Microbial recolonization and suppression of Rhizoctonia solani in a bedding-plant potting mix amended with recycled mix before aerated-steam treatment

Summary Some South Australian bedding-plant nurseries add recycled potting mix to fresh potting mix before aerated-steam treatment in an attempt to decrease fungal root diseases. To test the hypothesis that this addition of recycled potting mix affects microbial colonization and, consequently, the disease-suppressiveness of mixes treated with aerated steam, recycled potting mix was added to or withheld from fresh potting mix. The mixes were then treated with aerated steam at 60°C for 35 min or not treated. Their recolonization by actinomycetes, heat-resistant organisms, pseudomonads, and fungi was followed for 25 days. The addition of recycled potting mix frequently increased the numbers of actinomycetes and heat-resistant microbes recovered from the mixes, whether treated with steam or not, but decreased the numbers of aerobic bacteria. Fungal populations were rarely influenced by the addition of recycled potting mix. Pseudomonad populations dropped to undetectable levels after the aerated-steam treatment and failed to reach levels comparable to those in treatments without steam during the next 25 days. Organisms from each group were tested for in vitro antagonism to Rhizoctonia solani Kühn (AG-8). The proportion of inhibitory organisms varied with the microbial group, the mix treatment, and the time since mix treatment. Where aerated-steam treatment was applied, the addition of recycled potting mix rarely affected the development of Rhizoctonia disease symptoms on seedlings of Celosia argentea. The potential for improving the suppressiveness of aerated-steam-treated nursery mixes via microbial inoculation is discussed.     

Systemic Resistance Induced in Cucumber Against Pythium Root Rot by Source Separated Household Waste And Yard Trimmings Composts

Disease control with compost often is attributed to four factors including competition, antibiosis, parasitism and induced systemic resistance (ISR). Induction of systemic resistance by source separated household waste and yard trimmings compost against Pythium root rot of cucumber caused by Pythium ultimum was studied in a split-root bioassay. Split-root pairings were tested in root rot potting soil paired with potting soil, compost-amended potting soil suppressive to root rot paired with the potting soil, and compost-amended potting soil paired with the compost-amended potting soil. Only one side of the split roots was infested with P. ultimum. Root rot, based on dry and fresh root weights, was significantly reduced in split roots of plants produced in the conducive infested potting soil paired with the suppressive yard trimmings compost-amended mix. This suggested that systemic effects were induced in the roots by the suppressive compost against Pythium root rot. Growth of transplants germinated in the source separated household waste compost mix was significantly better than those germinated in the potting soil. Finally, root rot of plants germinated in the suppressive mix and then transplanted into the conducive mix was also significantly less severe than that of plants germinated in the conducive mix.     

Using the spermosphere model technique to describe the dominant nitrogen-fixing microflora associated with wetland rice in two Egyptian soils

Summary This study is an attempt to describe the dominant N₂-fixing microflora associated with the roots of wetland rice. Rice cultivar Giza 171 was grown in a phytotron on two alluvial Egyptian soils for 8 days, a stage when the nitrogenase activity of undisturbed plants reached a level of 245 × 10^–6 mol C₂H₄ h^–1 g^–1 dry weight of leaf. The roots and rhizosphere soils were then used for counting and isolating dominant diazotrophs. Counts and initial enrichment steps were carried out on a selective medium made of an axenic rice plantlet, the spermosphere model, incubated under 1 % acetylene. The counts were very high, exceeding 10⁸ bacteria g^–1 dry weight of rhizosphere soil. Enterobacteriaceae were dominant; most isolates were Enterobacter cloacae belonging to different biotypes in the two soils. Enterobacter agglomerans, Citrobacter freundii and Klebsiella planticola were also present as members of the dominant microflora. Azospirillum brasilense and Azospirillum lipoferum were present as well, but less abundant.     

Microbial enrichment to enhance the disease suppressive activity of compost

Compost amended soil has been found to be suppressive against plant diseases in various cropping systems. The level and reproducibility of disease suppressive properties of compost might be increased by the addition of antagonists. In the present study, the establishment and suppressive activity of two fungal antagonists of soil-borne diseases was evaluated after their inoculation in potting soil and in compost produced from different types of organic waste and at different maturation stages. The fungal antagonists Verticillium biguttatum, a mycoparasite of Rhizoctonia solani, and a non-pathogenic isolate of Fusarium oxysporum antagonistic to fusarium wilt, survived at high levels (10³–10⁵ CFU g^–1) after 3 months incubation at room temperature in green waste compost and in potting soil. Their populations faded out in the organic household waste compost, especially in the matured product. In bioassays with R. solani on sugar beet and potato, the disease suppressiveness of compost increased or was similar after enrichment with V. biguttatum. The largest effects, however, were present in potting soil, which was very conducive for the disease as well as the antagonist. Similar results were found in the bioassay with F. oxysporum in carnation where enrichment with the antagonistic F. oxysporum had a positive or neutral effect. We foresee great potential for the application of antagonists in agriculture and horticulture through enrichment of compost or potting soil with antagonists or other beneficial micro-organisms.     

Nematofauna associated with exotic and native leguminous plant species in West Africa: effect of<Emphasis Type="Italic"> Glomus intraradices</Emphasis> arbuscular mycorrhizal symbiosis

Ten leguminous trees, four exotic species (Australian Acacia) and six indigenous species (three Sahelian Acacia spp. and three Sesbania spp.), were grown for 4 months in a natural Sahelian soil inoculated with or without the endomycorrhizal fungus, Glomus intraradices. In control trials, the determinant factor structuring the soil nematode fauna was the plant species, related plants having a similar influence on the nematode community in the soil. Soil nematode abundance increased from exotic acacias (3.3 g^-1 dry soil) to native acacias (11.5 g^-1 dry soil) and Sesbania species (17.6 g^-1 dry soil). Plant feeding nematodes (mainly Scutellonema and Tylenchorhynchus) were significantly less abundant under exotic acacias (1.4 g^-1 dry soil) than under native acacias (7.2 g^-1 dry soil) or Sesbania species (7.3 g^-1 dry soil). Bacterial feeding nematode density increased from exotic acacias (1.2 g^-1 dry soil) to native acacias (3.0 g^-1 dry soil) and Sesbania species (7.7 g^-1 dry soil) as total densities. However, the differences in the structure of the nematode communities between plant groups were suppressed in the presence of the mycorrhizal fungus. In fact, no difference in nematode densities remained between plant groups when G. intraradices developed in several dominant taxa belonging to different trophic groups, particularly: Tylenchorhynchus, Apelenchina, Cephalobus and Dorylaimoidea. This study clearly indicated that inoculation with the arbuscular mycorrhizal fungus G. intraradices diminished the plant-specific effect on the structure of the soil nematode community.     

Effect of passage through the intestinal tract of detritivore earthworms (Lumbricus spp.) on the number of selected Gram-negative and total bacteria

Laboratory experiments were carried out to investigate the fate of bacteria during and after passage through the intestinal tract of detritivore earthworms. Earthworms (Lumbricus spp.) were fed with cattle dung inoculated 7 days previously with one of five different Gram-negative bacteria. Bacterial concentrations were determined 2 days later in dung and soil, and in gut material from different parts of the earthworm intestinal tract. A high percentage (28–82%) of the total bacteria (epifluorescence direct counts) in the earthworm gut content was culturable. The concentration of total heterotrophic aerobic bacteria did not vary significantly among the five different bacterial additions and the non-inoculated control. In earthworm casts the number of total heterotrophs per gram dry matter (2.1×10⁹) was higher than in soil (1.7×10⁸), but lower than in the dung (1.5×10¹⁰). The test-bacteria, however, showed different survival patterns along the earthworm intestinal tract. The concentrations of Escherichia coli BJ 18 and Pseudomonas putida MM 1 and MM 11 in earthworm casts were lower than in the ingested dung, while concentrations of Enterobacter cloacae A 107 and Aeromonas hydrophila DMU 115 in dung and casts were similar. Ent. cloacae, and to aminor extent E. coli, were reduced in numbers by several orders of magnitude in the pharynx and/or crop. In the hind gut, however, the concentration of Ent. cloacae had increased to the same level as in the ingested dung, while the concentration of E. coli remained low. Our observations indicate that the bacterial flora of ingested food materials changes qualitatively and quantitatively during gut transit.     

Impact of heavy metal amended sewage sludge on forest soils as assessed by bacterial and fungal biosensors

Bacterial and fungal bioluminescence-based biosensors were used as indicators of potential heavy metal toxicity to microorganisms in the needle litter of a mature Pinus radiata forest under heavy metal contaminated sewage sludge. Sewage sludge was amended with increasing concentrations of Cu, Ni and Zn and applied to the surface of a mature P. radiata forest. The response of the bacterial and fungal biosensors to soluble Cu, Ni and Zn in needle litter extracts was investigated. The bioluminescence response of the bacterial biosensor Escherichia coli HB101 pUCD607 declined as water-soluble Zn concentrations increased. The effective concentrations that gave a 50% reduction in bioluminescence (EC₅₀ values) for water-soluble Zn and total litter Zn were 1.3 mg l⁻¹ and 3700 mg kg⁻¹, respectively. The bioluminescence response of the fungal biosensor Armillaria mellea declined as soluble Cu concentrations increased. The EC₅₀ values for water-soluble Cu and total litter Cu were 0.12 mg l⁻¹ and 540 mg kg⁻¹, respectively. No decline in bioluminescence was noted for either the bacterial or fungal biosensor on exposure to increasing concentrations of water-soluble Ni. The use of a combination of bacterial and fungal biosensors offers a rapid and sensitive tool for assessing toxicity of heavy metals to microorganisms and, thus, elucidating the environmental impact of contaminants in sewage sludge on litter dwelling microorganisms.     

Identification of ergosterol in vesicular-arbuscular mycorrhizae

Summary Ergosta-5,7,22-tri-3-enol (ergosterol) was identified by gas chromatography-mass spectrometry in roots of berseem (Trifolium alexandrinum L., cv. Landsorte) and sweet corn (Zea mays L., cv. Honeycomb-F1) infected with the vesicular-arbuscular mycorrhizal (VAM) fungus Glomus intraradices. The fungal-derived compound ergosterol was determined quantitatively in root extracts using reverse-phase high performance liquid chromatography. The concentrations of ergosterol in VAM-infected roots reached 72 g^-1 dry material in berseem and 52 g^-1 in sweet corn after 80 days of growth, whereas concentrations in non-infected roots remained below 8 g^-1 dry weight. Additionally, phytosterols such as -sitosterol, campesterol, and stigmasterol were detected in both infected and non-infected roots. Ergosterol, as a characteristic fungal substance, is proposed as an indicator of fungal biomass in the early stages of VAM infection.     

Displacement of native rhizobia nodulating chickpea (Cicer arietinum L.) by an inoculant strain through soil solarization

Summary Soil solarization greatly reduced the native chickpea Rhizobium population. With inoculation, it was possible to increase the population of the Rhizobium in solarized plots. In the 1st year, 47% nodulation was obtained with chickpea inoculant strain IC 59 when introduced with a cereal crop 2 weeks after the soil solarization and having a native Rhizobium count of <10 g^-1 soil, and only 13% when introduced 16 weeks after solarization at the time the chickpeas were sown, with 2.0×10² native rhizobia g^-1 soil. In the non-solarized plots inoculated with 5.6×10³ native rhizobia g^-1 soil, only 6% nodulation was obtained with the inoculant. In the succeeding year, non-inoculated chickpea was grown on the same plots without any solarization or Rhizobium inoculation. The treatment that showed good establishment of the inoculant strain in year 1 formed 68% inoculant nodules. Other treatments indicated a further reduction in inoculant success, from 1%–13% to 1%–9%. Soil solarization thus allowed an inoculant strain to successfully displace the high native population in the field and can serve as a research tool to compare strains in the field, irrespective of competitive ability. In year 1, Rhizobium inoculation of chickpea gave increased nodulation and increased plant growth 20 and 51 days after sowing, and increased dry matter, grain yield, and grain protein yield at maturity. These beneficial effects of inoculation on plant growth and yield were not measured in the 2nd year.Submitted as Journal Article No. JA 945 by the International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru, Andhra Pradesh 502 324, India     

Competition between inoculated and indigenous Rhizobium/Bradyrhizobium spp. strains for nodulation of grain and fodder legumes in Pakistan

Summary The competitive ability of inoculated and indigenous Rhizobium/Bradyrhizobium spp. to nodulate and fix N₂ in grain legumes (Glycine max, Vigna unguiculata, Phaseolus vulgaris) and fodder legumes (Vicia sativa, Medicago sativa, and Trifolium subterraneum) was studied in pots with two local soils collected from two different fields on the basis of cropping history. The native population was estimated by a most-probable-number plant infectivity test in growth pouches and culture tubes. The indigenous rhizobial/bradyrhizobial population ranged from 3 to 2×10⁴ and 0 to 4.4×10³ cells g^-1 in the two soils (the first with, the second without a history of legume cropping). Inoculated G. max, P. vulgaris, and T. subterraneum plants had significantly more nodules with a greater nodule mass than uninoculated plants, but N₂ fixation was increased only in G. max and P. vulgaris. A significant response to inoculation was observed in the grain legume P. vulgaris in the soil not previously used to grow legumes, even in the presence of higher indigenous population (>10³ cells g^-1 soil of Rhizobium leguminosarum bv phaseoli). No difference in yield was observed with the fodder legumes in response to inoculation, even with the indigenous Rhizobium sp. as low as <14 cells g^-1 soil and although the number and weight of nodules were significantly increased by the inoculation in T. subterraneum. Overall recovery of the inoculated strains was 38–100%, as determined by a fluorescent antibody technique. In general, the inoculation increased N₂ fixation only in 3 out of 12 legume species-soil combinations in the presence of an indigenous population of rhizobial/bradyrhizobial strains.     

瓦克青霉F10-2对川楝树皮残渣纤维素酶解研究

以川楝树皮残渣为原料进行纤维素酶解研究,测定了不同培养时间培养基质中主要胞外酶活性的变化,并对发酵前后残渣结构进行扫描电镜观察和红外光谱分析。结果表明:瓦克青霉F10-2具有木质纤维素降解能力,酶解液中纤维素酶、半纤维素酶、木质素过氧化物酶和锰过氧化物酶活性在发酵的8～16d内分别达到最大值6.42U·g-1、7.62U·g-1、6.55U·g-1和3.33U·g-1。利用扫描电镜对降解后底物表面结构进行观察,可看到残渣表面变得疏松、柔软,且具有部分微孔。底物残渣傅立叶红外光谱分析表明,该菌株对残渣中各组分均有一定降解。固态发酵培养试验表明,培养24d后残渣中纤维素、半纤维素和木质素的降解率分别达到42.70%、33.96%和24.62%。     

Pre-inoculation with arbuscular mycorrhizal fungi suppresses root knot nematode (<Emphasis Type="Italic">Meloidogyne incognita</Emphasis>) on cucumber (<Emphasis Type="Italic">Cucumis sativus</Emphasis>)

A pot experiment was conducted to evaluate the influence of pre-inoculation of cucumber plants with each of the three arbuscular mycorrhizal (AM) fungi Glomus intraradices, Glomus mosseae, and Glomus versiforme on reproduction of the root knot nematode Meloidogyne incognita. All three AM fungi tested significantly reduced the root galling index, which is the percentage of total roots forming galls. Numbers of galls per root system were significantly reduced only in the G. intraradices + M. incognita treatment. The number of eggs per root system was significantly decreased by AM fungus inoculation, no significant difference among the three AM fungal isolates. AM inoculation substantially decreased the number of females, the number of eggs g⁻¹ root and of the number of eggs per egg mass. The number of egg masses g⁻¹ root was greatly reduced by inoculation with G. mosseae or G. versiforme. By considering plant growth, nutrient uptake, and the suppression of M. incognita together, G. mosseae and G. versiforme were more effective than G. intraradices.     

Gut load and food-retention time in the earthworms Lumbricus festivus and L. castaneus: A field study

Summary Lumbricus festivus and L. castaneus consume dung. In the field, below cow pats, their gut loads were about 0.15 and 0.14 g dry weight g^-1 ash-free dry weight of worm, respectively, but in free soil the loads were higher, about 0.21 and 0.19 g g^-1 ash-free dry weight of worm. The gut contents of dung were lighter than the total ingested material, at about 0.10 and 0.07 g dry weight g^-1 ash-free dry weight of worm, respectively. Field experiments showed that the retention time of dung ranged from >9 to 15 h for L. festivus, and from >3 to 6 h for L. castaneus. The experiments also indicated that L. festivus exploited 20- and 36-day-old dung in different ways, since the gut load was lower in those worms consuming 20-day-old dung than in those consuming 36- to 40-day-old dung. On the basis of these results the calculated consumption rate for L. festivus is 0.08 g dung day^-1 g live weight of worm^-1, and for L. castaneus 0.15 g dung day^-1, with retention times assumed to be at maximum, 15 h, for L. festivus and 6 h for L. castaneus. These calculations indicate that our field population of worms (75 g m^-2) consumes 10–15 t dung ha^-1 180 days^-1, corresponding to the amount of dung produced by 2–3 dairy cows.     

Population densities of clover rhizobia in Texas pastures and response to liming

Summary Clovers are widely used forage legumes on acidic soils in Texas and need inoculation with appropriate rhizobia when first introduced. Acidic soils are not conducive to survival of clover rhizobia. A survey of pastures was undertaken to determine the number of rhizobia present. The effect of liming acidic soils on the survival of clover rhizobia was also evaluated in the laboratory. The number of clover rhizobia was more than 100 cells g^-1 soil in 70% of the pastures surveyed but populations within pastures varied by more than two orders of magnitude. The number of years of clover production beyond 1 year did not affect the rhizobial population density. The soil pH of twelve samples was below 5.0 and six samples had populations of rhizobial lower than 100 g^-1 soil. Eleven out of sixteen samples from fields that had grown clover and had pH values above 6.0 had populations exceeding 1000 g^-1 soil and only three samples had populations lower than 100 g^-1 soil. Incubating indigenous or inoculated rhizobia in well-mixed soils having pH values of 5.1 or below resulted in populations declining to below 10 g^-1 soil in 6 weeks. Mixing of soils with pH values of up to 5.4 induced reduction of rhizobial numbers, possibly by destroying microsites. Liming of soils to increase pH values above 5.5 improved survival of native or inoculated rhizobia in most cases.     

Response of A-genome cotton germplasm to the seedling disease pathogens,Rhizoctonia solani and Pythium ultimum

Summary Approximately two hundred A-genome cotton (Gossypium arboreum L. and G. herbaceum L.) accessions were evaluated for resistance to the seedling disease pathogens Rhizoctonia solani Kühn [Thanatephorus cucumeris (A. B. Frank) Donk], and Pythium ultimum Trow. Susceptibility rating was based on a scale of 1 to 6 where 1 = no symptoms and 6 = dead. Variation was found among A-genome accessions in response to R. solani and P. ultimum, but none were highly resistant to these pathogens. As a group, the A-genome cottons were more susceptible to the pathogens than the G. hirsutum control.Abbreviations STV-A G. hirsutum Stoneville 506 with agar only - STV-NP G. hirsutum Stoneville 506 with non-pathogenic isolate - STV-P G. hirsutum Stoneville 506 with pathogenic isolate - A₁ G. herbaceum - A₂ G. arboreum - GRIN Genetic Resources Information Network     

Wood-ash fertilization and fire treatments in a Scots pine forest stand: Effects on the organic layer,microbial biomass,and microbial activity

We studied the reactions of humus layer (F/H) microbial respiratory activity, microbial biomass C, and the fungal biomass, measured as the soil ergosterol content, to the application of three levels of wood ash (1000, 2500, and 5000 kg ha^-1) and to fire treatment in a Scots pine (Pinus sylvestris L.) stand. Physicochemical measurements (pH, organic matter content, extractable and total C content, NH ₄ ⁺ and total N content, cation-exchange capacity, base saturation) showed similarity between the fire-treated plots and those treated with the lowest dose of wood ash (1000 kg ha^-1). The ash application did not change the level of microbial biomass C or fungal ergosterol when compared to the control, being around 7500 and 350 g g^-1 organic matter for the biomass C and ergosterol, respectively. The fire treatment lowered the values of both biomass measurements to about half that of the control values. The fire treatment caused a sevenfold fall in the respiration rate of fieldmoist soil to 1.8 l h^-1 g^-1 organic matter compared to the values of the control or ash treatments. However, in the same soils adjusted to a water-holding capacity of 60%, the differences between the fire treatment and the control were diminished, and the ash-fertilized plots were characterized by a higher respiration rate compared to the control plots. The glucose-induced respiration reacted in the same way as the water-adjusted soil respiration. The metabolic quotient, qCO₂, gradually increased from the control level with increasing applications of ash, reaching a maximum in the fire treatment. Nitrification was not observed in the treatment plots.     

Influence of arbuscular mycorrhizal fungi and salinity on growth,biomass, and mineral nutrition of<Emphasis Type="Italic"> Acacia auriculiformis</Emphasis>

The effect of salinity on the efficacy of two arbuscular mycorrhizal fungi, Glomus fasciculatum and G. macrocarpum, alone and in combination was investigated on growth, development and nutrition of Acacia auriculiformis. Plants were grown under different salinity levels imposed by 0.3, 0.5 and 1.0 S m^-1 solutions of 1 M NaCl. Both mycorrhizal fungi protected the host plant against the detrimental effect of salinity. The extent of AM response on growth as well as root colonization varied with fungal species, and with the level of salinity. Maximum root colonization and spore production was observed with combined inoculation, which resulted in greater plant growth at all salinity levels. AM fungal inoculated plants showed significantly higher root and shoot weights. Greater nutrient acquisition, changes in root morphology, and electrical conductivity of soil in response to AM colonization was observed, and may be possible mechanisms to protect plants from salt stress.     

Influence of the earthworm Aporrectodea trapezoides (Lumbricidae) on the colonization of alfalfa (Medicago sativa L.) roots by Rhizobium meliloti L5-30R and the survival of R. meliloti L5-30R in soil

A greenhouse study was performed to examine the ability of the earthworms Microscolex dubius and Aporrectodea trapezoides to transport Rhizobium meliloti L5-30R through soil. When R. meliloti L5-30R was inoculated into either ezi-mulch (a pelleted formulation of cereal-pea straw), oat hay, pea hay, or sheep dung and placed on the soil surface together with either A. trapezoides or M. dubius, >10⁴ colony-forming units (CFU) of R. meliloti L5-30R g^-1 soil were detected at 90 mm soil depth after 18 days. In the absence of earthworms, R. meliloti L5-30R was not detected at 90 mm soil depth after this time. In a second experiment using ezi-mulch as the inoculant material and in the presence of A. trapezoides (in a number equivalent to 471 or 785 m^-2), ca. 10³ CFU of R. meliloti L5-30R per 10 mm of alfalfa root were detected at 0–30, 30–60, and 60–90 mm soil depth after 18 days, while <3 CFU were detected per 10 mm of root in the absence of A. trapezoides. In a third experiment in which R. meliloti L5-30R was distributed evenly through soil at the start of the experiment, A. trapezoides (in a number equivalent to 157, 471, or 785 m^-2) significantly decreased the survival of L5-30R in soil after 40 days of incubation at 15°C, but not after 20 days. The decrease in survival of R. meliloti L5-30R was correlated with the density of A. trapezoides. These results demonstrate that A. trapezoides can increase root colonization of alfalfa by R. meliloti L5-30R, but may also reduce the ability of R. meliloti L5-30R to survive in soil.     

西花蓟马生长发育及其与寄主花化学物质的关系

为明确寄主对西花蓟马(Frankliniella occidentalis)生长发育的影响,采用非自由选择法,研究了西花蓟马在月季、康乃馨、百合、天竺葵及牵牛等5种植物花上的生长发育及存活差异,及其与寄主营养物质(可溶性蛋白质、糖)、次生物质(单宁酸、黄酮和总酚)含量的相关性。结果表明,西花蓟马在5种植物的花上不同阶段的生长发育及存活都有不同程度的显著性差异。总体来说,西花蓟马在月季花上发育最快(整个未成熟期为11.02 d),牵牛花上发育最慢(整个未成熟期为13.21 d);世代存活率在百合花上最高(84%),天竺葵上最低(76%);寄主的营养物质、次生物质含量也存在显著性差异。相关分析表明,西花蓟马的发育速率与寄主的可溶性蛋白质含量存在显著正相关关系(R=0.896,P=0.040),与单宁酸(R=-0.917,P=0.01)、黄酮(R=-0.921,P=0.014)及总酚含量(R=-0.905,P=0.013)存在显著的负相关关系,与可溶性含糖量无显著相关关系(R=0.40,P=0.505);西花蓟马的存活率与寄主的各类化学物质均无显著相关关系。因此,寄主花的蛋白质含量越高,对西花蓟马的生长发育越有利,而单宁酸、黄酮及总酚含量越高,则不利于其生长发育。     

Earthworms of different functional groups affect the fate of the Bt-toxin Cry1Ab from transgenic maize in soil

The fate of the insecticidal Cry1Ab protein from crop residues (leaves and roots) of the transgenic maize variety MON810 was studied in the presence and absence of two earthworm species (Lumbricus terrestris, Aporrectodea caliginosa; separate incubations) in soil microcosms. The recombinant Cry1Ab protein was quantified using a highly sensitive ELISA. Control microcosms received corresponding non-transgenic plant material. All earthworms survived in the microcosms over a period of 5 weeks, irrespective of whether they received MON810 or non-transgenic plant material. Weight loss was observed for both earthworm species, independent of the plant material or transgenic modification. A strong decline of immunoreactive Cry1Ab in plant residues (mean initial concentration approx. 5000 ng g⁻¹) of MON810 was observed in all treatments, but in microcosms with earthworms this decline was significantly higher with less than 10% of the initial Cry1Ab concentration remaining after 5 weeks. Cry1Ab concentrations in casts were only 0.1% of those found in remaining plant material of the respective microcosms. No immunoreactive Cry1Ab proteins were found in earthworm tissues (threshold of detection: 0.58 ng g⁻¹ fresh weight). No further decline was found for Cry1Ab concentrations in casts of A. caliginosa during a subsequent period of 3 months of incubation in bulk soil (<0.1 ng g⁻¹) after removal of the earthworms from the microcosms, while in casts of L. terrestris the concentration decreased from 0.4 to below 0.1 ng g⁻¹. In conclusion, this study demonstrates that earthworms enhance the decline of immunoreactive Cry1Ab proteins from maize residues.