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. Author manuscript; available in PMC: 2023 Jun 8.
Published in final edited form as: Nat Immunol. 2023 Jun;24(6):895–898. doi: 10.1038/s41590-023-01500-6

Table 1 |.

Knowledge gaps in skin microbiome research

Topics Gaps
Microbial interactions
  • How do different species of microorganisms influence each other’s colonization and function?

  • How do the different species of microorganisms collaborate to maintain a host’s homeostasis? What are the mechanisms that contribute to skin dysbiosis?

  • How does the skin microbiome reestablish new homeostasis once some commensals are removed or changed?

Interaction between microbiome and host
  • What are the age-, sex-, location-, or hormone-specific commensals? What are the underlying mechanisms?

  • What is the role of the host immune system during a change of commensals’ colonization? How do commensals interact with the innate and adaptive immune components?

  • How does a human body sense different commensal antigens? What are the receptors, the antigens, the antigen-presenting cells and the key signaling pathways?

Microbiome transmission and dynamics
  • How are commensals shared between family members, roommates, or between humans and pets? What are the benefits and potential harms?

  • What roles do the host and environmental factors have during this process?

  • How does microbiome transmission affect the dynamics and stability of microbiota?

Microorganisms and skin conditions
  • How do changes in cutaneous microbiota alter the skin microenvironment?

  • How does fungal or parasitic skin microorganisms modulate skin inflammatory diseases?

  • Would antibiotic treatment be a useful additional therapy for skin inflammatory, parasitic or fungal infectious diseases?

Implementing integration of strains in vivo
  • How can we induce sufficient production and directional diffusion of a microbial product of interest with the proper size and function?

  • What is the composition of the different microbial species colonizing the human bodysp;? Why do they colonize different areas? How can specific commensals be colonized in areas of interest?

  • How can colonization resistance of the skin microbiome be overcome at a sufficient density and reproducibly while heeding strain diversity?

  • Can we use components of the skin microbiome as therapeutic strategies to decolonize pathogens?