Functional diversity of c-di-GMP receptors in prokaryotic and eukaryotic systems

Cyclic bis-(3', 5')-dimeric guanosine monophosphate (c-di-GMP) is ubiquitous in many bacterial species, where it functions as a nucleotide-based secondary messenger and is a vital regulator of numerous biological processes. Due to its ubiquity, most bacterial species possess a wide range of downstream receptors that has a binding affinity to c-di-GMP and elicit output responses. In eukaryotes, several enzymes and riboswitches operate as receptors that interact with c-di-GMP and transduce cellular or environmental signals. This review examines the functional variety of receptors in prokaryotic and eukaryotic systems that exhibit distinct biological responses after interacting with c-di-GMP. Evolutionary relationships and similarities in distance among the c-di-GMP receptors in various bacterial species were evaluated to understand their specificities. Furthermore, residues of receptors involved in c-di-GMP binding are summarized. This review facilitates the understanding of how distinct receptors from different origins bind c-di-GMP equally well, yet fulfill diverse biological roles at the interspecies, intraspecies, and interkingdom levels. Furthermore, it also highlights c-di-GMP receptors as potential therapeutic targets, particularly those found in pathogenic microorganisms. Video Abstract Supplementary Information The online version contains supplementary material available at 10.1186/s12964-023-01263-5.


Introduction
Cyclic bis-(3' , 5')-dimeric guanosine monophosphate (c-di-GMP) is a nucleotide-based signaling molecule discovered in 1987 as an effective activator of cellulose synthase in Gluconacetobacter xylinus [1].Since then, c-di-GMP has been ubiquitously reported in bacterial species [2] as a universal secondary messenger that responds to various environmental and cellular cues [3].c-di-GMP plays regulatory roles in numerous cellular activities, including cell motility, biofilm formation and dispersion, cell division, differentiation, quorum sensing, and virulence [4].The intracellular concentration of c-di-GMP is controlled by diguanylate cyclases (DGCs) and phosphodiesterases (PDEs), respectively [5].DGCs (contain GGDEF domain) catalyze c-di-GMP production by consuming two GTP molecules, whereas PDEs (have EAL or HD-GYP domains) catalyze the degradation of c-di-GMP into a pGpG linear nucleotide or two GTP molecules [6].Signal transduction occurs through c-di-GMP binding to downstream receptors, triggered by sensing environmental or cellular cues [7].Recent advances in bioinformatics, molecular biology, structural biology, and biochemistry have identified several types of receptors in bacterial species that bind to c-di-GMP signaling molecules and regulate several cellular processes.The PilZ protein, which regulates flagellar motility, was the first c-di-GMP receptor identified [8].Moreover, PilZ proteins play key roles in cell aggregation by contributing to chemotaxis, biofilm formation, and colonization [9,10].
Proteins with GGDEF and EAL domains have been discovered as c-di-GMP receptors [11], in addition to various transcription-factor families and riboswitches located in the 5'-untranslated region of mRNA [12].Animals, humans, and other eukaryotic systems interact with bacteria in various ways, including symbiotic and nonsymbiotic associations [13].Bacterial c-di-GMP in these hosts can also serve as a nucleotide-based second messenger for various positive or negative cellular functions [14].Studies have shown that the host receptor interacts with c-di-GMP, activating host immune systems to defend against intracellular bacterial infections [15,16].
Understanding how the bacterial c-di-GMP functions as a universal signaling molecule at the interspecies, intraspecies, and interkingdom levels are essential due to its critical role in regulating various cellular processes.This review discusses several types of receptors that interact with c-di-GMP to perform various biological activities at the interspecies, intraspecies, and interkingdom levels.The evolutionary relationships between these receptors have been investigated to understand their c-di-GMP specificities.The residues of receptors implicated in c-di-GMP binding are also summarized.

Structural insight into the binding of c-di-GMP with their cognate receptors
The number of crystal structures of c-di-GMP receptors in alliance with c-di-GMP in various species is increasing [17].Based on these structures, three types of domains containing several c-di-GMP binding motifs have been articulated [18].Interestingly, the sorts of interactions between c-di-GMP and its receptors vary according to the type of c-di-GMP [19].c-di-GMP interacts with its receptor as a mono, di, or tetramer.The c-di-GMP structure can also achieve a stacked or extended form as a result of variations in their torsional or glycosidic angles.In c-di-GMP receptor dimers, guanine bases may be entirely or partially stacked or de-stacked, enabling them to interact with the hydrophobic amino acid residues of a receptor.Various non-covalent interactions between c-di-GMP and its diverse receptors include hydrogen bonds, π-π, polar-π, hydrophobic-π, cation-π, anion-π, C-H bond-π, and lone pair-π interactions [17].Each guanine base in c-di-GMP has Watson-Crick and Hoogsten edges that bind to glutamate or aspartate and arginine, respectively [20].Specifically, the arginine of the receptor forms a hydrogen bond with the N7 and O6 atoms of the guanine Hoogsteen edge.Contrastingly, guanine's N1 and N2 atoms at the Watson-Crick edge bind to aspartic acid and glutamate.Examples of these interactions are presented below.
The interaction between c-di-GMP and the MshEN receptor of Vibrio cholerae is an example of a hydrophobic interaction [21].MshEN contains a 53-residue long domain consisting of two 24-residue motifs [RLGXX(L) (V/I)XXG(I/F)(L/V)XXXXLXXXLXXQ] connected by a 5-residue spacer that accommodates c-di-GMP.The six well-conserved residues (in bold) play an important role in the c-di-GMP binding [21].The arginine (R9) in RLG interacts with Gua1 of c-di-GMP through stacking, whereas the leucine forms a hydrophobic triangular cluster with the L54 and L58 in the second motif.This cluster also involves hydrophobic CH-π interactions with Gua2 that stabilize protein-ligand interactions [21,22].Glycine residues from the conserved motif and the remaining non-conserved residues establish two hydrogen bonds with N7 and O6 of Gua1 at the Hoogsteen edge (Fig. 1A).The four-helix MshEN_N also forms a bundle structure maintained by hydrophobic residues in its core (Fig. 1B).
The stimulator of the interferon genes (STING) protein found in animals, mammals, and humans provides an example of arginine-guanine cation-π and guanine-guanine π-π interactions between c-di-GMP and its receptor [23].A single c-di-GMP molecule is symmetrically linked to the STING dimer, with each stack formed by two guanines (Fig. 1C).STING dimers contain a c-di-GMP binding pocket formed by α1, α3, and the loop formed by β2 and β3 (Fig. 1C).The four-layer stack is formed by the stack of the guanidinium group of arginine with the guanine base and the interaction of the long side chain of arginine with Y167 [20].It has been discovered that interactions between c-di-GMP and many residues, including P264, T263, E260, Y163, and S162, entail several Van der Waals interactions and hydrogen bonding [23].This four-layer stack consists of Tyr/Gua/Arg/Tyr interactions.Additionally, because the guanine bases are partly stacked, a compact core ring is adopted when c-di-GMP is connected to the STING interface.
The interaction between c-di-GMP and the anti-sigma factor RsiG in combination with the sigma factor σ WhiG at its interface involves lone pair-π interactions, polar-π interactions, and hydrophobic-π interactions [20].These interactions have been reported in Streptomyces venezuelae, where it sequesters sporulation σ WhiG , inhibiting the transcription of late sporulation genes [24]. Figure 1D shows interactions between the c-di-GMP dimer and σ WhiG , in addition to two EXXXSXXRXXXQXXXD motifs from the α1 and α6 helices of RsiG.The two antiparallel helices of RsiG are aligned together, and residues such as glutamic acid, arginine, and aspartic acid present in the EXXXSXXRXXXQXXXD motif establish hydrogen bonds with the two c-di-GMP monomers.The two extended guanines and the Gln residues within this motif have been seen to interact non-covalently.Additionally, a water molecule also helps to stabilize the c-di-GMP dimer by creating two hydrogen bonds with Gua1's N7 and O6 atoms in each c-di-GMP monomer, one with the carboxyl oxygen of adjacent D105 and the other with Gua3 in the second c-di-GMP monomer.S. venezuelae BldD is another receptor that interacts with c-di-GMP through π-π interaction and helps to transition hypha-spore forms by suppressing BldD regulon genes during vegetative growth [25] (Fig. 2).

Biological roles of c-di-GMP receptors in prokaryotic systems
In the bacterial system, c-di-GMP helps with the transduction of external (e.g., temperature, energy, surfaces, light, redox potential, respiratory electron acceptors, and several natural and synthetic chemicals) [26] or internal (generated during developmental progression or cellular division) [27] signals by binding to the effector component or receptor.These c-di-GMP-bound receptors/ effectors specifically interact with their targets, triggering a wide range of cellular processes.Moreover, c-di-GMP has demonstrated various biological functions, including motility, the formation and dispersion of biofilm, cell division, differentiation, quorum sensing, and virulence [4].Here, we discuss the functional consequences of the interaction of c-di-GMP with its effectors or receptors (Fig. 3).Table 1 summarizes the types of c-di-GMP receptors found in prokaryotic and eukaryotic systems and the outcome of their interactions in terms of biological Fig. 1 Hydrophobic interaction between c-di-GMP and MshEN receptor (A and B).Reproduced with permission from reference [21].Copyright, 2016, Springer Nature, (C) Interaction of c-di-GMP with the dimer of STING in the symmetry.Reproduced with permission from reference [23].Copyright, 2012, Elsevier Inc. and Copyright, and (D) The multiple non-covalent interactions of c-di-GMP dimer with the σ WhiG and two α helices of RsiG in Streptomyces venezuelae.Reproduced with permission from reference [20].Copyright, 2020, Elsevier Inc function.Table 1 also highlights the binding domains or motifs associated with interaction of c-di-GMP with its receptors.The outcome of this interaction is classified into the categories of control of transcription initiation and termination, control of translation, control of exopolysaccharide (EPS) synthesis and secretion, control of flagellar and type III secretion system assembly, control of cell cycle progression, proteolysis of target proteins, and involvement in the localization of target proteins [28].Detailed descriptions of the biological functions of these outcome reactions are provided below.

Biofilm formation and bacterial colonization
Bacteria use c-di-GMP signaling to transition from a motile to a solitary existence in response to environmental cues [133].Bacterial receptor proteins associate with c-di-GMP to create the extracellular cellulose matrix of biofilms [134].For instance, Bcam1349 protein from Burkholderia cenocepacia, combined with c-di-GMP, promotes pellicle and biofilm architecture progression [39].It has been shown that c-di-GMP increases the Bcam1349 protein's affinity for the promoter of a target gene, which results in the development of biofilms.In Pseudomonas aeruginosa, the binding of MapZ to c-di-GMP alters motility by controlling the switching frequency [91].This interaction is also related to enhanced adhesion during biofilm formation.Additionally, HapZ interacts with SagS in P. aeruginosa in a c-di-GMPdependent way to promote surface adhesion and biofilm formation [10].This is consistent with the role of SagS in controlling surface adhesion during the early stages of biofilm formation.In Escherichia coli, c-di-GMP stimulates biofilm formation by directly binding to PgaC and PgaD [57].The Pga machinery triggers the synthesis of poly-β-1, 6-N-acetylglucosamine, a biofilm component of E. coli.c-di-GMP also stimulates the expression of the gene encoding MrkH (a key factor in biofilm formation) in Klebsiella pneumoniae [60].Here, the C-terminal-and N-terminal domains of MrkH promote biofilm development upon the mediation of dimer association by c-di-GMP.Similarly, V. cholerae biofilm development is aided by VpsT-sensing c-di-GMP via extracellular matrix synthesis regulation [108].VpsT downregulates the motility genes of V. cholerae in a c-di-GMP-dependent fashion, leading to a sessile colony state.In addition, BrpT in V. vulnificus binds directly to c-di-GMP and promotes the expression of EPS, thereby improving cell surface adhesion [115].BolA interacts with c-di-GMP and promotes motility and biofilm formation, allowing E. coli to transition between planktonic and sessile lifestyles [59].Even in the presence of high c-di-GMP levels, the lack of BolA resulted in less robust biofilm development, emphasizing the importance of BolA in this regard.Alg44 in P. aeruginosa is involved in the biosynthesis of the EPS alginate via binding to c-di-GMP [75,76,135].It has also been demonstrated that c-di-GMP regulates polysaccharide polymerization and transport via Alg44.In Sinorhizobium meliloti, CuxR stimulates EPS production at high doses of c-di-GMP [99].TDE0214 protein produces a biofilm and exhibits virulence in the periodontal pathogen Treponema denticola via the c-di-GMP signaling cascade [105].Here, TDE0214 plays a significant role in cell adhesion and colonization during the early stages of biofilm formation.

Bacterial survival and adaptation
Several bacterial species respond to environmental fluctuations via the c-di-GMP signaling system [136].In addition, the presence of c-di-GMP in bacteria promotes host adaptation and persistence by regulating bacterial metabolism [137].Tlp1 from Azospirillum brasilense promotes motility by binding to c-di-GMP through its C-terminal PilZ domain.This allows the microaerobic A. brasilense to reach a hypoxic environment [31].ArgR from Mycobacterium bovis modulates c-di-GMP signaling to adapt to hypoxic environments [62].Specifically, c-di-GMP mitigates the autorepression of ArgR expression and promotes nitrite respiration, thereby increasing the viability of M. bovis in hypoxic environments.c-di-GMP in M. smegmatis enhances their antioxidant     resistance by binding to HpoR and LtmA [65,66].Here, c-di-GMP is upregulated by high levels of H 2 O 2 and enhances antioxidant resistance by specifically binding to HpoR, which induces DNA-binding activity.In addition, LtmA enhances the growth of M. smegamatis under high antioxidant stress levels, in contrast to HpoR.Borrelia burgdorferi, a tick-borne pathogen, also enhances its host adaptability by binding PlzA to c-di-GMP [35].These results are attributed to the effector mechanism that occurs through PlzA-c-di-GMP interaction [36].

Regulation of bacterial pathogenesis
c-di-GMP regulates factors that affect bacterial pathogenesis, including the expression of virulence genes, biofilm formation, and motility regulation [138].The diversity of c-di-GMP receptors and effectors contributes to bacterial lifestyle transformation by regulating multiple cellular processes [139].PlzC and PlzD in V. cholerae particularly cooperate with c-di-GMP to control the expression of the virulence genes and the production of biofilms [106].PlzC and PlzD proteins regulate downstream processes by binding to c-di-GMP.Additionally, VpsR is connected to c-di-GMP and activates aphA and vpsT to govern biofilm development and virulence factor production [109].FlrA controls the motility of V. cholerae by downregulating flagellar biosynthesis [110].Furthermore, c-di-GMP inhibits V. cholerae motility by promoting the formation of extracellular Vibrio polysaccharides.WspR from P. aeruginosa regulates biofilm development by binding to c-di-GMP [79].This is attributed to c-di-GMP, which restricts the mobility of the GGDEF domain of WspR.Furthermore, in the presence of c-di-GMP, P. aeruginosa reduces the expression of flagellar genes [86].This effect is enhanced in the presence of FleN.Finally, E. coli YcgR also binds to c-di-GMP to regulate flagellabased motility [8].

Regulation of enzyme activity
c-di-GMP may also bind to enzymes and thus regulate their activities [27].Cellulose production by pathogens is a key factor influencing virulence, since cellulose is a fundamental component of biofilm structures [140].In B. cenocepacia, c-di-GMP controls cellulose synthesis by increasing the binding of Bcam1349 to the cellulose synthase gene [39].BcsA controls cellulose synthesis in Erwinia amylovora in a c-di-GMPdependent fashion [53].Here, the allosteric binding of c-di-GMP to BcsA contributes to biofilm formation by activating cellulose biosynthesis.BcsE from E. coli maximizes cellulose production by binding to c-di-GMP through its DUF2819 domain [58].Additionally, BcsA and BcsB form a complex to activate c-di-GMP, thereby upregulating cellulose synthesis in E. coli [97].This occurs by activating the auto-inhibited enzyme by breaking the salt bridges that bind the gating loops controlling access to the active site and substrate coordination.Finally, GlgX from S. venezuelae interacts with c-di-GMP to stimulate the enzymatic hydrolyzation of glycogen [104].This indicates that the GlgX-c-di-GMP interaction is vital for controlling glucose availability in Streptomyces.

Biological roles of c-di-GMP receptors in eukaryotic systems
Bacterial c-di-GMP can interact with eukaryotic cell systems as well [104].c-di-GMP is used by eukaryotes as a pathogen presence indicator [27].In this regard, c-di-GMP modulates the response of the eukaryotic immune system to microbial pathogens [14].In mammals, STING acts as an immune sensor by inducing a type I interferon (IFN) response by binding to c-di-GMP [23,128].Furthermore, binding to c-di-GMP improves the interaction between the C-terminal domain of STING and TANK-binding kinase 1, resulting in IFN production [129] (Fig. 4).DDX41 (a c-di-GMP-detection pattern recognition receptor) encourages connections with STING, enhances STING's affinity for c-di-GMP, and activates IFNs [131].STING from Larimichthys crocea (a large yellow croaker) enhances its immunity against the infection caused by the parasite Cryptocaryon irritans, by acting as a receptor for c-di-GMP [125].During C. irritans infection, STING mediates the production of type I IFNs and inflammatory cytokines.In Itgax Cre Tmem173 Flox/Flox mice, c-di-GMP induces cytokine production by selectively activating cells expressing the mammalian c-di-GMP receptor MPYS (STING, MITA, and TMEM173) [126].In Jurkat cells, c-di-GMP binds to the P21 ras protein and stimulates CD4 receptor expression [127].Specifically, c-di-GMP binding to P21 ras maintains the protein in an active form following CD4 overexpression.In mammalian macrophages, coronin 1A and cyclophilin H bind to c-di-GMP and induce type I IFN expression, activating an inflammatory response [130].These findings suggest that mammalian macrophages detect and respond to c-di-GMP-induced inflammation.Finally, the membrane polypeptide of cellulose synthase from cotton fibers (Gossypium hirsutum) was characterized using the same c-di-GMP receptor as the cellulose synthase from Acetobacter xylinum [124].Plant cellulose synthase membrane polypeptides are identical to bacterial cellulose synthase subunits, allowing for the identification of genes responsible for cellulose synthesis in plants.

Evolutionary relationships between bacterial c-di-GMP receptors and identification of the bidirectional best hit
To investigate the evolutionary relationship of c-di-GMP receptors, a phylogenetic tree of receptors from several bacterial species was constructed (Fig. 5).Subsequently, the best bidirectional hit among these receptors was determined to demonstrate how these receptors from various bacterial species are clustered in the same branch of the tree.The bidirectional best hit helps to determine how the proteins share similar affinities for the same chemical (c-di-GMP).YcgR is recognized as a flagellar brake protein due to its role in controlling swarming and swimming in various flagellated bacterial species by interacting with c-di-GMP [141,142].YcgR from E. coli was found to be clustered with BrlR from P. aeruginosa in the same branch in the phylogenetic tree developed.In P. aeruginosa, BrlR regulates biofilm formation and multidrug efflux pump production, in addition to acting as a pyocyanin receptor [90].However, a sequence similarity analysis revealed no similarities between the two Fig. 5 Phylogenetic tree of the c-di-GMP receptors from different species of bacteria.The red-colored proteins promote biofilm formation, the blue-colored proteins promote bacterial survival and adaptability, the yellow-colored proteins promote bacterial pathogenicity, and the green-colored proteins promote enzyme activity proteins.Further, YcgR from E. coli was found to show 82.35% similarity to FlgZ from P. aeruginosa, indicating potentially similar binding specificities for c-di-GMPs and a role in flagellar motility (Table 2).
PlzA is a protein that binds to c-di-GMP (29.6 kDa, 261 amino acids) found in many species of Lyme disease spirochetes, such as Borreliella spp.Multiple mechanisms were hypothesized to influence borrelial activity previously.PlzAs from all Borreliella species were grouped together in the same branch.Moreover, LapD is a c-di-GMP-binding receptor that regulates cell surface attachment and biofilm formation [92].LapD from P. fluorescence was grouped in the same branch as CsrD from E. amylovora, CbrR from Campylobacter jejuni, and MrkH from K. pneumoniae.However, the sequence similarities indicated that CbrR and CsrD have 57.14%similarity, whereas MrkH has 66.67% similarity with BolA from E. coli and 50.00% similarity with PdtaS from M. tuberculosis.
Various proteins help regulate biofilm development by producing extracellular polymers such as alginate and cellulose [140].Several bacterial polymer-synthesizing proteins, such as cellulose and alginate synthases, were grouped in the same branch as well (Fig. 5).BcsA from Dickeya oryzae, which is involved in cellulose synthesis, showed 91.95% similarity with BcsA from E. amylovora (Table 2), yet lower similarities were exhibited with BcsA from E. coli (69.68%) and S. fredii (52.73%).The YdaK protein from Bacillus subtilis, which is involved in the production of putative EPS facilitating biofilm formation, was grouped in the same branch as that of the celluloseproducing proteins (Fig. 5).Additionally, YdaK from B. subtilis showed high similarity (87.94%) with the YdaK protein from B. velezensis (Fig. 5).Tlp1 from A. brasilense exhibits sustained motility after interacting with c-di-GMP via the PilZ domain and was found to be clustered along YkuI from B. subtilis.
Although the precise role of Ykul is unknown [143], a high degree of similarity (100.00%) between Yku1 and Tlp1 from A. brasilense suggests that it may also influence motility.WspR from P. aeruginosa, which is involved in biofilm production, was grouped in the same branch as the WspR from Lysobacter enzymogenes with a sequence similarity of 72.22%.BalD (controls the expression of sporulation genes in S. coelicolor) is found in the same branch as CdbA, which is required for viability in Myxococcus xanthus and plays a role in its chromosomal organization and segregation [70].Furthermore, a sequence similarity study showed 100.00% similarity between BalD and GlgX of S. venezuelae, which functions as a glycogen-debranching enzyme [104].GlgX is thought to be important in sporulation since a mutation in the glgX gene results in a strain that produces less spores than the wild-type strain [104].In the phylogenetic tree, GlgX from S. venezuelae was grouped in the same branch as PXO02374 from Xanthomonas oryzae and VpsT and GbpA from V. choloreae.CckA (cell cycle kinase) from Caulobacter vibrioides [48] is found in the same cluster as CdgR (controls cell size) from Synechocystis sp. and CuxR (regulates EPS synthesis) from S. meliloti [99].Surprisingly, CckA has a strong resemblance (71.43%) to CbrR (which regulates flagellar motility) in C. jejuni [44].

Evolutionary relationship between eukaryotic c-di-GMP receptors and identification of the bidirectional best hit
A phylogenetic tree of receptors of eukaryotic origin was also constructed (Fig. 6).The results revealed that STING from Drosophila melanogaster shares a high degree of similarity with STING from Mus musculus (100.00%),Homo sapiens (100.00%), and L. crocea (60.00%).In

Methodology: phylogenetic analysis and bidirectional best hit analysis
The sequences of all receptors were retrieved from the National Center for Biotechnology Information database.After multiple sequence alignments of c-di-GMP receptors, the phylogenetic trees were constructed using MEGA version 11 software [144].The Geneious ® 11.0.2 program was used to perform the bidirectional best hit among c-di-GMP receptors and multiple sequence alignment using the BLOSUM-65 matrix.

Conclusion and future perspectives
With recent advances in bioinformatics, structural biology, molecular biology, and biochemistry, the discovery of c-di-GMP receptors has expanded from prokaryotic to eukaryotic systems.Bacterial species use c-di-GMP signaling molecules in their natural environment through interactions with receptors, which are either membrane-bound or cytoplasmic.Bacteria are ubiquitous and can have either beneficial or detrimental Here, a phylogenetic tree of c-di-GMP receptors from bacterial and eukaryotic systems was created to understand distinct receptors that participate in diverse biological processes with similar c-di-GMP binding specificities.Several common receptors found in multiple bacterial species were found to be grouped in the same branch.A significant level of sequence similarity between the receptors in various bacterial genera implies shared specificities for c-di-GMP.The functionality of various bacterial species influenced upon binding receptor proteins with c-di-GMP is also clarified in this review.The following are the key aspects that must be addressed in future studies to better understand the mechanism of interaction between c-di-GMP and its receptors, as well as their diverse functional characteristics.
• The receptor in pathogenic bacteria and its response upon interacting with c-di-GMP, which is also associated with cell division and virulence, may constitute viable therapeutic targets for controlling microbial infections.• It is difficult to anticipate how the selectivity of c-di-GMP will change when receptors from prokaryotes and eukaryotes are present simultaneously within the cell.• The conditions under which the host receptor protein detects c-di-GMP need to be elucidated.• Interactions between c-di-GMP and c-di-GMP receptors of various species have been studied in vitro using techniques such as differential radial capillary action of ligand assays, pull-down assays, and capture compound experiments [25].These in vitro investigations should validate the binding interaction and affinity in the host system, followed by a study of the gene expression probing the response of the cell.• High-throughput screening of natural and synthesized compounds is required to antagonize the interaction between c-di-GMP and its receptor.• In vitro binding experiments have indicated that certain receptors also bind c-di-GMP.However, their biological functions remain unclear (Table 1) and require further in vivo studies.

Fig. 2
Fig. 2 Interaction of tetrameric c-di-GMP with the two subunits of BldD via C-terminal domain with the involvement of bipartite RXD-X 8 -RXXD signature.(A) Structural details of BldD dimer-(c-di-GMP) complex, (B) Top and bottom layer of BldD C-terminal domain-(c-di-GMP) contact, (C) Middle layers of two c-di-GMP dimers that are intercalated, and (D) c-di-GMP layers in side view.Reprinted with permission from reference [25].Copyright, 2014, Elsevier Inc

Fig. 3
Fig.3Interaction of c-di-GMP with different receptor proteins for controlling diverse biological roles in the bacterial system.The information obtained from the literature[28][29][30]

Fig. 4
Fig. 4 Downstream signaling induced by bacterial c-di-GMP binding to STING cognate receptors leads to the generation of type I IFNs through the IFN regulatory factor 3 and TANK-binding kinase 1 pathway.Reprinted with permission from the reference [129].Copyright, 2012 Elsevier Inc

Fig. 6
Fig. 6 Phylogenetic tree of the c-di-GMP receptors from different eukaryotic organisms including humans

Table 1
Different types of c-di-GMP receptors from prokaryotes and eukaryotes

Table 2
Bidirectional best hit of among c-di-GMP receptors from different bacterial species contrast, STING from M. musculus had a similarity of 88.95% with STING from H. sapiens.Protein helicase DDX41 from H. sapiens shares a high degree of similarity with H. sapiens coronin 1A (91.13%) and helicase from M. musculus (99.52%).The cyclophilin H proteins from H. sapiens and M. musculus were found in the same branch and showed 100.00% similarity.