Xerosis, commonly referred to as dry skin, is a common dermatological condition affecting almost a third of the population. Successful treatment of the condition traditionally involves the application of cosmetic products facilitating the moisturisation of the skin with a range of ingredients including glycerol and fatty acids. While the effectiveness of these treatments is not in question, limited information exists on the impact on the skin microbiome following use of these products and the improvement in skin hydration. Here, we describe improvements in skin barrier properties together with increased levels of cholesterol, ceramides and long-chain fatty acids following application of Body Lotion. Concomitant alterations in the skin microbiome are also seen via 16S rRNA metataxonomics, in combination with both traditional and novel informatics analysis. Following 5 weeks of lotion use, beneficial skin bacteria are increased, with improvements in microbiome functional potential, and increases in pathways associated with biosynthesis of multiple long chain fatty acids.

To assess the effects of enzymes and proteins in toothpastes to boost salivary defences and reduce oral bacteria growth and viability. An in vitro study to measure levels of hypothiocyanite in saliva after treatment with a toothpaste containing enzymes and proteins (colorimetric assay). A randomised, crossover in vivo study measuring, with biochemical assays, the effect of a toothpaste containing enzymes and proteins on the levels of hydrogen peroxide and lysozyme in saliva. In vitro studies to measure, using fluorescent dyes, the effects of enzymes and proteins on bacterial membrane integrity. In vitro microbiology studies measuring the effects of enzymes and proteins on planktonic bacterial growth, in vitro studies in single and multispecies biofilms measuring the effect of toothpaste with enzymes and proteins compared to control toothpaste. Levels of hypothiocyanite, hydrogen peroxide and lysozyme are boosted after application of a toothpaste containing enzymes and proteins. The enzymes and proteins adversely affect the bacterial membrane integrity in Streptococcus mutans and growth of planktonic S. mutans and Fusobacterium nucleatum. In a single species biofilm model the viability of S. mutans was significantly reduced and in a 7 species biofilm model bacterial viability was reduced for a biofilm grown on a pellicle pre-treated with toothpaste containing enzymes and proteins. The use of a toothpaste containing enzymes and proteins can boost the natural salivary defences by increasing the levels of lysozyme and hydrogen peroxide in vivo and hypothiocyanite in vitro and reduce the growth and viability of oral bacteria in microbiological models. The subtle effects reported here of enzymes and proteins in toothpastes on oral bacteria are consistent with both the gum health benefits reported for such toothpastes containing enzymes and proteins by Daly [1] and Pedersen [2] and the rebalancing of the oral microbiome reported by Adams [3].

Introduction. The importance of human saliva in aerosol-based transmission of SARS-CoV-2 is now widely recognized. However, little is known about the efficacy of virucidal mouthwash formulations against emergent SARS-CoV-2 variants of concern and in the presence of saliva. Hypothesis. Mouthwashes containing virucidal actives will have similar inactivation effects against multiple SARS-CoV-2 variants of concern and will retain efficacy in the presence of human saliva. Aim. To examine in vitro efficacy of mouthwash formulations to inactivate SARS-CoV-2 variants. Methodology. Inactivation of SARS-CoV-2 variants by mouthwash formulations in the presence or absence of human saliva was assayed using ASTM International Standard E1052-20 methodology. Results. Appropriately formulated mouthwashes containing 0.07 % cetylpyridinium chloride but not 0.2 % chlorhexidine completely inactivated SARS-CoV-2 (USA-WA1/2020, Alpha, Beta, Gamma, Delta) up to the limit of detection in suspension assays. Tests using USA-WA1/2020 indicates that efficacy is maintained in the presence of human saliva. Conclusions. Together these data suggest cetylpyridinium chloride-based mouthwashes are effective at inactivating SARS-CoV-2 variants. This indicates potential to reduce viral load in the oral cavity and mitigate transmission via salivary aerosols.

Bioprospecting is the discovery and exploration of biological diversity found within organisms, genetic elements or produced compounds with prospective commercial or therapeutic applications. The human skin is an ecological niche which harbours a rich and compositional diversity microbiome stemming from the multifactorial interactions between the host and microbiota facilitated by exploitable effector compounds. Advances in the understanding of microbial colonisation mechanisms alongside species and strain interactions have revealed a novel chemical and biological understanding which displays applicative potential. Studies elucidating the organismal interfaces and concomitant understanding of the central processes of skin biology have begun to unravel a potential wealth of molecules which can exploited for their proposed functions. A variety of skin-microbiome-derived compounds display prospective therapeutic applications, ranging from antioncogenic agents relevant in skin cancer therapy to treatment strategies for antimicrobial-resistant bacterial and fungal infections. Considerable opportunities have emerged for the translation to personal care products, such as topical agents to mitigate various skin conditions such as acne and eczema. Adjacent compound developments have focused on cosmetic applications such as reducing skin ageing and its associated changes to skin properties and the microbiome. The skin microbiome contains a wealth of prospective compounds with therapeutic and commercial applications; however, considerable work is required for the translation of in vitro findings to relevant in vivo models to ensure translatability.

The COVID-19 pandemic spurred research on the persistence of infectious SARS-CoV-2 and its surrogates, including bacteriophage Phi6, in environmental reservoirs. Despite the wide use of Phi6, side-by-side comparisons between Phi6 and SARS-CoV-2 are limited. Here, we quantified the persistence of SARS-CoV-2 and Phi6 on surfaces (PVC plastic and stainless steel), using an initial inoculum of 10 ³ plaque forming unit per surface, and evaluated the influence of four commonly used deposition solutions on viral persistence. In addition, we quantified the persistence of SARS-CoV-2 and Phi6 in water. Our findings revealed that Phi6 had a significantly longer half-life than SARS-CoV-2 in water and on surfaces. Phi6 persisted 34 hours in water compared with 13 hours for SARS-CoV-2. Viral persistence on surfaces was significantly influenced by the virus used and the deposition solution but not by the surface material. Phi6 remained infectious significantly longer than SARS-CoV-2 when the inoculation solution was culture media and saliva, leading to half-lives between 9 hours and 2 weeks for Phi6, compared to 0.5–2 hours for SARS-CoV-2. Using phosphate-buffered saline as a deposition solution led to half-lives shorter than 4 hours for both viruses on all surfaces. Our results indicate that bacteriophage Phi6 may lead to an overestimate of infectiousness for studies quantifying SARS-CoV-2 persistence on surfaces and water and highlight the importance of using appropriate deposition solutions when evaluating viral persistence on surfaces. IMPORTANCE: The COVID-19 pandemic spurred research on the persistence of SARS-CoV-2 and its surrogates. Here we highlight the importance of evaluating viral surrogates and experimental methodologies when studying pathogen survival in the environment.

The skin-associated microbiome plays an important role in general well-being and in a variety of treatable skin conditions. In this regard, endogenous antimicrobial peptides have both a direct and indirect role in determining the composition of the microbiota. We demonstrate here that certain small molecular species can amplify the antimicrobial potency of naturally occurring antimicrobial peptides. In this study, we have used niacinamide, a form of vitamin B3 naturally found in foods and widely used in cosmetic skincare products, and two of its structural analogs, to investigate their cooperativity with the human antimicrobial peptide LL37 on the bacterium Staphylococcus aureus. We observed a clear synergistic effect of niacinamide and, to some extent, N-methylnicotinamide, whereas isonicotinamide showed no significant cooperativity with LL37. Adaptively biased molecular dynamics simulations using simplified model membrane substrates and single peptides revealed that these molecules partition into the headgroup region of an anionic bilayer used to mimic the bacterial membrane. The simulated effects on the physical properties of the simulated model membrane are well correlated with experimental activity observed in real biological assays despite the simplicity of the model. In contrast, these molecules have little effect on zwitterionic bilayers that mimic a mammalian membrane. We conclude that niacinamide and N-methylnicotinamide can therefore potentiate the activity of host peptides by modulating the physical properties of the bacterial membrane, and to a lesser extent through direct interactions with the peptide. The level of cooperativity is strongly dependent on the detailed chemistry of the additive, suggesting an opportunity to fine-tune the behavior of host peptides.