scholarly journals Quantitation of Human Skin Surface Total Free Fatty Acids*

1968 ◽  
Vol 51 (6) ◽  
pp. 497-501
Author(s):  
Stephen J. Kraus
mBio ◽  
2016 ◽  
Vol 7 (1) ◽  
Author(s):  
Lindsey Bomar ◽  
Silvio D. Brugger ◽  
Brian H. Yost ◽  
Sean S. Davies ◽  
Katherine P. Lemon

ABSTRACTBacterial interspecies interactions play clinically important roles in shaping microbial community composition. We observed thatCorynebacteriumspp. are overrepresented in children free ofStreptococcus pneumoniae(pneumococcus), a common pediatric nasal colonizer and an important infectious agent.Corynebacterium accolens, a benign lipid-requiring species, inhibits pneumococcal growth duringin vitrococultivation on medium supplemented with human skin surface triacylglycerols (TAGs) that are likely present in the nostrils. This inhibition depends on LipS1, a TAG lipase necessary forC. accolensgrowth on TAGs such as triolein. We determined thatC. accolenshydrolysis of triolein releases oleic acid, which inhibits pneumococcus, as do other free fatty acids (FFAs) that might be released by LipS1 from human skin surface TAGs. Our results support a model in whichC. accolenshydrolyzes skin surface TAGSin vivoreleasing antipneumococcal FFAs. These data indicate thatC. accolensmay play a beneficial role in sculpting the human microbiome.IMPORTANCELittle is known about how harmlessCorynebacteriumspecies that colonize the human nose and skin might impact pathogen colonization and proliferation at these sites.We show thatCorynebacterium accolens, a common benign nasal bacterium, modifies its local habitatin vitroas it inhibits growth ofStreptococcus pneumoniaeby releasing antibacterial free fatty acids from host skin surface triacylglycerols. We further identify the primaryC. accolenslipase required for this activity. We postulate a model in which higher numbers ofC. accolenscells deter/limitS. pneumoniaenostril colonization, which might partly explain why children withoutS. pneumoniaecolonization have higher levels of nasalCorynebacterium. This work narrows the gap between descriptive studies and the needed in-depth understanding of the molecular mechanisms of microbe-microbe interactions that help shape the human microbiome. It also lays the foundation for futurein vivostudies to determine whether habitat modification byC. accolenscould be promoted to control pathogen colonization.


1957 ◽  
Vol 29 (6) ◽  
pp. 423-433 ◽  
Author(s):  
N. Nicolaides ◽  
George C. Wells

Metabolites ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 700
Author(s):  
Yohannes Abere Ambaw ◽  
Martin P. Pagac ◽  
Antony S. Irudayaswamy ◽  
Manfred Raida ◽  
Anne K. Bendt ◽  
...  

Malassezia are common components of human skin, and as the dominant human skin eukaryotic microbe, they take part in complex microbe–host interactions. Other phylogenetically related fungi (including within Ustilagomycotina) communicate with their plant host through bioactive oxygenated polyunsaturated fatty acids, generally known as oxylipins, by regulating the plant immune system to increase their virulence. Oxylipins are similar in structure and function to human eicosanoids, which modulate the human immune system. This study reports the development of a highly sensitive mass-spectrometry-based method to capture and quantify bioactive oxygenated polyunsaturated fatty acids from the human skin surface and in vitro Malassezia cultures. It confirms that Malassezia are capable of synthesizing eicosanoid-like lipid mediators in vitro in a species dependent manner, many of which are found on human skin. This method enables sensitive identification and quantification of bioactive lipid mediators from human skin that may be derived from metabolic pathways shared between skin and its microbial residents. This enables better cross-disciplinary and detailed studies to dissect the interaction between Malassezia and human skin, and to identify potential intervention points to promote or abrogate inflammation and to improve human skin health.


1963 ◽  
Vol 41 (5) ◽  
pp. 259-264 ◽  
Author(s):  
William M. Coon ◽  
Victor R. Wheatley ◽  
Franz Herrmann ◽  
Leona Mandol ◽  
Jean Gowdey

2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Philip W. Wertz

The primary purpose of the epidermis of terrestrial vertebrates is to produce the stratum corneum, which serves as the interface between the organism and the environment. As such, the stratum corneum provides a permeability barrier which both limits water loss through the skin and provides a relatively tough permeability barrier. This provides for a degree of resistance to mechanical trauma and prevents or limits penetration of potentially harmful substances from the environment. The stratum corneum consists of an array of keratinized cells embedded in a lipid matrix. It is this intercellular lipid that determines the permeability of the stratum corneum. The main lipids here are ceramides, cholesterol, and fatty acids. In addition, the skin surface of mammals, including humans, is coated by a lipid film produced by sebaceous glands in the dermis and secreted through the follicles. Human sebum consists mainly of squalene, wax monoesters, and triglycerides with small proportions of cholesterol and cholesterol esters. As sebum passes through the follicles, some of the triglycerides are hydrolyzed by bacteria to liberate free fatty acids. Likewise, near the skin surface, where water becomes available, some of the ceramides are acted upon by an epithelial ceramidase to liberate sphingosine, dihydrosphingosine, and 6-hydroxysphingosine. Some of the free fatty acids, specifically lauric acid and sapienic acid, have been shown to have antibacterial, antifungal, and antiviral activity. Also, the long-chain bases have broad spectrum antibacterial activity.


Metabolites ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 819
Author(s):  
Stefania Briganti ◽  
Mauro Truglio ◽  
Antonella Angiolillo ◽  
Salvatore Lombardo ◽  
Deborah Leccese ◽  
...  

Lipidomics is strategic in the discovery of biomarkers of neurodegenerative diseases (NDDs). The skin surface lipidome bears the potential to provide biomarker candidates in the detection of pathological processes occurring in distal organs. We investigated the sebum composition to search diagnostic and, possibly, prognostic, biomarkers of Alzheimer’s disease (AD) and Parkinson’s disease (PD). The observational study included 64 subjects: 20 characterized as “probable AD with documented decline”, 20 as “clinically established PD”, and 24 healthy subjects (HS) of comparable age. The analysis of sebum by GCMS and TLC retrieved the amounts (µg) of 41 free fatty acids (FFAs), 7 fatty alcohols (FOHs), vitamin E, cholesterol, squalene, and total triglycerides (TGs) and wax esters (WEs). Distributions of sebum lipids in NDDs and healthy conditions were investigated with multivariate ANOVA-simultaneous component analysis (ASCA). The deranged sebum composition associated with the PD group showed incretion of most composing lipids compared to HS, whereas only two lipid species (vitamin E and FOH14:0) were discriminant of AD samples and presented lower levels than HS sebum. Thus, sebum lipid biosynthetic pathways are differently affected in PD and AD. The characteristic sebum bio-signatures detected support the value of sebum lipidomics in the biomarkers search in NDDs.


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