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1.
Uptake of [14C]fenarimol (30 μM) by mycelium of wild-type Aspergillus nidulans was characterized by a rapid initial accumulation during the first 10 min of incubation with the fungicide and a subsequent gradual release with time. Uptake appeared to be the result of influx and efflux. Influx of fenarimol could not be inhibited by low temperature, anaerobiosis, starvation of mycelium, or incubation with several respiratory inhibitors and is, therefore, a passive process. Under identical test conditions efflux activity was severely inhibited and should, therefore, be regarded as an energy-dependent mechanism. After prolonged incubation (90 min) an equilibrium between influx and efflux was established, resulting in an energy-dependent permeability barrier, since uptake could instantaneously be enhanced by addition of oligomycin or N,N′-dicyclohexylcarbodiimide. It also indicates that efflux activity is inducible; this hypothesis is supported by the observation that pretreatment of mycelium with unlabeled fungicide prevented subsequent uptake of [14C]fenarimol. Uptake by fenarimol-resistant mutants J146, M193, and R264 of A. nidulans, all possessing the imaB gene for resistance, was relatively low and almost constant in time. In this case, uptake appeared to be considerably enhanced by low temperature, anaerobiosis, starvation of mycelium, and incubation with respiratory inhibitors. Low uptake by these mutants is ascribed to a higher energy-dependent efflux activity for fenarimol compared with the wild-type strain. Upon inhibition of the barrier activity, net uptake resulted from remaining passive influx, which in that case may be as high as in the wild-type strain. The results suggest that both wild-type and fenarimol-resistant mutants possess an energy-dependent efflux mechanism with different efficiencies to excrete fenarimol and probably other chemicals to which cross-resistance or collateral sensitivity is present.  相似文献   

2.
The effects of different incubation conditions on toxicity and uptake of imazalil by mycelium of a wild-type (003) and fungicide-resistant (R264) strain of Aspergillus nidulans were determined. In agar plate and liquid shake culture, imazalil was 200 and 40 times less toxic to the R264 strain, respectively, than to the wild-type strain. Inhibition of C-4 desmethyl sterol (ergosterol) biosynthesis occurred rapidly in mycelium of both strains at minimum growth inhibitory concentrations. Imazalil was neither detoxified nor converted into a toxic compound by mycelial suspension. Increased uptake of imazalil by the two strains occurred as concentrations of the fungicide were increased. However, the percentage uptake of imazalil by the wild-type strain was highest at the lowest concentration. These results suggest that binding in the wild-type strain involved a small number of high-affinity sites which became saturated as fungicide concentrations increased; and that at higher concentrations considerable nonspecific binding occurred in both strains. Uptake of imazalil during the initial 10 min of incubation was considerably lower in resistant than in the wild-type strain. However, upon prolonged incubation, both strains took up near equal amounts of fungicide. Uptake of fungicide by both strains was not inhibited by incubation at low temperature but was stimulated by respiratory inhibitors. These data support, in part, the hypothesis that resistance to imazalil, as reported previously for fenarimol (M. A. de Waard and J. G. M. van Nistelrooy, Pestic. Biochem. Physiol. 13, 255 (1980)), is based on reduced uptake of fungicide by mycelium of the resistant mutant.  相似文献   

3.
When the petioles of detached tobacco leaves (10–17 cm2) were incubated in aqueous solutions containing [14C]metalaxyl, uptake of the fungicide was dependent on the temperature and photoperiod. Detached leaves took up 78% more [14C]metalaxyl at 26°C than at 16°C. The rate of uptake in the light at 21°C was linear, but after an additional 20h in the dark, there was only twice as much fungicide in the leaves. Different sized leaves contained the same amount of fungicide per cm2 area. Uptake by detached leaves of the 14C-labelled anilide lactones ofurace and RE-26940 [2-methoxy-N-(tetrahydro-2-oxo-3-thienyl)acet-2′,6′-xylidide] was similar to that of metalaxyl. At the concentration of metalaxyl (66 ng ml?1) that controlled blue mould (Peronospora tabacina) on detached tobacco leaves, the amount of fungicide in the leaves was found to be 7.25 ng. Autoradiography showed that the distribution of [14C]metalaxyl in detached leaves after incubation for 23h was uniform, although higher concentrations of the label were present in the smaller veins of the leaves.  相似文献   

4.
Genetic control and mechanisms of resistance to tebuconazole, a sterol C14-demethylation inhibitor, were investigated in the phytopathogenic fungusNectria haematococca. Resistant mutants have been selected from the laboratory, following UV irradiation. They have been characterized through genetic crosses and mutations in at least three genes were found to be responsible for resistance. The genesTeb1, Teb2, andTeb3were clearly identified, a fourth gene calledTeb4could be hypothesized. Mutations at lociTeb2andTeb3induced pleiotropic effects such as reduced sporulation and growth rate, mycelium pigmentation (Teb2), or altered ascospore viability (Teb3). The resistance levels determined by mutations in the different genes were relatively low (below 10). When associated in double mutants, the additive effect was recorded. Cross-resistance toward other sterol C14-demethylation inhibitors was observed in all the resistant strains, except in theTeb4-carrying strain; moreover, for some C14-demethylation inhibitors hypersensitivity was expressed. A constitutive energy-dependent efflux seemed implicated in the mechanism of resistance for theTeb1-carrying strain and probably also for theTeb2andTeb3-carrying strains. However, theTeb4-carrying strain exhibited a kinetic of fungicide uptake similar to that of the wild-type strain. The sterol profile of theTeb4-carrying strain was similar to that of all the other resistant mutants and wild-type strains. Thus the resistance mechanism induced by mutation at theTeb4locus has not been found yet.  相似文献   

5.
The fitness of twelve fenarimol-resistant mutants of Aspergillus nidulans was tested with respect to spore germination, germ tube elongation, hyphal growth and sporulation. Half of the strains tested were isolated on triarimolcontaining media. The other strains were selected on imazalil-or cycloheximide-containing media (Van Tuyl, 1977).A number of mutant strains produced spores with unimpaired viability on synthetic medium. In other strains a reduction in spore viability was noticed. The rate of germ tube elongation of all resistant mutants was significantly lower than that of the wild-type strain. Mutant strains with a low degree of resistance always had an almost normal mycelial growth rate, whereas growth of some of the strains with a relatively high degree of resistance was significantly slower. Spore production on malt agar was highest in the wild-type strain and was found to be lower in fenarimol-resistant mutants. In most of the mutant strains tested a high degree of cross-resistance between fenarimol, imazalil and triadimefon was established; in some of them cross-resistance to these chemicals was low or even absent.Possible implications of the results described for the chance of development of resistance in phytopathogenic fungi to sterol biosynthesis-inhibiting fungicides are discussed.  相似文献   

6.
An enzymatic assay system has been developed to measure the relative potency of fungicides such as triadimefon, triarimol, triforine, and buthiobate as inhibitors of sterol 14-demethylation. The enzyme preparation used is the 8000g supernatant derived from a homogenate of an aerobically adapted, anaerobically grown, high sterol strain of Saccharomyces cerevisiae. After incubation of the enzyme with [2-14C]mevalonic acid and the fungicide the ratio, radioactivity in 4,4-dimethyl sterols/radioactivity in 4-demethyl sterols is determined. The higher this ratio is, the more efficient is the fungicide as an inhibitor of fungal sterol 14-demethylation. The ratio has been determined for a number of commercial fungicides and two series of triazole compounds. A similar assay system based on the 10,000g supernatant from a rat liver homogenate was also tested but gave an inaccurate assessment of the relative potency of fungicides as inhibitors of fungal sterol 14-demethylation.  相似文献   

7.
The acylalanine fungicides CGA 29212 and metalaxyl inhibit colony growth of Phytophthora megasperma f. sp. medicaginis at much lower concentrations than structurally related chloroacetanilide herbicides. Metolachlor, among the latter, shows the highest antifungal activity, followed by propachlor. Dimethachlor and alachlor are only weakly inhibitory. A metalaxyl- and CGA 29212-resistant strain of P. megasperma f. sp. medicaginis shows cross-resistance to metolachlor and propachlor, but levels of resistance are much lower than observed with CGA 29212 and metalaxyl. Cross-resistance does not occur to dimethachlor and alachlor. All compounds except metalaxyl inhibit uptake of [3H]uridine by mycelium, propachlor being most effective. Effects are similar with both a metalaxyl-sensitive and a -resistant strain. CGA 29212, metalaxyl, and metolachlor inhibit incorporation of [3H]uridine into RNA by mycelium of the sensitive strain at concentrations not inhibitory to uptake. Metalaxyl slightly affects incorporation by mycelium of the resistant strain; the other compounds have a more pronounced effect but only at concentrations inhibitory to uptake. Metalaxyl, CGA 29212, and propachlor do not induce leakage of radioactivity from mycelium of both strains when added at high concentrations to cultures previously incubated with [3H]uridine; under these conditions incorporation by mycelium of the metalaxyl-resistant strain is significantly more affected by CGA 29212 and propachlor than by metalaxyl. Endogenous RNA polymerase activity of isolated nuclei from a metalaxyl-sensitive strain is inhibited by CGA 29212, metalaxyl, and metolachlor but not by propachlor, dimethachlor, and alachlor. Neither compound has any effect on endogenous RNA polymerase activity of isolated nuclei from a metalaxyl-resistant strain. CGA 29212 and metolachlor evidently have a metalaxyl-type of action. The presence of cross-resistance of the metalaxyl-resistant strain to propachlor also indicates a metalaxyl-type of action for this compound, although this could not be confirmed by an inhibitory effect of propachlor on endogenous RNA polymerase activity. In addition to a metalaxyl-type of action, CGA 29212, metolachlor, and propachlor have a second one that is also present in dimethachlor and alachlor, which lack the metalaxyl-type of action. The second mechanism of action, involving inhibition of [3H]uridine uptake, is most prominent with propachlor and might be related to the primary mechanism of action in plants of the chloroacetanilide herbicides.  相似文献   

8.
Phthalimide fungicides (captafol, captan and folpet) enhanced the accumulation of fenarimol by the mycelium of a wild-type strain and a fenarimol-resistant strain of Aspergillus nidulans. The accumulation is ascribed to inhibition of active efflux of fenarimol from the mycelium. It is assumed that the synergistic action observed between the phthalimide fungicides and fenarimol with respect to fungitoxicity, was caused by the increased accumulation of fenarimol.  相似文献   

9.
The inherent resistance risk forMonilinia fructicola against sterol-biosynthesis inhibitors (SBIs) was estimated inin vitro andin vivo laboratory studies. Several mutant strains were selected on media amended with the triazole fungicides penconazole, etaconazole or the morpholine fungicide fenpropimorph.The potential forM. fructicola to develop resistance to the triazoles or to the morpholines was similar.The level of resistance attained did not differ for the two classes of fungicides after a single cycle of treatment with nitrosoguanidine (NTG). Attemps to select mutants with a higher level of resistance to penconazole after successive mutagenic treatments were successful. Most of the mutants were less fit than wild-type strains. Mutants with a low level of resistance had an almost normal mycelial growth rate, whereas growth of mutants with a higher level of resistance was significantly reduced. Spore production was highest in the wild-type strains, similar to the latter in a few resistant strains and less in most others. Only one mutant with an intermediate level of resistance could successfully compete in a mixed population with a wild type strain during successive infection cycles on peaches. Resistance was not stable in highly resistant mutants. Cross resistance to the inhibitors of 14-methylsterol demethylation (DMIs) tested was confirmedin vitro andin vivo for all mutant strains. One DMI-resistant mutant was also resistant to fenpropimorph and two fenpropimorph-resistant mutants were resistant to penconazole.  相似文献   

10.
 Laboratory mutants of Cochliobolus heterostrophus resistant to iprodione were obtained after chemical mutageneses. All the mutants were able to grow on the medium amended with iprodione 100 μg/ml. They showed positive cross-resistance to procymidone and fludioxonil and were sensitive to high osmolarity. Crosses between the mutant and a wild-type strain revealed that the fungicide resistance and osmotic sensitivity traits were inherited by their offspring in a 1 : 1 mutant/wild type ratio, indicating that the mutant phenotypes in these strains were due to alteration at a single gene locus. Results from allelism tests indicated that three genes (Dic1, Dic2, Dic3) conferred the mutant phenotypes. Among them, Dic1 mutant strains were classified into three types on the basis of their phenotypes. The first type was moderately resistant to the fungicides and less sensitive to osmotic stress than the other Dic1 mutant strains. The second type showed moderate fungicide resistance, but growth was inhibited under lower osmotic stress (50 mM KCl). The other Dic1 mutant strains grew well on medium containing iprodione and fludioxonil even at a concentration of 100 μg/ml and were highly sensitive to osmotic stress. The Dic2 and Dic3 mutant strains had moderate resistance to the fungicides with low-level osmotic sensitivity. The Dic1 gene was epistatic to Dic2 and Dic3 for fungicide resistance and hypostatic to them for osmotic sensitivity. These results suggest that the osmoregulatory system is involved in fungicide resistance in laboratory mutants of C. heterostrophus. Received: March 14, 2002 / Accepted: August 13, 2002  相似文献   

11.
The phenylpyrrole fungicide fenpiclonil inhibited the metabolism of glucose in mycelium of Fusarium sulphureum Schlecht at a concentration which only slightly inhibited mycelial growth (EC15). At the same concentration, fenpiclonil also inhibited accumulation and, to a greater extent, phosphorylation of 2-deoxy[U-14C]glucose in starved mycelium loaded with unlabelled 2-deoxyglucose. Fenpiclonil did not affect cell-free phosphorylation of 2-deoxyglucose or the ATP content of mycelium. Therefore, the primary mode of action of the fungicide may be based on inhibition of transport-associated phosphorylation of glucose. This may cause a cascade of metabolic events which eventually lead to fungal growth inhibition and death. One major event affected by inhibition of transport-associated phosphorylation is the accumulation of polyols, such as glycerol and mannitol, in mycelium. This was not observed in an osmotically sensitive, fenpiclonil-resistant laboratory isolate of the fungus.  相似文献   

12.
Mutants of Phytophthora parasitica Dast. more or less resistant to dimethomorph or metalaxyl were obtained by treating mycelium with ultraviolet radiation. Some metalaxyl-resistant mutants exhibited levels of resistance (i.e. the ratio between the EC50 values for the mutant and the wild-type strain) greater than 100, but those observed in the dimethomorph-resistant mutants never exceeded 25. Most mutants retained their resistance after sub-culturing on unamended agar medium. Single zoospore clones derived from a metalaxyl-resistant and a dimethomorph-resistant mutant, selected as amongst the most resistant, had levels of resistance similar to those of the parental strains. The metalaxyl-resistant mutants were also resistant to the related phenylamide fungicides, furalaxyl and benalaxyl, but remained sensitive to dimethomorph. The dimethomorph-resistant mutants were not resistant to phenylamide fungicides. The pathogenicity of some metalaxyl- or dimethomorph-resistant mutants on tobacco leaves was similar to that of the wild-type strains.  相似文献   

13.
Increasing adsorption of [14C]-labelled carbendazim in soil took place within a few weeks of incubation and was greatest in soil with a high organic matter content. Carbendazim was slowly decomposed in soil, mainly by soil microorganisms. After 250 days of incubation in two unsterilised soils, 13 and 5% respectively of added [14C]-carbendazim was recovered compared with 70 and 50% respectively from sterile soils; 4–8% of added carbendazim was recovered as 2-aminobenzimidazole (2-AB) from both unsterilised and sterile soil. After 270 days' incubation, 33 and 9% of 14C was recovered as 14CO2 from soil supplied with [14C]-carbendazim (20 and 100 mg/kg) respectively. Degradation started more rapidly when carbendazim was added to soil preincubated with the fungicide but the degradation rate was very low in all cases, indicating that the compound is a poor microbial energy source and that the degradation is a co-metabolic process. 2-AB was found as a degradation product although it appeared to be unstable in soil, decomposing rapidly after a lag period of about 3 weeks; small amounts remained in the soil for several months, however, presumably adsorbed on soil particles.  相似文献   

14.
The rapid effects of the thiocarbamate herbicide S-ethyl dipropyl thiocarbamate (EPTC) and the herbicide protectant N,N-diallyl-2,2-dichloroacetamide (DDCA) on macromolecular syntheses and glutathione (GSH) levels in maize cell cultures were studied to determine whether stimulation of GSH could be the primary mechanism of action of DDCA. EPTC (0.5 and 1 mM) reduced incorporation of radioactive precursors within 1 hr after treatment, and affected incorporation of [3H]acetate into lipids more than incorporation of [3H]adenosine into acid-precipitable nucleic acids, or [14C]protein hydrolysate into protein. [14C]EPTC was rapidly biotransformed within 8 hr by maize cell suspensions. Measureable decreases in GSH levels following treatment with 1 mM EPTC occurred after 15 hr. DDCA stimulated incorporation of [3H]acetate into lipids within 4 hr but did not affect incorporation of [14C]protein hydrolysate into protein or [3H]adenosine incorporation into nucleic acids. Measureable increases in GSH following DDCA treatment began after 12 hr. Treatment with EPTC and DDCA in combination inhibited incorporation of [3H]acetate into lipids less than EPTC given alone. Increases in GSH levels could be observed following pretreatments with glutathione precursors, but no protectant activity could be detected, in contrast to treatments with DDCA. It is suggested that DDCA has an initial rapid effect on lipid metabolism followed by a slower effect involving increases in cellular GSH.  相似文献   

15.
Corn (Zea mays L. single cross hybrid Mv 620) was germinated in a petri dish with addition of carbonyl[14C]EPTC (S-ethyl-N,N-dipropylthiocarbamate). The shoots and roots of 4-day-old seedlings were crushed and extracted in 80% methanol. On the chromatogram of the extract three radioactive peaks were found. The main peak was identified as S-(N,N-dipropylcarbamoyl)-glutathione. For the comparison of carbamoylating ability [14C]EPTC, [14C]EPTC-sulfoxide, and [14C]EPTC-sulfone were incubated with glutathione. Only EPTC-sulfone reacted in the 10-day incubation time. In aquatic solutions EPTC and EPTC-sulfoxide proved to be stable during the 10 days compared to EPTC-sulfone which quickly degraded, S-(N,N-Dipropylcarbamoyl)-glutathione was converted to S-(N,N-dipropylcarbamoyl)-cysteine in corn shoot homogenate. [14C]EPTC, [14C]EPTC-sulfoxide and [14C]EPTC-sulfone were added to corn shoot homogeneates and each of the three mixtures were analyzed by chromatography after 1 day incubation. EPTC was partly oxidized to EPTC-sulfoxide. EPTC-sulfoxide did not change and EPTC-sulfone produced similar metabolites as had been found in the germination experiment.  相似文献   

16.
Differential accumulation of [14C]imazalil and [14C]fenarimol by germlings of wild-type and DMI-resistant isolates ofPenicillium italicum was studied at various pH values. At pH 7 and 8 the low-resistant isolate E300–3 accumulated 22% and 35%, respectively, less imazalil than the wild-type isolate W5. Imazalil accumulation at pH 5 and 6 was similar. Isolate E300–3 also accumulated less fenarimol as compared with the wild-type isolate. This difference was much more obvious than for imazalil and was observed at all pH values tested. Differences in accumulation of both imazalil and fenarimol between low (E300–3), medium (H17) and high resistant (I33) isolates were not observed. These results suggest that decreased accumulation of DMIs is responsible for a low level of resistance only and that additional mechanisms of resistance might operate in isolates with a medium and high degree of resistance. With all isolates fenarimol accumulation was energy-dependent. This was not obvious for imazalil.The wild-type and DMI-resistant isolates had a similar plasma membrane potential as determined with the probe [14C]tetraphenylphosphonium bromide ([14C]TPP+). Various test compounds, among which ATPase inhibitors, ionophoric antibiotics and calmodulin antagonists, affected the accumulation of [14C]TPP+, [14C]imazalil and [14C]fenarimol. No obvious correlation between the effects of the test compounds on accumulation levels of the fungicides and [14C]TPP+ could be observed. These results indicate that the plasma membrane potential does not mediate the efflux of DMI fungicides byP. italicum.  相似文献   

17.
Growth of Penicillium digitatum was inhibited after a 40-min incubation in a culture medium containing 0.5 mM sec-butylamine, and the dry weight of the hyphae was 50% of the control value after 180 min. Respiration of the hyphae was reduced 13% after a 20-min contact with 0.5 mM sec-butylamine but this treatment did not influence the uptake of amino acids, glucose, or phosphate nor intensify the efflux of 33P- or 14C-labeled metabolites from the cells. The syntheses of cell walls and total lipids were inhibited 20–30% after a 90-min incubation with sec-butylamine, and nucleic acid synthesis was reduced to about 50% of the control value at this time. sec-Butylamine inhibited the incorporation of labeled carbon from [14C]glucose into the protein fraction of the hyphae to a greater degree than 14C derived from labeled proline, lysine, or leucine. These observations suggested that sec-butylamine interfered primarily with the intermediary metabolism of glucose rather than inhibiting a later stage of macromolecule synthesis. Hyphae incubated with [14C]glucose and sec-butylamine accumulated pyruvic acid to a level seven times greater than in control hyphae. Furthermore, sec-butylamine strongly inhibited 14CO2 evolution from hyphae metabolizing [14C]pyruvate whereas CO2 derived from acetate or glucose after a 45-min incubation was only slightly reduced by sec-butylamine. These observations implicate pyruvate oxidation as the primary site of sec-butylamine action in young hyphae of P. digitatum.  相似文献   

18.
The physiological mechanisms of resistance to carbaryl were investigated in a carbaryl-resistant strain of the fall armyworm, Spodoptera frugiperda (J. E. Smith). Piperonyl butoxide greatly reduced the resistance level from 90- to 6-fold, indicating that microsomal cytochrome P-450-dependent monooxygenases may play a major role in resistance. This finding is consistent with metabolic data in which the oxidative metabolism of carbaryl by midgut homogenates was five times more active in the resistant strain than in the susceptible strain. In addition, the resistant strain showed increased activities of microsomal hydroxylation and epoxidation compared to the susceptible strain. Cuticular penetration studies using [14C]carbaryl revealed that 55% of the applied radioactivity remained on the cuticle of resistant larvae while 32% remained on susceptible larvae 24 hr after topical treatment. The resistance appeared to be unrelated to target site insensitivity. It is concluded that the high level of resistance to carbaryl in this insect was mainly due to enhanced oxidative metabolism of the insecticide (via hydroxylation and epoxidation) with reduced cuticular penetration playing a very minor role, if any.  相似文献   

19.
Ethirimol, a hydroxypyrimidine fungicide active against powdery mildews only, inhibited the formation of appressoria during primary infection of barley powdery mildew, Erysiphe graminis f.sp hordei. It also affected other stages of mildew development. Several adenine analogs had similar effects and ethirimol-resistant mildew strains were generally cross-resistant to these. Adenine and adenosine reduced the fungitoxicity of ethirimol. During the formation of appressoria [3H]adenine was incorporated into RNA but [14C]glycine was not, suggesting that purine biosynthesis did not occur. Ethirimol inhibited this RNA synthesis and it is concluded that the fungicide may interfere with adenine metabolism at some site subsequent to its synthesis.  相似文献   

20.
An ergosterol-deficient mutant of Ustilago maydis was compared to the wild type in regard to morphology, growth rate, lipid content, and sensitivity to ergosterol biosynthetic inhibitors. Morphology of mutant sporidia is abnormal and resembles that of fenarimol-treated wild-type sporidia. Doubling time of mutant sporidia is 6.3 hr compared to 2.5 hr for the wild type. The mutant produces 24-methylenedihydrolanosterol, obtusifoliol, and 14α-methylfecosterol; ergosterol is absent. The sterols of the mutant are the same as those which accumulate in wild-type sporidia treated with the sterol C-14 demethylation inhibitors fenarimol, etaconazole, and miconazole. The level of free fatty acids is higher in the mutant than in wild-type cells. Growth of mutant sporidia is not inhibited by fenarimol, etaconazole, and miconazole, or by the sterol Δ14-reductase inhibitor azasterol A25822B at low concentrations which inhibit growth of wild-type sporidia. The residual growth rate of wild-type sporidia treated with low concentrations of the sterol C-14 demethylation inhibitors is about the same as that of untreated mutant sporidia. Therefore, the mutant would not be recognized as resistant in a wild-type population. The mutant is deficient in sterol C-14 demethylation and is similar in all properties studied to wild-type sporidia treated with sterol C-14 demethylation inhibitors. These findings support the contention that inhibition of sterol C-14 demethylation in U. maydis is the primary mode of toxicity of fenarimol, etaconazole, and miconazole. A secondary mode of toxicity is evident for miconazole and etaconazole at higher concentrations but is doubtful for fenarimol.  相似文献   

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