Skip to main content
Veterinary World logoLink to Veterinary World
. 2023 May 11;16(5):965–976. doi: 10.14202/vetworld.2023.965-976

Effect of dietary garlic (Allium sativum) on the zootechnical performance and health indicators of aquatic animals: A mini-review

Daniel Leonardo Cala Delgado 1,✉, Linda Lucia Castillo Caceres 2, Sebastián Alexander Cely Gómez 2, Aníbal Domínguez Odio 3
PMCID: PMC10420702  PMID: 37576751

Abstract

Considerable efforts have been made by modern aquaculture to mitigate the environmental damages caused by its practices while also attempting to improve the quality of the aquatic organisms by promoting alternatives, such as the use of natural products, like garlic (Allium sativum), and instead of chemical agents. Garlic has multiple properties, including antifungal, antibacterial, antiviral, antitoxic, and anticancer effects. In fish, the antiparasitic activity of garlic is one of the most reported effects in the literature, mainly using immersion baths for aquatic organisms. Using garlic also has an antimicrobial effect on the culture of aquatic organisms. Therefore, this review focuses on the impact of garlic on the health and production of aquatic organisms.

Keywords: Allium sativum, aquaculture, crustacean, salmonid, tilapia

Introduction

Aquatic animals and plant species have long been farmed for self-supply or commercial purposes. This practice is supported by over 2000 years of knowledge, thus determining its value as an income and protein source for people worldwide [1–4]. The consumption of aquatic products has been rapidly increasing [5], partially fueled by the world’s growing population and an increased interest in consuming healthy food [6]. However, this increase in production and consumption is not uniform globally. The geographic distribution of international trade shows that countries such as China, India, Egypt, Vietnam, Chile, and Norway account for 59% of the total fishing exports. In contrast, industrialized countries and geopolitical entities such as the United States, the European Union, and Japan import 71% of the international market’s fishing products [7, 8].

Urgent measures should be taken to increase, diversify, and optimize the current aquaculture production systems to meet the demand for protein consumption from aquatic species while lowering costs and minimizing resource utilization [2, 9].

The intensification of aquaculture practices leads to polyculture, high fish density per volume [10], and stress by overcrowding [1, 11], which favors the spread of infectious diseases [12]. Moreover, while each pathogen’s impact on aquatic health varies, they can all cause severe economic losses [13], because they affect the productive potential, require diagnosis and treatment, and can cause high mortality rates in aquatic species [14, 15].

These threats are managed by the use and abuse of synthetic chemical products, including antibiotics [16, 17]. These chemical products are harmful to the environment and human health because they bioaccumulate [18], accumulate in fish tissue [19], and promote the development of multidrug-resistant bacteria [20]. To reduce bacterial resistance, it is necessary to implement new strategies, which will avoid the use of traditional antimicrobial products [11] and favor the use of natural products [11, 21].

This environmental strategy encourages the generalized use of probiotics, prebiotics, postbiotics, and immunostimulants [22, 23], as well as the search for new natural alternatives regardless of their origin [24–28]. In addition, this strategy offers excellent opportunities to use herbal products, particularly those containing garlic (Allium sativum) [21, 29]. Therefore, this review focuses on the impact of garlic on the health and production of aquatic organisms.

Natural Aquaculture Products

One of humanity’s oldest practices is the use of therapeutic plants [27, 30]. Despite the achievements in healthcare accomplished over time, active plant ingredients and their biological activities remain invaluable resources for humans [31]. Recently, ancestral and modern knowledge have merged. Ancestral knowledge helped identify the medicinal properties of leaves, roots, seeds, barks, fruits, and flowers [32], whereas modern knowledge incorporated new techniques to explain and optimize the application of leaves, roots, seeds, barks, fruits, and flowers [33].

The interest in natural products is rising in the veterinary sector; however, despite the similarities in the use of medicinal plants in animals and humans, manufacturing of natural products for animal use remains a significant shortcoming of this sector. In general, products for terrestrial production animals and those related to health and nutrition dominate the veterinary herbal product market [34]. A peculiar characteristic of this sector is that it is not a part of the domain of large international biopharmaceutical companies related to animal health based in the United States, Germany, and France [35].

Various plants have shown promising results in aquatic production [29], with more than 250 plant species identified belonging to 75 families and 32 orders [32, 36]. In aquaculture, plant-based products and byproducts are administrated or incorporated through intraperitoneal [37] or intramuscular injection [38], oral administration [39], and immersion [40].

Nevertheless, oral administration and incorporation through diet are the most recommended and agreed-on methods in aquatic species because they do not cause stress and allow simultaneous treatment of many organisms with minimal effort and cost [41].

Besides their beneficial effects on disease control (Table-1) [41–62], plants can also improve production yields [42]; stimulate appetite [63] and the immune system [43, 64]; improve integral health [65]; exert anti-inflammatory [44], antistress [66], sedative, and anesthetic effects [67]; and prolong the shelf life of aquatic products [68]. Moreover, there are numerous therapeutic plants worth mentioning because they are used to treat bacterial and parasitic diseases affecting vital organs, such as the skin, gills, gut, and eyes [41, 45, 69].

Table-1.

Medicinal plants used in the production and processing of aquatic species and products.

Plant species Function Aquatic species Form Reference
Productive stage
 Urtica dioica Improves productive yields Immunostimulant Oncorhynchus mykiss C. auratus Powder Methanolic extract [43]
 Moringa Oleifera Antibacterial Immunostimulant Improves productive yields Carassius auratus gibelio Powder [42]
 Eugenia aromatica Anesthetic Amphiprion ocellaris Essential oil [46]
Anesthetic and sedative C. carpio [47]
 Vitex agnus-castus Immunostimulant C. auratus Hydro-ethanolic extract [48]
 Azadirachta indica Antiprotozoal Anabas testudineus Powder [49]
Antiparasitic C. auratus Ethanolic and aqueous extract [50]
 Chenopodium ambrosioides Anti-inflammatory Lutjanus peru Powder Methanolic extract [44]
 Curcuma longa Growth improvement Immunostimulant Antibacterial C. carpio Powder [51]
 Origanum heracleoticum Antibacterial Ictalurus punctatus Essential oil [52]
Growth stimulant
 Lippia berlandieri Antibacterial L. vannamei Essential oil [53]
Antibacterial Oreochromis mossambicus Essential oil [54]
Growth stimulant
 Kalopanax pictus Antibacterial Epinephelus bruneus Ethanolic extract [41]
 Scutellaria baicalensis Antibacterial Oplegnathus fasciatus Hydro-ethanolic extractw [41]
 Mentha piperita Antibacterial Lates calcarifer Powder [55]
Growth stimulant
Antiparasitic Oreochromis niloticus Essential oil [56]
 Caesalpinia sappan Antiparasitic C. auratus Methanolic extract [45]
 Lysimachia christinae
 Cuscuta chinensis
 Artemisia argyi
 Eupatorium fortune
 Cinnamomum cassia
 Lindera aggregate
 Pseudolarix kaempferi
 Piper longum
 Bupleurum chinensis
 Andrographis paniculata Growth stimulant and Immunostimulant L. vannamei Powder [57]
 Solanum procumbens Lour Immunostimulant [58]
 Bidens alba Improves productive yields Immunostimulant Antibacterial [59]
 Plectranthus amboinicus
 Eleutherine bulbosa Immunostimulant Antibacterial [60]
Processing stage
 Citrus sinensis Product preservation Parapenaeus longirostris Essential oil [61]
 Salvia officinalis Increase in the shelf life of fish burgers C. carpio [62]

C. auratus=Carassius auratus, C. carpio=Cyprinus carpio, L. vannamei=Litopenaeus vannamei

Garlic

Allium (Family: Amaryllidaceae) is a monocot genus having 800 species that are globally distributed, with different morphological and psychological characteristics [70]. Garlic has been used as a seasoning in food preparations and in traditional medicine to improve human health [70]. At the economic and commercial level, A. sativum is the most relevant species of the genus [71] and it is the most commonly used Allium species to treat common diseases, after onion (Allium cepa L.) [72].

Garlic has been shown to have antifungal, antibacterial, antiviral, antitoxic, and anticancer properties, among others [73–77]. Sulfur-containing bioactive compounds and sulfur-free phenolic compounds are responsible for these properties [63].

The proximate composition of garlic is 65% moisture, 27.5% carbohydrate, 4.7% fiber, 2%–3% organosulfur compounds, and 2% protein [78]. The sulfur-containing chemical compounds include ajoenes, thiosulfinates, vinilditine, sulfides, diallyl trisulfide, and cysteine [79]. Garlic also contains S-propyl-cysteine-sulfoxide and S-methyl cysteine-sulfoxide, which can produce more than 50 metabolites depending on the moisture content and temperature [80]. The secondary metabolites obtained from the cysteine accumulated in plants of the Allium genus are S-alqu(en)yl-cysteine sulfoxides; alliin, which transforms into allicin; N-acetylcysteine; S-allylcysteine; and S-allyl-mercapto cysteine [80, 81]. These active principles have antioxidant, anti-inflammatory, and anticancer properties [82].

Allicin is an unstable, volatile, and cytotoxic liposoluble organosulfur compound [83]. It is also garlic’s most important active component, with antiseptic, antiviral, antifungal, antiparasitic, and antibacterial properties [63, 84]. In addition, allicin and ajoene are the active components used in veterinary medicine and livestock production [85, 86], and their benefits and antiparasitic properties on the zootechnical performance of farm animals have been reported [63, 78–88].

The beneficial properties of garlic for the treatment of bacterial diseases caused by Gram-positive and Gram-negative bacteria are attributed to several thiosulfinates, including allicin [89, 90]. Garlic’s active components oxidize bacterial proteins [91] by reacting with low molecular weight thioles, such as glutathione, and changing the cellular redox potential into a more oxidized state, which induces cell apoptosis [92]. In addition, allicin’s lipophilic properties enhance its antimicrobial activity, allowing it to enter the cell through the bacterial cell wall [93].

Garlic also presents antiviral activity [94]. Allicin condenses into ajoene, a molecule with antiviral activity that blocks integrin-dependent processes in the infected cellular system [95]. Furthermore, allicin efficiently inhibits viral replication and stimulates the immune system through the host proteome [96], improving the host immune response through mechanisms involving interferon-gamma, tumor necrosis factor, interleukin (IL-12P70), and T-cells [83]. Moreover, another advantage of garlic is immunostimulation, which is attributed to organosulfur, polysaccharide, and fructan compounds [97].

The Use of Garlic in Aquatic Organisms

Garlic has been used in livestock production primarily to increase the indicators of zootechnical performance [98]. In aquaculture, garlic has been used for the same purpose [99, 100]. Its effects on zootechnical performance have been studied in different species of aquatic organisms [29]. Various garlic species have been used in aquaculture, for example, the alcoholic extract of Allium hirtifolium was used in feed of rainbow trout Oncorhynchus mykiss fingerlings [101]; this species has also been studied in Cyprinus carpio [102]. Other species, such as Allium stipitatum [63], Allium tuberosum [103], and Allium mongolicum [104], have been studied in the production of aquatic organisms.

Reported results and effects are different, for example, when the food formulation incorporated garlic (in a proportion of 40 g/kg), Asian sea bass (Lates calcarifer) grew faster than fish that were fed commercial diets [105]. Grouper (Epinephelus coioides) that was fed garlic supplemented diet (80 g/kg) and exposed to Vibrio alginolyticus, presented a significant increase in phagocytosis, superoxide anion production, and superoxide dismutase activity, indicating that garlic can increase the resistance against bacterial diseases and stimulate the immune system [102]. In addition, these values were higher in the groups that received a fresh garlic diet than in those that were given garlic powder [106]. Diets containing garlic (10 g/kg of food) increased resistance to Edwardsiella tarda infection in African sharptooth catfish (Clarias gariepinus) [107]. In narrow-clawed crayfish (Postantacus leptodactylus), the use of garlic powder included in the feed (1%–2%) has effects on growth and immunostimulant effects [108].

One of the most reported effects of garlic consumption on fish is its antiparasitic properties, which are achieved primarily by subjecting the aquatic organisms to immersion baths [109]. The effects of garlic extract on adult and oncomiracidia, production, development, and cumulative hatching of eggs of Neobenedenia spp. did not yield positive results in vitro [110]. However, another in vitro study demonstrated that 250 μL/L of aqueous garlic extract prevented the mobilization of Lernantropus kroyeri, which was isolated from European bass (Dicentrarchus labrax), for 60 min [111].

Furthermore, in vivo studies performed on Poecilia reticulata infected with Cryptocaryon irritans showed that an immersion bath containing garlic aqueous extract (250 or 500 μL/L) could reduce infection, particularly in the caudal fin [112]. In addition to the immersion baths, adding aqueous garlic extract (50 mL and 150 mL/kg) to the diet of L. calcarifer for 30 days reduced Neobenedenia spp. infection by 70% [113].

Garlic in Pisciculture

Pisciculture is a subset of aquaculture, which encompasses the production of all aquatic organisms. It is a collection of techniques and knowledge related to industrial fish farming. The Food and Agriculture Organization [9] has registered the production of 466 aquatic species, 92 genera, and 32 families for fish farming. However, global fish farming production mainly relies on nine species, five of which are carps, two of which are tilapia, and the rest are salmonids (Figure-1).

Figure-1.

Figure-1

Primary fish species contributing to global fish farming production. Source: FAO, 2020.

Carps

Carps belong to the Cyprinidae family, which includes important species for aquaculture due to their commercial value and distribution [114]. In the report of the Food and Agriculture Organization of the United Nations (FAO) 2020 [9], they composed 32% of the global freshwater aquaculture production.

Several factors can impact productive performance, such as the activity of digestive enzymes, structure, and gut microbiota [115]. Therefore, the implementation of products to improve nutrient absorption in fish has been thoroughly studied [116]. In this regard, it has been reported that adding ginger to the diet of the common carp (C. carpio) increases productive performance, which was attributed to an improvement in the digestion and absorption of dietary protein components due to the stimulation of gut protease secretion [117].

The use of garlic powder (0.5%, 1.0%, and 1.5% proportion) to supplement the diet of juvenile carps showed significant beneficial effects on weight gain, specific growth rate, and protein efficiency compared with the group that did not receive garlic powder-containing diet [118]. Moreover, adding 0.5% garlic powder to the diet of Carassius auratus improved the growth and survival of the juveniles [119].

In Ctenopharyngodon idella, the addition of 2% garlic powder in the diet significantly improved weight gain, food efficiency and food conversion indicators, and the percentage of protein in muscle when compared to fish with commercial diets without garlic powder [120]. Moreover, Adineh et al. [100] reported that the addition of 0.2% garlic and selenium nanoparticles to the diet of C. idella improved the activity of digestive enzymes, including amylase, protease, and lipase, which favored food assimilation and the subsequent improvement of growth indicators.

The immune system of fish is also affected by garlic. In C. carpio, the supplementation of commercial diets with garlic (5 g/kg) had a positive effect on the white cell count, especially on lymphocytes, and presented significantly higher productions of lysozyme and immunoglobulin M than the control groups fed commercial diets alone [121]. Another study on the same fish species has shown that 20 g/kg of garlic in the diet stimulates leukocyte production and phagocytosis [122].

Carps are prone to infectious diseases, and their first protective barrier is the skin mucus. It has been observed that when the C. auratus was fed a diet supplemented with 15 mL/kg of liquid garlic extract presented higher lysozyme, complement and alkaline phosphatase activity, and immunoglobulin and dissolved protein concentrations in skin mucus than the control groups. These results are reflected in their ability to inhibit the growth of Aeromonas hydrophila, Yersinia ruckeri, Micrococcus luteus, Streptococcus faecium, and Streptococcus iniae [123]. Using a commercial additive containing 2% garlic extract in the diet of C. carpio improved their resistance to experimental infection by A. hydrophila, resulting in a 100% survival rate compared to the 83% in the group that received the non-supplemented diet.

Ectoparasitic and endoparasitic infestations are common in carps [124]. C. carpio infested with Gyrodactylus elegans (Monogenean) and subjected to an immersion bath containing 8.37 mg/mL of garlic powder for 3 min reduced the parasite load by 14%. Moreover, 6 min of immersion with the same garlic concentration resulted in a 100% reduction of the parasite load [125].

Tilapia

Garlic has been known to promote the growth of aquatic organisms [125]. The supplementation of balanced commercial food with 14 g/kg of garlic for juvenile tilapia resulted in an increase in weight and average length; supplementation with 10 g/kg of garlic resulted in decreased conversion factor [126]. Tilapia zillii juveniles fed with a basal diet supplemented with garlic powder (20 g/kg) showed a weight gain of 32 g/fish and a food conversion factor of 1.27. In contrast, the control group only gained 22 g/fish and presented a conversion factor of 1.55 [127].

Replacing basic dietary ingredients with garlic leads to results contrary to those previously highlighted. The substitution of corn flour with 1.5% of garlic powder in the diet of Oreochromis niloticus juveniles (initial weight of 10 g) did not significantly alter the growth indicators or the food conversion factor when compared with the control group [128]. Furthermore, it is essential to note that a previous study revealed that the addition of garlic does not modify the proximate composition of the final product, which remained identical to that of the control group [128].

Studies have shown that as garlic concentration in food increases, the growth-promoting properties of natural garlic extract become evident. With an initial weight of 7 g, O. niloticus gained approximately 15 g/fish after consuming a diet containing 3% garlic powder. In contrast, the group that did not consume garlic gained 11 g [129]. This study also reported that 4% garlic powder in the diet has no negative impact on the fish’s health and does not disrupt the activity of the alanine transaminase and aspartate aminotransferase enzymes; these results can be attributed to A. sativum, which may cause stabilized cell membrane and protect the liver against deleterious agents and free radical-mediated toxic damages to the liver cells. This is reflected in the reduction of liver enzymes. A. sativum helps the liver to maintain its normal function by accelerating the regenerative capacity of its cells [129].

The addition of 4% garlic in the diets of O. niloticus revealed positive health effects. Mesalhy Aly et al. [130] demonstrated that in juveniles, garlic provides resistance against A. hydrophila and Pseudomonas flourescens. Furthermore, adding 1% garlic to the diet of O. niloticus juveniles increases their gut microbiota activity, favors resistance against experimental Streptococcus iniae infection, and reduces symptoms of diseases, such as exophthalmia, erratic swimming, and changes in pigmentation of the head. It also decreased the cumulative mortality rate, which was below 20% in the treated group and 80% in the control group [131].

In O. niloticus, experimentally infected with A. hydrophila, immersion baths containing 1%, 1.5%, and 2% liquid garlic extracts yielded positive results, indicating that immersion is an efficient method for using garlic to counteract the effect of bacterial diseases in tilapia. Moreover, garlic can be used to treat bacterial diseases, as well as parasitic diseases.

Abd El-Galil and Aboelhadid [132] performed culture experiments and studies under laboratory conditions to determine the effects of different methods of garlic administration to treat Trichodina and Gyrodactylus infestations (Table-2). It has been observed that a concentration of 800 ppm of raw garlic was effective in eliminating Trichodina spp. in O. niloticus juveniles weighing 3.6 g. However, the infection recurred after 14 days, possibly due to the organic matter produced by the garlic residue, which allows the parasites to survive in the culture water [133].

Table-2.

In vivo antiparasitic activity of garlic (Allium sativum).

Conditions Method Concentration Immersion time Results
Laboratory Therapeutic: Garlic oil immersion 2, 2.5, 3 ppm 24 h After 4 h of immersion, 100% of the parasites were eliminated.
1, 1.5 ppm 24 h After 4 h of immersion, 100% of the parasites were eliminated.
Culture Therapeutic: Garlic oil immersion 3 ppm 1 h (bath before seeding) 74%, 76%, and 55% of juveniles were free of parasites after 1 h, 14 h, and 7 days, respectively. Group without garlic=24% parasite-free juveniles.
Therapeutic: Macerated fresh garlic packed in permeable bags and added to the tank 300 g/m3 During the entire culture 31%, 79%, and 68% of juveniles were free of parasites after 1 h, 14 h, and 7 days, respectively.
Culture Preemptive: Garlic oil immersion 3 ppm 1 h (bath before seeding) Both treatments prevented parasite infection. Macerated garlic showed the best pre-emptive results.
Preemptive: Macerated fresh garlic packed in permeable bags and added to the tank 300 g/m3 During the entire culture

Source: Abd El-Galil and Aboelhadid [132]

Salmonids

The addition of garlic powder (5 and 10 g/kg) to the balanced food of O. mykiss improved their weight gain percentage, which increased as the concentration of garlic increased. In addition, this study found that the group on a supplemented diet (10 g/kg) had a daily weight gain of 2 g/fish and a food conversion factor of 1.1, whereas, in the control group, these values were 1.2 and 2.3 g/fish, respectively [134].

The effects of garlic extract could be related to the activity of the gut microbiota because it has been reported to increase the operational taxonomic units of Aeromonas, Deefgea, Exiguobacterium, and Mycoplasma. These bacterial species have been shown to improve intestinal absorption, resulting in improved growth indicators of fish fed commercial balanced food supplemented with 2% liquid garlic extract [135].

The efforts made to incorporate garlic into the diets of O. mykiss have led to microencapsulation studies, a methodology that aims to improve the properties of bioactive components. Microencapsulation of 2% garlic in trout diets improves their growth performance and decreases the food conversion factor compared to the control group; the effects of garlic on animal growth may be related to allicin; and garlic has been reported to induce intestinal villi growth and digestive enzyme activity, which may improve fish growth [100].

The experimental group of O. mykiss species fed a 5 and 10 g/kg garlic-supplemented diet were more resistant to the bacteria A. hydrophila compared to the control group, showing survival rates of 86% and 16%, respectively [129]. Similarly, O. mykiss juveniles fed garlic-supplemented food (5 and 10 g/kg) and subjected to experimental infection with Aeromonas salmonicida were more resistant to the infection compared to the control group and showed a significant increase in circulating lymphocytes [136]. This is because the active ingredients of garlic stimulate the production of defense cells and increased lymphocyte concentration indicates that there is an increased inflammatory response, that is, cell-mediated and/or humoral immunity [136].

Garlic has been used in pisciculture to treat systemic bacterial diseases and to decrease the activity and growth of Listeria spp. in raw Salmon salar intended for human consumption without modifying the sensory properties of the product [137]. Furthermore, garlic oil decreases the bacterial load of Salmonella enteritidis and Listeria monocytogenes during the storage of S. salar at 2°C [138].

Studies performed in S. salar production farms showed that garlic supplementation (10 g/kg) reduced sea lice infestation (Caligidae: Crustacea) [139]. In in vitro assays, liquid garlic extract (16.9 mg/mL) eliminates 100% of amoebas, which infest the gills and skin of O. mykiss [140]. Garlic is also effective against the parasite Ichthyophthirius multifiliis, with a concentration of 62 mg/L in water eliminating the theront stage of the parasite in 15 h, and concentrations of 117 and 570 mg/L eliminating the tomont stage of the parasite in 24 h [141].

Crustaceans

9.4 million tons of crustaceans are produced globally [9]. Similar to fish production, crustacean production systems are being expanded to contribute to food security and meet the demand for animal protein [12]. Therefore, crustaceans are a fundamental part of aquaculture. It is necessary to identify alternatives that will improve productivity indicators and can be used to prevent and treat bacterial and parasitic diseases while attempting to reduce the associated environmental impact [12].

Garlic has been used as a natural alternative to promote crustacean growth. Studies performed in Macrobrachium rosenbergii have shown that the addition of 1% garlic to their diet resulted in a higher survival rate (82%) and lower food conversion factor than the control group (66%), probably because the final weight of the treated and control groups was 2.33 g and 1.76 g, respectively [142]. Supplementation with garlic powder at 1% and 2% in the diet for narrow-clawed crayfish (P. leptodactylus) increased the growth indices and digestive enzymes activity, 2% elevated lysozyme, nitric oxide synthase, and phenoloxidase activities in the crayfish [108].

The addition of 2% garlic to the diet of Procambarus clarkii juveniles resulted in a weight gain of 1.2 g, whereas the control group gained 0.95 g. The study indicated that the best food conversion factor was found at concentrations of 2% and 3% garlic and also highlighted that the survival rate of the treated group was 50% higher than that of the control group [143]. Furthermore, Malar and Charles [144] observed that 2 months after adding 2% garlic concentration to the diet of Penaeus monodon, the survival rate increased from 77% (control group) to 87%. P. monodon showed similar growth improvement, and a 2% garlic concentration was reported as the optimal experimental concentration for the 1st and 2nd months of the study.

In whiteleg shrimp (Litopenaeus vannamei), dietary replacement with fish, meat, or bone flour with 3% garlic, improved growth and proximate composition even after 50% of the fish flour was replaced. These results indicate that garlic improves food consumption and the efficiency of utilization of proteins and amino acids [95]. The addition of 4% garlic for 2 months has been reported to have positive effects; however, a 6% concentration results in growth compared to the control group after 63 days of treatment [145]. Moreover, when compared to the control group, a 2% concentration has a positive effect on whiteleg shrimp growth, as do lower garlic concentrations (0.5% and 1%). This concentration also increased the conversion efficiency and, as a result, the food conversion factor; these effects might be due to an improvement in the immune system of the shrimp with a diet comprising 2% garlic concentration [146].

Among the diseases developed by shrimp, we found those caused by the white spot syndrome virus (WSSV) and Vibrio parahaemolyticus. It has been observed that shrimp fed with a 0.16% garlic-supplemented diet and exposed to WSSV and V. parahaemolyticus showed the highest survival rate after experimental infection [147]. Increasing the food garlic concentration to 2% and 4% for 30 days and exposing the crustaceans to V. parahaemolyticus improves their survival rate compared to the control group. This result could be attributed to the higher activity of superoxide dismutase and catalase observed in the treated group, as well as their ability to eliminate free radicals [148].

In in vitro experiments, liquid garlic extract at concentrations of 12.5%, 25%, and 50% reduced the growth of Gram-positive bacteria isolated from tiger shrimp (P. monodon), demonstrating the potential of garlic as a natural alternative in treating Gram-positive infections [149]. Furthermore, garlic exerts antiparasitic effects, for example, in L. vannamei infected by gregarines, the addition of mashed garlic (40 and 50 g/kg) to the diets decreased parasite load. Although it could not eliminate all the parasites, it controlled the infection [150, 151].

Conclusion

Several studies have evaluated garlic’s properties as a food supplement and as an extract for immersion baths used in the production of aquatic organisms, both in pisciculture and crustacean production. In addition, there is particular interest in research on certain fish species such as O. niloticus, C. carpio, and O. mykiss, as well as crustaceans such as the whiteleg shrimp.

Most studies focus on demonstrating garlic’s properties as a growth promoter that can directly impact productive performance indicators by improving food consumption and efficiency as well as the food conversion factor. These studies also highlight the high survival rates observed in aquatic organisms that consumed a garlic-supplemented diet after a bacterial or parasitic experimental infection.

The concentrations of garlic used to supplement food and that of liquid garlic extracts for immersion baths vary depending on the application and desired effect. However, most studies recommend concentrations between 2% and 4% both for food supplementation and immersion baths to treat animals infected with parasites, and these studies agree that high concentrations could cause harmful effects or may not benefit aquatic organisms.

Due to its properties and active components, garlic has become an effective alternative for use in the production of aquatic organisms in both continental water and seawater to improve productive performance indicators, increase bacterial resistance, and treat parasitic diseases. In addition, garlic has other functions and properties that this review could not describe in detail, such as immunostimulation or immunomodulation, antioxidant properties, stress-reduction abilities, and antiviral activity.

Authors’ Contributions

DLCD, SACG, and ADO: Conceptualization. DLCD and LLCC: Data curation. DLCD, LLCC, and ADO: Formal Analysis. DLCD: Funding acquisition. DLCD, SACG, and ADO: methodological implementation. DLCD, SACG, and LLCC: Drafted and revised the manuscript. All authors have read, reviewed, and approved the final manuscript.

Acknowledgments

The authors thank Crimson Interactive Pvt. Ltd. (Enago: https://www.enago.com/es/) for their assistance in manuscript translation and editing. The source of funding for this review was the Universidad Cooperativa de Colombia and Dirección Nacional de Investigación DINAI – ID INV3183.

Footnotes

The source of funding for this review was the Universidad Cooperativa de Colombia and Dirección Nacional de Investigación DINAI – ID INV3183.

Competing Interests

The authors declare that they have no competing interests.

Publisher’s Note

Veterinary World remains neutral with regard to jurisdictional claims in published institutional affiliation.

References

  • 1.El-Saadony M.T, Alagawany M, Patra A.K, Kar I, Tiwari R, Dawood M.A.O, Dharma K, Abdel-Latif H.M.R. The functionality of probiotics in aquaculture:An overview. Fish Shellfish Immun. 2021;117(33):36–52. doi: 10.1016/j.fsi.2021.07.007. [DOI] [PubMed] [Google Scholar]
  • 2.Ahmad A, Abdullah S.R.S, Hasan H.A, Othman A.R, Ismail N.I. Aquaculture industry:Supply and demand, best practices, effluent and its current issues and treatment technology. J. Environ. Manage. 2021;287(1):112271. doi: 10.1016/j.jenvman.2021.112271. [DOI] [PubMed] [Google Scholar]
  • 3.Naylor R.L, Hardy R.W, Buschmann A.H, Bush S.R, Cao L, Klinger D.H, Little D.C, Lubchenco J, Shumway S.E, Troell M. A 20-year retrospective review of global aquaculture. Nature. 2021;591(7851):551–563. doi: 10.1038/s41586-021-03308-6. [DOI] [PubMed] [Google Scholar]
  • 4.Food and Agriculture Organization (FAO) The State of World Fisheries and Aquaculture. Meeting the Sustainable Development Goals. Food and Agriculture Organization of the United Nations, Rome, Italy. 2018 [Google Scholar]
  • 5.Tacon A.G.J. Trends in global aquaculture and aquafeed production:2000-2017. Rev. Fish. Sci. Aquac. 2020;28(1):43–56. [Google Scholar]
  • 6.Liu Y, Chen J. In:Atlas of Global Change Risk of Population and Economic Systems. Singapore: Springer; 2022. Mapping global population changes; pp. 87–94. [Google Scholar]
  • 7.Food and Agriculture Organization (FAO), Fisheries Department, Fishery Information, Data and Statistics Unit. FishStatJ, a Tool for Fishery Statistics Analysis, Release:3.5.0, Universal Software for Fishery Statistical Time Series. Global Aquaculture Production:Quantity 1950-2017;Value 1950-2017;Global Capture Production. Food and Agriculture Organization, Rome, Italy. 2019:1950–2017. [Google Scholar]
  • 8.Velázquez-Durán V.M, Rosales-Ortega R. Governance of sustainable fisheries value chains:Between the global north and the global south. Estud. Soc. Rev. Aliment. Contemp. Desarro. Reg. 2020;30(56):e20992. [Google Scholar]
  • 9.Food and Agriculture Organization (FAO) The State of World Fisheries and Aquaculture 2020. Sustainability in Action. Meeting the Sustainable Development Goals. Food and Agriculture Organization of the United Nations, Rome, Italy. 2020 [Google Scholar]
  • 10.Newton R, Zhang W, Xian Z, McAdam B, Little D.C. Intensification, regulation and diversification:The changing face of inland aquaculture in China. Ambio. 2021;50(9):1739–1756. doi: 10.1007/s13280-021-01503-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Lieke T, Meinelt T, Hoseinifar S.H, Pan B, Straus D.L, Steinberg C.E.W. Sustainable aquaculture requires environmental-friendly treatment strategies for fish diseases. Rev. Aquac. 2020;12(2):943–965. [Google Scholar]
  • 12.Reverter M, Sarter S, Caruso D, Avarre J.C, Combe M, Pepey E, Pouyaud L, Vega-Heredía S, de Verdal H, Gozlan R.E. Aquaculture at the crossroads of global warming and antimicrobial resistance. Nat. Commun. 2020;11(1):1870. doi: 10.1038/s41467-020-15735-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Alexander C.P, Kirubakaran C.J.W, Michael R.D. Water soluble fraction of Tinospora cordifolia leaves enhanced the non-specific immune mechanisms and disease resistance in Oreochromis mossambicus. Fish Shellfish Immunol. 2010;29(5):765–772. doi: 10.1016/j.fsi.2010.07.003. [DOI] [PubMed] [Google Scholar]
  • 14.Kibenge F.S. Emerging viruses in aquaculture. Curr. Opin Virol. 2019;34(9):97–103. doi: 10.1016/j.coviro.2018.12.008. [DOI] [PubMed] [Google Scholar]
  • 15.Martínez-Lara P, Martínez-Porchas M, Gollas-Galván T, Hernández-López J, Robles-Porchas G.R. Granulomatosis in fish aquaculture:A mini review. Rev. Aquac. 2021;13(1):259–268. [Google Scholar]
  • 16.Lastauskienė E, Valskys V, Stankevičiūtė J, Kalcienė V, Gėgžna V, Kavoliūnas J, Ružauskas M, Armalytė J. The impact of intensive fish farming on pond sediment microbiome and antibiotic resistance gene composition. Front. Vet. Sci. 2021;8(8):673756. doi: 10.3389/fvets.2021.673756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Luu Q.H, Nguyen T.B.T, Nguyen T.L.A, Do T.T.T, Dao T.H.T, Padungtod P. Antibiotics use in fish and shrimp farms in Vietnam. Aquac. Rep. 2021;20(4):100711. [Google Scholar]
  • 18.Hedberg N, Stenson I, Pettersson M.N, Warshan D, Nguyen-Kim H, Tedengren M, Kautsky N. Antibiotic use in Vietnamese fish and lobster sea cage farms;implications for coral reefs and human health. Aquaculture. 2018;495:366–375. [Google Scholar]
  • 19.Ni L, Chen D, Fu H, Xie Q, Lu Y, Wang X, Zhao Y, Chen L. Residual levels of antimicrobial agents and heavy metals in 41 species of commonly consumed aquatic products in Shanghai, China, and cumulative exposure risk to children and teenagers. Food Control. 2021;129(2):108225. [Google Scholar]
  • 20.Jo H, Raza S, Farooq A, Kim J, Unno T. Fish farm effluents as a source of antibiotic resistance gene dissemination on Jeju Island, South Korea. Environ. Pollut. 2021;276:116764. doi: 10.1016/j.envpol.2021.116764. [DOI] [PubMed] [Google Scholar]
  • 21.Emeka U, Iloegbunam N.G, Gbekele-Oluwa A.R, Bola M. Natural products and aquaculture development. IOSR J. Pharm. Biol. Sci. 2014;9(2):70–82. [Google Scholar]
  • 22.Hoseinifar S.H, Yousefi S, Van Doan H, Ashouri G, Gioacchini G, Maradonna F, Carnevali O. Oxidative stress and antioxidant defense in fish:The implications of probiotic, prebiotic, and synbiotics. Rev. Fish. Sci. Aquac. 2020;29(2):198–217. [Google Scholar]
  • 23.Wangkahart E, Secombes C.J, Wang T. Studies on the use of flagellin as an immunostimulant and vaccine adjuvant in fish aquaculture. Front. Immunol. 2019;9:3054. doi: 10.3389/fimmu.2018.03054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Van Santen J.A, Jacob G, Singh A.L, Aniebok V, Balunas M.J, Bunsko D, Neto F.C, Castaño-Espriu L, Chang C, Clark T.N, Little J.L.C, Delgadillo D.A, Dorrestein P.C, Duncan K.R, Egan J.M, Galey M.M, Haeckl F.P.J, Hua A, Hughes A.H, Iskakova D, Khadilkar A, Lee J.H, Lee S, LeGrow N, Liu D.Y, Macho J.M, McCaughey C.S, Medema M.H, Neupane R.P, O'Donnell T.J, Paula J.S, Sanchez L.M, Shaikh A.F, Soldatou S, Terlouw B.R, Tran T.A, Valentine M, van der Hooft J.J.J, Vo D.A, Wang M, Wilson D, Zink K.E, Linington R.G. The natural products atlas:An open access knowledge base for microbial natural products discovery. ACS Cent. Sci. 2019;5(11):1824–1833. doi: 10.1021/acscentsci.9b00806. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Khalifa S.A.M, Elias N, Farag M.A, Chen L, Saeed A, Hegazy M.E.F, Moustafa M.S, Abd El-Wahed A, Al-Mousawi S.M, Musharraf S.G, Chang F.R, Iwasaki A, Suenaga K, Alajlani M, Göransson U, El-Seedi H.R. Marine natural products:A source of novel anticancer drugs. Mar. Drugs. 2019;17(9):491. doi: 10.3390/md17090491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Atanasov A.G, Zotchev S.B, Dirsch V.M, International Natural Product Sciences Taskforce. Supuran C.T. Natural products in drug discovery:Advances and opportunities. Nat. Rev. Drug. Discov. 2021;20(3):200–216. doi: 10.1038/s41573-020-00114-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Niero R, Cechinel F.V, Yunes R.A. Medicinal plants and phytomedicines. In: Cechinel F.V, editor. Natural Products as source of Molecules with Therapeutic Potential. Cham: Springer; 2018. [Google Scholar]
  • 28.Pogue R, Murphy E.J, Fehrenbach G.W, Rezoagli E, Rowan N.J. Exploiting immunomodulatory properties of β-glucans derived from natural products for improving health and sustainability in aquaculture-farmed organisms:Concise review of existing knowledge, innovation and future opportunities. Curr. Opin. Environ. Sci. Health. 2021;21(6):100248. [Google Scholar]
  • 29.Valenzuela-Gutierrez R, Lago-Leston A, Vargas-Albores F, Cicala F, Martínez-Porchas M. Exploring the garlic (Allium sativum) properties for fish aquaculture. Fish Physiol. Biochem. 2021;47(4):1179–1198. doi: 10.1007/s10695-021-00952-7. [DOI] [PubMed] [Google Scholar]
  • 30.Falzon C.C, Balabanova A. Phytotherapy:An introduction to herbal medicine. Prim. Care. 2017;44(2):217–227. doi: 10.1016/j.pop.2017.02.001. [DOI] [PubMed] [Google Scholar]
  • 31.Awad E, Awaad A. Role of medicinal plants on growth performance and immune status in fish. Fish Shellfish Immunol. 2017;67:40–54. doi: 10.1016/j.fsi.2017.05.034. [DOI] [PubMed] [Google Scholar]
  • 32.Reverter M, Tapissier-Bontemps N, Sasal P, Saulnier D. Use of medicinal plants in aquaculture. In: Austin B, editor. Diagnosis and Control of Diseases of Fish and Shellfish. India: Croydon Ltd; 2017. pp. 223–261. [Google Scholar]
  • 33.Azwanida N.N. A review on the extraction methods use in medicinal plants, principle, strength and limitation. Med. Aromat. Plants. 2015;4(3):196. [Google Scholar]
  • 34.Coipel R.Y, Odio A.D, Álvares O.M, Proenza R.T, Marrero I.G, Delgado D.L.C. Global market for veterinary herbal products during the 2018-2019 period. Braz. J. Vet. Res. Anim. Sci. 2021;58:e181002. [Google Scholar]
  • 35.Domínguez A, Polanco R, Cossío G, Morejón Y, Riquenes Y. Current trends and perspectives in veterinary vaccine production. Biotecnol. Apl. 2014;31(3):196–203. [Google Scholar]
  • 36.Doan H.V, Soltani E, Ingelbrecht J, Soltani M. Medicinal herbs and plants:Potential treatment of monogenean infections in fish. Rev. Fish. Sci. Aquac. 2020;28(2):260–282. [Google Scholar]
  • 37.Baba E, Uluköy G, Mammadov R. The effects of injected geophyte plant (Sternbergia candida) extract on the hemato-immunological parameters in gilthead seabream, Sparus aurata (L. 1758) Braz. Arch. Biol. Technol. 2021;64(1):e21210046. [Google Scholar]
  • 38.Swathy J.S, Mishra P, Thomas J, Mukherjee A, Chandrasekaran N. Nanometric neem oil emulsification through microfluidization, and its therapeutic potential against Aeromonas culicicola infection in Cyprinus carpio. Flavour Fragr. J. 2018;33(5):340–350. [Google Scholar]
  • 39.Hardi E.H, Nugroho R.A, Kusuma I.W, Suwinarti W, Sudaryono A, Rostika R. Borneo herbal plant extracts as a natural medication for prophylaxis and treatment of Aeromonas hydrophila and Pseudomonas fluorescens infection in tilapia (Oreochromis niloticus) F1000Res. 2018;7(6):1847. doi: 10.12688/f1000research.16902.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Abaho I, Masembe C, Akoll P, Jones C.L.W. The use of plant extracts to control tilapia reproduction:Current status and future perspectives. J. World Aquac. Soc. 2021;53(3):593–619. [Google Scholar]
  • 41.Harikrishnan R, Balasundaram C, Heo M. Impact of plant products on innate and adaptive immune system of cultured finfish and shellfish. Aquaculture. 2011;317(1):1–15. [Google Scholar]
  • 42.Zhang X, Sun Z, Cai J, Wang J, Wang G, Zhu Z, Cao F. Effects of dietary fish meal replacement by fermented moringa (Moringa oleifera Lam.) leaves on growth performance, nonspecific immunity and disease resistance against Aeromonas hydrophila in juvenile gibel carp (Carassius auratus gibelio var. CAS III) Fish Shellfish Immunol. 2020;102(3):430–439. doi: 10.1016/j.fsi.2020.04.051. [DOI] [PubMed] [Google Scholar]
  • 43.De Vico G, Guida V, Carella F. Urtica dioica (Stinging Nettle):A neglected plant with emerging growth promoter/immunostimulant properties for farmed fish. Front. Physiol. 2018;9:285. doi: 10.3389/fphys.2018.00285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Reyes-Becerril M, Angulo C, Sanchez V, Vázquez-Martínez J, López M.G. Antioxidant, intestinal immune status and anti-inflammatory potential of Chenopodium ambrosioides L. in fish:In vitro and in vivo studies. Fish Shellfish Immunol. 2019;86:420–428. doi: 10.1016/j.fsi.2018.11.059. [DOI] [PubMed] [Google Scholar]
  • 45.Huang A.G, Yi Y.L, Ling F, Zhang Q.Z, Wang G.X. Screening of plant extracts for anthelmintic activity against Dactylogyrus intermedius (Monogenea) in goldfish (Carassius auratus) Parasitol. Res. 2013;112(12):4065–4072. doi: 10.1007/s00436-013-3597-7. [DOI] [PubMed] [Google Scholar]
  • 46.Pedrazzani A.S, Neto A.O. The anaesthetic effect of camphor (Cinnamomum camphora), clove (Syzygium aromaticum) and mint (Mentha arvensis) essential oils on clown anemonefish, Amphiprion ocellaris (Cuvier 1830) Aquac. Res. 2016;47(3):769–776. [Google Scholar]
  • 47.Husen M.A, Sharma S. Anaesthetics efficacy of MS-222, Benzoak® vet, AQUI-S® and clove oil on common carp (Cyprinus carpio) fry. Inter. J. Res. Fish. Aquac. 2015;5(3):104–114. [Google Scholar]
  • 48.Rashmeei M, Shekarabi S.P.H, Mehrgan M.S, Paknejad H. Stimulatory effect of dietary chasteberry (Vitex agnus-castus) extract on immunity, some immune-related gene expression, and resistance against Aeromonas hydrophila infection in goldfish (Carassius auratus) Fish Shellfish Immunol. 2020;107(pt A):129–136. doi: 10.1016/j.fsi.2020.09.037. [DOI] [PubMed] [Google Scholar]
  • 49.Mondal P, Garai P, Chatterjee A, Saha N.C. Toxicological and therapeutic effects of neem (Azadirachta indica) leaf powder in hole-in-the-head (HITH) disease of fish Anabas testudineus. Aquac. Res. 2021;52(1):715–723. [Google Scholar]
  • 50.Kumari P, Kumar S, Ramesh M, Shameena S.S, Deo A.D, Rajendran K.V, Raman R.P. Antiparasitic effect of aqueous and organic solvent extracts of Azadirachta indica leaf against Argulus japonicus in Carassius auratus. Aquaculture. 2019;511:634175. [Google Scholar]
  • 51.Abdel-Tawwab M, Abbass F.E. Turmeric powder, Curcuma longa L., in common carp, Cyprinus carpio L., diets:Growth performance, innate immunity, and challenge against pathogenic Aeromonas hydrophila infection. J. World Aquac. Soc. 2017;48(2):303–312. [Google Scholar]
  • 52.Zheng Z.L, Tan J.Y.W, Liu H.Y, Zhou X.H, Xiang X, Wang K.Y. Evaluation of oregano essential oil (Origanum heracleoticum L.) on growth, antioxidant effect and resistance against Aeromonas hydrophila in channel catfish (Ictalurus punctatus) Aquaculture. 2009;292(3):214–218. [Google Scholar]
  • 53.Gracia-Valenzuela M.H, Orozco-Medina C, Molina-Maldonado C. Efecto antibacteriano del aceite esencial de orégano (Lippia berlandieri) en bacterias patógenas de camarón Litopenaeus vannamei. Hidrobiológica. 2012;22(3):201–206. [Google Scholar]
  • 54.Acar U, Kesbic O.S, Yilmaz A, Gultepe N, Turker A. Evaluation of the effects of essential oil extracted from sweet orange peel (Citrus sinensis) on growth rate of tilapia (Oreochromismossambicus) and possible disease resistance against Streptococcus iniae. Aquaculture. 2015;437(3):282–286. [Google Scholar]
  • 55.Talpur A.D. Mentha piperita (Peppermint) as feed additive enhanced growth performance, survival, immune response and disease resistance of Asian seabass, Lates calcarifer (Bloch) against Vibrio harveyi infection. Aquaculture. 2014;420(3):71–78. [Google Scholar]
  • 56.De Oliveira Hashimoto G, Neto F.M, Ruiz M.L, Acchile M, Chagas E, Chaves F.C.M, Martins M.L. Essential oils of Lippia sidoides and Mentha piperita against monogenean parasites and their influence on the hematology of Nile tilapia. Aquaculture. 2016;450(4):182–186. [Google Scholar]
  • 57.Yin X, Zhuang X, Liao M, Cui Q, Yan C, Huang J, Huang L, Luo W, Liu Y, Wang W. Andrographis paniculata improves growth and non-specific immunity of shrimp Litopenaeus vannamei, and protects it from Vibrio alginolyticus by reducing oxidative stress and apoptosis. Dev. Comp. Immunol. 2023;139(6):104542. doi: 10.1016/j.dci.2022.104542. [DOI] [PubMed] [Google Scholar]
  • 58.To T.T.H, Nhi N.T.H, Day P.V. Effect of Solanum procumbens lour. extract on survival, growth performances, immune responses and against Vibrio parahaemolyticus causing acute hepatopancreas necrosis disease in white leg shrimp (Litopenaeus vannamei) Indian J. Anim. Res. 2022;56(12):1513–1518. [Google Scholar]
  • 59.Huang H.T, Liao Z.H, Wu Y.S, Lin Y.J, Kang Y.S, Nan F.H. Effects of Bidens alba and Plectranthus amboinicus dietary supplements on nonspecific immune responses, growth, and resistance to Vibrio alginolyticus in white leg shrimp (Penaeus vannamei) Aquaculture. 2022;546(4):737306. [Google Scholar]
  • 60.Munaeni W, Widanarni W, Yuhana M, Setiawati M, Wahyudi A.T. Effect in white shrimp Litopenaeus vannamei of Eleutherine bulbosa (Mill.) Urb. Powder on immune genes expression and resistance against Vibrio parahaemolyticus infection. Fish Shellfish Immunol. 2020;102(4):218–227. doi: 10.1016/j.fsi.2020.03.066. [DOI] [PubMed] [Google Scholar]
  • 61.Alparslan Y, Yapıcı H.H, Metin C, Baygar T, Günlü A, Baygar T. Quality assessment of shrimps preserved with orange leaf essential oil incorporated gelatin. LWT Food Sci. Technol. 2016;72(3):457–466. [Google Scholar]
  • 62.Ehsani A, Hashemi M, Afshari A, Aminzare M, Raeisi M, Zeinali T. Effect of different types of active biodegradable films containing lactoperoxidase system or sage essential oil on the shelf life of fish burger during refrigerated storage. LWT Food Sci. Technol. 2020;117(4):108633. [Google Scholar]
  • 63.Shekarabi S.P.H, Javarsiani L, Mehrgan M.S, Dawood M.A.O, Adel M. Growth performance, blood biochemistry profile, and immune response of rainbow trout (Oncorhynchus mykiss) fed dietary Persian shallot (Allium stipitatum) powder. Aquaculture. 2022;548(3):737627. [Google Scholar]
  • 64.Elumalai P, Kurian A, Lakshmi S, Faggio C, Esteban M.A, Ringo E. Herbal immunomodulators in aquaculture. Rev. Fish. Sci. Aquac. 2020;29(1):33–57. [Google Scholar]
  • 65.Caipang C.M.A, Suharman I, Avillanosa A.L, Gonzales-Plasus M.M. Influence of phytogenic feed additives on the health status in the gut and disease resistance of cultured fish. IOP Conf. Ser. Earth Environ. Sci. 2021;695(1):012024. [Google Scholar]
  • 66.Souza C.D.F, Baldissera M.D, Baldisserotto B, Heinzmann B.M, Martos-Sitcha J.A, Mancera J.M. Essential oils as stress-reducing agents for fish aquaculture:A review. Front. Physiol. 2019;10(12):785. doi: 10.3389/fphys.2019.00785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Aydın B, Barbas L.A.L. Sedative and anesthetic properties of essential oils and their active compounds in fish:A review. Aquaculture. 2020;520(4):734999. [Google Scholar]
  • 68.Hussain M.A, Sumon T.A, Mazumder S.K, Ali M.M, Jang W.J, Abualreesh M.H, Sharifuzzaman S, Brown C, Lee H.T, Lee E.W, Hasan M.T. Essential oils and chitosan as alternatives to chemical preservatives for fish and fisheries products:A review. Food Control. 2021;129:108244. [Google Scholar]
  • 69.Ji J, Lu C, Kang Y, Wang G.X, Chen P. Screening of 42 medicinal plants for in vivo anthelmintic activity against Dactylogyrus intermedius (Monogenea) in goldfish (Carassius auratus) Parasitol. Res. 2012;111(1):97–104. doi: 10.1007/s00436-011-2805-6. [DOI] [PubMed] [Google Scholar]
  • 70.Ceccanti C, Rocchetti G, Lucini L, Giuberti G, Landi M, Biagiotti S, Guidi L. Comparative phytochemical profile of the elephant garlic (Allium ampeloprasum var. holmense) and the common garlic (Allium sativum) from the Val di Chiana area (Tuscany, Italy) before and after in vitro gastrointestinal digestion. Food Chem. 2021;338(5):128011. doi: 10.1016/j.foodchem.2020.128011. [DOI] [PubMed] [Google Scholar]
  • 71.Batiha G.E.S, Beshbishy A.M, Wasef L.G, Elewa Y.H.A, Al-Sagan A.A, El-Hack M.E.A, Taha A.E, Abd-Elhakim Y.M, Devkota H.P. Chemical constituents and pharmacological activities of garlic (Allium sativum L.):A review. Nutrients. 2020;12(3):872. doi: 10.3390/nu12030872. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Barnes J, Linda A.A, David J.P. Herbal Medicines. 3rd ed. United Kingdom: Pharmaceutical Press; 2007. [Google Scholar]
  • 73.Bocate K.P, Evangelista A.G, Luciano F.B. Garlic essential oil as an antifungal and anti-mycotoxin agent in stored corn. LWT. 2021;147(2):111600. [Google Scholar]
  • 74.Bhatwalkar S.B, Mondal R, Krishna S.B.N, Adam J.K, Govender P, Anupam R. Antibacterial properties of organosulfur compounds of garlic (Allium sativum) Front. Microbiol. 2021;12:613077. doi: 10.3389/fmicb.2021.613077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Rouf R, Uddin S.J, Sarker D.K, Islam M.T, Ali E.S, Shilpi J.A, Nahar L, Tiralongo E, Sarker S.D. Antiviral potential of garlic (Allium sativum) and its organosulfur compounds:A systematic update of pre-clinical and clinical data. Trends Food Sci. Technol. 2020;104(3):219–234. doi: 10.1016/j.tifs.2020.08.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Medina M.Á.T, Merinas-Amo T, Fernández-Bedmar Z, Font R, del Río-Celestino M, Pérez-Aparicio J, Moreno-Ortega A, Alonso-Moraga A, Moreno-Rojas R. Physicochemical characterization and biological activities of black and white garlic:In vivo and in vitro assays. Foods. 2019;8(6):220. doi: 10.3390/foods8060220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Farhat Z, Hershberger P.A, Freudenheim J.L, Mammen M.J, Blair R.H, Aga D.S, Mu L. Types of garlic and their anticancer and antioxidant activity:A review of the epidemiologic and experimental evidence. Eur. J. Nutr. 2021;60(7):3585–3609. doi: 10.1007/s00394-021-02482-7. [DOI] [PubMed] [Google Scholar]
  • 78.Gambogou B, Ouattara A.K, Taale E, Karou S.D, Ameyapoh Y.A, Simpore J. Garlic as alternative therapy to treat uropathogene bacteria in women with urinary tract infection in Lomé, Togo. Preprints. 2018;9(7):2018090077. [Google Scholar]
  • 79.Al-Snafi A.E. Pharmacological effects of Allium species grown in Iraq. An overview. Int. J. Pharm. Health Care Res. 2013;1(4):132–147. [Google Scholar]
  • 80.Zeng Y, Li Y, Yang J, Pu X, Du J, Yang X, Yang T, Yang S. Therapeutic role of functional components in alliums for preventive chronic disease in human being. Evid. Based Complement. Alternat. Med. 2017;2017(3):9402849. doi: 10.1155/2017/9402849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Souza G.A, Ebaid G.X, Seiva F.R.F, Rocha K.H.R, Galhardi C.M, Mani F, Novelli E.L.B. N-acetylcysteine an allium plant compound improves high-sucrose diet-induced obesity and related effects. Evid. Based Complement Altern. Med. 2011;2011(6):643269. doi: 10.1093/ecam/nen070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Cao X, Cao L, Ding L, Bian J.S. A new hope for a devastating disease:Hydrogen sulfide in Parkinson's disease. Mol. Neurobiol. 2018;55(5):3789–3799. doi: 10.1007/s12035-017-0617-0. [DOI] [PubMed] [Google Scholar]
  • 83.Salehi B, Zucca P, Orhan I.E, Azzini E, Adetunji C.O, Mohammed S.A, Banerjee S.K, Sharopov F, Rigano D, Sharifi-Rad J, Armstrong L, Martorell M, Sureda A, Martins N, Selamoğlu Z, Ahmad Z. Allicin and health:A comprehensive review. Trends Food Sci. Technol. 2019;86(1):502–516. [Google Scholar]
  • 84.Rad H.I, Arzanlou M, Omid M.R, Ravaji S, Doghaheh H.P. Effect of culture media on chemical stability and antibacterial activity of allicin. J. Funct. Foods. 2017;28(8):321–325. [Google Scholar]
  • 85.Liu C, Fan H, Guan L, Ma L, Ge R.L. Evaluation of allicin against alveolar echinococcosis in vitro and in a mouse model. Acta Parasitol. 2021;67(1):79–93. doi: 10.1007/s11686-021-00434-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Hayat S.U, Ali R, Khan A.H, ud Din I, Khan S, Ullah F, Hussain W, Shahzadi F, Khan R.A. Effect of garlic (Allium sativum) supplementation on growth performance and serum biochemistry of broiler chicks. Am. Acad. Sci. Res. J. Eng. Technol. Sci. 2022;85(1):287–300. [Google Scholar]
  • 87.El Fakahany A, Abdelmaabood A, Abd El Hamid A, Morsi A, Abououf E. In vitro and in vivo activity of allicin against Schistosoma mansoni. Benha Med. J. 2020;37(3):578–585. [Google Scholar]
  • 88.Zhong R, Xiang H, Cheng L, Zhao C, Wang F, Zhao X, Fang Y. Effects of feeding garlic powder on growth performance, rumen fermentation, and the health status of lambs infected by gastrointestinal nematodes. Animals (Basel) 2019;9(3):102. doi: 10.3390/ani9030102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Hashemi S.A, Ghorbanoghli S, Manouchehri A.A, Hatkehlouei M.B. Pharmacological effect of Allium sativum on coagulation, blood pressure, diabetic nephropathy, neurological disorders, spermatogenesis, antibacterial effects. AIMS Agric. Food. 2019;4(2):386–398. [Google Scholar]
  • 90.Nakamoto M, Kunimura K, Suzuki J.I, Kodera Y. Antimicrobial properties of hydrophobic compounds in garlic:Allicin, vinyldithiin, ajoene and diallyl polysulfides. Exp. Ther. Med. 2020;19(2):1550–1553. doi: 10.3892/etm.2019.8388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Müller A, Eller J, Albrecht F, Prochnow P, Kuhlmann K, Bandow J.E, Slusarenko A.J, Leichert L. Allicin induces thiol stress in bacteria through S-allylmercapto modification of protein cysteines. J. Biol. Chem. 2016;291(22):11477–11490. doi: 10.1074/jbc.M115.702308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Gruhlke M.C, Portz D, Stitz M, Anwar A, Schneider T, Jacob C, Schlaich N.L, Slusarenko A.J. Allicin disrupts the cell's electrochemical potential and induces apoptosis in yeast. Free Radic. Biol. Med. 2010;49(12):1916–1924. doi: 10.1016/j.freeradbiomed.2010.09.019. [DOI] [PubMed] [Google Scholar]
  • 93.Miron T, Rabinkov A, Mirelman D, Wilchek M, Weiner L. The mode of action of allicin:Its ready permeability through phospholipid membranes may contribute to its biological activity. Biochim. Biophys. Acta. 2000;1463(1):20–30. doi: 10.1016/s0005-2736(99)00174-1. [DOI] [PubMed] [Google Scholar]
  • 94.Xie Y, Chen Y, Guo Y, Huang Y, Zhu B. Allicin and glycyrrhizic acid display antiviral activity against latent and lytic Kaposi sarcoma-associated herpesvirus. Infect. Microbes Dis. 2020;2(1):30–34. [Google Scholar]
  • 95.Gökalp F. The inhibition effect of garlic-derived compounds on human immunodeficiency virus Type 1 and saquinavir. J. Biochem. Mol. Toxicol. 2018;32(11):e22215. doi: 10.1002/jbt.22215. [DOI] [PubMed] [Google Scholar]
  • 96.Mösbauer K, Fritsch V.N, Adrian L, Bernhardt J, Gruhlke M.C.H, Slusarenko A.J, Antelmann H. Allicin inhibits SARS-CoV-2 replication and abrogates the antiviral host response in the Calu-3 proteome. bioRxi. 2021;5(15):444275. [Google Scholar]
  • 97.Saif S, Hanif M.A, Rehman R, Riaz M. Garlic. In: Hanif M.A, Nawaz H, Khan M.M, Byrne H.J, editors. Medicinal Plants of South Asia. Ch. 23. Amsterdam: Elsevier; 2020. pp. 301–315. [Google Scholar]
  • 98.Ogbuewu I.P, Okoro V.M, Mbajiorgu E.F, Mbajiorgu C.A. Beneficial effects of garlic in livestock and poultry nutrition:A review. Agric. Res. 2019;8(4):411–426. [Google Scholar]
  • 99.Tazikeh T, Kenari A.A, Esmaeili M. Effects of fish meal replacement by meat and bone meal supplemented with garlic (Allium sativum) powder on biological indices, feeding, muscle composition, fatty acid and amino acid profiles of whiteleg shrimp (Litopenaeus vannamei) Aquac. Res. 2020;51(2):674–686. [Google Scholar]
  • 100.Adineh H, Harsij M, Jafaryan H, Asadi M. The effects of microencapsulated garlic (Allium sativum) extract on growth performance, body composition, immune response and antioxidant status of rainbow trout (Oncorhynchus mykiss) juveniles. J. Appl. Anim. Res. 2021;48(1):372–378. [Google Scholar]
  • 101.Ghafarifarsani H, Yousefi M, Hoseinifar S.H, Paolucci M, Lumsangkul C, Jaturasitha S, Van Doan H. Beneficial effects of Persian shallot (Allium hirtifolium) extract on growth performance, biochemical, immunological and antioxidant responses of rainbow trout Oncorhynchus mykiss fingerlings. Aquaculture. 2022;555(5):738162. [Google Scholar]
  • 102.Mahboub H.H, Rashidian G, Hoseinifar S.H, Kamel S, Zare M, Ghafarifarsani H, Algharib S.A, Moonmanee T, Van Doan H. Protective effects of Allium hirtifolium extract against foodborne toxicity of Zinc oxide nanoparticles in Common carp (Cyprinus carpio) Comp. Biochem. Physiol. C Toxicol. Pharmacol. 2022;257(2):109345. doi: 10.1016/j.cbpc.2022.109345. [DOI] [PubMed] [Google Scholar]
  • 103.Khan K.Y, Ali B, Zhang S, Stoffella P.J, Shi S, Xia Q, Cui X, Ali Z, Guo Y. Phytotoxic effects on chloroplast and UHPLC-HRMS based untargeted metabolomic responses in Allium tuberosum Rottler ex Sprengel (Chinese leek) exposed to antibiotics. Ecotoxicol. Environ. Saf. 2022;234(5):113418. doi: 10.1016/j.ecoenv.2022.113418. [DOI] [PubMed] [Google Scholar]
  • 104.Li M, Zhu X.M, Tian J.X, Liu M, Wang G.Q. Dietary flavonoids from Allium mongolicum regel promotes growth, improves immune, antioxidant status, immune-related signaling molecules and disease resistance in juvenile northern snakehead fish (Channa argus) Aquaculture. 2019;501(2):473–481. [Google Scholar]
  • 105.Abdelwahab A.M, El-Bahr S.M, Al-Khamees S. Influence of dietary garlic (Allium sativum) and/or ascorbic acid on performance, feed utilization, body composition and hemato-biochemical parameters of juvenile Asian Sea Bass (Lates calcarifer) Animals (Basel) 2020;10(12):2396. doi: 10.3390/ani10122396. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Huang H.T, Lee P.T, Liao Z.H, Huang C.T, Chen H.Y, Huang Z.G, Nan F.H, Wu Y.S. Raw garlic (Allium sativum) improves nonspecific immune responses and resistance against Vibrio alginolyticus infection in grouper (Epinephelus coioides) J. Mar. Sci. Technol. 2022;29(6):757–766. [Google Scholar]
  • 107.Abraham T.J, Ritu R. Effects of dietary supplementation of garlic (Allium sativum) extract on the resistance of Clarias gariepinus against Edwardsiella tarda infection. Iran. J. Fish. Sci. 2015;14(3):719–733. [Google Scholar]
  • 108.Rezaei O, Mehrgan M.S, Paknejad H. Dietary garlic (Allium sativum) powder improved zootechnical performance, digestive enzymes activity, and innate immunity in narrow-clawed crayfish (Postantacus leptodactylus) Aquac. Rep. 2022;24(7):101129. [Google Scholar]
  • 109.Armuelles-Bernal C, Cucala-García L, Barón-Sevilla B, Díaz-Jiménez L, Rubio-Godoy M, Hernández-Rodríguez M. Effect of garlic extract and diallyl sulfide immersion baths in the life stages of Zeuxapta seriolae, a parasite of California yellowtail (Seriola dorsalis) Aquac. Int. 2022;30(3):1261–1277. [Google Scholar]
  • 110.Trasviña-Moreno A.G, Ascencio F, Angulo C, Hutson K.S, Avilés-Quevedo A, Inohuye-Rivera R.B, Pérez-Urbiola J.C. Plant extracts as a natural treatment against the fish ectoparasite Neobenedenia sp. (Monogenea:Capsalidae) J. Helminthol. 2019;93(1):57–65. doi: 10.1017/S0022149X17001122. [DOI] [PubMed] [Google Scholar]
  • 111.Yildiz H.Y, Phan Van Q, Parisi G, Dam Sao M. Anti-parasitic activity of garlic (Allium sativum) and onion (Allium cepa) juice against crustacean parasite, Lernantropus kroyeri, found on European sea bass (Dicentrarchus labrax) Ital. J. Anim. Sci. 2019;18(1):833–837. [Google Scholar]
  • 112.Kim J.H, Fridman S, Borochov-Neori H, Sinai T, Zilberg D. Evaluating the use of garlic (Allium sativum) for the remedy of Cryptocaryon irritans in guppies (Poecilia reticulata) Aquac. Res. 2019;50(1):1–8. [Google Scholar]
  • 113.Militz T.A, Southgate P.C, Carton A.G, Hutson K.S. Dietary supplementation of garlic (Allium sativum) to prevent monogenean infection in aquaculture. Aquaculture. 2013;408–409(4):95–99. [Google Scholar]
  • 114.Wang Y, Lu Y, Zhang Y, Ning Z, Li Y, Zhao Q, Lu H, Huang R, Xia X, Feng Q, Liang X, Liu K, Zhang L, Lu T, Huang T, Fan D, Weng Q, Zhu C, Lu Y, Li W, Wen Z, Zhou C, Tian Q, Kang X, Shi M, Zhang W, Jang S, Du F, He S, Liao L, Li Y, Gui B, He H, Ning Z, Yang C, He L, Luo L, Yang R, Luo Q, Liu X, Li S, Huang W, Xiao L, Lin H, Han B, Zhu Z. The draft genome of the grass carp (Ctenopharyngodon idellus) provides insights into its evolution and vegetarian adaptation. Nat. Genet. 2015;47(6):625–631. doi: 10.1038/ng.3280. [DOI] [PubMed] [Google Scholar]
  • 115.Ahmadifar E, Sadegh T.H, Dawood M.A.O, Dadar M, Sheikhzadeh N. The effects of dietary Pediococcus pentosaceus on growth performance, hemato-immunological parameters and digestive enzyme activities of common carp (Cyprinus carpio) Aquaculture. 2020;516(1):734656. [Google Scholar]
  • 116.Abdel-Ghany H.M, Salem M.E.S. Effects of dietary chitosan supplementation on farmed fish;a review. Rev. Aquac. 2020;12(1):438–452. [Google Scholar]
  • 117.Mohammadi G, Rashidian G, Hoseinifar S.H, Naserabad S.S, Van Doan H. Ginger (Zingiber officinale) extract affects growth performance, body composition, haematology, serum and mucosal immune parameters in common carp (Cyprinus carpio) Fish Shellfish Immunol. 2020;99(1):267–273. doi: 10.1016/j.fsi.2020.01.032. [DOI] [PubMed] [Google Scholar]
  • 118.Chesti A, Chauhan R.S. Effect of inclusion of garlic (Allium sativum) on feed utilization and growth in Amur carp, Cyprinus carpio haematopterus. J. Pharm. Innov. 2018;7(3):249–252. [Google Scholar]
  • 119.Dadgar S, Seidgar M, Nekuiefard A, Valipour A.R, Sharifian M, Hafezieh M. Oral administration of garlic powder (Allium sativum) on growth performance and survival rate of Carassius auratus fingerlings. Iran. J. Fish. Sci. 2019;18(1):71–82. [Google Scholar]
  • 120.Liu H, Zhang S, Qiu M, Wang A, Ye J, Fu S. Garlic (Allium sativum) and Fu-ling (Poria cocos) mitigate lead toxicity by improving antioxidant defense mechanisms and chelating ability in the liver of grass carp (Ctenopharyngodon idella) Ecotoxicology. 2021;30(5):885–898. doi: 10.1007/s10646-021-02405-6. [DOI] [PubMed] [Google Scholar]
  • 121.Pashaki A.K, Zorriehzahra S.M.J, Ghasemi M, Rohani M.S, Hosseini S.M. Effects of dietary Garlic extract on some blood, immunity and growth parameters of Common Carp fingerlings (Cyprinus carpio) Iran. J. Aquat. Anim. Health. 2018;4(2):28–39. [Google Scholar]
  • 122.Isroni W, Bahri A.S, Maulida N. Increased immune response of carp (Cyprinus carpio L) by giving garlic (Allium sativum) powder extract. IOP Conf. Ser. Earth Environ. Sci. 2021;718(1):012032. [Google Scholar]
  • 123.Motlagh H.A, Safari O, Pourmozaffar S. Effect of garlic extract supplementation on growth performance, nonspecific immunity, and antibacterial activity of skin mucus in goldfish, Carassius auratus. Int. J. Aquat. Biol. 2021;9(6):350–359. [Google Scholar]
  • 124.Kashinskaya E.N, Simonov E.P, Andree K.B, Vlasenko P.G, Polenogova O.V, Kiriukhin B.A, Solovyev M.M. Microbial community structure in a host-parasite system:The case of Prussian carp and its parasitic crustaceans. J. Appl. Microbiol. 2021;131(4):1722–1741. doi: 10.1111/jam.15071. [DOI] [PubMed] [Google Scholar]
  • 125.Yavuzcan H, Bekcan S. Control of ectoparasitosis in carp (Cyprinus carpio) induced by Gyrodactylus elegans (Monogenea) with garlic (Allium sativum) and onion (Allium cepa) extracts. Ecocycles. 2020;6(1):10–17. [Google Scholar]
  • 126.Naqi J.A, Mateen A, Hussain D, Tahir H.M, Hussain S, Tabasum A. Effect of Allium sativum supplemented diets on growth and haematological responses in Nile Tilapia (Oreochromis niloticus) Pak. J. Zool. 2019;51(1):257–263. [Google Scholar]
  • 127.Jegede T. Effect of garlic (Allium sativum) on growth, nutrient utilization, resistance and survival of Tilapia zillii (Gervais 1852) fingerlings. J. Agric. Sci. 2012;4(2):269. [Google Scholar]
  • 128.Mahmoud R, Aziza A, Marghani B, Eltaysh R. Influence of ginger and garlic supplementation on growth performance, whole body composition and oxidative stress in the muscles of Nile tilapia (O. niloticus) Adv. Anim. Vet. Sci. 2019;7(5):397–404. [Google Scholar]
  • 129.Shalaby A.M, Khattab Y.A, Abdel Rahman A.M. Effects of garlic (Allium sativum) and chloramphenicol on growth performance, physiological parameters and survival of Nile tilapia (Oreochromis niloticus) J. Venom. Anim. Toxins Incl. Trop. Dis. 2006;12(2):172–201. [Google Scholar]
  • 130.Mesalhy Aly S, El Naggar G.O, Mohamed M.F, Mohamed W.E. Effect of garlic, Echinacea, organic green and vet-yeast on survival, weight gain, and bacterial challenge of overwintered Nile Tilapia fry (Orechromis niloticus) J. Appl. Aquac. 2010;22(3):210–215. [Google Scholar]
  • 131.Foysal M.J, Alam M, Momtaz F, Chaklader M.R, Siddik M.A.B, Cole A, Fotedar R, Rahman M.M. Dietary supplementation of garlic (Allium sativum) modulates gut microbiota and health status of tilapia (Oreochromis niloticus) against Streptococcus iniae infection. Aquac. Res. 2019;50(8):2107–2116. [Google Scholar]
  • 132.Abd El-Galil M.A, Aboelhadid S.M. Trials for the control of trichodinosis and gyrodactylosis in hatchery reared Oreochromis niloticus fries by using garlic. Vet. Parasitol. 2012;185(2–4):57–63. doi: 10.1016/j.vetpar.2011.10.035. [DOI] [PubMed] [Google Scholar]
  • 133.Chitmanat C, Tongdonmuan K, Nunsong W. The use of crude extracts from traditional medicinal plants to eliminate Trichodina sp. in tilapia (Oreochromis niloticus) fingerlings. Songklanakarin J. Sci. Technol. 2005;27(1):359–364. [Google Scholar]
  • 134.Nya E.J, Austin B. Use of garlic, Allium sativum, to control Aeromonas hydrophila infection in rainbow trout, Oncorhynchus mykiss (Walbaum) J. Fish Dis. 2009;32(11):963–970. doi: 10.1111/j.1365-2761.2009.01100.x. [DOI] [PubMed] [Google Scholar]
  • 135.Büyükdeveci M.E, Balcázar J.L, Demirkale İ, Dikel S. Effects of garlic-supplemented diet on growth performance and intestinal microbiota of rainbow trout (Oncorhynchus mykiss) Aquaculture. 2018;486(6):170–174. [Google Scholar]
  • 136.Breyer K.E, Getchell R.G, Cornwell E.R, Wooster G.A, Ketola H.G, Bowser P.R. Efficacy of an extract from garlic, Allium sativum, against infection with the furunculosis bacterium, Aeromonas salmonicida, in rainbow trout, Oncorhynchus mykiss. J. World Aquac. Soc. 2015;46(3):273–282. [Google Scholar]
  • 137.Pedrós-Garrido S, Clemente I, Calanche J.B, Condón-Abanto S, Beltrán J.A, Lyng J.G, Brunton N, Bolton D, Whyte P. Antimicrobial activity of natural compounds against Listeria spp. and their effects on sensory attributes in salmon (Salmo salar) and cod (Gadus morhua) Food Control. 2020;107(2):106768. [Google Scholar]
  • 138.Tosun Ş.Y, Alakavuk D.U, Ulusoy Ş, Erkan N. Effects of essential oils on the survival of Salmonella enteritidis and Listeria monocytogenes on fresh Atlantic salmons (Salmo salar) during storage at 2±1°C. J. Food Saf. 2018;38(1):e12408. [Google Scholar]
  • 139.Costello M.J. Boxshall G.A, Defaye D, editors. Review of methods to control sea lice (Caligidae:Crustacea) infestations on salmon (Salmo salar) farms. Pathogens of Wild and Farmed Fish:Sea Lice. Dublin, Irish Republic. 1993:219–252. [Google Scholar]
  • 140.Jensen H.M, Karami A.M, Mathiessen H, Al-Jubury A, Kania P.W, Buchmann K. Gill amoebae from freshwater rainbow trout (Oncorhynchus mykiss):In vitro evaluation of antiparasitic compounds against Vannella sp. J. Fish Dis. 2020;43(6):665–672. doi: 10.1111/jfd.13162. [DOI] [PubMed] [Google Scholar]
  • 141.Buchmann K, Jensen P.B, Kruse K.D. Effects of sodium percarbonate and garlic extract on Ichthyophthirius multifiliis theronts and tomocysts:In vitro experiments. N. Am. J. Aquac. 2003;65(1):21–24. [Google Scholar]
  • 142.Poongodi R, Bhavan P.S, Muralisankar T, Radhakrishnan S. Growth promoting potential of garlic, ginger, turmeric and fenugreek on the freshwater prawn Macrobrachium rosenbergii. Int. J. Pharm. Bio. Sci. 2012;3(4):914–926. [Google Scholar]
  • 143.Mona M.H, Rizk E.S.T, Salama W.M, Younis M.L. Efficacy of probiotics, prebiotics, and immunostimulant on growth performance and immunological parameters of Procambarus clarkii juveniles. J. Basic. Appl. Zool. 2015;69(C):17–25. [Google Scholar]
  • 144.Malar H.V, Charles P.M. Efficacy of garlic on the survival, growth and haematology of Penaeus Monodon post larvae. Int. J. Life Sci. Biotechnol. Pharma. Res. 2013;2(3):2250–3137. [Google Scholar]
  • 145.Kumar R.M, Rao A.C.S, Daggula N, Guguloth G, Das B.Y, Indhuri A. Growth promoter effect of ginger, garlic and fenugreek on Pacific White Leg Shrimp (Litopenaeus vannamei) Int. J. Curr. Microbiol. Appl. Sci. 2019;8(2):2993–3001. [Google Scholar]
  • 146.Pazir M.K, Pourshalkohi N.J, Rohani A. Evaluation of growth, survival, and health indices of Litopenaeus vannamei:Boone, 1931 fed diets containing different percentages of garlic powder (Allium sativum) Fish. Sci. Technol. 2018;7(4):287–293. [Google Scholar]
  • 147.Fierro-Coronado J.A, Luna-González A, Cáceres-Martínez C.J, Ruiz-Verdugo C.A, Escamilla-Montes R, Diarte-Plata G, Flores-Miranda M.D.C, Álvarez-Ruiz P, Peraza-Gómez V. Effect of medicinal plants on the survival of white shrimp (Penaeus vannamei) challenged with WSSV and Vibrio parahaemolyticus. Lat. Am. J. Aquat. Res. 2019;47(2):377–381. [Google Scholar]
  • 148.Chirawithayaboon P, Areechon N, Meunpol O. Hepatopancreatic antioxidant enzyme activities and disease resistance of Pacific white shrimp (Litopenaeus vannamei) fed diet supplemented with garlic (Allium sativum) extract. Agric. Nat. Resour. 2020;54(4):377–386. [Google Scholar]
  • 149.Nurtjahyani S.D, Hadra F. Antibacterial activity of garlic (Allium sativum) against Gram-positive bacteria isolated from tiger shrimp (Penaeus monodon) Asian Pac. J. Trop. Dis. 2016;6(1):46–48. [Google Scholar]
  • 150.Madhuri A.V, Rao D.S, Verma M.K, Naik J.K, Rao M.V.R. Treatment of gregarines sporozoites in shrimp with allicin an herbal preparation and control intermediate hosts with copper sulfate. Int. J. Fish Aquat. Stud. 2021;9(4):37–40. [Google Scholar]
  • 151.Nasr-Allah A, Gasparatos A, Karanja A, Dompreh E.B, Murphy S, Rossignoli C.M, Phillips M, Charo-Karisa H. Employment generation in the Egyptian aquaculture value chain:Implications for meeting the Sustainable Development Goals (SDGs) Aquaculture. 2020;520(1):734940. [Google Scholar]

Articles from Veterinary World are provided here courtesy of Veterinary World

RESOURCES