Wsv023 interacted with Litopenaeus vannamei γ-tubulin complex associated proteins 2, and decreased the formation of microtubules

A previous study found the key transcription factor of Litopenaeus vannamei PERK-eIF2α pathway cyclic AMP-dependent transcription factor 4 (LvATF4) was involved in the transcriptional regulation of white spot syndrome virus (WSSV) gene wsv023. Knocked-down expression of LvATF4 reduced the viral copy number and the cumulative mortality of WSSV-infected shrimp. These results suggested that wsv023 may be critical to WSSV infection but the precise function of wsv023 was still unknown. By using co-immunoprecipitation and pull-down assays, we show that wsv023 interacts with L. vannamei gamma complex-associated protein 2 (LvGCP2), which is the core protein of the γ-tubulin small complex. Knocked-down, the wsv023 gene significantly reduced the copy number of WSSV in L. vannamei muscle, as well as the cumulative mortality of infected shrimp. And PERK-eIF2α pathway inhibition also showed reduced virus copy number and abrogated shrimp mortality. Furthermore, overexpression of wsv023 inhibited the formation of microtubules in 293T cells. Flow cytometry revealed that WSSV infection similarly decreased the formation of microtubules in L. vannamei haemocytes. These findings suggested that wsv023 plays a role in microtubule organization in host cells, which in turn may be beneficial to WSSV.

decreased the formation of microtubules in L. vannamei haemocytes. These findings suggested that wsv023 plays a role in microtubule organization in host cells, which in turn may be beneficial to WSSV.

Introduction
Microtubules are essential components of the cytoskeleton that confers shape and function in eukaryotic cells. They also play a vital role in intracellular material transportation, organelle positioning, cell movement, signal transduction and cell division [1]. Microtubules should be ideally assembled using a special mode that is convenient for rapid reorganization and decomposition [2]. Research studies have shown that microtubules are formed by the arrangement of 13 parallel protofilaments that arise from the end-to-end aggregation of the α/β tubulin-dimers [3]. Microtubules are associated with various other proteins, such as dynein and kinesin, which are involved in the organization of the microtubule cytoskeleton [4].
Cells have specialized nucleation sites that are found in microtubule-organizing centres (MTOCs) [5]. All MTOCs contain γ-tubulin, which is homologous to α-tubulin and β-tubulin and is required for microtubule nucleation [6]. γ-tubulin is prevalent throughout the eukaryotes and is essential for normal microtubule organization in every organism. However, γ-tubulin is involved in nucleation of cells in non-MTOC sites, such as plant cells, which lack centrosome-like structures [7]. Thus, γ-tubulin seems to be critical to the initiation of new microtubules in vivo. γ-tubulin is part of a large complex consisting of several proteins, such as γ-tubulin, which is purified from Drosophila melanogaster embryos or Xenopus laevis eggs. This complex contains γ-tubulin complex protein (GCP) 2, GCP3, GCP4, GCP5, GCP6 and the neural precursor cell expressed developmentally downregulated protein 1 (NEDD1) that form a γ-tubulin ring (γ-TuRC). In γ-TuRC, γ-tubulin interacts with GCP2 and GCP3 and yields a stable 300 kDa subcomplex, called γ-tubulin smallcomplex (γ-TuSC) [8]. The assembly state of the γ-tubulin complex is important for its activity, and purified γ-TuSC has much lower microtubule-nucleating activity than intact γ-TuRC [3].
A previous investigation has determined that viral infections might influence microtubule organization in host cells. In the neuroblastoma cell line IMR32, a microtubule network was used as the transport system of a virus replication site and is involved in the release of mature Japanese encephalitis viruses [9]. A 60% decrease in particulate tubulin synthesis was reported in SV403T3 cells after transformation by SV40 virus compared to that in normal cells [10]. The matrix protein of the vesicular stomatitis virus interacted with tubulin in vivo and in vitro, suggesting that a cytopathic effect was caused by these interactions [11]. In herpes simplex virus-1 (HSV-1) infection disperses the location of miniaturized MTs in the cytoplasm, which in turn facilitates HSV-1 capsid migration to the site of envelopment after exiting the nucleus, thereby promoting efficient viral spread [12].
White spot syndrome virus (WSSV) is a rapidly replicating and extremely virulent shrimp pathogen that causes huge economic losses in shrimp aquaculture. Some studies have indicated that cytoskeleton modulation in shrimp cells might be linked to WSSV infection-driven microtubule modifications [13][14][15][16]. However, the relationship between WSSV infection and host cell microtubule modification remains unclear. This study proved that WSSV gene wsv023 interacted with Litopenaeus vannamei GCP2 (LvGCP2), the core member of γ-TuSC. Overexpression of wsv023 in 293T cells inhibited the formation of microtubules. Silencing expression of wsv023 significantly reduced the WSSV copy number in L. vannamei muscle and the cumulative mortality of WSSV-infected shrimp. These results suggest that WSSV possibly affects microtubule organization in the host cells via wsv023, thereby enhancing the infection process.

Co-immunoprecipitation and western blot assay
Expression vectors for full-length LvGCP2, eGFP with Flag-tag or wsv023, and GST with V5-tag were constructed for co-immunoprecipitation (Co-IP) assays. Briefly, Drosophila S2 cells were co-transfected with the expression plasmid pairs LvGCP2 (Flag)/wsv023 (V5), LvGCP2 (Flag)/GST(V5) and eGFP (Flag)/wsv023 (V5). Cells were harvested at 48 h post-transfection. S2 cells were lysed in NP-40 lysis buffer (Beyotime, China) on ice with a protease inhibitor cocktail (Roche Applied Science, Germany) and then incubated for 2 h at 4°C with anti-V5 or anti-Flag antibodies (Invitrogen, USA). The proteins were immunoprecipitated with Protein G Plus/protein A Agarose (Calbiochem, Germany). After incubation, the beads were washed three times with NP-40 lysis buffer, subjected to SDS-PAGE, and then electrotransferred to nitrocellulose membranes. Then western blot analyses were then performed. The blots were incubated for 2 h at room temperature (RT) in tris buffered saline with Tween-20 (TBST) with 5% bovine serum albumin and then for 1.5 h at RT with the anti-Flag or anti-V5 antibody. After washing three times with TBST, the membranes were incubated in TBST with 1/20 000 horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG antibody (Pierce, USA) for 1 h at RT. Signals were detected with Superstar ECL Plus (Pierce).

Pull-down assay
Prokaryotic expression vectors for N-terminal LvGCP2 (1 ∼ 450 aa, LvGCP2N) and the full-length open reading frame (ORF) of the wsv023 gene were constructed (for information on the primers used in the study, see table 1) by inserting the corresponding DNA fragments into pMAL-c2X (New England BioLabs, Inc.) and pET32a + (Novergen, USA), respectively. The recombinant proteins were expressed in Escherichia coli (BL21). The supernatants contained recombinant proteins, which were mixed together in the following pairs: MBP-LvGCP2N and 6×His-wsv023, MBP-LvGCP2N and 6×His-GST, and MBP-eGFP and 6×His-wsv023; each of these pairs were then incubated at 4°C in a vertical mixer for 4 h. The MBP and MBP-LvGCP2N were purified with amylose beads (New England BioLabs, Inc.), and 6×His-GST and 6×His-wsv023 were purified with Ni-NTA Agarose (Qiagen, USA), all according to the respective manufacturers' instructions. The beads were then collected, extensively washed and boiled in a sample buffer, followed by SDS-PAGE and then western blot assays.

Bioinformatics analysis
The GCP2 or GCP3 protein sequences from other species in the database were searched and analysed using the BLAST program (http://www.ncbi.nlm.nih.gov/BLAST/). Multiple sequence alignment was performed using the CLUSTALW program. Using MEGA 6.0 software, a neighbour-joining (NJ) phylogenetic tree was constructed based on the deduced amino acid sequences of LvGCP2 and other known GCP2 proteins. Bootstrap sampling was performed 10 000 times. Protein domains were predicted using the SMART program (http://smart.embl-heidelberg.de/).

Flow cytometry assay
293T cells were transfected with plasmids pcDNA-wsv023 and pcDNA-wsv220N250 (negative control, 1 ∼ 250 aa of WSSV membrane protein wsv220). After 48 h, the quantity of microtubules was examined using Tubulin Tracker™ Green kit (Life Technology, USA) following the manufacturer's instructions. A sufficient amount of staining solution (250 nM) was applied to cover the cells and then incubated for 30 min at 37°C. After incubation, the staining solution was removed, and the cells were rinsed three times in a buffer at 37°C. Then the cells were gently resuspended with Hank's balanced salt solution (HBSS) gently. Approximately 5 × 10 5 cells were applied to flow cytometry assay by BD accuri system (BD Biosciences, USA), and the fluorescence value of the cells were autokinetic calculated by BD accuri C6. Total RNAs and proteins of 293T cells from different groups were extracted, and the expression of Homo sapiens α-tubulin, β-tubulin and β-actin was detected by real-time RT-PCR and western blot. In the WSSV infection assay, haemocytes were collected from five shrimps in the phosphate buffered saline (PBS) injection group and the WSSV infection group at 72 h after treatment; the haemocytes were pooled together as one sample (n = 3). Litopenaeus vannamei haemocytes were prepared as described elsewhere [17].

Synthesis of double-stranded RNA
The DNA templates of the wsv023 gene for dsRNA-(designated as dsRNA-wsv023) synthesis were prepared via PCR using the primer pairs DsRNA-wsv023-T7-F/DsRNA-wsv023-R and DsRNA-wsv023-F/DsRNA-wsv023-T7-R (table 1). The DNA template for ssRNA synthesis consisted of annealed DNA oligonucleotides containing a T7 RNA polymerase promoter. For sense ssRNA synthesis, a DNA template containing a T7 RNA polymerase promoter at its 5 -end was employed, so the T7 RNA polymerase promoter sequence was added to 5 -end of the forward primer. For antisense ssRNA synthesis, the DNA template contained a T7 RNA polymerase promoter at its 3 -end, so a T7 RNA polymerase promoter sequence was added to the 5 -end of the reverse primer. The products        with the T7 promoter were confirmed by sequencing, and then subjected to in vitro transcription with the RiboMAX large-scale RNA production (Promega, USA) according to the instruction manual. The templates of the eGFP dsRNA (designated as dsRNA-eGFP) were prepared via PCR using the primer pairs DsRNA-eGFP-T7-F/DsRNA-eGFP-R and DsRNA-eGFP-F/DsRNA-eGFP-T7-R (table 1). The lengths of dsRNA-wsv023 and dsRNA-eGFP were 469 and 504 bp, respectively.

White spot syndrome virus challenge and preparation of templates for real-time RT-PCR analysis
To investigate the expression profiles of Lvα-tubulin, Lvβ-tubulin and Lvγ -tubulin in WSSV-infected shrimp, WSSV challenge was performed. Each healthy L. vannamei was injected intramuscularly at the second abdominal segment with 50 µl of a WSSV inoculum, which contained approximately 10 4 virions. Total RNA from the haemocytes was isolated at 0, 3,6,9,12,18,24,30,36,48,72 and 96 h post inoculation (hpi). From each sample, total RNA was extracted using RNeasy Mini Kit (Qiagen, Germany) and then reverse transcribed into cDNA by using PrimeScript RT Reagent Kit (TaKaRa, Japan). Then, real-time RT-PCR assay was performed on a LightCycler 480 System (Roche, Germany) using a reaction volume of 10 ml, which comprised 1 ml of cDNA template, 5 ml of 2× SYBR Premix Ex Taq™ II (Takara), and 500 nM of each primer. The optimized thermal cycling parameters were as follows: 95°C for 2 min to activate the polymerase, followed by 40 cycles at 95°C for 15 s, 60°C for 15 s and 72°C for 10 s. After performing the cycling protocol, the melting curves were obtained by increasing the temperature from 72°C to 95°C (0.5°C s −1 ) to denature the double-stranded DNA. The results were calculated using the 2 − Ct method after normalization to LvEF-1a (GenBank Accession No. GU136229) [18]. The primer sequences are presented in table 1.

Bioassay of white spot syndrome virus challenge tests in wsv023 knocked-down shrimp
Juvenile shrimp of 6 g mean body weight were obtained from the south base of a marine culture seed project (Zhanjiang, China) and screened for WSSV by PCR using WSSV-specific primers volume) of dswsv023, dseGFP, or PBS, respectively; 48 h later, 50 shrimp of each treatment were injected with 50 µl of PBS (negative controls), and another 50 shrimp were injected with tissue homogenate containing 10 4 virions (50 µl in volume) that was prepared from WSSV-infected shrimp following a published protocol [19]. The experiment was repeated three times. All shrimp were kept in culture tanks for approximately 7 days following infection. Cumulative mortality was recorded every 12 h.
To determine WSSV copy number, at each time point (a total of four time points), the muscles of five shrimp were collected and pooled into one sample. Three parallel samples were prepared. Then WSSV copy number was determined by real-time RT-PCR.
At 48 h after dseGFP or dswsv023 injection, a subsequent injection of WSSV-infected tissue homogenate was performed to examine the RNAi efficiency of wsv023, and shrimp were sacrificed on the third day after WSSV injection. Total RNA that was extracted from the haemocytes was reverse transcribed into cDNA using the PrimeScript RT reagent kit (TaKaRa) and then subsequently used as templates. LvEF1α was used as the internal reference. The primer sequences used in this assay are listed in table 1.

Bioassay of white spot syndrome virus challenge tests in PERK-eIF2α pathway inhibited shrimp
Salubrinal is a selective inhibitor of eIF2α dephosphorylation that inhibits endoplasmic reticulum-stress in cells. In a previous study, we showed that wsv023 is upregulated by the PERK-eIF2α pathway in L. vannamei [20]. In this study, shrimp (n = 100) were injected with Salubrinal (20 µM) or 0.1% dimethyl sulphoxide (DMSO). One hour later for each treatment, 50 shrimp were injected with tissue homogenate containing 1 × 10 4 virions (50 µl in volume), and 50 shrimp were injected with PBS. Cumulative mortality was recorded every 12 h. For the western blot assay and WSSV virion detection, an additional 120 shrimp were prepared with salubrinal (20 µM) or 0.1% DMSO injection plus WSSV infection.

Wsv023 interaction with LvGCP2
In our previous study, tandem affinity purification indicated that wsv023 probably interacted with LvGCP2. To verify whether wsv023 formed a complex with LvGCP2 in L. vannamei, co-IP and pull-down assays were conducted. The Wsv023 (V5) and LvGCP2 (Flag) proteins were co-expressed in S2 cells for the co-IP, which showed that wsv023 (V5) and LvGCP2 (Flag) co-precipitated with each other ( figure 1a). Furthermore, the MBP pull-down assay showed that MBP-LvGCP2N interacted with 6×His-wsv023 but not with 6×His-eGFP (V5) (figure 1b). In addition, MBP alone did not interact with wsv023 (figure 1b). These findings thus indicated that wsv023 interacted with LvGCP2.

Characterization of LvGCP2 and wsv023
The full-length cDNA of LvGCP2 was 3155 bp in size, which included an 88-bp 5 -untranslated region (UTR) and a 526-bp 3 -UTR with a poly(A) tail (electronic supplementary material, figure S1). The ORF of LvGCP2 was 2541 bp in size, which encodes a putative protein of 846 amino acids with a calculated molecular weight of 97 kDa. Conserved domain analysis using the SMART program showed that LvGCP2 contained a Spc97_Spc98 domain that apparently mainly consists of proteins that functioned in microtubule cytoskeleton organization. Multiple sequence alignment showed that the GCP2 proteins were conserved in all species tested (electronic supplementary material, figure S2). Furthermore, LvGCP2 showed a higher identity with vertebrate GCP2s than most of the invertebrate GCP2 proteins except for ZnGCP2; this result coincided with the results of phylogenetic analysis (electronic supplementary material, figure S1). Wsv023 did not show any conserved domain as analysed by SMART (http://smart.embl-heidelberg. de/), whereas BLAST analysis (http://blast.ncbi.nlm.nih.gov/Blast.cgi) revealed that wsv023 has similarities with GCP3s. Multiple sequence comparisons indicated that wsv023 had 20.6% and 16.0% identities with H. sapiens GCP3 (HsGCP3) and LvGCP3, respectively (electronic supplementary material figure S3). Considering the amino acids with similar properties, wsv023 showed 35.2% and 31.3% identity with HsGCP3 and LvGCP3, respectively (electronic supplementary material figure S3). Treatment with dsRNA-wsv023 on WSSV-infected shrimp effectively suppressed its expression in L. vannamei haemocytes as shown by RT-PCR assay ( figure 2a(i)). The shrimp treated with dsRNA-wsv023 had low cumulative mortality 72 h post WSSV infection. Shrimps treated with dsRNA-wsv023 and challenged with WSSV had a cumulative mortality of 60% at 168 hpi. By contrast, groups mock treated with dsRNA-eGFP or PBS had cumulative mortalities of 92% and 100% at 168 hpi, respectively ( figure 2a(ii)). The WSSV copy number in the wsv023 gene knocked-down groups was examined at 12, 24, 48 and 72 h after WSSV challenge (electronic supplementary material, table S1). At 12 hpi, the WSSV copy number in L. vannamei muscles showed no significant differences between the wsv023 knocked-down groups and the control groups (figure 2b). At 24 hpi, the copy number of wsv023 knocked-down groups showed significantly lower copy numbers than that in the PBS injection groups, except for the dsRNA-eGFP  injection group. At 48 and 72 hpi, wsv023 knocked-down groups had significantly lower WSSV copy number than the control groups (figure 2b). At 72 hpi, WSSV copy number in the PBS injection group was about 10-fold higher than that of the wsv023 knocked-down group, and at 48 and 72 hpi, WSSV copy number in dsRNA-eGFP treated groups was significantly higher than the wsv023 knocked-down groups too (figure 2B).

PERK-eIF2α pathway inhibition decreased white spot syndrome virus infection in shrimps
Western blot assay showed that 48 h after Salubrinal injection, phosphorylation of eIF2α was reduced in haemocytes of L. vannamei (figure 3a). At 24, 48 and 72 hpi, the WSSV copy number in L. vannamei muscle of the Salubrinal treatment group was significantly lower than that of the respective control groups (figure 3c). The shrimps treated with Salubrinal also had lower cumulative mortality than the control groups (figure 3b). The cumulative mortalities of the DMSO injection group, Salubrinal injection group, DMSO injection plus WSSV infection group and Salubrinal injection plus WSSV infection group at 168 hpi were 16%, 4%, 100% and 70%, respectively (figure 3b).

Wsv023 inhibited tubulin polymerization in 293T cells
TubulinTracker™ Green reagent (T34075) provides green fluorescent staining of polymerized tubulins, but not the unpolymerized tubulins in live cells. Wsv023 was overexpressed in 293T cells to investigate the function of wsv023. Flow cytometry analysis showed that wsv023 significantly decreased the average fluorescence values of the 293T cells, which was 20% less than that of the wsv220N250 expression groups (figure 4a). Western blot analysis showed that wsv023 did not affect the expression of α-tubulin and  (a) Western blot assay showed that Salubrinal injection reduced the phosphorylation of eIF2α compared with the control; (b) cumulative mortality was recorded every 12 h post-challenge. Data were derived from three independent experiments and shown as mean ± s.d. Differences in mortality levels between treatments were analysed by Kaplan-Meier plot (log-rank 2 test). Significant differences in L. vannamei mortality were marked with asterisks (** indicates p < 0.01); (c) DNA were collected from shrimp and detected WSSV copy numbers in each samples by quantity RT-PCR. Data were expressed as mean fold change (mean ± s.d., n = 3) from the untreated group, significant differences in L. vannamei mortality were marked with asterisks (** indicates p < 0.01).
β-tubulin ( figure 4b). Thus, the reduction in tubulin polymerization in 293T cells that overexpressed wsv023 was not influenced by the supply of α/β-tubulin. Given that γ-TuSC is critical for initiating all new microtubules [3], the present results suggested that wsv023 interacted with LvGCP2, and might therefore influence microtubule formation.

WSSV infection upregulates Lvα-tubulin and Lvβ-tubulin and inhibits microtubule formation
cDNA microarray analysis indicated that WSSV infection affects the expression of several genes that are relevant to microtubule formation [21]. Lvα-tubulin, Lvβ-tubulin and Lvγ -tubulin are primary components of L. vannamei microtubules. In the present study, RT-PCR analysis revealed that the expression of Lvα-tubulin (figure 5a(i)) and Lvβ-tubulin (figure 5a(ii)) in the haemocytes was upregulated after WSSV injection, whereas that of Lvγ -Tubulin (figure 5a(iii)) was not.

Discussion
Growing evidence indicates that WSSV infection modifies microtubule organization in host cells, yet more research is needed to make it clear. Blast analysis showed that wsv023 was similar to the GCP3 sequence of species such as H. sapiens. Other assays (Co-IP and pull-down) proved that wsv023 could interact with the core protein GCP2 of γ-TuSC in L. vannamei. Further, silencing wsv023 reduced WSSV copy number in muscle and cumulative mortality of WSSV-infected shrimp. Moreover, flow cytometry analysis revealed that wsv023 might play a role in inhibiting microtubule formation in host cells. These results indicate that wsv023 influences microtubule synthesis and organization in WSSV-infected cells in shrimp.
A total of 684, 531 and 507 putative ORFs have been identified on the WSSV-Th, WSSV-Cn and WSSV-Tn isolated genome, respectively [13,22]. Most of these ORFs encoded polypeptides that noticeably lacked sequence homology to known proteins. This limitation made it difficult for us to establish the functions of the WSSV proteins. As reported, wsv023 was expressed at the early stage of WSSV infection, suggesting that it might be indispensable for WSSV [21]. In our previous study, wsv023 was found to be upregulated by activating transcription factor 4, which is the basic region leucine zipper domain of the transcription factor of L. vannamei unfolded protein response [20], whereas its role in WSSV infection was still unclear. The wsv023 sequence was found to be similar to the N-terminal end of GCP3, which had 35.2% identity to HsGCP3 and 31.3% identity to LvGCP3. Surprisingly, wsv023 had higher identity with HsGCP3 than LvGCP3, and LvGCP2 had higher identity with mammal GCP2s than most insect GCP2s, except for Zootermopsis nevadensis GCP2 (ZnGCP2). These evidences suggest that wsv023 might be related to L. vannamei γ-TuSC.
GCP3 interacted with GCP2 through its N-terminal, interacted with γ-tubulins through its Cterminal, and formed the γ-TuSC, which is involved in microtubule growth initialization [23]. For some viruses, microtubules play a critical role in their infection, such as viral genome transport and envelope assembly; for other viruses, microtubules contribute to the immunologic process of host cells, such as phagocytosis vesicle transport, and microtubule formation should be depressed to support virus infection [24][25][26]. Thus, viruses develop different strategies to modify the microtubule organization of host cells to ensure successful infection. The most common strategy is to interact with a microtubule or its relevant complexes. Elongation protein zeta 1 promotes neurite extension through its interaction with microtubules; agnoprotein facilitates human polyomavirus John Cunningham virus propagation by inducing the dissociation of FEZ1 from microtubules [27]. Reovirus core protein μ2 determines the filamentous morphology of viral inclusion bodies by interacting with and stabilizing microtubules [28]. Furthermore, vaccinia virus proteins A10 L and L4R with MAP-like properties mediate the direct binding of viral cores to microtubules and disrupt microtubule organization and centrosome function [29]. In the present study, we demonstrated that the WSSV protein wsv023 interacts with LvGCP2, thereby indicating that it might influence microtubule formation in L. vannamei cells.
GCP2, GCP3 and two copies of γ-tubulins form γ-TuSC, which possess microtubule-nucleating activity and plays an important role in microtubule initiation [3]. Depletion of either GCP2 or GCP3 from D. melanogaster S2 cells eliminates the localization of γ-tubulin at the centrosomes and spindles; this elimination results in gross abnormalities in microtubule organization [30,31]. The formation of microtubules was inhibited by the overexpression of wsv023 in 293T cells, which suggests that the interaction between wsv023 and GCP2 could decrease microtubule-nucleating activity. The wsv023 product is similar to the N-terminal part of GCP3, which interacts with γ-tubulin at its C-terminal end. The wsv023-GCP2 complex prevented the formation of functional γ-TuSC but the effect of this interaction needs further investigation.
Previous reports have suggested that WSSV macromolecule transportation or morphological changes use the cytoskeletal framework of host cells. For example, studies have shown that WSSV infection upregulates the expression of tubulin α-1 chain, tubulin β-1 chain and microtubule-actin cross-linking factor 1, which is indicative of the relationship of WSSV infection and microtubule organization [14][15][16]. However, direct experimental evidence supporting these concepts is warranted. Flow cytometry analysis indicated that WSSV infection inhibits microtubule formation. In addition, knocked-down expression of wsv023 resulted in a decrease in WSSV copy number in the muscles of WSSV-infected L. vannamei, as well as in its cumulative mortality. These results provide evidences that wsv023-driven modifications in microtubule organization are also essential to WSSV infection.
In conclusion, this study indicates that wsv023 interacts with LvGCP2, and might disturb microtubule formation in shrimp haemocyte, promoting WSSV infection ( figure 6). Further study will focus on how WSSV may benefit from inhibiting microtubule organization.
Ethics. All the shrimps used in this study were obtained from the South base of the marine culture seed project (Zhanjiang, China). These animals were specifically raised for research purposes and China does not require any additional permit or permission. Because the experimental animals were invertebrates, no specific permits were required for this study; and there is no official recommendation for the use of shrimp for scientific purposes in China. Nevertheless, all our experimental procedures, including animal sacrifice, were designed to be as humane as possible, and all animals were treated so as to minimize suffering at all times.