Development and characterization of EST-derived SSR markers in the cereal cyst nematode <Emphasis Type="BoldItalic">Heterodera avenae</Emphasis>

The cereal cyst nematode Heterodera avenae is a pathogen of cereal crops and causes high yield losses worldwide. In this study, a collection of 37,348 expressed sequence tags (ESTs) of H. avenae was mined for EST-based simple sequence repeat (SSR) markers, which resulted in the identification of 5604 SSRs. A total of 210 pairs of SSR primers were further developed and used for validation of the amplification rate and assessment of the polymorphism. Eight SSR markers were finally identified and analyzed using 96 individual cysts of H. avenae sampled from three provinces in China. These loci were found to be moderately polymorphic with 3–8 alleles per locus. The observed and expected heterozygosity across the three populations ranged from 0.000 to 0.594 and from 0.000 to 0.731, respectively. The polymorphism information content (PIC) was medium and ranged from 0.080 to 0.562, with a mean of 0.409. The F _ST ranged from 0.1034 to 0.1550, indicating moderate genetic differentiation among the three H. avenae populations. These EST-SSR markers can be used to study population genetic diversity and the dispersal route of H. avenae in China.     

Cereal diseases caused by <Emphasis Type="Italic">Fusarium graminearum</Emphasis>: from biology of the pathogen to oxidative burst-related host defense responses

Small grain cereals, such as wheat, barley and oats are considered among the most important food sources. Plant-parasitic nematodes play a considerable role in decreasing cereal yields. The three-major species of cereal cyst nematodes (CCN) Heterodera avenae, H. latipons, and H. filipjevi are distributed worldwide and cause considerable damage. This review provides information regarding the global distribution of these nematode species, yield loss due to CCN, their biology and pathogenic relation to plants, identification and control through agricultural practices, biological agents and resistance breeding. As morphological identification of CCN is difficult and time-consuming, several molecular techniques for the identification of these CCN species have been developed in recent years. The restrictions on the use of nematicides demand for resistance to CCN. Resistance genes in several lines are known and are used in numerous breeding programmes against CCN; pyramiding these resistance genes into high yielding cultivars that could become commercially available for farmers is progressing.     

Presence of less-preferred hosts of the aphid parasitoids <Emphasis Type="Italic">Aphidius ervi</Emphasis> and <Emphasis Type="Italic">Praon volucre</Emphasis> reduces parasitism efficiency

Parasitoids are characterized by a defined range of hosts, either more specialist or generalist. Under natural conditions, females may encounter different host species on the same plant or in the same location. In this case, their preference for one host could influence their choice. However, the presence of less suitable hosts may also affect their choice and, in some cases, may reduce their interest in a patch where both preferred and less preferred hosts are available. The aim of the present study was to test the consequences of the simultaneous presence of three cereal aphids (Sitobion avenae Fabricius, Metopolophium dirhodum Walker, and Rhopalosiphum padi Linnaeus) on the parasitism by two of their parasitoids, Aphidius ervi Haliday and Praon volucre Haliday. Firstly, in the no-choice experiment, A. ervi parasitized on S. avenae at a significantly higher rate as compared to M. dirhodum, whereas no parasitism on R. padi was observed. P. volucre parasitized the three species of cereal aphids with a significant preference for S. avenae. Interestingly, when two or three host species were offered simultaneously in the same quantity to pairs of parasitoids, the level of parasitism was less than that observed for one host species alone. This observation exhibits a distractive effect on non-host species, from the defense mechanism of a non-suitable host or from the perception of bad quality patches. These results raise the question of the practical application of inundative release of parasitoids for biocontrol when several hosts are available simultaneously.     

Identification of <Emphasis Type="Italic">Globodera rostochiensis</Emphasis> and <Emphasis Type="Italic">G. pallida</Emphasis> in the Ukraine by PCR

Multiplex polymerase chain reaction was used to identify the potato cyst nematodes in soil samples from the Ukraine. The results show the occurrence of Globodera pallida in the Uzhhorod region (Zakarpatska oblast), where only G. rostochiensis had been previously reported. In the mixed potato cyst nematode (PCN) populations, G. pallida was less prevalent (2–5%) than G. rostochiensis (95–98%). A phylogenetic analysis based on ribosomal DNA internal transcribed spacer sequences showed that the Ukrainian population of G. pallida had >99% sequence identity with other G. pallida pa2/3 isolates from Europe. This study has demonstrated that polymerase chain reaction-mediated amplification of specific regions of the potato cyst nematode genome is not only highly effective as a species diagnostic tool but is also a sensitive method which can be used for taxonomic purposes with cyst collections which vary in age.     

Potential impacts of climate change on the threat of potato cyst nematode species in Great Britain

Potato cyst nematode (PCN) species have different temperature optima for various life cycle stages, therefore a risk assessment of the threat of PCN species under future climates is essential to guide adaptation strategies. Data defining the spatial coverage of potato crops in Great Britain were combined with probabilistic climate change data and a newly developed PCN life cycle model to project the future risk to potato crops from PCN. The model was based on the results of controlled environment experiments to investigate the effect of temperature on survival to female maturity using three PCN populations: Globodera pallida (Lindley) and G. rostochiensis from the James Hutton Institute PCN collection, and a field population of G. pallida (S‐Fife). It was found that projected increases in soil temperature could result in increased survival to female maturity for all three PCN populations, with greater increases expected for Scotland, followed by Wales then England. The largest projected increases in Scotland were for G. pallida, whereas G. rostochiensis showed the largest increases in Wales and England. The potential impact of several agronomic adaptation strategies on projected PCN risk were also investigated. The results from the model suggest that soil infestation levels would have to be reduced by up to 40% in order to negate projected increases in PCN risk, and that advancing the start date of the growing season or modifying planting patterns could be successful strategies to reduce future PCN risk.     

Managing potato cyst nematodes to minimize nematicide use1

Potato cyst nematodes (PCN), Globodera rostochiensis and G. pallida, are widespread in the ware potato-growing areas of the UK. Traditionally they were controlled by rotation but more intensive production methods have increased the PCN threat, especially from G. pallida. G. rosrochiensis has become less important since cultivars fully resistant to it were introduced but, where both species are present in a mixture, the G. pallida portion comes to dominate. It is possible to control G. pallida as effectively as G. rostochiensis if cultivars partially resistant to G. pallida are grown with nematicide treatment. Where nematicide is not used, control of G. pallida is more variable. In some years, some cultivars achieve good control but the results are not consistent. In general, G. pallida has increased on untreated plots about 5-fold in trials in the last 3 years.     

Host-suitability of black medick (<Emphasis Type="Italic">Medicago lupulina</Emphasis> L.) and additional molecular markers for identification of the pea cyst nematode <Emphasis Type="Italic">Heterodera goettingiana</Emphasis>

A survey was conducted in 16 fields cultivated with broad bean (Vicia faba L.) and garden pea (Pisum sativum L.) in nine localities of Apulia, southern Italy, to determine whether annual weeds were susceptible to the pea cyst nematode (PEACN), Heterodera goettingiana, and could therefore serve as alternate host for the nematode. The results of this study showed that black medick (Medicago lupulina L.) is a good host for the nematode increasing its population levels in the soil in the absence of the primary hosts. The identity of the PEACN was confirmed by integrative taxonomic approaches (classical, and molecular), resulting identical in all cases (broad bean and garden pea, as well as the spontaneous black medick infections). The phylogenetic analyses using ITS and coxI gene regions strongly support the identification of the populations of H. goettingiana from Italy. Also, ITS and coxI gene sequences were obtained from the same cyst, confirming the species identity in comparison to other nematodes and populations in the Goettingiana group, demonstrating that ITS and coxI gene regions of the PEACN are suitable molecular markers for accurate and unequivocal identification of the PEACN. Reproduction and histopathological analyses demonstrated a good host-suitability of black medick to the PEACN. This record enlarges the relatively narrow host-range of the pea cyst nematode and indicates the need to control M. lupulina to avoid the increase of the nematode population in the absence of the main host crop.     

Consistent action of two partially effective loci conferring resistance to Globodera pallida Pa2/3 across multiple nematode field populations

The potato cyst nematodes (PCN) Globodera rostochiensis and Globodera pallida are significant pests of potatoes worldwide. The most effective control methods are crop rotation and the deployment of resistant varieties. Complete resistance to G. rostochiensis based on a single resistance gene has successfully been integrated into many varieties. However, resistance to G. pallida has not been as successful to date, with current varieties only exhibiting partial resistance. Combining partially effective quantitative trait loci (QTLs) for resistance can increase the strength and breadth of the resistance. An additive effect on resistance has previously been demonstrated on combining two QTLs from Solanum tuberosum subsp. andigena (GpaIV^s_adg) and Solanum vernei (Gpa5). However, populations of G. pallida can be quite divergent and it was unclear whether the relative effects of the individual QTLs and the combined additive effect would be consistent across different G. pallida Pa2/3 populations. Using a mapping population segregating for both QTLs, the effect of the QTLs individually and combined was examined on four UK‐derived field populations of G. pallida pathotype Pa2/3, and the relative effects of the individual QTLs and the additive effect of the combination found to be consistent across all populations.     

Distribution and characterization of Dothistroma needle blight pathogens on <Emphasis Type="Italic">Pinus mugo</Emphasis> in Slovakia

The occurrence and distribution of Dothistroma needle blight (DNB) on Pinus mugo was studied in 2014–2015 around the Slovakia. In total, 42 localities were investigated both native and planted ones. Symptoms of DNB were observed on 35 localities only on planted shrubs. All these 35 localities are new P. mugo DNB stands. No DNB symptoms were observed in natural and naturally regenerated plantations. DNA was extracted from a total of 236 isolates and eight needle samples. Based on the ITS-rDNA comparisons and using species specific primers, both pathogenic Dothistroma species were detected: D. septosporum and D. pini. Isolates of D. septosporum had ITS sequences identical to D. septosporum from Europe and both mating types were identified with slight predominance of MAT2. The ratio of D. septosporum mating types varies significantly between sites, ranging from an equal proportion of each mating type to single mating type populations. D. pini ITS sequence grouped with D. pini from Ukraine, Russia and Switzerland and only MAT2 was found.     

PM 7/40(2): Globodera rostochiensis and Globodera pallida

Specific scope

This standard describes a diagnostic protocol for Globodera rostochiensis and Globodera pallida ¹ 1 Use of brand names of chemicals or equipment in these EPPO Standards implies no approval of them to the exclusion of others that may also be suitable.
.

Specific approval and amendment

This Standard was developed under the EU DIAGPRO Project (SMT 4‐CT98‐2252) by partnership of contractor laboratories and intercomparison laboratories in European countries. Approved as an EPPO Standard in 2003–09. Revision approved in 2009–09.

     

Integrative diagnosis of carrot cyst nematode (<Emphasis Type="Italic">Heterodera carotae</Emphasis>) using morphology and several molecular markers for an accurate identification

Cyst nematodes obtained from commercial carrot fields in Ontario (Canada) and northern and southern Italy were subjected to morphological and molecular examination. Morphology of cyst cone tops, males and second-stage juveniles (J2) indicated the nematode species was the Carrot Cyst Nematode (CaCN), Heterodera carotae. The sequence of the Internal Transcribed Spacer (ITS), D2-D3 region of the 28S gene of ribosomal RNA, cytochrome oxidase I of mitochondrial DNA (coxI), and a heat shock protein gene (hsp90), from single cysts were also examined. Sequences of ITS and D2-D3 placed all the nematodes with Heterodera carotae and other Heterodera spp. belonging to the Goettingiana group in the same clade. The novel nine coxI sequences obtained also clustered in a well-supported phylogenetic clade for H. carotae. Similarly, the six new hsp90 sequences of H. carotae generated in this study were placed in a well-supported clade (PP = 1.00) together with other two sequences of H. carotae from Greece. Restriction Fragment Length Polymorphism (RFLP) of ITS-PCR products gave a restriction pattern for RsaI different than H. carotae but the other 6 restriction patterns were similar as described in former research. A diagnostic conventional PCR method was developed based on a primer set to be specific for H. carotae using coxI sequence. These primers were also used in real time PCR to generate a melt curve specific to H. carotae. Limit of detection for CaCN in conventional PCR reaction was a single J2.     

Population differentiation of <Emphasis Type="Italic">Puccinia coronata</Emphasis> between hosts –implications for the epidemiology of oat crown rust

The fungus Puccinia coronata Corda. is the causal agent of crown rust on oats (Avena sativa) and grasses and the disease is a major problem in oat production causing devastating yield losses. The population biology of P. coronata in oat fields and on the aecial host in central Sweden was studied to get a deeper understanding of the role of the aecial hosts in the epidemiology of the disease. Samples were collected from the aecial hosts common buckthorn (Rhamnus cathartica) and alder buckthorn (Frangula alnus), and three adjacent spring oat (Avena sativa) fields. Microsatellite markers were used to evaluate the relationships between populations sampled from the different hosts. According to our results F. alnus can be excluded as a part of the oat crown rust disease cycle. The results further show that samples collected from the aecial host were genetically separate from the population sampled in adjacent oat fields. Concurrently, the genotypic variation of P. coronata observed within oat fields was high. No population differentiation was observed within or between samples collected from different fields within the region, suggesting that airborne spores from other than the sampled specimens of the aecial hosts were contributing to the genetic diversity of P. coronata f. sp. avenae in the selected oat fields.     

Genetic structure of <Emphasis Type="Italic">Pyrenophora teres</Emphasis> f. <Emphasis Type="Italic">teres</Emphasis> and <Emphasis Type="Italic">P. teres</Emphasis> f. <Emphasis Type="Italic">maculata</Emphasis> populations from western Canada

Infection by Pyrenophora teres f. teres (Ptt) or P. teres f. maculata (Ptm), the causal agents of the net and spot forms of net blotch of barley, respectively, can result in significant yield losses. The genetic structure of a collection of 128 Ptt and 92 Ptm isolates from the western Canadian provinces of Alberta (55 Ptt, 27 Ptm), Saskatchewan (58 Ptt, 46 Ptm) and Manitoba (15 Ptt, 19 Ptm) were analyzed by simple sequence repeat (SSR) marker analysis. Thirteen SSR loci were examined and found to be polymorphic within both Ptt and Ptm populations. In total, 110 distinct alleles were identified, with 19 of these shared between Ptt and Ptm, 75 specific to Ptt, and 16 specific to Ptm. Genotypic diversity was relatively high, with a clonal fraction of approximately 10 % within Ptt and Ptm populations. Significant genetic differentiation (PhiPT = 0.230, P = 0.001) was found among all populations; 77 % of genetic variation occurred within populations and 23 % between populations. Lower, but still significant genetic differentiation (PhiPT = 0.038, P = 0.001) was detected in Ptt, with 96 % of genetic variation occurring within populations. No significant genetic differentiation (PhiPT = 0.010, P = 0.177) was observed among Ptm populations. Isolates clustered in two distinct groups conforming to Ptt or Ptm, with no intermediate cluster. The high number of haplotypes observed, combined with an equal mating type ratio for both forms of the fungus, suggests that P. teres goes through regular cycles of sexual recombination in western Canada.     

The use of isoelectric focusing as a tool in the identification and management of potato cyst nematode populations1

Isoelectric focusing on thin layers of polyacrylamide or agarose gels may be used to separate proteins from the potato cyst nematodes Globodera rostochiensis and G. pallida. General protein patterns may be used to identify the two species, even from single cysts. Densitometry of species-specific protein bands may be used to assess the proportions of G. rostochiensis and G. pallida in potato cyst nematode samples. Staining for the enzymes phosphoglucomutase and phosphoglucose isomerase also revealed species-specific patterns, and variation among G. pallida populations was observed. Thus calculations of coefficients of similarity based on six enzymes, phosphoglucose isomerase, phosphoglucomutase, glycerol-3-phosphate dehydrogenase, enolase, hexokinase and malate dehydrogenase and the construction of a dendrogram for several Northern Ireland populations indicated clear separations between G. pallida (Pa1), G. pallida (Pa3) and G. rostochiensis (Ro1). The use of the technique of isoelectric focusing as a routine research and advisory tool in nematology, and as a means of further understanding the genetic basis of pathotype schemes, is discussed.     

Characterization of virulence reactions for Heterodera avenae populations from two localities in Algeria

Heterodera avenae is widely distributed in areas where most cereal crops are produced in Algeria. However, the virulence of the Algerian populations of this nematode on individual cereal species and cultivars has not been well documented. The virulence of H. avenae populations from Tiaret and from Oued Smar were tested under natural outdoor conditions and in an in vitro test to determine reactions of nine barley, oat and wheat cultivars selected from the International differential assortment for identifying pathotypes of H. avenae. All nine cereal differentials expressed the same reactions to both populations. The nematodes reproduced well on the barley cultivar ‘Emir’ and the wheat cultivar ‘Capa’. Resistant entries included the barley cultivars ‘Siri’, ‘Ortolan’ and ‘Morocco’, the oat cultivars ‘Nidar II’ and ‘A. sterilis I.376’, and the wheat cultivars ‘Loros’ and ‘AUS10894’. This matrix of reactions indicated that H. avenae populations from both locations were characterized as H. avenae Group 1 pathotypes but did not conclusively distinguish among pathotypes Ha21, Ha31 or Ha81. The Cre1 gene was identified as a potentially valuable source of resistance when developing wheat cultivars intended for release into these localities.     

Quantification of Globodera rostochiensis and G. pallida in mixed populations using species-specific thermostable proteins

A method has been developed to quantify species ratios in mixed populations. The method is based on the separation of species-specific thermostable proteins by SDS-PAGE. Densitometric analyses of the 17 kD protein ofGlobodera pallida and the 18 kD protein ofG. rostochiensis revealed a high correlation (R ²=0.93) with the species ratio in the mixed samples. Within the limits of 10 to 90% of each species, one can estimate with 95% reliability the species composition with 3 to 6% deviation.Samenvatting Een methode is ontwikkeld om de samenstelling van soortenmengsels vanGlobodera rostochiensis enG. pallida te kwantificeren. Bij deze methode wordt gebruik gemaakt van de soort-specifieke thermostabiele eiwitten die met behulp van SDS-PAGE gescheiden worden. De kleurintensiteit van het 17 kD eiwit vanG. pallida en het 18 kD eiwit vanG. rostochiensis is per gel-laan bepaald m.b.v. een densitometer en heeft een lineair verband met de soortsverhouding in de mengsels (R ²=0.93). Binnen het bereik van 10 tot 90% van elke soort kan men met deze ijklijn met 95% betrouwbaarheid de soortsamenstelling bepalen op 3 tot 6% nauwkeurig.     

Models of incomplete selection for virulence of potato cyst nematodes caused by sex determination that depends on host resistance

Sex determination of potato cyst nematodes (Globodera rostochiensis andG. pallida) is strongly affected by host resistance. Larvae may develop more frequently into males in case of poorly compatible host parasite combinations than in case of fully compatible combinations. As a consequence, the number of males on a resistant host may be higher in case of a virulence than in case of virulence. To development into females, in contrast, virulence is more advantageous. According to logical reasoning, these conflicting interests of the two sexes may give rise to an equilibrium frequency of virulent nematodes, and therewith to incomplete selection for virulence when a resistant host is grown during a long period. This incomplete selection would manifests itself as durable partial resistance of the host.This new idea was studied theoretically for a host that is completely resistant to avirulent females on the basis of a gene-for-gene relationship. One calculation route to the equilibrium frequency of virulent nematodes was a numerical approach, by means of computer simulation, and the other route was an analytical approach, i.e. algebraic derivation.In case of excess of virulence allele a, the resistant host may even select for avirulence, according to the models. The equilibrium frequency of virulent nematodes equals 0.5/(1-α), where α represents the proportion of eggs that develop into males in case of virulence (aa) divided by that proportion in case of avirulence (Aa). If α≥0.5, then selection for virulence becomes complete. Consequences for purification of potato cyst nematodes to complete virulence are discussed.     

Infection of <Emphasis Type="Italic">Sorghum bicolor</Emphasis>, selected grass species and <Emphasis Type="Italic">Zea mays</Emphasis> by G<Emphasis Type="Italic">loeocercospora sorghi</Emphasis>, causal pathogen of zonate leaf spot

Zonate leaf spot (Gloeocercospora sorghi) is a common disease in Sorghum bicolor producing areas of the U.S., but little is known about its biology, virulence and severity on S. bicolor, Zea mays, and related crop grassweeds. Greenhouse studies were conducted to determine and compare the virulence and severity of G. sorghi on 10 commercially available sorghum hybrids, four Z. mays hybrids and selected grassweed species including Sorghum bicolor (grain sorghum and shattercane biotypes) and Sorghum halepense (Johnsongrass), two of the most problematic arable weeds. Plants from the respective species were inoculated with a local G. sorghi isolate and maintained in a dew-chamber at 24 °C for 24 h and then incubated under greenhouse conditions for 4 weeks. Plants were observed for lesion expression and rated using a modified Horsfall-Barrett scale (0–10). The first symptoms of infection were visible within 24 h following inoculation on shattercane and S. bicolor hybrids. Symptoms consisted of small, non-diagnostic purple lesions on the leaves. Results showed that S. bicolor, S. halepense and shattercane were susceptible to G. sorghi. All other species tested in this study were not infected. More particularly, disease severity, increased from a rating of 3 to 10 on sorghum and from 2 to 7 on S. halepense between 2 and 23 days after inoculation, respectively. However, disease severity on shattercane increased rapidly from 3.5 to 10 between 2 and 8 days after inoculation, respectively. Among the sorghum hybrids tested, FFR-322 appeared to be the most resistant to G. sorghi while Pioneer 83G66 appeared to be the most susceptible. Z. mays hybrids were not infected by the fungus used in this study. G. sorghi could be used effectively to manage shattercane and S. halepense infestations occurring in Z. mays and S. bicolor fields consisting of specific G. sorghi-resistant hybrids.     

Evaluation of PCR,IEF and ELISA techniques for the detection and identification of potato cyst nematodes from field soil samples in England and Wales

Effective management of potato cyst nematodes (PCNs) requires simple, rapid and accurate identification and quantification of field populations. Soil samples from a survey of 484 fields in potato rotations in England and Wales were used to compare the identification and quantification of PCNs using IEF, PCR, ELISA and bait plant tests. The cyst counts and bait plant test revealed that 64.3% of field samples contained PCNs. Bait plant tests increased the detection rate of PCNs in field samples by 4–6.4%. This means that some infestations are cryptic and would not normally be detected by standard counts. IEF, PCR and ELISA methods distinguished between Globodera rostochiensis and G pallida and were able to register mixed populations; however they were not in full agreement. All methods suggested that G pallida is the dominant species in the field samples tested. The PCR results indicated that 66% of field samples contained pure G pallida, 8% contained pure G rostochiensis and 26% contained mixtures of the two species. Estimates of the relative process times taken per sample in the PCR, IEF and ELISA techniques are given. © 2001 Society of Chemical Industry     

Hsp90 gene, an additional target for discrimination between the potato cyst nematodes, Globodera rostochiensis and G. pallida, and the related species, G. tabacum tabacum

The heat-shock gene, Hsp90, was targeted as a new variable genomic region to supplement other DNA-based tests for identification and discrimination of Globodera pallida, G. rostochiensis and G. tabacum tabacum. Populations of the potato cyst nematodes, G. pallida and G. rostochiensis (PCN), originating from Canada, France, Belgium and USA, together with two populations of G. tabacum tabacum from the USA and France were used for the amplification of a fragment of the Hsp90 gene. General and specific primers and probes for each species were derived from the consensus and non-consensus regions of the aligned sequences, respectively. A triplex conventional PCR assay, using a general forward and reverse or three specific reverse primers, as well as a real-time PCR using general primers and specific TaqMan probes, were developed. Melting curve analysis and restriction fragment polymorphisms using high resolution electrophoresis were explored for identifying PCR amplicons that characterized and discriminated the three Globodera species in both pure and mixed samples. Results from the different molecular assay strategies confirmed the usefulness of Hsp90 as a new additional gene target and showed that several different test options could be used for discrimination of PCN.