Interaction of hookworm 14-3-3 with the forkhead transcription factor DAF-16 requires intact Akt phosphorylation sites

Background Third-stage infective larvae (L3) of hookworms are in an obligatory state of developmental arrest that ends upon entering the definitive host, where they receive a signal that re-activates development. Recovery from the developmentally arrested dauer stage of Caenorhabditis elegans is analogous to the resumption of development during hookworm infection. Insulin-like signaling (ILS) mediates recovery from arrest in C. elegans and activation of hookworm dauer L3. In C. elegans, phosphorylation of the forkhead transcription factor DAF-16 in response to ILS creates binding cites for the 14-3-3 protein Ce-FTT-2, which translocates DAF-16 out of the nucleus, resulting in resumption of reproductive development. Results To determine if hookworm 14-3-3 proteins play a similar role in L3 activation, hookworm FTT-2 was identified and tested for its ability to interact with A. caninum DAF-16 in vitro. The Ac-FTT-2 amino acid sequence was 91% identical to the Ce-FTT-2, and was most closely related to FTT-2 from other nematodes. Ac-FTT-2 was expressed in HEK 293T cells, and was recognized by an antibody against human 14-3-3β isoform. Reciprocal co-immunoprecipitations using anti-epitope tag antibodies indicated that Ac-FTT-2 interacts with Ac-DAF-16 when co-expressed in serum-stimulated HEK 293T cells. This interaction requires intact Akt consensus phosphorylation sites at serine107 and threonine312, but not serine381. Ac-FTT-2 was undetectable by Western blot in excretory/secretory products from serum-stimulated (activated) L3 or adult A. caninum. Conclusion The results indicate that Ac-FTT-2 interacts with DAF-16 in a phosphorylation-site dependent manner, and suggests that Ac-FTT-2 mediates activation of L3 by binding Ac-DAF-16 during hookworm infection.


Background
Hookworm infection is one of the most common chronic illnesses in the world, with an estimated 740 million infections [1]. The developmentally arrested third-stage infective larvae (L3) of hookworms resume development in response to a host-specific signal encountered during invasion. This cue initiates a signaling pathway that results in expression of genes required for development and molting to the L4 and subsequent adult stage. This signaling pathway represents a potential target for intervention in the hookworm life cycle as a means of preventing infection.
When non-feeding arrested L3 of the canine hookworm Ancylostoma caninum are incubated with serum components in vitro, they resume feeding within 12 hrs [2,3]. While they do not molt in vitro, "activation" by serum induces the release of molecules associated with infection, including proteases and activation-associated secretory proteins (ASPs) [4][5][6][7], and differential gene expression [8]. Hookworm L3 activation is mediated by an insulin-like signaling (ILS) pathway, similar to recovery from the analogous dauer stage of the free-living nematode Caenorhabditis elegans [9,10]. This dauer stage is morphologically, behaviorally, and functionally analogous to the hookworm L3, and recovery from it has been proposed as a model for the hookworm infective process [11,12]. The molecular biology of dauer recovery is well-defined, and has provided a useful framework for investigation of the molecular biology of hookworm infection.
Recovery from dauer in C. elegans is mediated by an insulin-like signaling (ILS) pathway [13]. Replete environmental conditions initiate a signaling cascade through an insulin growth factor 1 (IGF-1)-like receptor (encoded by the daf-2 gene), a phosphatidylinositol 3-kinase (PI3-K, age-1), and protein kinase B/Akt [14][15][16][17][18][19][20]. One of the key downstream targets of ILS is the forkhead/FOXO transcription factor DAF-16. Under dauer-inducing conditions, DAF-16 is located primarily in the nucleus, where it binds to target genes and mediates entry into and maintenance of dauer [15,21]. ILS during recovery causes the phosphorylation of DAF-16 by the serine/threonine kinase Akt [18], thereby creating binding sites for 14-3-3 proteins [22]. Binding of 14-3-3 to phosphorylated DAF-16 results in translocation of DAF-16 from the nucleus to the cytoplasm, and expression of genes associated with growth and development [23,24]. The 14-3-3 proteins are highly conserved ~30 kDa acidic dimeric proteins found in all eukaryotes. They function in cell signaling, cell cycle regulation, intracellular trafficking, and other process by modulating protein-protein interactions [22]. Typically organisms contain several isoforms, and homo-or heterodimers bind to phosphoserine-or phosphothreonine-containing motifs [25]. All forms of 14-3-3 share a similar tertiary structure, the dimer contact residues are highly conserved, and each monomer is capable of binding a phosphopeptide independently [25]. There are two isoforms of 14-3-3 in C. elegans, ftt-2 and par-5, but only ftt-2 is involved in regulation of DAF-16. Specific knockdown by RNAi of ftt-2, but not par-5, caused increased transcription of DAF-16 target genes [26].
Activation of hookworm L3 requires ILS [13,27], and recently the ortholog of Ce-DAF-16 was identified from the hookworms A. caninum and A. ceylanicum and shown to bind to a conserved DNA binding element [28]. Given the conservation of this pathway and the similarity between L3 activation and dauer recovery, we asked whether Ac-DAF-16 was regulated by a 14-3-3 protein as well. We report here that the ortholog of Ce-FTT-2 from A. caninum interacts with Ac-DAF- 16 in vivo, and that this interaction requires intact Akt phosphorylation sites on DAF- 16. This provides further support for the use of dauer recovery as a model for larval activation during the hookworm infective process.

Cloning and characterization of Ac-ftt-2
A consensus sequence of a cluster of eight A. caninum expressed sequence tag (EST) sequences homologous to 14-3-3 proteins was used to design oligonucleotide primers to isolate the complete Ac-ftt-2 cDNA from A. caninum. Using a hemi-nested strategy, the 5' end was isolated using the conserved nematode spliced leader sequence [29] as the forward primer, coupled with two nested gene-specific reverse primers in successive PCR reactions. The second reaction produced an amplicon of approximately 600 bp that contained the SL sequence and overlapped the 5' end of the A. caninum EST sequence. A similar strategy was used to isolate the 3' end from an A. caninum cDNA library. A reverse primer complementary to the flanking T7 sequence in the vector was used with two nested forward primers to generate an amplicon of approximately 700 bp that contained a poly d(A) tail, and overlapped the EST and the 5' end sequences. New primers were designed to amplify the entire coding sequence of A. caninum 14-3-3 cDNA, which was cloned into pET28 vector and confirmed by DNA sequencing of both strands. The fulllength cDNA sequence was deposited in GenBank (accession number FJ842376).
The full-length 14-3-3 cDNA contained the conserved 22 nucleotide nematode SL at the 5' end [30], which was followed by 33 untranslated nucleotides and an ATG codon encoding the starting methionine at nucleotide 56. The cDNA is predicted to encode an open reading frame of 249 amino acids, ending with a TAA termination codon at nucleotide 803, and followed by a 327 bp 3'-untranslated region. A canonical AATAAT polyadenylation signal [31] was located 11 bp upstream of the poly (dA) tail (nucleotides 1116 to 1121). The deduced amino acid sequence has a predicted mass of 28174 Da and a calculated pI of 4.87. The hookworm 14-3-3 lacks a secretory signal peptide [32], and contains a nuclear export signal (LxxxLxL) [33] at amino acids 223 to 229, consistent with a role in nuclear transport [34].

Transfection and immunoprecipitation of Ac-FTT-2 from HEK 293 cells
Given the high level of conservation in 14-3-3 molecules, we tested whether an antibody against the human β isoform of 14-3-3 could detect Ac-FTT-2. As shown in Figure  2A, the 14-3-3β antibody recognized a single band in lysates of both untreated and serum-stimulated (activated) A. caninum L3 by Western blot. Next, we expressed recombinant Ac-FTT containing a V5 epitope tag in HEK293 cells. Western blotting of cell lysates indicated that Ac-FTT-2 was expressed in mammalian cells (Fig. 2B). An anti-V5 body recognized a single band of the appropriate size in lysates of cells transfected with pcDNA3.1V5/ Ac-ftt-2 plasmid, but not in lysates from cells transfected with empty vector. The 14-3-3β antibody recognized two bands in the transfected cells, and a single band in the mock transfected cells. The lower molecular weight band, present in both transfected and mock cells, is endogenous 14-3-3, while the higher molecular weight band is the expressed FTT-2/V5 fusion protein, which migrates more slowly in the gel because of the attached epitope tag. This indicates that recombinant Ac-FTT-2 can be expressed in mammalian cells, and recognized by an antibody against the epitope tag and an anti-human 14-3-3 antibody.
Dauer recovery in C. elegans is mediated by 14-3-3 through regulation of DAF-16 subcellular localization and transcriptional activities [26]. This regulation is dependent on insulin-like signalling [23]. Because the resumption of development associated with infection in hookworms is analogous to dauer recovery [11,37], we hypothesized that DAF-16 is regulated by 14-3-3 in response to ILS as in dauer recovery in C. elegans. Previously, we demonstrated that Ac-DAF-16 binds to and drives transcription from a conserved hookworm DAF-16 DNA binding element in mammalian cells [38]. As hookworms have yet to be transfected with foreign DNA, we again used mammalian cells to examine interactions between Ac-FTT-2 and Ac-DAF-16.
As shown in Figure 3A, anti-FLAG agarose pulled down both a 64 kDa FLAG-tagged DAF-16 and the V5-tagged recombinant Ac-FTT-2 from co-transfected cells (lanes 3), but only recombinant DAF-16 from cells singly transfected with Ac-daf-16 (lane 1). As expected, anti-FLAG agarose did not pull down any protein from the Ac-ftt-2 singly transfected cells (lane 2). Conversely, anti-V5 agarose precipitated both proteins from co-transfected cells, but only recombinant 14-3-3 from cells singly transfected with the The phylogenetic relationship between Ac-FTT-2 and selected 14-3-3 protein family members Figure 1 The phylogenetic relationship between Ac-FTT-2 and selected 14-3-3 protein family members. A. Alignment of Ac-FTT-2 with C. elegans 14-3-3 proteins. Shading indicates residues that are identical (black) or similar (gray) to Ac-FTT-2. Amino acid residues that directly contact phosphate groups of targets are marked with an arrow. Protein sequences were aligned using CLUSTAL W software and displayed using BOXSHADE software located on the Swiss EMBnet server [74]. B. Neighbor joining tree of representative 14-3-3 proteins. Proteins were aligned using CLUSTAL W software on the Swiss EMBnet server [74]. Amino acid distances were calculated using the Poisson correction model in the MEGA program version 3.1 [75]. Major   Ac-ftt-2 construct, and nothing from cells expressing recombinant Ac-DAF-16 only (Fig. 3B). This indicates that Ac-FTT-2 interacts with Ac-DAF-16 in mammalian cell culture, and suggests that a similar interaction occurs in worms.

Intact phosphorylation sites are required for the FTT-2 -DAF-16 interaction
Interaction of 14-3-3 with Ce-DAF-16 requires phosphorylation of specific serine or threonine residues by the protein kinase Akt (Cahill et al., 2001). To determine if the predicted Akt phosphorylation sites are important for the interaction of hookworm 14-3-3 and DAF-16, recombinant Ac-DAF-16 proteins with the phosphorylation sites mutated to alanine were tested for their ability to co-IP recombinant FTT-2 when co-expressed in HEK293 cells. Anti-FLAG M2 resin co-immunoprecipitated recombinant Ac-FTT-2 and wild type FLAGtagged DAF-16 from cells expressing both proteins ( Figure  4). However, mutation of serine107 to alanine (S107A) completely abolished the interaction with Ac-FTT-2, either singly or in combination with mutations at the other Akt phosphorylation sites (S107A:T312A, S107A:S381A, or triple). Mutation of threonine 312 (T312A) alone or in combination with mutations at the other sites also severely diminished the interaction with FTT-2 However, mutation of serine 381 (S381A) had no effect on the interaction with 14-3-3 ( Figure 4). These data indicate that serine107 and threonine312 are essential for the interaction of Ac-DAF-16 with Ac-FTT-2.

Secretion of Ac-FTT-2
Hookworm L3 activated in vitro by incubation with serum components under host-like conditions release multiple proteins, including the activation associated secretory proteins 1 and 2 (ASP-1 and ASP-2) [5,6] and a metalloprotease [4]. Adult worms release molecules associated with feeding and survival in the host intestine, including anticoagulants [39], ASPs [40] and protease inhibitors [41]. To determine if Ac-FTT-2 was secreted, we took advantage of the cross-reactivity with the anti-human 14-3-3β antibody to examine ESP from L3 and adult stages by Western blot. As seen in Figure 5A, 14-3-3β antibody failed to detect any bands in non-activated, activated L3, or adult ESP (lanes 1-3), but recognized recombinant Ac-FTT-2 expressed in HEK293 cells (lane 4). As a control, L3 ESP were probed with ASP-1 antiserum, which detects a band in activated but not non-activated ESP ( Figure 5B, lanes 1-3) [5]. Furthermore, antiserum against Ac-TMP-1, known to be released in adult ESP [42], detected Ac-TMP in the adult ESP ( Figure 5B, lanes 4 and 5), indicating that the ESP contained secreted proteins. These data indicate that Ac-FTT-2 is not released in detectable amounts by either activated L3 or adult A. caninum.

Discussion
When hookworm L3 infective stage larvae encounter and invade a permissive host, developmental pathways are initiated by host-specific signals and lead to the maturation of larvae into adult parasites. The molecular details of this process are unknown, but clues to hookworm developmental processes have been revealed by studies of the related free-living nematode C. elegans. Specifically, dauer recovery in C. elegans has been compared to the transition to parasitism in hookworms [11,37], and they share several conserved pathways and molecules [27,38,43,44]. Despite these similarities, detailed mechanistic knowledge of the molecular biology of the transition to parasitism is difficult to obtain due to the inability of hookworms to complete their life cycle in vitro. For this reason, the regulation and function of hookworm molecules must be studied indirectly, using heterologous systems. This and a previous study [38] represent the first applications of a mammalian cell culture system to investigate hookworm molecular biology. This system will allow us to investigate molecular mechanisms of hookworm infection for the first time.
Dauer recovery in C. elegans is mediated by ILS signaling in response to improving environmental conditions [13]. ILS activates the serine/threonine kinase Akt/PKB, which in turn phosphorylates the forkhead transcription factor DAF-16 on multiple serine/threonine residues [18]. Phosphorylation of DAF-16 creates binding sites for the 14-3-3 family protein FTT-2 and translocates DAF-16 to the cytoplasm [23,26], thereby allowing a pattern of gene expression associated with reproductive development. Previously, we isolated an ortholog of DAF-16 from the hookworm A. caninum, and demonstrated that it bound to and drove transcription from a conserved DAF-16 binding element when expressed in mammalian cells [38]. The similarity between A. caninum and C. elegans ILS and recovery from dauer arrest led us to hypothesize that ILS plays a similar role in hookworms. To investigate the regulation of Ac-DAF-16 by 14-3-3, we isolated the FTT-2 ortholog from A. caninum, and co-expressed it with Ac-DAF-16 in HEK293 cells Most organisms contain multiple isoforms of 14-3-3, including seven in mammals, two in Drosophila and yeast, and 15 in plants [45]. Several isoforms have been identified in platyhelminths of the genera Echinococcus and Schistosoma [46,47]. To date, no nematodes have been shown to encode more than two FTT-2 isoforms. Sequence comparison and phylogenetic analysis indicated that the hookworm 14-3-3 was most closely related to FTT-2 molecules from C. elegans and other nematodes. Despite 86% sequence identity between 14-3-3 isoforms FTT-2 and PAR-5 in C. elegans, only FTT-2 affects dauer recovery. RNAi knockdown of Ce-ftt-2 enhanced dauer formation at permissive temperatures in dauer constitutive daf-2 mutants, increased nuclear localization of DAF-16, and promoted transcription of several DAF-16 target genes [26]. The high level of sequence conservation of Ac-FTT-2 with Ce-FTT-2 suggested that this isoform was most likely to interact with Ac-DAF-16 in hookworms. While FTT-2 affects dauer formation in C. elegans, PAR-5 also weakly interacts with Ce-DAF-16, suggesting a possible role in aspects of DAF-16 function other than those listed above [26]. Indeed, over-expression of Ce-FTT-2 and PAR-5 extend lifespan in a DAF-16-dependent manner, and both interact with SIR-2.1 and DAF-16 in C. elegans [48]. While our data suggest that Ac-FTT-2 shares similar functions with Ce-FTT-2, we can not rule out a function in infection for another isoform of 14-3-3 in hookworms.
Once we identified the appropriate 14-3-3 ortholog from A. caninum, we introduced Ac-ftt-2 cDNA into mammalian expression vectors and expressed epitope tagged fusion protein in HEK293 cells. The native and recom-binant hookworm FTT-2 protein expressed in HEK293 cells was recognized by an antibody against the β isoform of human 14-3-3. The antibody also detected an endogenous 14-3-3 protein in 293 cells, as indicated by the lower molecular weight band that is also present in cells transfected with empty vector. This antibody will permit further investigation of Ac-FTT-2 function in vitro and with native worm protein.
Ce-DAF-16 has been demonstrated to interact with 14-3-3 previously [26]. To determine if Ac-FTT-2 interacted with Ac-DAF-16, we co-expressed both proteins in HEK293 cells and performed reciprocal co-IPs using antibodies against the epitope tags on the recombinant proteins. We were able to successfully IP both proteins using both antibodies from serum stimulated cells, indicating that FTT-2 interacts with DAF-16.
Typically, FOXO family proteins have three Akt phosphorylation sites, with sites P1 and P2 flanking the DNA binding domain in the N-terminal half of the molecule, and site P3 in the C-terminal half. In FOXO-4, as in Ac-DAF-16, the P1 and P2 sites are required for interaction with the 14-3-3 protein [49]. Binding of the 14-3-3 to these sites is believed to mask the DNA binding domain, thereby interrupting the FOXO/DAF-16 function. Interestingly, this differs from the FTT-2/DAF-16 interaction in C. elegans, where the analogous N-terminal P1 site and the Cterminal P3 site are required for interaction [23]. Our results demonstrate the requirement of Akt phosphorylation sites for 14-3-3/DAF-16 association, and suggest that Ac-14-3-3 binds to phosphorylated Ac-DAF-16 to mediate ILS, as occurs in C. elegans. Further investigations are underway to confirm this hypothesis.
14-3-3 proteins have been reported from a growing number of helminth parasites. In nematodes, aside from C. elegans and now A. caninum, the only other well characterized 14-3-3 proteins are from the root-knot nematode Meloidogyne incognita [50]. Partial sequences from EST databases have been reported from Strongyloides stercoralis, Haemonchus contortus [46], and the hookworm of humans Necator americanus [51]. A 29 kDa protein in ESP from the adult stage of the ovine stomach worm Teladorsagia circumcincta was identified as a 14-3-3 protein [52]. The complete descriptive and functional characterization of these proteins remains to be performed.
More is known about the 14-3-3 proteins of platyhelminths. Multiple isoforms and sub-isoforms have been identified and characterized in Schistosoma and Echinococcus species [46,47]. In S. mansoni, 14-3-3ε-1 interacts with the TGF-β Type 1 receptor and enhances TGF-β signaling [53]. TGF-β signaling is required for dauer formation Absence of Ac-FTT-2 in excretory/secretory products of adult and L3 Ancylostoma caninum (although not recovery) in C. elegans [13,54], and the TGF-β receptor ligand DAF-7 has been identified from A. caninum [44]. Also, TGF-β signaling has been implicated in the reactivation of tissue-arrested A. caninum L3 [55]. Demonstration of a functional role for Ac-FTT-2 in TGF-β signaling awaits further characterization of this pathway in hookworms. The 14-3-3 proteins of platyhelminths are associated with the tegument, or are actively secreted, making them available as targets of the host immune system and therefore potential vaccine antigens [47,56]. In S. mansoni, all three isoforms of 14-3-3 are expressed during infection and induce antibody production by the host [57]. The 14-3-3ζ isoform has shown some protection against schistosome challenge infections, eliciting worm reductions ranging from 25 to 65% [58][59][60][61]. The greatest success of a 14-3-3 as an anti-parasite vaccine antigen was in Echinococcus multilocularis, where vaccination with the 14-3-3ζ isoform resulted in a 97% reduction in parasite load following challenge in a mouse [47,62]. Recombinant 14-3-3ζ reduced nitric oxide production from activated macrophages in vitro [63], and may contribute to the immunosuppressive effect associated with alveolar cyst infection [47,64].
The FTT-2 ortholog in the root-knot nematode M. incognita is synthesized in the dorsal esophageal gland cell and present in stylet secretions [50,65]. In this parasite, stylet secretions play a role in the induction and maintenance of the feeding site within the plant host [66]. 14-3-3 proteins in ESP suggest an extra-corporeal function, including potentially influencing host immune responses [47,64]. Hookworms are known to release abundant ESP from both activated L3 [4][5][6] and adult stages [41,42]. Minimally, release of 14-3-3 by a life history stage would be a prerequisite for a vaccine antigen. However, we could not demonstrate Ac-FTT-2 in either larval or adult ESP, indicating that unlike some other helminth 14-3-3 proteins, Ac-FTT-2 is not secreted. Therefore it is unlikely that this protein interacts with the host immune system. It is more likely that it is part of endogenous signaling pathways, including ILS downstream of Akt.

Conclusion
In conclusion, we report the identification and cloning of a 14-3-3 protein family member, Ac-FTT-2, from the canine hookworm A. caninum. Ac-FTT-2 is most closely related to Ce-FTT-2, a protein that mediates the effects of ILS in C. elegans. We demonstrated that Ac-FTT-2 interacts with the forkhead transcription factor Ac-DAF-16 when co-expressed in mammalian cells, and that this interaction requires intact Akt phosphorylation sites at serine 107 and threonine 312. Our data suggest that, as in C. elegans dauer recovery, the interaction of Ac-FTT-2 with phosphorylated Ac-DAF-16 mediates the effects of ILS on development, and therefore might play an important role in the hookworm infective process. Further investigations into the role of FTT-2 and DAF-16 in hookworm recovery will provide insights into the early, critical events of hookworm infection, and possibly novel intervention strategies for the prevention of hookworm disease.

Parasites
The Baltimore strain of A. caninum (U.S. National Parasite Collection accession 100655.00) was maintained in beagles as described previously [67]. The beagles were housed and treated according to a protocol approved by the George Washington University Institutional Care and Use Committee. Infective L3 were recovered from coproculture by a modified Baermann technique and stored at room temperature in buffer BU (50 mM Na 2 HPO 4 /22 mM KH 2 PO 4 /70 mM NaCL, pH 6.8) for up to one month [68], or snap-frozen in liquid N 2 and stored at -80 C until lysates were prepared.

In vitro larval activation and collection of excretory/ secretory products
Ancylostoma caninum L3 were activated under host-like conditions as described previously [6]. Briefly, approximately 5000 decontaminated L3 were incubated at 37C, 5% CO 2 for 24 hr in 0.5 ml RPMI 1640 tissue culture medium supplemented with 25 mM HEPES (pH 7.0) and antibiotics (RPMI-c) in individual wells of 24-well tissue culture plates. L3 were activated by the addition of 10% (v/v) of a less than 10 kDa ultrafiltrate of canine serum and 15 mM S-methyl-glutathione (GSM, Sigma Chemical, St. Louis, MO) in RPMI-c. Non-activated L3 were incubated with RPMI-c medium alone. The percentage of L3 feeding (or "activated") was determined as described elsewhere [2] Following incubation, medium containing L3 was transferred to microcentifuge tubes and centrifuged at 13,000 rpm for 5 min. The supernatant containing the excretory/ secretory products (ESP) was collected and concentrated by ultrafiltration using Centricon YM-10 cartridge (Millipore). The retentate was washed with 0.5 mL PBS, and concentrated 10-fold for electrophoresis.

Ac-FTT-2 amplification and cloning
A consensus sequence derived from a cluster of eight expressed sequence tags encoding an A. caninum 14-3-3 (AC01065) [69] was used to design specific forward and reverse oligonucleotide primers for PCR. The Ac-ftt-2 cDNA ends were amplified in two separate PCR reactions. For the 5' end, the reverse primer R2 (5'-AAATTGA-GAGCGAGGCCAAGGCG-3'), the forward nematode spliced leader primer SL (5'-GGTTTAATTACCCAAG TTT-GAG-3') and first strand cDNA [70] were incubated in a PCR reaction for 35 cycles of 1 min at 94 C, 1 min at 57 C, and 2 min at 72, followed by a final extension for 4 min at 72 C. The 3' end was isolated using a nested strategy from an A. caninum L3 directional cDNA library constructed in Lambda ZAP II [71]. The first reaction employed the forward primer FTT-F1 (5'-GAACTCGTGTTGAG-GGCCAAGC-3') together with a primer complementary to the T7 promoter site in the vector flanking the 3' end of the cDNA insert site (5'-TAATACGACTCACTATAG-3'). The primers and 1 μl of cDNA library were incubated in a PCR reaction of 1 min at 94 C, 1 min at 55 C, and 2 min at 72 C, and a final extension for 5 min at 72 C. The first round reaction was diluted 1:10 and used as template in a second reaction containing the nested forward primer FTT-F2 (5'-CGAGCTGGAGAGTTATTT CGTCG-3') and reverse primer T7-NEST (5'-ACTCACTATAG-GGCGAATTG-3'), using identical cycling conditions. Amplicons of approximately 550 bp (5' end) and 900 bp (3'end) were gel purified, cloned using the pGEM-T Easy TA cloning kit (Promega, Madison, WI), and the DNA sequence of both strands determined. The DNA sequences of the 5' and 3' end clones were aligned and combined to give the 1165-bp full-length composite sequence of Ac-ftt-2, including a 32-bp poly-d(A) tail.
The composite sequence was used to design primers to amplify and clone the full-length coding sequence. Forward primer FTT-FX (5'-TTAGGATCCATG GCCGAT AACAAGGATGAACTCG-3') containing a 5'BamHI restriction site (underlined) and FTT-RX (5'-GATCTCGAG-GAATCAGATCATA TGGGTTTAATTGGC-3') with a 5' XhoI restriction site were incubated in a PCR with A. caninum L3 first strand cDNA for 35 cycles of 95 C for 1 min, 55 C for 1 min, and 72 C for 2 min, followed by a final 5 min extension at 72 C. The amplicon was digested for 18 h at 37 C with 20 units each of XhoI and BamHI restriction enzymes (New England Biolabs, Beverley, MA) in BamHI buffer, gel purified and ligated into pET28a (Novagen, Gibbstown, NJ) which had been digested with the same enzymes. The ligation products were transformed into E. coli DH5α competent cells by standard methods, and the constructs confirmed by DNA sequencing.
The full length coding sequence of A. caninum 14-3-3 cDNA (Ac-ftt-2) in pET28a was used as a template to amplify the insert for subcloning into a mammalian expression vector. Forward primer FTT-FX and reverse primer FTT-RX2 (5'-ATAACTCGAGAT TGGCAC CCTCTC-CTTGC-3') containing a XhoI site were incubated in a PCR reaction with 12 ng of plasmid DNA for 35 cycles of 95 C for 1 min, 55 C for 1 min, and 72 C for 2 min, followed by a 5 min extension at 72 C. An amplicon of approximately 700 bp was purified by Nucleospin column (Clon-Tech, Palo Alto, CA), and 2.5 μg of the product digested with XhoI and BamHI restriction enzymes as above. The gel purified insert was ligated into the mammalian expression vector pcDNA3.1-V5/His (Invitrogen, Carlsbad, CA) cut with the same enzymes, and the ligation products were transformed as above. Positive colonies were confirmed by colony PCR using FX and RX2 primers, and the DNA sequence of both strands determined. All DNA concentrations were determined spectrophotometrically (Nanodrop, Thermo Fisher Scientific, Waltham, MA).

Transfection of human embryonic kidney 293 cells
Growing human embryonic kidney 293 (HEK293) cells were re-suspended in fresh, pre-warmed RPMI 1640 containing 10% FBS (Biowhittaker, Walkersville, MD), 2 mM L-glutamine (Mediatech, Herndon, VA), 100 IU/mL penicillin (Mediatech, Herndon, VA), and 100 μg/ml streptomycin (Mediatech, Herndon, VA), and evenly distributed into individual wells of a 6-well tissue culture plate. Medium was added to a final volume of 2 mL in each well and the plate was incubated overnight at 37 C, 5% CO 2 . The medium from each well was then replaced with fresh pre-warmed RPMI without disturbing attached cells and incubated for 2 h at 37 C. The cells were transfected with 4 μg of pcDNA3.1V5/Ac-ftt-2 plasmid DNA or empty pcDNA3.1V5 vector (mock) using Metafectene (Bionex, Munich) and incubated at 37°C for 48 h. Following incubation, media were removed and 2 mL of lysis buffer (20 mM Tris-HCl pH 7.5, 50 mM NaCl, 5 mM CHAPS, 1% Triton X-100, and 0.1% SDS) were added to each well to lyse the cells. Cell lysates were vortexed for 1 minute in microcentrifuge tubes, then frozen overnight at -80 C. Samples were thawed, vortexed again and centrifuged at room temperature for 5 min at 2300 × g. The supernatants were collected and stored at -20 C. Total protein concentrations were determined by bicinchoninic acid method (Micro BCA, Thermo Fisher) according to the manufacturer's protocol.
Co-transfections were performed as above with 2 μg each of pcDNA3.1V5/Ac-ftt-2 and pCMV4FLAG/Ac-daf-16 encoding the A. caninum forkhead transcription factor DAF-16 [38], or 2 μg each of the expression constructs and the corresponding empty vector. Cells were incubated overnight, followed by 20% serum treatment for 24 h, and lysates prepared.

Immunoprecipitation of recombinant Ac-FTT from HEK 293 cell lysate
To determine if we could immunoprecipitate hookworm recombinant Ac-FTT-2, 5 μL of anti-V5 antibody (Invitrogen) were incubated for 16 h at 4 C with lysates of mock or Ac-ftt-2 transfected HEK 293 cells in a total volume of 500 μL of PBS-T (0.1% Tween-20). Protein A-agarose (Invitrogen) was pre-cleared with PBS-T and incubated with the antibody-antigen complexes for 1.5 h at 22 C with rotation. Following centrifugation for 30 s at 2300 × g, the supernatant was removed and stored frozen as the unbound sample, and the agarose complexes washed by rotation 3 × 5 min with 1 mL PBS-T. The agarose-antibody-antigen complexes were separated by SDS-PAGE and visualized by Western blot with HRP conjugated αhuman 14-3-3β antibody or α-V5/HRP as described above.
Reciprocal co-immunoprecipitation with α-V5 and α-FLAG using HEK293 cell lysates HEK293 cells co-transfected with Ac-daf-16 and Ac-ftt-2 were lysed with 200 μL of cold buffer containing 50 mM NaCl, 50 mM Tris-HCl pH7.5, 0.1% NP-40, 5 mM EDTA, 1× Phosphatase Inhibitor Cocktail II (Calbiochem), and 1× Halt Protease Inhibitor cocktail (Pierce). Lysates were centrifuged at 4 C for 10 min at 10,000 × g, and the protein concentration of the supernatants determined by Micro BCA. Forty μg of anti-FLAG M2 resin (Sigma, St. Louis, MO) was prepared according to manufacturer's directions, added to ~1 mg of cell lysates, and mixed by rotation overnight at 4 C. Tubes were centrifuged for 30 s at 8200 × g and washed 3 times in TBS (50 mM Tris HCl pH7.4, 150 mM NaCl). Co-immunoprecipitation (co-IP) complexes were separated by 4-20% gradient SDS-PAGE and transferred to PVDF membrane for 7.5 min in an iBlot apparatus (Invitrogen). Following blocking, the membrane was probed with anti-V5/HRP (1:5000 dilution) at 22 C for 2 h. The membrane was washed 3 times in PBS-T and 2 times in distilled deionized water (ddH 2 O), dried, and incubated with ECL solution as above. Following visualization, the membrane was stripped with Restore buffer (Pierce) and blocked overnight in 5% NFDM in PBS-T at 4 C. The stripped membrane was re-probed with a specific Ac-DAF-16 polyclonal antiserum (1:20,000 dilution) [38], and visualized as above. The reciprocal co-IP was performed as above, using anti-V5 resin (Sigma) to pull-down protein complexes, and anti-DAF-16/anti-rabbit IgG-HRP and anti-V5/HRP to probe the membranes.

Effect of phosphorylation on Ac-FTT-2 interaction with Ac-DAF-16
To determine the importance of phosphorylation at the predicted Akt phosphorylation sites for the interaction between 14-3-3 and Ac-DAF-16, the serine or threonine residue at each site was changed to alanine by site-directed mutagenesis. Using a Quickchange Site-Directed mutagenesis kit (Stratagene, La Jolla, CA), mutant Ac-DAF-16 plasmids were constructed in which each site was mutated separately (S107A, T312A, S381A), in pairs (S107A/ T312A; S107A/S381A; T312A/S381A), or at all three phosphorylation sites (3A). The mutated plasmid constructs were confirmed by DNA sequencing.
HEK293 cells were co-transfected with 2 μg of pcDNA3.1V5/Ac-ftt-2 and 2 μg of wild-type or mutant pCMV4FLAG/Ac-daf-16 as above. Mock cells received 4 μg of empty pcDNA3.1/V5-His vector. After 24 hrs incubation, the cells were fed with 20% serum and grown overnight. Following cell lysis, co-IPs were performed using anti-FLAG agarose, separated by electrophoresis, and visualized by Western blot with anti-V5/HRP antibody as above. After stripping, the gel was re-probed with DAF-16 antiserum to visualize Ac-DAF-16.

Preparation of lysates from frozen A. caninum L3 larvae
Ancylostoma caninum L3 were activated by incubating with canine serum fractions and S-methylglutathione as described above [6]. Approximately 100,000 frozen nonactivated and activated L3 A. caninum larvae were ground to fine powder with a sterile mortar and pestle pre-chilled with liquid N 2 . The powder was added to 500 μL of cold PBS plus 1% EDTA, 1% Halt Protease Inhibitor Cocktail, and 1% Phosphatase Inhibitor Cocktail II and mixed by inversion. The lysates were centrifuged at 16,100 × g for 6 min at 4 C. Aliquots of the supernatants were removed to determine protein concentration by Micro BCA, and the remaining supernatants were stored at -20 C until needed.
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