Algae and Their Metabolites as Potential Bio-Pesticides

An increasing human population necessitates more food production, yet current techniques in agriculture, such as chemical pesticide use, have negative impacts on the ecosystems and strong public opposition. Alternatives to synthetic pesticides should be safe for humans, the environment, and be sustainable. Extremely diverse ecological niches and millions of years of competition have shaped the genomes of algae to produce a myriad of substances that may serve humans in various biotechnological areas. Among the thousands of described algal species, only a small number have been investigated for valuable metabolites, yet these revealed the potential of algal metabolites as bio-pesticides. This review focuses on macroalgae and microalgae (including cyanobacteria) and their extracts or purified compounds, that have proven to be effective antibacterial, antiviral, antifungal, nematocides, insecticides, herbicides, and plant growth stimulants. Moreover, the mechanisms of action of the majority of these metabolites against plant pests are thoroughly discussed. The available information demonstrated herbicidal activities via inhibition of photosynthesis, antimicrobial activities via induction of plant defense responses, inhibition of quorum sensing and blocking virus entry, and insecticidal activities via neurotoxicity. The discovery of antimetabolites also seems to hold great potential as one recent example showed antimicrobial and herbicidal properties. Algae, especially microalgae, represent a vast untapped resource for discovering novel and safe biopesticide compounds.


Introduction
The term algae encompasses a wide range of photosynthetic organisms that are found primarily in freshwater and marine environments, although certain representatives can thrive in terrestrial niches, either on their own or by developing symbiotic relationships with other organisms [1,2]. Larger eukaryotic algae, such as seaweeds, are called macroalgae, while smaller unicellular eukaryotes are collectively referred to as microalgae. On the other hand, cyanobacteria (blue-green algae) represent the prokaryotic clade of this highly tides, peptides, polysaccharides, phlorotannins, diterpenes, sterols, quinones, lipids, glycerols, have been found to exhibit antibacterial action [14,31]. However, in some stances, the specific compounds with antibacterial properties are not fully elucidated, the activity is collectively attributed to algal extracts. Also, as most studies focus on antibacterial properties of algal extracts on human pathogens, information on plant p ogens is scarce but is constantly being enriched. An excellent example of algal extr with antibacterial action comes from the brown marine alga Sargassum wightii (Table  The methanolic extracts of this species showed maximum antibacterial acti against the plant pathogen Pseudomonas syringae, to prevent leaf spot disease of the dicinal herb Gymnema sylvestre [32]. Similar in vitro activity against the phytopathog bacterium Xanthomonas oryzae was observed by the macroalgae Gracilaria edulis, Sargas wightii, and Enteromorpha flexuosa [16]. The compound that was responsible for this ac in the brown alga Sargassum wightii was the sulphoglycerolipid 1-O-palmitoyl-3-O sulpho-a-quinovopyranosyl)-glycerol ( Figure 1) from the methanolic extract [33]. plant pathogens Xanthomonas campestris and Erwinia carotovora were also inhibited in v by the methanol-soluble and insoluble extracts of Ulva fasciata [34]. The spray applica of aqueous extracts from the brown algae Cystoseira myriophylloides and Fucus spiralis nificantly reduced Crown gall disease incidence that was caused by the bacterial patho Agrobacterium tumefaciens in greenhouse tomato plants (Solanum lycopersicum) [18]. The sponse was related to oxidative burst mechanisms since the treated plants exhibited nificantly greater activity levels of the plant defense enzymes polyphenol oxidase and roxidase. The methanolic extract of the marine brown algae Sargassum latifolium, Hy clathrus clathratus, and Padina gymnospora showed antibacterial activity against the s borne phytopathogenic bacteria Ralstonia solanacearum and Pectobacterium carotovor The extract of Padina gymnospora, which showed the most potent effect, was domina by palmitic and oleic acids ( Figure 1) [35].  In most documented cases, the antibacterial activity is against human or animal pathogens. In terms of agricultural practices, this is important for pathogenic bacteria that are associated with livestock. However, such agents could be further tested as potential candidates for plant protection applications, leaving ample room for future research [19,[36][37][38][39][40][41][42][43][44][45][46][47]; such are the cases of the tetrabrominated diphenyl ether-like 2-(2 ,4 -dibromophenoxy)-4,6-dibromoanisole ( Figure 2) that was isolated from the green alga Cladaphora fascicularis that showed bactericidal action against Escherichia coli, Bacillus subtilis, and Staphylococcus aureus [38], and tetracyclic brominated diterpenes such as 3-hydroxy-1-deoxy-bromotetraspaerol ( Figure 3) from the red alga Sphaerococcus coronopifolius that exhibited antibacterial activity against a panel of S. aureus strains [36]. Interestingly, ethyl acetate extracts from two cyanobacterial species, Anabaena variabilis and A. circinalis, were effective against bacterial fish pathogens belonging to the genus Aeromonas, proving to be useful in aquaculture applications [48]. Moreover, as most of the published studies focus on macroalgae or cyanobacteria's antimicrobial activity, microalgae could constitute another exciting prospect for future research. NK: not known.
Microorganisms 2022, 10, 307 5 of 32 bromotetraspaerol ( Figure 3) from the red alga Sphaerococcus coronopifolius that exhib antibacterial activity against a panel of S. aureus strains [36]. Interestingly, ethyl ac extracts from two cyanobacterial species, Anabaena variabilis and A. circinalis, were e tive against bacterial fish pathogens belonging to the genus Aeromonas, proving to be ful in aquaculture applications [48]. Moreover, as most of the published studies focu macroalgae or cyanobacteria's antimicrobial activity, microalgae could constitute ano exciting prospect for future research.    . The chemical structure of active compounds that were isolated from Sphaerococcus coronopifolius, Plocamium cartilagineum, Plocamium telfairiae, and Prasiola crispa.

Antiviral Action
Plant viruses are a serious threat to agricultural crops, affecting product quality and yields and resulting in severe economic losses [30]. Their management is heavily dependent on synthetic chemical products, but natural compounds are continuously gaining ground. In this respect, natural compounds from algae that exhibit antiviral properties could Microorganisms 2022, 10, 307 6 of 32 be valuable resources. Among them are various polysaccharides, such as laminarins, agarans, alginate, carrageenans, and sulphated fucans, that can function as elicitors of defense mechanisms, as well as proteins, lipids, tannins, and terpenoids [10,13,30,50,51]. Polysaccharides are the most common compounds in algal extracts that induces antiviral responses in plants. For example, sodium alginate ( Figure 4) from marine algae exhibited strong inhibitory activity against the tobacco mosaic virus (TMV) that was isolated from systemically-infected leaves of Nicotiana tabacum L. var bright yellow [21] (Table 2).  Apart from polysaccharides, lectins (carbohydrate-binding proteins) that were isolated from the marine alga Ulva pertusa also showed antiviral action against tobacco mosaic virus (TMV) [53,54]. Similarly, lipids that were extracted from 11 algal species displayed antiviral activity against TMV on Nicotiana tabacum cv. Xanthi-nc. The brown alga Cystoseira balearica and the red alga Lophocladia lallemandii showed the highest inhibitory activity [19]. Aqueous and ethanolic extracts from the brown alga Durvillaea antarctica suppressed damage that was caused by TMV in tobacco leaves [17]. Moreover, an exciting application in livestock animals refers to the use of sulphated polysaccharides from the algae Ulva clathrata and Cladosiphon okamuranus in inhibiting Newcastle Disease Virus (NDV) infection in poultry [55].
Research for algal compounds with antiviral effects in plants has yielded significant results in the past years and remains promising for discovering new biopesticide products. However, as expected, algal antiviral research is mainly concentrated around human pathogens. Algal extracts have been studied extensively for their inhibitory action against important human viruses, such as human immunodeficiency virus (HIV), human papilloma virus (HPV), hepatitis B virus (HBV), herpes simplex virus types 1 and 2 (HSV-1, HSV-2), and diverse strains of Dengue virus (DENV-2) [56][57][58][59][60][61][62][63][64], suggesting that there are still many research opportunities in the field of algal antiviral products.    Inhibition of cell-cell fusion [55] NK: not known.
The degree of inhibition increased with alginate concentration and was higher when the alginate polymer had a lower mannuronate to guluronate ratio [21]. Another polysaccharide, i.e., kappa/beta-carrageenan ( Figure 4) from red marine alga Tichocarpus crinitus, reduced tobacco mosaic virus (TMV) infection in Xanthi-nc tobacco leaves by 87 percent [52]. The same compound stimulated lytic processes against PVX particles in the leaves of Datura stramonium [22]. Methanolic extracts from six algal species also showed inhibitory effects against PVX by more than 80%. Among them, the extract from Fucus gardneri contained the polysaccharide alginate, which showed 95% success in suppressing PVX infection via aggregation of the virus particles [23].
Apart from polysaccharides, lectins (carbohydrate-binding proteins) that were isolated from the marine alga Ulva pertusa also showed antiviral action against tobacco mosaic virus (TMV) [53,54]. Similarly, lipids that were extracted from 11 algal species displayed antiviral activity against TMV on Nicotiana tabacum cv. Xanthi-nc. The brown alga Cystoseira balearica and the red alga Lophocladia lallemandii showed the highest inhibitory activity [19]. Aqueous and ethanolic extracts from the brown alga Durvillaea antarctica suppressed damage that was caused by TMV in tobacco leaves [17]. Moreover, an exciting application in livestock animals refers to the use of sulphated polysaccharides from the algae Ulva clathrata and Cladosiphon okamuranus in inhibiting Newcastle Disease Virus (NDV) infection in poultry [55].
Research for algal compounds with antiviral effects in plants has yielded significant results in the past years and remains promising for discovering new biopesticide products. However, as expected, algal antiviral research is mainly concentrated around human pathogens. Algal extracts have been studied extensively for their inhibitory action against important human viruses, such as human immunodeficiency virus (HIV), human papilloma virus (HPV), hepatitis B virus (HBV), herpes simplex virus types 1 and 2 (HSV-1, HSV-2), and diverse strains of Dengue virus (DENV-2) [56][57][58][59][60][61][62][63][64], suggesting that there are still many research opportunities in the field of algal antiviral products.
The extract, which was directly applied on tomato plants, completely inhibited the growth of the fungus Sclerotinia sclerotiorum [20]. The aqueous extracts of three brown algae Cystoseira myriophylloides, Laminaria digitata, and Fucus spiralis, that were applied as spray or drench, had a protective effect against Verticillium wilt disease that was caused by the fungus Verticillium dahliae, in greenhouse tomato seedlings [18]. In tomato leaves that were infected with Botrytis cinerea, organic extracts from the brown alga Lessonia innamomic reduced the frequency and extent of necrotic lesions, while aqueous and ethanolic extracts from the red alga Gracillaria chilensis were effective against Phytophthora innamomic, showing dose and time-dependent responses [17]. Methanolic extracts of the sea brown algae Sargassum latifolium and Padina gymnospora showed antifungal activity against phytopathogenic fungus species such as Fusarium solani and Rhizoctonia solani in addition to antibacterial activity [35]. Notably, the antifungal activity of alkaline extracts of Ulva lactuca, Sargassum filipendula, and Gelidium serrulatum has been linked to the increase in plant defense enzymes activity and the overexpression of key marker genes of plant defense pathways [49].
De Corato et al. [68] performed in vitro and in vivo tests of extracts from two brown and three red macroalgae against three phytopathogenic fungi. The compounds that were identified in the extracts included twenty fatty acids, three types of polysaccharides (laminarans, fucoidans, and alginates) (Figure 4), and three types of phlorotannins (phlorethols, fucophloretols, and eckols) ( Figure 2). Regarding lipids, palmitic acid, linoleic acid, and arachidonic acid were found at the highest concentrations in most extracts. The quantity of fatty acids corresponded to most of the total dry weight of the crude extracts and could be linked to the antifungal activity [68]. Lipids that were extracted from 10 algal species inhibited the germination of Phoma tracheiphila, a pathogenic fungus that causes a disease known as Mal secco on citrus trees. More specifically, the inhibition effect of the brown alga Cystoseira balearica and the green alga Codium effusum reached 100% [19].
Various algal oligo-or polysaccharides have demonstrated antifungal activity against plant pathogens either directly or indirectly, by activating plant defense mechanisms [78][79][80][81][82][83][84]. The cell wall polysaccharide laminarin ( Figure 4) that was purified from the brown algae Laminaria digitata induced a defense response in grapevine leaves against the fungus Botrytis cinerea, effectively reducing the infection. In addition, grapevine plants that were sprayed on the leaves with laminarin were protected against the fungus Plasmopara viticola [85]. Polysaccharides from Anabaena sp., Ecklonia sp., and Jania sp. showed inhibitory action against Botrytis cinerea, effectively protecting strawberry fruits from infection in in vitro experiments [86]. Similar polysaccharide-rich extracts from green (Ulva lactuca and Caulerpa sertularioides) and brown (Padina gymnospora and Sargassum liebmannii) macroalgae induced resistance in tomato plants against the necrotrophic fungus Alternaria solani [87]. The water-soluble heteropolysaccharide ulvan ( Figure 4) from Ulva sp. extracts significantly reduced the severity of Glomerella leaf spot (GLS) disease, caused by the fungus Colletotrichum gloeosporioides on the leaves of apple plant seedlings (Malus domestica). The induced resistance was associated with increased peroxidase activity, revealing that although ulvan does not exhibit antimicrobial activity, its action is associated with plant defense mechanisms [88].   Extracts and powders of the green seaweeds Ulva fasciata and Enteromorpha flexuosa inhibited the growth or affected the microsclerotia formation of the soil-borne fungi, Macrophomina phaseolina and Fusarium solani, that infect cucumber plants. The identification of iron-monocarbonyl and their functional groups, such as amine and ether in the extracts, could suggest a potential antifungal role for these compounds [89]. Similar compounds were also identified in the chloroform extracts from the red macroalgae Gracilaria confervoides that exhibited inhibitory action against three soil-borne pathogenic fungi of cucumber: Rhizoctonia solani, Fusarium solani, and Macrophomina phaseolina [75].
The methanolic extract of the brown alga Sargassum vulgare contained phenolic acids and flavonoids that may be responsible for the antifungal action that was observed against Pythium aphanidermatum, the causative agent of Pythium leak disease in potato [90]. Phenolic acids and phytoalexins were among the 18 compounds that were detected in the acetone extract of the brown alga Sargassum wightii. The extract exhibited antifungal activity against Rhizoctonia solani, the causative agent of rice sheath blight [91].

Nematocidal Action
The extracts and compounds from micro-and macroalgae are also effective against plant-parasitic nematodes that are responsible for the annual loss of 10-25% of worldwide crop production [92] (Table 4). Brominated diterpenes that were isolated from the marine red alga Jania rubens were effective against Allolobophora caliginosa [93]. Different concentrations of methanolic extracts from the Nostoc strain ATCC 53,789 either killed or slowed the development of the nematode C. elegans [20]. Dry powders from three macroalgae species, Spatoglossum variabile, Stokeyia indica, and Melanothamnus afaqhusainii displayed a suppressive effect on the rootknot nematode Meloidogyne incognita by reducing the gall formation and preventing nematode penetration in the roots of eggplant and watermelon [65]. Similar effects against the nematode Meloidogyne javanica were identified in okra, sunflower, and tomato after treatment with aqueous and ethanolic extracts of the marine macroalgae Sargassum tenerrimum, S. swartzii, S. wightii, Spatoglossum variabile, Melanothamnus afaqhusainii, and Halimeda tuna [24,94]. Algal extracts showed relatively similar suppressive effects with a carbofuran nematicide; however, the best result was obtained when extracts from Spatoglossum variabile were applied together with the synthetic product [24]. The marine alga Stoechospermum polypodioides was also effective against Meloidogyne javanica, causing 80% mortality, the strongest effect among 21 species of algae that were examined for their nematocidal action [95]. A reduction in root-knot nematode infestation using macroalgal extracts has been previously reported in tomato [96]. There are two commercially available products that are derived from the marine macroalgae Ascophyllum nodosum and Ecklonia maxima, that affected the hatching and sensory perception of the root-knot nematodes Meloidogyne chitwoodi and M. hapla. The alkaline extract from the brown marine alga A. nodosum showed a stronger inhibitory effect compared to the extract from the brown alga E. maxima, which in certain cases enhanced the infectivity of the nematodes [97]. Extracts of A. nodosum have shown inhibitory action against other nematodes, such as Radopholus similis, Meloidogyne incognita, and Belonolaimus longicaudatus, infecting citrus, tomato, and centipede grass, respectively [98][99][100][101].

Insecticidal-Acaricidal Action of Algae
Marine macroalgae extracts exhibit insecticidal/acaricidal activity and can be used in integrated pest management applications as environmentally friendly approaches for arthropod population control. These botanical biopesticides are safer than synthetic products and are equally or more effective since they display different modes of action. Therefore, their targets are less likely to develop resistance against them [102,103]. There are a large number of publications describing the pesticidal or repellent action of algal extracts against different arthropods that are either agricultural pests or related to human and animal health [25,26,[104][105][106][107][108][109][110][111][112][113][114][115]. The bioactive compounds that were identified in the extracts, as expected, cover a broad range of chemical structures, including polysaccharides, phenolics, proteins, terpenes, lipids, and halogenated compounds [116]. For example, two halogenated monoterpenes (mertensene and violacene) ( Figure 3) that were extracted from the red alga Plocamium cartilagineum, and the mertensene derivatives, dibromomertensene, and dihydromertensene, showed strong insecticidal activity against the tomato moth Tuta absoluta and the cereal aphid, Schizaphis graminum [104] (Table 5).   [112] Water and ethanol extracts from the cyanobacterium Arthrospira platensis (syn. Spirulina platensis) and the brown alga Sargassum vulgar contained phenols, tannins, and alkaloids. Further analysis of phenols in A. platensis revealed the presence of the phenolic compounds: quercetin, kaempferol, and resorcinol ( Figure 2), which could be related to the insecticidal action of the extracts [27]. An evaluation of the ethanolic extracts of the macroalgal species (Caulerpa sertularioides, Laurencia johnstonii, and Sargassum horridum) revealed insecticidal and repellent activities against Asian citrus psyllid adults (Diaphorina citri). The chemical composition of the three extracts showed phenols, alkaloids, terpenes, tannins, flavonoids, saponins, and anthraquinones, which are associated with insecticidal and repellent activity [109]. In certain cases, algal extracts exhibit different insecticidal effects, depending on the insect species and on the developmental stages of the target insect. For instance, the acetone extract of Ulva lactuca was the most potent extract against Culex pipiens. In the case of the cotton leafworm, Spodoptera littoralis, ethanolic and chloroform extracts acted as larvicides, methanolic and ethanolic extracts resulted in the highest pupation inhibition, whereas etheric and methanolic extracts strongly inhibited larval growth and adult emergence [117]. In terms of agricultural pests, more research has focused on the insecticidal activity of algal extracts against the cotton insect pests of the genera Dysdercus and Spodoptera. Algal extracts of various species, including Caulerpa scalpelliformis [118], Padina pavonica [115], Sargassum tenerrimum [114], Sargassum vulgar [27], Ulva fasciata, and U. lactuca [105] were effective against these agricultural pests by causing nymphal mortality, adult mortality, abnormal development, or reducing adult lifespan, fecundity, and hatchability [14,106]. As observed throughout the text, algal extracts could be used against more than one target type (antimicrobial, insect, mite, etc.). Therefore, apart from the antifungal action, the methanolic extracts of the cyanobacterium Nostoc strain ATCC 53,789 also killed larvae of the moth Helicoverpa armigera [20].
The volatile oils from Actinotrichia fragilis, Liagora ceranoides, and Colpomenia sinuosa were hydrodistilled and contained different aliphatic alcohols and long-chain hydrocarbons as the major components. They caused 55-90% and 60-80% mortality to pests of stored products Oryzaephilus mercator and Tribolium castaneum, respectively, at a dose of 12 µL/L air after 48 h of fumigation exposure [119].
The volatile oils of A. fragilis caused 80-90% mortality in both T. castaneum and O. mercator and consisted of 49% aliphatic alcohols, mainly 1-dodecanol (39.6%) [119]. The insecticidal activity of 1-dodecanol was suggested to be related to the developing cuticle, producing a disruption in the cuticular tanning process [120].

Herbicidal Activity
Natural bioherbicides have become a useful tool for the integrated management of herbaceous weeds, a major problem in agriculture that are known for impairing the growth of cultivated plants and effectively reducing crop yields [121]. Various algal metabolites, such as cyanotoxins that exhibit cytotoxicity, have been considered as potential candidates for herbicidal activity [6]. In many documented cases, cyanotoxins have ecological role as allelochemicals, inhibiting competitive macrophytes, algae, and microbes [122][123][124][125]. Such is the case in the recovery of indole alkaloid norharmane ( Figure 5) from the cyanobacterium Synechocystis aquatilis, which inhibited the growth of the cyanobacteria Microcystis aeruginosa and Oscillatoria limnetica, and that of the green algae Chlorella vulgaris and Ulothrix sp. [126] ( Table 6). of grass seedlings by reducing culm height and inhibiting root development, even though it did not affect the initial germination of the seeds [20]. However useful, one of the limitations of cyanobacterial toxins is their potential toxic effects against non-target organisms, including humans, animals, and plants, and their bioaccumulation in the food chain. Therefore, designing candidate agricultural products that make use of toxins should always take into consideration the adverse effects to non-target organisms [122,124].

Plant Growth Stimulation (Biostimulators and Biofertilizers) and Bioprotection
Algal extracts and compounds are valuable resources that display a wide range of beneficial effects on cultivated plants. Such effects include improved seed germination, plant growth, crop performance and yield, post-harvest shelf-life, and protection against biotic and abiotic factors [135][136][137][138][139]. Compounds with growth-stimulating activities include polysaccharides, minerals, trace elements, growth hormones, betaines, and sterols [137].
Alkaline extracts of Ascophyllum nodosum enhanced the development of the mycorrhizal fungus Rhizophagus irregularis in terms of spore germination, germ tube   [20] Although this action was not against land crop weeds but algal blooms, it has been found that norharmane can also inhibit the germination of weeds, such as Avena fatua and Plantago lanceolata; suppress the growth of Portulaca oleracea, Echinochloa crus-galli and Amaranthus retroflexus; and damage the metabolism in Arabidopsis thaliana [28]. Cyanobacterin (a chlorinated γ-lactone) ( Figure 5) is another allelopathic substance that was isolated from the freshwater cyanobacterium Scytonema hofmanni that is highly toxic to other cyanobacteria and eukaryotic algae by interrupting photosynthetic electron transport [29]. There are two other structurally different cyanobacterins that were identified in Nostoc linckia that specifically inhibit electron transport in photosystem II [127,128]. A series of metabolites, such as nostocyclamide, nostocine A and nostocarboline ( Figure 5) that were isolated from a Nostoc sp., exhibited toxic action against algae [129][130][131]. Another type of toxin, microcystins (for an example see Figure 5) that were isolated from Microcystis aeruginosa, inhibits the growth of aquatic plants, such as Myriophyllum variifolium and Lemna japonica [132,133]. A sugar, 7-deoxy-sedoheptulose (7dSh) ( Figure 5) that was isolated from the cyanobacterium Synechococcus elongatus, inhibited the growth of various pho-totrophic organisms, including cyanobacteria as well as yeasts and plants [134]. Moreover, the methanolic extract of the Nostoc strain ATCC 53,789 hindered the development of a mixture of grass seedlings by reducing culm height and inhibiting root development, even though it did not affect the initial germination of the seeds [20]. However useful, one of the limitations of cyanobacterial toxins is their potential toxic effects against non-target organisms, including humans, animals, and plants, and their bioaccumulation in the food chain. Therefore, designing candidate agricultural products that make use of toxins should always take into consideration the adverse effects to non-target organisms [122,124].

Plant Growth Stimulation (Biostimulators and Biofertilizers) and Bioprotection
Algal extracts and compounds are valuable resources that display a wide range of beneficial effects on cultivated plants. Such effects include improved seed germination, plant growth, crop performance and yield, post-harvest shelf-life, and protection against biotic and abiotic factors [135][136][137][138][139]. Compounds with growth-stimulating activities include polysaccharides, minerals, trace elements, growth hormones, betaines, and sterols [137].
Alkaline extracts of Ascophyllum nodosum enhanced the development of the mycorrhizal fungus Rhizophagus irregularis in terms of spore germination, germ tube length, and hyphal branching. The application of the extracts improved the formation of mycorrhizal associations, increased root colonization, arbuscular maturity, and the size of greenhouse-grown Medicago truncatula plants [140]. An Ascophyllum nodosum extract significantly improved the root, shoot, and fruit biomass productivity parameters by positively influencing the rhizospheric bacterial and fungal communities that are associated with pepper and tomato plants [141]. Additionally, beneficial effects of an alkaline extract of A. nodosum were observed in tomato and sweet pepper plants. The foliar application of the extract significantly improved the plant height, leaf number, root length, dry biomass, and increased the leaf chlorophyll content under greenhouse conditions. The extract also reduced disease severity that was caused by pathogenic fungal and bacterial species by 50% under field conditions [142]. The effect of the extract was associated with the induction of plant defense-related enzymes, the production of phenolic compounds, and the activation of genes that were related to auxin, gibberellin, and cytokinin biosynthesis [142]. Plant growth regulators, such as auxin, gibberellic acid, cytokinin, and cytokinin-like compounds, have been isolated from various algal species, including A. nodosum, Ecklonia maxima, and Fucus serratus [143][144][145][146]. The application of A. nodosum extract on turf and forage grasses resulted in increased amounts of antioxidant compounds and activity of antioxidant enzymes, therefore, helping plants overcome oxidative stress [147].
Various Chlorella species have exhibited similar beneficial effects on the development of cultivated plants. Chlorella extracts showed a growth-promoting effect in a variety of crops, including onion, lettuce, cabbage, turnip, wheat, and maize [148][149][150]. A similar effect was also observed in sugar beet with the application of extracts from Chlorella vulgaris and Scenedesmus quadricauda [151]. Lettuce, tomato, and cucumber seeds that were treated with extracts of Chlorella vulgaris were characterized by enhanced germination, higher shoot, and root weights [152,153]. A combination of algal species or compounds could result in more effective microalgae-based fertilizers. For example, powders from Nannochloropsis biomass and filamentous microalgae (Ulothrix and Klebsormidium spp.) effectively enhanced tomato plant growth and improved the fruit quality [154].
Apart from eukaryotic algae, cyanobacteria have also been identified as effective plant biofertilizers. In this respect, composts that were amended with Anabaena variabilis and A. laxa resulted in enhanced soil organic carbon, nitrogen fixation, significant improvement in growth, yield, fruit quality parameters, nitrogen, phosphorus, and zinc content [73]. Anabaena variabilis and a Nostoc sp. increased seed germination, plant height, leaf length, and grain yield, when they were applied as biofertilizers on rice seeds or plants [155,156]. Treatment with Anabaena laxa resulted in 25% enhanced germination in cumin, while Calothrix elenkinii enhanced the root and shoot length significantly in cumin, fennel, and coriander [157]. Filtrates of Calothrix ghosei, a Nostoc sp. and Hapalosiphon intricatus, enhanced the germination, radicle, and coleoptile length in experiments with wheat seeds. Analysis of the filtrates revealed the presence of several amino acids, such as histidine, and auxin-like compounds [158]. The foliar application of seaweed extracts of Macrocystis pyrifera, Bryothamnion triquetrum, Ascophyllum nodosum, Grammatophora spp., and Macrocystis integrifolia improved the quality of cucumber fruits by increasing the antioxidant capacity of the plant [159]. Moreover, supplementation with Arthrospira platensis (Spirulina platensis) biomass enhanced the plant growth and improved the seed germination of leafy vegetables, including Eruca sativa, Ameranthus gangeticus, Brassica oleracea, and Brassica rapa [160].
The utilization of algal substances could also provide significant benefits to crops in overcoming various types of abiotic stress. Extracts of the brown macroalga Ascophyllum nodosum significantly increased the tolerance of Arabidopsis thaliana to freezing temperatures, both in vitro and in vivo. The effect was also characterized by reduced tissue, membrane, and chlorophyll damage. Tolerance to freezing stress was also observed when plants were treated only with the lipophilic fraction of the extracts, suggesting that the effect could be associated with its components [161]. Moreover, the extract of Ascophyllum nodosum improved the fresh and dry weight of shoots and roots of Zea mays that were grown in phosphorous-limited conditions [162]. Vitis vinifera plants that were treated with algal extracts exhibited high tolerance against water stress. The extract significantly enhanced potassium and calcium fluxes, improved plant growth, and the accumulated macronutrients in the plant organs [163].
Similarly, Chlorella vulgaris induced tolerance against water stress in Vicia faba plants [164]. Extracellular products of the cyanobacterium Scytonema hofmanni counteracted the effects of salt stress in rice plants. Contrary to salt-stressed plants, treated plants had a higher shoot weight and length, carotenoid content, root weight, and total free porphyrin [165]. A similar effect was induced by Dunaliella salina exopolysaccharides, which alleviated the salt stress on tomato plants. The treated plants were also characterized by higher length and weight of their shoot and root systems, higher K + concentration, and K + /Na + ratio [166]. Treating water-stressed whole grains of wheat plants with water extracts of Chlorella ellipsoida and Spirulina maxima resulted in increased total carotenoid, tocopherol, phenolic, and protein contents [167]. Algal extracts are also effective in activating mechanisms that protect plants from oxidative stress, which is caused by the accumulation of reactive oxygen species (ROS), such as the superoxide anion (O − 2 .) and hydrogen peroxide (H 2 O 2 ). This response is mainly associated with antioxidant compounds, such as carotenoids, cytokinins, αtocopherol, and ascorbic acid, as well as the activation of enzymes with antioxidant activity, including peroxidase, superoxide dismutase, glutathione reductase, catalase, and ascorbate peroxidase [14,137,138,147,164,166,168].

Mechanism of Action of Algal Metabolites
The mechanisms of action of the majority of algal metabolites against agricultural pests are not known, and mechanism studies are usually performed against medically important organisms [169]. However, the available information on potentially biopesticidal algal metabolites is presented below.

Inhibition of Photosynthesis
Research on allelopathy between different algal species/genera has led to the discovery of novel secondary metabolites with various modes of action [170]. Among them, photosynthesis inhibitors can potentially be used in higher plants, due to the similarity of photosynthetic apparatus between algae and plants. One of the first photosynthesis inhibitors was isolated from the cyanobacterium Scytonema hofmanni UTEX B 2349. Cell extracts or spent medium of this cyanobacterium inhibited the growth of other cyanobacteria and green algae [171]. This led to the isolation of a halogenated secondary metabolite called cyanobacterin ( Figure 5) [171]. Cyanobacterin was ineffective against all eukaryotic algae and eubacteria [171,172]. Further work demonstrated thylakoid damage in transmission electron micrographs of Synechococcus sp. ATCC 27,146 cells that were exposed to the minimum effective dose of 4.6 µM cyanobacterin. Cyanobacterin also inhibited light-dependent oxygen evolution in the same cyanobacterium, suggesting specific action on photosynthetic electron transport [172]. Cyanobacterin was toxic to aquatic Lemna species and terrestrial angiosperms [29]. Similar to Synechococcus sp. ATCC 27146, photosynthetic electron transport was inhibited by cyanobacterin in purified pea chloroplasts. Both cyanobacteria and plant studies suggested that the potential site of action of cyanobacterin was a site in PSII ( Figure 6) [29]. The site of action proved to be different from the site of action of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), which is the quinone binding protein (Q B ) of PSII [173]. Cyanobacterin did not have any effect on PSI activity [29]. A cyanobacterin-resistant strain of the cyanobacterium Anacystis nidulans R2 was selected through mutagenesis with nitrosoguanidine. The mutant was not resistant to 3-(3,4dichlorophenyl)-1,1-dimethylurea, or DCMU and the authors concluded that cyanobacterin inhibited electron flow from quinone-A to quinone-B [174]. The toxicity of cyanobacterin to non-target organisms was studied in Daphnia magna. LC 50 (48-h) of cyanobacterin in D. magna and was approximately 1.37 µg mL −1 , suggesting caution if this metabolite would ever be used as a herbicide [175]. A secondary metabolite, named cyanobacterin LU-1, that was isolated from Nostoc linckia CALU 892, also inhibited the growth of cyanobacteria and algae ( Figure 6). This metabolite inhibited the O2 evolution in Synechococcus sp. PCC 7942 cells in a light-dependent manner. However, its structure and site of action seems to be different compared to cyanobacterin from Scytonema hofmanni. Mutants of Synechococcus sp. PCC 7942 and Anabaena variabilis ALU 458 that were resistant to cyanobacterin LU-1 were also resistant to DCMU, suggesting binding to quinone-B by cyanobacterin LU-1. This metabolite (5 mg) was non-toxic to mice by intraperitoneal injection [127].
The spent culture medium and the cell-free extract of an Oscillatoria strain that was isolated from a lake in India inhibited the growth of several cyanobacteria and algae. Ether extract of this strain inhibited oxygenic photosynthesis in Anacystis nidulans [176], and the growth of angiosperm plants, presumably through inhibition of electron transport at a site that was different than those of cyanobacterin and DCMU [177]. The cell-free extracts were non-toxic to mice. The active metabolites in ether extract seemed to consist of saturated fatty acids [177].
Nostocarboline ( Figure 5) from Nostoc 78-12A is a β-carboline alkaloid inhibiting A secondary metabolite, named cyanobacterin LU-1, that was isolated from Nostoc linckia CALU 892, also inhibited the growth of cyanobacteria and algae ( Figure 6). This metabolite inhibited the O 2 evolution in Synechococcus sp. PCC 7942 cells in a lightdependent manner. However, its structure and site of action seems to be different compared to cyanobacterin from Scytonema hofmanni. Mutants of Synechococcus sp. PCC 7942 and Anabaena variabilis ALU 458 that were resistant to cyanobacterin LU-1 were also resistant to DCMU, suggesting binding to quinone-B by cyanobacterin LU-1. This metabolite (5 mg) was non-toxic to mice by intraperitoneal injection [127].
The spent culture medium and the cell-free extract of an Oscillatoria strain that was isolated from a lake in India inhibited the growth of several cyanobacteria and algae. Ether extract of this strain inhibited oxygenic photosynthesis in Anacystis nidulans [176], and the growth of angiosperm plants, presumably through inhibition of electron transport at a site that was different than those of cyanobacterin and DCMU [177]. The cell-free extracts were non-toxic to mice. The active metabolites in ether extract seemed to consist of saturated fatty acids [177].
Nostocarboline ( Figure 5) from Nostoc 78-12A is a β-carboline alkaloid inhibiting cholinesterase [178]. Nostocarboline and its derivatives inhibit the growth of cyanobacteria and green algae. The inhibitory activity seemed to be related to the inhibition of photosynthesis in cyanobacteria, since this alkaloid was not active against non-photosynthetic bacteria [129]. Further work proved nostocarboline to be a mammalian serine protease inhibitor. Therefore, photosynthetic inhibition in cyanobacteria and algae by nostocarboline might be related to the inhibition of serine proteases in cyanobacteria and algae [179].
Fischerellin A (Figure 1) was isolated from the cyanobacterium Fischerella muscicola UTEX 1829, which inhibited the growth of cyanobacteria and green algae. It did not affect the growth of bacteria. Fischerellin specifically inhibited the photosynthetic electron transport involving PSII in the cyanobacterium Anabaena sp. P9 (Figure 1) [180] and in the aquatic macrophyte Lemna minor [181]. Later, Srivasatava et al. [182] demonstrated that fischerellin inactivated the reaction centre of PSII and modified the PSII antenna architecture. Apart from its herbicidal effect, fischerellin effectively inhibited the growth of the fungi/oomycetes Uromyces appendiculatus, Erysiphe graminis, Phytophthora infestans, and Pyricularia oryzae [181].

Induction of Plant Defense Responses
Exposure to pathogens triggers several defense-related pathways in plants. This is achieved through signal molecules called elicitors that are recognized by receptors on the plant cell membrane [183]. Elicitors may originate from the pathogen or from the plant itself [67,85], or they may be a molecule from a non-pathogenic unrelated organism [183].
The principal cell wall polysaccharides from marine macroalgae, ulvans, alginates, fucans, laminarin, and carrageenans, can activate defense mechanisms in plants against pathogens (Figure 7). This response is mainly associated with the generation of oxidative burst and the activation of the salicylic acid (SA), ethylene, and jasmonic acid (JA) signalling pathways [50].
Therefore, this property allows algae and their compounds to be used as plant protectants [184]. One advantage of algal elicitors is that, contrary to pathogens, they don't usually induce cell death in plants [85]. One notable example is carrageenans (Figure 4) that are found in the cell wall of red algae. Mercier et al. [185] compared the elicitor responses of the pathogen oomycete Phytophthora parasitica var. nicotianae and, Anabaena variabilis ALU 458 that were resistant to cyanobacterin LU-1 were to DCMU, suggesting binding to quinone-B by cyanobacterin LU-1. This mg) was non-toxic to mice by intraperitoneal injection [127].
The spent culture medium and the cell-free extract of an Oscillatoria s isolated from a lake in India inhibited the growth of several cyanobacteria an extract of this strain inhibited oxygenic photosynthesis in Anacystis nidulans growth of angiosperm plants, presumably through inhibition of electron site that was different than those of cyanobacterin and DCMU [177]. The ce were non-toxic to mice. The active metabolites in ether extract seemed to c rated fatty acids [177].
Nostocarboline ( Figure 5) from Nostoc 78-12A is a β-carboline alkal cholinesterase [178]. Nostocarboline and its derivatives inhibit the growth o ria and green algae. The inhibitory activity seemed to be related to the inhi tosynthesis in cyanobacteria, since this alkaloid was not active against non-p bacteria [129]. Further work proved nostocarboline to be a mammalian se inhibitor. Therefore, photosynthetic inhibition in cyanobacteria and algae b line might be related to the inhibition of serine proteases in cyanobacteria an Fischerellin A (Figure 1) was isolated from the cyanobacterium Fische UTEX 1829, which inhibited the growth of cyanobacteria and green algae. It the growth of bacteria. Fischerellin specifically inhibited the photosynt transport involving PSII in the cyanobacterium Anabaena sp. P9 (Figure 1) [1 aquatic macrophyte Lemna minor [181]. Later, Srivasatava et al. [182] dem fischerellin inactivated the reaction centre of PSII and modified the PSII ant ture. Apart from its herbicidal effect, fischerellin effectively inhibited the fungi/oomycetes Uromyces appendiculatus, Erysiphe graminis, Phytophthora Pyricularia oryzae [181].

Induction of Plant Defense Responses
Exposure to pathogens triggers several defense-related pathways in p achieved through signal molecules called elicitors that are recognized by re plant cell membrane [183]. Elicitors may originate from the pathogen or f itself [67,85], or they may be a molecule from a non-pathogenic unrelated or The principal cell wall polysaccharides from marine macroalgae, ulva fucans, laminarin, and carrageenans, can activate defense mechanisms in pathogens (Figure 7). This response is mainly associated with the generatio burst and the activation of the salicylic acid (SA), ethylene, and jasmonic ac ling pathways [50].
Therefore, this property allows algae and their compounds to be used as ants [184]. One advantage of algal elicitors is that, contrary to pathogens, they induce cell death in plants [85]. One notable example is carrageenans (Figu found in the cell wall of red algae. Mercier et al. [185] compared the elicitor re pathogen oomycete Phytophthora parasitica var. nicotianae and, Ƙ-, Ɩ-, and λ-ca tobacco plants. After infiltration into the mesophyll layer of tobacco leaves, caused desiccation and necrosis in the infiltrated area in 24 h. Enzymes that a -, Microorganisms 2022, 10, x FOR PEER REVIEW defense pathways, including sesq II, were induced, but the activities ways were activated in plants by t roscopic changes that were simila served. However, complete necro erpene cyclase, chitinase, and pro transcript abundance continued f pathogen, JA, ethylene, and SA p tions [185]. The same authors sug be initiated by receptors on the pl Similarly, Sangha et al. [186] induction of defense responses in ogenic fungus Sclerotinia sclerotio to infection, the ones that were tr related genes were induced in th activity were detected in plants th acid that is secreted by the fungu sponses of the plant to Ɩand λ-ca Laminarin, a linear β-1,3 glu algae [187]. Incubation of tobacco responses, including rapid alkali tion of the phenylpropanoid path lyase (PAL) activity at 4 h, caffei h, and a strong increase in SA f induced, as demonstrated by lip hours of incubation with laminar NN plants with laminarin result lated (PR) proteins (PR1, PR2, PR3 defense reactions protected the to carotovora subsp. carotovora, whic duced defense responses in grape cium uptake, alkalinization of th protein kinases. The defense resp defense-related genes, such as 9 phenylalanine ammonia lyase (P ing protein (Pgip), basic class I, a β-1,3-glucanases gene Glu1, and production of antimicrobial phyt tected grapevine against Botrytis The presence of β-1,3-glucan hta and Chryosophyceae, and in opens new avenues of research f -, and λ-carrageenans in tobacco plants. After infiltration into the mesophyll layer of tobacco leaves, the pathogen caused desiccation and necrosis in the infiltrated area in 24 h. Enzymes that are involved in defense pathways, including sesquiterpene cyclase, chitinase, and proteinase inhibitor type II, were induced, but the activities usually disappeared in 24 h. JA, ethylene, and SA pathways were activated in plants by the pathogen. After the application of λ-carrageenan, macroscopic changes that were similar to the ones that are induced by the pathogen were observed. However, complete necrosis was not recorded. Among the defense genes, sesquiterpene cyclase, chitinase, and proteinase inhibitor type II were induced in plants, and high transcript abundance continued for at least a week for the latter two genes. Similar to the pathogen, JA, ethylene, and SA pathways were activated in plants, albeit for longer durations [185]. The same authors suggested that the perception of algal polysaccharides might be initiated by receptors on the plasma membrane.
Similarly, Sangha et al. [186] investigated the effects of Microorganisms 2022, 10, x FOR PEER REVIEW defense pathways, including sesquiterpene cyclase, chitina II, were induced, but the activities usually disappeared in ways were activated in plants by the pathogen. After the ap roscopic changes that were similar to the ones that are ind served. However, complete necrosis was not recorded. Am erpene cyclase, chitinase, and proteinase inhibitor type II w transcript abundance continued for at least a week for the pathogen, JA, ethylene, and SA pathways were activated tions [185]. The same authors suggested that the perceptio be initiated by receptors on the plasma membrane. Similarly, Sangha et al. [186] investigated the effects induction of defense responses in Arabidopsis thaliana ecoty ogenic fungus Sclerotinia sclerotiorum. While λ-carrageen to infection, the ones that were treated with Ɩ-carrageenan related genes were induced in the former. Additionally, activity were detected in plants that were treated with λ-c acid that is secreted by the fungus for infection. The aut sponses of the plant to Ɩand λ-carrageenans and to the hi Laminarin, a linear β-1,3 glucan ( Figure 4) is a long-te algae [187]. Incubation of tobacco cv BY cells with lamina responses, including rapid alkalinization of the culture m tion of the phenylpropanoid pathway that was demonstr lyase (PAL) activity at 4 h, caffeic acid O-methyltransfera h, and a strong increase in SA from 6 h to 48 h. Similar induced, as demonstrated by lipoxygenase (LOX) activit hours of incubation with laminarin. On the other hand, in NN plants with laminarin resulted in the induction of fo lated (PR) proteins (PR1, PR2, PR3, and PR5), which have a defense reactions protected the tobacco leaves against inf -and λ-carrageenans on the induction of defense responses in Arabidopsis thaliana ecotype Col-0 against the phytopathogenic fungus Sclerotinia sclerotiorum. While λ-carrageenan-treated plants were resistant to infection, the ones that were treated with Microorganisms 2022, 10, x FOR PEER REVIEW defense pathways, including sesquiterpene cyclase, chitinase, and p II, were induced, but the activities usually disappeared in 24 h. JA, ways were activated in plants by the pathogen. After the application roscopic changes that were similar to the ones that are induced by served. However, complete necrosis was not recorded. Among the erpene cyclase, chitinase, and proteinase inhibitor type II were indu transcript abundance continued for at least a week for the latter tw pathogen, JA, ethylene, and SA pathways were activated in plants, tions [185]. The same authors suggested that the perception of algal be initiated by receptors on the plasma membrane.
Similarly, Sangha et al. [186] investigated the effects of Ɩand induction of defense responses in Arabidopsis thaliana ecotype Col-0 ogenic fungus Sclerotinia sclerotiorum. While λ-carrageenan-treated to infection, the ones that were treated with Ɩ-carrageenan were su related genes were induced in the former. Additionally, increase activity were detected in plants that were treated with λ-carrageena acid that is secreted by the fungus for infection. The authors attri sponses of the plant to Ɩand λ-carrageenans and to the higher sulf Laminarin, a linear β-1,3 glucan ( Figure 4) is a long-term storag algae [187]. Incubation of tobacco cv BY cells with laminarin trigge responses, including rapid alkalinization of the culture medium an tion of the phenylpropanoid pathway that was demonstrated by a lyase (PAL) activity at 4 h, caffeic acid O-methyltransferase up-reg h, and a strong increase in SA from 6 h to 48 h. Similarly, the fa induced, as demonstrated by lipoxygenase (LOX) activity that wa hours of incubation with laminarin. On the other hand, infiltration -carrageenan were susceptible. JA pathway-related genes were induced in the former. Additionally, increased oxalase and oxidase activity were detected in plants that were treated with λ-carrageenan, offsetting the tions [185]. The same authors suggested that the perception of algal polysaccharides might be initiated by receptors on the plasma membrane.
Similarly, Sangha et al. [186] investigated the effects of Ɩand λ-carrageenans on the induction of defense responses in Arabidopsis thaliana ecotype Col-0 against the phytopathogenic fungus Sclerotinia sclerotiorum. While λ-carrageenan-treated plants were resistant to infection, the ones that were treated with Ɩ-carrageenan were susceptible. JA pathwayrelated genes were induced in the former. Additionally, increased oxalase and oxidase activity were detected in plants that were treated with λ-carrageenan, offsetting the oxalic acid that is secreted by the fungus for infection. The authors attributed the different responses of the plant to Ɩand λ-carrageenans and to the higher sulfation in the latter [186].
Laminarin, a linear β-1,3 glucan ( Figure 4) is a long-term storage compound in brown algae [187]. Incubation of tobacco cv BY cells with laminarin triggered multi-step defense responses, including rapid alkalinization of the culture medium and H2O2 release, induction of the phenylpropanoid pathway that was demonstrated by a strong Phe ammonialyase (PAL) activity at 4 h, caffeic acid O-methyltransferase up-regulation at 2 h until 25 h, and a strong increase in SA from 6 h to 48 h. Similarly, the fatty acid pathway was induced, as demonstrated by lipoxygenase (LOX) activity that was induced within four hours of incubation with laminarin. On the other hand, infiltration of tobacco cv Samsun NN plants with laminarin resulted in the induction of four families of pathogenesis-related (PR) proteins (PR1, PR2, PR3, and PR5), which have antimicrobial activities. All these defense reactions protected the tobacco leaves against infection by the bacterium Erwinia carotovora subsp. carotovora, which causes soft rot disease [188]. Similarly, laminarin induced defense responses in grapevine (Vitis vinifera L.), which included H2O2 release, calcium uptake, alkalinization of the culture medium, and induction of mitogen-activated protein kinases. The defense responses in the grapevine also included the upregulation of defense-related genes, such as 9-lipoxygenase (Lox) and glutathione-S-transferase (Gst), phenylalanine ammonia lyase (Pal), stilbene synthase 1 (Sts1), polygalacturonase-inhibiting protein (Pgip), basic class I, acidic class III, and acidic class IV chitinase genes, class I β-1,3-glucanases gene Glu1, and serine protease (Pin) genes. Laminarin also caused the production of antimicrobial phytoalexins in the grapevine. These defense reactions protected grapevine against Botrytis cinerea and Plasmopara viticola infections [85].
The presence of β-1,3-glucans in the unicellular eukaryotic members of Bacillariopyhta and Chryosophyceae, and in Nannochloropsis gaditana of Eustigmatophyceae [189,190] opens new avenues of research for their effects in plant defense metabolism. It also provides an opportunity to mass culture these microalgae, preferably within a biorefinery approach, where β-1,3-glucan-separated biomass can be used for other purposes (e.g., feed supplement, pigment source, biofuel feedstock).
An extract of Ulva spp. was tested as an elicitor in Medicago truncatula. After the application of Ulva extract, the expression patterns of mainly defense-related genes were undertaken using a macroarray. In addition to the aforementioned defense-related genes, the upregulation of genes for the cell wall proteins calmodulin, ribonuclease, and aquaporin was observed. Genes that were involved in carbon and nitrogen metabolism were not down-regulated, suggesting that the induction of defense genes did not affect primary metabolism. The Ulva extract protected M. truncatula against the fungal pathogen Colletotrichum trifolii, which causes anthracnose disease [67].
-and λ-carrageenans and to the higher sulfation in the latter [186]. Laminarin, a linear β-1,3 glucan ( Figure 4) is a long-term storage compound in brown algae [187]. Incubation of tobacco cv BY cells with laminarin triggered multi-step defense responses, including rapid alkalinization of the culture medium and H 2 O 2 release, induction of the phenylpropanoid pathway that was demonstrated by a strong Phe ammonia-lyase (PAL) activity at 4 h, caffeic acid O-methyltransferase up-regulation at 2 h until 25 h, and a strong increase in SA from 6 h to 48 h. Similarly, the fatty acid pathway was induced, as demonstrated by lipoxygenase (LOX) activity that was induced within four hours of incubation with laminarin. On the other hand, infiltration of tobacco cv Samsun NN plants with laminarin resulted in the induction of four families of pathogenesis-related (PR) proteins (PR1, PR2, PR3, and PR5), which have antimicrobial activities. All these defense reactions protected the tobacco leaves against infection by the bacterium Erwinia carotovora subsp. carotovora, which causes soft rot disease [188]. Similarly, laminarin induced defense responses in grapevine (Vitis vinifera L.), which included H 2 O 2 release, calcium uptake, alkalinization of the culture medium, and induction of mitogen-activated protein kinases. The defense responses in the grapevine also included the upregulation of defense-related genes, such as 9-lipoxygenase (Lox) and glutathione-S-transferase (Gst), phenylalanine ammonia lyase (Pal), stilbene synthase 1 (Sts1), polygalacturonase-inhibiting protein (Pgip), basic class I, acidic class III, and acidic class IV chitinase genes, class I β-1,3-glucanases gene Glu1, and serine protease (Pin) genes. Laminarin also caused the production of antimicrobial phytoalexins in the grapevine. These defense reactions protected grapevine against Botrytis cinerea and Plasmopara viticola infections [85].
The presence of β-1,3-glucans in the unicellular eukaryotic members of Bacillariopyhta and Chryosophyceae, and in Nannochloropsis gaditana of Eustigmatophyceae [189,190] opens new avenues of research for their effects in plant defense metabolism. It also provides an opportunity to mass culture these microalgae, preferably within a biorefinery approach, where β-1,3-glucan-separated biomass can be used for other purposes (e.g., feed supplement, pigment source, biofuel feedstock).
An extract of Ulva spp. was tested as an elicitor in Medicago truncatula. After the application of Ulva extract, the expression patterns of mainly defense-related genes were undertaken using a macroarray. In addition to the aforementioned defense-related genes, the upregulation of genes for the cell wall proteins calmodulin, ribonuclease, and aquaporin was observed. Genes that were involved in carbon and nitrogen metabolism were not downregulated, suggesting that the induction of defense genes did not affect primary metabolism. The Ulva extract protected M. truncatula against the fungal pathogen Colletotrichum trifolii, which causes anthracnose disease [67].
Tobacco leaves that were treated with sulphated fucans (Figure 4) exhibited defensive responses against the tobacco mosaic virus. The oligofucans, in this case, also stimulated the SA pathway and the expression of pathogenesis-related proteins [191].
During a fungal infection, some plant species recognize the chitin (poly-(1→4)-βlinked N-acetyl-D-glucosamine) components in fungal cell walls and induce lignification as a defense mechanism to prevent further fungal damage. This was initially demonstrated in wounded wheat leaves when crab and fungal chitin, chitosan, and ethylene glycol chitin were applied as elicitors [192]. Later work demonstrated the induction of chitinase in melon seedlings upon treatment with varying concentrations of chitin oligosaccharides. The same study suggested the hexamer or heptamer chitin oligomer as the optimal size for maximum chitinase activity [193]. Kaku et al. [194] identified a high-affinity binding protein for chitin in the plasma membrane of rice cells. The knockdown of the receptor gene by RNA interference shut down the chitin-induced defense responses. Further work demonstrated that, in addition to this membrane receptor glycoprotein, a receptor kinase was also required for chitin-based elicitor response in rice [195].
Chitin is naturally found in the exoskeletons of crustaceans and the cell walls of fungi. Industrial production of chitin utilizes crustaceans, such as crabs and shrimp. The isolation of chitin from these sources is a lengthy process, including treatment with HCl and then with NaOH, increasing the cost of production [196]. Less known is the presence of chitin in some algal groups, such as green algae and diatoms [197]. Especially some diatom species from the Cyclotella and Thallassiosira genera synthesize chitin as nanofibers and extrude through pores on the frustule. The extruded chitin nanofiber is in the form of β-chitin, which is easier to dissolve and modify compared to α-chitin [198]. Moreover, extruded chitin can be readily isolated from the culture medium.
Within a biorefinery approach, a diatom biomass can be produced to obtain various valuable chemicals, including lipids and chitin [199]. The leftover diatom frustules will also have the potential to be used as an insecticide. Diatomaceous earth (DE) is formed from fossilized diatoms dating back 20 to 80 million years. DE contains about 50% moisture and up to 94% silica of dry weight. After mining, the moisture is reduced, and the DE is milled to reduce the particle size to between 10-50 µm. DE is safe for humans, and among many uses, it is also an effective insecticide. After application, DE dust is picked up by insect bodies, where DE damages the wax coat of insects. This results in water loss from the body of insects, causing desiccation and death [200]. Therefore, leftover diatom frustules would be a valuable side product, where all components of diatom biomass can be utilized.   [201]. Salicylic acid (SA) biosynthesis starts with chorismate in the chloroplast and SA is transported into the cytosol [202]. Ethylene (ET) biosynthesis starts with methionine and ET is recognized by receptors on the endoplasmic reticulum. All three pathways eventually lead to defense gene expression and evidence suggest crosstalk between these pathways [203].

Inhibition of Quorum Sensing
Although algal extracts or metabolites exert antimicrobial properties, knowledge on the mechanism of action of these substrates against plant pathogens is limited. A notable example is the production of halogenated furanones by the red alga Delisea pulchra. Early investigations revealed that D. Pulchra produced secondary metabolites that prevented fouling on its surface [204]. These secondary metabolites, namely halogenated furanones, were proposed to biomimic acylated homoserine lactones (AHLs) [205], which are signalling molecules that are involved in quorum sensing for the colonization of Gram-negative bacteria [206]. This led Manefield et al. [207] to test a synthetic halogenated furanone for the inhibition of N-3-oxohexanoyl-L-homoserine lactone (3-oxo-C6-HSL) in the plant pathogen Erwinia carotovora subsp. carotovora. Its metabolite 3-oxo-C6-HSL regulated the  [201]. Salicylic acid (SA) biosynthesis starts with chorismate in the chloroplast and SA is transported into the cytosol [202]. Ethylene (ET) biosynthesis starts with methionine and ET is recognized by receptors on the endoplasmic reticulum. All three pathways eventually lead to defense gene expression and evidence suggest crosstalk between these pathways [203].

Inhibition of Quorum Sensing
Although algal extracts or metabolites exert antimicrobial properties, knowledge on the mechanism of action of these substrates against plant pathogens is limited. A notable example is the production of halogenated furanones by the red alga Delisea pulchra. Early investigations revealed that D. Pulchra produced secondary metabolites that prevented fouling on its surface [204]. These secondary metabolites, namely halogenated furanones, were proposed to biomimic acylated homoserine lactones (AHLs) [205], which are signalling molecules that are involved in quorum sensing for the colonization of Gram-negative bacteria [206]. This led Manefield et al. [207] to test a synthetic halogenated furanone for the inhibition of N-3-oxohexanoyl-L-homoserine lactone (3-oxo-C6-HSL) in the plant pathogen Erwinia carotovora subsp. carotovora. Its metabolite 3-oxo-C6-HSL regulated the production of extracellular degradative enzymes and a carbapenem antibiotic, where both processes help the bacterium to infect terrestrial plants [207]. The results suggested that the halogenated furanone inhibited carbapenem production and reduced the production of extracellular enzymes, the exact mechanisms of which were not clear. Other work demonstrated that D. pulchra furanones might displace AHL from its binding site, which is a transcriptional activator (i.e., Lux R protein) [208,209]. Follow-up work by Manefield et al. [210] failed to detect furanone binding to the LuxR protein that is expressed in E. coli. Instead, their results showed decreased concentrations of cytoplasmic LuxR protein when furanone is added, which led them to suggest halogenated furanones interacted with LuxR causing conformational change for rapid degradation.

Neurotoxicity
Although there is a lack of information regarding the mechanism of action of algal metabolites against agricultural pest insects, limited work that was performed with other insects might provide some clues. Watanabe et al. [215] reported the insecticidal activities of two halogenated monoterpenes, aplysiaterpenoid A and telfairine (Figure 3), from the red alga Plocamium telfairiae. Aplysiaterpernoid A and telfairine caused 60% and 80% mortality in the German cockroach (Blatella germanica), respectively. Telfairine also caused random firings in the central nervous system, similar to the effects of (1246/35)-1,2,3,4,5,6-hexachlorohexane (γ-BHC), an organochlorine insecticide. Their modelling studies suggested that both aplysiaterpenoid A and telfairine might act on the picrotoxinin receptors of insects.
Extracts of the macroalga Prasiola crispa were shown to possess insecticidal properties in fruit fly (Drosophila melanogaster) and cockroach (Nauphoeta cinerea) [216]. In a follow-up study, Prasiola crispa extracts and its phytosterols, namely β-sitosterol, campesterol and stigmasterol (Figure 3), exhibited insecticidal activities in the cockroach Nauphoeta cinerea [217]. To understand the mechanism of action of the extracts and isolated compounds, the authors performed acetylcholinesterase activity assays, semi-isolated heart preparations to determine heartbeats, grooming activity assays, and cockroach neuromuscular function assays. The cockroach brain preparations did not reveal any acetylcholinesterase activity. However, the algal extract caused a significant and reversible drop in the heartbeats in the cockroach semi-isolated heart preparations and a significant change in the grooming activity. The extracts and the aforementioned phytosterols also caused neuromuscular inhibition, which was reduced by the application of phentolamine, an octopamine receptor inhibitor. Altogether, these results suggested the involvement of octopaminergic-cholinergic pathways in the insecticidal activity of this Antarctic macroalga [217].

Production of Antimetabolites
An antimetabolite may bind to an enzyme as the native substrate does; however, it is not converted to a functional product. Therefore, antimetabolites may compete with the natural substrates and may block an enzyme's catalytic activity. Brilisauer et al. [134] observed growth inhibition of the cyanobacterium Anabaena variabilis ATCC 29,413 by the spent culture media of the cyanobacterium Synechococcus elongatus PCC 7942. The isolation and chemical characterization of the extracellular inhibitory compounds proved the presence of 7-deoxysedoheptulose (7dSh) ( Figure 5). Incubation of A. variabilis with puri-fied 7dSh resulted in the accumulation of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) in cells, which is the natural substrate of 3-dehydroquinate (DHQ) synthase. The results suggested that 7dSh was the antimetabolite of DAHP, the native substrate of the DHQ synthase in the shikimate biosynthesis pathway [134,218]. Accordingly, the inhibition of this pathway disturbed protein synthesis by inhibiting aromatic amino acid biosynthesis [134]. The shikimate pathway occurs in bacteria, fungi, and plants, but not in animals [219]. As expected, 7dSh inhibited the growth of Saccharomyces cerevisiae and Arabidopsis thaliana. No cytotoxicity was detected in mammalian cells, potentially making 7dSh an ideal antibacterial, antifungal, or herbicidal compound.

Blocking Virus Entry into the Plant
Sodium alginate (Figure 4) is a commercial gelling product that is obtained from brown seaweeds [220]. Sano et al. [21] investigated the inhibitory activity of alginate on the infection of tobacco leaves with tobacco mosaic virus (TMV). This polysaccharide did not inactivate TMV. However, its application on leaves reduced TMV infectivity, with the reduction being proportional to the salginate concentration and stiffness of the polysaccharide. The addition of sodium alginate caused TMV particles to form large aggregates on the cell surface, blocking TMV RNA entry into the plant cells. The authors also suggested that anions of the polysaccharide might have interacted with the cationic amino groups of TMV, preventing interaction with the anionic phosphate groups of the cell membrane.

Conclusions
Extensive research in the past decades on macro-and microalgal species has resulted in the discovery of an impressive array of extracts and bioactive compounds with pesticidal action for application in agricultural practices. These compounds have been used effectively as standalone treatment against agricultural pests, but their full potential can be revealed by combining them with other techniques in the context of integrated pest management. Moreover, even though a lot of progress has been recorded so far in deciphering their mode of action, more knowledge is expected to be produced in the future in this regard. Conservative estimates suggest the number of current algal species to be over 70,000 [221]. Yet, only a small number of these species have been investigated for their effects on other organisms (e.g., antimicrobial effects), mainly in the area of medicine. Concerning the long evolutionary history of algae and their distribution in highly diverse ecological settings from freshwaters to terrestrial ecosystems, one can expect a myriad of different metabolites from algae. This seems to be the case with novel secondary metabolites that are continuously reported from various algal species. Based on the discovery of active metabolites in medicine, where most of the work is done, similar results against plant pathogens can be expected. A limited number of biopesticidal extracts or compounds from algae have usually been reported from seaweeds or cyanobacteria. Therefore, macro-and microalgae represent a large untapped resource for the discovery of novel biopesticide compounds.