Analysis of protease activity in <Emphasis Type="Italic">Aspergillus flavus</Emphasis> and <Emphasis Type="Italic">A. parasiticus</Emphasis> on peanut seed infection and aflatoxin contamination

Aspergillus flavus and A. parasiticus are aflatoxin-producing fungi that can infect peanut seeds in field crops. An association between A. parasiticus proteolytic enzyme activities and peanut fungal infection was examined. For this study, a model of inductive and non-inductive culture media to produce A. parasiticus extracellular protease before infection was used. These A. parasiticus cultures were used to infect peanut seeds of cultivars resistant and susceptible to aflatoxin contamination. Peanut seeds of both cultivars exposed to fungi grown on casein medium (inductive medium) showed higher internal and external infection and a higher fungal protease content than those observed on potato dextrose agar (PDA) and sucrose medium (non-inductive media). A further study showed higher fungal colonisation and aflatoxin contamination in seeds of the resistant cultivar pre-incubated with Aspergillus extracellular proteases than in those incubated without proteases. Moreover, protease activities affected the viability of non-infected resistant cultivar seeds, inhibiting germination and radicle elongation and enhancing seed tissue injury. The results strongly suggest that protease production by A. parasiticus is involved in peanut seed infection and aflatoxin contamination resulting in seed tissue damage, affecting seed viability and facilitating the access of fungi through the testa. The analysis of fungal extracellular proteases formed on peanut seed during infection showed that A. flavus and A. parasiticus produced metallo and serine proteases; however, there were differences in the molecular masses of the enzymes between both species. The greatest activity in both species was by serine protease, that could be classified as subtilase.     

Factors associated with the incidence of Aspergillus section Flavi and aflatoxin contamination of peanuts in the Busia and Homa bay districts of western Kenya

The aim of this study was to identify agronomic, ecological and sociocultural factors that could be modified to reduce the risk of aflatoxin contamination of peanuts from western Kenya. Presence of fungi within section Flavi of the genus Aspergillus and levels of total aflatoxin were determined for 436 peanut samples from the Busia and Homa bay districts. A total of 1458 cultures of Aspergillus flavus or A. parasiticus isolated from the samples were assayed for production of aflatoxin B₁, B₂, G₁ and G₂. Associations among the incidences of fungal species, incidences of samples with ≥10 μg kg^?1 aflatoxin, production of specific aflatoxin types and various agronomic, ecological and sociocultural factors were modelled with chi‐squared and logistic regression methods. The predominant species were A. flavus L‐strain (78% incidence), A. flavus S‐strain (68%) and A. niger (65%). Occurrence of A. caelatus, A. alliaceus and A. tamarii in Kenya was also documented. Samples from the Busia district were three times (odds ratio = 3·01) as likely to contain ≥10 μg kg^?1 of total aflatoxin as were samples from the Homa bay district, while samples containing A. flavus S‐strain were 96% more likely to exceed this threshold compared with samples from which this fungus was not isolated. Grading, planting improved cultivars and membership of a producer marketing group were negatively associated with the incidence of A. flavus, while crop rotation was negatively correlated with the incidence of B aflatoxins. These sociocultural factors can be modified to reduce the risk of peanut contamination with aflatoxin.     

Description of a strain from an atypical population of Aspergillus parasiticus that produces aflatoxins B only,and the impact of temperature on fungal growth and mycotoxin production

In this study, an atypical strain of Aspergillus parasiticus is described. This strain, reported from Portuguese almonds, was named Aspergillus parasiticus B strain. The strain is herein characterised at the morphological and physiological levels, and compared with the typical A. parasiticus strain and other similar species in section Flavi. Previously published morphological and molecular data support that the B strain is very closely related to the A. parasiticus type strain. However, while A. parasiticus typically produces aflatoxins B and G, B strain produces aflatoxins B only. Furthermore, this atypical strain showed to differ from the typical strain in the fact that higher growth (colony diameter) and aflatoxin B1 production were observed at 25?ºC than at 30?ºC, whereas the opposite was observed for the typical strain. This strain can become a major food safety concern in colder regions where the typical A. parasiticus strains are not well adapted.     

Pod wart disease of peanuts

Peanut pod wart, a relatively new disease to peanut culture, was first reported in Israel in 1988 attacking peanut plants and causing dark warts on the pod. The causal agents are variousStreptomyces spp. Scanning electron microscopy showed a significant difference between healthy and diseased tissues of the exocarp and mesocarp layers of the pod; there were no effects on the endocarp layer. The mesocarp cells of infected tissue were smaller and more compressed than those of healthy tissue. In most cases two cells under the peak of the wart were extremely large and the cells growing from them toward the surface were uneven, forming the shape of a fan. The pathogen could be isolated from the soil and rhizosphere, but in the pod it was found only in the waited tissue. The microorganisms isolated from the warts belong to different groups ofStreptomyces spp.; subsequent pathogenicity tests proved their virulence to a limited host range. In potato, these isolates ofStreptomyces spp. caused deep pitted scab; in peanuts they caused warts. Peanut seeds which developed in infected pods were free of the pathogen if the shell was undamaged. However, the pathogen is surface seedborne, and contaminated seeds during the mechanical cracking process.     

不同轮作模式对花生病虫害及产量的影响

为探明水旱轮作模式对花生土传病虫害及其产量的影响,设水旱轮作不施药、水旱轮作减施药、旱旱轮作常规施药和旱旱轮作不施药(CK)4种处理,于2014—2016年对花生果腐病、白绢病和蛴螬虫害的发生情况进行调查,并对花生产量及其构成因素进行考种分析。结果表明,水旱轮作不施药处理的花生果腐病病情指数和发病率分别较CK显著降低90.40%和96.55%,防控效果达96.34%;水旱轮作减施药处理对花生果腐病的防控效果为81.49%;旱旱轮作常规施药处理对花生果腐病无防控效果。水旱轮作和旱旱轮作常规施药处理对白绢病均无防控效果。水旱轮作不施药、水旱轮作减施药和旱旱轮作常规施药处理对蛴螬的防控效果分别为63.80%、65.50%和66.20%。水旱轮作不施药与旱旱轮作常规施药处理相比,株结果数、株果重和产量分别显著降低15.03%、12.14%和6.33%,株饱果数和出仁率分别显著提高13.88%和3.01%,株根瘤个数显著提高166.22%;水旱轮作减施药与旱旱轮作常规施药处理相比,株结果数、株果重、产量、百仁重和出仁率均无显著差异,株饱果数显著提高14.33%,株根瘤个数显著提高122.97%。表明水旱轮作模式对花生果腐病和蛴螬有较理想的防控效果,且使花生产量结构明显优化,根瘤菌数量显著提高。     

四粒红花生物料特性试验与测定

以新疆中西部地区林果套种模式下的‘四粒红’花生为研究对象,在田间调研的基础上,应用微控电子万能试验机、MS-70红外线水分测定仪和ZRQF-F30J手持式数显热球风速计等试验设备,研究花生在挖掘铺放晾晒过程中含水率,秧柄节点、果柄节点与果柄拉伸力,花生荚果破碎力以及花生荚果、茎秆和叶片在不同含水率下的风力悬浮速度范围。本研究初步确定了最佳的收获时间为花生晾晒后5～7 d,此时花生秧蔓、果柄、花生荚果的含水率分别为34.5%降至24.0%、22.0%降至16.0%、14.0%降至9.0%,果柄、秧柄节点、果柄节点的拉伸力分别为14.95～15.10、12.50～12.90、8.45～8.60 N,花生荚果侧面、荚果正面、荚果立面破碎力分别为45.0 N降至41.0 N、86.5 N降至70.3 N、42.0 N降至36.1 N,花生荚果、茎秆、花生叶片的风力悬浮速度分别为5.82～6.97、2.43～2.77、1.97～2.44 m·s^-1,研究结果为后续花生收获机械设计、研制提供参考。     

Cloning and characterization of an NBS-LRR resistance gene from peanuts (Arachis hypogaea L.)

The nucleotide-binding site (NBS)-leucine-rich repeat (LRR) gene family accounts for the largest number of known disease resistance genes and is one of the largest gene families in plant genomes. In this study, resistance gene analogs (RGAs) were isolated from peanuts based on the NBS domain. A full-length cDNA, PnAG₃, was obtained by rapid amplification of cDNA ends (RACE). Sequence analysis indicated that the length of PnAG₃ was 1882 bp, which included a complete open reading frame of 1335 bp that encoded for the PnAG₃ protein composed of 444 amino acids. Multiple analyses showed that this protein had homology with known resistance proteins, the highest being 48.01% with a resistance protein from Arachis cardenasii. The polypeptide has a typical non-TIR-NBS-LRR gene structure. Real-time fluorescence quantitative PCR analysis showed that after Aspergillus flavus infection, expression of the PnAG₃ gene in J11 (A. flavus-resistant species) increased by 16.68, 11.16 and 25.96 in the seed coat, kernel and pericarp, respectively. However, it only increased 2–3 times in JH1012 (A. flavus-sensitive species). Cloning of the putative resistance gene from peanut provides a basis for studying the structure and function of peanut disease resistance-related genes and disease resistance genetic breeding in peanuts.     

Period of susceptibility of almonds to aflatoxin contamination during development in the orchard

Almonds can be contaminated with aflatoxins, produced mainly by Aspergillus flavus and A. parasiticus. Infection can be facilitated by insect injuries during hull split, which begins four to six weeks before harvest. Within this period, it is unknown which kernel stages are most susceptible to aflatoxin contamination. Developing almonds of the Nonpareil cultivar were inoculated weekly with a spore suspension of A. flavus or A. parasiticus for five weeks after hull split in 2013. The almonds were infested with eggs of the lepidopteron navel orangeworm (NOW) (Amyelois transitella) before each spore inoculation. Aflatoxin levels were quantified at harvest using HPLC. Aflatoxin contamination was consistently higher in NOW-damaged kernels, although aflatoxins were also detected in undamaged kernels at each inoculation date. Insect injury is not required for kernel infection but it is a key risk factor for high aflatoxin contamination. Laboratory inoculations were also performed on Nonpareil almond kernels collected during the summers of 2013 and 2015. Aflatoxin levels were significantly lower on dried almonds but the ability to produce aflatoxins was restored when almonds were incubated with high humidity or when the Aspergillus species were inoculated on almond meal agar amended with ground kernels. Therefore, aflatoxins can accumulate in kernels with low a_w, should sufficient moisture favors aflatoxin production. In our field experiment, the orchard micro-climate had sufficient humidity to enable aflatoxin production in both damaged and undamaged dried kernels.     

Infection process of Stagonosporopsis tanaceti in pyrethrum seed and seedlings

Ray blight disease of pyrethrum (Tanacetum cinerariifolium) is caused by Stagonosporopsis tanaceti, with infected seed being a major means of transmission of this fungal pathogen. The infection process of S. tanaceti in pyrethrum seed and seedlings was determined. Infection hyphae only infected the outer and inner layers of the seed coat and not the embryo of naturally infected pyrethrum seed. During the process of germination of infected seed, S. tanaceti from the seed coat infected the developing embryo and cotyledon, resulting in pre‐ and post‐emergence death, depending on the level of infection in the seed coat. Pre‐emergence death occurred due to disintegration of the infected embryo, which was replaced by hyphae and extracellular anthocyanin‐like material (EAM) at 7 days after incubation (dai). Post‐emergence death occurred after both epidermal and cortical tissues of infected cotyledons at the crown/hypocotyl region disintegrated due to colonization by hyphae. Moreover, most of the tissues of the vascular bundles and cortical tissues contained heavy depositions of EAM at 10–14 dai. In 6‐week‐old infected seedlings, hyphae were confined to the epidermis and the cortical tissues at the crown/hypocotyl regions; the vascular bundles of both infected and uninfected regions, and cortical tissues of the uninfected regions of the seedlings were completely free from infection hyphae and EAM. These findings provide a better understanding of the early stages of the disease cycle of S. tanaceti and will lead to improved control measures for seedborne infection using seed treatments.     

球毛壳ND35菌株在宿主植物上的侵染定殖

为了解球毛壳Chaetomium globosum ND35菌株在宿主植物上的侵染定殖方式和途径,以毛白杨组培苗为宿主植物,借助光学显微镜、扫描电镜、透射电镜,结合免疫荧光标记技术,研究了球毛壳ND35菌株子囊孢子萌发后在毛白杨上的侵染行为及其菌丝在组培苗根部的定殖。结果显示,子囊孢子萌发后形成的菌丝,能从杨树苗根、茎部表面细胞间的缝隙侵入或在根表面形成附着胞,进而形成侵染钉直接从表皮细胞侵入,在叶部主要从气孔侵入叶片内部。侵入根部的菌丝主要定殖于表皮细胞、外皮层细胞和细胞间隙,未进入内皮层和维管束组织。     

Plasmodiophora brassicae -induced expression of pyk20, an Arabidopsis thaliana gene with glutamine-rich domain

The expression of the pyk20 gene of Arabidopsis thaliana, which encodes a protein containing a glutamine-rich domain is up-regulated during Plasmodiophora brassicae infection. Transgenic A. thaliana plants harbouring a β-glucuronidase (uid A) reporter gene under the control of the pyk20 gene promoter were grown in soil and infected with P. brassicae resting spores. GUS expression in non-infected plants was found in stipules, apical meristem, leaf vascular tissues, vascular tissue of roots and in the root tips. After infection with P. brassicae, GUS staining was observed in the root hairs during primary infection and in galls in roots and hypocotyls during secondary infection phase. GUS expression during primary infection was also detected in a small number (approx. 0.01%) of zoosporangia. Sections of the GUS-stained galls showed reporter gene expression in infected and non-infected tissues. Northern-blot analysis using a pyk20 cDNA clone as a probe confirmed responsiveness of the pyk20 gene to P. brassicae infection.     

Surface characteristics of necrotrophic secondary hyphae produced by the bean anthracnose fungus, Colletotrichum lindemuthianum

During infection of bean (Phaseolus vulgaris), the hemibiotrophic anthracnose pathogen, Colletotrichum lindemuthianum, initially produces biotrophic primary hyphae that are large-diameter and entirely intracellular, followed by necrotrophic secondary hyphae that are narrower and either intercellular or intracellular. In the present study, transmission electron microscopy of infected tissues prepared by high-pressure freezing and freeze-substitution showed that secondary hyphae have much thinner cell walls (25–40 nm) than primary hyphae (100–130 nm) and are not surrounded by an extracellular matrix. Immunofluorescence labelling with a panel of monoclonal antibodies showed that glycoproteins which are present on conidia, germ-tubes, appressoria, primary hyphae and mycelium grown in vitro are absent from the surface of secondary hyphae. Chitin, detected with the lectin wheat germ agglutinin, was the only surface component shared by secondary hyphae and the other fungal cell types. The results suggest that the fungal cell surface becomes modified during necrotrophic growth, with none of the glycoproteins associated with earlier stages of the infection process being produced.     

Epidemiology of dark leaf spot caused by Alternaria brassicicola and A. brassicae in organic seed production of cauliflower

In organic seed production of Brassica vegetables, infections by Alternaria brassicicola and A. brassicae can cause severe losses of yield and seed quality. Four field experiments with or without artificial inoculation with A. brassicicola were conducted in organically managed seed‐production crops of cauliflower cv. Opaal RZ in 2005 and 2006 in the Netherlands. The development of A. brassicicola and A. brassicae on pod tissues and developing seeds was followed and seed quality was assessed. Alternaria brassicicola was externally present on 1·2% of the seeds 14 days after flowering and observed internally within 4 weeks after flowering. In both seasons, seed colonization by the pathogen increased slowly until maturation but sharply increased during maturation. A similar pattern was found for the colonization of pod tissues by A. brassicicola as quantified by TaqMan‐PCR. The incidence of A. brassicicola on mature seeds reached 70–90%. Internal colonization was found for 62–80% of the seeds. External and internal seed colonization by A. brassicae was much lower, with incidences below 3%. The quality of harvested seeds was generally low, with less than 80% of seeds able to germinate. Seed quality was not affected by warm water treatments. It was concluded that A. brassicicola and A. brassicae have the potential to infect pods and seeds soon after flowering. For the production of high quality seeds, producers must prevent such early infections. Therefore, new control measures are needed for use in organic cropping systems.     

An Efficient Inoculation Method for Colonization of Chinese Cabbage Seedlings by the Root Endophytic Fungus Heteroconium chaetospira

To develop an efficient method to inoculate Chinese cabbage seedlings with the root endophytic fungus Heteroconium chaetospira, an appropriate nursery soil and glucose concentration for the nutrient medium for fungal colonization were determined. A grid-sheet method was established for estimating the degree of colonization of entire roots by the fungus. The fungus colonized at high frequencies when peat moss was used as the rooting medium. Colonization was highest (75%) when peat moss was amended with 0.1% glucose. Under these conditions, fungal hyphae developed intracellularly in root cortical cells. In contrast, under high glucose conditions, fungal colonization was restricted mostly to intercellular regions of epidermal or cortical root tissues. Here, hyphae formed inter- or intracellular microsclerotia. Received 19 August 2002/ Accepted in revised form 5 December 2002     

Use of Fusarium graminearum transformed with gfp to follow infection patterns in barley and Arabidopsis

The fungal pathogen Fusarium graminearum attacks the seed spikes of barley and wheat, causing sterility, reduced seed weight and accumulation of mycotoxins. To explore infection patterns in barley and in the Arabidopsis model system, the green fluorescent protein gene (gfp) was used to transform F. graminearum. Inoculation of intact barley spikes resulted in rapid colonization of the brush hairs (ovary epithelial hairs) at the extruded seed tip within 7 h. Colonization followed a pattern of rapid basipetal growth along the pericarp epithelium (interior to the lemma and palea), accompanied by slower growth inward through the pericarp and testa. However, at 16 days after infection the aleurone and starchy endosperm remained uninfected, despite heavy colonization of the pericarp. Colonization of the outer lemma also occurred but was much slower. No increase in amylase enzyme activities was found, discounting the possibility that F. graminearum utilizes gibberellin-induced host enzymes to tap the endosperm for nutrients. The transformed Fusarium strain readily infected Arabidopsis thaliana leaves and produced copious spores within distant leaves. Results show the utility of gfp in tracing the growth of this pathogen, without misinterpretation due to contaminating fungi, and for resistance studies utilizing the Arabidopsis model system.     

Infection of wheat spikes by <Emphasis Type="Italic">Fusarium avenaceum</Emphasis> and alterations of cell wall components in the infected tissue

The infection process of Fusarium avenaceum on wheat spikes and the alteration of cell wall components in the infected host tissue were examined by means of electron microscopy and cytochemical labelling techniques following spray inoculation at growth stage (GS) 65 (mid-flowering). Macroconidia of the pathogen germinated with one to several germ-tubes 6–12 h after inoculation (hai) on host surfaces. The germ-tubes did not penetrate host tissues immediately, but extended and branched on the host surfaces. Hyphal growth on abaxial surfaces of the glume, lemma and palea was scanty 3–4 days after inoculation (dai) and no direct penetration of the outer surfaces of the spikelet was observed. Dense mycelial networks formed on the inner surfaces of the glume, lemma, palea and ovary 36–48 hai. Penetration of the host tissue occurred 36 hai by infection hyphae only on the adaxial surfaces of the glume, lemma, palea and upper part of ovary. The fungus penetrated the cuticle and hyphae extended subcuticularly or between the epidermal wall layers. The subcuticular growth phase was followed by penetration of the epidermal wall, and hyphae spread rapidly inter- and intracellularly in the glume, lemma, palea and ovary. During this necrotrophic colonization phase of the wheat spike, a series of alterations occurred in the host tissues, such as degeneration of cytoplasm and cell organelles, collapse of host cells and disintegration of host cell walls. Immunogold labelling techniques showed that cell walls of spike tissues contained reduced amounts of cellulose, xylan and pectin near intercellular hyphae or infection pegs compared to walls of healthy host tissues. These studies suggest that cell wall degrading enzymes produced by F. avenaceum facilitated rapid colonization of wheat spikes. The different penetration properties of abaxial and adaxial surfaces of the spikelet tissues as well as the two distinct colonization strategies of host tissues by F. avenaceum are discussed. The penetration and colonization behaviour of F. avenaceum in wheat spikelets resembled that of F. culmorum and F. graminearum, although mycotoxins produced by F. avenaceum differed from those of the latter two Fusarium species.     

Effects of some commercial herbicides on rhizobia and their symbiosis with peanuts

Four herbicides commonly used in Israel for controlling weeds in peanuts were evaluated under field and screenhouse conditions. Terbutryn (Terbutrex 50, w.p.), ethalfluralin (Sonalan 333, e.c.), dinitramine (Cobex 240, e.c.) and alachlor (Alapaz 480, e.c.), used at recommended levels, had no adverse effect on nodulation rate, nitrogenase activity, total nitrogen of peanut tops or pod yield, compared with control (inoculated but herbicide non-treated) plants. Studies were conducted to determine the relative toxicity in vitro of the herbicides on each of four Rhizobium strains used for commercial peat inoculant production. The results showed that at up to 94 μg g^?1 the herbicides has no inhibitory effect on the growth of rhizobia. The sensitivity of Rhizobium strains to different rates of the chemicals decreased in the order: dinitramine>alachlor>ethalfluralin>terbutryn. It was found that various strains differ in their sensitivity to the herbicides tested.     

Efficacy of certain agrochemicals on Aspergillus spp. and subsequent aflatoxin production in rice

Efficacy of certain fungicides and non-conventional chemicals against Aspergillus spp. contamination and subsequent aflatoxin production in rice was investigated. Among the 10 fungicides tested, carbendazim, contaf plus, folicur, propiconazole and saaf completely inhibited the growth of all Aspergillus spp. and aflatoxin B₁ (AFB1) production at 1 g or ml/kg concentration. Of the five non-conventional chemicals tested, benzoic acid effectively inhibited the mycelial growth of Aspergillus flavus (72%) at 4 g/kg, completely inhibited the Aspergillus parasiticus and Aspergillus niger even at 1 g/kg and Aspergillus ochraceus at 4 g/kg concentration. Vanillin completely reduced the AFB1 production at 4 g/kg of seed followed by sodium chloride with out inhibiting the mycelial growth. This study reveals that fungicides and non-conventional chemicals had effectively inhibited the mycelial growth of Aspergillus spp. and AFB1 production in rice.     

Local infection associated with vascular bundles: the colonization of coconut palm leaflets by two <Emphasis Type="Italic">Camarotella</Emphasis> species

Two Camarotella (Phyllachoraceae) species, C. torrendiella and C. acrocomiae are the causative agents of small (SV) and large verrucosis (LV), respectively, which are important diseases affecting Brazilian coconut palms. The small verrucosis produces necrotic lesions in coconut palm leaflets, whereas LV just produces chlorosis. Semi-thin sections of asymptomatic leaflets and of leaves presenting stromata in different development stages were compared through light microscopy in order to characterize the colonization process of these two coconut palm verrucosis agents. Camarotella torrendiella initially colonized the adaxial epidermal cells and the cells underlying the epidermis close to the vascular bundles. In latter colonization stages, the hyphae of C. torrendiella remained limited to the underlying necrotic tissue adjacent to the mature stromata, mostly in the intracellular spaces and in the collapsing cells of necrotized tissues around the vascular bundles. This species does not colonize intracellular intact fiber cells, xylem vessels or phloem sieve tube elements. In contrast, C. acrocomiae presented a typical biotrophic parasitism model such as that of some gramineous Phyllachora spp. High densities of C. acrocomiae hyphae were found inside intact sieve tube elements; however, with no evidence of cellular death. The extensive hyphal colonization by C. acrocomiae within sieve tube elements was also observed in tertiary and quaternary bundles, as well as in anastomosing vascular bundles. The dependence of both species on the colonization sites associated with vascular bundles indicates the need for additional studies about these intricate host-pathogen relationships. These studies could be important to define new strategies to control coconut palm verrucosis diseases.