一株合欢枯萎病拮抗菌的分离鉴定及盆栽防治试验

合欢枯萎病是导致多年生合欢衰弱和死亡的主要因素之一,目前尚无有效的防治手段。本研究通过平板对峙法和含毒培养基法分离筛选健康合欢植株根际土壤中的潜在拮抗菌,结合形态学特征和双基因系统发育分析对拮抗菌进行鉴定,并通过盆栽试验验证拮抗菌株对合欢枯萎病的防治效果。结果表明,经过初筛得到11株对合欢枯萎病具有潜在拮抗作用的菌株,其中菌株5-2的抑制作用最为显著。对峙培养6d,菌株5-2对尖孢镰刀菌Fusariumoxysporum和腐皮镰刀菌Fusariumsolani的抑制率分别为76.88%和84.08%,两种病原菌在含6.67%拮抗菌孢悬液(孢子浓度1.0×10⁷个/mL)的平板上生长均受到显著抑制。显微观察发现菌株5-2可缠绕病原菌菌丝体并寄生生长,盆栽试验表明菌株5-2对尖孢镰刀菌和腐皮镰刀菌具有优良的拮抗作用,防治效果达78.26%和57.89%。通过形态学和ITS-TEF1双基因系统发育分析,菌株5-2鉴定为康宁木霉Trichodermakoningii。综上所述,菌株5-2对合欢枯萎病具有良好的防治效果,可作为合欢枯萎病生防菌剂的候选菌株资源。     

烟草尖孢镰刀菌拮抗真菌的筛选鉴定及促生作用研究

为获得烟草镰刀菌根腐病拮抗真菌菌株,试验以河南省豫中烟区烟草根际土壤为试材,以主要致病菌尖孢镰刀菌Fusarium oxysporum为主要靶标,采用稀释涂布平板法分离获得土壤真菌371株,平板对峙培养法测定获得1株具有明显抑制效果的拮抗菌株,利用形态学和分子生物学的方法将其鉴定为棘孢木霉Trichoderma asperellum Tr-0111。抑制效果测定表明,该菌株对尖孢镰刀菌的抑制率最高可达93.13%,对根串珠霉菌、拟茎点霉、链格孢菌等其他8种烟草病原菌均具有较强的抑制效果。促生作用测定结果表明,菌株发酵液使烟草种子萌发率提高5.34%,烟苗根长增长率为62.39%,对盆栽烟草的最大叶面积和地上部鲜重也具有显著的促生效果。为进一步相关机理的研究和生防菌剂的研制奠定了基础。     

拮抗尖孢镰刀茵的木霉菌筛选方法评估

利用11株不同木霉菌株分别比较对峙培养法、病原菌存活率测定法、生防菌分泌物降解病原菌测定法、浸种抑菌萌发试验法及种苗接种活体筛选法对抑制黄瓜枯萎病尖孢镰刀菌Fusariumoxysporum的拮抗木霉菌的筛选效率。试验表明不同的筛选方法获得拮抗木霉菌菌株的结果差异较大,其中病原菌存活率测定法与种苗活体接种筛选法结果一致性较高,可推荐作为生防木霉菌株初筛的有效方法。     

土壤环境条件对威百亩熏蒸防治黄瓜枯萎病的影响

为探究威百亩在不同土壤环境条件下的消毒效果,采用离体和活体方法研究施药量、覆膜熏蒸时间、土壤相对含水量及土壤温度对威百亩熏蒸防治黄瓜枯萎病的作用效果。结果表明,25℃条件下,威百亩12 mg(a.i.)/kg土壤熏蒸消毒,对尖孢镰刀菌Fusarium oxysporum的抑制率为78.82%,对黄瓜枯萎病的防治效果为87.03%,且对作物安全无药害;威百亩对尖孢镰刀菌的熏蒸抑制作用随着熏蒸时间的增加而增强,土壤熏蒸10 d后对尖孢镰刀菌的抑制率为95.21%;土壤相对含水量为30%和50%时,威百亩对黄瓜枯萎病的防治效果分别为72.32%和82.14%,含水量过高或过低均不利于药效的发挥,而且还会对作物产生药害反应。威百亩的熏蒸效果随着土壤温度的升高而增强,在25、30、35℃时对黄瓜枯萎病的防治效果分别为80.18%、98.20%和100.00%。表明威百亩结合日光消毒温度大于25℃、土壤相对含水量为30%或50%、熏蒸10~15 d可有效控制土壤中尖孢镰刀菌引起的黄瓜枯萎病。     

具防病并提高植物耐旱功能的小链霉菌HS57的筛选

本研究旨在寻找防治黄瓜枯萎病并提高植物抗逆能力的多功能菌株。从连作田健康黄瓜根际土中分离筛选到1株放线菌HS57。平板对峙法测定菌株HS57对尖孢镰刀菌、茄病镰刀菌和立枯丝核菌的抑制作用,平皿对扣共培养法测定其挥发性物质对尖孢镰刀菌的抑制作用,温室盆栽法测定其对黄瓜枯萎病的防病效果及对小麦耐旱能力的影响,结合菌株形态特征和16S rRNA基因序列分析对其进行鉴定。结果表明,菌株HS57可抑制3种病原菌生长,其中对尖孢镰刀菌的抑制率为52.4%;其挥发性物质对尖孢镰刀菌的抑制率为32.1%。浓度为10⁷个/mL的HS57孢子悬浮液浸种对黄瓜枯萎病的防效最好,为51.0%;小麦种子经浓度为10⁷、10⁸个/mL的HS57孢子悬浮液浸种,麦苗经连续7 d缺水处理后再浇水,比对照恢复得更好。初步鉴定HS57菌株为小链霉菌Streptomyces parvus,是一株非常有潜力的多功能菌株。     

稻曲病菌拮抗菌的筛选及拮抗活性测定

从对稻曲病菌具有拮抗能力的18株芽孢杆菌中选出拮抗作用较强的2个菌株A1、H-51,分别对稻曲病菌进行抑菌率、致畸性、孢子萌发影响以及对水稻促生性试验。结果表明,拮抗菌2个菌株的发酵液对稻曲病菌最大抑制率分别为67.66％和62.87％,对病菌分生孢子的萌发抑制率分别为77.37％和59.74％,但对水稻促生作用不明显。     

三株拮抗细菌的鉴定及抑菌作用研究

为了充分发掘和利用有益微生物资源,本文以草莓根腐尖孢镰刀菌Fusariumoxysporum为靶标菌,从草莓根际土壤中分离筛选得到3株拮抗细菌,通过培养性状与形态特征、生理生化特征以及16SrDNA同源序列比对分析进行了鉴定,菌株1-9和9—4为多粘类芽孢杆菌Paenibacilluspolymyxa、菌株12—4为枯草芽孢杆菌Bacillussubtilis。这3株细菌对草莓根腐尖孢镰刀菌的抑菌作用进行了初步的研究,结果表明,3株拮抗细菌对草莓根腐尖孢镰刀菌的生长有很好的抑制作用,镜下观察对菌丝有致畸作用,其培养滤液还能够抑制草莓根腐病尖孢镰刀菌分生孢子的产生与萌发。     

河北廊坊大豆枯萎病病原镰刀菌的分子鉴定

 为明确河北廊坊中国农科院植保所试验基地大豆孢囊线虫病田内大豆枯萎病病原镰刀菌的种类,对362份罹病枯萎大豆植株进行病原真菌分离,得到335株真菌;使用镰刀菌通用引物鉴定出镰刀菌(Fusarium spp.) 279株,占分离菌株83.3%;镰刀菌特异性引物、测序等分子生物学技术结合形态学特征进一步鉴定镰刀菌种类,鉴定出尖孢镰刀菌(F. oxysporum)189株,占分离菌株56.4%;茄病镰刀菌(F. solani)67株占20.0%、禾谷镰刀菌(F. graminearum)16株占4.8%、木贼镰刀菌(F. equiseti)3株、层出镰刀菌(F. proliferaum)2株、燕麦镰刀菌(F. avenaceum)和厚孢镰刀菌(F. chlamydosporum)各1株;致病性测试结果表明数量最多的尖孢镰刀菌(F. oxysporum)中约92.8%菌株具有不同程度的致病力;这些结果表明该试验基地大豆枯萎病的优势病原菌为尖孢镰刀菌(F. oxysporum);研究结果可为大豆枯萎病的防治提供科学依据,并为大豆孢囊线虫与尖孢镰刀菌复合侵染大豆的研究奠定基础。     

贝莱斯芽胞杆菌ZZBV-3的鉴定及其对草莓根腐病的防效

为获得草莓根腐病原菌尖孢镰刀菌Fusarium oxysporum的优良拮抗菌,以草莓种植基地的土壤为拮抗菌来源,通过室内测定不同菌株的抑菌活性,筛选抑菌率最高的菌株,在此基础上对所筛菌株进行分类鉴定,并评价其抑菌谱和防效.结果表明,从土壤中分离获得39株拮抗菌,筛选出3株对尖孢镰刀菌具有明显抑制作用的菌株.其中,菌株...     

防风根腐病拮抗真菌的筛选鉴定及生防作用研究

从防风根际土壤中筛选得到1株对根腐病具有良好防治效果的拮抗菌株MR-47,基于形态学、ITS序列分析方法对菌株MR-47进行鉴定,确定该菌株为桃色顶孢霉Acremonium persicinum（GenBank No. OK287149.1）。通过对峙培养、显微镜观察,探究了菌株MR-47对木贼镰刀菌Fusarium equiseti的抑菌机理;基于盆栽试验,明确菌株MR-47的定殖能力及防病促生效果。结果表明,菌株MR-47对木贼镰刀菌抑菌率达69.26%,病原菌菌丝出现缢缩、膨大、扭曲、畸形等现象;对尖孢镰刀菌、腐皮镰刀菌等多种病原真菌表现出了良好的广谱抑菌活性;在土壤中定殖35 d内,最大定殖量为8.38×10⁶ CFU/g,最低为5.57×10⁶ CFU/g;MR-47对防风根腐病防效达75.05%。因此,桃色顶孢霉MR-47在防风根腐病的病害管理方面具有较好的开发价值及应用潜力。     

黄淮海夏玉米主产区穗腐病病原菌的分离鉴定

为明确我国黄淮海夏玉米主产区玉米穗腐病的病原菌种类、优势种群及虫害、年度、省份对病原菌的影响,以形态学为基础,结合分子生物学方法对2013、2015年随机采自河南、河北、山东3省的155份玉米穗腐病样品进行分离鉴定。结果表明,引起黄淮海夏玉米主产区玉米穗腐病的主要致病菌为镰孢菌Fusarium spp.,包括拟轮枝镰孢F.verticillioides、禾谷镰孢F.graminearum、层出镰孢F.proliferatum、木贼镰孢F.equiseti及藤仓镰孢F.fujikuroi,分离频率分别为49.7%、28.4%、12.3%、3.9%和1.3%;其次为木霉菌Trichoderma spp.,包括哈茨木霉T.harzianum、绿色木霉T.viride和棘孢木霉T.asperellum,分离频率分别为8.4%、3.2%和5.2%;青霉菌Penicillium spp.分离频率较低,为14.2%;曲霉菌Aspergillus spp.包括黑曲霉A.niger和黄曲霉A.flavus,分离频率分别为2.6%和1.9%。研究表明,黄淮海主产区玉米穗腐病优势病原菌为拟轮枝镰孢、禾谷镰孢和木霉菌,不同省份不同年度间病原菌种类及优势病原菌存在差异,虫害能加重玉米穗腐病的发生。     

Fusarium Redolens f.sp asparagi, Causal Agent of Asparagus Root Rot, Crown Rot and Spear Rot

Two Fusarium species, F. oxysporum f.sp. asparagi and F. proliferatum, are known to be involved in the root and crown rot complex of asparagus. We have investigated reports on the involvement of F. redolens, a third species, which until recently was considered conspecific with F. oxysporum because of morphological similarities. RFLP analysis of the rDNA internal transcribed spacer region and AFLP fingerprinting identified eight strains from asparagus unambiguously as F. redolens. Four of these were tested and found to be pathogenic to asparagus either in this study (two strains) or in a previous one in which they were classified as F. oxysporum (three strains). Disease symptoms and disease development were the same as with F. oxysporum f.sp. asparagi and F. proliferatum. Present data and literature reports identify F. redolens as a host-specific pathogen involved in root, crown and spear rot of asparagus. The pathogen is formally classified as F. redolens Wollenw. f.sp. asparagi Baayen.     

The Elegans fusaria causing wilt disease of carnation. I. Taxonomy

The distinction of the wilt disease pathogen of carnationFusarium (oxysporum var.)redolens fromF. oxysporum (var.oxysporum) is considered. Previous reports that isolates of both taxa cause indistinguishable diseases in carnation are confirmed.F. (oxysporum var.)redolens andF. oxysporum were found to form one variable complex on morphological criteria. Apparently, host specialization rather than morphological variation reflects the evolutionary relationships in theFusarium sectionElegans. The distinction ofF. redolens fromF. oxysporum does therefore not seem justified, neither at specific nor at varietal level.Samenvatting Het onderscheid tussenFusarium (oxysporum var.)redolens enF. (oxysporum var.)oxysporum als verwekkers van verwelkingsziekte bij anjer wordt ter discussie gesteld. Fytopathologisch onderzoek bevestigde vermeldingen in de literatuur dat voor anjer pathogene isolaten van beide soorten ziekten veroorzaken die niet te onderscheiden zijn; dit is ook bekend voor andere gewassen. Op morfologische gronden blekenF. (oxysporum var.)redolens enF. oxysporum één variabel complex te vormen. Kennelijk geeft de pathogene specialisatie inFusarium sectieElegans de evolutionaire verwantschappen beter weer dan de morfologische variatie. Het onderscheiden vanF. redolens naastF. oxysporum is daarom noch als soort, noch als variëteit gerechtvaardigd.     

Efficacy of bacterial antagonists and different commercial products against Fusarium wilt on rocket

Seven experimental trials were carried out to evaluate the efficacy of the bacterial strains Achromobacter xylosoxydans AM1 and Serratia sp. DM1 obtained from suppressive soils and from soilless used rockwool substrates (Pseudomonas putida FC6B, Pseudomonas sp. FC7B, Pseudomonas putida FC8B, Pseudomonas sp. FC9B and Pseudomonas sp. FC24B) against Fusarium wilt on rocket caused by Fusarium oxysporum ff. spp. raphani and conglutinans. Along with these strains, two commercial bioproducts (RootShield—Trichoderma harzianum T22; Cedomon—Pseudomonas chlororaphis MA342) were also tested. Different application strategies such as soil treatment (trials I to VI; 10⁷ and 10⁸ CFU ml⁻¹) and root dipping (trial VII; 10⁸ and 10⁹ CFU ml⁻¹) were performed in a glasshouse in order to test the efficacy of the bacterial strains against Fusarium oxysporum ff. spp. raphani and conglutinans. The lowest disease incidence (16.7%) was observed with the application of Achromobacter sp. AM1, Serratia sp. DM1 at 10⁸ CFU ml⁻¹ and Pseudomonas sp. FC9B at 10⁷ CFU ml⁻¹ against F. oxysporum f. sp. conglutinans (experiment I). Maximum plant biomass (5.0 g/plant) was registered in Serratia sp. DM1 at 10⁸ CFU ml⁻¹ treated plants in trial IV. The trials against F. oxysporum f. sp. raphani (experiment II) showed that the application of Pseudomonas sp. FC7B, P. putida FC8B at 10⁸ CFU ml⁻¹ and P. chlororaphis MA342 at 7.5 × 10⁶ CFU ml⁻¹ significantly reduced disease incidence to values ranging between 87% and 92%. The highest plant biomass was recorded with the application of Achromobacter sp. AM1 and P. putida FC6B at 10⁷ CFU ml⁻¹ (3.9 to 4.2 g) carried out 7 days before the artificial inoculation of the pathogens (trial IV). The present study showed the potential biocontrol activity of the bacterial strains Achromobacter sp. AM1, Serratia sp. DM1 and Pseudomonas sp. FC9B against F. oxysporum f. sp. conglutinans and of Pseudomonas sp. FC7B, P. putida FC8B, P. chlororaphis MA342, Achromobacter sp. AM1 and P. putida FC6B against F. oxysporum f. sp. raphani. Growth-promoting activity of biocontrol bacteria used during the trials was observed.     

Fusarium wilt on sweet basil: Cause and sources in southeastern Spain

This study concerned a new disease detected in 1997 in southeastern Spain — Fusarium wilt in basil (Ocimum basilicum L.), caused byFusarium oxysporum f.sp.basilici. Its importance was evaluated at two locations in the Almería area, where 14% of the plants presented symptoms of the disease after 4 months of cropping. The search for sources of the disease inoculum was centered on the health of the seeds and the polypropylene trays that were reused for plant production. Analysis of four lots of seeds from Germany and Italy showed that two of them harboredF. oxysporum f.sp.basilici. This finding was confirmed by the analysis of seeds collected from diseased plants. Furthermore, analysis of three reused trays revealed the presence of the pathogen on them and it was concluded that the trays acted as the source of dispersion of the mycosis. http://www.phytoparasitica.org posting July 14, 2004.     

Development of PCR assays to Tri7 and Tri13 trichothecene biosynthetic genes, and characterisation of chemotypes of Fusarium graminearum, Fusarium culmorum and Fusarium cerealis

Fusarium graminearum, Fusarium culmorum and Fusarium cerealis are major causal agents of Fusarium Head Blight (scab) which is a disease of global significance in all cereal growing areas. These fungi produce trichothecene mycotoxins, principally nivalenol (NIV) and deoxynivalenol (DON). Genes Tri13 and Tri7 from the trichothecene biosynthetic gene cluster convert DON to NIV (Tri13) and NIV to 4-acetyl-NIV (Tri7). We have developed positive–negative PCR assays based on these two genes, which accurately indicate a DON or NIV chemotype in F. graminearum, F. culmorum and F. cerealis. These assays are useful in assessing the risk of trichothecene contamination, and can be informative in epidemiological studies. All NIV chemotype isolates studied have functional copies of both Tri13 and Tri7, and all DON-producing isolates have both genes disrupted or deleted. We have identified several mutations in these genes, which are conserved across F. graminearum lineage, RAPD and SCAR groupings and between the three species. There appears to be evidence of inter-species hybridisation within the trichothecene biosynthetic gene cluster.     

Surveys of cereal diseases and pests in the Netherlands. 3. Monographella nivalis and Fusarium spp. in winter wheat fields and seed lots

Data from surveys of winter wheat fields in the period 1974–1986 and of seed lots in the period 1962–1986 and identifications of diseases on plant samples were compiled to describe the occurrence of snow mould (Monographella nivalis) andFusarium spp. On average,M. nivalis dominated overFusarium spp. The complex ofFusarium spp. constituted mainly ofF. culmorum, followed byF. avenaceum andF. graminearum. M. nivalis was dominant in May on stem-bases and in July on leaves and leaf sheaths. On seedsM. nivalis predominated only in years with low temperatures in July and August.Average brown footrot infection in the field was 4% tillers in May and 5% culms in July. Brown footrot intensity in July was high in cropping seasons with high precipitation in October and with low temperatures in October, November and December. In July during the early eighties, an average of 8% of leaves and 6% of flag leaf sheaths were infected byM. nivalis. Average ear blight incidence was 1.2% glumes infected. Seed contamination by these pathogens averaged 16% in the years 1962–1986. The contamination was high in years with high precipitation in June, July and August. Aspects of cv. resistance and yield loss are illustrated.     

Extracts of killedPenicillium chrysogenum Induce resistance against Fusarium wilt of melon

Dry fungal biomass ofPenicillium chrysogenum (dry mycelium), a waste product of the pharmaceutical industry, was extracted with water and applied to the roots of melon plants before or after inoculation withFusarium oxysporum f.sp.melonis (Font). Seedlings (4–6 days after emergence) treated with either acidic dry mycelium extract (DME) or neutralized dry mycelium extract (NDME) were protected against challenge infection withFom. A single drench with 2–5% DME applied 12–72 h before inoculation provided significant control of the disease compared with water-drenched, challenged seedlings. No protection was seen in plants treated 0–6 h before inoculation or 0–48 h after inoculation. Neither DME nor NDME (0.5–5%) had any effect on fungal growthin vitro, which implied that disease controlin vivo was mediated by induced resistance. The resistance induced by DME protected melon plants not only against race 1,2, but also against the three other races of the pathogen, indicating a race-non-specific resistance againstFom. Both DME and NDME significantly increased peroxidase activity and free L-proline content in seedlings 12 h and 48 h after soil drench, respectively. Resistance to Fusarium wilt was significantly associated with elevated levels of peroxidase activity but not with free L-proline content. Thus, peroxidase might be involved in the defense mechanisms activated by DME or NDME. http://www.phytoparasitica.org posting Aug. 31, 2001.     

Genetic Analysis of the Role of Trichothecene and Fumonisin Mycotoxins in the Virulence of Fusarium

The phytotoxicity of the Fusarium trichothecene and fumonisin mycotoxins has led to speculation that both toxins are involved in plant pathogenesis. This subject has been addressed by examining virulence of trichothecene and fumonisin-nonproducing mutants of Fusarium in field tests. Mutants were generated by transformation-mediated disruption of genes encoding enzymes that catalyze early steps in the biosynthesis of each toxin. Two economically important species of Fusarium were selected for these studies: the trichothecene-producing species Fusarium graminearum, which causes wheat head blight and maize ear rot, and the fumonisin-producing species F. verticillioides, which causes maize ear rot. Trichothecene-non-producing mutants of F. graminearum caused less disease than the wild-type strain from which they were derived on both wheat and maize, although differences in virulence on maize were not observed under hot and dry environmental conditions. Genetic analyses of the mutants demonstrated that the reduced virulence on wheat was caused by the loss of trichothecene production rather than by a non-target mutation induced by the gene disruption procedure. Although the analyses of virulence of fumonisin-non-producing mutants of F. verticillioides are not complete, to date, the mutants have been as virulent on maize ears as their wild-type progenitor strains. The finding that trichothecene production contributes to the virulence of F. graminearum suggests that it may be possible to generate plants that are resistant to this fungus by increasing their resistance to trichothecenes. As a result, several researchers are trying to identify trichothecene resistance genes and transfer them to crop species.     

Effect of antagonistic<Emphasis Type="Italic">Fusarium</Emphasis> spp. and of different commercial biofungicide formulations on Fusarium wilt of lettuce

Five experimental trials were carried out to test different biological control agents against Fusarium wilt of lettuce, cause byFusarium oxysporum f.sp.lactucae. In the presence of a very high disease incidence, the best results in terms of disease control as well as increased growth response were shown byTrichoderma harzianum T 22 (RootShield), which, at 3 gl ⁻¹ of substrate, provided very consistent results.F. oxysporum IF 23 gave good disease control but in two out of five trials reduced the biomass produced. Less consistent, but still significant results were provided byF oxysporium MSA 25, at 3 gl ⁻¹ of substrate, and byTrichoderma viride TV 1. The twoF. oxysporum agents Fo 251/2 and Fo 47 and the mixture ofT. harzianum + T. viride (Remedier) partially reduced disease incidence but were less effective than the above mentioned. Less interesting results were offered byStreptomyces griseoviridis (Mycostop). The results obtained show that biological control can play a role in the management of Fusarium wilt of lettuce.