Two apolipoproteins in salmon louse (Lepeophtheirus salmonis), apolipoprotein 1 knock down reduces reproductive capacity

The salmon louse, Lepeophtheirus salmonis is an ectoparasite of salmonid fish in the Northern Hemisphere, causing large economical losses in the aquaculture industry and represent a threat to wild populations of salmonids. Like other oviparous animals, it is likely that female lice use lipoproteins for lipid transport to maturing oocytes and other organs of the body. As an important component of lipoproteins, apolipoproteins play a vital role in the transport of lipids through biosynthesis of lipoproteins. Apolipoproteins have been studied in detail in different organisms, but no studies have been done in salmon lice. Two apolipoprotein encoding genes (LsLp1 and LsLp2) were identified in the salmon lice genome. Transcriptional analysis revealed both genes to be expressed at all stages from larvae to adult with some variation, LsLp1 generally higher than LsLp2 and both at their highest levels in adult stages of the louse. In adult female louse, the LsLp1 and LsLp2 transcripts were found in the sub-epidermal tissue and the intestine. RNA interference-mediated knockdown of LsLp1 and LsLp2 in female lice resulted in reduced expression of both transcripts. LsLp1 knockdown female lice produced significantly less offspring than control lice, while knockdown of LsLp2 in female lice caused no reduction in the number of offspring. These results suggest that LsLp1 has an important role in reproduction in female salmon lice.


Introduction
Lipoproteins are lipid-protein complexes involved in the transport of lipids to various tissues of animals through circulation. The central core of a lipoprotein particle consists of neutral lipids surrounded by a single layer of phospholipid molecules, plus unesterified cholesterol and apolipoproteins. As an important structural component of the lipoproteins, apolipoproteins play an essential role in the biogenesis of lipoproteins, and also act as ligand for low density lipoprotein (LDL) receptor [1]. Apolipoproteins belong to the large lipid transfer (LLT) protein superfamily [2] which is further divided into three subfamilies: apolipoproteins (apo), vitellogenin (Vit) and clotting protein (CP) and finally the microsomal triglyceride transfer protein (MTP). Apo family include vertebrate apolipoprotein B (apo-B), insect apolipophorin-II/I (apoLp-II/I), crustacean large discoidal lipoproteins (dLPs) and apolipocrustacein (apoCr). Vit and CP family includes Vit from vertebrates and invertebrates and CP of the crustaceans while the MTP family includes MTPs from all the vertebrates and invertebrates [2][3][4][5][6]. Apolipoproteins are involved in the transport of lipids among different tissues of animal body [7][8][9]. Vit is the main yolk protein found in egg-laying animals, supplying nutrients including lipids to developing larvae [10,11]. MTP is found in both vertebrates and invertebrates and is involved in the biosynthesis of LLT proteins such as apoliproteins and Vit [12][13][14].
Mammals have several different classes of lipoproteins [1], characterized by their lipid composition and apolipoproteins. Apo-B is the main protein in all lipoproteins except the high-density lipoprotein (HDLP) [15,16]. The two apo-B containing lipoproteins, chylomicron and very low-density lipoprotein (VLDL) are involved in the transport of triacylglycerides (TAGs) from their sites of synthesis or storage to peripheral tissues for uptake through the activity of lipoprotein lipase [for details, see refs [1,17,18]] However, remnants of these lipoproteins are taken up by the liver or by peripheral tissues through LDL receptors.
The salmon louse, Lepeophtheirus salmonis, is a marine ectoparasitic crustacean, found on salmonids in the Northern Hemisphere. It feeds on blood, mucus, and skin of the host [42] and causes economic loss in the salmon farming industry as well as represents a threat to wild salmonids [43][44][45]. The life cycle of salmon louse consists of eight developmental stages, each stage separated by a molt [46][47][48]. The first two naupliar stages and the third infective copepodid stage are planktonic and rely on yolk for energy. The infective copepodids must locate and settle on a suitable host before all yolk reserves are exhausted. Following the copepodid stage there are two chalimi, two preadult and one adult stage. Female salmon lice produce eggs continuously throughout their adult life. Oocytes are produced in the ovaries and transported through the oviducts to the genital segment where developing eggs accumulate large amounts of yolk proteins [49,50] and lipids. Previous studies have shown that eggs and larvae (nauplius II) of L. salmonis contain triacylglycerol (TAG) as a main neutral lipid and phosphatidylcholine and phosphatidylethanolamine as major polar lipids [51,52]. Recent studies in L. salmonis have shown that maternal lipids supplied to the maturing eggs during vitellogenesis are essential for growth and development of larvae [53]. Presence of lipophorin receptor [54] in ovaries and eggs suggest internalization of lipoproteins mediated through endocytosis, but the transport of lipids to the growing oocytes is undescribed.
In this study, two predicted apolipoproteins LsLp1 and LsLp2 were characterized at the molecular level and their impact on development of eggs and larva were investigated by RNA interference in female salmon lice.

Collection of animals
A laboratory strain of salmon lice, Lepeophtheirus salmonis [55] was maintained on Atlantic salmon (Salmo salar) in tanks, supplied with a continuous flow of seawater with a temperature of 10 • C and a salinity of 34.5 ppt. Fish were hand-fed daily with commercial dry pellets. Nauplii I/II and free-living copepodids were obtained from eggs hatched in the incubators with the same supply of seawater. Attached chalimi, and mobile stages of lice, pre-adult I/II males and females, adult males and young adult females (newly molted) and mature egg-producing females were sampled directly from the host fish. Before lice collection, fish were anesthetized with a mixture of benzocaine (60 mg/l) and methomidate (5 mg/l) in seawater. All the experiments were carried out according to the Norwegian animal welfare legislations.
Five biological replicates were collected for each stage of salmon lice for the analysis of stage-specific quantitative reverse transcription PCR (RT-qPCR). Each biological replicate contained 100 animals for nauplius I, nauplius II and planktonic copepodids, 10 animals for chalimus I and chalimus II, and one animal for pre-adult I male and female, pre-adult II male and female, adult male and female. For reverse transcription PCR (RT-PCR), four tissues (sub-epidermal, intestine, ovary and maturing eggs) were dissected from at least 10 female lice. Animal samples and dissected tissue samples were collected in RNAlater TM (Ambion) and either used immediately or stored overnight at 4 • C before long-term storage at − 20 • C.

Extraction of RNA and synthesis of cDNA
TRI reagent (Sigma-Aldrich) was used to extract the total RNA from the samples stored in RNAlater TM (Ambion). The extracted RNAs were diluted in RNAse-free water (Invitrogen) and final concentration and quality of the RNA was determined using Nanodrop ND-1000 spectrophotometer (NanoDrop Technologies). The isolated RNA from each sample was treated with DNaseI, amplification grade (Invitrogen) according to the manufacturer's instructions. 140, 250 ng of total DNasetreated RNA was used for cDNA synthesis with Affinity Script QPCR cDNA synthesis kit (Stratagene). The synthesized cDNA was diluted 10 times with nuclease-free and stored at − 20 • C for further use. For RT-PCR, 1 μg of total RNA was reverse transcribed using a qScript cDNA SuperMix (Quanta Bioscience).

Identification of lipoproteins, SDS-PAGE and mass spectrophotometry
Lipoproteins from adult male (n=50) and female (n=25) lice were purified according to the procedure previously described in [22,56,57]. Briefly, male and female animals were homogenized separately in ice cold phosphate buffer saline (PBS; 0.10 M sodium phosphate, pH 7.0, and 0.15 M NaC1) in the presence of protease-inhibitor cocktail (Sigma-Aldrich). The homogenates were centrifuged at 4500 g for 30 min at 4 • C to remove all the debris and supernatants were collected. Afterwards, each recovered supernatant of 7 ml was mixed with potassium bromide to set the final concentration of solution to 0.4 g/ml, overlaid with 0.9% sodium chloride solution to make up the final volume to 10 ml and re-centrifuged (Beckman SW 41 Ti Rotor) at 40000 rpm for 20 h. After centrifugation, four individual fractions were identified in the centrifuge tubes, collected separately from the top and dialyzed against PBS to remove potassium bromide. Apolipoproteins in the fractions were separated by electrophoresis in gradient (3-7%) SDS polyacrylamide gels, loaded with 5 ul of sample from each fraction. The gels were stained with Coomasie Blue R-250 (Bio-Rad), and molecular weights of the apolipoproteins were estimated by comparing with Precision Plus Protein™ Dual Color Standards (10-250 kD) (Bio-Rad). From the top fraction (fraction 1) the stained protein bands were excised from the gel, digested with trypsin and the peptides analysed using the ESI-QToF mass spectrometer. Digestion of proteins, purification of peptides and sequencing analysis were carried out at the Proteomics Unit at the University of Bergen (PROBE).

In situ hybridization and RT-PCR
Apolipoprotein mRNA was localized in sections of salmon lice by in situ hybridization according to the previously described procedures [66,67]. Single stranded Digoxigenin (DIG) labelled antisense and sense RNA probes were synthesized by in vitro transcription from PCR-derived templates using the DIG RNA labelling kit (Roche). Primers used for the synthesis of sense and antisense RNA probes are listed in Table 1. Quality and concentration of probes were determined by gel electrophoresis (1% agarose gel) and spectrometry (Nanodrop ND-1000) respectively. Paraffin embedded sections of adult females were baked at 60 • C for 20 min followed by deparaffinization of sections with Histoclear (National Diagnostic). After deparaffinization, the tissue sections were rehydrated digested with proteinase-K (0.1 μg/ml) for 18 min and fixed with 4% formaldehyde. The fixed Sections were dehydrated and hybridized with DIG-labelled RNA probes (1500 ng/100 μl) overnight at 65 • C. Finally, all the sections were incubated with anti-DIG-alkaline phosphatase Fab fragments (Roche) and visualized using the nitroblue tetrazolium (0.2 mM) and 5-bromo-4-chloro-3-indolyl phosphate (0.2 mM) from Roche. A sense probe was used as a negative control. Pictures were obtained with an Zeiss Axio ScopeA1.
Total RNA isolated from different tissues of female lice were used for cDNA synthesis (as described above) and diluted 20 times with nuclease free water. 2 ul samples of diluted cDNA were used as a template for RTreactions using Gotaq DNA polymerase (Promega) with primer concentrations of 10 μM in 25 uL of each PCR reaction. A total of 35 cycles were performed and PCR products were run on 1% agarose gels in TAEbuffer and stained with GelredTM (Biotum). Agarose gels were visualized with UV-light in a gel doc imaging system from Biorad.

RT-qPCR analysis
RT-qPCR was carried out on Applied Biosystem 7500 Real-Time PCR system using PowerUp SYBR Green Master Mix (Applied Biosystem) according to the manufacturer's instructions. Primers used in RT-qPCR are listed in Table 1. Standard curves were generated using a two-fold serial dilution (six dilutions) of cDNA to estimate the RT-qPCR assay efficiency. The conditions for RT-qPCR were: 50 • C for 2 min, 95 • C for 2 min, 40 cycles of 95 • C for 15 s and 60 • C for 1 min. At the end of the amplification cycles, melting curve analysis were performed at 60-95 • C. As the efficiency of the assay ranged from 95% to 100%, all the assays were carried out simultaneously for LsLp1, LsLp2 and the reference gene using the same cDNA and master mix along with two negative controls, a non-template control (NTC) and a no reverse transcriptase control (-RT). Salmon louse Elongation factor 1 alpha (ef1α) which has previously been validated as a reference gene [68] was used and has stable expression in all the developmental stages of salmon louse. All samples were run in duplicates and Ct (cycle threshold) values were averaged. The expression levels of LsLp1 and LsLp2 were normalized with the expression level of ef1α, and the relative expression of LsLp1 and LsLp2 was calculated with 2 − ΔΔCT method [69]. Control group was selected as a calibrator to analyse the relative expression levels of LsLp1 and LsLp2 in RNAi experiments, whereas, relative expression levels of LsLp1 and LsLp2 were determined in various developmental stages of salmon louse using copepodids as a calibrator. For RNAi experiments, unpaired T-test was used to determine if control and LsLp1 and LsLp2 knock downed groups were differently expressed and a p-value of 0.05 was chosen as threshold. One-way ANOVA test (p< 0.05) was used to calculate the statistical significance of the LsLp1 and LsLp2 expression differences among different developmental stages of salmon louse. To synthesize dsRNA targeting each gene, two pairs of primers (with and without the T7 bacteriophage promoter sequence (5 ′ TAATACGACTCACTATAGGGAGA) were used to generate templates ( Table 1). For LsLp1, a fragment of 633 bp (nucleotides 2215 to 2847 from the start codon) was selected. In case of LsLp2, a fragment of 568 bp (nucleotides 3960 to 4527 from the start codon) was used. Sense and anti-sense RNAs were produced by in vitro transcription with T7 RNA polymerase as described in the protocol of Megascript RNAi kit (Ambion). The two single-stranded RNAs were mixed together to produce the dsRNA and store at − 20 • C for long time use. The final concentration of dsRNA was measured with Nanodrop ND 1000 Spectrophotometer. A fragment of 850 bp from cod trypsin (CPY185) was used as a control [50].

Knock down of LsLp1 and LsLp2 in pre-adult female lice
To knock down the apolipoproteins, RNA interference (RNAi) were conducted in the pre-adult II female lice as described previously [50] and effects of RNAi were assessed in mature adult females, 30-32 days post injection. Two RNAi experiments were conducted separately with fragments targeting LsLp1 and LsLp2, whereas a third experiment included a combination of the two fragments targeting both genes. Control groups were included in all RNAi experiments, with injections of dsRNA complementary to cod trypsin (CPY185) as a negative control. Details regarding RNAi experiments are shown in Table 2. For RNAi experiments, dsRNA fragments were diluted to a final concentration of 600 ng/μl and dsRNA solution was visualized with bromophenol blue dye during injection. On the day of injections, pre-adult II female lice were carefully picked with forceps from fish host. Female lice (n=30) were injected with 0,5 μl of dsRNA solution in the cephalothorax and left to recover in seawater at 10 • C for 3-4 h. Afterwards, equal numbers of dsRNA treated female and untreated male lice were put back on each fish and kept in single fish tanks. A total of three host fish were used for each treatment group in each experiment. All RNAi experiments were terminated when control dsRNA injected female lice had become adults and produced their second pair of egg-strings. All female lice along with egg-strings were photographed and examined for changes in gross morphology. Subsequently, the egg-strings were gently removed with forceps, placed into individual hatching incubators and monitored daily to record hatching and developmental progress. Copepodids developed from eggs produced by females treated with target and control dsRNAs were counted at 9 dph (days post hatching) when fully developed to copepodids. All females recovered from RNAi experiments were collected in RNA later (Ambion) for RT-qPCR analysis. The lengths of egg-strings were measured and numbers of hatched copepodids from each pair of egg-string were also counted.   Table 1). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Sequence analysis and similarities to other apolipoproteins
From the salmon lice genome database, two cDNA sequences encoding L. salmonis apolipoprotein 1 (EMLSAG00000011090) and apolipoprotein 2 (EMLSAG00000011091) were identified, designated as LsLp1 and LsLp2, respectively. The genomic organization revealed that the LsLp1 gene is composed of eleven exons spanning 14 kb whereas; LsLp2 consists of seven exons and span nearly 12 kb (Fig. 1A). LsLp1 and A BLASTP search in the NCBI database revealed that LsLp1 shared

Domain architecture and peptide sequencing
SMART annotation revealed that the predicted amino acid sequence of LsLp1 contain three structural domains (Fig. 1B). A LpD-N (lipoprotein N-terminal domain, SM00638) domain also known as vitellogenin-N domain (pfam01347) was found at the N-terminus of the protein. Next to LpD-N, a DUF1943 (domain of unknown function, pfam09172) was found. A DUF1081 domain (PF06448) of unknown function was also found in the central region of the protein. In LsLp2, a single von Willebrand-factor type-D domain (VWD) (pfam00094) was found at the C-terminus of the protein (Fig. 1B). The predicted furin cleavage site (RNKR) was found in both LsLp1 and LsLp2 sequences (Fig. 1B). Furing cleavage sites indicate that LsLp1 produced two subunits of 75 kDa and 120 kDa and LsLp2 produced two subunits of 37 kDa and 208 kDa from the N-terminal side. SDS-PAGE analysis of isolated lipoproteins from adult males and females showed two prominent protein bands (A and B) of approximately 170 and 100 kDa (Fig. 1C). Moreover, recovered

Phylogenetic analysis
A maximum likelihood phylogenetic analysis was carried out to reveal the evolutionary relationship between LsLp1 and members of LLTP superfamily from other species (Fig. 2). Phylogenetic analysis was based on LpD-N domain sequences. LsLp2 lacks the LpD-N domain and is therefore excluded from analysis. The analysis showed that members of LLTP superfamily found in extracellular circulation such as apolipoproteins (apo B-100, apoLp-II/I, apoCr and dLp), Vit and CP grouped separately from MTP which is an intracellular protein (Fig. 2). Moreover, LsLp1 and predicted apolipoprotein (apo) of closely related copepod, Caligus rogercresseyi were closely grouped together with dLp from crustaceans along with insect apoLp-II/I and crustacean apoCr (Fig. 2). Further results showed that two already known vitellogenins (Vit1 and Vit2) from L. salmonis [49] were grouped together with vitellogenins from other organisms. Similarly, MTP of L. salmonis was grouped together with MTPs from other organisms (Fig. 2).

Expression of LsLp1 and LsLp2
Transcriptional analysis of salmon lice revealed expression of both LsLp1and LsLp2 in all the tested developmental stages (Fig. 3). A significant higher expression was observed in adult stages as compared to other stages (one-way ANOVA, (p< 0.05)). However, high variations in the expression levels of both LsLp1 and LsLp2 were observed between biological replicates in adult females.

Expression of LsLp1 and LsLp2 in the sub-epidermal tissue and intestine of adult female lice
To determine the site of expression of LsLpR1 and LsLpR2, in situ hybridizations were performed on sections of adult female lice. As shown in Fig. 4A-B, LsLp1 and LsLp2 were detected in the sub-epidermal tissue also known as sub-cuticular tissue [49,70]. Moreover, RT-PCR was also performed using cDNA from four tissues (sub-epidermal, intestine, ovaries and vitellogenic oocytes) of the adult female lice. Results from the RT-PCR confirmed that both genes were expressed in the sub-epidermal tissue as well as the intestine of the lice (Fig. 4C).

RNA interference (RNAi)
To investigate the functional role of LsLp1 and LsLp2 in the reproduction of adult female salmon lice, RNA interference (RNAi) was carried out using double-stranded RNA (dsRNA). Knock down of LsLp1 and LsLp2 were performed in pre-adult II female lice either separately or in combination ( Table 2) and analysed by RT-qPCR in adult females, 30-32 days post injection. A significant (Unpaired T-test, p<0.05) downregulation of LsLp1 and LsLp2 in dsRNA treated groups were found as compared to control groups (Fig. 5). The levels of LsLp1 and LsLp2 transcripts were reduced by 80% and 95% respectively compared to their control groups when lice were injected separately. Similarly, the levels of LsLp1 and LsLp2 were reduced by 92-94% compared with control animals when lice were injected by the combination of LsLp1 and LsLp2 dsRNAs.
No changes in survival or gross morphology between control and any target dsRNA treated group were observed ( Table 2). Females treated with LsLp1 dsRNA produced significantly (Unpaired T-test, p<0.05) shorter egg-strings compared to control group (Fig. 6A-B and 7A). Similarly, the number of hatched copepodids per adult female was significantly lower (reduced by 35%, Unpaired T-test, p<0.05) in the LsLp1 dsRNA treated group compared to the control group (Fig. 7B). Females treated with LsLp2 dsRNA produced egg strings of reduced length (Fig. 6C-D and 7A), but no difference were observed in the average number of copepodids hatched from these egg-strings compared to control group (Fig. 7B). Combined treatment with LsLp1+LsLp2 dsRNAs produced significantly (Unpaired T-test, p<0.05) shorter eggstrings compared to lice in the control group (Fig. 6C, E and 7A). The average number of copepodids produced were lowered (reduced by 36%) compared to control group animals and significant difference (Unpaired, T-test, p<0.05) was found between LsLp1 and LsLp2 dsRNA treated and control dsRNA treated group (Fig. 7B). Columns demonstrate mean expression level, error bars show standard deviation and asterisk represents significant difference (Unpaired T-test, p<0.05) in mRNA levels of LsLp1 or LsLp2 between the control group (n = 5) and the knocked down group (n = 5) in each experiment.

Discussion
Apolipoproteins are essential structural components of lipoproteins [1] and thus play an integral role in the lipid metabolism. There has previously been a lot of research done on apolipoproteins from mammals and insects. Few studies, however, have focused on crustaceans. In crustaceans, HDL-BGBP is the main lipid transporter in decapods, more recently two dLp subunits highly capable of binding to lipids have been found in crayfish, but the functions remain unclear [4,37,38,71]. Here, in salmon louse, we identified two apolipoproteins LsLp1 and LsLp2 and RNAi experiments in female lice suggest a role of LsLp1 in reproduction.
Salmon louse apolipoprotein LsLp1 showed the highest amino acid similarity with apolipoproteins from insects and crustaceans but also similarity with vitellogenin and MTP. Domain architecture showed that LsLp1 has three domains; LpD-N, DUF1943 and DUF1081 (Fig. 1B) which classify LsLp1 in the family of LLT proteins that include vertebrate apolipoprotein B, insect apoLipophorin-II/I and large lipid transfer particle, apolipocrustacein and clotting proteins from crustaceans [2,6,72]. Moreover, several members of LLT protein family also contain VWD domain at the C-terminus [2,6,29]. In LsLp1, VWD domain was absent, similar to apolipoprotein B from the vertebrates and BGBP-dLp of crayfish [5,6]. In contrast to LsLp1, LsLp2 contained only the VWD domain and shared high sequence similarity with C-terminal amino acids of apolipoproteins and vitellogenins (Fig. 1B).
Several members of LLT protein family are cleaved posttranslationally at consensus sites of furin [73] as seen in insect apoLp II/I [74] and crustacean dLp/HDL-BGBP [5]. Insect apoLp-II/I cleaved by furin, give two apolipoproteins: apoLp-I, ~240 kDa and apoLp-II, ~80 kDa [26,29,75]. In crustacean crayfish, two putative furin cleavage sites have been identified in the dLp/HDL-BGBP [5] that result in two subunits of dLp (large and small) and one HDL-BGBP. Similar to apolipoproteins, proteolytic cleavage sites have been identified in Vits from different organisms [76][77][78]. Here in salmon louse, a furin cleavage site has been predicted in both apolipoproteins (Fig. 1B) similar to apolipoproteins from other organisms. Moreover, the apolipoproteins purified from both sexes of salmon lice showed two major and several weak protein bands (Fig. 1C). Peptides recovered from the two major protein bands were sequenced and shown to have LsLps1 and LsLp2 origin. These findings indicated that LsLps1 and LsLp2 were recovered from animal extracts as cleaved products possibly from the action of furin-type protease as reported for other apolipoproteins.
Based on previous phylogenetic analyses, three main families of LLT proteins, apolipoproteins, Vit/CP and MTP have been identified. Our phylogenetic analysis included sequences from copepod apolipoproteins, Vits, and MTP, as well as those from other organisms used in previous studies. According to our phylogenetic analysis, the LsLp1 belongs to the family of apolipoproteins, together with crustacean dLp and insect apoLp II/I (Fig. 2). These results suggested that LsLp1 may have the same lipid transport function as apolipoproteins in other organisms. Furthermore, two already known vitellogenins [49] from salmon lice were grouped together with Vits from insects and CPs from crustaceans. In conclusion, our studies further support the notion that LsLp1 shares similar properties with apolipoproteins rather than Vits or CP from other organisms.
The higher expression of LsLp1 and LsLp2 was observed in the adult stages of the salmon louse (Fig. 3) compare to the other stages. This was similar to the findings in other organisms, where expression of apolipoproteins has been observed in both males and females [40,79]. In mature adult females, both apolipoproteins were expressed but with large variation compared to males. The reason for this variation between biological replicates is unclear, but could possibly be due to the cyclic nature of egg production, which are produced in batches.
In vertebrates such as human, apo-B synthesis take place in the intestine and liver [80]. In insects, apoLp II/I are synthesized in the fat body, which is a functional analogue of the mammalian liver [19,74]. In insects, apolipophorin is produced in the fat body and released into the hemolymph in lipoproteins. From here lipoproteins particles are loaded with lipids from the gut and further transported to other tissues including the fat body; the fat body also functions as a storage site for lipids [81][82][83]. The site of lipid deposition is variable in insects and depend on the developmental stage and their activity [22]. For example, in larvae of M. sexta most lipids are delivered to the fat body, whereas in adults, lipids are mobilized from fat body to flight muscle. In A.gambiae most of the lipids are stored in the ovary [8,22,84,85]. Other than fat body, the expression of lipophorin has also been observed in the brain of L. migratoria. In crustaceans, HDL-BGBP and dLp originate from a common precursor and it is reasonable to assume that both proteins have the same expression sites such as hepatopancreas, intestine, muscle tissues and hemocytes [4]. Antibody staining for dLp verified similar expression as HDL-BGBP in hepatopancreas [4]. In salmon lice, expression of LsLp1 and LsLp2 were found in sub-cuticular tissue and in the intestine (Fig. 4). The expression of apolipoproteins such as vitellogenins have been reported in the same tissue as found for LsLp1 and LsLp2 [49]. The expression analysis of different tissues of female louse suggests that LsLp1 and LsLp2 are synthesized by the sub-epidermal tissue and the intestine and involved in the recruitment of lipids to different lice tissues. Lipid staining results suggest a major transport of lipids in adult female lice to the ovaries and developing oocytes in the genital segment [53,54]. Therefore, it is speculated that lipids from intestine are taken up by apolipoproteins produced in intestine or sub-cuticular tissues, and transported to the ovaries and oocytes via the hemolymph.
In egg-laying insects, there are few experimental data from RNA interference that demonstrate that apolipoproteins are involved in the transport of lipids to different tissues, particularly to ovaries and growing oocytes. In tsetse fly (Glossina morsitans morsitans), RNAi targeting gmmlp (apoII/I) resulted in low lipid levels in the hemolymph, delayed oocytes development and extended larval gestation [86]. Knockdown of Lp gene in the fat body increased the amount of neutral lipids in the midgut of Drosophila which suggest its role as a lipid transporter [87]. In Anopheles, apolipophorin precursor was silenced during Plasmodium invasion and contribution of apolipophorin precursor in both mosquito egg development and ookinetes survival was demonstrated [88]. Silencing of apoLp II/I in Locusta migratoria significantly reduced lipid contents in the cuticle surface including alkanes and methyl alkanes [29]. To evaluate the importance of apolipoproteins in reproduction of L. salmonis, RNAi based knockdown in female lice at the pre-adult II stage were analysed as eggs produced (length of egg-strings) and live copepodids 9 days after hatching. Females injected with LsLp1 dsRNA either alone or in combination with LsLp2, gave reduced number of offspring. Reproductive output was unchanged in LsLp2 silenced females and similar to the control group.
In conclusion; in L. salmonis the two predicted apolipoprotein genes LsLp1 and LsLp1 are expressed in all live stages, strongest in adults and localized in intestines and sub-epidermal cells. RNAi knock down suggest that L. salmonis apolipoproteins take part in lipid transport from intestines to tissues like maturing oocytes, and that LsLp1 but not LsLp2 is important for normal production of offspring.

Declaration of competing interest
☒ The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.