Introduction
Extreme environments can lead to some highly diverse marine
microorganisms. With this diversity comes a whole range of biomolecules that
may not be produced by their less extreme relatives, which can be of use, for
example, in microbial biotechnology or pharmaceuticals. Gugliandolo, et al. (2013) used the example of the
herpes simplex virus type 2 (HSV-2) which is attributed as one of the most
common and continuously occurring viral infections in humans, particularly due
to the persistent latency of the virus after the first infection. Unfortunately
with recurrent use of drug treatments, viral resistance comes hand in hand.
This requires new variations of HSV fighting treatments to battle the new
resistant strains. Isolation of a novel strain of Bacillus licheniformis T14 can yield new exopolysaccharides (EPSs)
with antiviral properties useful for the production of these alternate
treatments. The benefits extend to the thermophilic nature of the vent-dwelling
bacteria, where proliferation rates would be much greater than its mesophilic
or psychrophilic counterparts.
Methods
Isolation of B.
lichenformis strain T14 occurred from a thermal fluid sample obtained from a
shallow submarine vent of Panarea Island in the Eolian Islands, Italy. EPS1 was
obtained after 48h of incubation from culture medium and purified using gel
chromatography before characterisation of physiochemical properties. Human peripheral
blood mononuclear cells (PBMC) were collected from healthy blood donors, washed
in RPMI 1640 medium and cultured at 37°C. The PBMC were treated with 200, 300
and 400 micrograms per millilitre (ug ml-1) of EPS1 and incubated
for 24h at 37°C. Cytoxicity tests were done on PBMC and WISH cells, and
colorimetric assays were done to determine the effect of the concentrations on
the viability of the cells. In another series of experiments, the PBMC and WISH
cells were plated and treated with EPS1 at the concentrations of 200, 300 and
400 ug ml-1 and incubated at 37°C for 24h. The plates were then
frozen and thawed three times to cause the intracellular virus to release.
Results
PBMC show a dose-dependent cytoxicity relationship with EPS1.
48h post treatment indicates that cytoxicity was not found at concentrations of
400 ug ml-1 or below, but above cytoxicity increased with higher
concentrations of EPS1. EPS1 exhibited antiviral properties on HSV-2 (PMBC) at
300 and 400 ug ml-1 but not with lower concentrations, whereas with
the WISH cell line, no significant inhibition was found at any concentration. High
levels of cytokines were detected in EPS1-treated PBMC supernatants but on
samples then infected with HSV-2, there was a significant down regulation of cytokine
production.
Discussion
The EPS that B.
licheniformis T14 produces contains both fructose and fucose. Fucose
containing polysaccharides are highly marketable due to their rarity and value
in pharmaceuticals and cosmetics, and have attributes including anti-inflammatory,
anticarcinogenic, and immunomodulatory properties. EPS1 provides a knowledge
that damaging immunological disorders caused by HSV-2 could be reversed. The
key of this biomolecule is the relative ease of cultivation, particularly with B. licheniformis T14’s affinity to
thrive at variable temperatures, pH’s and salinities due to its high stress
tolerance which is attributed to organisms that exist in such extreme
environments. The potential of this research is huge, and this paper presents
vital data for the deriving of novel biomolecules for use in medicine and
biotechnology, especially with resistant pathogenic strains on the rise. The
author’s conclusions send a positive message to those afflicted with
reoccurring viral infections and also the potential of strains of
microorganisms yet undiscovered in the oceans and the ability they may have to
produce biomolecules that can be used to aid in medical and pharmaceutical applications.
Ref: Gugliandolo, C., Spanò, A., Lentini, V., Arena, A. &
Maugeri, T. L. (2013) Antiviral and immunomodulatory effects of a novel bacterial
exopolysaccharide of shallow marine vent origin. Journal of Applied Microbiology. 116(4), 1028-1034. doi:10.1111/jam.12422
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