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Volume 5, Issue 3 (Suppl)

J Infect Dis Ther, an open access journal

ISSN:2332-0877

Infectious Diseases 2017

August 21-23, 2017

3

rd

Annual Congress on

Infectious Diseases

August 21-23, 2017 San Francisco, USA

Apple cider vinegar (ACV®) displays potent antibiotic activity directly against

Escherichia coli and

Candida albicans

and within

in vitro

monocytes exposed to microbes by inhibiting inflammatory

cytokine secretion

Darshna Yagnik

Middlesex University, UK

Introduction:

Extraintestinal pathogenic Escherichia coli (E-coli) are the most frequent cause of blood borne, urinary tract

and hospital acquired infections.

Candida albicans

infection can also pose a huge threat especially following transplantation

and to immune compromised patients. Globally there has never been a more desperate time for novel anti-microbial agents to

target microbes and multi drug resistance from bacterial or fungal associated infections.

Aim:

The aim of this study was to investigate the potential anti-microbial effects of ACV®. We used microbial strains:

E. coli

strain 6571,

C. albicans

strain 90828 purchased from ATCC.

Methodology:

We tested the effect of commercial ACV® directly on microbial cultures over a 24 hour period, measuring

inhibition zones. We also looked at whether ACV® could have an anti-inflammatory effect

in vitro

. This was tested using human

blood derived monocytes which were incubated with microbes and AVC®. The collected supernatants were analyzed for pro-

inflammatory cytokine secretion by ELISA.

Results:

When monocytes were cultured with both microbes they secreted TNFα and IL-1β. ACV® was able to significantly

inhibit E-coli growth demonstrated by the results of direct co-culture with each of the microbial inoculums and ACV® in

varying concentrations. The zone of inhibition with the addition of ACV® to each of the microbes varied dose dependently

ACV® concentration. For

Candida albicans

undiluted ACV® had the strongest effect, whereas on E-coli cultures, the most

potent effect was visible at lower dilutions including 1/1000 dilution of the neat solution (p<0.05). When monocytes were

cultured with both microbes they secreted inflammatory cytokines (TNFα, IL-1β) ACV® was effective in significantly inhibiting

inflammatory cytokine secretion in human peripheral blood monocytes cultured with

E. coli

and

Candida albicans

Conclusion and significance:

ACV® displayed potent anti-microbial and anti-inflammatory activity against

E. coli

and

Candida

albicans

. We propose that ACV® could be potentially therapeutic in cases of antibiotic resistance and sepsis.

Biography

Darshna Yagnik is a Lecturer of Immunology and Biomedical Sciences at Middlesex University. Her research is based on human

in vitro

models of mononuclear

cell differentiation and their role in inflammatory pathways and particularly the resolution phase of inflammation.

d.yagnik@mdx.ac.uk

Darshna Yagnik, J Infect Dis Ther 2017, 5:3 (Suppl)

DOI: 10.4172/2332-0877-C1-026