- Open Access
Linalool, derived from Cinnamomum camphora (L.) Presl leaf extracts, possesses molluscicidal activity against Oncomelania hupensis and inhibits infection of Schistosoma japonicum
- Fan Yang†1, 2,
- Erping Long†1, 2,
- Juhua Wen†1, 3,
- Lei Cao†1, 2,
- Chengcheng Zhu1, 2,
- Huanxin Hu1, 2,
- Ying Ruan1, 2,
- Kamolnetr Okanurak4,
- Huiling Hu1, 2,
- Xiaoxia Wei1, 2,
- Xiangyun Yang1, 2,
- Chaofan Wang1, 2,
- Limei Zhang1, 2,
- Xiaoying Wang1, 2,
- Pengyu Ji1, 2,
- Huanqin Zheng1, 2,
- Zhongdao Wu1, 2Email author and
- Zhiyue Lv1, 2Email author
© Yang et al.; licensee BioMed Central Ltd. 2014
- Received: 30 May 2014
- Accepted: 20 August 2014
- Published: 29 August 2014
Schistosomiasis japonicum remains a considerable economic and public health concern in China, the Philippines and Indonesia. Currently available measures to control the unique intermediate host Oncomelania hupensis are frequently associated with severe side effects. Previous studies have demonstrated that linalool-rich extracts from various plants exhibited promising biological activities including cytotoxic, anti-microbial and anti-parasitic properties.
We identified the components of leaf extracts from Cinnamomum camphora by gas chromatography coupled to mass spectrometry (GC-MS) and investigated molluscicidal and larvicidal effects of linalool against O. hupensis and Schistosoma japonicium. The ultrastructural alterations in gills, salivary gland, stomach and hepatopancreas of snails were observed under the light microscope and transmission electron microscope, and lesions to tegument of cercaria were examined under a light microscope and fluorescence microscope. We then evaluated the effects of linalool on skin penetration and migration of schistosomula and adult survival by measurement of worm burden and egg counts in Balb/C mice infected with linalool-treated cercariae.
In the present work, 44 components were identified from the leaf extracts of C. camphora, of which linalool was the most abundant constituent. Linalool exhibited the striking molluscicidal and larvicidal effects with LC50 = 0.25 mg/L for O. hupensis and LC50 = 0.07 mg/L for cercaria of S. japonicium. After exposure to linalool, damage to the gills and hepatopancreas of the snails, and to the tegument and body-tail joint of cercariae was apparent. In addition, linalool markedly reduced the recovered schistosomulum from mouse skin after challenge infection, and therefore decreased the worm burden in infected animals, but not fecundity of female adults of the parasite.
Our findings indicated that linalool might be a novel chemotherapeutic agent against S. japonicium and the snail intermediate host.
- Oncomelania hupensis
- Schistosoma japonicum
- Molluscicidal activity
- Schistosomicidal property
- Cinnamomum camphora
Schistosomiasis japonicum, a parasitic disease caused by Schistosoma janponcium that live in snail-infested fresh water, remains one of the most prevalent parasitic infections with 413,000 people suffering from the plague in 7 provinces of China (Hubei, Hunan, Jiangxi, Anhui, Jiangsu, Sichuan and Yunnan). Endemicity of schistosomiasis japonicum is governed by socioeconomic and behavioral determinants, and the distribution of the snail intermediate host Oncomelania hupensis, which mainly spread in the Yangtze River valley and mountains or hills in southwest China. Though O. hupensis control by molluscicides is one of the main strategies to reduce the worm transmission in the snail population in infected areas, the synthetic niclosamide (2′, 5-dichloro-4′-nitrosalicylanilide) is the only effective molluscicide recommended by World Health Organization. Studies on the molluscicidal efficacies of natural products of plant origin have been promoted due to the high cost and environmental contamination of synthetic molluscicides, and the possible development of snail resistance[3–5].
Extracts from several species of the Cinnamomum have shown to be one of the most promising sources of new bio-efficacy against fungus[6, 7], bacteria and insect pests, and compounds for treatment of infectious diseases, autoimmune diseases and cancer. There are few reports on molluscicidal activity of leaf extracts from C. camphora against O. hupensis[13, 14]. The schistosomicidal effect of the extracts form C. camphora and the underlying mechanisms that account for their activity and active components, however, remain largely unelucidated. In this study, therefore, we identified the active component of extracts from leaves of C. camphora and elevated the molluscicidal effect against O. hupensis and the schistosomicidal activity.
Compounds, leaves and experimental animals
Linalool was purchased from Sigma–Aldrich Chemical Co., China. Niclosamide and wild adult negative snails of O. hupensis were gifts from Leading Office of Schistosomiasis Control of Hanchuan County, Hubei Province, China, and the positive snails were kindly presented by Prof. Shiping Wang, Department of Parasitology, Xiangya School of Medicine, the Central South University (Changsha, China). The two kinds of snails were confirmed by cercaria shedding test in our laboratory and reared under standard laboratory conditions. The leaves of C. camphora were collected in July 2011 from North Campus, Sun Yat-sen University, China. Voucher samples were deposited in Sun Yat-sen University Department of Parasitology collection with a reference number of 2011060018. Eight-week-old Balb/C mice were purchased from the Laboratory Animal Center of Sun Yat-sen University (Guangzhou, China). The mice infected with cercariae were used to determine the inhibition of cercarial penetration and protective effect of linalool against S. japonicum. All of the procedures involving animals and their care in this study were approved by the Institutional Animal Care and Use Committee of Sun Yat-sen University in accordance with institutional guidelines for animal experiments.
SC-CO2 extraction and GC-MS analysis
The fresh healthy leaves of C. camphora were picked from the sunlit branches of trees. Air-dried leaves (100 g) of the tree were powdered and extracted according to the protocol in previously published articles[15, 16] with minor modifications in a supercritical CO2 extraction apparatus (HA121-50-12, Huaan Supercritical Fluid Extraction Ltd., China). The sample was extracted with supercritical fluid CO2 at 25 MPa at 45°C for 4 hours and at the desired flow rate 15 L/h.
The components of extraction (0.5 μL), clear and of golden color, were quantified and identified by a QP2010 gas chromatography-mass spectrometry (GC-MS, Shimadzu Corporation, Japan). Injector temperatures were set at 280°C and the initial GC column temperature was held at 40°C for 5 min, then increased to 250°C at a rate of 5°C/min and maintained for 5 min at this final temperature. Helium was used as the carrier gas at 0.8 mL/min. The transfer line temperature was 230°C. Electron impact mass spectra were scanned at 70 ev in the mass range of 40-600 units. Compounds were identified by comparison of their mass spectra with those of NIST05 library data of the GC-MS system.
Molluscicidal activities of extracted samples and linalool against O. hupensis were evaluated following protocols in previously described studies[17, 18]. Briefly, 30 negative snails per group were placed in a 250-ml wide-necked bottle and maintained for 6 h, 12 h, 18 h, 24 h, 30 h, 36 h, 42 h, 48 h, 54 h, 60 h, 66 h, 72 h, 78 h, 84 h, 90 h or 96 h in one of the following solutions: i) a diluted extracts (ranging from 0.25 to 8.0 mg/L) containing 1% (v/v) ethanol, ii) diluted linalool (ranging from 0.1 to 3.2 mg/L) containing 1% (v/v) ethanol, iii) extract-free dechlorinated tap water containing 1% (v/v) ethanol (negative control group), and iv) extract-free dechlorinated tap water containing 0.5% (w/v) niclosamide (positive control group). The death was confirmed by the absence of snail heart beats for 2 min under Olympus microscope and the sum of the dead was used to estimate the lethal concentration (LC)50 and LC90 values for the periods of 24 h, 48 h and 96 h exposure to the leaf extract or linalool. All experiments were repeated three times under the same experimental conditions.
Light and transmission electron microscopy study
For light microscopy, O. hupensis were fixed in 10% phosphate-buffered formalin solution and processed in paraffin blocks. Serial sections (5-μm thick) of the gills, salivary gland, stomach and hepatopancreas were cut, mounted on glass slides and stained with hematoxylin-eosin. They were observed using a compound light microscope (Olympus, Japan). Digital images were captured with the affiliated software of the microscope.
For electron microscopy, hepatopancreas was dissected out from three linalool treated and untreated snails, respectively and the separated samples were fixed in 2.45% glutaraldehyde and 2.45% paraformaldehyde in 0.1 M sodium cacodylate buffer (pH 7.4) at room temperature for 5 h and then at 4°C overnight. The tissues were washed in 0.1 M sodium cacodylate buffer (pH 7.4) at room temperature for 3 h and postfixed in 2% OsO4 at room temperature for 2 h. The specimens were washed in 0.1 M sodium cacodylate buffer (pH 7.4) at room temperature for 3 h and dehydrated with graded ethanol series and embedded in TAAB epoxy resin (Agar Scientific Ltd.). Semithin sections (80 nm) were mounted onto Formvar-coated slot grids, then contrasted with uranyl acetate and lead citrate, and examined under a Zeiss EM 902 transmission electron microscope. Semithin sections (90 nm) from the staining with uranyl acetate and lead citrate was obtained using an ultramicrotome (PowerTomeXL, RMC, Tucson, USA). Specimens were examined under a transmission electron microscopy (H-7650, Hitachi, Tokyo, Japan).
Cercaria shedding assay
Activity assay measured on cercaria release was conducted at room temperature with a 9-h light period to determine the effect of linalool on the ability of cercaria releasing from infected O. hupensis by the number of the shedding cercariae within 6 hours and the time for the first cercarial release from the snails. The snails were transferred from the aquaria into Corning Costar® 6-well cell culture microplates (one snail/cell) and maintained in a diluted linalool containing 1% (v/v) ethanol or dechlorinated tap water containing the same concentration of ethanol (negative control). The microplates were observed under microscopes (Olympus, Japan) at 10-minute intervals until the released sercariae were found and the time was recorded. Six hours after the first cercarial release, the snails and cercariae were sacrificed with an incubation of the culture microplates at 80°C for 15 min. The sum of the dead cercariae at the bottom of the microplates were counted under microscopes (Olympus, Japan).
The cercariae of S. japonicum were procured from experimentally infected O. hupensis at room temperature and 100 ± 2 larvae were selected and exposed to the diluted linalool with dechlorinated tap water containing 1% (v/v) ethanol or dechlorinated tap water containing 1% (v/v) ethanol for 6 hours in 6-well cell culture microplates, and number of the dead cercariae was counted at 30-minute intervals. Sinking down of cercariae without movement within one minute give indication of death of the larvae, and to estimate LC50 and LC90 of linalool exposure for 30 min, 120 min and 360 min. The morphological characteristics of worms were observed under light microscope after different treatments as described above.
Detection of tegument integrity by fluorescent probe
The effect of linalool on integrity of the cercarial tegument was evaluated using detection of tegumentary protein SjCa8, a cercariae specific molecule, which has been described by Lv et al.. Briefly, after treatment with different compound for 30 min, and subsequent three washes (5 min each) with 1 × PBS, cercariae were incubated for 45 min at 37°C in PBS containing 5% bovine serum albumin (BSA, Sigma). The worms were treated for 45 min at 37°C with the primary antibodies (1:500 dilution) to recombinant SjCa8 prepared in our laboratory. After an additional washing step, parasites were incubated for 1 h at room temperature with Cy3-conjugated anti-mouse IgG diluted at 1:100, washed thrice and then observed under an FV 500-IX81 laser scanning confocal system (Olympus, Japan) with Krypton/Argon laser and appropriate filters.
Skin penetration and tissue migration assay
Twenty four Balb/C mice were randomly allocated to three groups with eight mice in each group. All mice were infected percutaneously with 30 S. japonicum cercariae. Prior to the infection of animals, the cercariae were exposed for 15 min to 0.1 mg/L, 1 mg/L linalool, or dechlorinated tap water containing 1% (v/v) ethanol, respectively. The mice were sacrificed 30 min after the challenge and the shaved skins exposed to the larvae were cut into pieces and then cultured for 24 h at 37°C, 5% CO2 in 6-well cell culture microplates in RPMI 1640 medium supplemented with antibiotics (100 U/ml of penicillin and 100 μg/ml of streptomycin) and 10% fetal calf serum (Invitrogen, USA) in quintuplicate. The penetrated larvae were collected and counted to evaluate the linalool's effect on skin penetration and migration by cercariae.
Worm recovery and tissue sampling
Twenty four Balb/C mice (8 mice/group) were challenged with cercariae after treatment as the protocol of "Skin penetration and tissue migration assay". Forty-five days after the challenge infection, the adult worm recovery and tissue sampling were performed according to our previously described study. In brief, all mice were sacrificed by cervical dislocation and adult worms were recovered from hepatic portal system and mesenteric veins. The percentage of worm reduction for each group was calculated according to the following formula: % reduction = (1-mean number of worms in experimental mice/mean number of worms in challenge control mice) × 100. The livers and intestines of mice from all groups were collected and weighed, and a known portion (0.5 g) of the intestine and liver from each animal were fixed and serial sections was prepared as description above for routine histopathological examination of granuloma in the organs. Moreover, same part of livers and intestines were completely digested with potassium hydroxide (4%) overnight at 37°C on a rocking platform. The eggs in the digest were put on the glass slide and counted under light microscopy. The calculation of egg reduction rate for each gram of liver or intestine was based on the following formula: % reduction = [(average number of eggs/g liver or intestine in control group - average number of eggs/g liver or intestine in experimental group)/average number of eggs/g liver or intestine in control group] × 100. Egg reduction rate for each adult female was calculated as following formula: egg reduction rate for each adult female (%) = [(average number of eggs/g liver or intestine/number of female in control group - average number of eggs/g liver or intestine/number of female in experimental group)/average number of eggs/g liver or intestine/number of female in control group] × 100.
Data were expressed as the mean ± standard deviation (SD) and *P < 0.05, determined by Student’s t test (GraphPad Prism 5), was considered significant. LC50, LC90 and their respective 95% confidence limit (95% CL) were obtained by nonlinear regression using the SPSS program version 16.0.
SC-CO2 extraction and GC-MS analysis
Components in the leaf extract of C. camphora with their molecular weight, molecular formula and relative content
Component of volatile oil
Relative content (%)
linalool, Z-pyranic acid
Molluscicidal effects against O. hupensis
Molluscicidal activity of C. camphora leaf extracts and linalool against O. hupensis after 96 h exposure (mg/L)
C. camphora leaf extracts
LC50 (95% CL)
LC90 (95% CL)
Light microscope and TEM study of snails treated with linalool
Cercaria shedding assay
The time of the first cercarial release from each infected snail grouped as above was recorded individually and the difference between the groups was not statistically significant (P > 0.05, Figure 5B).
Cercaricidal activity of 6 h exposure to linalool (mg/L)
LC50 (95% CL)
LC90 (95% CL)
Detection of tegument integrity
To determine whether linalool exhibited damage to integrity of cercariael tegument, we used immunofluorescence to localize a cercaria-specific tegumental protein SjCa8 as described above. Thirty minutes after treatment with linalool (0.1 mg/L), a majority of living cercariae began to shed their tails and the detached tails started to grow a large number small bulbous structures throughout whole tail region. Moreover, fluorescence-labeled particles were leaked from the head-tail junctions of the linalool-treated larvae and visualized under a fluorescence microscope in comparison to untreated parasites (Figure 7).
Skin penetration assay
Protective efficacy against challenge infection
Treatment and protection
Egg number/g liver
Egg number/g liver
Egg number/g intestine
Egg number/g intestine
/female worm (×104)
/female worm (×104)
11.50 ± 1.93
11.50 ± 1.60
23.25 ± 3.24
4.73 ± 1.02
4.14 ± 0.81
5.71 ± 0.98
5.01 ± 0.82
0.1 mg/l linalool
8.38 ± 1.92
8.5 ± 1.69
16.88 ± 3.48
3.54 ± 0.90
4.25 ± 0.62
4.37 ± 0.60
5.39 ± 0.97
1.0 mg/l linalool
4.50 ± 1.60
4.63 ± 1.41
9.13 ± 3.00
1.98 ± 0.66
4.50 ± 0.91
2.00 ± 0.76
4.47 ± 0.75
Hepatic and intestine egg reduction
Parasitic diseases, including malaria, schistosomiasis, filariasis and Chagas disease, remain a major public health threat affecting more than 30% of the human population in the world. Unfortunately, parasite infection can hardly be prevented by vaccination in most instance and many parasites have become resistant to the available pharmaceutical medicines. There is an increasing awareness of the potential of natural products from plants, which may lead to the development of much-needed new anti-parasitic drugs, with interesting biological activities of cytotoxic and anti-parasitic properties[22–25]. Cinnamomum extracts have been identified as preferred natural antiparasitic agents for the treatment of ectoparasitic louse and mite, entoparasites of Dactylogyrus intermedius (a parasitic helminth), Tetratrichomonas gallinarum and Histomonas meleagridis (protozoan parasites), and malaria vector of Anopheles gambiae. No systematic evaluation of molluscicidal or cercaricidal activity of C. camphora extracts against O. hupensis or S. japonicium has been carried out. In this study, we characterized the promising molluscicidal effect of C. camphora against schistosomiasis vector snail (O. hupensis) and identified the chemical composition of exacts of C. camphora leaves by GC-MS analysis. Taken into consideration of the highest abundance of C. camphora leaf extracts and known molluscicidal activities against schistosomiasis and fascioliasis vector snails of Biomphalaria alexandrina, Bulinus truncatus and Lymnneae natalensis, linalool investigated in the present report exhibited a highly significant molluscicidal effect on O. hupensis, the unique intermediate host of S. japonicum, as compared to control. The most evident histopathological alterations occurred in the hepatopancreas, the main metabolic and detoxification organ in molluscs, and the gills, which are involved in the transport of respiratory gases and regulation of ionic and osmotic balances in snails. Severe damage to these two organs, therefore, likely lead to a disruption of the osmoregulation and a reduction of oxygen consumption, which are critical to snail survival[34, 35].
Interestingly, linalool also displayed a considerable cercaricidal activity against S. japonicium accompanied with an inhibition of larvae shedding from snails and an obvious damage to tegumental integrity of cercariae exposed to the compound. The tegument of cercariae is a thin syncytial layer that covers the whole worm, which constitutes the major host-parasite interface after transformation of schistosomula and serves as a barrier preventing the loss of fluid, proteins and ions from breakage between body-tail joint and maintaining osmotic balance during penetration into and migration in the skin of hosts[36, 37]. Hence, the disruption of cercarial tegument by exposure to linalool will impair the crucial functions of larval tegument in immune evasion and parasite survival, which was coincident with the results of a significant reduction of recovered larvae in skin penetration assay and adult worm burden in animal challenge experiment. Nevertheless, linalool exhibited inapparent ovicidal properties on S. japonicum according to the similar egg counts in liver or intestine per female adult in all infected animals in this study.
Linalool, a monoterpene alcohol, is the most abundant component of C. camphora leaf extracts tested by GC-MS in this study and the major constituents of Aniba rosaeodora, Arisaema franchetianum, Arisaema lobatum, Croton cajucara and Ocimum forskolei essential oils[38–41]. Linalool-rich extracts from various plants present properties against bacteria, viruses, insects and parasites (protozoa and helminths)[45–47, 40] and the results presented in this work further support the molluscicidal and anti-parasite activity of linalool-rich exacts from plants. The extreme molluscicidal and cercaricidal properties of linalool offer a chance to develop a new lead compound for novel anti-schistosomal drugs.
In summary, in this work we first report linalool, the most abundant components from Cinnamomum camphora leaf extracts and a potentially important target for development of natural and novel agents for the control of schistosomiasis. Our analysis of molluscicidal activity and cercaricidal property of linalool against Oncomelania hupensis and Schistosoma japonicium, respectively, provide insights into antiparasitic treatment of this eco-friendly compound. Perhaps most striking are the characteristics of linalool that apparently causes damages to gills and hepatopancreas of the snails, and disruption of cercarial tegument. The results reported here should catalyze future studies of linalool and development of an alternative anti-schistosomal drug.
Yang Fan, Long Erping, Wen Juhua and Cao Lei are joint first authors.
We are grateful to Pro. Wang Shi Ping and Mr. Zhang Zhi Hai for their kind donation of O. hupensis. This work was supported by a grant from the National Basic Research Program of China (grant no. 2010CB530004), the National Natural Science Foundation of China (grant no. 30771888, 81371836 and 30800966), the 111 Project (grant no. B12003) and Research Fund for Students of Sun Yat-sen University (2011, 2013).
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