Effects of Herbicides on Fusarium solani f. sp. glycines and Development of Sudden Death Syndrome in Glyphosate-Tolerant Soybean

ABSTRACT Sudden death syndrome of soybean, caused by Fusarium solani f. sp. glycines, is a disease of increasing economic importance in the United States. Although the ecology of sudden death syndrome has been extensively studied in relation to crop management practices such as tillage, irrigation, and cultivar selection, there is no information on the effects of herbicides on this disease. Three herbicides (lactofen, glyphosate, and imazethapyr) commonly used in soybean were evaluated for their effects on the phenology of F. solani f. sp. glycines and the development of sudden death syndrome in four soybean cultivars varying in resistance to the disease and in tolerance to glyphosate. Conidial germination, mycelial growth, and sporulation in vitro were reduced by glyphosate and lactofen. In growth-chamber and greenhouse experiments, there was a significant increase in disease severity and frequency of isolation of F. solani f. sp. glycines from roots of all cultivars after application of imazethapyr or glyphosate compared with the control treatment (no herbicide applied). Conversely, disease severity and isolation frequency of F. solani f. sp. glycines decreased after application of lactofen. Across all herbicide treatments, severity of sudden death syndrome and isolation frequency were lower in disease-resistant than in susceptible cultivars. Results suggest that glyphosate-tolerant and -nontolerant cultivars respond similarly to infection by F. solani f. sp. glycines after herbicide application.     

Interactions Between the Soybean Cyst Nematode and Fusarium solani f. sp. glycines Based on Greenhouse Factorial Experiments

ABSTRACT The soybean cyst nematode, Heterodera glycines, and the fungus that causes sudden death syndrome (SDS) of soybean, Fusarium solani f. sp. glycines, frequently co-infest soybean (Glycine max) fields. The interactions between H. glycines and F. solani f. sp. glycines were investigated in factorial greenhouse experiments with different inoculum levels of both organisms on a soybean cultivar susceptible to both pathogens. Measured responses included root and shoot dry weights, H. glycines reproduction, area under the SDS disease progress curve, and fungal colonization of roots. Both H. glycines and F. solani f. sp. glycines reduced the growth of soybeans. Reproduction of H. glycines was suppressed by high inoculum levels but not by low levels of F. solani f. sp. glycines. The infection of soybean roots by H. glycines did not affect root colonization by the fungus, as determined by real-time polymerase chain reaction. Although both pathogens reduced the growth of soybeans, H. glycines did not increase SDS foliar symptoms, and statistical interactions between the two pathogens were seldom significant.     

Molecular detection of Fusarium solani f. sp. glycines in soybean roots and soil

A polymerase chain reaction (PCR)-based method was developed to detect DNA of Fusarium solani f. sp. glycines , the cause of soybean sudden death syndrome. Two pairs of primers, Fsg1/Fsg2 designed from the mitochondrial small subunit ribosomal RNA gene, and FsgEF1/FsgEF2 designed from the translation elongation factor 1-α gene, produced PCR products of 438 and 237 bp, respectively. Primer specificity was tested with DNA from 82 F. solani f. sp. glycines , 55 F. solani non-SDS isolates, 43 isolates of 17 soybean fungal pathogens and the oomycete Phytophthora sojae , and soybean. The sensitivity of primer Fsg1/Fsg2 was 10 pg while that of FsgEF1/FsgEF2 was 1 ng when using F. solani f. sp. glycines total genomic DNA or down to 10³ macroconidia g⁻¹ soil. Nested PCR increased the sensitivity of the PCR assay 1000-fold to 10 fg using primers Fsg1/Fsg2, and 1 pg using primers FsgEF1/FsgEF2. F. solani f. sp. glycines DNA was detected in field-grown soybean roots and soil by PCR using either single pairs of primers or the combination of two pairs of primers. The occurrence of F. solani f. sp. glycines was determined using nested PCR for 47 soil samples collected from soybean fields in 20 counties of Illinois in 1999. F. solani f. sp. glycines was detected in soil samples from all five Illinois Agricultural Statistic Districts including 100, 89, 50, 92 and 50% of the samples from East, Central, North-east and West Districts, respectively.     

Molecular Differentiation of Fusarium solani f. sp. glycines from Other F. solani Based on Mitochondrial Small Subunit rDNA Sequences

Fusarium solani is a soilborne plant pathogen that infects many different hosts. Within the species, there is some specialization, and a number of forma specialis have been described based on host affiliation. One of these, F. solani f. sp. glycines, infects soybean and causes sudden death syndrome. To differentiate between F. solani f. sp. glycines and other F. solani isolates, a partial sequence of the mitochondrial small subunit (mtSSU) rRNA gene was amplified by polymerase chain reaction and sequenced from 14 F. solani f. sp. glycines and 24 F. solani isolates from various plant hosts. All F. solani f. sp. glycines isolates had identical sequences. A single, unique insertion of cytosine occurred in all F. solaniisolates but not in any of the F. solani f. sp. glycines isolates. Two major lineages, distinguished by sequence divergence and the presence or absence of multiple insertions, occurred in F. solani isolates. Cladistic analysis produced a single most-parsimonious tree with three major clades. The first clade contained all F. solani f. sp. glycines isolates. A second clade grouped together all of the F. solani isolates that had only a single nucleotide insertion difference from the first clade. Genetic distance between these two clades was 0.016. A third clade was formed by five F. solaniisolates that had multiple insertions. Isolates in the third clade had a genetic distance of 0.040 from the first and second clades. Based on the sequence data, it is likely that F. solani f. sp. glycineshas a shorter evolutionary history than other F. solaniisolates that have either single or multiple nucleotide insertions. The differences in nucleotide insertions in part of the mtSSU rRNA gene between F. solani f. sp. glycinesand other F. solani isolates provide a direct and reliable way to distinguish isolates of F. solani.     

Pathogenicity of Fusarium solani f.sp. cucurbitae race 1 to courgette

Fusarium solani f. sp.cucurbitae race 1 causes foot rot in courgette (Cucurbita pepo). The pathogen could be distinguished fromFusarium solani from sweet pepper (Capsicum annuum) both morphologically and in its host range.In inoculation experiments all nine cultivars of the six species of Cucurbitaceae tested were susceptible. Courgette Green became diseased after inoculation with a spore suspension by root dipping or adding the suspension to the soil around the stem base or spraying the whole plant with it.Both wounded and young plants died more quickly than unwounded and older plants. With low inoculum densities the plants were affected more slowly than with high densities and the differences in susceptibility of the Cucurbitaceae tested were more pronounced.From infected courgette seeds the fungus could be reisolated until 6 months after harvest.This is the first record of this pathogen in courgettes in the Netherlands.Samenvatting Fusarium solani f. sp. cucurbitae fysio 1 is de oorzaak van een voetrot in courgette. Het pathogeen is morfologisch en door middel van een waardplantenreeks goed vanF. solani uit paprika te onderscheiden.In inoculatieproeven waren de getoetste Cucurbitaceae in meer of mindere mate gevoelig voorF. solani f. sp.cucurbitae. Bij courgette Green werden zowel gedompelde, als aangegoten, als bespoten planten door het pathogeen aangetast. Zowel verwonde als niet-verwonde planten werden aangetast als ook planten van verschillende leeftijden. Niet-verwonde en ook oudere planten stierven minder snel af dan verwonde en jongere planten. Bij lagere inoculumdichtheden werden de planten minder snel aangetast dan bij hogere dichtheden en waren de verschillen in vatbaarheid voor het pathogeen tussen de getoetste Cucurbitaceae duidelijker.Uit courgette zaad, dat met het pathogeen was besmet, kon de schimmel tot 6 maanden na zaadwinning opnieuw worden geïsoleerd.Dit is de eerste melding van dit pathogeen in courgette in Nederland.     

Suppression of Fusarium solani f. sp. phaseoli on Bean by Aluminum in Acid Soils

ABSTRACT The severity of bean root rot caused by Fusarium solani f. sp. phaseoli in vitro was studied with regard to exchangeable soil aluminum for 25 soil samples collected from northeastern Honshyu island, Japan. Of these, 24 were Andosols, typically acidic and of volcanic ash origin. Disease severity was assessed based on the number of lesions produced by the pathogen on a 6-cm section of bean stem buried and incubated for 8 days at 25 degrees C in artificially infested soil samples. The number of lesions differed considerably among soil samples. In all soils in which disease incidence was very low, macroconidial germination was strongly inhibited. The inhibition was observed in all soil samples with exchangeable aluminum contents of at least 0.4 meq/100 g of soil, although it is unclear if this concentration is the lowest limit for inhibition. When soil pH was 5.6 or lower, higher amounts of exchangeable aluminum were detected from soils in which the major clay mineralogy was chloritized 2:1 minerals, while no or limited amounts of aluminum were detected from soils in which the major clay mineralogy was allophane/imogolite. Macroconidial germination and disease incidence are thus closely related to clay mineralogy, which regulates the behavior of exchangeable aluminum.     

Genetic diversity in Fusarium oxysporum f.sp. dianthi and Fusarium redolens f.sp. dianthi

Pathogenic isolates were selected representing all known vegetative compatibility groups (VCGs) and races of Fusarium oxysporum sensu lato from Dianthus spp. On basis of differences in the internal transcribed spacer region of the ribosomal DNA, six VCGs were classified as F. oxysporum f.sp. dianthi and four as F. redolens f.sp. dianthi. All VCGs of F. oxysporum f.sp. dianthi were characterized by unique restriction fragment length polymorphisms (RFLPs), unique overall esterase profiles, and unique virulence spectra, supporting a clonal lineage concept. Two VCGs of F. oxysporum f.sp. dianthi nevertheless comprised more than one race, but races within the same VCG shared the same distinct overall virulence spectrum. VCGs belonging to F. redolens f.sp. dianthi also had unique RFLPs and unique virulence spectra, but had grossly identical esterase profiles. Three new races (9, 10 and 11) are described for F. oxysporum f.sp. dianthi, and four for F. redolens f.sp. dianthi. Two races previously considered lost were recovered; race 7 was identified as a member of VCG 0021 of F. oxysporum f.sp. dianthi while race 3 was identified as a distinct VCG and race of F. redolens f.sp. dianthi. A summary of races and VCGs in F. oxysporum f.sp. dianthi and F. redolens f.sp. dianthi is presented.     

Fusarium solani f.sp.cucurbitae andF. oxysporum f.sp.niveum inoculum densities in tunisian soils and their effect on watermelon seedlings

Populations ofFusarium solani f.sp.cucurbitae (Fsc) andFusarium oxysporum f.sp.niveum (Fon) in naturally infested soil of watermelon fields were counted by the soil dilution method with subsequent pathogenicity tests. Inoculum density varied within the same region from one field to another, ranging between 9 and 1600 CFU g^?1 soil forFsc and from 0 to 200 CFU g^?1 soil forFon. Fusarium crown- and root-rot-diseased seedlings were observed in most soils (93%); however, Fusarium wilt was observed in only 34% of soil samples. The disease incidence on cv. ‘Giza’ (Y) increased significantly with inoculum density in the soil (X) (P<0.001). ForFsc, the relationship between inoculum density and disease incidence was characterized by the equation Y=0.0005X+0.165 (R²=0.67). ForFon, the equation was Y=0.003X?0.0014 (R²=0.88). Based on these equations, the estimated inoculum densities required to cause 50% disease incidence (DI₅₀) on cv. Giza plants was 670 and 171 CFU g^?1 soil forFsc andFon, respectively.     

几丁质酶与大豆抗胞囊线虫关系初步研究

 几丁质酶作为病原物和寄主植物相互作用中的一种重要蛋白质,已成为在植物抗病虫害研究中的热点。线虫卵壳及表皮的主要组成成分是几丁质,与真菌病原物一样,植物被线虫侵染时,可产生几丁质酶^[1]。     

生防菌与茄病镰刀菌在黄瓜根际动态变化

应用荧光定量PCR和稀释分离法检测了枯草芽孢杆菌Bacillus subtilis和木霉菌Trichoderma spp.与茄病镰刀菌Fusariumsolani f.sp.cucurbitae在黄瓜根际动态变化及其对黄瓜根腐病的防治效果。结果表明,施用500×木霉菌肥、100×枯草芽孢杆菌7d后对黄瓜根腐病的防效分别为100%和92.5%,14和28d的防效分别为96.71%、86.76%和85.35%、79.24%;100×枯草芽孢杆菌初始拷贝数为130787 copys/μL,7d内枯草芽孢杆菌拷贝数下降到51161 copys/μL,14和28d时数量开始上升到295139和680556 copys/μL。木霉菌肥的变化趋势与枯草芽孢杆菌相同;用枯草芽孢杆菌和木霉菌肥防治黄瓜根腐病后,茄病镰刀菌变化趋势一致,初始拷贝数分别为2.61和15.34 copys/μL,7d内茄病镰刀菌DNA拷贝数增加明显,100×枯草芽孢杆菌和木霉菌DNA拷贝数分别为11.22和20.9 8copys/μL,之后茄病镰刀菌数量保持平稳。经过稀释分离法分离2种生防菌和茄病镰刀菌的数量,变化趋势与荧光定量PCR检测趋势相似。因此使生防菌快速定殖是提高其对土传病害防治效果的重要因素之一。     

Fusarium solani f. sp. passiflorae: a new forma specialis causing collar rot in yellow passion fruit

The aim of this study was to characterize a Fusarium population obtained from yellow passion fruit (YPF) with collar rot using pathogenicity, morphocultural characteristics and molecular tests. Pathogenicity and disease severity were assessed in six plant species: YPF, zucchini, tomato, bean, soya bean and cucumber. Potato dextrose agar medium (PDA) was used to determine mycelial growth at five temperatures (15–35°C). The colour produced by isolates was also determined on PDA at 25°C. Synthetic nutrient agar medium was used to evaluate: (i) type of mycelium and phialides; (ii) size, shape and number of septa from conidia; and (iii) production of chlamydospores and perithecia. Molecular tests consisted of sequencing the ITS–5·8S rDNA region and elongation factor 1α (EF‐1α) gene. The isolates caused large lesions on YPF, zucchini and tomato, with YPF having the highest mean disease severity and being the only one that showed wilt symptoms and death of the plant. Thus the isolates showed host specificity. Maximum mycelial growth occurred at 25°C and the predominant colour was bluish‐white. The isolates produced long phialides, dense aerial mycelium, oval microconidia with a mean size of 9·5 × 2·6 μm, macroconidia of 32·7 × 3·4 μm with 3·3 septa, and chlamydospores; only one isolate lacked perithecia. Phylogenetic trees of the ITS region and EF‐1α gene showed that isolates from YPF formed a distinct group within the F. solani group and the formae speciales of F. solani. It is proposed to name all isolates from YPF as F. solani f. sp. passiflorae.     

种子处理诱导大豆抗胞囊线虫病的生防细菌筛选与鉴定

国内研究了简单芽孢杆菌Bacillussimplex包衣处理大豆种子,诱导大豆植株抗胞囊线虫的侵染。采用温室盆栽试验,对研究室通过2年田间试验筛选出的3株生防细菌进行复筛,获得最优菌株Sneb545;为了阐明其作用方式,设计了裂根试验验证菌株Sneb545诱导大豆产生抗胞囊线虫的能力,并对菌株Sneb545进行种水平鉴定。结果表明,菌株Sneb545处理种子后可以诱导苗期大豆对第一代胞囊线虫产生明显的抗性,线虫入侵总数显著降低,较对照降低72．63％,胞囊抑制率达70．63％;裂根试验结果证明,菌株Sneb545能够诱导大豆对胞囊线虫产生很强的抗性,菌株Sneb545在挑战根系中接种后,应答根系中胞囊线虫入侵量降低51．27％,土壤中胞囊减少65．82％;经形态学特征、生理生化试验测定及16SrDNA序列同源性分析,确定该菌株为简单芽孢杆菌。     

Fusarium solani f. sp. cucurbitae race 1, a potential pathogen of grafted watermelon production in Spain*

A crown, root and fruit rot of squash (Cucurbita maxima and Cucurbita moschata) has been observed in eastern provinces of Spain over the past 4 years. Isolations from the crown of symptomatic plants and fruits yielded primarily a Fusarium solani that was identified as F. solani f. sp. cucurbitae race 1 on the basis of pathogenicity tests and disease symptoms in the field. In Spain, more than 90% of watermelon plants are grafted, using different Cucurbita hybrids (C. maxima × C. moschata) as rootstocks. In 1998, some grafted watermelon plants were first found to be affected by F. s. cucurbitae race 1. The purpose of this study was to evaluate the pathogenicity of this fungus on several rootstocks commonly used for grafting watermelon (Brava, Titan, Shintoza, RS‐841, TZ‐148 and TW‐1) in order to prevent a possible spread of this fungus that could cause serious economic losses in watermelon production. None of them proved to be resistant.     

Fine Structure of the Early Interaction of Lily Roots with Fusarium oxysporum f.sp. lilii

The early interaction of lily roots with the cortical rot pathogen Fusarium oxysporum f.sp. lilii was studied using roots of lily bulblets grown in Hoagland's solution, inoculated with the pathogen, and sampled up to 48h later. Conidia produced germ tubes within 6h, which extended towards and into the mucilage covering the root elongation zone, and along and into the anticlinal grooves and middle lamellae of epidermal cells. By 24–48h, infecting hyphae had reached the periclinal walls and intercellular spaces between the epidermis and the outermost cells of the cortex. Penetration of intercellularly growing hyphae directly across host cell walls was not observed; invasion of the cell lumen only occurred by gradual infringing of hyphae upon successive primary wall layers. Non-cellulosic wall appositions rich in vesicles and covered by a cellulosic protective-like layer were formed in response to approaching hyphae in resistant cv.Connecticut King, but rarely in susceptible cv. Esther which seemed more susceptible to plasmolysis and rot. Finger-like projections of the appositions into the host cell cytoplasm likely represent early stages of transfer cell formation.     

Effect of the herbicides EPTC and linuron on cotton diseases caused by Rhizoctonia solani and Fusarium oxysporum f. sp. vasinfectum

The herbicides EPTC and linuron applied to soil in the field at three different concentrations X₂X, 1X, and 2X of recommended dose) decreased post-emergence, but not pre-emergence daraping-off in cotton incited by Rhizoctonia solani. Both herbicides at the two high concentrations significantly reduced wilt incited by Fusarium oxysporum f. sp. vasinfectum. Both herbicides reduced germination of chlamydospores of Fusarium in natural soil, but not in steamed soil. The 2X concentration of EPTC and linuron reduced the saprophytic activity of R. solani in soil. The effects of EPTC and linuron on post-emergence damping-off and wilt were attributed Ic their ability to suppress the saprophytic ability of R. solani and chlamydospore germinability of Fusarium in soil, respectively.     

Synergism in the interaction of Fusarium virguliforme with Heterodera glycines in sudden death syndrome of soybean

Journal of Plant Diseases and Protection - Sudden death syndrome (SDS) of soybean caused by Fusarium virguliforme has increased in geographical distribution in the North Central region of the U.S....     

Effect of light on sporulation ofalternaria porri f. sp.solani and ofstemphylium botr yosum f. sp.lycopersici in vivo

The highest spore production ofStemphylium botryosum f. sp.lycopersici on tomato leaves during a 24-h wetting period occurred in continuous darkness, and ofAlternaria porri f. sp.solani on potato leaves in a 12-h dark period which had been preceded by a 12-h light period. Sporulation of both pathogens was inhibited by illumination during the entire wetting period or during the last 12 h of it. In inhibitory conditions spore yield increased with a decrease in the incubation temperature and as tested withA. porri f. sp. solani, also with lowered light intensity.