Photorhabdus belongs to the family Enterobacteriaceae and is a Gram-negative bacterium symbiotically associated with the gut of Heterorhabditis, an entomopathogenic nematode (Forst et al., 1997). It is the only well-known terrestrial bioluminescent bacterium reported from the gut of IJs (infective juveniles) in EPNs. In the case of Heterorhabditidae, IJs do ambush, and they do not move in search of host and enter its body through natural openings (Figure 1). Once, it reaches the blood system of the host, the IJs regurgitates 50–200 bacterial cells (Ciche and Ensign, 2003) to conquer the immune system of the host and kill the host with septicemia. The IJs reproduce and multiply a few generations inside the host. The dead host raises the challenge of the Photorhabdus as it has to successfully compete with saprophytic scavengers, such as protists, other bacteria, nematodes, fungus, and even insects (Waterfield et al., 2009). In response, this symbiont produces a wide range of bioactives to cope up with the challenges for successful establishment and survival (Lulamba et al., 2021). Based on phenotypic characterization and DNA relatedness, Photorhabdus has been classified broadly into three species, i.e., Photorhabdus luminescens, Photorhabdus asymbiotica, and Photorhabdus temperata. This classification has been confirmed through limited microarray analysis (Marokhazi et al., 2003), genomic studies, and multilocus sequence typing (Duchaud et al., 2003; Gerrard et al., 2004). More recently, Machado et al. (2018) have proposed Photorhabdus subspecies to the species level and described one novel Photorhabdus bodei sp. and new Photorhabdus laumonii subspecies based on whole genome study. Photorhabdus species are facultative anaerobic and highly motile rods (Peel et al., 1999). All species produce a unique thin line of annular hemolysis on blood agar and grow well at 28°C. The clinical isolates grow from a temperature range of 37–42°C (Hapeshi et al., 2020). All the strains show bioluminescence on both liquid medium and agar plates, which peaks at exponential phase. The development of Heterorhabditis requires exogenous sterols (Chitwood, 1999), which are provided by the Photorhabdus to ensure successful symbiosis. Photorhabdus produces iso-branched fatty acids (BCFAs) through bkdABC operon (Joyce et al., 2008) for the nematode partner. For nematode nutrition, Photorhabdus produces CipA, CipB (crystalline inclusion proteins), and secondary metabolites, such as stilbene (ST), called 3,5-dihydroxy-4-isopropylstilbene (Joyce et al., 2008). Photorhabdus is the only non-plant organism that produces STs, a polyketide molecule. The biochemical pathway for the production of ST is different from that of plants and is well characterized (Williams et al., 2005; Joyce et al., 2008). InPtNC19, phosphopantethienyl (PPANT) transferase (ngrA gene) is vital for secondary metabolite synthesis, as well as nematode growth and reproduction (Ciche et al., 2001). In Photorhabdus, almost 6% genome is occupied by genes involved in secondary metabolite production, which is much greater than that of Streptomyces, the model organism for the production of secondary metabolite (Duchaud et al., 2003). Streptomyces uses 3.8% genome only and is a source of more than 90% clinically important antibiotics (Waterfield et al., 2009). This emphasizes the significant potential of Photorhabdus as a source of novel bioactive compounds. Studies have reported that Photorhabdus expresses two virulence factors, i.e., Tca (toxin complex A) and PrtA (metalloprotease) (Daborn et al., 2001; Silva et al., 2002). Recently, studies have also reported antimicrobial activities of compounds isolated from Photorhabdus species strain ETL in association with Heterorhabditis zealandica (Lulamba et al., 2021).

An overview of general mode of action of these compounds against different insect pest is shown in Figure 2.

A new cyclic lipopeptide, phototemtide A (1), was isolated from Escherichia coli expressing the biosynthetic gene cluster pttABC from Photorhabdus temperata Meg1. This new cyclic lipopeptide has three more minor derivatives. It has been reported that this peptide has weak antiprotozoal activity with IC₅₀ = 9.8 μM, against deadly plasmodium species Plasmodium falciparum (Zhao et al., 2020). New peptide drugs have gained attention due to their easy synthesis, low toxicity, fewer side effects, and rapid elimination (Du et al., 2015). The quantity of market active constituents is very less due to unpleasant side effects and observed resistance (Weinke et al., 1991; Steketee et al., 1996; Plowe, 2005; Uhlemann and Krishna, 2005). This compound is selectively effective against Plasmodium falciparum and maybe a potential antiprotozoal alternative in the future.

A cyclic peptide photoditritide, which was isolated from Photorhabdus temperata Meg1, which contains two rare amino acid D-homoarginine residues and encoded by pdtS gene. The gene pdtS codes for non-ribosomal peptide synthetase having six modules with 18 domains in all. It showed weak antiprotozoal activity against causative agent of African sleeping sickness, i.e., Trypanosoma brucei rhodesiense with IC₅₀ = 13 μM (Zhao et al., 2019). Peptides containing homoarginine, a non-proteinogenic amino acid, have been reported from many marine organisms, such as cyanobacteria, actinomycetes, and sponge, but photoditritide is the only example of peptide containing homoarginine derived from entomopathogenic bacteria (Bonnington et al., 1997; Saito et al., 2001; Cha et al., 2012; Zhao et al., 2019).

This is a class of natural products produced by Photorhabdus luminescens TT01. Many derivatives of this class have been synthesized by modifying PAL gene and antB gene in Photorhabdus luminescens mutant (BMM901), such as cyclohexanedione (CHD) and dialkylresorcinol (DAR) derivatives (Joyce et al., 2008; Kronenwerth et al., 2014). The biosynthesis of isopropylstilbene from Photorhabdus varies from plant stilbene biosynthesis, whereby two acyl moieties become condensed to form a resorcinol ring (Ferrer et al., 2008; Joyce et al., 2008; Fuchs et al., 2013). Synthetic derivatives, such as 12–14 and 1 and 6, were reported to be more effective against Trypanosoma cruzi (causes Chagas disease) and Plasmodium falciparum (causes malaria), respectively. Some chemically synthesized derivatives were more active against Trypanosoma cruzi (LC₅₀ = 8.80 μM) and Leishmania donovani (LC₅₀ = 3.71 μM) (Kronenwerth et al., 2014). This potent class of antiprotozoal compounds can meet the needs of pharmaceutical sector in the future.

Photorhabdus luminescens, an entomopathogenic bacterium bears a flag of producing the largest and continuous non-ribosomal peptide synthetase among bacteria (Bode et al., 2015). It possesses a fully functional uninterrupted gene that could produce 15 consecutive modules encoded by kol gene (plu2670, 49.1 kbp). Many gene clusters of its genome are involved in biosynthesis of diverse natural products (Duchaud et al., 2003; Yin et al., 2015). Photorhabdus luminescens produces kolossin A, a d-/l-pentadecapeptide biosynthetic product of non-ribosomal peptide synthetase. It has been reported that stereoisomer of Kolossin A, displays high activity against the causative agent of African sleeping sickness, i.e., Trypanosoma brucei rhodesiense (IC₅₀ = 2.7μM), Plasmodium falciparum (IC₅₀ = 16.1μM), and T. brucei r. (IC₅₀ = 8.9μM) (Bode et al., 2015). This class of antiprotozoal compounds can prove to be useful for drug discovery against deadly protozoal diseases in the near future (Figure 3 and Table 1).

Photorhabdus Temperata M1021 Produces Benzaldehyde as an Insecticidal, Antimicrobial, and Antioxidant Compound.

Antimicrobial activity was assessed by MIC values ranging from 6 to 10 mM for bacterial strains and 6–10 mM for fungal strains, i.e., Phytophthora capsici (IC₅₀ = 5.7 mM), Corynespora cassiicola (IC₅₀ = 8.1 mM), and Rhizoctonia solani (IC₅₀ = 6.0 mM) (Ullah et al., 2015). Studies claim that the interaction of benzaldehyde with the cell surface triggers cell membrane disintegration and intracellular constituent release, which leads to cell death (Cheng et al., 2009).

These classes of compounds are phenolics. It has been reported that seven derivatives of stilbene, i.e., 3-hydroxy-2-isopropyl-5-phenethylphenyl carbamate,2-(1-hydroxypropan-2-yl)-5-[(E)-2-phenylethenyl]benzene-1,3-diol, 2-(1-hydroxypropan-2-yl)-5-[2-phenylethyl]benzene-1,3-diol, 2-ethyl-5-(2-phenylethyl) benzene-1,3-diol, 2-isopropyl-5-[2-phenylethyl]benzene-1, 3-diol, 2-isopropyl-5- [(E)-2-phenylethenyl]benzene-1,3-diol, and 2-ethyl-5-[(E)-2-phenylethenyl]benzene-1,3-diol showed antifungal activity against four phytopathogenic fungi, such as Rhizoctonia solani Kuhn, Pythium aphanidermatum, Fusarium oxysporum, and Exserohilum turcicum (Paul et al., 1981; Fuchs et al., 2013). Out of these seven derivatives, 3-hydroxy-2-isopropyl-5-phenethylphenyl carbamate strongly inhibits Pythium aphanidermatum mycelium at EC₅₀ = 2.8 and 2.7 μg/ml, respectively. The presence of acyl amino group in the former and isopropyl group in the latter contributed to inhibitory activity of these compounds.

This class of compound is a small molecule possessing antibiotic properties and food preservative (US patent doc numbers 6036986; 6042861) (Si et al., 2006; Wong et al., 2008; Chen et al., 2011; Hakkim et al., 2012). It has been reported that TCA is a necessary precursor for biosynthesis of the antibiotic stilbene (Williams et al., 2005; Eleftherianos et al., 2007; Chalabaev et al., 2008). Studies have established that TCA produced by Photorhabdus luminescens shows antimycotic activity against two important plant pathogens belonging to two fungal genera Colletotrichum and Fusicladium. In vitro studies have confirmed the toxicity of TCA against Colletotrichum gloeosporioides, Colletotrichum acutatum, Colletotrichum fragariae, and Fusicladium effusum (Bock et al., 2014). Recently, researchers have discovered phenylalanine ammonia-lyase (PAL) gene from Photorhabdus luminescens DSM 3368, which has enhanced the value of this strain for the production of TCA at commercial level (Zhang et al., 2021; Figure 4 and Table 1).

This novel compound belongs to the luminmycin metabolite family and is produced by Photorhabdus asymbiotica in laboratory culture. Photorhabdus asymbiotica has a unique, biphasic lifestyle as both a symbiotic and pathogenic bacterium. Genomic analysis revealed several synthetic gene clusters capable of producing secondary metabolites. Photorhabdus asymbiotica can produce cytotoxic derivatives, such as glidobactin A, luminmycin D, and luminmycin A. These compounds show cytotoxicity against pancreatic cells (IC₅₀ = 0.11 μM) and inhibit proteasome (IC₅₀ = 0.38 μM) (Theodore et al., 2012). Sequencing and annotation of the Photorhabdus asymbiotica (ATCC43949) genome have also been reported (Wilkinson et al., 2009). Recently, studies have reported cepafungin 1 and (GLNPs) glidobactin A produced by Photorhabuds laumondii as potent anticancer agents (Zhao et al., 2021).

This novel compound epoxide 1, is also known as 2-isopropyl-5-(3-phenyl-oxiranyl)-benzene-1,3-diol. It was isolated from Galleria mellonella larvae infected with Photorhabdus luminescens C9-Heterorhabditis megidis 90 symbiont complexes (tripartite interaction, insect-nematode, and bacterium). Epoxide 1 has been derived from 2-isopropyl-5-(2-phenylethenyl)-benzene-1,3-diol (Hu et al., 1997, 1998). Epoxide 1 was active against Bacillus subtilis, Escherichia coli, Streptococcus pyogenes, and a drug-resistant, clinical strain of Staphylococcus aureus (RN4220) with minimum inhibitory concentrations in the range of 6.25–12.5 μg/ml. Epoxide 1 was cytotoxic against human cancer cell lines, MCF-7 wt, H460, and Jurkat, with GI (50) of 2.14, 0.63, and 0.42 μM, respectively, but was less toxic on normal, mouse splenic lymphocytes with a GI (50) of 45.00 μM (Hu et al., 2006).

Lumizinones are produced exclusively from the pathogenic form, a phenotypic variant of Photorhabdus, which is associated with insect pathogenesis and nematode development. Photorhabdus. This compound inhibits calpain protease activity at IC₅₀ = 3.9 μM (Park and Crawford, 2016). Calpain is a heterodimer having two subunits, i.e., regulatory subunit (30 kDa) and catalytic subunit (80 kDa). It belongs to the intracellular cysteine proteases family, Ca²⁺-dependent, and distributed in the cytoplasm of cells and tissues in eukaryotes (Sato and Kawashima, 2001; Goll et al., 2003; Park and Crawford, 2016). Calpains are associated with cancer like schwannomas and meningiomas, renal cell carcinoma, colorectal adenocarcinoma, squamous carcinomas of the skin, prostate cancer, endometrial cancer, uterine sarcomas and carcinosarcomas, uterine cervical, neoplasiamelanoma, gastric cancer, laryngeal, colorectal, and pancreatic cancer (Kimura et al., 1998; Braun et al., 1999; Yoshikawa et al., 2000; Mamoune et al., 2003; Reichrath et al., 2003; Rios-Doria et al., 2003; Lakshmikuttyamma et al., 2004; Frances et al., 2007; Lee et al., 2007, 2008; Moretti et al., 2009; Fong et al., 2010; Salehin et al., 2010; Moreno et al., 2011; Figure 5 and Table 1).

These quinones are derived from anthracene and are widely used in cosmetics, food, dyes, and pharmaceuticals. Over the years, many anthraquinone derivatives have been identified from bacteria, plants, insects, and fungi having a wide array of bioactivity like anticancer, laxation, neuroprotective, antimalaria, and anti-inflammatory effects (Bonadonna et al., 1969; Monks et al., 1992; Van Gorkom et al., 2002; Pankewitz et al., 2007; Wang et al., 2007; Batista et al., 2009; Kim et al., 2009; Gessler et al., 2013; Lim et al., 2017; Wu et al., 2017).

Recently, Photorhabdus temperata has been reported as a source of anti-neuroinflammatory and neuroprotective drug leads, such as 1, 3, 8-trihydroxy-9, 10-anthraquinone, and 3, 8-dihydroxy-1-methoxy-9, 10-anthraquinone. An earlier compound has shown significant protection of hippocampal neuronal cells (HT22) at 75 μM in mouse against glutamate-induced cell death (5 mM) caused via lipid peroxidation, Ca²⁺ influx, and inhibiting reactive oxygen species production. Both the compounds have also been reported to suppress neuroinflammation induced by interferon γ in microglial cells (BV2) of mouse at a concentration of 10 ng/ml through reduction of interleukin-6, TNF (tumor necrosis factor-α), and nitric oxide (Yang et al., 2018; Figure 6 and Table 1).

It is a 12-member macrolactam ring system that is linked with a fatty acid tail, terminally branched, and having additional methyl moiety. This compound has been reported to be produced by Photorhabdus luminescens. This compound is similar to one of the strongest proteasome inhibitors Glidobactin A (GlbA) (Oka et al., 1988; Shoji et al., 1990; Groll et al., 2008).

Photorhabdus asymbiotica-produced compound luminmycin D is also a potent proteasome inhibitor at IC₅₀ value equal to 0.38 μM (Theodore et al., 2012).

This is a simplest aromatic aldehyde made up of benzene ring and formyl components. Photorhabdus temperata M1021 has been reported to produce this compound (Ullah et al., 2015). This compound shows antimicrobial properties against Bacillus anthracis RSC-9 (IC₅₀ = 5.0 mM), Pantoea conspicua RSC-6 (IC₅₀ = 6.1 mM), Enterobacter cowanii RSC-3 (IC₅₀ = 4.5 mM), Citrobacter youngae RSC-5 (IC₅₀ = 7 mM), and Bacillus aryabhattai RSC-7 (IC₅₀ = mM).

This compound has been reported from Photorhabdus temperata Meg1. This compound shows antimicrobial potential against bacterium Micrococcus luteus at an MIC value equal to 3.0 μM (Zhao et al., 2019).

This compound has been isolated from Photorhabdus luminescens. Studies have reported that this compound (2-isopropyl-5-(3-phenyl-oxiranyl)-benzene-1, 3-diol) is active against Escherichia coli, Streptococcus pyogenes, Bacillus subtilis, and Staphylococcus aureus (RN4220) at an inhibitory concentration ranging from 6.25 to 12.5 μg/ml (Hu et al., 2006; Figures 3, 4 and Table 1).

This is an insecticidal compound produced by Photorhabdus temperata M1021. Studies have shown that it caused 100% mortality in G. mellonella at 8 mM concentration. It is toxic to insects and inhibited PO activity from 15 to 80% at different concentrations (Ullah et al., 2015).

This class of molecule is an amidoglycosyl- and vinyl-isonitrile-functionalized tyrosine derivative produced by Photorhabdus luminescens. This compound targets the innate immune system of the insect through a key component called phenoloxidase in G. mellonella and has emerged as a potential lead for the formation of insecticides (Crawford et al., 2012).

This compound is a simple urea compound produced by Photorhabdus luminescens. Studies have shown that it inhibits juvenile hormone epoxide hydrolase (JHEH), which is an important enzyme in the growth and development of insects. This makes it a more suitable chemical with insecticidal properties (Nollmann et al., 2015b).

This is a small molecule having antibiotic properties and is produced by Photorhabdus luminescens in both in vivo as well as in vitro conditions. Cinnamic acid is a precursor of ST and is catalyzed by an enzyme encoded by stlA gene, which is a Photorhabdus gene (Eleftherianos et al., 2007). Studies have shown that this compound shows a wide range of antimicrobial activity and defends dead insects from microbe invasion (Hu and Webster, 2000; Williams et al., 2005).

This class of compound has been isolated from Photorhabdus luminescens in dead G. mellonella larvae. This compound minimizes the competition between different microbes by inhibiting the growth of a wide range of bacterium (Li et al., 1995; Hu et al., 1998). This hypothesis is well supported in in vitro studies, but in vivo shreds of evidence are very less and have been questioned by Dutky (1959, 1974), Paul et al. (1981), Akhurst (1982), Li et al. (1995), Forst and Nealson (1996) and Jarosz (1996).

This compound was isolated from Photorhabdus temperata and has shown reliable insecticidal activity against G. mellonella (Figure 7 and Table 1).

Phospholipase A₂ (PLA₂) plays a key role in imparting immunity to insects as it releases arachidonic acid (AA) via its catalytic activity from phospholipids (Burke and Dennis, 2009). AA acts as precursor molecule in synthesis of eicosanoid. Eicosanoids are oxygenated C₂₀ polyunsaturated fatty acids. These eicosanoids are grouped into three main categories, namely, prostaglandins (PGs), epoxyeicosatrienoic acids (EETs), and leukotrienes (LTs) (Stanley, 2014). Cyclooxygenase, monooxygenases, and lipoxygenase oxygenate AA into PGs, EETs, and LTs, respectively (Stanley and Kim, 2019). However, in the case of terrestrial insects, linoleic acid (LA) is present, which becomes converted into AA with the help of elongase and desaturase enzymes (Hasan et al., 2019). Furthermore, PGs and LTs, in turn, activate phenol oxidase (PO) via formation of proPo and antimicrobial gene expression (AMP) (Shrestha and Kim, 2008; Shrestha et al., 2011). This PO catalyzes the process of melanization, which is a crucial event that leads to insect mortality (Castillo et al., 2011). Bioactive compounds rhabduscin have the ability to destruct the host’s epithelium and inhibit the catalytic activity of PLA₂ (Figure 2).

Gibberellins represent a group of tetracyclic compounds, diterpenoid compounds consisting of four isoprene units having an ent-gibberellane ring skeleton. It plays an essential role in germination, stem elongation, flowering, dormancy, sex expression, induction of enzymes, and senescence of fruit and leaf. This compound has been reported to be produced by Photorhabdus temperata M1021, a symbiont of entomopathogenic nematodes. Various bioactive GAs reported from Photorhabdus temperata M1021 through GC/MS-SIM analyses are GA1, GA3, GA4, GA7, GA9, GA12, and GA20 (Ullah et al., 2014b). GAs initiate cellular totipotency, seed germination, and plant growth (Großelindemann et al., 1992; Hedden and Kamiya, 1997; Table 1).

These pigments are secondary metabolites having carbonyl and methylene groups, or have precursors with this group. Studies have reported these compounds from Photorhabdus luminescens strain TT01 and linked these compounds with antibiotic activity (Ffrench-Constant et al., 2003).

Bacteriocin is a protein, which is produced by one species of bacteria to inhibit some other strain. Studies have shown that Photorhabdus aeruginosa produces R-type pyocins having modified tail fibers, which strongly bind to bacterial surfaces and advocate antibacterial activity (Eleftherianos, 2009). Photorhabdicins are compounds having structures similar to R-type pyocins, have been reported from K122 and W14 strains of Photorhabdus, and possess a vital role against microbes (Ffrench-Constant et al., 2003) (Figure 8).

This is another type of bacteriocin reported to be produced by the W14 strain of Photorhabdus luminescens (Sharma et al., 2002). It carries many killer proteins to counter the effect of many other bacteria strains (Sharma et al., 2002).

It is a class of antibiotics produced via biosynthetic pathways in cephamycins, penicillins, and cephalosporins (Williamson et al., 1985; Bycroft et al., 1988). It was reported that Photorhabdus luminescens TT01 possess a group of eight genes (cpmH to cpmA), which are responsible for carbapenem-like antibiotic production. This compound was found effective against Escherichia coli, Enterobacter cloacae, and Klebsiella pneumonia (Derzelle et al., 2002).

Many Anthraquinone (AQ) pigments have been reported from Photorhabdus (Richardson et al., 1988; Li et al., 1995). Two gene clusters (plu4186-plu4194) have been identified for the production of type II PKS, which is predicted to form an AQ heptaketide backbone (Duchaud et al., 2003). These compounds possess antibiotic potential (Richardson et al., 1988; Sztaricskai et al., 1992; Li et al., 1995; Brachmann et al., 2007). Two more anthraquinone derivatives, i.e., 1,3-dimethoxy-8-hydroxy-9,10-anthraquinone (major) and 3,8-dimethoxy-1-hydroxy9,10-anthraquinone (minor) have been reported from Photorhabdus luminescens (Li et al., 1995).

Among the hydroxystilbene family, 1,3-dihydroxy-2-(isopropyl)-5-(2-phenylethenyl) benzene (ST) is an important molecule. This is a small multifunctional compound produced by only one bacterium, i.e., Photorhabdus luminescens, and shows antibacterial properties (Akhurst, 1982; Richardson et al., 1988; Li et al., 1995; Williams et al., 2005). ST epoxide, another related compound having powerful antibiotic potential, has also been reported from Photorhabdus species (Hu et al., 2006). stlA gene is responsible for the production of stilbene antibiotic molecules (Williams et al., 2005). Reports of antibiotic, 3,5-dihydroxy-4-isopropylstilbene from Photorhabdus luminescens are also available (Li et al., 1995).

This compound is a precursor of the antibiotic 3,5-dihydroxy-4-isopropylstilbene (ST) (Williams et al., 2005; Eleftherianos et al., 2007). Antioxidant as well as antibacterial activities of this compound have been reported (Korkina, 2007). Photorhabdus luminescens studies have linked Hca enzyme with ST synthesis and CA utilization (Chalabaev et al., 2008).

This compound is a catechol-type siderophore produced by Photorhabdus luminescens having the structure 2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-oxazole-4-carboxylic acid [4-(2,3-dihydroxybenzoylamino)-butyl]-amide (Ciche et al., 2003). Purified photobactin also shows antibiotic activity (Paul et al., 1981; Akhurst, 1982; Richardson et al., 1988).

The bacteria of the genus Photorhabdus is also a source of many compounds having unknown functions or multifunctions. Studies have reported new pentapeptides known as GameXPeptides A (22) from Photorhabdus luminescens TTO1. These peptides are of unknown nature (Nollmann et al., 2015a). In Photorhabdus asymbiotica PB68.1, a library of photohexapeptides (23) has been generated after activating phpS, which is a silent gene. The photohexapeptide compound belongs to the rare linear D-/L-peptide family, which also includes feglymycin, kolossin (A), and gramicidin A (Zhao and Bode, 2019; Figure 8 and Table 1).