Microbial Bioactives

Microbial Bioactives | Online ISSN 2209-2161
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Marine Actinobacteria as Emerging Anti-Infective Resources for Acne Vulgaris: A Systematic Review–Driven Perspective on Microbial Dysbiosis, Antimicrobial Resistance, and Novel Therapeutic Opportunities

Abstract 1. Introduction 2. Materials and Methods 3. Results 4. Discussion 5. Limitations 6. Conclusion References

Amena Khatun Manica 1*, Shahadat Hossain 2

+ Author Affiliations

Microbial Bioactives 9 (1) 1-8 https://doi.org/10.25163/microbbioacts.9110619

Submitted: 17 December 2025 Revised: 12 February 2026  Accepted: 20 February 2026  Published: 22 February 2026 


Abstract

Acne vulgaris (AV) is a chronic inflammatory disorder of the pilosebaceous unit that affects a large proportion of adolescents and adults worldwide, imposing substantial physical, psychological, and social burdens. The disease is closely associated with alterations in the skin microbiome, particularly involving Cutibacterium acnes, Staphylococcus aureus, and Staphylococcus epidermidis. Conventional acne therapies rely heavily on topical and systemic antibiotics, retinoids, and hormonal agents; however, their long-term use is limited by adverse effects and the accelerating emergence of antimicrobial resistance. These challenges highlight an urgent need for alternative, resistance-conscious therapeutic strategies. This study synthesizes evidence from a systematic review and meta-analytic perspective to evaluate marine actinobacteria as a promising source of novel anti-infective compounds relevant to AV management. Marine actinobacteria, shaped by extreme and diverse oceanic environments, possess exceptional biosynthetic potential and produce structurally unique secondary metabolites with antibacterial, antibiofilm, and quorum-sensing inhibitory activities. The reviewed evidence demonstrates substantial activity of marine actinobacteria-derived compounds against S. aureus and S. epidermidis, including multidrug-resistant strains, through both growth inhibition and virulence attenuation mechanisms. Notably, the analysis reveals a critical research gap: despite extensive activity against staphylococcal species, there is a striking lack of reported marine actinobacterial metabolites specifically targeting C. acnes. This finding is particularly significant given the historical success of actinobacteria-derived antibiotics in acne therapy. Overall, the review underscores the untapped potential of marine actinobacteria as a foundation for developing next-generation acne treatments that prioritize microbial balance, reduced resistance pressure, and innovative mechanisms of action.

Keywords: Acne vulgaris; marine actinobacteria; Cutibacterium acnes; antimicrobial resistance; antibiofilm activity; quorum sensing inhibition; skin microbiome

References

Arasu, M. V., Valli, K., Radhakrishnan, R., Duraipandiyan, V., Al-Dhabi, N. A., & Ignacimuthu, S. (2013). Marine polyketide metabolites. Chemosphere, 90, 479–487. https://doi.org/10.1016/j.chemosphere.2012.07.037

Balasubramanian, S., Skaf, J., Holzgrabe, U., Bharti, R., Förstner, K. U., Ziebuhr, W., Humeida, U. H., Abdelmohsen, U. R., & Oelschlaeger, T. A. (2018). A new bioactive compound from the marine sponge-derived Streptomyces sp. SBT348 inhibits staphylococcal growth and biofilm formation. Frontiers in Microbiology, 9, 1473. https://doi.org/10.3389/fmicb.2018.01473

Brandwein, M., Steinberg, D., & Meshner, S. (2016). Microbial biofilms and skin. NPJ Biofilms and Microbiomes, 2, 3. https://doi.org/10.1038/npjbiofilms.2016.3

Cai, W., Chen, Q. Y., Dang, L. H., & Luesch, H. (2017). Apratoxin S10, a dual inhibitor of angiogenesis and cancer cell growth to treat highly vascularized tumors. ACS Medicinal Chemistry Letters, 8(9), 1007–1012. https://doi.org/10.1021/acsmedchemlett.7b00192

Cheng, Y. B., Jensen, P. R., & Fenical, W. (2013). Cytotoxic and antimicrobial napyradiomycins from two marine-derived Streptomyces strains. European Journal of Organic Chemistry, 2013(17), 3751–3757. https://doi.org/10.1002/ejoc.201300349

Cheng, Y.-B., He, H.-Y., Tian, X., Li, X.-L., & Li, Y.-Q. (2013). Napyradiomycins. European Journal of Organic Chemistry, 3751–3757. https://doi.org/10.1002/ejoc.201300305

Cho, E., Kwon, O. S., Chung, B., Lee, J., Sun, J., Shin, J., & Oh, K. B. (2020). Antibacterial activity of chromomycins from a marine-derived Streptomyces microflavus. Marine Drugs, 18(10), 522. https://doi.org/10.3390/md18100522

Chung, B., Kwon, O. S., Shin, J., & Oh, K. B. (2020). Antibacterial activity and mode of action of lactoquinomycin A from Streptomyces bacillaris. Marine Drugs, 19(1), 7. https://doi.org/10.3390/md19010007

de La Hoz-Romo, M. C., Díaz, L., & Villamil, L. (2022). Marine actinobacteria as antibacterial sources for acne vulgaris. Antibiotics, 11, 965. https://doi.org/10.3390/antibiotics11070965

de Sousa, I. C. V. D., Silva, M. T., & Almeida, L. R. (2020). FMX-101 for acne. Expert Opinion on Pharmacotherapy, 21, 741–746. https://doi.org/10.1080/14656566.2020.1721461

Dholakiya, R. N., Patel, J. J., & Desai, H. G. (2017). Marine actinobacteria bioactivity. Frontiers in Microbiology, 8, 2420. https://doi.org/10.3389/fmicb.2017.02420

Elsayed, Y., Hassan, A. M., & Fahmy, M. H. (2018). Rhodococcus metabolites. Phytochemical Analysis, 29, 543–548. https://doi.org/10.1002/pca.2763

Farrah, G., & Tan, E. (2016). Oral antibiotics in acne. Dermatologic Therapy, 29, 377–384. https://doi.org/10.1111/dth.12398

Fournière, M., Dupont, M., & Thomas, D. (2020). Skin microbiota sentinels. Microorganisms, 8, 1752. https://doi.org/10.3390/microorganisms8111752

Gannesen, A. V., Kozlova, L., & Petrov, A. (2019). Biofilm matrix of Cutibacterium acnes. Frontiers in Microbiology, 10, 1284. https://doi.org/10.3389/fmicb.2019.01284

Gavriilidou, A., Papatheodorou, G., & Dimitrios, P. (2021). Marine sponge bacteria. Marine Drugs, 19, 75. https://doi.org/10.3390/md19020075

Heng, A. H. S., & Chew, F. T. (2020). Systematic review of the epidemiology of acne vulgaris. Scientific Reports, 10, 5754. https://doi.org/10.1038/s41598-020-62529-7

Hifnawy, M. S., El-Gendy, M. A., & Abdel-Razek, A. G. (2020). Co-cultivation induced metabolites. Marine Drugs, 18, 243. https://doi.org/10.3390/md18050243

Horbert, R., Pinchbeck, B., Jäger, E., Schlüter, J., Stumpf, D., Ciesielski, D., Thiem, F., Schollmeyer, D., & Proschak, E. (2014). Optimization of potent DFG-in inhibitors of platelet-derived growth factor receptor β (PDGF-Rβ) guided by water thermodynamics. Journal of Medicinal Chemistry, 58(1), 170–182. https://doi.org/10.1021/jm500373x

Hughes, C. C., Fenical, W., & Jensen, P. R. (2008). Marinopyrroles. ChemInform, 629–631. https://doi.org/10.1002/chin.200840228

Iniyan, A. M., Mary, T. R. J., Joseph, F. J. R. S., Kannan, R. R., & Vincent, S. G. P. (2016). Cell wall distracting anti-methicillin-resistant Staphylococcus aureus compound PVI331 from a marine sponge-associated Streptomyces. Journal of Applied Biomedicine, 14(4), 273–283. https://doi.org/10.1016/j.jab.2016.04.003

Jiao, W. H., Yuan, W., Li, Z. Y., Li, J., Li, L., Sun, J. B., Gui, Y. H., Wang, J., Ye, B. P., & Lin, H. W. (2018). Anti-MRSA actinomycins D1–D4 from the marine sponge-associated Streptomyces sp. LHW52447. Tetrahedron, 74(41), 5914–5919. https://doi.org/10.1016/j.tet.2018.08.023

Kim, M. C., Li, Z., Cullum, R., Molinski, T. F., Eid, M. A. G., Hebishy, A. M. S., Faraag, A. H. I., Abdel Moneim, A. E., Abdelfattah, M. S., & Fenical, W. (2022). Chlororesistoflavins A and B, chlorinated benzopyrene antibiotics produced by the marine-derived actinomycete Streptomyces sp. strain EG32. Journal of Natural Products, 85(2), 270–275. https://doi.org/10.1021/acs.jnatprod.1c01084

Kock, I., Meyers, P., & Schwalbe, H. (2005). Marine Streptomycete antibiotics. Journal of Antibiotics, 58, 530–534. https://doi.org/10.1038/ja.2005.111

Kwon, H. C., Kauffman, C. A., Jensen, P. R., & Fenical, W. (2006). Marinomycins A–D, antitumor antibiotics of a new structure class from a marine actinomycete of the recently discovered genus Marinispora. Journal of the American Chemical Society, 128(5), 1622–1632. https://doi.org/10.1021/ja0558948

Lim, H. J., Kim, H. J., & Lee, J. S. (2022). Ligiamycins from marine bacteria. Marine Drugs, 20, 93. https://doi.org/10.3390/md20020093

Liu, L. L., Xu, Y., Han, Z., Li, Y. X., Lu, L., Lai, P. Y., Zhong, J. L., Guo, X. R., Zhang, X. X., & Qian, P. Y. (2012). Four new antibacterial xanthones from the marine-derived actinomycetes Streptomyces caelestis. Marine Drugs, 10(11), 2571–2583. https://doi.org/10.3390/md10112571

Mary, T. R. J., Kannan, R. R., Iniyan, A. M., Ramachandran, D., & Vincent, S. G. P. (2020). Cell wall distraction and biofilm inhibition of marine Streptomyces-derived angucycline in methicillin-resistant Staphylococcus aureus. Microbial Pathogenesis, 150, 104712. https://doi.org/10.1016/j.micpath.2020.104712

Miao, L., Qian, S., Qi, S., Jiang, W., & Dong, K. (2021). Culture medium optimization and active compounds investigation of an anti-quorum sensing marine actinobacterium Nocardiopsis dassonvillei JS106. Microbiology, 90(1), 112–123. https://doi.org/10.1134/S0026261721010070

Miller, B. W., Torres, J. P., Tun, J. O., Flores, M. S., Forteza, I., Rosenberg, G., Haygood, M. G., Schmidt, E. W., & Concepcion, G. P. (2020). Synergistic anti-methicillin-resistant Staphylococcus aureus (MRSA) activity and absolute stereochemistry of 7,8-dideoxygriseorhodin C. The Journal of Antibiotics, 73(5), 290–298. https://doi.org/10.1038/s41429-019-0275-8

Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., & PRISMA Group. (2009). PRISMA statement. PLoS Medicine, 6, e1000097. https://doi.org/10.1371/journal.pmed.1000097

Newaz, A. W., Rahman, M., & Karim, M. (2022). Streptoindoles. Tetrahedron, 104, 132598. https://doi.org/10.1016/j.tet.2022.132598

O'Neill, J., Smith, P., & Thompson, R. (2016). Review on antimicrobial resistance. Revue. https://revue.revuesonline.com/article.jsp?articleId=22904

Paderog, M. J. V., Santos, L., & Fernandez, R. (2020). Marine Streptomyces vs MRSA. Frontiers in Microbiology, 11, 743. https://doi.org/10.3389/fmicb.2020.00743

Palomo, S., González, I., de la Cruz, M., Martín, J., Tormo, J. R., Anderson, M., Hill, R. T., Vicente, F., Reyes, F., & Genilloud, O. (2013). Sponge-derived Kocuria and Micrococcus spp. as sources of the new thiazolyl peptide antibiotic kocurin. Marine Drugs, 11(4), 1071–1086. https://doi.org/10.3390/md11041071

Pham, J. V., Kim, S., Cho, H., & Park, J. (2019). Microbial natural products. Frontiers in Microbiology, 10, 1404. https://doi.org/10.3389/fmicb.2019.01404

Platsidaki, E., Dessinioti, C., & Gaitanis, G. (2018). Cutibacterium acnes and acne pathogenesis. F1000Research, 7, 1953. https://doi.org/10.12688/f1000research.16781.1

Ryu, M. J., Hillman, P. F., Lee, J., Hwang, S., Lee, E. Y., Cha, S. S., Yang, I., Oh, D. C., Nam, S. J., & Fenical, W. (2021). Antibacterial meroterpenoids, merochlorins G–J from the marine bacterium Streptomyces sp. Marine Drugs, 19(11), 618. https://doi.org/10.3390/md19110618

Santos, J. D., Almeida, R. F., Costa, P. R., & Oliveira, F. S. (2019). Actinomycetales from sponges. Frontiers in Microbiology, 10, 727. https://doi.org/10.3389/fmicb.2019.00727

Shen, X., Liu, Y., Wang, Z., & Zhang, Q. (2020). Meroterpenoids. Biomolecules, 10, 1187. https://doi.org/10.3390/biom10081187

Sung, A. A., Lee, H., Kim, J., & Park, S. (2017). Marine Streptomyces co-cultures. Marine Drugs, 15, 250. https://doi.org/10.3390/md15080250

Tuchayi, S. M., Kilani, R., & Goldberg, D. (2015). Acne vulgaris. Nature Reviews Disease Primers, 1, 15029. https://doi.org/10.1038/nrdp.2015.29

Veale, C. G. L., Roya, Z., Young, R. M., Morrison, J. P., Manoja, P., Lobb, K. A., Reiner, N. E., Andersen, R. J., & Davies-Coleman, M. T. (2015). Synthetic analogues of the marine bisindole deoxytopsentin: Potent selective inhibitors of MRSA pyruvate kinase. Journal of Natural Products, 78(2), 355–362. https://doi.org/10.1021/np500755v

Wang, J. N., Zhang, H. J., Li, J. Q., Ding, W. J., & Ma, Z. J. (2018). Bioactive indolocarbazoles from the marine-derived Streptomyces sp. DT-A61. Journal of Natural Products, 81(4), 949–956. https://doi.org/10.1021/acs.jnatprod.7b01058

Wu, B., Wiese, J., Schmaljohann, R., & Imhoff, J. (2016). Biscogniauxone, a new isopyrrolonaphthoquinone compound from the fungus Biscogniauxia mediterranea isolated from deep-sea sediments. Marine Drugs, 14(11), 204. https://doi.org/10.3390/md14110204

Yin, Q., Liang, J., Zhang, W., Zhang, L., Hu, Z. L., Zhang, Y., & Xu, Y. (2019). Butenolide, a marine-derived broad-spectrum antibiofilm agent against both gram-positive and gram-negative pathogenic bacteria. Marine Biotechnology, 21(1), 88–98. https://doi.org/10.1007/s10126-018-9861-1

Yu, M., Liu, X., & Zhang, Q. (2019). Marine actinomycete co-cultures. Frontiers in Microbiology, 10, 915. https://doi.org/10.3389/fmicb.2019.00915


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