- Research article
- Open Access
Establishing a reference array for the CS-αβ superfamily of defensive peptides
BMC Research Notes volume 9, Article number: 490 (2016)
“Invertebrate defensins” belong to the cysteine-stabilized alpha-beta (CS-αβ), also known as the scorpion toxin-like, superfamily. Some other peptides belonging to this superfamily of defensive peptides are indistinguishable from “defensins,” but have been assigned other names, making it unclear what, if any, criteria must be met to qualify as an “invertebrate defensin.” In addition, there are other groups of defensins in invertebrates and vertebrates that are considered to be evolutionarily unrelated to those in the CS-αβ superfamily. This complicates analyses and discussions of this peptide group. This paper investigates the criteria for classifying a peptide as an invertebrate defensin, suggests a reference cysteine array that may be helpful in discussing peptides in this superfamily, and proposes that the superfamily (rather than the name “defensin”) is the appropriate context for studying the evolution of invertebrate defensins with the CS-αβ fold.
CS-αβ superfamily sequences were identified from previous literature and BLAST searches of public databases. Sequences were retrieved from databases, and the relevant motifs were identified and used to create a conceptual alignment to a ten-cysteine reference array. Amino acid sequences were aligned in MEGA6 with manual adjustments to ensure accurate alignment of cysteines. Phylogenetic analyses were performed in MEGA6 (maximum likelihood) and MrBayes (Bayesian).
Across invertebrate taxa, the term “defensin” is not consistently applied based on number of cysteines, cysteine spacing pattern, spectrum of antimicrobial activity, or phylogenetic relationship. The analyses failed to reveal any criteria that unify “invertebrate defensins” and differentiate them from other defensive peptides in the CS-αβ superfamily. Sequences from various groups within the CS-αβ superfamily of defensive peptides can be described by a ten-cysteine reference array that aligns their defining structural motifs.
The proposed ten-cysteine reference array can be used in addition to current nomenclature to compare sequences in the CS-αβ superfamily and clarify their features relative to one another. This will facilitate analysis and discussion of “invertebrate defensins” in an appropriate evolutionary context, rather than relying on nomenclature.
Defensin nomenclature has a complex history (Table 1). “Defensins” originally referred to a set of three human neutrophil peptides that show activity against Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Cryptococcus neoformans, and herpes simplex virus, type 1 . The general term “defensin” seemed appropriate due to the broad spectrum of activity. These peptides are 29–30 amino acids long, contain six cysteines that form three disulfide bonds, and are homologous to a group of six peptides from rabbit neutrophils [2, 3].
The term “insect defensin” was proposed by Lambert et al. in their description of two small cysteine-rich peptides from Phormia terranovae (phormicins) . These peptides, along with sapecins identified a year earlier, showed activity primarily against Gram-positive bacteria and appeared to have some sequence homology to the mammalian defensins [4, 5]. It is now clear that observed similarities between insect and mammalian defensins are most likely due to convergence, but the name “defensin” has been retained [6, 7]. Two antifungal peptides with similarity to defensins were isolated from radish , and the term “plant defensin” was proposed after cloning of the full-length sequences for these peptides, which have eight cysteines instead of six . While invertebrate peptides are the focus of this study, plant defensins are part of the same superfamily and the similarity of drosomycin from Drosophila to plant peptides has been acknowledged since it was first described .
The structure that unifies the invertebrate and plant defensins is the cysteine-stabilized alpha-beta (CS-αβ) motif established by Cornet et al. for Phormia defensin A (phormicin A), which has an alpha helix followed by two antiparallel beta sheets, and is stabilized by three disulfide bonds . Two of the three bonds correspond to a smaller structural motif that had been previously described in toxic peptides from arthropods, the cysteine-stabilized α-helix (CSH) . Sequences with this fold also tend to have the γ-core motif, an enantiomeric motif of 8–16 amino acids generally containing a conserved GXC or CXG and forming a β-hairpin structure . This motif is found not only in sequences with the CSH and CS-αβ motifs, but in nearly all groups of cysteine-containing defense peptides [13, 14].
Invertebrate defensins and other peptides containing the CS-αβ fold form the CS-αβ superfamily of proteins, also known as the scorpion toxin-like superfamily in the SCOP  and new SCOP2  databases. This superfamily includes five families of defensive peptides: long-chain scorpion toxins, short-chain scorpion toxins, defensin MGD-1, insect defensins, and plant defensins [15, 16]. Charybdotoxin from the deathstalker scorpion was identified and described around the same time as mammalian and insect defensins [17, 18], but its antimicrobial activity wasn’t tested until much later . The superfamily may have originated from myxobacterial sequences that contain the CSH motif . Although the GXC/CXG of the γ-core motif is missing, Anaeromyxobacter dehalogenans defensin-like peptide (AdDLP) has a defensin-like structure and activity against Plasmodium berghei, in spite of showing no other antimicrobial or hemolytic activity thus far .
A protein’s nomenclature generally reflects its characteristics and how it is related to other proteins. Ideally, proteins named as part of a group share important characteristics and/or a common evolutionary history not shared with other proteins. As additional members of the CS-αβ superfamily have been identified from fungi as well as mollusks, nematodes, annelids, and other invertebrate taxa, the nomenclature and associated criteria have become confusing at best. A peptide named as a “defensin” may have six or eight cysteines with varying antimicrobial activities. Depending on the taxonomic group, a peptide with the characteristics of “invertebrate defensins” may have 4–12 cysteines and be called a mycin, macin, mytilin, myticin, antibacterial factor, defensin-like peptide/protein, or drosomycin-like antifungal peptide (Table 1). The clearest demonstration of the inconsistent and confusing nomenclature is the cremycins from Caenorhabditis remanei. These peptides are described as drosomycin-like antifungal peptides, but their sequences are not particularly drosomycin-like and only one of the two tested (of 15 total) has antifungal activity . To further confuse the nomenclature, invertebrate big defensins are not part of the CS-αβ superfamily, but are more likely related to vertebrate defensins . This paper investigates the criteria for classifying a peptide as an invertebrate defensin, suggests a reference cysteine array that may be helpful in discussing peptides in the CS-αβ superfamily, and proposes that the superfamily is the appropriate context for studying the evolution of invertebrate defensins with the CS-αβ fold.
Results and discussion
CS-αβ reference array
It is often the case that the first, and possibly only, information available for a CS-αβ peptide is its sequence, with activity and structure studied later or not at all. While sequence comparison may seem straightforward, different members of this superfamily have different numbers and bonding patterns of cysteines. For example, insect defensins are described as having the pattern C1–C4, C2–C5, C3–C6; nematode ABFs have C1–C5, C2–C6, C3–C7, C4–C8. From these descriptions, it isn’t clear that the first three disulfide bonds of nematode ABFs are structurally the same as the three found in insect defensins (i.e., C4 of insect defensins aligns with C5 of nematode ABFs). Most CS-αβ peptides have 6–10 cysteines, so I aligned sequences to a ten-cysteine array. C3, C4, C8, and C9 correspond to the CSH motif ; the addition of C2 and C6 completes the CS-αβ fold . The C of the GXC in the γ-core motif is generally C6. CS-αβ sequences were aligned to this array using these cysteines as guides to facilitate comparison of cysteine spacing patterns (Fig. 1a; Additional file 1: Figure S1). Additional cysteines at the N or C-terminus of the conserved array are represented by additional filled boxes. In the case there are additional cysteines within the conserved array, they are represented as “C.” For example, two filled boxes with “2C” in between would be interpreted as “CXXCC,” with “C2C” in between as “CCXXCC,” and with “2C1” in between as “CXXCXC.” It is unlikely that established names for peptides will be changed for consistency, and revising names will make reading previous literature confusing. A reference array for comparing these sequences that can be used in addition to current nomenclature is a reasonable solution.
Nomenclature is not consistent with cysteine pattern
Figure 1a shows the names and cysteine patterns of selected members of the CS-αβ superfamily aligned to the proposed reference array. The representative sequences were chosen to highlight the inconsistency in naming of these peptides, and a more complete alignment can be found in Additional file 1: Figure S1. The structures for several of these have been reported and are shown in Fig. 1b–m.
Sapecin A and other typical insect defensins have six cysteines corresponding to C2–C4, C6, C8, and C9 of the reference array (Fig. 1a, b). The n-loop is variable, with 4-16 amino acids separating C2 from C3. Some previous work proposed three categories of insect defensins: (1) “classical insect-type defensins” (CITDs) with longer n-loops restricted primarily to phylogenetically recent insect orders, (2) “ancient invertebrate-type defensins” (AITDs) with shorter n-loops found in primitive insect taxa as well as other invertebrates, and (3) “plant/insect-type defensins” (PITDs) that have a fourth disulfide bond found in plants and Drosophila [6, 23, 24]. Given that a single insect species may have both CITDs and AITDs, this classification is confusing and of limited utility. Examples show that “defensin” is not consistently applied to either long or short n-loop insect sequences (Fig. 1a: Acalolepta luxuriosa, Bombyx mori, Galleria mellonella, and Sarcophaga peregrina). A recent review  combined CITDs and AITDs into “arthropod and mollusk-type six-cysteine defensins,” but a combination of literature and database searches shows sequences from nematodes, tardigrades, velvet worms, crustaceans, and fungi with cysteine arrays consistent with this spacing (Additional file 1: Figure S1). Charybdotoxin and other short-chain scorpion toxins in the CS-αβ superfamily also have this cysteine pattern, and the structure of charybdotoxin is similar to that of sapecin (Fig. 1a–c) [26, 27]. The scorpion Leiurus quinquestriatus produces both charbydotoxin and a defensin with a very similar cysteine pattern (Fig. 1a) [17, 18, 28]. Therefore, it is not possible to determine whether a six-cysteine CS-αβ sequence with the typical insect spacing is a toxin or an antimicrobial peptide, let alone whether it is called a defensin, defensin-like peptide/protein, cysteine-rich peptide/protein, or a name derived from the species (gallerimycin, sapecin, etc.).
The additional cysteines in drosomycin (Fig. 1d)  and most plant defensins (represented by RsAFP1, Fig. 1e)  correspond to C1 and C10 of the reference array. Other than the drosomycin family in Drosophila and plant defensins, only one nematode sequence seems consistent with this spacing (NEMBASE: PSC02929). Zhu and Gao reported a family of drosomycin-type antifungal peptides (DTAFPs) from Caenorhabditis remanei called “cremycins” . However, all 15 cremycins have only six cysteines (instead of the eight found in drosomycin), and their spacing is consistent with insect defensins (Fig. 1a; Additional file 1: Figure S1) . Long-chain scorpion toxins, such as from Centruroides sculpturatus, also have additional cysteines corresponding to C1 and C10 that form a fourth disulfide bond, but the sequence spacing is characterized by a long C-terminal extension between C9 and C10 that is not present in drosomycin and plant defensins (Fig. 1a, d–f) [31, 32]. Two Hypsibius (tardigrade) and four Schistosoma (trematode) sequences fit this pattern (Additional file 1: Figure S1), suggesting they might have toxic activity instead of or in addition to antimicrobial activity.
In contrast to the relative homogeneity of plant defensins, seven families of fungal defensins/defensin-like peptides (DLPs) have been identified [23, 24]. The cysteine number and spacing of families 1, 2, 6, 7, and some of 3 is consistent with the insect spacing, while the patterns for most members of 3, and families 4 and 5 are found almost exclusively in fungi (Fig. 1a; Additional file 1: Figure S1). Plectasin (in fDLP family 1) has an n-loop similar in length to sapecin A, but may form additional β-sheets (Fig. 1b, g) .
Mollusks and nematodes both express CS-αβ sequences with eight cysteines corresponding to C2–C6, C8, C9, and C10. In mollusks, most work has focused on mussels and oysters, leading to three groups that fit this pattern (defensins, myticins, and mytilins; Fig. 1a; Additional file 1: Figure S1). The nearly identical spacing for mollusk defensins and myticins makes this an ineffective means of differentiation; however, mytilin B has longer β-sheets than MGD-1 (Fig. 1h, i) [34, 35] and the GXC motif aligns with C7 of the reference array instead of C6. Nematode sequences with a similar cysteine pattern and structure to mollusk defensins with eight cysteines have been traditionally called “antibacterial factors” (ABFs) instead of “nematode defensins” (Fig. 1a, h, j; Additional file 1: Figure S1). Nematode CS-αβ peptides tend to have a longer n-loop, but this is not always the case (Fig. 1a; Additional file 1: Figure S1). A sequence from the sponge Suberites domuncula is referred to as an ASABF-type antimicrobial peptide , but is arguably just as similar to mollusk defensins and myticins (Fig. 1a). Some eight-cysteine potassium-channel toxins from scorpions are also consistent with the mollusk/nematode cysteine pattern and structure (represented by Maurotoxin, Fig. 1a, k) . Since there doesn’t seem to be a consensus that “defensin” should apply only to six-cysteine sequences, there seems to be no reason that nematode “antibacterial factors” could not be referred to as “nematode defensins.”
In contrast to the majority of nematode sequences, ASABF 6-Cys-alpha has only six cysteines; however, the cysteines correspond to C3–C6, C8, and C9 of the reference array instead of the six found in typical insect defensins. The missing cysteines do not correspond to a disulfide bond-forming pair, so the authors suggest the bonding pattern may be different compared to most invertebrate defensins . The structure will have to be experimentally determined to address this possibility.
The macins are a family of peptides that have not usually been included in analyses of defensins and defensin-like peptides, but clearly have the CS-αβ fold. Macins were originally described from annelids [39, 40] and have been reported from the cnidarian Hydra magnipapillata [40, 41], the mussels Hyriopsis cumingii  and Mytilus galloprovincialis , and the giant African land snail, Achatina fulica . The addition of a fourth bond formed by C1 and C7 as seen in hydramacin (Fig. 1a, l)  may be a defining characteristic of macins. In ten-cysteine macins such as theromacin, the fifth bond is formed by C5 and C10 (Fig. 1a, m) . Diverse invertebrate taxa have sequences with 8–12 cysteines consistent with the macin pattern (Additional file 1: Figure S1) . Due to uncertainty regarding the presence of pro-peptides, some of these may have nine cysteines (Additional file 1: Figure S1). These peptides may act as dimers, as has been suggested for the scorpion lipolysis activating peptide LVP1 (a peptide similar to scorpion sodium-channel toxins; Additional file 1: Figure S1) .
Nomenclature is not consistent with specific antimicrobial activity
It is reasonable to suggest that invertebrate defensins and related peptides be named based on their spectrum of antimicrobial activity rather than by features of their primary sequence. A barrier to classification and naming of CS-αβ sequences by function is that not all peptides are tested for activity prior to reporting. Of those that are, there is a great deal of variability in the extent of antimicrobial activity testing. Some peptides are tested against a wide variety of organisms, but others are only tested against a representative species in the pathogen group the peptide is suspected to be active against. Representative peptides used to illustrate the lack of nomenclature consistency are shown in Table 2; Additional file 2: Table S1 summarizes available antimicrobial activity for the CS-αβ peptides considered in this study.
The first insect defensins reported (sapecin A, phormicin, and royalisin from Apis mellifera royal jelly) had six cysteines and were primarily active against Gram-positive bacteria, although results from assays with yeast and fungi were only reported for phormicin [4, 5, 46–49]. Drosophila expresses both a six-cysteine defensin with activity against Gram-positive bacteria  and the eight-cysteine drosomycin with antifungal activity and similarity to plant defensins (which are predominantly antifungal) . Since insect defensins were thought to be characterized by activity against Gram-positive bacteria, an antifungal peptide from Heliothis virescens was named “heliomicin” . However, both gallerimycin and Galleria defensin from Galleria mellonella show antifungal activity and no antibacterial activity [51, 52]. The situation in arachnids is similar; both Scapularisin 3 and Scapularisin 6 from Ixodes scapularis have antifungal activity, but Scapularisin 6 also has activity against Gram-positive bacteria . A defensin from the scorpion Leiurus quinquestriatus has activity against Gram-positive but not Gram-negative bacteria , while charybdotoxin from the same species has been shown to be active against Gram-positive and Gram-negative bacteria as well as yeast . Therefore, one can deduce little regarding the antimicrobial activity of an arthropod CS-αβ peptide based on the name.
Mollusk peptides also show little correlation between nomenclature and antimicrobial activity. Mollusk defensins, myticins, and mytilins tend to have predominantly Gram-positive activity, but MGD-1 and Myticin B also show some activity against Gram-negative bacteria and fungi [34, 54–56], while Myticin A has shown no additional antimicrobial activity . Mytilins all seem to show activity against Gram-positive bacteria, with mytilins A–D also active against Gram-negative bacteria, and mytilins B and D showing antifungal activity [57, 58]. To the best of my knowledge, antimicrobial activities of mytimacins from mussels have not been published yet. Other macins (hydramacin, neuromcain, theromacin, and mytimacin-AF) have shown primarily antibacterial activity, with antifungal testing being rather limited [39–41, 44].
In nematodes, Ascaris suum antibacterial factor (ASABF) has activity against Gram-positive and Gram-negative bacteria , while Caenorhabditis elegans antibacterial factor 2 (Ce-ABF2) also has activity against yeast . The activity of several additional ABFs in each species has not been reported, including that for the six-cysteine peptide with proposed disulfide bond rearrangement (ASABF-6Cys-α) . The sponge ASABF-like peptide has activity against Gram-positive and Gram-negative bacteria, fungi, yeast, and is hemolytic . Antimicrobial activity has been tested for two of the fifteen cremycins, reported to be drosomycin-type antifungal peptides: cremycin-5 showed antifungal activity, but cremycin-15 showed antibacterial activity without any antifungal activity .
Although the primary concern of this study is invertebrate defensins, some invertebrate sequences most closely resemble CS-αβ peptides from plants or fungi. The cysteine number and spacing is much more consistent in plants than in invertebrates and most plant defensins studied have shown antifungal activity; however these peptides are not all called defensins (Additional file 2: Table S1). For example, Raphanus sativus antifungal peptide (RsAFP1), Zea mays gamma-2-zeathionin (also called PDC-1), Medicago sativa defensin 1 (MsDEF1), and Nicotiana alata defensin 1 (NaD1) all have antifungal activity [8, 61–67]. Some plant defensins have additional activities against bacteria, oomycetes, or bruchid larvae (Additional file 2: Table S1). Brazzein, initially identified as a sweet-tasting protein from Pentadiplandra brazzeana , has been shown to have activity against Gram-positive and Gram-negative bacteria as well as yeast . The antimicrobial activity of fungal defensins has only been reported for plectasin and micasin; both have activity against Gram-positive bacteria and micasin is also active against Gram-negative bacteria [24, 33].
If nomenclature based on activity is desirable, then each peptide needs to either be tested extensively prior to reporting or specific antimicrobial activities need to be correlated with sequence features. The γ-core motif has been hypothesized to be a signature of cysteine-rich antimicrobial peptides . Only a few studies have examined the γ-core in isolation, and have shown either antibacterial activity [69, 70] or both antibacterial and antifungal activity [55, 71]. Interestingly, in studies where the fragment was compared to the complete peptide, the isolated γ-core had a greater spectrum of activity than the complete peptide [55, 69, 71]. While the majority of CS-αβ peptides have a γ-core sequence, it is not absolutely necessary for activity. Sapecin B from Sarcophaga peregrina does not have a clear γ-core sequence, but has activity against Gram-positive bacteria . An 11-amino acid fragment of sapecin B (7R-17K) upstream of the region corresponding to the γ-core shows activity against not only Gram-positive bacteria, but also Gram-negative bacteria and yeast . The defensins from the beetles Allomyrina dichotoma, Oryctes rhinoceros, and Copris tripartitus have clear γ-core motifs [74–76], but the fragments studied and found to have antibacterial activity are similar to those from sapecin B [73, 75–77]. Peptides corresponding approximately to these regions of tenecin 1 and longicin do not have antimicrobial activity [69, 78]. Experimental conversion of navidefensin2-2 into a peptide with toxic activity suggested that defensins with the motif KCXN in the γ-core (with C being C6 of the reference array) were likely to have toxic activity if the n-loop is short to prevent steric hindrance during binding to the channel . Consistent with this hypothesis, both charybdotoxin and defensin from Leiurus have short n-loops, but charybdotoxin has the sequence “GKCMN” while the defensin has “GYCAG.” Charybdotoxin also has antimicrobial activity, so while the short n-loop and KCXN motif may be sufficient to indicate toxic activity, the characteristics suggesting antimicrobial activity are less clear. Drosomycin-like defensin (DLD) from humans has activity specifically against filamentous fungi, despite the sequence not having conventional CSH, CS-αβ, or γ-core motifs .
Nomenclature does not necessarily reflect phylogeny
The similarity in cysteine pattern and pre-cursor arrangement led to the suggestion that mollusk defensins and nematode ABFs might have a common ancestor , while an exon-shuffling mechanism was proposed to explain variability between arthropod and mollusk defensins . Differences in gene structure and the large number of events that would be necessary for exon shuffling to accommodate the nematode sequences led to both the conclusion that convergent evolution was more likely  and that there was insufficient evidence to support either model . Rodríguez de la Vega and Possani point out that the lack of defensins reported from basal taxa (such as annelids and merastomatans) and sister groups (including crustaceans, cephalopods, gastropods, and spiders) complicates establishing invertebrate defensins as orthologs . More recently, complete defensin sequences have been reported from five spider species  and the gastropod Haliotis discus .While sequences that look like typical arthropod or mollusk defensins have not been reported from annelids, macins have been reported from the annelids Hirudo medicinalis  and Theromyzon tessulatum , as well as from the gastropod Achatina fulica . Although not yet characterized, database searches reveal CS-αβ sequences in the crustaceans Daphnia pulex and Litopenaeus vannamei, the gastropods Aplysia californica and Littorina saxatalis, and the tardigrades Hypsibius dujardini and Milnesium tardigradum. As sequencing continues, there is a reasonable expectation that CS-αβ peptides from additional invertebrate taxa will be identified.
The scorpion-toxin like superfamily in the SCOP databases includes both short and long-chain scorpion toxins, insect defensins, plant defensins, and the mollusk defensin MGD-1 [15, 16]. A phylogenetic analysis suggests that the long-chain scorpion sodium channel toxins may have evolved from antifungal defensins . Based on the conserved cysteines and structural information, nematode ABFs and macins are clearly part of this superfamily [41, 88]. Sequences from two myxobacterial species (A. dehalogenans and Stigmatella aurantiaca) have been identified that may represent the ancestor of the CS-αβ peptides . These sequences have four cysteines that are consistent with the CSH motif, and there is a plausible mechanism for mutations in AdDLP generating the cysteines that form the third disulfide bond of the CS-αβ motif . Testing of recombinant AdDLP has shown no antibacterial or antifungal activity, but has shown activity against Plasmodium berghei .
Ideally, invertebrate defensins would form a monophyletic group within the superfamily, suggesting that all sequences called “invertebrate defensin” are more closely related to each other than to sequences with other names. Alignments of CS-αβ sequences have to be manually adjusted to ensure the conserved cysteines are accurately positioned, and short sequence length as well as low levels of sequence similarity make it difficult to generate well-resolved trees with well-supported clades. A maximum likelihood phylogenetic analysis of 250 CS-αβ sequences did not produce a well-resolved tree with major clades reflecting taxonomy or nomenclature (Fig. 2, all bootstrap values retained to highlight the low degree of support for the majority of clades). A few small clades were supported at ≥70 (Fig. 2, red bootstrap values). Decreasing the cut-off to ≥50 (orange bootstrap values) added a few more small clades or an additional sequence to a clade ≥70, but did not result in clades defining major groups. There were some identifiable groupings with little to no support, but even these did not necessarily contain all group members previously identified (Fig. 2).
Bayesian analyses of the same dataset also resulted in poorly resolved trees with few well-supported clades, and the runs did not converge (average standard deviation of split frequencies was >0.1; trees not shown). In an effort to increase the phylogenetic signal, a Bayesian analysis was performed using the same set of sequences with added information regarding insertions/deletions (relative to AdDLP) and pro-peptide presence or absence N-/ C-terminal to the mature peptide, an increase in the number of generations, and a decrease in the temperature parameter. These changes did not significantly improve tree resolution and the runs still did not converge (average standard deviation of split frequencies = 0.142989; Fig. 3). This analysis did support the macins as a separate group (Fig. 3, posterior probability = 0.99). The cysteine patterns of two sequences identified in the BLAST searches were most similar to the macin group (Archispirostreptus gigas [GenBank: FN197329] and Peripatopsis sedwicki [GenBank: FN237260]; Additional file 1: Figure S1); however, their cysteine spacings deviate from those of the majority of macins and the Bayesian analysis did not place them with this group (Fig. 3). The analysis also identified a group of six-cysteine scorpion toxins, although not all six-cysteine scorpion toxin sequences were placed in this clade, and several small groups contained two to four sequences (Fig. 3). Of note, the analysis supported the similarity of drosomycin and human DLD (Fig. 3, posterior probability = 0.91), despite DLD’s lack of signature motifs for this superfamily.
Many papers reporting defensins perform phylogenetic analyses, but most use a limited number of sequences from closely-related species and many do not show measures of support. The analysis arguing for convergent evolution included only ABFs from A. suum and C. elegans, two insect defensins, one tick defensin, one scorpion sequence, and MGD-1, and showed no measures of support for the resulting clades . A study of defensins from Ixodes ricinus included a phylogenetic analysis of sequences from ticks, scorpions, insects, plants, mollusks, and snakes; clades corresponding to these major groups were fairly well supported, with the exception of one scorpion sequence placed in the tick clade and the two mollusk sequences distributed between the insect and scorpion groups . However, no nematode sequences were included, and the rationale for inclusion of 34 snake defensins was unclear since these are not part of the CS-αβ superfamily and are not likely to share a common ancestor with this group.
A recent review classified invertebrate defensins into five categories: arthropod and mollusk-type 6-cysteine defensins, mollusk-type 8-cysteine defensins, nematode-type 8-cysteine defensins, invertebrate big defensins, and invertebrate β-defensin-like peptides . Only the first three categories are part of the CS-αβ superfamily, and while the analysis identifies the major groups, the bootstrap values are low for major clades . Unfortunately, the only nematode sequences included are the ASABFs and CeABFs, which represent only some of the diversity of nematode defensins . Broad analyses such as this are likely to be biased by nomenclature—the analysis included five groups of “defensins,” two of which are not considered to be evolutionarily related, while sequences like drosomycin and the macins were omitted. When studying relationships between invertebrate defensins in the CS-αβ superfamily, sequences from other groups in the superfamily are likely to provide a more appropriate evolutionary context than sequences based on the name “defensin.”
A reference array for the superfamily may facilitate peptide comparisons
Since there are no clear sequence or activity criteria for classification as an invertebrate defensin, it seems reasonable to consider newly identified CS-αβ sequences in the context of the superfamily. Most sequences in the superfamily have six, eight, or ten cysteines. Using a reference array with ten cysteines, the insect defensins would be described as C2–C6, C3–C8, C4–C9 and the nematode ABFs would be described as C2–C6, C3–C8, C4–C9, C5–C10, making their similarity explicit. Drosomycin and plant defensins would then be described as C2–C6, C3–C8, C4–C9, C1–C10, which clearly shows the difference in the fourth disulfide bridge compared to the nematode ABFs. The ten-cysteine theromacin can then be described as C2–C6, C3–C8, C4–C9, C1–C7, C5–C10. Since the structures of many peptides have not been experimentally verified, bonds inferred from homology can be put in parentheses or brackets. For additional cysteines or cases for which the bonding is not known or inferred, these can be listed in parentheses as well. For example, the structure of mytimacin 5 has not been reported, but from the reference array (Fig. 1) it can be described as (C2–C6, C3–C8, C4–C9, C1–C7, C5–C10, C3/4–C10/); in this case, the bonding is inferred based on similarity to theromacin, with C3/4 located between C3 and C4, and C10/ located after C10 that would be hypothesized to form an additional bond.
It should be possible to clearly define the characteristics of an invertebrate defensin based on invertebrate peptides currently classified as defensins; however, this is not the case. Depending on taxonomic group, a peptide classified as an “invertebrate defensin” may have six or eight cysteines and a variety of biological activities, while a similar (sometimes nearly indistinguishable) peptide with 4–12 cysteines may be called a mycin, macin, mytilin, myticin, antibacterial factor, antifungal peptide, defensin-like peptide/protein, cysteine-rich peptide/protein, or drosomycin-type antifungal peptide. Since it is unlikely that established names of peptides will be changed even if a unified nomenclature is proposed, a reasonable alternative is to establish a system for comparing and discussing these peptides that can be used in addition to peptide names. The proposed reference array clarifies similarities between peptides within the superfamily. Researchers studying invertebrate defensins in the CS-αβ superfamily should be aware that relying exclusively on the term “defensin” to identify sequences for inclusion in phylogenetic analyses has no evolutionary basis, and should instead look at the superfamily for evolutionary context.
CS-αβ sequences used for analysis
CS-αβ sequences used in the analyses were identified from previous BLAST searches of invertebrate taxa performed in this lab, published analyses, and reviews of scorpion toxins , nematode CS-αβ sequences , plant defensins , fungal defensins/defensin-like peptides [23, 24], spider defensins , and insect defensins  identified in PubMed searches. The query sequences used in BLAST searches are shown in Additional file 4: Table S3. Amino acid sequences were obtained from GenBank and the Protein Database (PDB) available on the NCBI website, Swiss-Prot/Uni-ProtKB , NEMBASE4 , and WormBase (version WS250, http://www.wormbase.org) . Sequences were viewed in EditSeq (LaserGene 12 Core Suite, DNASTAR, Madison, WI, USA) and saved in FASTA format. If only a nucleotide sequence was available, this was translated in EditSeq; sequences without database entries that were shown in a publication were entered into EditSeq manually. The complete set of sequences considered in the analyses can be found in Additional file 5: Table S4. Structures for Fig. 1 were downloaded from the Molecular Modeling Database (MMDB)  and viewed with the Cn3D macromolecular structure viewer (version 4.3.1).
Sequences encoding the mature peptide were aligned in MEGA6  with manual adjustments to ensure accurate alignment of the cysteines. Representatives were chosen from groups of highly similar sequences to reduce the number of sequences for the analyses shown in Fig. 2 and 3. The “Find BestDNA/Protein Models” algorithm identified the WAG + G + I model as the best fit for the data. This model was used for the maximum likelihood analysis with 1000 bootstrap replicates; all sites were used (Fig. 2). Alignments were exported in Nexus (PAUP) format, and the file used as input for MrBayes 3.2 . Since AdDLP is hypothesized as an ancestor of this group, insertions and deletions relative to AdDLP in the full alignment were coded for six areas: (1) AdDLP has three amino acids upstream of C2, so 3aa = 1, <3aa = 0, >3aa = 2; (2) AdDLP has a total of 17 gap spaces between C2 and C3, so 17 = 1, <17 = 0, >17 = 2; (3) AdDLP has three amino acids between C3 and C4 (standard for the motif), so 3aa = 1, <3aa = 0, >3aa = 2; (4) AdDLP has a total of 11 gap spaces between the position of C6 and C8, so 11 = 1, <11 = 0, >11 = 2; (5) AdDLP has one amino acid between C8 and C9 (standard for the motif), so 1aa = 1, <1az = 0, >1aa = 2; and (6) AdDLP has nine amino acids after C9, so 9aa = 1, <9aa = 0, >9aa = 2. N- and C-terminal propeptides were encoded as present = 1 and absent = 0. All missing or unknown data was coded as (-). These data were manually entered into the Nexus file in WordPad. The data was partitioned into protein, indel, and pro(peptide) partitions for analysis. In MrBayes, “lset rates = invgamma” and “prset = aamodel pr = mixed” was applied to the protein partition, “lset rates = gamma” was applied to the indel and pro partitions. The “ratepr” parameter was set to “variable” to allow rates to vary across partitions. For the tree shown in Fig. 3, the number of generations was increased to two million and the temperature decreased to 0.5. Analyses with only one million generations and varying temperature parameters did not give drastically different trees (not shown). The tree was visualized in FigTree1.4 (available from http://tree.bio.ed.ac.uk/software/figtree/) with levels of support shown as posterior probabilities.
Ganz T, Selsted ME, Szklarek D, Harwig SSL, Daher K, Bainton DF, et al. Defensins: natural peptide antibiotics of human neutrophils. J Clin Invest. 1985;76:1427–35.
Selsted ME, Harwig SSL, Ganz T, Schilling JW, Lehrer RI. Primary structures of three human neutrophil defensins. J Clin Invest. 1985;76:1436–9.
Selsted ME, Brown DM, DeLange RJ, Harwig SSL, Lehrer RI. Primary structures of six antimicrobial peptides of rabbit peritoneal neutrophils. J Biol Chem. 1985;260(8):4579–84.
Lambert J, Keppi E, Dimarcq JL, Wicker C, Reichhart JM, Dunbar B, et al. Insect immunity: isolation from immune blood of the dipteran Phormia terranovae of two insect antibacterial peptides with sequence homology to rabbit lung macrophage bactericidal peptides. PNAS. 1989;86:262–6.
Matsuyama K, Natori S. Purification of three antibacterial proteins from the culture medium of NIH-Sape-4, an embryonic cell line of Sarcophaga peregrina. J Biol Chem. 1988;263(32):17112–6.
Dimarcq J-L, Bulet P, Hetru C, Hoffmann J. Cysteine-rich antimicrobial peptides in invertebrates. Biopolymers. 1998;47:465–77.
Shafee TMA, Lay FT, Hulett MD, Anderson MA. The defensins consist of two independent, convergent protein superfamilies. Mol Biol Evol. 2016;33(9):2345–56.
Terras FRG, Schoofs HME, De Bolle MFC, van Leuven F, Rees SB, Vanderleyden J, et al. Analysis of two novel classes of plant antifungal proteins from radish (Raphanus sativus L.) seeds. J Biol Chem. 1992;267(22):15301–9.
Terras FRG, Eggermont K, Kovaleva V, Raikhel NV, Osborn RW, Kester A, et al. Small cysteine-rich proteins from radish: their role in host defense. Plant Cell. 1995;7:573–88.
Fehlbaum P, Bulet P, Michaut L, Lagueux M, Broekaert WF, Hetru C, et al. Septic injury of Drosophila induces the synthesis of a potent antifungal peptide with sequence homology to plant antifungal peptides. J Biol Chem. 1994;269(52):33159–63.
Cornet B, Bonmatin JM, Hetru C, Hoffmann JA, Ptak M, Vovelle F. Refined three-dimensional solution structure of insect defensin A. Structure. 1995;3(5):435–48.
Kobayashi Y, Takashima H, Tamaoki H, Kyogoku Y, Lambert P, Kuroda H, et al. The cysteine-stabilized α-helix: a common structural motif of ion-channel blocking neurotoxic peptides. Biopolymers. 1991;31:1213–20.
Yount NY, Yeaman MR. Multidimensional signatures in antimicrobial peptides. Proc Natl Acad Sci USA. 2004;101(19):7363–8.
Yount NY, Yeaman MR. Structural congruence among membrane-active host defense polypeptides of diverse phylogeny. Biochim Biophys Acta. 2006;1758:1373–86.
Murzin AG, Brenner SE, Hubbard T, Chothia C. SCOP: a structural classification of proteins database for the investigations of sequences and structures. J Mol Biol. 1995;247:536–40.
Andreeva A, Howorth D, Chothia C, Kulesha E, Murzin A. SCOP2 prototype: a new approach to protein structure mining. Nucleic Acid Res. 2014;42(D1):D310–4.
Miller C, Moczydlowski E, Latorre R, Phillips M. Charybdotoxin, a protein inhibitor of single Ca2+-activated K+ channels from mammalian skeletal muscle. Nature. 1985;313:316–8.
Gimenez-Gallego G, Navia MA, Reuben JP, Katz GM, Kaczorowski GJ, Garcia ML. Purification, sequence, and model structure of charybdotoxin, a potent selective inhibitor of calcium-activated potassium channels. Proc Natl Acad Sci USA. 1988;85:3329–33.
Zhu S. Evidence for myxobacterial origin of eukaryotic defensins. Immunogenetics. 2007;59(12):949–54.
Gao B, del Carmen Rodriguez M, Lanz-Mendoza H, Zhu S. AdDLP, a bacterial defensin-like peptide, exhibits anti-Plasmodium activity. Biochem Biophys Res Commun. 2009;387:393–8.
Zhu S, Gao B. Nematode-derived drosomycin-type antifungal peptdies provide evidence for plant-to-ecdysozoan horizontal transfer of a disease resistance gene. Nat Commun. 2014;5:3154.
Zhu S, Gao B. Evolutionary origin of β-defensins. Dev Comp Immunol. 2013;39:79–84.
Zhu S. Discovery of six families of fungal defensin-like peptides provides insights into origin and evolution of the CSαβ defensins. Mol Immunol. 2008;45:828–38.
Zhu S, Gao B, Harvey PJ, Craik DJ. Dermatophytic defensin with antiinfective potential. PNAS. 2012;109(22):8495–500.
Tassanakajon A, Somboonwiwat K, Amparyup P. Sequence diversity and evolution of antimicrobial peptides in invertebrates. Dev Comp Immunol. 2015;48:324–41.
Hanzawa H, Shimada I, Kuzuhara T, Komano H, Kohda D, Inagaki F, et al. 1H nuclear magnetic resonance study of the solution conformation of an antibacerial protein, sapecin. FEBS Lett. 1990;269(2):413–20.
Bontems F, Roumestand C, Gilquin B, Ménez A, Toma F. Refined Structure of charybdotoxin: common motifs in scorpion toxins and insect defensins. Science. 1991;254(5037):1521–3.
Cociancich S, Goyffon M, Bontems F, Bulet P, Bouet F, Menex A, et al. Purification and characterization of a scorpion defensin, a 4 kDa antibacterial peptide presenting structural similarities with insect defensins and scorpion toxins. Biochem Biophys Res Commun. 1993;194(1):17–22.
Landon C, Sodano P, Hetru C, Hoffmann J, Ptak M. Solution structure of drosomycin, the first inducible antifungal protein from insects. Protein Sci. 1997;6:1878–84.
Fant F, Vranken W, Broekaert W, Borremans F. Determination of the three-dimensional solution structure of Raphanus sativus antifungal protein 1 by 1H NMR. J Mol Biol. 1998;279:257–70.
Babin DR, Watt DD, Goos SM, Mlejnek RV. Amino acid sequences of neurotoxic protein variants from the venom of Centruroides sculpturatus Ewing. Arch Biochem Biophys. 1974;164(2):694–706.
Cook WJ, Zell A, Watt DD, Ealick SE. Structure of variant 2 scorpion toxin from Centruroides sculpturatus Ewing. Protein Sci. 2002;11(3):479–86.
Mygind PH, Fischer RL, Schnorr KM, Hansen MT, Sönksen CP, Ludvigsen S, et al. Plectasin is a peptide antibiotic with therapeutic potential from a saprophytic fungus. Nature. 2005;437:975–80.
Yang Y-S, Mitta G, Chavanieu A, Calas B, Sanchez JF, Roch P, et al. Solution structure and activity of the synthetic four-disulfide bond Mediterranean mussel defensin (MGD-1). Biochemistry. 2000;39:14436–47.
Roch P, Yang Y, Toubiana M, Aumelas A. NMR structure of mussel mytilin, and antiviral-antibacterial activities of dereived synthetic peptides. Dev Comp Immunol. 2008;32(3):227–38.
Wiens M, Schröder HC, Korzhev M, Wang XH, Batel R, Müller WEG. Inducible ASABF-type antimicrobial peptide from the sponge Suberites domuncula: microbicidal and hemolytic activity in vitro and toxic effect on molluscs in vivo. Mar Drugs. 2011;9(10):1969–94.
Blanc E, Sabatier JM, Kharrat R, Meunier S, El Ayeb M, Van Rietschoten J, et al. Solution structure of maurotoxin, a scorpion toxin from Scorpio maurus, wtih high affinity for voltage-gated potassium channels. Proteins. 1997;29(3):321–33.
Minaba M, Ueno S, Pillai A, Kato Y. Evolution of ASABF (Ascaris suum antibacterial factor)-type antimicrobial peptdies in nematodes: putative rearrangement of disulfide bonding patterns. Dev Comp Immunol. 2009;33(11):1147–50.
Tasiemski A, Vandenbulcke F, Mitta G, Lemoine J, Lefebvre C, Sautière PE, et al. Molecular characterization of two novel antibacterial peptdies inducivle upon bacterial challenge in an annelid, the leech Theromyzon tessulatum. J Biol Chem. 2004;279(30):30973–82.
Jung S, Sönnichsen FD, Hung C-W, Tholey A, Boidin-Wichlacz C, Haeusgen W, et al. Macin family of antimicrobial proteins combines antimicrobial and nerve repair activities. J Biol Chem. 2012;287(17):14246–58.
Jung S, Dingley AJ, Augustin R, Anton-Erxleben F, Stanisak M, Gelhaus C, et al. Hydramacin-1, structure and antibacterial activity of a protein from the basal metazoan hydra. J Biol Chem. 2009;284(3):1896–905.
Xu Q, Wang G, Yuan H, Chai Y, Xiao Z. cDNA sequence and expression analysis of an antimicrobial peptide, theromacin, in the triangle-shell pearl mussel Hyriopsis cumingii. Comp Biochem Physiol B Biochem Mol Biol. 2010;157:119–26.
Gerdol M, De Moro G, Manfrin C, Venier P, Pallavicini A. Big defensins and mytimacins, new AMP families of the Mediterranean mussel Mytilus galloprovincialis. Dev Comp Immunol. 2012;36:390–9.
Zhong J, Wang W, Yang X, Yan X, Liu R. A novel cysteine-rich antimicroial peptide from the mucus of the snail of Achatina fulica. Peptides. 2013;39:1–5.
Soudani N, Gharbi-Chihi J, Srairi-Abid N, Martin-El Yazidi C, Planells R, Margotat A, et al. Isolation and molecular characterization of LVP1 lipolysis activating peptide from scorpion Buthus occitanus tunetanus. Biochim Biophys Acta. 2005;1747(1):47–56.
Lamberty M, Ades S, Uttenweiler-Joseph S, Brookhart G, Bushey D, Hoffmann JA, et al. Isolation from the lepidopteran Heliothis virescens of a novel insect defensin with potent antifungal activity. J Biol Chem. 1999;274(14):9320–6.
Lamberty M, Zachary D, Lanot R, Bordereau C, Robert A, Hoffmann JA, et al. Constitutive expression of a cysteine-rich antifungal and a linear antibacterial peptide in a termite insect. J Biol Chem. 2001;276(6):4085–92.
Bulet P, Cociancich S, Reuland M, Sauber F, Bischoff R, Hegy G, et al. A novel insect defensin mediates the inducible antibacterial activity in larvae of the dragonfly Aeschna cyanea (Paleoptera, Odonata). Eur J Biochem. 1992;209:977–84.
Fujiwara S, Imai J, Fujiwara M, Yaeshima T, Kawashima T, Kobayashi K. A potent antibacterial protein in royal jelly. Purification and determination of the primary structure of royalisin. J Biol Chem. 1990;285(19):11333–7.
Dimarcq J-L, Hoffmann D, Meister M, Bulet P, Lanot R, Reichhart J-M, et al. Characterization and transcriptional profiles of a Drosophila gene encoding an insect defensin. Eur J Biochem. 1994;221(1):201–9.
Lee YS, Yun EK, Jang WS, Kim I, Lee JH, Park SY, et al. Purification, cDNA cloning and expression of an insect defensin from the great wax moth, Galleria mellonella. Insect Mol Biol. 2004;13(1):65–72.
Schuhmann B, Seitz V, Vilcinskas A, Podsiadlowski L. Cloning and expression of gallerimycin, an Antifungal peptide expressed in immune response of greater wax moth larve, Galleria mellonella. Arch Insect Biochem Physiol. 2003;53(3):125–33.
Tonk M, Cabezas-Cruz A, Valdés JJ, Rego ROM, Chrudimská T, Strnad M, et al. Defensins from the tick Ixodes scapularis are effective against phytopathogenic fungi and the human bacterial pathogen Listeria grayi. Parasit Vectors. 2014;7:554.
Hubert F, Noël T, Roch P. A member of the arthropod defensin family from edible Mediterranean mussels (Mytilus galloprovincialis). Eur J Biochem. 1996;240(1):302–6.
Romestand B, Molina F, Richard V, Roch P, Granier C. Key role of the loop connecting the two beta strands of mussel defensin in its antimicrobial activity. Eur J Biochem. 2003;270:2805–13.
Mitta G, Hubert F, Noël T, Roch P. Myticin, a novel cystein-rich antimicrobial peptide isolated from haemocytes and plasma of the mussel Mytilus galloprovincialis. Eur J Biochem. 1999;265(1):71–8.
Charlet M, Chernysh S, Philippe H, Hetru C, Hoffmann JA, Bulet P. Innate immunity. Isolation of several cyteine-rich antimicrobial peptides from the blood of a mollusc, Mytilus edulis. J Biol Chem. 1996;271(36):21808–13.
Mitta G, Vandenbulcke F, Hubert F, Salzet M, Roch P. Involvement of Mytilins in mussel antimicrobial defense. J Biol Chem. 2000;275(17):12954–62.
Kato Y, Komasku S. ASABF, a novel cysteine-rich antibacterial peptide isolated from the nematode Ascaris suum. J Biol Chem. 1996;271(48):30493–8.
Kato Y, Aizawa T, Hoshino H, Kawano K, Nitta K, Zhang H. abf-1 and abf-2, ASABF-type antimicrobial peptide genes in Caenorhabditis elegans. Biochem J. 2002;361(Pt2):221–30.
Osborn RW, De Samblanx GW, Thevissen K, Goderis I, Torrekens S, Van Leuven F, et al. Isolation and characterisation of plant defensins from seeds of Asteraceae, Fabaceae, Hippocastanaceae, and Saxigragaceae. FEBS Lett. 1995;368(2):257–62.
Kushmerick C, de Souza Castro M, Cruz JS, Bloch C Jr., Beirão PSL. Functional and structural features of γ-zeathionins, a new class of sodium channel blockers. FEBS Lett. 1998;440(3):302–6.
Kant P, Liu WZ, Pauls KP. PDC1, a corn defensin peptide expressed in Escherichia coli and Pichia pastoris inhibits the growth of Fusarium graminearum. Peptides. 2009;30(9):1593–9.
Gao A-G, Hakimi SM, Mittanck CA, Wu Y, Woerner BM, Stark DM, et al. Fungal pathogen protection in potato by expression of a plant defensin peptide. Nat Biotechnol. 2000;18:1307–10.
Spelbrink RG, Dilmac N, Allen A, Smith TJ, Shah DM, Hockerman GH. Differential antifungal and calcium channel-blocking activity among structurally related plant defensins. Plant Physiol. 2004;135:2055–67.
Allen A, Snyder AK, Preuss M, Nielsen EE, Shah DM, Smith TJ. Plant defensins and virally encoded fungal toxin KP4 inhibit plant root growth. Planta. 2008;227(2):331–9.
Lay FT, Brugliera F, Anderson MA. Isolation and properties of floral defensins from ornamental tobacco and petunia. Plant Physiol. 2003;131:1283–93.
Ming D, Hellekant G. Brazzein, a new high-potency thermostable sweet protein from Pentadiplandra brazzeana B. FEBS Lett. 1994;355:106–8.
Lee KH, Hong SY, Oh JE, My Kwon, Yoon JH, Lee Jh, et al. Identification and characterization of the antimicrobial peptide corresponding to C-terminal β-sheet domain of tenecin 1, an antibacterial protein of larvae of Tenebrio molitor. Biochem J. 1998;334:99–105.
Wang Y, Zhu S. The defensin gene family expansion in the tick Ixodes scapularis. Dev Comp Immunol. 2011;35:1128–34.
Gao B, Zhu S. Identification and characterization of the parasitic wasp Nasonia defensins: positive selection targeting the functional region? Dev Comp Immunol. 2010;34(6):659–68.
Yamada K, Natori S. Purification, sequence and antibacterial activity of two novel sapecin homologues from Sarcophaga embryonic cells: similarity of sapecin B to charybdotoxin. Biochem J. 1993;291:275–9.
Yamada K, Natori S. Characterization of the antimicrobial peptide derived from sapecin B, an antibacterial protein of Sarcophage peregrina (flesh fly). Biochem J. 1994;298:623–8.
Miyanoshita A, Hara S, Sugiyama M, Asaoka A, Taniai K, Yukuhiro F, et al. Isolation and characterization of a new member of the insect defensin family from a beetle, Allomyrina dichotoma. Biochem Biophys Res Commun. 1996;220(3):526–31.
Ishibashi J, Saido-Sakanaka H, Yang J, Sagisaka A, Yamakawa M. Purification, cDNA cloning and modification of a defensin from the coconut rhinoceros beetle, Oryctes rhinoceros. Eur J Biochem. 1999;266(2):616–23.
Hwang JS, Lee J, Kim YJ, Bang HS, Yun EY, Kim SR, et al. Isolation and characterization of a defensin-like peptide (Coprisin) from the dung beetle, Copris tripartitus. Int J Pept. 2009;2009:136284.
Saido-Sakanaka H, Ishibashi J, Sagisaka A, Momotani E, Yamakawa M. Synthesis and characterization of bactericidal oligopeptides designed on the basis of an insect anti-bacterial peptide. Biochem J. 1999;338:29–33.
Tsuji N, Battsetseg B, Boldbaatar D, Miyoshi T, Xuan X, Oliver JH Jr, et al. Babesial vector tick defensin against Babesia sp. parasites. Infect Immun. 2007;75(7):3633–40.
Zhu S, Peigneur S, Gao B, Umetsu Y, Ohki S, Tytgat J. Experimental conversion of a defensin into a neurotoxin: implications for origin of toxic function. Mol Biol Evol. 2014;31(3):546–59.
Simon A, Kullberg BJ, Tripet B, Boerman OC, Zeeuwen P, van der Ven-Jongekrijg J, et al. Drosomycin-like defensin, a human homologue of Drosophila melanogaster drosomycin with antifungal activity. Antimicrob Agents Chemother. 2008;52(4):1407–12.
Zhang H, Kato Y. Common structural properties specifically found in the CSαβ-type antimicrobial peptides in nematodes and mollusks: evidence for the same evolutionary origin? Dev Comp Immunol. 2003;27(6–7):499–503.
Froy O, Gurevitz M. Arthropod and mollusk defensins–evolution by exon-shuffling. Trends Genet. 2003;19(12):684–7.
Froy O. Convergent evolution of invertebrate defensins and nematode antibacterial factors. Trends Microbiol. 2005;13(7):314–9.
Rodriguez de la Vega RC, Possani LD. On the evolution of invertebrate defensins. Trends Genet. 2005;21(6):330–2.
Baumann T, Kuhn-Nentwig L, Largiadèr CR, Nentwig W. Expression of defensins in non-infected araneomorph spiders. Cell Mol Life Sci. 2010;67(15):2643–51.
De Zoysa M, Whang I, Lee Y, Lee S, Lee JS, Lee J. Defensin from disk abalone Haliotis discus discus: molecular cloning, sequence characterization and immune response against bacterial infection. Fish Shellfish Immunol. 2010;28:261–6.
Zhu S, Gao B, Tytgat J. Phylogenetic distribution, functional epitopes and evolution of the CSαβ superfamily. Cell Mol Life Sci. 2005;62(19–20):2257–69.
Aizawa T, Hoshino H, Fujitani N, Koganesawa N, Matsuura A, Miyazawa M, et al. Structural analysis of an antibacterial peptide derived from a nematode. In: Shiroiri T, editor. Peptide science 2000. Hiratsuka: The Japanese Peptide Society; 2001. p. 269–72.
Tonk M, Cabezas-Cruz A, Valdés JJ, Rego ROM, Grubhoffer L, Estrada-Peña A, et al. Ixodes ricinus defensins attack distantly-related pathogens. Dev Comp Immunol. 2015;53(2):358–65.
Tarr DEK. Distribution and characteristics of ABFs, cecropins, nemapores, and lysozymes in nematodes. Dev Comp Immunol. 2012;36(3):502–20.
Carvalho AdO, Gomes VM. Plant defensins and defensin-like peptides-biological activities and biotechnological applications. Curr Pharm Des. 2011;17:427–4293.
Yi HY, Chowdhury M, Huang YD, Yu XQ. Insect antimicrobial peptides and their applications. Appl Microbiol Biotechnol. 2014;98(13):5807–22.
UniProt Consortium. UniProt: a hub for protein information. Nucleic Acid Res. 2015;43(Database issue):D204–12.
Elsworth B, Wasmuth J, Blaxter M. NEMBASE4: the nematode transcriptome resource. Int J Parasitol. 2011;41(8):881–94.
Harris TW, Baran J, Bieri T, Cabunoc A, Chan J, Chen WJ, et al. WormBase 2014: new views of curated biology. Nucleic Acid Res. 2014;42(Database issue):D789–93.
Madej T, Lanczycki CJ, Zhang D, Thiessen PA, Geer RC, Marchler-Bauer A, et al. MMCB and VAST+: tracking structural similarities between macromolecular complexes. Nucleic Acid Res. 2014;42(Database issue):D297–303.
Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: molecular evolutionary genetics analysis. Mol Biol Evol. 2013;30(12):2725–9.
Ronquist F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19(12):1572–4.
Matsuyama K, Natori S. Molecular cloning of cDNA for sapecin and unique expression of the sapecin gene druring development of Sarcophaga peregrina. J Biol Chem. 1988;263(32):17117–21.
Tian C, Gao B, del Carmen Rodriguez M, Lanz-Mendoza H, Ma B, Zhu S. Gene expression, antiparasitic activity, and functional evolution of the drosomycin family. Mol Immunol. 2008;45(15):3909–16.
Mitta G, Vandenbulcke F, Hubert F, Roch P. Mussel defensins are synthesised and processed in granulocytes then released into the plasma after bacterial challenge. J Cell Sci. 1999;112:4233–42.
Roch P, Beschin A, Bernard E. Antiprotozoan and antiviral activities of non-cytotoxic truncated and variant analogues of mussel defensin. Evid Based Complement Alternat Med. 2004;1(2):167–74.
Bílikova K, Huang SC, Lin IP, Šimuth J, Peng CC. Structure and antimicrobial activity relationship of royalisin, an antimicrobial peptide from royal jelly of Apis mellifera. Peptides. 2015;68:190–6.
Hynes WL, Ceraul SM, Todd SM, Seguin KC, Sonenshine DE. A defensin-like gene expressed in the black-legged tick, Ixodes scapularis. Med Vet Entomol. 2005;19(4):339–44.
Mitta G, Hubert F, Dyrynda EA, Boudry P, Roch P. Mytilin B and MGD2, two antimicrobial peptides of marine mussels: gene structure and expression analysis. Dev Comp Immunol. 2000;24(4):381–93.
Lee E, Kim JK, Shin S, Jeong KW, Shin A, Lee J, et al. Insight into the antimicrobial activities of coprisin isolated from the dung beetle, Copris tripartitus, revealed by structure-activity relationships. Biochim Biophys Acta. 2013;1282(2):271–83.
Lee J, Lee D, Choi H, Kim HH, Kim H, Hwang JS, et al. Structure-activity relationships of the intramolecular disulfide bonds in coprisin, a defensin from the dung beetle. BMB Rep. 2014;47(11):625–30.
Moon HJ, Lee SY, Kurata S, Natori S, Lee BL. Purification and molecular cloning of cDNA for an inducible antibacterial protein from larvae of the coleopteran, Tenebrio molitor. J Biochem. 1994;116(1):53–8.
Rahman MM, Tsuji N, Boldbaatar D, Battur B, Liao M, Umemiya-Shirafiju R, et al. Structural characterization and cytolytic activity of a potent antimicrobial motif in longicin, a defensin-like peptide in the tick Haemophysalis longicornis. Parasitology. 2010;72(2):149–56.
I thank Alexandra Rogers for manuscript comments and her ongoing efforts to characterize the defensins, and Angelina Zehrbach for BLAST searches to identify new CS-αβ superfamily members.
The author declares that she has no competing interests.
Availability of supporting data
The datasets supporting the results of this article are included within the article and its additional files.
Ongoing antimicrobial peptide research is supported by intramural funding from the Midwestern University Office of Research and Sponsored Programs (ORSP). ORSP had no role in study design, data collection, analysis, and interpretation, or manuscript preparation.
Alignment of CS-αβ superfamily sequences with reference array. Alignment to a ten-cysteine reference array based on the cysteines forming the CSH motif (C3–C8, C4–C9) and the third bond completing the CS-αβ fold (C2–C6). The GXC of the γ-core is usually at C6, except for mytilins (C7). A filled square indicates presence of the indicated cysteine and numbers in unfilled blocks represent the number of intervening amino acids. Sequences are grouped based on the basic cysteine patterns observed and within these by major taxonomic group (listed in column A). Additional cysteines at the N or C-terminus of the conserved array are represented by additional filled boxes. Additional cysteines within the conserved array are represented as “C.” Major taxonomic groups are color-coded: Annelida (dark rose), Arachnida (light orange), Bacteria (black), Bivalvia (light blue), Cnidaria (light grey), Crustacea (peach), Echinodermata (pink), Fungi (light green), Gastropoda (blue), Hexapoda (orange), Myriapoda (dark orange), Nematoda (lavender), Onychophora (light purple), Plantae (green), Platyhelminthes (light rose), Porifera (dark grey), and Tardigrada (yellow).
Antimicrobial activity of CS-αβ peptides. Peptides are listed in alphabetical order by species within major taxonomic groups. The activity column lists activity against Gram-positive bacteria (G+), Gram-negative bacteria (G−), filamentous fungi (F), yeast (Y), and protozoa (P), as well as cytotoxic (C) and hemolytic (H) activity. The peptide has the activity shown if the abbreviation is shown without parentheses, and has been tested but not shown to have the activity if shown in parentheses. If a dominant activity has been determined, the abbreviation is shown in bold; any activity not shown has not been tested for that peptide.
Representative CS-αβ sequences used for phylogenetic analysis. Accession numbers are shown for each sequence used in the analysis. The “Tree Label” column corresponds to the names shown in Fig. 2 and 3. The “Sequences Represented” column shows information for sequences excluded from the analysis based on similarity to the representative sequence. In cases where a sequence is represented by more than one accession number, the sequence used is shown in bold.
Accession numbers for query sequences used in BLAST searches.
CS-αβ sequences considered in this study. In cases where a sequence is represented by more than one accession number, the sequence used is shown in bold.
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Tarr, D.E.K. Establishing a reference array for the CS-αβ superfamily of defensive peptides. BMC Res Notes 9, 490 (2016). https://doi.org/10.1186/s13104-016-2291-0
- Antimicrobial peptide
- CS-αβ superfamily
- Fungal defensin
- Invertebrate defensin
- Invertebrate immunity
- Plant defensin
- Scorpion toxin