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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Mar. Sci.</journal-id>
<journal-title>Frontiers in Marine Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Mar. Sci.</abbrev-journal-title>
<issn pub-type="epub">2296-7745</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fmars.2023.1290879</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Marine Science</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Nano-liposome of thyme essential oil promotes growth performance, antioxidant and immune responses to aeromonad septicemia in Nile tilapia, <italic>Oreochromis niloticus</italic>, fingerlings</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Yousefi</surname>
<given-names>Morteza</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/902623"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
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</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Hoseini</surname>
<given-names>Seyyed Morteza</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/117802"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Ghadamkheir</surname>
<given-names>Maryam</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Mahboub</surname>
<given-names>Heba H.</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1656415"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Vatnikov</surname>
<given-names>Yury Anatolyevich</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Kulikov</surname>
<given-names>Evgeny Vladimirovich</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Sotnikova</surname>
<given-names>Elena Dmitriyevna</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
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</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Veterinary Medicine, RUDN University</institution>, <addr-line>Moscow</addr-line>, <country>Russia</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Inland Waters Aquatics Resources Research Center, Iranian Fisheries Sciences Research Institute, Agricultural Research, Education and Extension Organization</institution>, <addr-line>Gorgan</addr-line>, <country>Iran</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Economics and Organization of Agricultural Production, Institute of Land Management, State University of Land Use Planning</institution>, <addr-line>Moscow</addr-line>, <country>Russia</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Aquatic Animal Medicine, Faculty of Veterinary Medicine, Zagazig University</institution>, <addr-line>Zagazig</addr-line>, <country>Egypt</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Bin Xia, Qingdao Agricultural University, China</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Yunfei Sun, Shanghai Ocean University, China; Mansour Torfi Mozanzadeh, South Iran Aquaculture Research Center, Iran</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Morteza Yousefi, <email xlink:href="mailto:myousefi81@gmail.com">myousefi81@gmail.com</email>; Seyyed Morteza Hoseini, <email xlink:href="mailto:seyyedmorteza.hoseini@gmail.com">seyyedmorteza.hoseini@gmail.com</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>30</day>
<month>11</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>10</volume>
<elocation-id>1290879</elocation-id>
<history>
<date date-type="received">
<day>08</day>
<month>09</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>15</day>
<month>11</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Yousefi, Hoseini, Ghadamkheir, Mahboub, Vatnikov, Kulikov and Sotnikova</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Yousefi, Hoseini, Ghadamkheir, Mahboub, Vatnikov, Kulikov and Sotnikova</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Nano-encapsulation protects essential oils and increases their efficiency, compared to bulk forms. Hence in the present study, four diets (328 g/kg crude protein and 4402 kcal/kg gross energy) containing 0 (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), and 100 mg/kg (100TV) thyme, <italic>Thymus vulgaris</italic>, essential oil nano-liposomes (TV-NP) were offered to Nile tilapia fingerlings (initial weight of 4.27 &#xb1; 0.05&#xa0;g) at water temperature of 26.46 &#xb1; 0.43&#xb0;C, followed by intraperitoneal infection by <italic>Aeromonas hydrophila</italic>. Three hundred and sixty healthy fish were stocked in 12 tanks (60 L), 30 fish per tank, with daily water renewal rate of 40%. Each diet was offered to three tanks for 70 days. The fish were sampled at the end of feeding period and 12&#xa0;h after the bacterial challenge. Compared to CTL, 50TV and 100TV treatments exhibited significant elevations in growth rate (14-17%; P&lt;0.001), intestinal activities of amylase (9-19%; P=0.004), lipase (13-26%; P&lt;0.001), protease (20-23%; P=0.001), and post-challenge survival (26-27%; P=0.001). Plasma lysozyme (14-15% P&lt;0.001) and complement (5.1-5.4%; P=0.004) activities significantly increased in 25TV and 50TV, but decreased (lysozyme: 19%, complement 5.9%) in 100TV before the challenge; however, all TV-NP treatments showed similar lysozyme and complement activities after the challenge that were higher than CTL. 50TV and 100TV treatments also showed a decrease in lipid peroxidation (23-26%; P&lt;0.001) and highest glutathione peroxidase activity (17-18%; P=0.001) and pre-challenge superoxide dismutase (21%; P=0.046) and catalase (15-17%; P=0.001) activities. Expression of tumor necrosis factor-alpha (11-fold, P&lt;0.001), inerleukin-1 beta (5-fold, P&lt;0.001), and transforming growth factor-beta (31-fold; P=0.001) in head kidney significantly increased in 100TV before the challenge. After the challenge, the transcripts of the cytokines significantly increased in all treatments and the highest expressions were observed in 50TV and 100TV treatments (62-148-fold). In conclusion, dietary 50-100 mg/kg TV-NP can be considered as a new feed additive in tilapia culture, as it improves growth rate, antioxidant capacity, and disease resistance in the fish.</p>
</abstract>
<kwd-group>
<kwd>disease</kwd>
<kwd>nano-technology</kwd>
<kwd>
<italic>Thymus vulgaris</italic>
</kwd>
<kwd>aquaculture</kwd>
<kwd>cytokine</kwd>
<kwd>antioxidant</kwd>
</kwd-group>
<contract-sponsor id="cn001">RUDN University<named-content content-type="fundref-id">10.13039/501100018647</named-content>
</contract-sponsor>
<counts>
<fig-count count="5"/>
<table-count count="4"/>
<equation-count count="3"/>
<ref-count count="75"/>
<page-count count="12"/>
<word-count count="5572"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Marine Fisheries, Aquaculture and Living Resources</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<title>Introduction</title>
<p>Due to the ever-increasing population of the world, food security and protein consumption per capita are one of the most important global challenges. In this regard, aquaculture is one of the important food production industries with rapid growth during the recent decades (<xref ref-type="bibr" rid="B61">Subasinghe et&#xa0;al., 2009</xref>). Because of rapid growth and tolerating captivity, Nile tilapia, <italic>Oreochromis niloticus</italic>, is one of the important aquaculture species that is reared in many countries (<xref ref-type="bibr" rid="B18">Gabriel, 2019</xref>). Modern aquaculture is based on increasing the density of cultivation and production. But the increase in density causes stress in fish and the outbreak of various diseases (<xref ref-type="bibr" rid="B3">Akdemir et&#xa0;al., 2017</xref>). <italic>Aeromonas hydrophila</italic> is a gram-negative bacteria that can cause various diseases in fish, including Nile tilapia (<xref ref-type="bibr" rid="B53">Shirajum Monir et&#xa0;al., 2020</xref>). It is one of the most common pathogens in tilapia aquaculture and can cause significant economic losses. Some of the diseases caused by <italic>A. hydrophila</italic> in tilapia include hemorrhagic septicemia, fin rot, and skin ulcers. These diseases can lead to decreased growth rates, increased mortality, and reduced marketability of the fish (<xref ref-type="bibr" rid="B47">Noga, 2011</xref>).</p>
<p>The use of antibiotics to control livestock diseases is very limited due to environmental pollution, consumer health (<xref ref-type="bibr" rid="B69">Zargar et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B64">Yilmaz et&#xa0;al., 2022</xref>), and the emergence of resistant strains of various bacteria, including <italic>A. hydrophila</italic> (<xref ref-type="bibr" rid="B35">Li et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B70">Zdanowicz et&#xa0;al., 2020</xref>). For this reason, the main strategy in aquaculture is to increase the health and immunity of fish and prevent the occurrence of diseases. Improve in feed quality and using functional feeds can increase fish health and disease resistance (<xref ref-type="bibr" rid="B17">Favero et&#xa0;al., 2020</xref>). Various feed additives have been found to improve growth performance, antioxidant capacity, immune strength, and disease resistance in aquaculture fish (<xref ref-type="bibr" rid="B33">Lee et&#xa0;al., 2015</xref>). Among them, herbal additives have gained great attentions, because of their natural origin, growth promotion, immunostimulation, and pathogen elimination, which can augment fish health and decrease the use of antibiotics (<xref ref-type="bibr" rid="B27">Hoseinifar et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B74">Zhu, 2020</xref>).</p>
<p>Thyme, <italic>Thymus vulgaris</italic>, essential oil has been shown to have potential benefits in aquaculture and fish nutrition. It contains a range of bioactive compounds, including thymol, carvacrol, and p-cymene, which have antimicrobial, antioxidant, and anti-inflammatory properties (<xref ref-type="bibr" rid="B55">Silva et&#xa0;al., 2021</xref>). Studies have demonstrated that adding thyme essential oil/extract to fish feed can improve growth performance, antioxidant capacity, immune function, and resistance against diseases, including Aeromonas septicemia (<xref ref-type="bibr" rid="B46">Navarrete et&#xa0;al., 2010</xref>; <xref ref-type="bibr" rid="B26">Hoseini and Yousefi, 2019</xref>; <xref ref-type="bibr" rid="B68">Zargar et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B30">Khalil et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B19">Ghafarifarsani et&#xa0;al., 2022</xref>). One of the limitations of using essential oils in aquaculture is their stability, high light sensitivity and strong organoleptic characteristic (<xref ref-type="bibr" rid="B40">Luis et&#xa0;al., 2019</xref>). Nanotechnology is one of the approaches to resolve these problems. Various nanoparticles of essential oils have been found to improve fish growth performance, health, and disease resistance (<xref ref-type="bibr" rid="B59">Souza et&#xa0;al., 2017a</xref>; <xref ref-type="bibr" rid="B58">Souza et&#xa0;al., 2017b</xref>; <xref ref-type="bibr" rid="B1">Abdel-Tawwab et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B52">Sheikh Asadi et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B20">Gheytasi et&#xa0;al., 2021</xref>). It has been demonstrated that nano-emulsion of thyme essential oil can excrete anti-bacterial effects against <italic>A. hydrophila</italic>, both <italic>in vitro</italic> and <italic>in vivo</italic> in Nile tilapia, <italic>Oreochromis niloticus</italic>, concurrent with elevation of serum immunoglobulin M, lysozyme, and interleukin-1 beta (il-1b) and preventing mortality after an experimental bacterial challenge (<xref ref-type="bibr" rid="B51">Salam et&#xa0;al., 2021</xref>). Another studies revealed protection of Nile tilapia against <italic>Streptococcus iniae</italic> infection by dietary administration of nano-emulsion of thyme essential oil, which was accompanied by lower inflammation and stress (<xref ref-type="bibr" rid="B31">Korni et&#xa0;al., 2023</xref>). Hence, nanoparticle of thyme essential oil is a promising prophylactic agent against opportunistic bacterial pathogens.</p>
<p>Type of nanoparticle substantially affects its functions. Nano-liposomes are known for their protection of essential oils and slow release, which increase the essential oils anti-bacterial activity (<xref ref-type="bibr" rid="B16">Fajardo et&#xa0;al., 2022</xref>). Moreover, slow releasing results in the release of essential oil along the gastrointestinal tract, when nano-liposomes are orally administered. Thus, the present study aimed to extend the knowledge regarding the benefits of nanoparticles of thyme essential oil in Nile tilapia by applying nano-liposomes over a long time (70&#xa0;d) and monitoring the fish growth performance, humoral innate immunity responses, hepatic antioxidant status, and head kidney immune-related genes&#x2019; expression, before and after infection with <italic>A. hydrophila</italic>.</p>
</sec>
<sec id="s2" sec-type="materials|methods">
<title>Materials and methods</title>
<sec id="s2_1">
<title>Preparation of thyme essential oil nano-liposome (TV-NP)</title>
<p>First, 0.5&#xa0;g of whey powder was poured into a 100-mL beaker and 7 mL of distilled water were added to it and placed in a bain-marie at a temperature of 50&#xb0;C for 12&#xa0;h and after cooling with phosphate buffer was adjusted to pH=6 (<xref ref-type="bibr" rid="B41">Lutz et&#xa0;al., 2009</xref>).</p>
<p>The organic phase was prepared by adding 0.1&#xa0;g of lecithin to 1 mL of olive oil and mixing. The aqueous phase was prepared by adding 0.2&#xa0;g of glycerol in 2 mL of distilled water and incubating for 2&#xa0;h in a Bain-Marie (55&#xb0;C). The organic phase was added drop-wise to the aqueous phase; then 60 ppm of thyme essential oil (purchased from Dr. Soleymani pharmacy, Gorgan, Iran) was added to it and the pH of the solution was adjusted to pH=6 with phosphate buffer (<xref ref-type="bibr" rid="B43">Mohammadi et&#xa0;al., 2016</xref>). Finally, the obtained solution was added to the whey powder solution and placed in an ultrasonic homogenizer for 5&#xa0;min to prepare TV-NP. The product was powdered using a freeze-dryer. The characteristics of nano-liposomes were examined by scanning electron microscope (KYKY, EM-3200, China) and particle size analyzer (Malvern model MS1002, UK) and shown in <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref>.</p>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>Particle size analysis <bold>(A-C)</bold> and scanning electron microscope photograph <bold>(D)</bold> of the nano-liposomes.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-10-1290879-g001.tif"/>
</fig>
</sec>
<sec id="s2_2">
<title>Diets</title>
<p>A control diet without TV-NP (CTL) and three diets containing 25 (25TV), 50 (50TV), or 100 (100TV) mg/kg TV-NP were prepared in this study (<xref ref-type="bibr" rid="B7">Besharat et&#xa0;al., 2021</xref>). Feedstuffs (<xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>) were mixed and pasted after moisturizing with 400 mL/g water. The paste was pelleted using a meat grinder and dried against a fan blow. The diets were analyzed according to <xref ref-type="bibr" rid="B5">AOAC (2005)</xref>.</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Feedstuffs, dietary composition and biochemical composition of the experimental diets.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left">Ingredients</th>
<th valign="top" align="left">Amount (g/kg)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Corn meal<sup>1</sup>
</td>
<td valign="top" align="left">102</td>
</tr>
<tr>
<td valign="top" align="left">Wheat meal<sup>2</sup>
</td>
<td valign="top" align="left">275</td>
</tr>
<tr>
<td valign="top" align="left">Soybean meal<sup>3</sup>
</td>
<td valign="top" align="left">202</td>
</tr>
<tr>
<td valign="top" align="left">Poultry byproduct<sup>4</sup>
</td>
<td valign="top" align="left">382</td>
</tr>
<tr>
<td valign="top" align="left">Corn oil</td>
<td valign="top" align="left">9</td>
</tr>
<tr>
<td valign="top" align="left">Sunflower oil</td>
<td valign="top" align="left">9</td>
</tr>
<tr>
<td valign="top" align="left">Mineral premix<sup>5</sup>
</td>
<td valign="top" align="left">10</td>
</tr>
<tr>
<td valign="top" align="left">Vitamin premix<sup>6</sup>
</td>
<td valign="top" align="left">5</td>
</tr>
<tr>
<td valign="top" align="left">Methionine<sup>7</sup>
</td>
<td valign="top" align="left">3</td>
</tr>
<tr>
<td valign="top" align="left">Lysine<sup>8</sup>
</td>
<td valign="top" align="left">3</td>
</tr>
<tr>
<th valign="top" colspan="2" align="left">Proximate composition (g/kg)</th>
</tr>
<tr>
<td valign="top" align="left">Moisture</td>
<td valign="top" align="left">91.5</td>
</tr>
<tr>
<td valign="top" align="left">Crude protein</td>
<td valign="top" align="left">389</td>
</tr>
<tr>
<td valign="top" align="left">Crude fat</td>
<td valign="top" align="left">100</td>
</tr>
<tr>
<td valign="top" align="left">Crude ash</td>
<td valign="top" align="left">54.8</td>
</tr>
<tr>
<td valign="top" align="left">Crude fiber</td>
<td valign="top" align="left">40.0</td>
</tr>
<tr>
<td valign="top" align="left">Crude energy (kcal/kg)</td>
<td valign="top" align="left">4402</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>1 Crude protein 8.9%; crude fat 3.5%; crude ash 5.3%; crude fiber 2.6%.</p>
</fn>
<fn>
<p>2 Crude protein 11.1%; crude fat 1.5%; crude ash 2.3%; crude fiber 2.5%.</p>
</fn>
<fn>
<p>3 Crude protein 44.3%; crude fat 1.88%; crude ash 5.32%; crude fiber 3.68%.</p>
</fn>
<fn>
<p>4 Crude protein 63%; crude fat 16%; crude ash 6%; crude fiber 4%.</p>
</fn>
<fn>
<p>5 Amineh Gostar Co. (Tehran, Iran). The premix provided the following amounts of vitamin to the diets (per kg): A: 1600 IU; D3: 500 IU; E: 20 mg; K: 24 mg; B3: 12 mg; B5: 40 mg; B2: 10 mg; B6: 5 mg; B1: 4 mg; H: 0.2 mg; B9: 2 mg; B12: 0.01 mg; C: 60 mg; Inositol: 50 mg.</p>
</fn>
<fn>
<p>6 Amineh Gostar Co. (Tehran, Iran). The premix provided the following amounts of minerals to the diets (per kg): Se: 0.15 mg; Fe: 2.5 mg; Co: 0.04 mg; Mn: 5 mg; Iodate: 0.05 mg; Cu: 0.5 mg; Zn: 6 mg; Choline: 150 mg.</p>
</fn>
<fn>
<p>7 CheilJedang Co., Seoul, Korea.</p>
</fn>
<fn>
<p>8 CheilJedang Co., Seoul, Korea.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s2_3">
<title>Experimental protocol</title>
<p>In this study, 360 Nile tilapia (initial weight of 4.27 &#xb1; 0.05&#xa0;g) were purchased from a private sector (Kashan, Iran) and transferred to the laboratory (University of Gonbad-e-Kavoos, Gonbad, Iran). The fish were healthy, approved by no morphological abnormality and macroscopic signs of diseases (no wounds and patchy redness, normal coloration, and healthy fins). After 7&#xa0;d acclimation in a 1 m<sup>3</sup> tank and feeding with CTL diet, the fish were allocated into 12 tanks filled with 60 L water. Each of the above-mentioned diet was offered to three tanks for 70&#xa0;d at a daily ration of 4% of biomass. All tanks were continuously aerated and their water was daily renewed by 40%. Water temperature, pH, dissolved oxygen, total alkalinity, and un-ionized ammonia were 26.46 &#xb1; 0.43&#xb0;C, 7.64 &#xb1; 0.15, 6.70 &#xb1; 0.38 mg/L, 401.80 &#xb1; 9.31mg CaCO<sub>3</sub>/L, and 0.059 &#xb1; 0.016 mg/L, respectively. Feed amounts were adjusted every other week by measuring the tanks&#x2019; biomasses.</p>
<p>And the end of the feeding trial, fish final weight, specific growth rate (SGR), weight gain (WG), and feed conversion ratio (FCR) were calculated according to the following formula:</p>
<disp-formula>
<mml:math display="block" id="M1">
<mml:mrow>
<mml:mtext>Weight&#x2004;gain</mml:mtext>
<mml:mo>&#xa0;</mml:mo>
<mml:mo stretchy="false">(</mml:mo>
<mml:mo>%</mml:mo>
<mml:mo stretchy="false">)</mml:mo>
<mml:mo>=</mml:mo>
<mml:mn>100</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:mo stretchy="false">[</mml:mo>
<mml:mo stretchy="false">(</mml:mo>
<mml:mtext>final&#x2004;weight</mml:mtext>
<mml:mo>&#x2212;</mml:mo>
<mml:mtext>initial&#x2004;weight</mml:mtext>
<mml:mo stretchy="false">)</mml:mo>
<mml:mo stretchy="false">/</mml:mo>
<mml:mtext>initial&#x2004;weight</mml:mtext>
<mml:mo stretchy="false">]</mml:mo>
</mml:mrow>
</mml:math>
</disp-formula>
<disp-formula>
<mml:math display="block" id="M2">
<mml:mrow>
<mml:mtext>Feed&#x2004;conversion&#x2004;ratio</mml:mtext>
<mml:mo>&#xa0;</mml:mo>
<mml:mo stretchy="false">(</mml:mo>
<mml:mtext>FCR</mml:mtext>
<mml:mo stretchy="false">)</mml:mo>
<mml:mo>=</mml:mo>
<mml:mtext>feed&#x2004;intake</mml:mtext>
<mml:mo stretchy="false">/</mml:mo>
<mml:mo stretchy="false">(</mml:mo>
<mml:mtext>final&#x2004;weight</mml:mtext>
<mml:mo>&#x2212;</mml:mo>
<mml:mtext>initial&#x2004;weight</mml:mtext>
<mml:mo stretchy="false">)</mml:mo>
</mml:mrow>
</mml:math>
</disp-formula>
<disp-formula>
<mml:math display="block" id="M3">
<mml:mrow>
<mml:mtext>Specific&#x2004;growth&#x2004;rate</mml:mtext>
<mml:mo>&#xa0;</mml:mo>
<mml:mo stretchy="false">(</mml:mo>
<mml:mtext>SGR</mml:mtext>
<mml:mo>;</mml:mo>
<mml:mo>%</mml:mo>
<mml:mo stretchy="false">/</mml:mo>
<mml:mtext>d</mml:mtext>
<mml:mo stretchy="false">)</mml:mo>
<mml:mo>=</mml:mo>
<mml:mn>100</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:mo stretchy="false">[</mml:mo>
<mml:mo stretchy="false">(</mml:mo>
<mml:msub>
<mml:mrow>
<mml:mtext>ln</mml:mtext>
</mml:mrow>
<mml:mrow>
<mml:mtext>final&#x2004;weight</mml:mtext>
</mml:mrow>
</mml:msub>
<mml:mo>&#x2212;</mml:mo>
<mml:msub>
<mml:mrow>
<mml:mtext>ln</mml:mtext>
</mml:mrow>
<mml:mrow>
<mml:mtext>initial&#x2004;weight</mml:mtext>
</mml:mrow>
</mml:msub>
<mml:mo stretchy="false">)</mml:mo>
<mml:mo stretchy="false">/</mml:mo>
<mml:mn>60</mml:mn>
<mml:mo stretchy="false">]</mml:mo>
</mml:mrow>
</mml:math>
</disp-formula>
</sec>
<sec id="s2_4">
<title>Bacterial challenge</title>
<p>
<italic>A. hydrophila</italic> (ATCC 7966) was obtained from the Iranian Biological Resource Center (Tehran, Iran) and cultured on TSA medium and suspended in 0.85% NaCl solution. Thirteen fish per tank were used for the bacterial challenge, and remaining fish were removed from the tanks and stocked in another 2000-L tank. The fish were anesthetized by eugenol (50 mg/L) and injected intraperitoneally. Each fish was injected by 250 &#xb5;L of bacterial suspension with a cell density of 1 &#xd7; 10<sup>7</sup> cell/mL. A batch of 10 fish from the CTL tanks were injected by 250 &#xb5;L of phosphate buffer as negative control. The injected fish were returned to their corresponding tanks and mortality was daily observed at 6.00, 14.00, and 22.00 for 14&#xa0;d.</p>
</sec>
<sec id="s2_5">
<title>Sampling and analysis</title>
<p>At the end of the feeding trial, three fish from each tank were caught and anesthetized (50 mg/L eugenol). Blood samples were collected from the fish by caudal puncture, using heparinized syringes. Then, the fish were killed by spinal cord dissecting and pieces of anterior/middle intestine, liver, and head kidney were sampled and immediately frozen in liquid nitrogen. Then the remaining fish were challenged by <italic>A. hydrophila</italic> and blood, liver, and head kidney were sampled again 12&#xa0;h after challenge.</p>
</sec>
<sec id="s2_6">
<title>Intestinal digestive enzymes</title>
<p>The intestine samples were homogenized in cold buffer (phosphate buffer, pH 7.0) at a ratio of 1:3 (w:v). Enzyme extract was obtained by centrifugation at 4&#xb0;C (13000&#xa0;g; 15&#xa0;min). Protease activity was determined based on AZO-casein method using a spectrophotometer as described before (<xref ref-type="bibr" rid="B29">Iversen and J&#xf8;rgensen, 1995</xref>). Amylase activity was determined according to <xref ref-type="bibr" rid="B62">Winn-Deen et&#xa0;al. (1988)</xref>, based on the decomposition of starch. Lipase activity was determined using 1, 2-O-dilauryl-rock-glycero-3-glutaric acid- (6-methyl-resorophine)-ester emulsion as substrate (<xref ref-type="bibr" rid="B28">Iijima et&#xa0;al., 1998</xref>). Soluble protein concentration was determined based on the Bradford method (<xref ref-type="bibr" rid="B8">Bradford, 1976</xref>).</p>
</sec>
<sec id="s2_7">
<title>Plasma immune parameters</title>
<p>The whole blood samples were centrifuged (5000&#xa0;g, 7&#xa0;min) to separate plasma; the plasma kept at -70&#xb0;C until analysis. Plasma lysozyme activity was measured using <italic>Micrococcus luteus</italic> as the target. To 1 mL of the bacterium suspension (in phosphate buffer, pH 6.2) was added 30 &#xb5;L of the plasma samples and decrease in optical density (550 nm) was recorded for 5&#xa0;min. Each 0.001 decrease in optical density was considered as one unit of lysozyme activity (<xref ref-type="bibr" rid="B14">Ellis, 1990</xref>). Plasma alternative complement (ACH50) activity was determined as hemolytic capacity of the samples. Serially diluted plasma samples were mixed with sheep erythrocyte in EGTA-magnesium-veronal buffer containing gelatin. After 90&#xa0;min incubation in room temperature, hemolysis rate was determined at 412 nm. ACH50 activity was calculated according to <xref ref-type="bibr" rid="B63">Yano (1992)</xref>.</p>
</sec>
<sec id="s2_8">
<title>Hepatic antioxidant parameters</title>
<p>The hepatic samples were homogenized using a mortar and mixed with three volumes of cold phosphate buffer (pH 7.0). The mixture was then centrifuged at 4&#xb0;C (13000&#xa0;g; 15&#xa0;min) and the supernatant was used for analysis. Commercial kits (Zellbio Co., Deutschland, Germany) were used for superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and malondialdehyde (MDA). SOD activity was determined according to hydroxylamine method. CAT activity was determined according to decomposition of hydrogen peroxide over time. GPx activity was determined based on the decomposition of hydrogen peroxide using reduced glutathione (GSH) and the reaction on the remaining GSH with dinitrobenzoic acid. Malondialdehyde (MDA) content was determined based on the reaction with thiobarbituric acid at 95&#xb0;C. Soluble protein concentration was determined based on the Bradford method (<xref ref-type="bibr" rid="B8">Bradford, 1976</xref>).</p>
</sec>
<sec id="s2_9">
<title>Head kidney gene expressions</title>
<p>A commercial kit was used for extraction of RNA (Denazist Co., Tehran, Iran), which was then treated by DNase I (Thermo Fisher Scientific, Waltham, MA, USA). The RNA quality was confirmed by agarose gel. Then, cDNA was synthetized using a commercial kit. Specific primers of tumor necrosis factor-alpha (<italic>tnf-a</italic>), <italic>il-1b</italic>, and transforming growth factor-beta (<italic>tgf-b</italic>) were used (<xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref>) for gene expression assessments. RT-PCR method and a SYBER GREEN kit was used for quantification of RNA in the samples. Beta-actin (<italic>b-actin</italic>) was used as the housekeeping gene. Ct of the target and housekeeping genes were determined and used for gene expression analysis. The expressions of the genes were presented as fold changes relative to the CTL treatment, based on <xref ref-type="bibr" rid="B39">Livak and Schmittgen (2001)</xref>.</p>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption>
<p>Sequence, amplicon, and accession number of specific primers used for transcriptomic analysis.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left">Gene</th>
<th valign="top" align="left">Primer name</th>
<th valign="top" align="left">Sequences</th>
<th valign="top" align="left">Amplicon</th>
<th valign="top" align="left">Accession number</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" rowspan="2" align="left">
<italic>tnf-a</italic>
</td>
<td valign="top" align="left">TNFa-F</td>
<td valign="middle" align="left">GTCGTCGTGGCTCTTTGTTTA</td>
<td valign="top" rowspan="2" align="center">113</td>
<td valign="top" rowspan="2" align="left">AY428948.1</td>
</tr>
<tr>
<td valign="top" align="left">TNFa-R</td>
<td valign="middle" align="left">GTGTTCTTCGCCTTTAGTGCT</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">
<italic>il-1b</italic>
</td>
<td valign="top" align="left">IL1b-F</td>
<td valign="middle" align="left">CATCATAATGGCGGATGTGCTG</td>
<td valign="top" rowspan="2" align="center">125</td>
<td valign="top" rowspan="2" align="left">XM_019365842</td>
</tr>
<tr>
<td valign="top" align="left">IL1b-R</td>
<td valign="middle" align="left">AATGTGCTGTGTTCGCAGTT</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">
<italic>tgf-b</italic>
</td>
<td valign="middle" align="left">TGFb-F</td>
<td valign="middle" align="left">ATACGGAGTAACGTCGGGGA</td>
<td valign="top" rowspan="2" align="center">149</td>
<td valign="top" rowspan="2" align="left">NM_001311325</td>
</tr>
<tr>
<td valign="middle" align="left">TGFb-R</td>
<td valign="middle" align="left">GTGACAAAGCGAGATGCCAG</td>
</tr>
<tr>
<td valign="top" rowspan="2" align="left">
<italic>b-actin</italic>
</td>
<td valign="middle" align="left">Actin-F</td>
<td valign="middle" align="left">ATGGTGGGTATGGGTCAGAAA</td>
<td valign="top" rowspan="2" align="center">139</td>
<td valign="top" rowspan="2" align="left">XM_003443127.5</td>
</tr>
<tr>
<td valign="middle" align="left">Actin-R</td>
<td valign="middle" align="left">AGGTGTGATGCCAGATCTTCT</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s2_10">
<title>Statistical analysis</title>
<p>Data of growth performance and digestive enzymes activities were analyzed by polynomial contrast analysis to find relationship between the TV concentration and the tested parameters. Among the models, linear was the most significant one, thus was used for all parameters. Significant differences among the treatments were determined by contrast analysis. Post-challenge survival data were arcsin-transformed and analyzed by contrast test to find significant differences among the treatments. Hepatic antioxidant, humoral immune-related, and kidney transcriptomic parameters were analyzed by repeated measure two-way ANOVA (time &#xd7; dietary TV). Hepatic GPx and MDA exhibited no significant responses to the interaction of time and dietary TV levels, thus main effects of dietary TV were determined by contrast analysis. The other parameters exhibited significant responses to the interaction of time and dietary TV levels, thus pair comparisons were performed by contrast analysis to find significant differences among the treatment combinations. All analysis were performed in SPSS v.22 at the significance level of 0.05.</p>
</sec>
</sec>
<sec id="s3" sec-type="results">
<title>Results</title>
<p>There were significant relationships between the dietary TV levels and fish final weight, weight gain, and SGR, but not FCR. These parameters were not significantly different between the CTL and 25TV treatments, which showed significantly lower values compared to 50TV and 100TV treatments. Weight gain and SGR were similar between the 50TV and 100TV treatments, but the later exhibited significantly higher final weight (<xref ref-type="table" rid="T3">
<bold>Table&#xa0;3</bold>
</xref>).</p>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption>
<p>Growth performance, feed efficiency, and survival of Nile tilapia after 70-d feeding with diets containing 0 g/kg (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), or 100 g/kg (100TV) TV-NP.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="bottom" align="left"/>
<th valign="bottom" align="left">CTL</th>
<th valign="bottom" align="left">25TV</th>
<th valign="bottom" align="left">50TV</th>
<th valign="bottom" align="left">100TV</th>
<th valign="bottom" align="left">Linear contrast P-value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="bottom" align="left">Initial weight (g)</td>
<td valign="bottom" align="left">4.08 &#xb1; 0.10</td>
<td valign="bottom" align="left">4.37 &#xb1; 0.01</td>
<td valign="bottom" align="left">4.22 &#xb1; 0.11</td>
<td valign="bottom" align="left">4.40 &#xb1; 0.08</td>
<td valign="bottom" align="left">&#x2013;</td>
</tr>
<tr>
<td valign="bottom" align="left">Final weight (g)</td>
<td valign="bottom" align="left">20.3 &#xb1; 0.36 a</td>
<td valign="bottom" align="left">21.7 &#xb1; 0.99 a</td>
<td valign="bottom" align="left">26.2 &#xb1; 0.29 b</td>
<td valign="bottom" align="left">28.7 &#xb1; 0.33 c</td>
<td valign="bottom" align="left">&lt;0.001</td>
</tr>
<tr>
<td valign="bottom" align="left">Weight gain (%)</td>
<td valign="bottom" align="left">399 &#xb1; 17.1 a</td>
<td valign="bottom" align="left">396 &#xb1; 22.8 a</td>
<td valign="bottom" align="left">523 &#xb1; 23.1 b</td>
<td valign="bottom" align="left">551 &#xb1; 13.5 b</td>
<td valign="bottom" align="left">&lt;0.001</td>
</tr>
<tr>
<td valign="bottom" align="left">FCR</td>
<td valign="bottom" align="left">1.38 &#xb1; 0.04</td>
<td valign="bottom" align="left">1.38 &#xb1; 0.09</td>
<td valign="bottom" align="left">1.33 &#xb1; 0.03</td>
<td valign="bottom" align="left">1.29 &#xb1; 0.01</td>
<td valign="bottom" align="left">0.202</td>
</tr>
<tr>
<td valign="bottom" align="left">SGR (%/d)</td>
<td valign="bottom" align="left">2.29 &#xb1; 0.05 a</td>
<td valign="bottom" align="left">2.28 &#xb1; 0.06 a</td>
<td valign="bottom" align="left">2.61 &#xb1; 0.05 b</td>
<td valign="bottom" align="left">2.67 &#xb1; 0.03 b</td>
<td valign="bottom" align="left">&lt;0.001</td>
</tr>
<tr>
<td valign="bottom" align="left">Feed intake (g/fish)</td>
<td valign="bottom" align="left">22.4 &#xb1; 0.07</td>
<td valign="bottom" align="left">23.8 &#xb1; 0.62</td>
<td valign="bottom" align="left">29.3 &#xb1; 0.56</td>
<td valign="bottom" align="left">31.3 &#xb1; 0.37</td>
<td valign="bottom" align="left">&#x2013;</td>
</tr>
<tr>
<td valign="bottom" align="left">Survival (%)</td>
<td valign="bottom" align="left">100</td>
<td valign="bottom" align="left">100</td>
<td valign="bottom" align="left">100</td>
<td valign="bottom" align="left">100</td>
<td valign="bottom" align="left">&#x2013;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Different letters within a row show significant differences among the treatments (contrast analysis; P&lt; 0.05; n = 3).</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>There were significant relationships between the dietary TV levels and intestinal amylase, lipase, and protease activities. These parameters were not significantly different between the CTL and 25Tv treatments, which showed significantly lower values compared to 50TV and 100TV treatments. 50TV and 100TV treatments exhibited the highest amylase and lipase activities, respectively; but there was no significant difference in protease activity between these treatments (<xref ref-type="table" rid="T4">
<bold>Table&#xa0;4</bold>
</xref>).</p>
<table-wrap id="T4" position="float">
<label>Table&#xa0;4</label>
<caption>
<p>Intestinal digestive enzymes&#x2019; activities of Nile tilapia after 70-d feeding with diets containing 0 g/kg (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), or 100 g/kg (100TV) TV-NP.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="bottom" align="left"/>
<th valign="bottom" align="left">CTL</th>
<th valign="bottom" align="left">25TV</th>
<th valign="bottom" align="left">50TV</th>
<th valign="bottom" align="left">100TV</th>
<th valign="bottom" align="left">Linear contrast <italic>P</italic>-value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="bottom" align="left">Amylase (U/mg pr.)</td>
<td valign="bottom" align="left">37.7 &#xb1; 1.32 a</td>
<td valign="bottom" align="left">38.3 &#xb1; 0.67 a</td>
<td valign="bottom" align="left">44.7 &#xb1; 0.63 c</td>
<td valign="bottom" align="left">41.1 &#xb1; 1.03 b</td>
<td valign="bottom" align="left">0.004</td>
</tr>
<tr>
<td valign="bottom" align="left">Lipase (U/mg pr.)</td>
<td valign="bottom" align="left">1.76 &#xb1; 0.05 a</td>
<td valign="bottom" align="left">1.81 &#xb1; 0.05 a</td>
<td valign="bottom" align="left">1.99 &#xb1; 0.03 b</td>
<td valign="bottom" align="left">2.21 &#xb1; 0.06 c</td>
<td valign="bottom" align="left">&lt;0.001</td>
</tr>
<tr>
<td valign="bottom" align="left">Protease (U/mg pr.)</td>
<td valign="bottom" align="left">4.20 &#xb1; 1.13 a</td>
<td valign="bottom" align="left">4.48 &#xb1; 0.12 a</td>
<td valign="bottom" align="left">5.15 &#xb1; 0.10 b</td>
<td valign="bottom" align="left">5.06 &#xb1; 0.13 b</td>
<td valign="bottom" align="left">0.001</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Different letters within a row show significant differences among the treatments (contrast analysis; P&lt; 0.05; n = 3).</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>The negative control groups showed no mortality during the 14-d post-challenge. Post-challenge survival rates were significantly different among the treatments. Survival rates in CTL and 25TV were similar (53.3 and 56.7%, respectively) and significantly lower than 50TV and 100TV treatments (76.7 and 80.0%, respectively). There was no significant difference in the post-challenge survival rate between 50TV and 100TV treatments (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>).</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Survival of Nile tilapia after 70-d feeding with diets containing 0 g/kg (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), or 100 g/kg (100TV) TV-NP and challenged by <italic>A. hydrophila</italic>. Different letters show significant differences in cumulative mortality among the treatments, 14 day after the infection (contrast analysis; P&lt; 0.05; n = 3).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-10-1290879-g002.tif"/>
</fig>
<p>There were interaction effects of dietary TV and bacterial challenge on the hepatic SOD and CAT activities. Before the challenge, 50TV and 100TV exhibited significantly higher SOD and CAT activities, compared to the CTL. The challenge significantly increased SOD activity in all treatments, but there were no significant differences among the dietary treatments after the challenge. CAT activities significantly increased in CTL and 25TV treatments, after the challenge. 50TV and 100TV exhibited significantly lower CAT activity, compared to CTL, after the challenge (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>).</p>
<p>Dietary TV and bacterial challenge significantly affected the hepatic GPx activity and MDA concentration. Both parameters exhibited significant elevations after the challenge. TV-treated fish presented significantly high GPx activity and lower MDA levels, compared to the CTL. The highest GPx and lowest MDA values were observed in 50TV and 100Tv treatments (<xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3</bold>
</xref>).</p>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Hepatic antioxidant parameters of Nile tilapia after 70-d feeding with diets containing 0 g/kg (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), or 100 g/kg (100TV) TV-NP and challenged by <italic>A. hydrophila</italic>. Grey bars: pre-challenge; black bars: post-challenge. SOD and CAT: Different lowercase and uppercase letters above the bars show significant differences among the treatments, before challenge and after challenge, respectively. Asterisks show significant differences between pre-challenge and post-challenge (contrast analysis; P&lt; 0.05; n = 3). GPx and MDA: Different letters above the bars show significant differences among the treatments (contrast analysis; P&lt; 0.05; n = 3).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-10-1290879-g003.tif"/>
</fig>
<p>There were interaction effects of dietary TV and bacterial challenge on the plasma lysozyme and ACH50 activities. Before the challenge, 25TV and 50TV exhibited significantly higher lysozyme and ACH50 activities, whereas, compared to the CTL. At this time, 100TV exhibited significantly lower lysozyme and ACH50 activities, whereas, compared to the CTL. The challenge significantly decreased lysozyme activity in CTL and 50TV, had no significant effects on lysozyme activity in 25TV, and significantly increased lysozyme activity in 100TV treatments. The challenge induced no significant changes in ACH50 activities in CTL, 25TV, and 50TV, but significantly increased it in 100TV treatment. All TV-treated fish had similar plasma lysozyme and ACH50 activities, which were significantly higher than CTL, after the challenge (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>).</p>
<fig id="f4" position="float">
<label>Figure&#xa0;4</label>
<caption>
<p>Plasma innate immune-related parameters of Nile tilapia after 70-d feeding with diets containing 0 g/kg (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), or 100 g/kg (100TV) TV-NP and challenged by <italic>A. hydrophila</italic>. Grey bars: pre-challenge; black bars: post-challenge. Different lowercase and uppercase letters above the bars show significant differences among the treatments, before challenge and after challenge, respectively. Asterisks show significant differences between pre-challenge and post-challenge (contrast analysis; P&lt; 0.05; n = 3).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-10-1290879-g004.tif"/>
</fig>
<p>There were interaction effects of dietary TV and bacterial challenge on the head kidney <italic>tnf-a</italic>, <italic>il-1b</italic>, and <italic>tgf-b</italic> expressions. Before the challenge, 100TV treatment exhibited significantly higher expression of <italic>tnf-a</italic>, <italic>il-1b</italic>, and <italic>tgf-b</italic>, compared to CTL. The bacterial challenge significantly up-regulated the expression of these genes in all treatments and the highest expressions were observed in 50TV and 100TV treatments (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5</bold>
</xref>).</p>
<fig id="f5" position="float">
<label>Figure&#xa0;5</label>
<caption>
<p>Head kidney expression of immune-related genes of Nile tilapia after 70-d feeding with diets containing 0 g/kg (CTL), 25 mg/kg (25TV), 50 mg/kg (50TV), or 100 g/kg (100TV) TV-NP and challenged by <italic>A. hydrophila</italic>. Grey bars: pre-challenge; black bars: post-challenge. Different lowercase and uppercase letters above the bars show significant differences among the treatments, before challenge and after challenge, respectively. Asterisks show significant differences between pre-challenge and post-challenge (contrast analysis; P&lt; 0.05; n = 3).</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-10-1290879-g005.tif"/>
</fig>
</sec>
<sec id="s4" sec-type="discussion">
<title>Discussion</title>
<p>Nano-encapsulation is a reliable method to protect essential oils against degradation and enhance their efficiency in fish nutrition. This study showed that dietary 50-100 mg/kg TV-NP can improve growth rate in Nile tilapia. There is no study on Nile tilapia assessing the effects of nanoparticles of thyme essential oil on growth performance of this species. However, 10 g/kg bulk essential oil of thyme was shown to improve growth performance of Nile tilapia under normal conditions or exposed to waterborne copper (<xref ref-type="bibr" rid="B2">Ahmed et&#xa0;al., 2022</xref>). Furthermore, adding 10-20 g/kg thyme meal to diet resulted in no change in growth performance of Nile tilapia (<xref ref-type="bibr" rid="B66">Zaki et&#xa0;al., 2012</xref>; <xref ref-type="bibr" rid="B30">Khalil et&#xa0;al., 2020</xref>) and Mozambique tilapia, <italic>Oreochromis mossambicus</italic> (<xref ref-type="bibr" rid="B65">Y&#x131;lmaz et&#xa0;al</xref>.). Considering the essential oil yield of thyme (<xref ref-type="bibr" rid="B4">Alavi-Samani et&#xa0;al., 2015</xref>), these concentrations of thyme meal correspond to 83-166 mg/kg thyme essential oil, which are close to the concentrations used in this study. Thus, it is speculated that nano-liposome technique can improve the benefits of thyme in Nile tilapia. However, other differences between the TV-NP and thyme meal should not be neglected and further studies are needed to address this topic. The present results are in line with a study assessed the effects of cinnamon nanoparticle on growth performance of Nile tilapia, which found growth promotion at 3 g/kg dietary nanoparticle (<xref ref-type="bibr" rid="B1">Abdel-Tawwab et&#xa0;al., 2018</xref>).</p>
<p>Increase in digestive enzymes&#x2019; activity can be a reason for growth promotion in fish fed supplemented diets. It is supposed that increase in the activity of these enzymes leads to better digestion. It has been shown that thyme essential oil improves growth performance concurrent with increase in the intestinal activity of digestive enzymes in common carp, <italic>Cyprinus carpio</italic> (<xref ref-type="bibr" rid="B19">Ghafarifarsani et&#xa0;al., 2022</xref>), which supports the present finding. The exact mechanisms of elevation of digestive enzymes are not clear, but it could be a direct effects of TV-NP on enzyme synthesis and release from pancreas, which needs further investigations. Moreover, intestinal microbes are another source of digestive enzymes and TV-NP might change the composition of microbiota, considering the antimicrobial effects of thyme ingredients (<xref ref-type="bibr" rid="B54">Sienkiewicz et&#xa0;al., 2012</xref>). But this topic needs to be investigated in fish.</p>
<p>Bacterial infections induce severe oxidative stress caused by reactive oxygen/nitrogen species. This leads to activation of the antioxidant system to protect host cells. The nuclear factor erythroid 2-related factor 2 (Nrf2)/Kelch-like ECH-associated protein 1 (Keap1) signaling pathway responds to oxidative stress and regulates the antioxidant system (<xref ref-type="bibr" rid="B12">Elbialy et&#xa0;al., 2023</xref>). Infection of fish with <italic>A. hydrophila</italic> has been reported to down-regulate <italic>nrf2</italic> transcript and increase reactive oxygen species concentrations in the kidney (<xref ref-type="bibr" rid="B67">Zang et&#xa0;al., 2020</xref>). A study on Nile tilapia has reported decreases in SOD and GPx activities accompanied by an increase in MDA (lipid peroxidation) concentration after <italic>A. hydrophila</italic> infection (<xref ref-type="bibr" rid="B45">Moustafa et&#xa0;al., 2020</xref>), suggesting the induction of oxidative stress due to weakness of the enzymatic antioxidant system. However, lipid peroxidation has been observed in Nile tilapia and largemouth bass, <italic>Micropterus salmoides</italic>, infected with <italic>A. hydrophila</italic>, along with increase in SOD and/or CAT; increase in these enzymes&#x2019; activities have been accompanied by higher post-infection survival (<xref ref-type="bibr" rid="B22">Gong et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B32">Kuebutornye et&#xa0;al., 2020</xref>). Thyme essential oil mainly contains thymol and carvacrol, two well-known antioxidants (<xref ref-type="bibr" rid="B21">Giannenas et&#xa0;al., 2012</xref>; <xref ref-type="bibr" rid="B25">Hashemipour et&#xa0;al., 2013</xref>). Dietary supplementation of 10-20 g/kg of this essential oil has been found to improve antioxidant capacity and reduce lipid peroxidation in rainbow trout, <italic>Oncorhynchus mykiss</italic> (<xref ref-type="bibr" rid="B57">S&#xf6;nmez et&#xa0;al., 2015</xref>), and common carp (<xref ref-type="bibr" rid="B19">Ghafarifarsani et&#xa0;al., 2022</xref>); the later also exhibited improved survival after <italic>A. hydrophila</italic> infection. This suggests TV-NP may be more efficient than non-protected essential oil in strengthening the antioxidant system. In the present study, the highest post-infection survivals were accompanied by lower lipid peroxidation (MDA levels), and elevations in GPx, andpre-infection SOD/CAT activities. Thus, antioxidant-stimulating capacity of TV-NP can be considered as one of the mediators of improved resistance against <italic>A. hydrophila</italic> infection. Interestingly, CAT activities in the 50TV and 100TV treatments were lower than CTL, despite lower lipid peroxidation in these treatments. CAT decomposes hydrogen peroxide at high concentrations, but low concentrations of hydrogen peroxide are detoxified by GPx (<xref ref-type="bibr" rid="B60">Spolarics and Wu, 1997</xref>; <xref ref-type="bibr" rid="B50">Rocha et&#xa0;al., 2015</xref>; <xref ref-type="bibr" rid="B11">Djordjevi&#x107; et&#xa0;al., 2022</xref>); thus, it can be speculated that 50TV and 100TV experienced lower concentration of hydrogen peroxide that led to lower lipid peroxidation.</p>
<p>Plasma lysozyme is a component of the soluble humoral immune system that attacks both gram-positive (directly) and gram-negative (in contribution with other actors) bacteria (<xref ref-type="bibr" rid="B56">Song et&#xa0;al., 2021</xref>). The decrease in the plasma lysozyme activity after the challenge may be as a result of the production of lysozyme inhibitors by <italic>A. hydrophila</italic>. Gram-negative bacteria have an ability to escape from lysozyme attack by producing periplasmic proteins that inactivate lysozyme (<xref ref-type="bibr" rid="B36">Liu et&#xa0;al., 2015</xref>) and <italic>A. hydrophila</italic> has been found possessing periplasmic lysozyme inhibitors (<xref ref-type="bibr" rid="B34">Leysen et&#xa0;al., 2011</xref>). Similar to the present results, <xref ref-type="bibr" rid="B13">El-Houseiny et&#xa0;al. (2021)</xref> found decrease in lysozyme activity in Nile tilapia seven days after an experimental infection with <italic>A. hydrophila</italic>. Wuchang bream, <italic>Megalobrama amblycephala</italic>, showed similar decrease in lysozyme activity 48&#xa0;h after an experimental infection with <italic>A. hydrophila</italic> (<xref ref-type="bibr" rid="B37">Liu et&#xa0;al., 2012</xref>). It was shown that thyme essential oil can increase serum and mucosal lysozyme activities in rainbow trout (<xref ref-type="bibr" rid="B68">Zargar et&#xa0;al., 2019</xref>) and common carp (<xref ref-type="bibr" rid="B19">Ghafarifarsani et&#xa0;al., 2022</xref>), which support the present results. However, the present results show that pre-challenge plasma lysozyme activity is not a suitable predictor of survival after <italic>A. hydrophila</italic> infection, as shown in 100TV treatment. This result is similar to that obtained in rainbow trout (<xref ref-type="bibr" rid="B68">Zargar et&#xa0;al., 2019</xref>).</p>
<p>Complement proteins have various roles in the fish innate and adaptive immune defenses such as opsonization, cell lysis, B cell activation, and inflammation (<xref ref-type="bibr" rid="B6">Bavia et&#xa0;al., 2022</xref>). Pathogens possess adaptive mechanisms to escape from the complement system. <italic>A. hydrophila</italic> has metaloproteins that degrade the C3 component of the complement system in fish, thus inhibit alternative complement responses (<xref ref-type="bibr" rid="B9">Chen et&#xa0;al., 2019</xref>). Such decrements in ACH50 activity have been reported in Nile tilapia <xref ref-type="bibr" rid="B13">El-Houseiny et&#xa0;al. (2021)</xref> and olive barb, <italic>Systomus sarana</italic> (<xref ref-type="bibr" rid="B10">Das et&#xa0;al., 2011</xref>), respectively, 7 and 2&#xa0;d after infection with <italic>A. hydrophila</italic>. Similar results have been reported for other gram negative pathogens;&lt;24&#xa0;h post-infection with <italic>Flavobacterium columnare</italic> (<xref ref-type="bibr" rid="B49">Ravindra et&#xa0;al., 2019</xref>) or 48&#xa0;h post-infection with <italic>Edwardsiella tarda</italic> (<xref ref-type="bibr" rid="B44">Mohanty and Sahoo, 2010</xref>). In the present study, there was a decrease in ACH50 activity in CTL treatment after the infection, but not statistically significant. This might be related to the sampling time, as the above studies show that ACH50 response to infection is time-dependent. Thus, it is speculated that <italic>A. hydrophila</italic> may suppress ACH50 activity in Nile tilapia, but further studies are needed for confirmation. Essential oil of thyme has been found to increase mucosal ACH50 in common carp (<xref ref-type="bibr" rid="B19">Ghafarifarsani et&#xa0;al., 2022</xref>) and C<sub>3</sub> mRNA in rainbow trout (<xref ref-type="bibr" rid="B68">Zargar et&#xa0;al., 2019</xref>), but none of them were predictor of survival after <italic>A. hydrophila</italic> infection. The present results also confirmed this, as 100TV had the lowest ACH50 activity before challenge but expressed the highest survival after the challenge.</p>
<p>Inflammation is critical for proper immune function and pathogen clearance in fish. Pro-inflammatory cytokines are the mediators of inflammation with a wide range of effects. Tumor necrosis factor-alpha and il-1b are two major pro-inflammatory cytokines that respond at early stages on infection (reviewed by <xref ref-type="bibr" rid="B75">Zou and Secombes (2016)</xref>). They have diverse but overlapping functions in fish including stimulating resting macrophages to actively explore foreign germs and engulf them. Interleukin-1 beta acts as a chemo-attractant for leukocyte and tnf-a increases macrophage survival after phagocytosis (<xref ref-type="bibr" rid="B75">Zou and Secombes, 2016</xref>). Studies have shown that increase in these two cytokines (protein or transcript) is necessary for resistance against <italic>A. hydrophila</italic> in fish (<xref ref-type="bibr" rid="B10">Das et&#xa0;al., 2011</xref>; <xref ref-type="bibr" rid="B22">Gong et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B72">Zhang et&#xa0;al., 2020</xref>), including Nile tilapia (<xref ref-type="bibr" rid="B45">Moustafa et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B13">El-Houseiny et&#xa0;al., 2021</xref>). Furthermore, it has been shown that <italic>A. hydrophila</italic>-resistance Nile tilapia expresses higher <italic>tnf-a</italic> and <italic>il-b</italic> transcript, compared to non-resistance individuals (<xref ref-type="bibr" rid="B15">El-Magd et&#xa0;al., 2019</xref>), suggesting the importance of these cytokines in Aeromonas septicemia control. Transforming growth factor-beta has been traditionally known as an anti-inflammatory and immunosuppressive cytokine (<xref ref-type="bibr" rid="B42">Maehr et&#xa0;al., 2013</xref>). But recent findings have demonstrated that this cytokine has active roles in immune responses and disease resistance (<xref ref-type="bibr" rid="B48">Qi et&#xa0;al., 2016</xref>). Head kidney leukocytes of Nile tilapia have exhibited up-regulations in <italic>tgf-b</italic> transcript, following lipopolysaccharide and poly I:C stimulations (<xref ref-type="bibr" rid="B71">Zhan et&#xa0;al., 2015</xref>). Macrophages isolated from goldfish, <italic>Carassius auratus</italic>, head kidney exhibited up-regulations in <italic>tgf-b</italic> transcript in response to lipopolysaccharide and recombinant TNF-a stimulations (<xref ref-type="bibr" rid="B23">Haddad et&#xa0;al., 2008</xref>). It seems that tgf-b controls inflammation induced by pro-inflammatory cytokines like tnf-a and il-1b, which has been confirmed in Nile tilapia (<xref ref-type="bibr" rid="B24">Han et&#xa0;al., 2020</xref>) and other species such as common carp (<xref ref-type="bibr" rid="B73">Zhang et&#xa0;al., 2017</xref>), obscure puffer, <italic>Takifugu obscurus</italic> (<xref ref-type="bibr" rid="B38">Liu et&#xa0;al., 2020</xref>), and largemouth bass (<xref ref-type="bibr" rid="B22">Gong et&#xa0;al., 2019</xref>). The present results are supported by these studies. Thyme essential oil has been found up-regulating <italic>il-1b</italic> transcript in head kidney of rainbow trout that resulted in higher post-infection (<italic>A. hydrophila</italic>) survival, suggesting that the essential oil may improve immune response against the disease by inducing inflammation. But, this has not been always the case, as administration of thyme essential oil and its nano-emulsion resulted in lower transcript of <italic>tnf-a</italic> and higher <italic>tgf-b</italic> in head kidney, accompanied by lack of mortality after an experimental streptococcusis in Nile tilapia. Thus, the present results show that TV-NP improves survival of Nile tilapia by stimulating pro-inflammatory cytokines that improve cell-mediated immunity, but at the same time, induces anti-inflammatory cytokine (<italic>tgf-b</italic>) to control detrimental effects inflammation on host cells.</p>
<p>In conclusion, TV-NP at 50-100 mg/kg successfully promoted growth rate of Nile tilapia, which seems to be related to increase in the intestinal digestive enzymes. Moreover, these concentrations improved the fish survival after challenge with <italic>A. hydrophila</italic>. Based on the results, improved disease resistance was likely related to improved antioxidant function and cytokine responses after infection.</p>
</sec>
<sec id="s5" sec-type="data-availability">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec id="s6" sec-type="ethics-statement">
<title>Ethics statement</title>
<p>The animal study was approved by Bioethics Commission of Agrarian and Technological Institute, RUDN University (Protocol &#x2116; 12 dated November 14, 2022. The study was conducted in accordance with the local legislation and institutional requirements.</p>
</sec>
<sec id="s7" sec-type="author-contributions">
<title>Author contributions</title>
<p>MY: Conceptualization, Data curation, Funding acquisition, Supervision, Writing &#x2013; review &amp; editing. SMH: Conceptualization, Formal Analysis, Project administration, Writing &#x2013; original draft. MG: Formal Analysis, Methodology, Resources, Writing &#x2013; original draft. HHM: Conceptualization, Data curation, Methodology, Writing &#x2013; review &amp; editing. YAV: Conceptualization, Supervision, Writing &#x2013; original draft. EVK: Data curation, Methodology, Visualization, Writing &#x2013; original draft. EDS: Formal Analysis, Methodology, Writing &#x2013; original draft.</p>
</sec>
</body>
<back>
<sec id="s8" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This publication has been supported by the RUDN University Scientific Projects Grant System, project &#x2116; &#x201c;202196-2-000&#x201d;.</p>
</sec>
<sec id="s9" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
<p>The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.</p>
</sec>
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<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
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