Aquaculture as a fast-growing industry provides almost half of fish on our dining
table. However, the bacterial disease in aquaculture causes enormous lost every year.
To cure bacterial disease, antibiotics have been applied into feedings of cultured
animals. The usage of antibiotics has brought many problems, including water pollution,
drug residue and growing of antibiotic resistant bacteria. Traditional Chinses medicine
(TCM) has been used for thousands of years with various pharmacology functions.
Additionally, the TCM has characters of low toxicity, low price and environmentally
friendly, which makes it an ideal replacement of antibiotic in aquaculture.
A high throughput screening method, called starting growth time (SGT), was
applied as screening platform to find the TCM extracts with anti-bacterial effect. Four
kinds of pathogenic bacterial strains that commonly found in South China sea, e.g.
Aeromonas hydrophila, Edwardsiella tarda, Vibrio alginolyticus and Vibrio harveyi,
were chosen as experimental bacteria. According to our screening result, the water
extract of S̲cutellaria b̲aicalensis a̲erial part, named as SBA, inhibited the growth of experimental bacteria in time- and dose- dependent manners. The chemical
components of SBA were further tested by HPLC, and scutellarin and baicalin were
tended to be the main components. The chemical profile of SBA was similar with its
medicinal part, e.g. the root of S. baicalensis (Scutellaria Radix). The stem and leaf
(aerial part) S. baicalensis are considered as waste during the production of root. Thus,
the usage of SBA as an additive in aquaculture feeding could be a new way to recycle the waste.
Siganus fuscescens (rabbit fish) was chosen as experimental animal to test the
effect of SBA in fish. SBA was included in the feeding of rabbit fish. The total fish output
and its nutritive value were determined. Feeding the fish with different doses of SBA
for a month, the body length and weight were significantly increased after intake of
standard feed containing 1% SBA. In parallel, the expressions of alkaline phosphatase
and growth-related factors in bone, liver and muscle of 1% SBA-fed fish were markedly
increased, suggesting the beneficial effects of SBA. The composition of amino acid
and fatty acid in fish muscle, after intaking of 1% SBA containing feed, was altered. In
SBA-fed fish muscle, the amounts of threonine and methionine were increased; while
the amount of leucine was decreased, as compared with control group. The amounts
of fatty acids, including docosahexaenoic acid, phosphatidylcholine and phosphatidylethanolamine, were increased in the 1% SBA-fed fish, while the amounts of
triglycerides were decreased. The results indicated the growth promoting activity of
SBA in an in vivo culture of rabbit fish, as well as to increase the nutritive values of the
meat.
SBA was included in the feeding of rabbit fish and tested its anti-bacterial and
anti-inflammatory effect in vivo under bacterial contamination. Here, SBA was mixed
into the feedings of rabbit fish that was cultured with a mixture of pathogenic bacteria. After 2 days of feeding, the mRNAs from fish tissues were extracted. The expression
of inflammatory cytokines in these tissues were measured by qPCR. The expression
levels of COX-2, IL-1β and TNF-α were markedly reduced in the present of SBA. The
gut microbiota of rabbit fish, after intake of the SBA, was determined as well. The gut
content of fish was collected for the extraction and sequenced of 16S rDNA. The results
indicated that the intake of SBA showed strong anti-bacterial effect, which inhibited the
growth of pathogenic bacteria, i.e. Deltaproteobacteria and Fusobacteria. In contrast
to antibiotic (enrofloxacin), the growth of probiotics, e.g. Erysipelotrichia, was promoted
after intake of SBA.
Two cell lines isolated from rabbit fish were established to reveal the anti-inflammatory mechanism of SBA. One epidermal cell line was derived from dorsal fin
of rabbit fish and named as r̲abbit f̲ish f̲in (RFF) cell line. Another cell line was isolated
and from the head kidney of rabbit fish, corresponding to a new macrophagic cell line, named as r̲abbit f̲ish m̲acrophage (RFM). These cell lines were tested for growth in
different temperatures and serum concentrations, and the best growing condition was
at 20% serum at 28 °C. In cultured RFF and RFM cells, amplification of 18S rDNA from
genomic DNA confirmed their proper identities. After 30
th passage of cultures, the RFF
cells were exposed to challenge of inflammation, triggered by LPS, and hypoxia,
mimicked by CoCl
2. Cultured RFF cells showed robust sensitive responses to
inflammation and hypoxia in directing the expressions of cytokines and hypoxia
inducible factor-1α (HIF-1α). Application of SBA inhibited the expression of LPS-induced inflammatory cytokines, i.e. IL-1β, IL-6, as well as the signaling of NF-κB. SBA
suppressed the LPS-induced transcription of NF-κB subunit, triggered by LPS. The
application of CoCl
2 in cultured RFF cells triggered the hypoxia-induced cell death and
up regulation of HIF-1α. As expected, the applied SBA in cultures prevented the hypoxia-induced signaling.
The isolated RFM cell was identified by immunostaining of CD 68, confirmed the
identity as macrophagic cell. Cultured RFM cells were exposed to challenge of
inflammation, as triggered by LPS, showing highly sensitive responses to inflammation,
including release of nitric oxide, expression of cytokine, and activation of phagocytosis.
In order to test the effect of SBA, the SBA and its effective flavonoids, i.e. baicalin and
scutellarin, were applied in LPS-treated RFM cells. Application of SBA, baicalin or
scutellarin, inhibited the expressions of LPS-induced inflammatory cytokines, i.e. IL-1β,
TNF-α, as well as the signaling of transcription factor NF-κB. Our results show the
establishment of RFF and RFM cell lines may be served as an ideal in vitro model in
drug screening relating to inflammation and hypoxia.
The application of SBA on other aquaculture fish species, e.g. Epinephelus
fuscoguttatus (groupers) or Oreochromis niloticus (tilapia) was carried out as well.
Here, the addition of SBA in their feeding could promote the growth of groupers and
tilapia. In addition, the addition of SBA enhanced the immune function by promoting
the activity of lysozyme and expression of anti-inflammatory cytokines, including IL-4,
IL-10 and TGF-β. These findings proved that application of SBA as a feeding additive can be extended to other fish species.
Our investigations showed the anti-bacterial and anti-inflammatory effect of SBA
in vitro and in vivo, as well as its potential effect to promote the uptake of nutrients.
The superiority of using this herbal extract in comparing to antibiotic was illustrated
here, and which further suggested the possible development of recycling the waste
product of S. baicalensis in fish aquaculture. Thus, the re-cycle of waste products
during the farming of S. baicalensis herb in serving as fish feeding should be encouraged.
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