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.     

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.     

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.     

Soil suppressiveness against the disease complex of the soybean cyst nematode and sudden death syndrome of soybean

The ecology of the complex of soybean cyst nematode (SCN) and sudden death syndrome (SDS) of soybean was investigated under soybean monoculture in two field experiments from 2003 to 2007. Initially, susceptible soybean 'Spencer' was planted while inoculating Fusarium virguliforme into nonfumigated or preseason-fumigated plots (methyl bromide, MB, at 450 kg/ha), and SCN and SDS were monitored. In one field, SCN population densities declined in nonfumigated but increased in fumigated plots. After years of limited SDS in 2003 and 2004, SDS developed later in nonfumigated than fumigated plots. In 2006 in the greenhouse, nondisturbed or disturbed soil cores (10-cm diameter, 30-cm depth) from field plots received two two-level factors: (i) nonfumigated or fumigated (1,070 kg/ha MB); and (ii) noninoculated or inoculated with 9,000 second-stage juveniles of SCN. At harvest, nonfumigated cores from nonfumigated plots had fewer nematodes and less SDS regardless of disturbance or inoculation than the corresponding fumigated cores and any cores from fumigated plots. In the second field, SCN became detectable after 2003 during the monoculture in nonfumigated plots and lagged in fumigated plots; both treatments had low levels of SDS. Exploiting the suppressiveness of the first field could allow for biological control of SDS and SCN in soybean production.     

Morphological and molecular characterization of the sudden-death syndrome pathogen of soybean in Brazil

Brazilian Fusarium isolates causing soybean sudden death syndrome (SDS) were characterized by comparing them with other Fusarium isolates associated with soybean root rot, as well as F. solani f.sp. glycines isolates associated with the disease in the USA, using molecular (mitochondrial and nuclear rDNA), morphological, cultural and pathogenic characteristics. On the basis of pathogenicity data, and restriction fragment length polymorphism and sequence analysis of the rDNA internal transcribed spacer (ITS) regions, isolates formed a group distinct from nonSDS F. solani isolates, as well as other Fusarium species. ITS sequence analysis also revealed that Brazilian isolates were distinct from the majority of SDS pathogens from the USA ( Fusarium virguliforme ) and conformed to Fusarium tucumaniae .     

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。     

Biological Control Efficiency of Fusarium Wilt of Tomato by Nonpathogenic Fusarium oxysporum Fo-B2 in Different Environments

ABSTRACT Efficiency of nonpathogenic Fusarium oxysporum Fo-B2 for the biological control of Fusarium wilt of tomato, caused by F. oxysporum f. sp. lycopersici CU1, was examined in different environments: a growth chamber with sterile soil-less medium, a greenhouse with fumigated or nonfumigated soil, and nonfumigated field plots. Inoculation of Fo-B2 onto tomato roots significantly reduced the severity of disease, but the efficiency of disease suppression decreased as the experimental environment became less controlled. Relationships between the recovery of Fo-B2 from hypocotyls and the disease severity indicated that the biocontrol agent was most effective when it colonized vascular tissues intensively. Moreover, the degree of Fo-B2 colonization was greatly reduced when the seedlings were grown in nonfumigated soil. Dose-response models (negative exponential, hyperbolic saturation, and logistic) were fit to observed data collected over a range of inoculum densities of the pathogen and the antagonist; the logistic model provided the best fit in all environments. The ratios of an 50% effective dose parameter for Fo-B2 to that of CU1 increased as the environment became less controlled, suggesting that environmentally related efficiency reduction impacted the antagonist more than the pathogen. The results suggest that indigenous soil microbes were a primary factor negatively influencing the efficiency of Fo-B2. Therefore, early establishment of the antagonist in a noncompetitive environment prior to outplanting could improve the efficacy of biological control.     

山东省大豆根腐病病原菌及其生物学研究

 1988-1989年采集山东大豆根腐病标样553个,经分离接种证明,致病菌有茄病镰刀菌[Fusarium solani(Mart.)Sacc.]、尖孢镰刀菌(F.oxysporum Schl.)和木贼镰刀菌[F.equiseti(Corda)Sacc.]三种,以茄病镰刀菌的分离频率最高,致病力最强,为主要致病菌。并对其培养特性、形态特征、寄主范围和光照、温度及pH对生长的影响进行了研究,根据这些研究结果,将大豆根腐病主要致病菌定名为茄病镰刀菌大豆专化型[Fusarium solani(Mart.)Sacc.f.sp.glycines Li et Luo],本专化型过去没有报告。     

Incidence of soil-borne plant pathogens isolated from barley and winter wheat, and other crops in the rotation, on Prince Edward Island

Barley and winter wheat were sampled over 3 years to characterize soil-borne organisms involved with cereal crown and root disease complexes. Winter wheat crowns were infected more often by Fusarium avenaceum and F. sambucinum than barley crowns. Bipolaris sorokiniana and F. graminearum were more common in crown tissue of barley underseeded with clover than in winter wheat crowns. In roots, the incidence of F. avenaceum was highest in winter wheat. In soil, populations of Rhizoctonia solani and F. sambucinum were higher in winter wheat than barley underseeded with ryegrass. Stunt nematodes (Tylenchorhynchus spp.) were greatest in winter wheat and barley underseeded with ryegrass. The incidence of F. avenaceum in roots of winter wheat correlated positively with the severity of crown and root rot symptoms. The severity of barley crown and root rot correlated positively with the incidence of R. solani in crowns, F. avenaceum in crowns and roots, B. sorokiniana in roots, and numbers of stunt nematodes in the soil. The incidence of soil-borne organisms was also recorded in annual ryegrass. soybean, potato, pea, and clover which were grown in rotation with barley and winter wheat. The incidence of R. solani and F. avenaceum was highest in clover crown tissue, and F. sambucinum was prevalent in soybean hypocotyls. Soil population levels of R. solani, F. avenaceum , and stunt nematodes were greatest in ryegrass and pea soil just prior to ploughing down or harvesting these crops, respectively.     

Biological Control of Pathogens Causing Root Rot Complex in Field Pea Using Clonostachys rosea Strain ACM941

ABSTRACT Pea root rot complex (PRRC), caused by Alternaria alternata, Aphanomyces euteiches, Fusarium oxysporum f. sp. pisi, F. solani f. sp. pisi, Mycosphaerella pinodes, Pythium spp., Rhizoctonia solani, and Sclerotinia sclerotiorum, is a major yield-limiting factor for field pea production in Canada. A strain of Clonostachys rosea (syn. Gliocladium roseum), ACM941 (ATCC 74447), was identified as a mycoparasite against these pathogens. When grown near the pathogen, ACM941 often was stimulated to produce lateral branches that grew directly toward the pathogen mycelium, typically entwining around the pathogen mycelium. When applied to the seed, ACM941 propagated in the rhizosphere and colonized the seed coat, hypocotyl, and roots as the plant developed and grew. ACM941 significantly reduced the recovery of all fungal pathogens from infected seed, increased in vitro seed germination by 44% and seedling emergence by 22%, and reduced root rot severity by 76%. The effects were similar to those of thiram fungicide, which increased germination and emergence by 33 and 29%, respectively, and reduced root rot severity by 65%. When soil was inoculated with selected PRRC pathogens in a controlled environment, seed treatment with ACM941 significantly increased emergence by 26, 38, 28, 13, and 21% for F. oxysporum f. sp. pisi, F. solani f. sp. pisi, M. pinodes, R. solani, and S. sclerotiorum, respectively. Under field conditions from 1995 to 1997, ACM941 increased emergence by 17, 23, 22, 13, and 18% and yield by 15, 6, 28, 6, and 19% for the five respective pathogens. The seed treatment effects of ACM941 on these PRRC pathogens were greater or statistically equivalent to those achieved with thiram. Results of this study suggest that ACM941 is an effective bioagent in controlling PRRC and is an alternative to existing chemical products.     

贵州省大豆孢囊线虫的发生与分布

大豆孢囊线虫病是威胁大豆生产的重大病害之一。2015-2016年,采用随机取样的方法对贵州省大豆孢囊线虫的发生和分布情况进行了调查。调查范围包括贵阳、六盘水、安顺、毕节、黔西南和遵义等6个地区下辖的14个县(区),共采集土样287份。调查结果表明,贵州省大豆孢囊线虫的总检出率为28.2%,其中毕节地区的大方县和赫章县孢囊检出率最高,分别达到46.7%和45.0%,而在遵义市、贵阳市和黔西南州孢囊检出率为0。六盘水地区的水城县孢囊发生量最大,平均孢囊数为3.4个/200g土,最大孢囊数达到17个/200g土;安顺地区的镇宁和关岭县大豆孢囊线虫发生程度最轻,每200g土样平均孢囊数分别为0.3和0.2个,最大孢囊数仅为2个/200g土。分离的孢囊主要形态特征与大豆孢囊线虫一致,并且ITS序列与甘肃大豆孢囊线虫种群序列一致性达100%。根据形态学观察和ITS序列分析比对,将贵州省采集到的孢囊线虫鉴定为大豆孢囊线虫。本研究结果可为有效防控贵州省大豆孢囊线虫病提供依据。     

Interactions of Pratylenchus thornei and Fusarium oxysporum f. sp. ciceris on Chickpea

ABSTRACT Fusarium oxysporum f. sp. ciceris and the root-lesion nematode Pratylenchus thornei coinfect chickpeas in southern Spain. The influence of root infection by P. thornei on the reaction of Fusarium wilt-susceptible (CPS 1 and PV 61) and wilt-resistant (UC 27) chickpea cultivars to F. oxysporum f. sp. ciceris race 5 was investigated under controlled and field conditions. Severity of Fusarium wilt was not modified by coinfection of chickpeas by P. thornei and F. oxysporum f. sp. ciceris, in simultaneous or sequential inoculations with the pathogens. Root infection with five nematodes per cm(3) of soil and 5,000 chlamydospores per g of soil of the fungus resulted in significantly higher numbers of propagules of F. oxysporum f. sp. ciceris with the wilt-susceptible cultivar CPS 1, but not with the wilt-resistant one. However, infection with 10 nematodes per cm(3) of soil significantly increased root infection by F. oxysporum f. sp. ciceris in both cultivars, irrespective of fungal inoculum densities (250 to 2,000 chlamydospores per g of soil). Plant growth was significantly reduced by P. thornei infection on wilt-susceptible and wilt-resistant chickpeas in controlled and field conditions, except when shorter periods of incubation (45 days after inoculation) were used under controlled conditions. Severity of root necrosis was greater in wilt-susceptible and wilt-resistant cultivars when nematodes were present in the root, irrespective of length of incubation time (45 to 90 days), densities of nematodes (5 and 10 nematodes per cm(3) of soil), fungal inocula, and experimental conditions. Nematode reproduction on the wilt-susceptible cultivars, but not on the wilt-resistant one, was significantly increased by F. oxysporum f. sp. ciceris infections under controlled and field conditions.     

Interactions Between Meloidogyne artiellia, the Cereal and Legume Root-Knot Nematode, and Fusarium oxysporum f. sp. ciceris Race 5 in Chickpea

ABSTRACT In the Mediterranean Basin, Fusarium oxysporum f. sp. ciceris and the root-knot nematode Meloidogyne artiellia coinfect chickpea. The influence of root infection (after inoculation with 20 nematode eggs and second-stage juveniles per gram of soil) by two M. artiellia populations, from Italy and Syria, on the reaction of chickpea lines and cultivars with partial resistance to Fusarium wilt (CA 252.10.1.OM, CA 255.2.5.0, CPS 1, and PV 61) and with complete resistance to F. oxysporum f. sp. ciceris race 5 (CA 334.20.4, CA 336.14.3.0, ICC 14216 K, and UC 27) was investigated under controlled conditions. In genotypes with partial resistance, infection by M. artiellia significantly increased the severity of Fusarium wilt, irrespective of the fungal inoculum density (3,000 or 30,000 chlamydospores per gram of soil), except in cultivar CPS 1 at the lower fungal inoculum density. In genotypes with complete resistance to Fusarium wilt, infection by M. artiellia overcame the resistance to F. oxysporum f. sp. ciceris race 5 in CA 334.20.4 and CA 336.14.3.0 but not in ICC 14216 K, irrespective of the fungal inoculum density, and overcame the resistance in UC 27 only at the higher inoculum density. Infection by the nematode significantly increased the number of propagules of F. oxysporum f. sp. ciceris race 5 in root tissues of genotypes with complete resistance to Fusarium wilt, compared with roots that were not inoculated with the nematode, irrespective of the fungal inoculum density, except in ICC 14216 K, in which this effect occurred only at the higher inoculum density. Reproduction of an M. artiellia population from Syria in the absence of F. oxysporum f. sp. ciceris race 5 was significantly higher than that of a population from Italy in all tested chick-pea genotypes except ICC 14216 K. However, there was no significant difference between the reproduction rates of the two nematode populations in plants infected with F. oxysporum f. sp. ciceris race 5, irrespective of the fungal inoculum density and the reaction of the genotypes to the fungus.     

Phytosanitary importance of Heterodera glycines for South-east Asian countries

Heterodera glycines is not known to occur in South-east Asian countries except in Indonesia. Specific surveys carried out recently in central India indicate absence of the nematode. The region has a large area under cultivation of soybean, and also other crop and wild hosts. H. glycines causes annual yield losses of about half a million metric tons in 10 major soybean-growing countries. Asia has to import half its demand of soybeans, mainly from North America and Brazil, where H. glycines occurs. Spread is mainly through soil mixed with seeds, or by spillage of grain. A preliminary pest risk analysis suggests that the South-east Asian region is suitable for the introduction and spread of H. glycines . Management practices are suggested to delay its introduction.     

Temporal dynamics of root and foliar severity of soybean sudden death syndrome at different inoculum densities

Temporal dynamics of soybean sudden death syndrome (SDS) root and foliar disease severity were studied in growth chamber experiments on susceptible plants exposed to different inoculum densities (0, 10⁰, 10¹, 10², and 10³ conidia g⁻¹ soil) of Fusarium virguliforme. The monomolecular model provided the best fit to describe the progress of root and foliar disease severity over time. Disease severity and area under disease progress curve (AUDPC) both increased in response to increasing inoculum density (P < 0.01), particularly for foliar symptoms. Rate of disease progress increased as inoculum densities increased for both root and foliar disease severities. The incubation period for root and foliar disease severity ranged from 9 to 18 and 15 to 25 days, respectively. Significant differences in root rot severity were most easily detected during the early stages of infection, whereas root rot and foliar severities were only weakly correlated when both were assessed simultaneously at later stages of disease development. Root rot severity assessments performed 15 to 20 days after inoculation (DAI) were most highly correlated (r > 0.9, P < 0.01) with foliar disease severity assessments performed 30 to 50 DAI. Root biomass was reduced by up to 67% at the three highest inoculum densities, indicating the aggressiveness that F. virguliforme possesses as a root rot pathogen on soybeans.     

Relationships Between Tillage and Spatial Patterns of Heterodera glycines

ABSTRACT The dynamics of Heterodera glycines spatial patterns were studied under different tillage systems in two naturally infested soybean fields in Iowa from 1994 to 1997. At each location, there were four different tillage treatments (conventional tillage, reduced tillage, ridge tillage, and no tillage). Soil samples were taken from 98 contiguous quadrats (5.2 m(2)) per plot in the fall of 1994, before any tillage was performed, and in the spring of the following 3 years shortly after planting. Cysts were extracted from soil samples by elutriation and counted, and eggs were extracted from cysts and enumerated. Spatial patterns of H. glycines populations were characterized by geostatistical analysis and variance-to-mean (VM) ratios. Semivariance values were calculated for cyst and egg densities and semivariograms were constructed. In general, there was greater spatial dependence among cyst populations than egg populations. In one field with a strongly aggregated initial H. glycines population, tillage practices resulted in changes in spatial patterns of H. glycines populations, characterized by spherical-model semivariogram parameters (sill, nugget effect, and range of spatial dependence). These parameters indicated increasing aggregation over time in no tillage and ridge tillage treatments, but decreasing aggregation in reduced and conventional tillage treatments. There was an increase of 350% in sill values (maximum semivariance) for cyst populations after 3 years of no tillage, but in the conventional tillage treatment, sill values remained unchanged or decreased over time as tillage was implemented. Semivariograms for cyst and egg population densities revealed strong anisotropy (directional spatial dependence) along soybean rows, coincident with the direction of tillage practices. VM ratios for cyst counts increased each year in the no tillage and ridge tillage treatments, but decreased for 2 years in reduced tillage and conventional tillage treatments. Final VM ratios for cyst and egg counts were highest in the no tillage treatment. In a second field, with low initial aggregation of H. glycines populations, there was little measurable change in semivariogram parameters after 3 years of no tillage, but in the conventional tillage treatment, populations became less aggregated, as the range, sill, and the proportion of the sill explained by spatial dependence decreased for cyst population densities. Our results indicated that in soybean fields with initially aggregated populations of H. glycines, no tillage and ridge tillage systems promoted aggregation of the nematode population, whereas conventional and reduced tillage systems resulted in a less aggregated spatial pattern.     

河北省大豆孢囊线虫分子鉴定及其分布

2003年,在河北省邯郸、邢台、石家庄、保定、秦皇岛、唐山、张家口等地采集大豆根际土壤样品65份,应用大豆孢囊线虫特异性引物对采集的孢囊线虫进行了分子鉴定,结果表明从邯郸的永年、磁县、峰峰,邢台的南和、广宗、清河,保定的南大园、西马池、望都、定州,石家庄的栾城、鹿泉、平山及石家庄市郊,秦皇岛的抚宁、昌黎,唐山的迁西、迁安、丰润的大豆和张家口的红云豆上采集的孢囊线虫的孢囊及其二龄幼虫均为大豆孢囊线虫;卢龙和滦县的样品中没有发现大豆孢囊线虫的孢囊及其二龄幼虫,且孢囊的检出率与二龄幼虫的检出率的趋势一致。     

Pathogenicity and toxicity of Fusarium tucumaniae and Fusarium crassistipitatum to soybean and Arabidopsis thaliana

Sudden death syndrome (SDS) of soybean is a fungal disease caused by at least four distinct Fusarium species: F. tucumaniae, F. virguliforme, F. brasiliense, and F. crassistipitatum. All four species are present in Argentina. These fungi are soilborne pathogens that only colonize roots and cause root necrosis. However, damage also reaches the aboveground part of the plant, and foliar chlorosis and necrosis, followed by premature defoliation, can be observed. Although the pathogenicity and phytotoxicity of F. virguliforme has been well characterized, knowledge regarding disease development by other fungal species is scarce. In this study, two plant species, soybean (Glycine max) and Arabidopsis thaliana, and isolates from two fungal species, F. tucumaniae and F. crassistipitatum, were used to comparatively analyse the fungal pathogenicity and the phytotoxicity of volatile organic compounds (VOCs) and cell-free culture filtrates. Fungal inoculation had a significant effect on plant growth, regardless of the plant species. In addition, infected soybean plants showed disease incidence and foliar and root symptoms. Inhibition of A. thaliana growth was not due to VOCs emitted by fungi. Instead, both pathogens were shown to produce toxins that caused typical SDS foliar symptoms in soybean and root length reduction in A. thaliana. As far as we know, this is the first report that demonstrates that F. tucumaniae and F. crassistipitatum affect A. thaliana growth and emit VOCs, and that F. crassistipitatum produces toxins.     

Soybean Brown Stem Rot, Phytophthora sojae, and Heterodera glycines Affected by Soil Texture and Tillage Relations

ABSTRACT Investigations were conducted to determine whether the effects of tillage practices on the prevalence of brown stem rot of soybean (caused by Phialophora gregata), Heterodera glycines, and Phytophthora sojae were confounded by soil texture in samples collected in the fall of 1995 and 1996. Soil and soybean stem samples, along with tillage information, were collected from 1,462 randomly selected fields in Illinois, Iowa, Minnesota, Missouri, and Ohio in collaboration with the National Agricultural Statistics Service. The incidence of brown stem rot was determined from 20 soybean stem pieces collected from each field in a zigzag pattern. The detection frequency of P. sojae (expressed as percent leaf disks colonized) and population densities of H. glycines were determined from soil cores also collected in a zigzag pattern. The soil samples were grouped into various textural classes, and the effect of soil texture and tillage relations on the activities of each pathogen were determined. Both tillage and soil texture affected the incidence of brown stem rot; however, there was no interaction between tillage and soil texture. Conservation tillage had a greater (P < 0.05) incidence of brown stem rot in clay loam and silty clay loam than did conventional tillage. The detection frequency of P. sojae was not affected by tillage, but a tillage x texture interaction (P = 0.013) indicated that the effect of tillage depended on soil texture. There was a greater (P < 0.05) detection frequency of P. sojae in conservation tillage than in conventional tillage in silt loam and loam soils. However, in sandy loam, the detection frequency of P. sojae was greater (P = 0.0099) in conventional tillage than in conservation tillage. Population densities of H. glycines were significantly affected by both tillage and soil texture, but overall, there was no tillage x texture interaction. There was an inverse relationship between population densities of H. glycines and percent clay (r = -0.81, P = 0.01) in no-till fields, but little or no change in nematode densities was observed with increasing clay content in tilled fields. Population densities of H. glycines were less (P < 0.05) in no-till fields than in tilled fields in silty clay loam and clay soils. There was no difference in H. glycines densities between the tillage categories in soils sandier than silty clay loam or clay. The findings emphasize the need for cautious interpretation of the effects of tillage practices on diseases and pathogens in the absence of information on soil texture.