Scientifically grounded · Dermatology-informed · No marketing claims
Definition
The skin microbiome is the collection of bacteria, fungi, viruses, and microorganisms living on the skin surface that help protect against pathogens, regulate immunity, and maintain skin barrier function. A balanced skin microbiome is essential for preventing eczema, acne, rosacea, and chronic sensitivity.
Quick Answer — What Is the Skin Microbiome?
The skin microbiome is the vast community of microorganisms — bacteria, fungi, viruses, and microscopic mites — that live on and within the skin's surface, directly shaping how your skin behaves day to day. Far from being something to eliminate, most of these microorganisms are harmless or actively beneficial. They compete against harmful pathogens, help regulate immunity, support the skin barrier, and maintain the slightly acidic environment that keeps skin balanced. When this community is disrupted — by harsh cleansers, antibiotics, stress, or the wrong skincare ingredients — the consequences show up directly on your skin.
If your skin has been "fine" for years and suddenly becomes reactive, congested, or sensitive for no obvious reason — your microbiome is often the first place to look.
The skin microbiome: a living ecosystem of bacteria, fungi, viruses, and mites that actively supports skin health.
At a Glance
| What it is | The community of microorganisms living on the skin surface |
| Key residents | Bacteria, fungi, viruses, Demodex mites |
| Most beneficial bacterium | Staphylococcus epidermidis |
| Most disruptive bacterium | Staphylococcus aureus |
| Ideal skin pH for balance | 4.5 – 5.5 (slightly acidic) — see acid mantle guide |
| Linked conditions when disrupted | Eczema, acne, rosacea, psoriasis |
| Supported by | Prebiotics, postbiotics, pH-balanced care, ceramides |
| Disrupted by | Harsh cleansers, antibiotics, fragrance, over-exfoliation, stress |
The Bottom Line
- The skin microbiome is not dirt. It is a living ecosystem that plays an active role in skin health — supporting the barrier, regulating immunity, and defending against harmful microorganisms.
- The most important bacterial species for skin health is Staphylococcus epidermidis — it produces antimicrobial compounds, supports barrier repair, and actively competes against harmful bacteria.
- The skin microbiome and the skin barrier are interdependent. A disrupted barrier allows harmful bacteria in; those bacteria then further disrupt the barrier. Breaking this cycle requires working on both simultaneously.
- Eczema, acne, rosacea, and psoriasis all have well-documented microbiome associations — not as a cause of the condition, but as a contributing factor that worsens symptoms when the balance is lost.
- The most evidence-supported way to support the microbiome is not to add probiotics, but to stop disrupting it: pH-balanced cleansers, no unnecessary antibacterials, no fragrance, and a functioning skin barrier.
- Prebiotics and postbiotics in skincare show more consistent evidence than live topical probiotics, which struggle to survive in standard cosmetic formulations.
In This Article
- What is the skin microbiome?
- Who lives there — the key players
- What does the skin microbiome do?
- The microbiome–barrier connection
- The skin microbiome and common skin conditions
- What disrupts the skin microbiome?
- Signs your skin microbiome may be out of balance
- How to support your skin microbiome
- Prebiotics, probiotics, and postbiotics — what the evidence says
- Best skincare for supporting the skin microbiome
- Frequently asked questions
- Conclusion
For most of skincare history, bacteria on the skin were treated as a problem to be eliminated. Antibacterial soaps, alcohol toners, and harsh cleansers were considered thorough and effective. The goal was a "clean" skin surface.
We now know this was precisely wrong. The skin surface is not sterile — and it should not be. It is home to trillions of microorganisms that perform functions no skincare product can replicate: defending against pathogens, supporting the immune system, maintaining pH balance, and actively reinforcing the skin barrier.
The science of the skin microbiome has transformed dermatological thinking over the past two decades. Understanding it changes not just what you put on your skin — but what you should stop putting on it.
01 — The Concept
What Is the Skin Microbiome?
The word "microbiome" refers to the complete community of microorganisms living in a particular environment — their collective genes, metabolic activity, and interactions with the host. The skin microbiome is this community as it exists on and within the skin's surface.
The skin is the human body's most microbially diverse organ. Research estimates that one square centimetre of skin can host up to one million microorganisms. Across the entire skin surface, the total number is estimated in the trillions. These microorganisms exist in distinct communities that vary based on body site — the face, scalp, armpits, and forearms each host different microbial populations, shaped by local temperature, humidity, sebum levels, and pH.
Most of these microorganisms are permanent residents — called commensals — that have co-evolved with human skin over millions of years. They are not passing through. They are part of the skin's normal functioning. The minority that cause problems — called pathogens or opportunistic pathogens — typically only cause harm when the balance of the community shifts in their favour.
02 — The Residents
Who Lives There — The Key Players
The skin microbiome is dominated by bacteria, but also includes fungi, viruses, and microscopic mites. Understanding the key players — and what they do — explains why balance matters more than total elimination.

Staphylococcus epidermidis — the most protective commensal on the skin surface — alongside other key microbiome residents.
| Organism | Role in healthy skin | What happens when it overgrows |
|---|---|---|
| Staphylococcus epidermidis | Produces antimicrobial peptides; competes against S. aureus; supports barrier repair; helps regulate immune response | Generally harmless even at higher levels — one of the most beneficial skin commensals |
| Staphylococcus aureus | Low-level presence in healthy skin (rare); may be absent entirely | Releases enzymes and toxins that break down the skin barrier; worsens eczema inflammation; triggers immune activation |
| Cutibacterium acnes (formerly P. acnes) | Produces fatty acids from sebum that maintain acid mantle; low-level presence is normal | Certain strains, when dominant in follicles, contribute to acne inflammation — not a single-cause relationship |
| Malassezia (yeast) | Normal resident on sebum-rich areas (face, scalp); part of healthy skin ecology at low levels | Overgrowth associated with dandruff, seborrhoeic dermatitis, and folliculitis; context-dependent |
| Corynebacterium spp. | Dominant in moist skin areas; contribute to skin odour processing; generally commensal | Usually harmless; rarely problematic in immunocompetent individuals |
| Demodex mites | Microscopic mites living in hair follicles; low levels are normal in adults | Higher densities associated with rosacea; relationship is correlational and still being studied |
03 — The Function
What Does the Skin Microbiome Do?
The skin microbiome performs several functions that are difficult — or impossible — to replicate with skincare ingredients alone. These are not passive effects. They are active, ongoing biological processes happening on your skin right now.
1. Competitive exclusion — crowding out pathogens
Beneficial bacteria occupy the physical space on skin and consume available nutrients, leaving less room and fewer resources for harmful pathogens to establish themselves. This is called competitive exclusion — and it is one of the most fundamental mechanisms of microbiome protection. Remove the beneficial bacteria through over-cleansing or antibiotics, and the space they occupied becomes available for whatever comes next.
2. Antimicrobial production
S. epidermidis and other commensal bacteria produce natural antimicrobial compounds — including bacteriocins and serine proteases — that directly inhibit the growth of pathogens like S. aureus and certain fungal species. This is a biological defence system that no synthetic preservative system can fully replicate.
3. Immune regulation
The skin microbiome communicates directly with keratinocytes and immune cells in the epidermis, helping to calibrate the skin's immune response. A diverse, balanced microbiome supports immune tolerance — the ability to not react to harmless substances. A disrupted microbiome is associated with heightened immune reactivity — the skin overreacting to things it would normally ignore. This is the microbiological basis of sensitisation and the "suddenly reactive skin" phenomenon that many people experience. For more on how this affects sensitive skin, see our full guide.
4. Acid mantle maintenance
Several commensal bacteria produce organic acids as metabolic byproducts — including lactic acid and short-chain fatty acids. These contributions help maintain the skin surface's slightly acidic pH (4.5–5.5). When the microbiome is disrupted, this contribution is lost, and the acid mantle pH can drift upward — impairing barrier repair enzymes and creating conditions where S. aureus thrives more easily.
5. Barrier support
The microbiome and the skin barrier are in constant chemical communication. Commensal bacteria produce compounds that stimulate ceramide synthesis, support keratinocyte function, and reinforce tight junction integrity. The relationship is bidirectional — a healthy barrier supports a healthy microbiome, and a healthy microbiome supports a healthy barrier. Read our guide to ceramides in skincare for more on how to support this from the barrier side.
04 — The Connection
The Microbiome–Barrier Connection
The skin microbiome and the skin barrier are not separate systems — they are deeply interdependent. Understanding their relationship explains why so many skin conditions are so difficult to resolve when only one is addressed.
| Scenario | What happens to the barrier | What happens to the microbiome |
|---|---|---|
| Healthy, balanced state | Intact lipid matrix; low TEWL; stable acid mantle | Diverse, commensal-dominant; S. epidermidis active |
| Barrier disrupted first | Lipids depleted; TEWL elevated; pH rises | S. aureus colonises the alkaline, open surface; diversity falls |
| Microbiome disrupted first | S. aureus enzymes break down barrier lipids; tight junctions degraded | Beneficial bacteria unable to recolonise disrupted surface |
| Both disrupted — chronic state | Persistent high TEWL; chronic inflammation; reactive skin | Low diversity; S. aureus dominant; immune dysregulation |
This is the cycle seen in eczema: barrier disruption allows S. aureus to colonise, which releases toxins that further damage the barrier, which allows more colonisation. Research confirms that S. aureus can be detected on the skin of eczema patients even in clinically clear, non-flaring skin — meaning the microbiome imbalance persists even when symptoms appear resolved.
The practical implication: supporting only the barrier without addressing the microbiome — or vice versa — is an incomplete approach for chronically reactive or eczema-prone skin. Both systems need to be supported simultaneously. For a deeper look at TEWL measurement and barrier function, see our TEWL explainer.
05 — Skin Conditions
The Skin Microbiome and Common Skin Conditions
The research connecting microbiome balance to visible skin conditions has grown substantially in the past decade. The relationships are not simple cause-and-effect — they are bidirectional, with each condition both influencing and being influenced by the microbiome.
Microbiome dysbiosis contributes to four major skin conditions — but the relationship is bidirectional in each case.
Eczema (atopic dermatitis)
Evidence: Strong
S. aureus colonises the skin of approximately 90% of people with moderate-to-severe atopic dermatitis, compared to around 5–30% in people without the condition. This colonisation is not a coincidence — it is a driver. S. aureus produces serine proteases and toxins that directly break down ceramides, degrade tight junctions, and trigger immune pathways that sustain the inflammatory cycle. Reducing S. aureus colonisation — through microbiome-supportive care rather than broad-spectrum antibiotics — is now recognised as a meaningful component of eczema management.
Acne (acne vulgaris)
Evidence: Moderate-to-strong
The relationship between Cutibacterium acnes (C. acnes) and acne is more nuanced than previously understood. It is not simply that C. acnes causes acne — the organism is present on all skin types, including clear skin. What matters is strain diversity and relative dominance. Acne-prone skin shows reduced diversity within C. acnes strains and overrepresentation of certain inflammatory strains. Approaches that preserve overall microbiome diversity — rather than eliminating C. acnes entirely — are increasingly favoured in dermatological research.
Rosacea
Evidence: Emerging
Rosacea is associated with elevated levels of Demodex mites — which, at higher densities, may trigger immune responses in susceptible individuals — and with altered bacterial populations on facial skin. The microbiome differences seen in rosacea are consistently observed but causality is not yet fully established. What is clear is that microbiome-disruptive products — high-alcohol toners, harsh exfoliants, fragrance — consistently worsen rosacea symptoms.
Psoriasis
Evidence: Emerging-to-moderate
Psoriatic skin shows reduced microbiome diversity compared to healthy controls, with shifts in bacterial communities both at plaques and in uninvolved skin. Research into the gut-skin axis suggests that gut microbiome imbalance may also contribute to systemic inflammation that manifests in psoriasis — though this remains an area of active investigation.
06 — Disruption
What Disrupts the Skin Microbiome?
The skin microbiome is remarkably resilient — it can recover from short-term disruption. But repeated or sustained disruption shifts its composition in ways that take significantly longer to resolve. Most common disruptors are in the bathroom cabinet.
| Disruptor | Mechanism | Impact level |
|---|---|---|
| Alkaline soaps and harsh cleansers | Raise skin pH above 6.0; disrupt acid mantle; alter the chemical environment commensal bacteria depend on | High |
| Topical antibiotics | Eliminate broad microbial populations, not just target pathogens; create space for resistant organisms | High |
| Oral antibiotics | Reduce both gut and skin microbiome diversity; effects can persist for months after a course ends | High |
| Fragrance (synthetic and natural) | Recognised in dermatological literature as a well-documented contributor to sensitisation; antimicrobial properties in some compounds disrupt commensal bacteria | Moderate-high |
| Over-exfoliation | Removes corneocytes that commensal bacteria colonise; disrupts barrier that microbiome depends on | Moderate |
| Antimicrobial preservatives (certain) | Broad-spectrum antimicrobials in some formulations may suppress commensal as well as harmful bacteria | Moderate |
| High-concentration alcohol (denat) | Antimicrobial; strips surface microbiome alongside surface lipids | Moderate |
| Chronic stress | Cortisol alters skin pH and sebum composition; changes the nutrient environment that shapes bacterial populations | Moderate |
| UV exposure | Alters skin surface chemistry; suppresses local immune surveillance; associated with shifts in microbial diversity | Moderate |
| Poor sleep | Impairs skin barrier repair; indirectly affects the surface environment the microbiome inhabits | Low-moderate |
07 — Signs
Signs Your Skin Microbiome May Be Out of Balance
Microbiome imbalance — called dysbiosis — does not always announce itself clearly. Many of its signs overlap with other skin concerns, which is why it is frequently missed or misattributed.
| What you notice | What it may indicate about the microbiome |
|---|---|
| Skin that was stable becomes suddenly reactive | Loss of microbial diversity; reduced immune tolerance; often follows a course of antibiotics or a period of stress |
| Recurring small breakouts in new areas | Commensal bacteria no longer controlling C. acnes distribution; acid mantle disruption |
| Skin that stings or reacts to gentle products | Reduced barrier integrity driven by microbial imbalance; immune hypersensitivity from reduced tolerance |
| Persistent redness or warmth without obvious cause | Low-level immune activation — consistent with S. aureus presence or reduced commensal protection |
| Flaking or rough texture that is not dryness | May reflect dysbiosis affecting normal skin shedding (desquamation) — the microbiome plays a role in this process |
| Eczema that improves, then consistently returns | Classic pattern of incomplete microbiome restoration — barrier addressed, but S. aureus colonisation persisting |
08 — Support Protocol
How to Support Your Skin Microbiome
The most important insight from microbiome research is counterintuitive: the best way to support your skin microbiome is mostly about what you stop doing, not what you add. The microbiome has been managing itself successfully for the entirety of human evolution — it mainly needs you to stop disrupting it.
Microbiome-Supportive Skincare Protocol
The single highest-impact change. An SLS-free cleanser at pH 4.5–6.0 cleans effectively without stripping the commensal community or disrupting the acid mantle. Cleanse once daily at night; morning rinse with water is sufficient for most skin types.
Reserve antibacterial ingredients for specific clinical purposes. For daily cleansing, a gentle surfactant-based formula is more microbiome-compatible and achieves effective mechanical cleansing without wholesale microbial disruption.
If you are currently exfoliating daily or more than 3 times per week, this alone may be the primary driver of microbiome disruption. Reducing to 1–2 times per week — using a mild AHA at appropriate pH — allows the commensal community to re-establish between sessions.
A functioning skin barrier is the platform the microbiome lives on. Ceramide-based moisturisers, applied while skin is still slightly damp, help maintain the surface chemistry that commensal bacteria require. The microbiome cannot rebalance on a chronically disrupted barrier.
Fragrance — both synthetic and many natural essential oils — is recognised in dermatological literature as a well-documented contributor to sensitisation and microbiome disruption. Replacing fragranced products with fragrance-free alternatives reduces a significant ongoing stressor on the commensal community.
Prebiotics — ingredients that selectively feed beneficial bacteria — represent the most evidence-consistent approach to actively supporting the microbiome topically. Beta-glucan, inulin, and certain fermented extracts have shown capacity to support microbial balance without disrupting the commensal community.
09 — Ingredients
Prebiotics, Probiotics, and Postbiotics — What the Evidence Actually Says
The terms "probiotic," "prebiotic," and "postbiotic" have migrated from gut health into skincare — often with more marketing ambition than scientific rigour. Here is what the current evidence supports.
Prebiotics — the most consistently supported
Prebiotics are ingredients that selectively feed beneficial bacteria without being consumed themselves. In skincare, this typically means complex sugars, fermented extracts, and certain plant-derived compounds that S. epidermidis and other beneficial bacteria can metabolise, while S. aureus is less able to utilise.
Examples with evidence of skin microbiome support include inulin, beta-glucan, oat-derived compounds, and certain fermented botanical extracts. These can be incorporated into standard cosmetic formulations at effective concentrations. They do not require live bacteria to be present — they work by selectively shifting the nutrient environment.
Probiotics (live) — limited by formulation stability
The appeal of putting live beneficial bacteria directly on the skin is intuitive. The challenge is that most live bacteria cannot survive in cosmetic formulations — they require specific temperatures, pH conditions, and absence of preservatives that are incompatible with shelf-stable products. Some encapsulation technologies are emerging to address this, but the evidence for topical live probiotics in standard skincare formulations remains limited and inconsistent.
Postbiotics — the emerging category with real promise
Postbiotics are the beneficial metabolic byproducts produced when bacteria ferment substrates — including antimicrobial peptides, organic acids, enzymes, and cell wall fragments. These are biologically active compounds that retain functional properties without requiring live organisms to be present. Fermented ingredients — including fermented lactobacillus filtrate, fermented saccharomyces extracts, and others — are increasingly used in skincare formulations with growing evidence that they support barrier function, skin comfort, and microbial balance. This is the category that Bold Purity's AquaBlur™ and SkinReset™ PDRN Serum draw on in their formulation approach.
| Type | What it is | Evidence level | Practical rating |
|---|---|---|---|
| Prebiotic | Feeds beneficial bacteria selectively | Moderate-to-strong for microbiome support | ⭐⭐⭐⭐ — formulation-stable, consistent |
| Probiotic (live) | Live beneficial microorganisms applied topically | Limited — stability challenges in cosmetic formats | ⭐⭐ — promising concept, unresolved delivery |
| Postbiotic | Beneficial byproducts of bacterial fermentation | Emerging-to-moderate — growing body of evidence | ⭐⭐⭐⭐ — stable, bioactive, increasingly well-studied |
10 — Best Skincare for the Skin Microbiome
Best Skincare for Supporting the Skin Microbiome
Microbiome-supportive skincare is not a single product — it is a layered approach that addresses each stage of your routine. The sequence matters: a microbiome-disruptive cleanser undoes every subsequent step. Below are the three product categories with the highest evidence base, and how Bold Purity's formulations address each one.
A microbiome-supportive routine addresses cleansing pH, hydration layer chemistry, and barrier-repair actives in sequence.
AquaBlur™ Bubble Toner Serum
Fragrance-free, formulated at skin-compatible pH. Nano-encapsulated humectants hydrate the surface without disrupting the acid environment commensal bacteria depend on. The step that bridges cleansing and actives without a microbiome cost.
Shop AquaBlur™ →SkinReset™ PDRN Serum
PDRN (polydeoxyribonucleotide) supports cellular repair and skin barrier restoration — the structural foundation the microbiome requires to rebalance. Fragrance-free, clinically formulated for reactive and mature skin.
Shop SkinReset™ →CellMorph 500 Microneedling Serum
Formulated to support dermal matrix renewal and barrier integrity at a structural level. Used alongside a microbiome-supportive base routine, it addresses the deeper skin architecture that determines long-term barrier resilience.
Shop CellMorph →11 — FAQ
Frequently Asked Questions
What is the skin microbiome?
The skin microbiome is the community of microorganisms — bacteria, fungi, viruses, and mites — that live on and within the skin's surface. Most of these microorganisms are harmless or actively beneficial, supporting barrier function, regulating immunity, and protecting against harmful pathogens. The microbiome varies across different body sites, skin types, and individuals.
What does the skin microbiome do?
It competes with harmful pathogens for space and nutrients, produces antimicrobial compounds that limit bacterial overgrowth, helps regulate the skin's immune response, supports the acid mantle by contributing to the skin's slightly acidic pH, and interacts directly with the skin barrier to support its structural integrity.
What disrupts the skin microbiome?
The most common disruptors are harsh cleansers and soaps that alter skin pH, antibiotics (topical and oral), over-exfoliation, synthetic fragrance, certain preservatives, chronic stress, poor sleep, dietary changes, and environmental factors including pollution and UV exposure. Each of these shifts the balance of the microbiome away from beneficial species.
Is the skin microbiome linked to eczema and acne?
Yes — both conditions have well-documented microbiome associations. In eczema, Staphylococcus aureus overgrowth on disrupted skin worsens inflammation and barrier disruption. In acne, an imbalance in Cutibacterium acnes strains contributes to follicular inflammation. Both conditions may benefit when microbiome balance is supported alongside other approaches.
Do probiotics in skincare actually work?
The evidence for live probiotics in topical skincare is still developing — most live bacteria cannot survive in standard cosmetic formulations. What research more consistently supports is the use of prebiotics and postbiotics, alongside microbiome-friendly formulation principles such as appropriate pH and avoiding harsh antimicrobial ingredients.
How can I support my skin microbiome?
The most evidence-supported approach is to reduce unnecessary disruption: use pH-balanced, fragrance-free cleansers, avoid antibacterial soaps for daily use, reduce over-exfoliation, and support the skin barrier with ceramide-based moisturisers. Prebiotics in topical formulations can help feed beneficial bacteria.
What is the difference between prebiotics, probiotics, and postbiotics in skincare?
Prebiotics selectively feed beneficial skin bacteria — examples include inulin and beta-glucan. Probiotics are live microorganisms — their stability in cosmetic formulations is limited. Postbiotics are beneficial byproducts of bacterial fermentation, including peptides and organic acids, and these are increasingly used in skincare with growing evidence of benefit for barrier function and microbial balance.
Can you repair the skin microbiome?
Yes — the skin microbiome can recover, but the timeline depends on the severity and duration of disruption. Short-term disruption (a single course of antibiotics, a week of harsh cleansing) can resolve within weeks with microbiome-supportive care. Chronic disruption — sustained over months or years — may take considerably longer and may not fully restore to its previous composition. The most effective approach combines removing disruptors (fragrance, alkaline cleansers, antibacterials) with supporting the skin barrier and introducing prebiotic-containing formulations.
How long does the skin microbiome take to heal?
Research on antibiotic-induced microbiome disruption suggests partial recovery within 2–4 weeks for short-term disruption, though full restoration of bacterial diversity may take months. For chronic disruption associated with conditions like eczema, the microbiome requires consistent, long-term support rather than a short intervention. Signs of improvement — reduced reactivity, better moisture retention, calmer skin — often appear before full microbial diversity is restored.
Is microbiome skincare worth it?
The most evidence-supported microbiome skincare is not about adding exotic ingredients — it is about avoiding disruptive ones. Switching to fragrance-free, pH-balanced, non-antibacterial products represents the highest-impact change most people can make. Adding prebiotic-containing formulations provides additional support. Live probiotic skincare shows limited evidence in standard formulations, but postbiotic ingredients (fermented extracts, bacterial metabolites) have a growing evidence base and are formulation-stable.
Does washing your face damage the skin microbiome?
Washing the face with the wrong cleanser can significantly disrupt the skin microbiome. Alkaline bar soaps, SLS-heavy foaming cleansers, and antibacterial washes raise skin pH above the acid mantle range (4.5–5.5), creating conditions unfavourable to beneficial commensals and more hospitable to S. aureus. A pH-balanced, SLS-free, fragrance-free cleanser used once daily (evening) with a water rinse in the morning is the most microbiome-compatible approach.
12 — Conclusion
The Microbiome Is Not a Problem to Solve. It Is a System to Support.
The shift in understanding from "bacteria on skin are bad" to "bacteria on skin are essential" is one of the most significant changes in dermatological thinking of the past two decades. And it has direct, practical implications for what you do — and stop doing — every day.
Most skincare routines that cause long-term problems do so not because of what they fail to add, but because of what they continuously strip away. The commensal community that has lived on human skin for millions of years is extraordinarily good at its job — it just needs a surface that is not being disrupted faster than the microbiome can recover.
Less disruption, pH-compatible products, no fragrance, a functioning skin barrier. These are not complex interventions. But they are the ones the science most consistently supports — and they are the foundation on which everything else in a skincare routine should be built.
Microbiome-Compatible Skincare
Aquablur™ Bubble Toner Serum is formulated without fragrance, at a skin-compatible pH, with humectants that support surface hydration without disrupting the acid environment the skin's commensal community depends on.
Explore Aquablur™ →The microbiome may recover — but diversity takes time
Research on antibiotic-induced microbiome disruption shows that skin bacterial diversity can take weeks to months to partially recover after a course of topical or oral antibiotics — and may not fully return to its previous composition. This is one reason why skin that was stable before a round of antibiotics sometimes never quite returns to its previous state. Supporting the barrier and creating microbiome-compatible conditions during and after antibiotic treatment — fragrance-free products, pH-balanced care, prebiotic ingredients — is a strategy with growing evidence in the dermatological literature.
Scientific References
- Grice, E.A., & Segre, J.A. (2011). The skin microbiome. Nature Reviews Microbiology, 9(4), 244–253. PubMed →
- Nakatsuji, T., et al. (2017). Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis. Science Translational Medicine, 9(378). PubMed →
- Byrd, A.L., Belkaid, Y., & Segre, J.A. (2018). The human skin microbiome. Nature Reviews Microbiology, 16(3), 143–155. PubMed →
- Kong, H.H., et al. (2012). Temporal shifts in the skin microbiome of atopic dermatitis patients and healthy controls. Genome Research, 22(5), 850–859. PubMed →
- Fitz-Gibbon, S., et al. (2013). Propionibacterium acnes strain populations in the human skin microbiome associated with acne. Journal of Investigative Dermatology, 133(9), 2152–2160. PubMed →
- Prescott, S.L., et al. (2017). The skin microbiome: impact of modern environments on skin ecology, barrier integrity, and systemic immune programming. World Allergy Organization Journal, 10(1), 29.
- Williams, M.R., & Gallo, R.L. (2015). The role of the skin microbiome in atopic dermatitis. Current Allergy and Asthma Reports, 15(11), 65.
- Dekio, I., et al. (2005). Detection of potentially novel bacterial components of the human skin microbiota using culture-independent molecular profiling. Journal of Medical Microbiology, 54(12), 1231–1238.
- Rosenfeldt, V., et al. (2004). Effect of probiotic Lactobacillus strains in children with atopic dermatitis. Journal of Allergy and Clinical Immunology, 111(2), 389–395.
- Elias, P.M., & Schmuth, M. (2009). Abnormal skin barrier in the etiopathogenesis of atopic dermatitis. Current Allergy and Asthma Reports, 9(4), 265–272.
- Belkaid, Y., & Segre, J.A. (2014). Dialogue between skin microbiota and immunity. Science, 346(6212), 954–959. PubMed →
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