24. Yamaguchi T, Costabel U, McDowell A et al. Immunohistochemical detection of potential microbial antigens in granulomas in the diagnosis of sarcoidosis. J. Clin. Med. 10(5), 983 (2021).
  • 25. Isshiki T, Homma S, Eishi Y et al. Immunohistochemical detection of Propionibacterium acnes in granulomas for differentiating sarcoidosis from other granulomatous diseases utilizing an automated system with a commercially available PAB antibody. Microorganisms 9(8), 1668 (2021). • Focuses on prevalence and detection methods of C. acnes in sarcoidosis and other granulomatous diseases.
  • 26. Wright JL, Lin DW, Stanford JL. Circumcision and the risk of prostate cancer. Cancer 118(18), 4437–4443 (2012).
  • 27. Price LB, Liu CM, Johnson KE et al. The effects of circumcision on the penis microbiome. PLOS ONE 5(1), e8422 (2010).
  • 28. McDowell A, McLaughlin J, Layton AM. Is Cutibacterium (previously Propionibacterium) acnes a potential pathogenic factor in the aetiology of the skin disease progressive macular hypomelanosis? J. Eur. Acad. Dermatol. Venereol. 35(2), 338–344 (2021). • Discusses the detection of C. acnes subsp. elongatum in patients with progressive macular hypomelanosis and results of antibacterial therapy of the disease.
  • 29. Aubin GG, Lavigne JP, Foucher Y et al. Tropism and virulence of Cutibacterium (formerly Propionibacterium) acnes involved in implant-associated infection. Anaerobe 47, 73–78 (2017).
  • 30. Namdari S, Nicholson T, Abboud J et al. Comparative study of cultures and next-generation sequencing in the diagnosis of shoulder prosthetic joint infections. J. Shoulder Elbow Surg. 28(1), 1–8 (2019).
  • 31. Torrens C, Marí R, Alier A, Puig L, Santana F, Corvec S. Cutibacterium acnes in primary reverse shoulder arthroplasty: from skin to deep layers. J. Shoulder Elbow Surg. 28(5), 839–846 (2019).
  • 32. Brüggemann H, Salar-Vidal L, Gollnick HPM, Lood R. A Janus-faced bacterium: host-beneficial and -detrimental roles of Cutibacterium acnes. Front. Microbiol. 12, 673845 (2021). •• Reviews important disease associations of C. acnes.
  • 33. Coenye T, Spittaels KJ, Achermann Y. The role of biofilm formation in the pathogenesis and antimicrobial susceptibility of Cutibacterium acnes. Biofilm 4, 100063 (2021).
  • 34. Ciofu O, Moser C, Jensen PØ, Høiby N. Tolerance and resistance of microbial biofilms. Nat. Rev. Microbiol. 20(10), 621–635 (2022).
  • 35. Capoor MN, Ruzicka F, Schmitz JE et al. Propionibacterium acnes biofilm is present in intervertebral discs of patients undergoing microdiscectomy. PLOS ONE 12(4), e0174518 (2017).
  • 36. McDowell A. Over a decade of recA and tly gene sequence typing of the skin bacterium Propionibacterium acnes: what have we learnt? Microorganisms 6(1), 1 (2017).
  • 37. Barnard E, Nagy I, Hunyadkürti J, Patrick S, McDowell A. Multiplex touchdown PCR for rapid typing of the opportunistic pathogen Propionibacterium acnes. J. Clin. Microbiol. 53(4), 1149–1155 (2015).
  • 38. Lomholt HB, Scholz CFP, Brüggemann H, Tettelin H, Kilian M. A comparative study of Cutibacterium (Propionibacterium) acnes clones from acne patients and healthy controls. Anaerobe 47, 57–63 (2017).
  • 39. Aarhus University. SLST for Cutibacterium acnes (formerly Propionibacterium acnes) (2022). http://medbac.dk/slst/pacnes (Accessed 10 August 2022).
  • 40. Shah RA, Hsu JI, Patel RR, Mui UN, Tyring SK. Antibiotic resistance in dermatology: the scope of the problem and strategies to address it. J. Am. Acad. Dermatol. 86(6), 1337–1345 (2022). •• Summarizes current and new approaches to treating dermatological infections, including acne.
  • 41. Maraki S, Mavromanolaki VE, Stafylaki D, Kasimati A. Antimicrobial susceptibility patterns of clinically significant gram-positive anaerobic bacteria in a Greek tertiary-care hospital, 2017–2019. Anaerobe 64, 102245 (2020).
  • 42. Broly M, Ruffier d'Epenoux L, Guillouzouic A et al. Propionibacterium/Cutibacterium species-related positive samples, identification, clinical and resistance features: a 10-year survey in a French hospital. Eur. J. Clin. Microbiol. Infect. Dis. 39(7), 1357–1364 (2020).
  • 43. Alkhawaja E, Hammadi S, Abdelmalek M, Mahasneh N, Alkhawaja B, Abdelmalek SM. Antibiotic resistant Cutibacterium acnes among acne patients in Jordan: a cross sectional study. BMC Dermatol. 20(1), 17 (2020).
  • 44. Sheffer-Levi S, Rimon A, Lerer V et al. Antibiotic susceptibility of Cutibacterium acnes strains isolated from Israeli acne patients. Acta Derm. Venereol. 100(17), adv00295 (2020).
  • 45. Aoki S, Nakase K, Hayashi N, Nakaminami H, Noguchi N. Increased prevalence of doxycycline low-susceptible Cutibacterium acnes isolated from acne patients in Japan caused by antimicrobial use and diversification of tetracycline resistance factors. J. Dermatol. 48(9), 1365–1371 (2021).
  • 46. Castellanos Lorduy HJ, Pérez Cely HC, Casadiego Rincón EJ, Henao Riveros SC, Colorado CL. Cutibacterium acnes tetracycline resistance profile in patients with acne vulgaris, in a Colombian dermatologic center. Actas Dermosifiliogr. (Engl. Ed.) doi: 10.1016/j.ad.2021.05.004 (2021) (Epub ahead of print).
  • 47. Zhang J, Yu F, Fu K et al. C. acnes qPCR-based antibiotics resistance assay (ACQUIRE) reveals widespread macrolide resistance in acne patients and can eliminate macrolide misuse in acne treatment. Front. Public Health 10, 787299 (2022).
  • 48. Heng AHS, Chew FT. Systematic review of the epidemiology of acne vulgaris. Sci. Rep. 10(1), 5754 (2020).
  • 49. European Committee on Antimicrobial Susceptibility Testing. Breakpoint tables for interpretation of MICs and zone diameters (2022). www.eucast.org
  • 50. Nakase K, Aoki S, Sei S et al. Characterization of acne patients carrying clindamycin-resistant Cutibacterium acnes: a Japanese multicenter study. J. Dermatol. 47(8), 863–869 (2020).
  • 51. Haidari W, Bruinsma R, Cardenas-de la Garza JA, Feldman SR. Sarecycline review. Ann. Pharmacother. 54(2), 164–170 (2020).
  • 52. Woodburn KW, Jaynes J, Clemens LE. Designed antimicrobial peptides for topical treatment of antibiotic resistant acne vulgaris. Antibiotics (Basel) 9(1), 23 (2020).
  • 53. Castillo DE, Nanda S, Keri JE. Propionibacterium (Cutibacterium) acnes bacteriophage therapy in acne: current evidence and future perspectives. Dermatol. Ther. (Heidelb.) 9(1), 19–31 (2019).
  • 54. Janus SE, Durieux JC, Hajjari J, Carneiro H, McComsey GA. Inflammation-mediated vitamin K and vitamin D effects on vascular calcifications in people with HIV on active antiretroviral therapy. AIDS 36(5), 647–655 (2022).
  • 55. Podgórska A, Puścion-Jakubik A, Markiewicz-Żukowska R, Gromkowska-Kępka KJ, Socha K. Acne vulgaris and intake of selected dietary nutrients – a summary of information. Healthcare (Basel) 9(6), 668 (2021).