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| Read ARTICLES OF INTEREST Extracts from Studies on Antimicrobiol effects of essential oils Twenty plant oils and extracts were investigated, using a broth microdilution
method, for activity against C. albicans, Staph. aureus and E.
coli. The lowest minimum inhibitory concentrations were 0.03%
(v/v) thyme oil against C. albicans and E. coli and 0.008%
(v/v) vetiver oil against Staph. aureus. . Methods and Results: Bergamot ethanolic fractions were
tested to be effective against Gram-negative bacteria (Escherichia coli,
Pseudomonas putida, Salmonella enterica), Significance and Impact of the
Study: Bergamot peel is a potential source of natural antimicrobials that
are active against Gram-negative bacteria. Thyme essential oil - studies have shown it effective against food-borne pathogens, namely Salmonella enteriditis, Eschericia coli, Staphylococcus aureus, Listeria monocytogenes, and Campylobacter jejuni, was tested. Also showed wide antibacterial activity against microbes with developed resistance to antibiotics such as MRSA and vancomycin-resistant Enterococcus faeciu The Carrot essential oil ( Daucus carota L.) is reported
antimicrobial against the human enteropathogen Campylobacter jejuni. Growth
of all the C. jejuni, Campylobacter coli, and Campylobacterlari strains
tested, including one multidrug resistant C. jejuni, was inhibited to
the same extent Testing virgin coconut oil and fluconazole for inhibition on Candida albicans, Candida glabrata, Candida tropicalis, Candida parapsilosis, Candida stellatoidea , and Candida krusei. C. albicans had the highest inhibition to coconut oil (100%), at 1:4 dilution, while fluconazole had same effect at 1:2 dilution. It is noteworthy that coconut oil was active against species of Candida at 100% concentration compared to fluconazole. Coconut oil should be used in the treatment of fungal infections in view of emerging drug-resistant Candida species.
------------------------------------------------------------------------------- Staph Infections Patients with atopic dermatitis exhibit increased susceptibility
to cutaneous infections, especially pathological colonization with superantigen-secreting
Staphylococcus aureus. Recent attention has been focused
on antimicrobial peptides, especially on cathelicidin and human beta-defensin-2,
which are under-expressed in atopic skin. Antimicrobial lipids from the
stratum corneum are also major contributors to cutaneous antimicrobial
defense. The major classes of stratum corneum lipids with antimicrobial
activity are free fatty acids, glucosylceramides, and free sphingosines.
Diminished levels of free sphingosines in the stratum corneum have recently
been detected in atopic dermatitis and have been associated with the pathological
colonization of atopic skin with Staphylococcus aureus. The superantigen
staphylococcal enterotoxin B has been shown to reduce the suppressive
effect of regulatory T cells on T-cell proliferation, thus augmenting
T-cell activation in patients with atopic dermatitis. The killing
of superantigen-secreting bacterial strains with topically applied antimicrobial
lipids offers new antiseptic and immunomodulatory options for
the treatment and secondary prevention of atopic dermatitis. Staphylococcus aureus (S. aureus) often colonizes on the skin of patients
with atopic dermatitis. It is known that superantigens which are staphylococcal
enterotoxins can activate T cells without processing by antigen presenting
cells. It has been suggested that activated T cells release various cytokines
which may exacerbate or prolong the cutaneous inflammation associated
with atopic dermatitis. Reduction of bacterial colonization from
skin lesions (caused by S aureus) has been reported to be effective in
the treatment of atopic dermatitis. Therefore, antimicrobial
therapy using antibiotics may be a treatment option for atopic dermatitis
in selected patients. in vitro tests to determine the action mechanism
of antibiotics in the treatment of atopic dermatitis found that antibiotics
with inhibitory effect on protein synthesis can suppress the production
of superantigen.
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