Promoting role of an endophyte on the growth and contents of kinsenosides and flavonoids of Anoectochilus formosanus Hayata, a rare and threatened medicinal Orchidaceae plant

Promoting role of an endophyte on the growth and contents of kinsenosides and flavonoids of Anoectochilus formosanus Hayata, a rare and threatened medicinal Orchidaceae plant 1 2 first-author 1 3 1 4 1 corresp ‡Corresponding Author ‡Corresponding Author †E-mail:sxguo1986@163.com †E-mail:sxguo1986@163.com sxguo1986@163.com Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China Department of Pharmaceutical Affairs, Beijing Chao-Yang Hospital, Beijing 100020, China Department of Pharmaceutical Affairs, Beijing Chao-Yang Hospital, Beijing 100020, China School of Traditional Chinese Material Medica, Shenyang Pharmaceutical University, Shenyang 110161, China School of Traditional Chinese Material Medica, Shenyang Pharmaceutical University, Shenyang 110161, China Anoectochilus formosanus , commonly known as “Jewel Orchid”, is a Chinese folk medicine used to treat hypertension, diabetes, and heart disease. The existence of A. formosanus is currently threatened by habitat loss, human and animal consumption, etc. The highly potent medicinal activity of A. formosanus is due to its secondary metabolites, especially kinsenosides and flavonoids. This orchid also has a unique mycorrhizal relationship. Most adult orchids rely on endophytes for mineral nutrition and have complex interactions with them, which are related to plant growth, yield and changes in secondary metabolites. This study investigated the promoting role of F-23 fungus (genus Mycena ) on the biomass and contents of kinsenosides and flavonoids of A. formosanus in pot culture. The following were observed after 10 weeks of symbiotic cultivation: increased shoot height, shoot dry weight, and leaf numbers by 16.6%, 31.3%, and 22.5%, respectively; increased contents of kinsenosides, isorhamnetin-3- O -β- D -rutinoside, and isorhamnetin-3- O -β- D -glucopyranoside by 85.5%, 226.1%, and 196.0%, respectively; some hyphae in epidermal cells dyed red and/or reddish brown by safranine; and, significantly reduced number of starch grains in cortical cells. Moreover, F-23 fungus significantly improved the kinsenoside and flavonoid contents of A. formosanus . These findings supported the reports that endophytes can alter the production of secondary metabolites in their plant hosts, although further physiological, genetic and ecological analyses are warranted. Anoectochilus formosanus Endophyte Secondary metabolite Kinsenoside Flavonoid Introduction 1 Anoectochilus formosanus Hayata, commonly known as “Jewel Orchid” (Cavestro, 1994 1994 ) because of its beautiful foliage (Teuscher, 1978 1978 ), is a terrestrial orchid widely distributed in Taiwan and Fujian Province of China, and Japan (State Administration of Traditional Chinese Medicine, 1999 1999 ). It has been used as a Chinese folk medicine for many years (Fujian Institute of Traditional Chinese Medicine, 1982 1982 ) to treat hypertension, diabetes, heart disease, lung and liver diseases, nephritis (Mak et al., 1990 1990 ; Huang et al., 1991 1991 ; Chiu and Chang, 1995 1995 ; Zheng et al., 1996 1996 ; Shih et al., 2002 2002 ), and other diseases (Lin et al., 1993 1993 ; Chan et al., 1994 1994 ; Du et al., 2001 2001 ; Shih et al., 2001 2001 ). The existence of A. formosanus is currently being threatened by its low seed germination rate, habitat loss and degradation, animal consumption, indiscriminate collection, and increasing demand by humans. Its wild sources are gradually decreasing (Zhang et al., 2010 2010 ). Consequently, the prices of its fresh and dry states have increased to approximately CNY 320 and 3 200 per kilogram, respectively (Shiau et al., 2002 2002 ), thereby limiting its clinical application. In a previous study, we used a micro-propagation technique for the large-scale production of A. formosanus to protect the wild population of this rare and threatened orchid species. The results demonstrate that A. formosanus maintains high genetic fidelity even after a 5-year propagation in vitro (Zhang et al., 2010 2010 ). The highly potent medicinal activity of A. formosanus is due to its secondary metabolites, especially kinsenosides. Kinsenosides were first isolated from A. koshunensis by Ito et al. ( 1993 1993 ) and shown to have antihyperliposis and antihyperglycemic effects (Du et al., 2001 2001 ; Zhang et al., 2007 2007 ). Orchids also have a unique mycorrhizal relationship (Bernard, 1902 1902 ). The mycobionts of most adult orchids have been mainly assigned to the form group Rhizoctonia (Roberts, 1999 1999 ), as well as to other fungal groups such as Agaricales or Ascomycetes. The characteristic poorly developed root systems of most adult orchids are believed to rely on endophytes for mineral nutrition (Smith and Read, 1997 1997 ) and have complex interactions with fungal endophytes. Despite all these interactions, fungal endophytes have been related to host plant growth, yield, fitness, and stress responses (Andrade-Linares et al., 2011 2011 ). Most research work on A. formosanus focuses on the large-scale production using the micro-propagation technique and the analyses of their chemical constituents, as well as the bioactivities and therapeutic applications. Little is known about the interaction between A. formosanus and fungus, especially the promoting role of fungus on the growth and contents of secondary metabolites of A. formosanus . A total of 69 strains isolated from Anoectochilus , Dendrobium , and Cypripedium were screened, among which 16 strains were selected for further analysis. Based on pot culture experiments under greenhouse conditions, one strain, namely F-23, was found to have the ability to increase the biomass of A. formosanus . Moreover, F-23 fungus was once identified and shown to be a mycorrhizal fungus of Dendrobium officinale , which might be of potential use to the mass cultivation of D. officinale under artificial conditions (Zhang et al., 2011 2011 ). The present study was aimed to identify the growth-promoting endophytes (F-23) of A. formosanus . We investigated the promoting role of F-23 fungus on the biomass and contents of kinsenosides and flavonoids of A. formosanus in pot culture. The findings help elucidate the effect of endophytes on the production of secondary metabolites in their orchid host plants. Materials and methods 1 Plant and fungal materials 2 A. formosanus Hayata belongs to Anoectochilus of Orchidaceae. After surface sterilization, above-ground parts of A. formosanus samples collected from Fujian Province, China, were cut into small pieces of stems with an axillary bud about 1 cm, and cultured in sterile micropropagation medium (MM) containing MS (Murashige and Skoog, 1962 1962 ) basic medium and supplemented with 0.5 mg/L naphthaleneacetic acid (NAA), 1 mg/L 6-benzyl adenine (6BA), 1 g/L activated charcoal, and 30 g/L sucrose. The medium was solidified with 10 g/L agar and then incubated at (25±2) °C under a 12-h photoperiod and a photosynthetic photon flux density of 50 μmol/(m 2 ∙s) (Zhang et al., 2010 2010 ). After four months of micropropagation in vitro, the aseptic in vitro micropropagated plants of A. formosanus were transferred to fresh MM without NAA and 6BA and cultured for another two weeks. The above aseptic in vitro micropropagated plants were grown in a greenhouse for two weeks with a mean temperature, daily radiation, and humidity of 23.3 °C, 20.5 mol/m 2 , and 62.5%, respectively. These in vitro micropropagated plants were used as plant materials for further experiments. F-23 fungus isolated from the roots of D. officinale was collected from subtropical forests in Xishuangbanna, Yunnan Province, China. Phylogenetic analysis of the internal transcribed spacer (ITS) region of ribosomal DNA (rDNA) indicated that F-23 fungus (GenBank accession No. FJ544251) belongs to the genus Mycena (Zhang et al., 2011 2011 ). F-23 fungus was grown in 90-mm Petri dishes containing potato dextrose agar in the dark for two weeks at 25 °C. To prepare the inocula, the hyphae of F-23 were transplanted to culture bottles containing sterile substrate containing wheat bran and cottonseed husk (1/1), and grown in the dark for four weeks at 25 °C (Zhang et al., 2011 2011 ). The mock inoculum had no hyphae and contained only wheat bran and cottonseed husk (1/1). Plant inoculation 2 The aseptic in vitro micropropagated plants were transferred to 8 cm×8 cm×9 cm plastic pots filled with a humus soil/vermiculite mixture (HVM; 1/1), and then inoculated with the above F-23 inoculum or mock inoculum. The plastic pots were initially filled with HVM to one-third of its capacity, and then a thin layer of oak leaves cut into 1 cm×1 cm pieces was evenly sprinkled on the HVM. Afterwards, a thin layer of raw sawdust of pine was sprinkled on the oak leaves. The inoculum (3 g) in small pieces was sprinkled on the sawdust, and A. formosanus plants were arranged on the inoculated sawdust. The roots were covered with HVM and buried 1 cm away from the pots’ edge. Each pot was thoroughly drenched with tap water until excess water flowed out from the drainage holes. Control plants were added to the mock inoculum and subjected to the same inoculation procedure as above. Each group consisted of 10 pots with 3–5 in vitro micropropagated plants in a pot. The pots were supplied with tap water every other day. All materials including the HVM, oak leaves, and sawdust were sterilized at 122 °C for 2.5 h prior to experiments. Interaction studies 2 After 10 weeks of growth in the greenhouse, 20 plants from each treatment group were harvested. Endophyte strains were isolated from the roots of plant hosts, and all strains were subjected to further phylogenetic analysis of the ITS region of rDNA. The shoot height (namely the main stem height) and number of leaves were recorded, whereas stems (namely above-ground parts) were bagged and dried at 40 °C for dry mass determination. Fresh roots of the remaining plants were fixed in formalin-acetic acid-alcohol. All samples were observed and photographed (ZEISS Axiolmager A1, Germany) after a series of routine light microscope observations following the protocol of Feder and O′Brien ( 1968 1968 ). This protocol involved dehydration in a graded ethanol series, embedding in paraffin, staining with safranine and fast green, and sealing with Canada gum. Kinsenoside content 2 High-performance liquid chromatography (HPLC) was carried out on a Waters™ 600E controller (USA) with an evaporative light scattering detector (Waters 2420, USA) and an autoinjector (Waters 2707, USA). HPLC was performed under the following conditions: drift tube temperature, 45 °C; gas flow, 30 pounds per square inch (psi; 1 psi=6.895 kPa); YMC-Pack Polyamine II, 250 mm×4.6 mm i.d.; particle size, 5 μm; column temperature, 25 °C; and, 77.5% CH 3 CN, 1 ml/min. The dried powders of A. formosanus from each treatment were passed through a mesh sieve (250±9.9 μm), accurately weighed (100 mg), transferred into 5 ml of centrifuge tubes containing 2 ml of methanol, and marinated for one night. Given the unstable chemical nature of kinsenosides (i.e., they easily decompose at high temperatures), extraction was performed for 45 min by ultrasonication (HHSY11-Ni, China) at low temperatures (4–15 °C). The extracts were centrifuged at 10 000 r/min for 10 min. After removing the supernatant, 2 ml of deionized water was added to the residue and the extraction was performed again by ultrasonication for 45 min, followed by centrifugation at 10 000 r/min for 10 min. The supernatant was collected and 2 ml of deionized water was added to the residue. The extraction and centrifugation procedures were repeated, and the supernatants were combined. The final solution was fixed at 10 ml and filtered through a 0.45-μm membrane. The injection volume of each sample solution was 20 μl. Three individual samples from each group (inoculated and non-inoculated with F-23) were extracted and analyzed by the proposed method. Two replicates of each extract were prepared. The relative standard deviation (RSD, presented as standard deviation (SD)/mean) was calculated as a measurement of method repeatability. Flavonoid compound content 2 The HPLC system consisted of a Waters™ 600E controller, a photodiode array detector (Waters 2996, USA), an autoinjector (Waters 2707, USA), and a Venusil ASB C 18 column (250 mm×4.6 mm i.d.; particle size, 5 μm). The mobile phase consisted of water containing 15% CH 3 CN and 0.5% acetic acid (A) and CH 3 CN (B). The gradient program was as follows: 0–15 min, 0–12% B; 15–25 min, 12%–18% B; 25–45 min, 18%–30% B, followed by column re-equilibration with 40% methanol for 15 min. The flow rate was 1 ml/min, the column temperature was 40 °C, and the detection wavelength was 365 nm. Stock solutions of isorhamnetin-3- O -β- D -rutinoside (Bu-h, 1.64 mg/ml) and isorhamnetin-3- O -β- D -glucopyranoside (Bu-d, 0.53 mg/ml) were prepared in methanol. For calibration, working standard solutions were prepared by diluting the stock solution with appropriate quantities of methanol, and then stored at 4 °C and brought to room temperature before use. The pretreatment of A. formosanus for each treatment was the same as that described in Section 2.3. Prior to the addition of methanol, all centrifuge tubes were cooled to room temperature to compensate for solvent loss. The conditions of centrifugation and filtration, as well as the injection volume and RSD calculation value were the same. Data analysis 2 The experiment of plant inoculation was performed in a completely randomized block design and each group (inoculated and non-inoculated with F-23) consisted of 10 pots with 3–5 in vitro micropropagated plants in a pot. This experiment was repeated three times. Plant growth responses, including the shoot height, shoot dry weight, and leaf number, were analyzed with SPSS 16.0 software. Statistical comparisons between inoculated and non-inoculated plants were carried out by Tukey’s post-hoc test and one way analysis of variance (ANOVA) according to the least significant difference ( P < 0.05). Results 1 Effect of F-23 fungus on A. formosanus vegetative growth 2 All A. formosanus plants inoculated and non-inoculated with F-23 fungus were harvested 10 weeks after cultivation to determine the influence of the endophyte F-23 on the shoot growth of A. formosanus plants. Results showed that F-23 fungus significantly affected the A. formosanus in vitro micropropagated plants in pot (Table 1 1 ), and that F-23 plants appeared more vigorous than the controls (Fig. 1a 1a ). The shoot height and shoot dry weight of F-23-colonized A. formosanus plants increased by 16.6% and 31.3%, respectively, whereas the leaf numbers were 22.5% higher compared with controls (Table 1 1 ). Phylogenetic analysis of the ITS region of rDNA indicated that all strains isolated from the roots of plant hosts were F-23, which belongs to genus Mycena . Values are presented as the mean±SD, n =20. Control: plants not inoculated with F-23 fungus; F-23: plants infected with the fungal endophyte F-23. All P < 0.05 vs. control Group Shoot height (cm) Shoot dry weight (g) Leaf number Control 8.66±1.64 0.067±0.009 2.36±0.63 F-23 10.1±0.96 0.088±0.005 2.89±0.78 (a) A. formosanus plants inoculated with F-23 appeared more vigorous than the controls at the end of the incubation period in pots. (b, c) A. formosanus roots of the control group (b) and the F-23 group (c) viewed under a dissecting microscope after a 10-week inoculation. (d, e) Light micrographs of transverse section of roots showing starch grains in the control group (d) and root hairs and outermost layer cells dyed in red (arrow) by safranine and few starch grains (star) in the F-23 group (e). (f) Transverse section of the control showed that the root surface of the control had no hyphae and remained green. (g, h) Transverse section of A. formosanus roots infected with F-23 showing aged hyphae dyed reddish brown (g) and an outermost cell layer dyed red (h) (Note: for interpretation of the references to color in this figure legend, the reader is referred to the web version of this article) Interaction of F-23 fungus with the root of A. formosanus 2 After 10 weeks of symbiotic cultivation, the plants infected with the fungal endophyte F-23 were more vigorous than the controls (Fig. 1a 1a ). The root surface of A. formosanus inoculated with F-23 fungus had a more remarkable change in color than the control. White hyphae were observed under a dissecting microscope on the surface of A. formosanus roots, which became khaki after 10 weeks of interaction between the endophyte F-23 and A. formosanus root (Fig. 1c 1c ), whereas the root surface of the control had no hyphae and remained green (Fig. 1b 1b ). The cortical cells of the control roots of A. formosanus contained more starch grains than that of the transverse section of A. formosanus roots infected with F-23 (Fig. 1d 1d ). In addition, a transverse section of A. formosanus roots infected with F-23 show root hairs and outermost layer cells dyed in red by safranine (Fig. 1e 1e ). The transverse section showed that aged hyphae in root hairs and outermost layer cells were dyed reddish brown by safranine (Fig. 1g 1g ), and fresh hyphae in outermost layer cells were red (Fig. 1h 1h ), whereas the root hairs and outermost layer cells of the control had no change of color (Fig. 1f 1f ). Moreover, several root hairs spread on the root surface of the control, which was not inoculated with hyphae (Fig. 1b 1b ). The outermost cell layer of the roots collapsed because of the infection with hyphae, and some hyphae were observed in the outermost cell layer and its adjacent cells (Figs. 1g and 1h 1g and 1h ). Effects of F-23 fungus on the kinsenoside content of A. formosanus 2 The correlation coefficient of kinsenoside was R 2 =0.9995, and the linear injection volume ranged from 5.78 to 57.8 μg. The chromatographic retention time ( t R ) of kinsenoside was 3.89 min, whereas the t R values of the control and F-23 groups were 3.873 and 3.877 min, respectively. The kinsenoside content of F-23 group was 85.5% higher than that of the control (Table 2 2 ). The RSD values of kinsenosides in these samples were less than 5.0% (Table 2 2 ), which showed acceptable variation within the measurement of the method. Values of RSD are presented as SD/mean ( n =3) Growths of A. formosanus non-inoculated and inoculated with F-23 fungus are as control and F-23, respectively Group t R (min) Kinsenosides content (mg/g) RSD * * (%)  Control 3.873 73.709 3.02  F-23 3.877 136.759 1.87 Effects of F-23 fungus on flavonoid compound content of A. formosanus 2 The t R values of Bu-h, control, and F-23 groups were 19.209, 19.167, and 19.233 min, respectively. The t R values of Bu-d, control, and F-23 groups were 20.567, 20.550, and 20.583 min, respectively. The Bu-h content of the F-23 group was increased by 226.1%, whereas the Bu-d content was 196.0% higher than that of the control (Table 3 3 ). The RSD of the kinsenoside in these samples was less than 5.1%, which showed acceptable variation within the measurement of the method. Values of RSD are presented as SD/mean ( n =3) Growths of A. formosanus non-inoculated and inoculated with F-23 fungus are as control and F-23, respectively 2 Group 2 Bu-h 2 Bu-d 2 RSD * * (%) t R (min) Content (μg/g) t R (min) Content (μg/g) Control 19.167 47.425 20.550 166.647 2.37 F-23 19.233 154.639 20.583 493.336 2.83 Chromatographic data also showed that some unknown flavonoids apart from Bu-h and Bu-d existed in both samples, especially in the F-23 group (Table 4 4 ). The F-23 group had one unknown flavonoid at t R =10–15 min, whereas the control had two unknown flavonoids at t R =10–15 and 25–30 min. In addition, with the exception of the newly found unknown flavonoid in the F-23 group at 21.317 min, the chromatographic peak areas all increased by different percentages as follows (compared with the control at the same t R values): 40.6% at 10–15 min, 182.2% at 15–20 min, 215.5% and 193.5% at 20–25 min, 60.3% and 1179.2% at 30–35 min, and 57.2% at 35–40 min (Table 4 4 ). t R : chromatographic retention time; NAP: no absorption peak at 365 nm. Growths of A. formosanus non-inoculated and inoculated with F-23 fungus are as control and F-23, respectively 2 Group 2 10–15 min 2 15–20 min 2 20–25 min 2 25–30 min 2 30–35 min 2 35–40 min t R (min) Area t R (min) Area t R (min) Area t R (min) Area t R (min) Area t R (min) Area Control 10.800 3 082 16.633 17 518 20.850 8 239 21.267 15 979 31.800 14 599 38.883 19 928 11.467 7 813 22.517 2 627 23.617 3 832 32.883 3 234 F-23 10.917 4 334 16.700 49 438 20.883 25 994 NAP NAP 31.917 23 397 38.967 31 318 NAP NAP 21.317 24 298 NAP NAP 32.933 41 368 22.533 7 709 Discussion 1 Orchids belong to the largest plant family, which was estimated to comprise more than 25 000 species worldwide (Jones, 2006 2006 ). Various orchid species are economically important, including terrestrial species, epiphytes, and lithophytes. Some orchids are used as food and drink flavoring, and others are used as important natural medicines. Orchids also have a huge horticultural market worth 100 million dollars annually in the USA alone (Griesbach, 2002 2002 ). Although terrestrial species account for only one-third of orchids, almost half of extinct orchid species are terrestrial herbaceous perennials according to the International Union for Conservation of Nature. These perennials are most likely to be at a greater extinction risk because of increased threats to their existence, especially under the current climatic change scenarios (Swarts and Dixon, 2009 2009 ). However, research on the unique mycorrhizal relationships of orchids (Bernard, 1902 1902 ) considerably lags behind research on other important mycorrhizal types, particularly the arbuscular mycorrhiza. Accordingly, in this study we observed the growth and contents of secondary metabolites of A. formosanus inoculated with F-23 fungus in open pot cultures. As described by Imhof et al. ( 2013 2013 ), mycoheterotrophic plants lack chlorophyll and depend on an intimate association between their underground organs and fungi. These fungi were considered to be connected to photosynthetic plants for carbon compounds and some of them involved may also increase access to soil-derived nutrients. Our results showed that F-23 fungus significantly affected A. formosanus in vitro micropropagated plants in pots. Tang and Guo ( 2004 2004 ) demonstrated that an endophyte of Epulorhiza sp. can increase the survival rate, fresh weight, dry weight, and activities of four enzymes (chitinase, β-1,3-glucanase, polyphenol oxidase, and phenylalanine ammonia-lyase) of A. formosanus in open pot cultures. The contents of fructose, sucrose, polysaccharide, and total soluble sugar were also enhanced when Epulorhiza sp. was present but not when no inoculum was added (Tang et al., 2008 2008 ). Therefore, we hypothesized that the increase in A. formosanus biomass may be due to F-23 fungus by increasing the enzyme activities and photosynthesis of the host plant. It is becoming increasingly clear that soil microbial communities comprised of a vast array of bacteria, fungi, nematodes, and other organisms, are not passively determined but actively regulated by plants (Sugiyama et al., 2012 2012 ). Light micrographs of the interactions between A. formosanus root and F-23 fungus showed that the number of starch grains was significantly reduced in cortical cells, which was reported for the first time. Some reddish brown aged hyphae were observed in the outermost layer of cells and adjacent cells. Several reasons have been suggested for the decomposition of starch grains in cortical cells. First, the decomposition of starch grains may provide carbon for endophyte growth. Second, it may enable continued fungal colonization because N, P, and water continue to flow from the fungal partner, although carbon exchange is essentially reversed with photosynthate in adult photosynthetic orchids (Dearnaley, 2007 2007 ). Third, under the promoting role of the endophyte, the decomposition of starch grains may provide the carbon required for the growth of the host plant A. formosanus itself. In addition, all the abovementioned reasons may simultaneously occur because nutrient exchange in photosynthetic orchids is highly complex (Selosse et al., 2004 2004 ; Cameron et al., 2006 2006 ). Plants secrete both high- and low-molecular weight compounds from their roots, whose exudates function not only as nutrients for soil microbes but also as signal molecules in plant-microbe interactions (Sugiyama and Yazaki, 2012 2012 ). Studies of the changes in secondary host metabolites as an effect of orchid mycorrhizal relationships are limited. Nevertheless, reports that endophytes can alter the production of secondary metabolites in their plant hosts are increasing. Chen et al. ( 2006 2006 ) found that the production of alkaloids in Dendrobium candidum protocorms can be induced by a fungal elicitor. Our study showed a significant increase in kinsenosides and flavonoids in A. formosanus when co-cultured with F-23 fungus. Sugiyama and Yazaki ( 2012 2012 ) demonstrated that flavonoids and strigolactones in root exudates serve as signal molecules to establish the symbiotic interactions between legume plants and rhizobia or/and arbuscular mycorrhizal fungi, while root exudates also function to acidify surrounding soils to acquire phosphate. Moreover, Demain and Fang ( 2000 2000 ) demonstrated that secondary metabolites, including a heterogeneous group of chemically different natural products, may be related to survival functions for the producing organism. 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Bencaologic review, resource survey and taxonomic identification We are grateful to Prof. Hai-hong HUANG (Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, China) for supplying the kinsenosides, and to Prof. Chun-lan WANG (Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, China) for supplying the flavonoids Bu-h and Bu-d. Compliance with ethics guidelines Fu-sheng ZHANG, Ya-li LV, Yue ZHAO, and Shun-xing GUO declare that they have no conflict of interest. This article does not contain any studies with human or animal subjects performed by any of the authors. 10.1631/jzus.B1300056 Project supported by the National Natural Science Foundation of China (No. 31070300) and the National High-Tech R&D Program (863) of China (No. 2008AA09Z405) 2013-02-25 2013-08-13 2013-05-10 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2013 2013 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 09 14