Background

Clonorchis sinensis (C. sinensis), a human liver fluke, is one of the major food-borne parasites in China [1,2]. 15–20 millions people are infected with C. sinensis and 1.52 millions show symptoms or complications mainly in China, Korea, East Russia, and Vietnam [1]. C. sinensis infection is thought to be a significant risk factor of cholangiocarcinoma and hepatocellular carcinoma in humans [3-5], and thus is included in control programs of neglected tropical diseases by WHO [2].

To efficiently adapt to the host, a parasite mainly changes its metabolism and morphology throughout a complex life cycle [6-8]. C. sinensis lives in the bile environment which is mainly made up of water, lecithin, cholesterol, fatty acids and bile salts [9,10]. All enzymes involved in the pathway of fatty acid beta oxidation moderately expressed in the transcriptome of C. sinensis adults [11], while they were not integrally expressed in blood fluke of human, Schistosoma japonicum (S. japonicum) [12]. It was hinted that these two types of parasites adopted a different metabolic mode of fatty acid production in different living environments. Their main sources of energy might be also different from each other. The mechanisms involved in why C. sinensis can survive in the bile environment containing relatively higher lipid have not yet been elucidated.

Eukaryotic thiolases have key roles in many vital biochemical pathways, including the beta oxidation pathway of fatty acid degradation and various biosynthetic pathways. Thiolase of Caenorhabditis elegans (C. elegans) has been demonstrated to play a key role in delaying aging of the worm and is required for lifespan extension [13,14]. It was documented that thiolase of Homo sapiens abolished the BNIP3 (a unique pro-apoptosis protein) induced apoptosis, which provided a possible linkage between fatty acid metabolism and apoptosis of cells [15]. Thiolases share a common evolutionary origin and a high degree of sequence similarity [16,17]. In the present study, we identified acetoacetyl-CoA thiolase of C. sinensis (CsACAT), a homologue of thiolase. The thiolytic cleavage activity of CsACAT was successively assayed. Whether CsACAT was related to survival of the adult worm in the lipid environment of bile duct was also investigated. The collective information will be a cornerstone for learning about CsACAT and its role in C. sinensis survival and development in the bile duct environment containing lipid.

Methods

Ethics statement

Male Sprague–Dawley (SD) rats (7 weeks old) and New Zealand rabbits (2 months old) were purchased from the Animal Centre of Sun Yat-Sen University (Guangzhou, China) and raised strictly in accordance with National Institutes of Health on animal care and ethical guidelines. The experimental procedures were approved by the animal care and use committee of Sun Yat-Sen University (Permit Numbers: SCXK (Guangdong) 2009–0011).

Parasite collection

Metacercariae of C. sinensis were isolated from experimentally infected freshwater fish Pseudorasbora parva in our ecological pool as previously described [18]. Each rat was orally infected with 50 metacercariae. 8 weeks after infection, the rats were sacrificed and C. sinensis adults were recovered from the livers.

Sequence analysis of CsACAT

The full-length complementary DNA (cDNA) of CsACAT (GenBank accession No. GAA52468.1) was screened from the genome and transcriptome database of C. sinensis [11] by using BLAST program provided by The National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov/). InterPro-Scan and Swiss-Model provided by Expert Protein Analysis System (http://www.expasy.org/tools/) were used to analyze the conserved domains and spatial structure of CsACAT [19]. Deduced amino acid sequences alignment and dendrogram analysis of CsACAT with homologues from other species were carried out by using the software of Vector NTI.

Quantitative real-time PCR (Q-PCR)

To investigate mRNA levels of CsACAT at different developmental stages of C. sinensis, total RNA was extracted from adult worms, metacercariae or eggs using TRIZOL reagent (Invitrogen, USA) according to the manufacturer’s instructions. cDNA synthesis was performed with First Strand cDNA Synthesis Kit (Fermentas, Canada) and oligo (dT)18 primer by using 2 μg of total RNA. Relative mRNA levels were quantified on a BIORAD iQ5 instrument (BioRad, USA) by using 100 ng of cDNA with the SYBR Premix ExTaq Kit (TaKaRa, Japan) according to the recommendations. 5′-CGTCATCTGTGCGGGCGGTAT-3′ and 5′-TTGGCGTAGGCGTCCTGCTCT-3′ were employed to amplify specific fragments of CsACAT. β-actin from C. sinensis (Cs β-actin, GenBank accession No. EU109284) was used as an internal control (323 bp) [20]. The forward and reverse primers were 5′-ACCGTGAGAAGATGACGCAGA-3′ and 5′-GCCAAGTCCAAACGAAGAATT-3′. The real-time PCR procedure was as follows: 95°C for 30 s, 40 cycles of 95°C for 5 s, and 60°C for 20 s. The melting curves were analyzed automatically by collection of the fluorescence signals. Bio-Rad iQ5 software was used to analyze the data according to 2−ΔΔCt method [21].

Preparation of antiserum of excretory/ secretory proteins from C. sinensis (CsESPs) and CsACAT

CsESPs were collected from isolated adult worms according to the method previously described [22].

Forward primer 5′-GTCGGATCCATGGGTGGTCTGAGT-3′ with restriction site of BamH I (italic) and reverse primer 5′-CTCCTCGAGTTACCCAACCGGATGAC-3′ with restriction site of Xho I (italic) were employed to amplify open reading frame (ORF) of CsACAT by PCR. The amplification condition was 94°C for 30 s, 58°C for 45 s and 72°C for 1 min for 30 cycles, plus 72°C for 10 min. Specific PCR products were purified, digested with BamH I and Xho I, and ligated into pET-28a (+) plasmid digested with the same endonuclease. The recombinant plasmid pET-28a (+)-CsACAT were confirmed by DNA sequencing and transformed into E. coli, BL21 (DE3). E. coli BL21 cells harboring the recombinant plasmid were inoculated in 6 L of Luria-Bertani broth medium containing 50 μg/ml of kanamycin and cultured for about 3 h. The expression of CsACAT was induced with 0.5 mM isopropyl-β-D-thiogalactopyranoside (IPTG) for 4 h at 30°C. Recombinant CsACAT (rCsACAT) was purified with His-Bind Purification kit (Novagen, USA), and then analyzed using 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by Coomassie blue staining.

The concentration of rCsACAT or CsESPs was determined by bicinchoninic acid assay (BCA, Novagen, USA). 200 μg of rCsACAT or CsESPs were emulsified with an equal volume of complete Freund’s adjuvant and injected subcutaneously to each SD rat. Each rat was given 100 μg of protein, emulsified with equivalent incomplete Freund’s adjuvant, for three booster injections at 2-week intervals [23]. Anti-serum was collected every 2 weeks. Sera from naïve rats were also collected to use as a control.

Immunohistochemical localization of CsACAT in C. sinensis

Newly isolated C. sinensis adults were fixed with 4% formaldehyde, embedded in paraffin wax and sliced into 3–5 μm-thick sections using a microtome (Microm, Germany). The sections were then dewaxed and dehydrated. The slides were blocked with goat serum overnight at 4°C and incubated with rat anti-rCsACAT sera (1:400 dilutions) at room temperature for 2 h. Sera from naïve rats (1:400 dilutions) were used as a negative control. The slides were washed with phosphate buffered saline (PBS) containing 0.1% Tween-20 (PBST) three times and then incubated with goat anti-rat IgG labeled with red fluorescent Cyanine dye 3 (1:400 dilutions, Cy3, Proteintech, USA) at room temperature for 1 h in the dark. 0.1% bovine serum albumin (BSA) in PBST was used as dilution buffer. After washing with PBST, fluorescence microscopy (ZEISS, Goettingen, Germany) was used in the visualization of antibody staining.

Culture of C. sinensis adults with gradient lecithin

Adult worms newly recovered from infected rats were washed with sterilized PBS (pH 7.4) containing antibiotics (100 μg/ml of penicillin and 100 U/ml of streptomycin). The worms were then incubated in different concentrations of lecithin (L-α-Phosphatidylcholine, Sigma-P5394, Sigma, USA). Lecithin was firstly dissolved with 100% alcohol in a water bath maintained at 56°C and diluted with PBS to prepare the culture medium with final concentrations of lecithin of 6 mmol/L, 0.6 mmol/L and 0.06 mmol/L. The final concentration of alcohol was the same for all concentrations of culture medium i.e. 0.6%. 0.6% alcohol in PBS was used as a negative control. Finally, the mixture was homogenized using an ultrasonic instrument (285 W, 180 s, Scientz IID, China). 10 adult worms were incubated in a single well of a 6-well flat-bottom plate (Corning, USA), with 3 ml of the mixture (which was replaced every 24 hours). The worms were monitored under the microscope (Leica, Germany) for 5 min and intact live worms were counted after 12 h, 18 h, 24 h, 36 h, 48 h, and 72 h respectively. Worms with no muscle contraction or no movement after consecutive 5 shoots was recorded as dead [3,24]. All of the independent experiments were repeated in triplicate. Living adult worms were then respectively washed with 50 mM Tris–HCl (pH 7.0, buffer A) and kept in TRIZOL for total RNA extraction or sonicated in 2 ml of buffer A and then centrifuged at 12,000 g for 15 min. The supernatants were kept at 4°C for determination of protein concentration, activity assay and western blotting analysis.

Enzymatic activity assay of rCsACAT

The thiolytic assay of rCsACAT was performed using the method previously described [25,26]. The standard reaction system contained 50 mM Tris–HCl, 20 mM MgCl2, 60 μM CoA (C4282, SIGMA, USA), 10 μM acetoacetyl-CoA (A1625, SIGMA, USA) and 40 mM KCl in a final volume of 0.3 mL [27]. The changes of absorption value at 303 nm were detected 10 min after addition of 0.1 μg of rCsACAT in the presence of KCl. The optimal pH and temperature of thiolytic reaction of rCsACAT were determined. The enzymatic activity of naïve ACAT in total worm extracts was measured in the optimal pH and temperature.

Western blotting analysis

rCsACAT (5 μg), total worm extracts (50 μg), ESPs (30 μg) were subjected to 12% SDS-PAGE and then electro-transferred onto polyvinylidene difluoride (PVDF) membrane (Whatman, UK) at 100 V for 1 h in a Trans-Blot transfer cell (BIO-RAD, USA). The membranes were blocked with 5% (w/v) skimmed milk in PBS for 2 h at room temperature and then probed with mouse anti-His tag monoclonal antibody (Novagen, USA) at 1:2,000 dilutions, rat anti-rCsACAT serum (1:200), rat anti-CsESPs serum (1:200) or serum from C. sinensis-infected rat (1:200) at 4°C overnight, respectively. After washing with PBS, the membranes were successively incubated with HRP-conjugated rabbit anti-rat or rabbit anti-mouse IgG at 1:2000 dilutions (Proteintech Group, Chicago, USA) at room temperature for 1 h. The blots were visualized by enhanced chemiluminescence (ECL) method.

Hyperlipidemic diet animal models with infection of C. sinensis

New Zealand rabbits (male) were randomly divided into two groups, a hyperlipidemic diet group and a basal diet group. Hyperlipidemic diet was composed of chow diet (78.8% w/w), pig oil (10% w/w), powdered egg yolk (10% w/w), cholesterol (1% w/w) and bile salt (0.2% w/w) [28]. Lipid levels in their sera were measured 1 month after the treatment. The concentrations of total cholesterol (TC), triglycerides (TG), high density lipoprotein (HDL) and low density lipoprotein (LDL) were measured by enzymatic methods with automated analyzer (Hitachi 7180, Hitachi, Japan). When the rabbits were confirmed as hyperlipidemic, they were intragastrically infected with 150 metacercariae. One and a half months after the infection, the rabbits were sacrificed and C. sinensis adults were recovered from the infected livers. The worms were prepared for detection of mRNA and protein levels of CsACAT by using quantitative real-time PCR and western blotting mentioned above. The total proteins of adult worms from each group were subjected to western blotting analysis in the same quantity as a rigorous control. In addition, serum samples were taken when rabbits were starved for 2 hours. Lipids levels in serum and bile from each rabbit were measured.

Statistical analysis

Statistical analysis was performed with SPSS 13.0 Software (SPSS, München, Germany) using either Student t-test or one-way ANOVA when appropriate. Results represented means ± s.d. of triplicates per experimental condition. p-value <0.05 was considered as significant.

Results

Sequence analysis of CsACAT

The ORF of CsACAT encoding 284 amino acids contained highly conserved motifs of thiolase-like region. The thiolase folds or representative functional domain of the thiolase superfamily were identified in spatial structures of CsACAT. There were significant similarities among tertiary structures of ACAT from C. sinensis, Homo sapiens, and C. elegans (Additional file 1: Figure S1A). Multi-sequence alignment analysis indicated that the deduced amino acid sequence of CsACAT shared 56%, 55%, 55%, 52%, and 51% identity with those of Drosophila melanogaster (XP_002057374.1), Homo sapiens (BAA01387.1), Trichinella spiralis (XP_003380495.1), Ascaris suum (ADY43074.1), and C. elegans (NP_495455.2). A phylogenetic analysis showed that CsACAT was homologous with groups of trematodes such as S. japonicum and nematodes such as C. elegans (Additional file 1: Figure S1B). The mammalian ACAT formed a major clade with ACAT from bird and fish. The insect ACAT grouped a clade from others.

Expression, purification, and identification of CsACAT

The ORF of CsACAT was cloned into pET-28a (+) expression vector and the recombinant plasmids were confirmed by sequencing. The IPTG induced rCsACAT was purified and analyzed by SDS-PAGE, showing a single band with molecular mass of approximately 30 kDa (Figure 1A). Western blotting (Figure 1B) indicated that rCsACAT could be probed by mouse anti-His tag monoclonal antibody, rat anti-CsACAT serum, rat anti-CsESPs serum, and serum from C. sinensis-infected rat at a clear band about 30 kDa, while rCsACAT could not be blotted with serum from pre-immunized rat. CsESPs and total proteins of worm could also be probed by rat anti-CsACAT serum but not by serum from pre-immunized rat. In addition, the optimum enzymatic activity of rCsACAT was at pH 7.5 and 37°C (Additional file 2: Figure S2).

Figure 1
figure 1

Expression, purification and characterization of Cs ACAT. (A) rCsACAT was identified by 12% SDS-PAGE. Protein molecular weight markers (lane M), lysate of E. coli containing pET28a (+) without induction (lane 1) and with induction by IPTG (lane 2), lysate of E. coli containing pET28a (+)-CsACAT without induction (lane 3) and with induction by IPTG (lane 4), supernatant (lane 5) and precipitant (lane 6) of lysate of E. coli containing the recombinant plasmid after induction, the purified recombinant CsACAT protein (lane 7). (B) Western blotting analysis of CsACAT. Lane 1–4, rCsACAT probed with naive serum, anti-His tag monoclonal antibody, rat anti-rCsACAT serum and serum from C. sinensis-infected rat; lane 5–6, CsESPs probed with naive serum and rat anti-rCsACAT serum; lane 7–8, total proteins of adult worm probed with naive serum and rat anti-rCsACAT serum; lane 9, purified rCsACAT blotted with rat anti-CsESPs serum.

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Expression pattern of CsACAT

The specific fluorescences were specifically localized in the vitellarium and sub-tegumental muscle layer of the adult worm by using rat anti-rCsACAT serum, while no specific fluorescence was observed in sections treated with naive serum (Figure 2A). The result of quantitative real-time PCR demonstrated that mRNA of CsACAT was observed at life stages of adult worm, metacercaria and egg of C. sinensis. The mRNA level of CsACAT in egg was higher than that in metacercaria (2.93-fold, p < 0.05) or adult worm (10.16-fold, p < 0.01) (Figure 2B).

Figure 2
figure 2

Expression pattern of Cs ACAT. (A) Immunolocalization of CsACAT in C. sinensis adult. Panel a and b, sections treated with anti-rCsACAT serum and specific fluorescences distributed in the vitellarium and sub-tegumental muscular layer of the adult worm; Panel c and d, sections treated with naive serum. No fluorescence was detected. M, sub-tegumental muscular layer; V, vitellarium. Magnification for the adult worm was × 100. (B) mRNA level of CsACAT at different developmental stages of C. sinensis by quantitative real-time PCR. The specific mRNA fragment of CsACAT was observed among the stages. The quantities were normalized with Cs β-actin and analyzed by means of the 2−ΔΔCt ratio.

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Survival rate of adult worms cultured in lecithin

In gradient concentrations of lecithin from 6 mM to 0.06 mM, the survival rate of adult worms declined in a time-dependent manner from 18 h. The survival rate of 6 mM lecithin group was statistically the highest. The survival rates were 87.0 ± 6.0% in 6 mM, 57.9 ± 7.1% in 0.6 mM, 54.8 ± 5.0% in 0.06 mM lecithin, and 45.2 ± 5.0% in the control group at 48 h. At 72 h, the survival rates were 38.8 ± 2.0% in 6 mM lecithin, 0% in 0.6 mM, 0% in 0.06 mM lecithin and 0% in the control group (Figure 3).

Figure 3
figure 3

Survival rate of adult worms cultured in lecithin. (A) Survival rates of adult worms in all groups were decreased in a time-dependent manner. (B) Survival rates of worms in different concentrations of lecithin at 48 h. All data are presented as mean ± SD, *p < 0.05, **p < 0.01.

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Enzymatic activity and expression level of CsACAT in adult worms incubated in lecithin

Living worms were collected 48 h after incubation in lecithin and subjected to crude extraction to examine enzymatic activity of CsACAT. The CsACAT activity in newly recovered worms taken from rats was set as 100%. The enzymatic activity of CsACAT from worms cultured in 6 mM lecithin showed a highest activity of 40.19% compared with other groups (Table 1). Both mRNA and protein levels of CsACAT were higher in 6 mM lecithin and 0.6 mM lecithin groups compared with those of the control group by Q-PCR (Figure 4A) and Western blotting (Figure 4B-C).

Table 1 Enzymatic activity of Cs ACAT in adult worms incubated with different concentrations of lecithin
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Figure 4
figure 4

Expression level and enzymatic activity of Cs ACAT in adult worms incubated in lecithin. (A) mRNA levels of CsACAT in worms cultured with different concentrations of lecithin were evaluated by quantitative real-time PCR. (B) Crude proteins extracted from worms cultured in 6 mM (Lane 1), 0.6 mM (Lane 2), 0.06 mM (Lane 3) of lecithin and control group (Lane 4) were probed with rat anti-rCsACAT serum. (C) Optical density analysis of the protein levels. The optical density was calculated by Tanon Gis software and analyzed by Student’s t test, *p < 0.05.

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Expression level of CsACAT in adult worm recovered from hypercholesteremia rabbit models

The total cholesterol (TC) levels in sera from rabbits fed a hyperlipidemic diet were much higher than those of the basal diet group after 30 days (Additional file 3: Figure S3A). It verified the successful construction of hypercholesteremia rabbit models. 6 weeks after infection with C. sinensis, TC levels in sera and bile collected from the hypercholesteremia rabbits were much higher than those of rabbits fed with basal diet. TG levels showed no statistical difference in the sera and bile between the two groups (Additional file 3: Figure S3B-C). More worms were recovered from livers of hypercholesteremia rabbits than from the basal diet group (Figure 5A). The mRNA and protein levels of CsACAT were higher in the worms extracted from hypercholesterolemic rabbits than those of the control group (Figure 5B-D).

Figure 5
figure 5

Worm burden in rabbit models and expression level of Cs ACAT in the worms. (A) Worm burden in hypercholesteremia or basal diet fed rabbits 6 weeks after C. sinensis infection. All data are presented as mean ± SD, *p < 0.05, **p < 0.01. (B) The mRNA level of CsACAT in adult worms extracted from hypercholesteremia or basal diet fed rabbits, normalized with Cs β-actin. (C) The protein levels of CsACAT in adult worms of the two groups. Lane 1–3, total proteins of worms recovered from basal diet treated rabbits probed with rat anti-rCsACAT serum. Lane 4–6, total proteins of worms recovered from hypercholesteroemic rabbits blotted with rat anti-rCsACAT serum. (D) Optical density analysis of the protein levels in Figure 5C. The optical density was calculated by Tanon Gis software and analyzed by Student’s t test, *p < 0.05.

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Discussion

ACAT is a member of the thiolases superfamily. Thiolases function in both degradative and synthetic pathways of fatty acids. In the degradative direction, ACAT can catalyze the thiolytic cleavage of acetoacetyl-CoA molecules into two molecules of acetyl-CoA [26]. The optimal thiolytic activity of rCsACAT to cleave acetoacetyl-CoA was at pH 7.5 and 37°C (Additional file 2: Figure S2) and native CsACAT had thiolytic activity too (Table 1), confirming that CsACAT is a member of the thiolase family.

ESPs released by C. sinensis adults are complex, including proteases, antioxidant enzymes and metabolic enzymes, which play important roles in the reaction between the parasite and the host [22,29]. The crude extracts of worms and CsESPs could be blotted with rat anti-rCsACAT sera at a specifically single band. rCsACAT could be probed with rat anti-CsESPs and sera from infected rats. The results indicated that CsACAT was an ingredient of CsESPs as well as a circulating antigen. CsACAT was specifically localized at the vitellarium and sub-tegumental muscle layer in adult worms by immunofluorescence. The localizations have close relationships with lipid metabolism and energy consumption. The mRNA level of CsACAT in egg was much higher than those in adult worms and metacercariae. Fatty acid catabolism was documented to be essential for egg production in schistosomes [30] and might also be of importance in C. sinensis. Collectively, it was the first report on the molecular characterizations of CsACAT, which was a cornerstone for further investigation of its role in physiology of C. sinensis.

C. sinensis adults survive in a bile environment which contains lipids (lecithin, cholesterol and fatty acids). As mentioned, mapped to Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways of gene models, enzymes functioning in fatty acid metabolism were completely intact and expressed in C. sinensis while not in S. japonicum [11,12]. Enzymatic activity of these enzymes and their roles in physiology and parasitism of C. sinensis were worth clarifying. We firstly investigated the influences of different levels of lipids on CsACAT and the fluke in vivo and in vitro.

Lecithin and cholesterol are the major lipids in human bile. The concentrations of lecithin and cholesterol in human bile are 4.1-9.3 mM [31] and 1.6-8.3 mM [32], respectively. On the one hand, it was difficult to imitate the physical concentration of cholesterol due to solidification of the solution at 37°C in vitro, therefore, adult worms were cultured in gradient concentrations of lecithin from 0.06 mM to 6 mM. On the other hand, in vivo lecithin could be converted into free fatty acid by lyso-phospholipases of C. sinensis, which have previously been confirmed to be components of CsESPs and to be responsible for the activity [33,34]. It might be a way to supply free fatty acids for C. sinensis as materials for beta-oxidation in the bile environment after transportation by the fatty acid binding protein (FABP) [30,34]. As a result, the survival rate of adult worms in 6 mM lecithin was statistically higher than those in 0.6 mM, 0.06 mM lecithin and controls at 48 h. Simultaneously, the enzymatic activity of CsACAT to convert acetoacetyl-CoA molecules into two molecules of acetyl-CoA in worms cultured in 6 mM lecithin was the highest in the four groups, as well as the expression level of CsACAT. Moreover, more worms were recovered from hypercholesteremia animal models with higher TC levels in the bile. The expression level of CsACAT in the worms was also higher than that of the basal diet group. The results in vivo and in vitro implied that C. sinensis might sense lipid levels and survive better in the bile environment with higher lipid levels. The findings suggested that hypercholesteremia might increase the risk of infections of C. sinensis.

In vitro, lecithin in mixed micelles attenuates the cytotoxicity of bile salts on Caco-2 cells [4]. It has been documented that abundant fat oxidation could delay aging of C. elegans [35]. In C. elegans, function loss of thiolase gene kat-1 causes accelerated aging. The effect of kat-1 might be a consequence of an influence on fatty acid oxidation [13,14,36,37]. CsACAT converts acetoacetyl-CoA molecules into two molecules of acetyl-CoA and the latter may enter into the tricarboxylic acid cycle (TCA cycle) for energy production. Our transcriptome [11] and unpublished data showed that the enzymes involved in the TCA cycle intactly expressed in the adult stage. C. sinensis might utilize lipids by up-regulating expression and enzymatic activity of CsACAT to enhance beta oxidation pathways of fatty acid as an energy resource to survive longer, which might contribute to the higher survival rate of adult worms in an environment with a higher level of lipids.

Collectively, in the present study, we identified and characterized CsACAT, and investigated its potential role in survival of the worm in the bile duct. The expression level and enzymatic activity of CsACAT were up-regulated with the enhancement of lipid concentration in vivo and in vitro. Simultaneously, the survival rates of adult worms were increased. Our findings suggested that as a parasitic organism in a bile environment, C. sinensis might modulate the expression and enzymatic activity of CsACAT, an enzyme involved in fatty acid metabolism, for energy or physical requirements to efficiently adapt to surviving in the bile duct of the host.

Conclusions

In summary, our results implied that C. sinensis might sense lipid levels and survive better in the bile environment with higher lipid levels. CsACAT, an enzyme involved in fatty acid metabolism, might play an important role in the efficient adaption of C. sinensis to the bile environment with lipids in host.