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1.
The effect of the amendment of nutrient solutions with soluble potassium silicate on the response of cucumber (cv. Corona) root and hypocotyl tissues infected by Pythium ultimum was examined by light and electron microscopy, and by energy dispersive X-ray analysis (EDX). Plants were grown in 0 or 1·7 m Si-amended nutrient solutions, and root and hypocotyl samples were collected at different times after inoculation with P. ultimum. By 48 h after infection, striking differences in the expression of defence reactions were observed between Si-amended and Si-free cucumber plants. Treatment of plants with Si markedly stimulated the accumulation of an electron-dense, phenolic-like material in infected host tissues, and significantly increased the percentage of cells filled with this material. Fungal hyphae colonizing occluded host cells were seriously damaged, and were often reduced to empty hyphal shells. Additionally, Si-treated cucumber plants responded to P. ultimum infection by forming electron-dense layers along primary and secondary cell walls, as well as over pit membranes of xylem vessels. EDX analysis failed to reveal the presence of silica deposits in P. ultimum-infected plants grown in Si-supplemented media. Our results suggest that a relationship exists between Si treatment, resistance to P. ultimum attack, and expression of plant defence mechanisms.  相似文献   

2.
The possible involvement of salicylic acid in systemic acquired resistance ofCucumis sativus againstSphaerotheca fuliginea was studied. Cucumber plants were inoculated with tobacco necrosis virus on the cotyledons and the level of endogenous salicylic acid in the first true leaf was determined by gas chromatography. Salicylic acid increased continously from the second day after virus inoculation to the fifth day, when the same leaf was inoculated withSphaerotheca fuliginea. In healthy plants, the efficiency of exogenous salicylic acid in inducing resistance was assayed by applying aqueous solutions at different times beforeSphaerotheca fuliginea inoculation. To evaluate the level of induced resistance, the following parameters were examined by light microscopy: percentage of conidial germination, length of the hyphae derived from single conidia, number of haustoria, percentage of epidermal cells with lignified walls and of necrotic cells underlying fungal hyphae. In treated plants conidial germination was reduced, the total length of the hyphae was shorter, the number of haustoria was lower and the haustorium-containing epidermal cells had more frequently lignified walls. Moreover, an evident increase in callose deposition was observed leading to the formation of oversized papillae around the penetration pegs. These results indicate that the application of salicylic acid before inoculation withSphaerotheca fuliginea reduces the intensity of the infectious process and that salicylic acid is involved in the expression of systemic resistance in cucumber challenged by the biotrophic pathogenSphaerotheca fuliginea.  相似文献   

3.
It is our working hypothesis that suppression of the activity of glycoprotein non-specific elicitors (NSE) from fungal cell walls is required in establishment of basic compatibility in the Cladosporium fulvum-tomato system. A suppressor of NSE-induced necrosis on tomato leaves was partially purified from intercellular fluid (IF) obtained from C. fulvum infected, or uninoculated, leaves. The suppressor was stable to treatment with heat, protease, glucosidase, galactosidase, laminarinase, periodate, and mild acid (0·1 N HCl) and base (0·01 N NaOH). Addition of the chelators, EDTA (15 mM) or EGTA (2 mM), to IF resulted in a marked reduction in suppressor activity. Suppressor activity was partially reduced by dialysis of IF, but activity was lost upon dialysis by prior treatment of IF with urea, or with protease which was then inactivated by heating. Activity of a low molecular weight suppressor, partially purified by dialysis and Sephadex G-25 column chromatography, corresponded with a carbohydrate peak. Pectinase or pectinase-generated oligogalacturonides from polypectate suppressed activity of NSE. However, incubation of NSE with pectinase, followed by heat treatment before assay, did not affect NSE activity. It is suggested that low molecular weight suppressor molecules may originate from action of pectolytic enzymes on host cell walls. In addition to these low molecular weight suppressor, native IF, but not heat treated IF, contained proteins that on in vitro incubation with NSE slowly reduced its ability to induce necrosis.  相似文献   

4.
Leaf tissue harvested from cucumber plants (Cucumis sativus L.) expressing induced resistance against the powdery mildew fungus Podosphaera xanthii (syn. Sphaerotheca fuliginea, Castagne; Braun and Shishkoff) was extracted and analyzed for phytoalexin compounds. Fluorescence microscopy was then used to observe the production of these compounds in planta, and laser scanning confocal microscopy observations were made to locate the subcellular sites of phytoalexin accumulation. Phytochemical analyses and fluorescence microscopy observations revealed the production of autofluorescent C-glycosyl flavonoid phytoalexins within the epidermal tissues of disease-resistant plants undergoing fungal ingress. Phytoalexin production was triggered by the combination of an eliciting/inoculation treatment, and tissue autofluorescence of color characteristic of the phytoalexins reached a maximum 48 h after elicitation prior to subsiding following the collapse of the pathogen. After a second eliciting treatment, disease-resistant plants produced phytoalexins more rapidly in response to fungal challenge. At the cellular level, autofluorescent C-glycosyl flavonoid phytoalexins were observed associated with the plasma membrane of infected epidermal cells immediately following elicitation. In the hours that preceded the collapse of conidial chains, phytoalexins accumulated inside the haustorial complexes of the pathogen within the epidermal cells of disease-resistant plants. Taken together, the results of this study show the timely synthesis of C-glycosyl flavonoid phytoalexins at precise subcellular locations as a key defense reaction used by cucumber to create incompatible interactions with powdery mildew.  相似文献   

5.
采用喷雾法研究了大黄酚对黄瓜白粉病的生物活性及其在黄瓜组织中的内吸传导性。结果表明,大黄酚对黄瓜白粉病菌具有较高毒力,感染白粉病的叶片经200 mg/L的大黄酚处理2 d后,霉状物变褐色,病斑枯死。扫描电子显微镜观察显示,黄瓜白粉病菌经大黄酚处理后,菌丝和分生孢子梗扭曲、变形,分生孢子塌陷。盆栽试验表明,利用大黄酚防治黄瓜白粉病具有较长的持效期,黄瓜子叶上喷施100 mg/L的大黄酚,20 d后接种病原菌,其防效仍达84.83%,与有效成分500 mg/L的硫磺悬浮剂防效相近。此外,大黄酚在黄瓜组织中具有一定的跨层传导性,其横向传导性较弱,几乎无向顶及向基的传导性。  相似文献   

6.
The cucumber pathogen Cladosporium cucumerinum produces one endo-polygalacturonase and at least two exo-polygalacturonases during growth in a liquid medium containing citrus pectin as the carbon source. The endo-polygalacturonase was purified nine-fold by ion-exchange chrumatography and gel filtration. The enzyme elicits lignification in cucumber hypocotyls down to a concentration of about 0·08 units ml−1 which corresponds to about 70 ng protein ml−1. It also releases elicitors of lignification from polygalacturonic acid and cucumber cell walls. The enzyme has a pH-optimum between 5·0 and 5·5, a molecular weight of about 38 000 and contains neutral hexose and protein in a ratio of 15:85 (w/w). The endo-polygalacturonase elicits lignification equally effectively in susceptible as in resistant cucumber hypocotyl segments, and releases about the same amount of elicitor from the cell walls of resistant and susceptible cucumber hypocotyls. This does not exclude the involvement of endo-polygalacturonase in the lignification reaction of resistant cucumber plants towards C. cucumerinum, but the specificity of the reaction must apparently be determined by other molecules.  相似文献   

7.
Powdery mildew, caused by Podosphaera pannosa, is a very common disease in greenhouse potted roses, resulting in poor marketing value and hence economic losses. Alternatives to chemical control are necessary, and therefore the ability of silicon (Si) applied to roots to control the disease was investigated, as well as the mechanisms behind the observed disease reductions. Four genotypes of miniature potted roses representing different genetic backgrounds and susceptibility to disease were studied. Plants were watered with a nutrient solution containing either 3·6 mm Si (100 ppm) supplied as K2SiO3 (Si+) or no Si (Si?) before inoculation with P. pannosa. Si application increased leaf Si content two‐ to four‐fold compared to control plants. Confocal microscopy showed that Si deposition was larger in Si+ than in Si? plants and that deposition mainly occurred in the apoplast, particularly in epidermal cell walls. Si application delayed the onset of disease symptoms by 1–2 days and disease severity was reduced by up to 48·9%. The largest reduction was found in the two most resistant genotypes, which also had the highest increase in Si uptake. The Si‐induced disease protection was accompanied by increased formation of papillae and fluorescent epidermal cells (FEC) as well as deposition of callose and H2O2, especially at the sites of penetration and in FEC, which are believed to represent the hypersensitive response. Si treatment reduced powdery mildew development by inducing host defence responses and can therefore be used as an effective eco‐friendly disease control measure.  相似文献   

8.
The polygalacturonases (PG) and oxalic acid produced by Sclerotinia sclerotiorum in infected soybean hypocotyls were investigated as elicitors of the phytoalexin glyceollin I.Purification to homogeneity through isoelectrofocusing and ion-exchange fast protein liquid chromatography revealed three endo-PG isoenzymes (PG-I, PG-II and PG-IV) and one exo-PG (PG-III) in 6-day-old etiolated soybean hypocotyls infected with the B-24 isolate of S. sclerotiorum.PG-I and PG-III, in the range of concentrations tested (0·15–1·2 reducing units ml−1), did not act as elicitors of glyceollin I synthesis. Some elicitor activity was shown by PG-II at 0·6–1·2 reducing units ml−1. PG-IV, at lower doses (0·038–0·30 reducing units ml−1), was even more effective in inducing phytoalexin synthesis. However higher concentrations of PG-IV induced tissue softening and decreased phytoalexin accumulation.PG-II and PG-IV released heat-stable elicitors from purified soybean cell walls supporting the evidence that uronides are intermediate inducers in elicitation by endo-PGs. Oxalic acid was an active elicitor of glyceollin I over the range of concentrations tested (0·31–20 m ) with the maximum at a concentration of 5 m . The inability of oxalic acid to release uronides from purified cell walls makes it unlikely that uronide intermediate elicitors are involved in elicitation by oxalic acid.  相似文献   

9.
A spray inoculation of the first leaf of 2-leaf stage cucumber plants with a non-pathogenic isolate of Alternaria cucumarina or Cladosporium fulvum before a challenge inoculation with the pathogen Sphaerotheca fuliginea induced systemic resistance to powdery mildew on leaves 2–5. Systemic resistance was expressed by a significant (p < 0.05) reduction in the number of powdery mildew colonies produced on each leaf of the induced plants, as compared with water-sprayed plants. Systemic resistance was evident when a prior inoculation with each of the inducing fungi was administered 1, 3 or 6 days before the challenge inoculation with S. fuliginea. Increasing the inoculum concentration of A. cucumarina or C. fulvum enhanced the systemic protection and provided up to 71.6% or 80.0% reduction, respectively, in the number of colonies produced on upper leaves, relative to controls. Increasing the inoculum concentration of S. fuliginea used for challenge inoculation, increased the number of powdery mildew colonies produced on both induced and non-induced plants. Pre-treated plants, however, were still better protected than controls, indicating that the level of systemic protection was related to the S. fuliginea inoculum concentration. The induction of systemic resistance against powdery mildew by biotic agents, facilitates the development of a wide range of disease management tools.  相似文献   

10.
Stemphylium botryosum pathogenic on alfalfa (Medicago sativa) produced a phytotoxin in a defined liquid medium which caused symptoms similar in sequence and appearance to stemphylium leafspot lesion development on attached alfalfa leaflets. The molecular weight of the phytotoxin was estimated to be 19500 by gel filtration chromatography. Treatment of partially purified phytotoxin with proteinase K or subtilisin resulted in loss of phytotoxic activity. Action of the proteases in inducing loss of phytotoxicity was inhibited by phenylmethylsulphonyl fluoride. Concentrated culture filtrates were fractionated by chromatofocusing, HPLC ion-exchange and gel filtration. Gel filtration also was followed by non-denaturing electrophoresis or isoelectric focusing (IEF). Analysis of sequential fractions from each procedure by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) indicated that phytotoxic activity was consistently coincident with the presence of two major polypeptides (Mr = 26900 ± 2%; 19500 ± 4%) and a triplet of polypeptides (Mr = 15500). The constant association between the three polypeptides suggested an intermolecular interaction during fractionation. The phytotoxic activity eluted from the chromatofocusing column between pH 5·79 and 5·43 whereas IEF estimated the isoelectric point to be between 5·40 and 5·02.Immobilized concanavalin A and wheat germ lectin failed to bind phytotoxicity. Proteolytic activity in some phytotoxic gel filtration fractions was reduced by addition of phenyl-methylsulphonyl fluoride and separated from phytotoxicity by non-denaturing electrophoresis, indicating that phytotoxicity was not due to serine protease activity.Pathogenicity tests of the cool-temperature biotype on 20 plant species representing eight plant families resulted in a compatible interaction only on M. sativa and M. polymorpha. In contrast, sensitivity to the phytotoxin was observed on both pathogen-resistant and susceptible alfalfa clones along with all other plants tested with the exception of Triticum aestivum, Zea mays, Apium graveolens and Melilotus officinalis, indicating non-host-specificity of the phytotoxic polypeptides produced by the cool-temperature biotype.  相似文献   

11.
Microspectrophotometry was performed on intact, pigmented vesicle-like inclusions within living sorghum cells that were accumulating phytoalexins as a response to attempted fungal infection. The results indicate that the deoxyanthocyanidin phytoalexins are present in inclusions. Moreover, the phytoalexin concentration within a single inclusion, based on luteolinidin, was calculated to be 0·15 m. The amounts of luteolinidin and apigeninidin in cells involved in the phytoalexin response at individual infection sites were also determined. The data showed that luteolinidin accumulated to levels of 0·48–1·20 ng/cell whereas apigeninidin accumulated to levels of 0·24–0·91 ng/cell. The results of both analyses confirmed that at the infection site the deoxyanthocyanidins accumulate to levels in substantial excess of those required for inhibition of the fungus Colletotrichum graminicola.  相似文献   

12.
The protective activity of a crude extract prepared from the green macroalga, Ulva armoricana, previously shown to induce plant defence responses, was evaluated on three plant species, common bean, grapevine and cucumber, cultivated in the greenhouse and inoculated with three powdery mildew pathogens Erysiphe polygoni, E. necator and Sphareotheca fuliginea respectively. Chemical analyses showed that the extract was enriched in ulvans, which are green algae polysaccharides essentially composed of uronic acid and sulphated rhamnose. Weekly applications were performed by spraying of the green algal extract at various dilutions on bean, grapevine and cucumber leaves. A significant effect (50% protection) was observed using a dilution corresponding to about 3 g l−1 dry matter and up to 90% reduction of symptom severity was obtained for the highest concentration (1/9 dilution, 6 g l−1 dry matter) for the three plant species. To study the natural variability of the protective activity, five extracts prepared from algae batches harvested at different year periods were evaluated. Although polysaccharide composition varied among batches, all extracts elicit a reporter gene regulated by a defence-gene promoter in a transgenic tobacco line, and protect cucumber plants against powdery mildew infection. Together, these data demonstrate that U. armoricana is a reproducible source of active compounds which can be used to efficiently protect crop plants against powdery mildew diseases.  相似文献   

13.
Two chitinase encoding EcoRI fragments from the enteric soil bacterium Serratia marcescens were cloned. From a genomic library of 5686 transductants, 21 expressed chitinase activity as indicated by clearing of a chitin-containing medium. The chitinase encoding clones could be divided into two groups. Four had an 18kb EcoRI fragment and 17 had a 9·4 kb EcoRI fragment. In Southern hybridization experiments the 18kb fragment showed no homology to the 9·4 kb fragment and restriction enzyme maps indicated no similarity. Triparental mating with fluorescent Pseudomonas spp. yielded transconjugants that expressed chitinase activity, inhibited growth of Fusarium oxysporum f. sp. redolens germ tubes and reduced disease of radish caused by the same fungus.  相似文献   

14.
Infection of groundnut leaves with the early leaf spot pathogen Cercospora arachidicola leads to a marked increase in extracellular 1,3-β-glucanase activity, limited to the infected tissue. Three isoforms of low molecular weight and extreme pI values, typical of pathogenesis-related proteins, were induced. These β-glucanases, when acting together, were capable of degrading the pathogen cell wall in vitro. Glucanases from homogenates of infected leaf tissue were partially purified by ion-exchange chromatography to give enzymes with molecular weights of 35, 32 and 20 kDa and pI values of 3·8, 3·6 and > 9, respectively. They were electrophoretically identical to the β-glucanases found in the intercellular washing fluid. Treatment of groundnut plants with 200 μM mercuric chloride induced the accumulation of identical extracellular β-glucanases. During the course of the infection an increase in peroxidase activity was also observed, but chitinase activity remained more or less constant.  相似文献   

15.
Cotton carpel tissue (35–45 days post-anthesis) that had been treated with a mixture of xylanolytic hydrolases derived from Aspergillus flavus was subjected to immunocytochemical analysis. Microscopic examination of treated tissues revealed severe degradation of the secondary wall structure. Control tissue cells revealed the presence of high concentrations of xylans/arabinoxylans throughout the cell wall, as well as significant concentrations of arabinogalactan proteins in secondary wall structure. Carpel cells treated with a mixture of A. flavus-produced xylanolytic hydrolases showed a much reduced presence of labeling by xylan-specific antibodies on the inner wall surface, suggesting a severe loss of these plant polysaccharides in the secondary wall structure. Carpel exposure to a purified 14 kD endoxylanase from A. flavus also resulted in a severe reduction of xylans from secondary wall structure, although penetration of the tissue was not as dramatic. Arabinogalactan proteins were not as severely affected by the xylanolytic hydrolases. Comparison of control tissue with hydrolase-treated tissue stained with toluidine blue revealed an apparent reduction in wall thickness, supporting the conclusion of secondary wall structure degradation. Interestingly, the pectins could only be detected in the samples treated with xylanolytic enzymes, indicating that the pectins were being masked by xylans. These results are consistent with the conclusion that the xylanolytic hydrolase complex of A. flavus is a critical factor for host cell wall maceration and may represent another important fungal virulence factor, in addition to pectolytic hydrolase activities.  相似文献   

16.
Persistence of resistance to fungicides in Sphaerotheca fuliginea   总被引：2，自引：0，他引：2  
Isolates ofSphaerotheca fuliginea collected in 1981–1983 in cucumber glasshouses in the Netherlands were tested for their sensitivity to benzimidazole fungicides, dimethirimol, dinocap and pyrazophos.Resistance to dinocap was not observed, although this fungicide has been used for over 30 years. Resistance to benzimidazole fungicides and dimethirimol has been persistent since these fungicides were withdrawn for control of cucumber powdery mildew more than 10 years ago. Although pyrazophos has only been used incidentally after 1977, the level of resistance has not decreased.Factors possibly involved in the persistence of resistance and implications for disease control in practice are discussed.Samenvatting De gevoeligheid voor twee benzimidazool-fungiciden en dimethirimol, dinocap en pyrazofos werd getoetst vanSphaerotheca fuliginea isolaten die in 1981–1983 verzameld waren in komkommerkassen in Nederland. Resistentie tegen dinocap werd niet waargenomen, ofschoon dit fungicide al meer dan 30 jaar wordt gebruikt.De resistentie tegen benzimidazool-fungiciden en dimethirimol, die meer dan 10 jaar geleden werden teruggetrokken voor de bestrijding vanS. fuliginea, was persistent. Hoewel pyrazofos slechts incidenteel gebruikt is sinds 1977, is het resistentieniveau niet teruggelopen. Factoren die mogelijk betrokken zijn bij de persistentie van resistentie en de gevolgen voor de ziektebestrijding worden besproken.  相似文献   

17.
The infection process of Fusarium avenaceum on wheat spikes and the alteration of cell wall components in the infected host tissue were examined by means of electron microscopy and cytochemical labelling techniques following spray inoculation at growth stage (GS) 65 (mid-flowering). Macroconidia of the pathogen germinated with one to several germ-tubes 6–12 h after inoculation (hai) on host surfaces. The germ-tubes did not penetrate host tissues immediately, but extended and branched on the host surfaces. Hyphal growth on abaxial surfaces of the glume, lemma and palea was scanty 3–4 days after inoculation (dai) and no direct penetration of the outer surfaces of the spikelet was observed. Dense mycelial networks formed on the inner surfaces of the glume, lemma, palea and ovary 36–48 hai. Penetration of the host tissue occurred 36 hai by infection hyphae only on the adaxial surfaces of the glume, lemma, palea and upper part of ovary. The fungus penetrated the cuticle and hyphae extended subcuticularly or between the epidermal wall layers. The subcuticular growth phase was followed by penetration of the epidermal wall, and hyphae spread rapidly inter- and intracellularly in the glume, lemma, palea and ovary. During this necrotrophic colonization phase of the wheat spike, a series of alterations occurred in the host tissues, such as degeneration of cytoplasm and cell organelles, collapse of host cells and disintegration of host cell walls. Immunogold labelling techniques showed that cell walls of spike tissues contained reduced amounts of cellulose, xylan and pectin near intercellular hyphae or infection pegs compared to walls of healthy host tissues. These studies suggest that cell wall degrading enzymes produced by F. avenaceum facilitated rapid colonization of wheat spikes. The different penetration properties of abaxial and adaxial surfaces of the spikelet tissues as well as the two distinct colonization strategies of host tissues by F. avenaceum are discussed. The penetration and colonization behaviour of F. avenaceum in wheat spikelets resembled that of F. culmorum and F. graminearum, although mycotoxins produced by F. avenaceum differed from those of the latter two Fusarium species.  相似文献   

18.
We investigated the in vitro and in vivo effects of some pesticides on rainbow trout erythrocyte glucose-6-phosphate dehydrogenase enzyme. The enzyme was purified 1691-fold with a specific activity of 16.235 U/mg protein and a yield of 63%. Cypermethrin, and propoxur inhibited glucose-6-phosphate dehydrogenase enzyme in vitro and deltamethrin inhibited both in vivo and in vitro. The obtained IC50 values for deltamethrin, cypermethrin, and propoxur were 0.63, 1.02, and 12 mM, respectively. The activity of the control was determined as 5.17 ± 0.62 U/g Hb in in vivo studies. The enzyme activities of the groups treated with 0.25 g/L deltamethrin were measured at 6, 12, 24, 48, and 72 h, and found to be 4.32 ± 0.47, 3.57 ± 0.39, 3.47 ± 0.45, 2.86 ± 0.37, and 2.31 ± 0.32 U/g Hb. In vivo experiments showed that deltamethrin significantly inhibited the G6PD enzyme activity after the 48th h (p < 0.05).  相似文献   

19.
To determine whether light quality affects the incidence of disease, we exposed cucumber (Cucumis sativus L. cv. Jinyan No. 4) plants at the 4-leaf stage to white and other monochromatic lights and tested the effects on plant response to Sphaerotheca fuliginea, defence-related gene expression and metabolic changes. Exposure to red light resulted in higher levels of H2O2 and salicylic acid (SA), and stronger expression of defence genes such as PR-1 than exposure to white or other monochromatic lights. In comparison, plants grown under purple and blue light had higher activities of phenylalanine ammonia-lyase (PAL) and polyphenoloxidase (PPO) and higher level of flavonoids than plants grown under other lights. Furthermore, plants grown under red light were more resistant whilst plants grown under other monochromatic lights were less resistant to Sphaerotheca fuliginea than plants grown under white light. These results suggest a role of red light in light-enhanced resistance, which correlates with enhanced SA-dependent signaling pathway.  相似文献   

20.
Extracellular endopolygalacturonase, purified from the pathogenic fungus Fusarium moniliforme, consists of four molecular forms (38, 41·5, 45, and 48·5 kDa, respectively. Three forms (38, 41·5, and 45 kDa) were purified to homogencity by FPLC on a Mono S column followed by electroelution after SDS-PAGE. The N-terminal amino acid sequences of each of the three forms, and of a mixture containing all four forms were shown to be identical to that predicted from the nucleotide sequence of the endopolygalacturonase gene previously cloned from F. moniliforme. Enzymatic deglycosylation experiments revealed the presence of N-linked, high mannose oligosaccharide side-chains on all four forms of endo polygalacturonase. Hydrogen fluoride catalysed chemical deglycosylation of the polygalacturonase mixture yielded a single polypeptide with an apparent molecular mass of 36·2 kDa. Southern blot analysis, carried out at high stringency with an endopolygalacturonase-specific probe on genomic DNA digested with three different restriction enzymes, showed a single hybridizing restriction fragment in all three digests. A single 2·0 Mb chromosome hybridized with the endo polygalacturonase-specific probe, as shown by Southern blot analysis of F. moniliforme chromosomes separated by CHEF electrophoresis. Northern blot analysis revealed only one mRNA species 1350 nt encoding endo polygalacturonase. These data indicate that a single gene encodes the endopolygalacturonases of F. moniliforme.  相似文献   

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