RNA interference and plant parasitic nematodes

RNA interference (RNAi) has recently been demonstrated in plant parasitic nematodes. It is a potentially powerful investigative tool for the genome-wide identification of gene function that should help improve our understanding of plant parasitic nematodes. RNAi should help identify gene and, hence, protein targets for nematode control strategies. Prospects for novel resistance depend on the plant generating an effective form of double-stranded RNA in the absence of an endogenous target gene without detriment to itself. These RNA molecules must then become available to the nematode and be capable of ingestion via its feeding tube. If these requirements can be met, crop resistance could be achieved by a plant delivering a dsRNA that targets a nematode gene and induces a lethal or highly damaging RNAi effect on the parasite.     

Neurobiology of plant parasitic nematodes

The regulatory constraints imposed on use of chemical control agents in agriculture are rendering crops increasingly vulnerable to plant parasitic nematodes. Thus, it is important that new control strategies which meet requirements for low toxicity to non-target species, vertebrates and the environment are pursued. This would be greatly facilitated by an improved understanding of the physiology and pharmacology of these nematodes, but to date, these microscopic species of the Phylum Nematoda have attracted little attention in this regard. In this review, the current information available for neurotransmitters and neuromodulator in the plant parasitic nematodes is discussed in the context of the more extensive literature for other species in the phylum, most notably Caenorhabditis elegans and Ascaris suum. Areas of commonality and distinctiveness in terms of neurotransmitter profile and function between these species are highlighted with a view to improving understanding of to what extent, and with what level of confidence, this information may be extrapolated to the plant parasitic nematodes.     

The soil as an environment for plant parasitic nematodes

British arable soils are uniform in texture to plough depth but vary in structure and the content of new organic matter according to recent cultivations. Subsoils are less uniform and little influenced by cultivations. Although remarkably uniform in structure and outward appearance nematodes vary greatly in length and girth. Root ectoparasites live wholly in the soil but root endoparasites may spend only brief periods there. Nematodes that spend much time in the soil surface are subject to a harsher microclimate than those inhabiting deeper layers. The movement and activity of nematodes in soil is influenced by the thickness of water films, the amount of pore space with dimensions the nematodes can traverse, the stability and packing of aggregates, the oxygen consumption of competing organisms and the rate of supply. Other factors of which little is known are the degree of continuity of the usable spaces and their tortuosity. The moisture characteristic curve which relates water withdrawn to the suction pressure (matric potential) applied is a useful tool which enables the space available to a given nematode to be related to its cross-sectional diameter. Although total pore space and usable pore space are correlated in a general way with each other and with texture (e.g.% sand), and bulk density is correlated with pore space within textural classes, none of these measures can be substituted for an estimate of the usable pore space appropriate to the size of the nematode being studied. For most purposes the solid matrix of arable soils can be regarded as an inert skeleton supporting the pore space. The stability of the matrix is therefore an important parameter, determining changes of space and time. Little is known about the distribution of macro-voids in soils and rapid methods of assessing them are needed. These may be more important for and more easily used by long nematodes than short ones. For nematodes living near the soil surface diurnal temperature fluctuations may be large. Their movement and activity should be related to temperature fluctuations via the Q₁₀-curve. For nematodes living deeper in the soil diurnal fluctuations are unimportant. So development can be mirrored by curves of accumulated temperature in day degrees above basal development temperature. Unlike the pattern of rainfall accumulation, which varies from place to place and year to year, and must greatly affect nematode multiplication, crop damage and activity, the pattern of temperature accumulation is remarkably stable. Differences from place to place and year to year are moderated by the changes in sowing date they impose. Consequently a nematode species and the host plant it infests usually develop together under similar soil climatic conditions from planting date onwards. In real soils the spaces in which nematodes live are partly filled by water in winter but are progressively drained as the season advances and become air filled. Then water films are too thin to permit movement except while the soil is draining after rainfall. Therefore the duration of activity is proportional to rainfall, and total activity throughout development is proportional to accumulated rainfall after discounting amounts too small to penetrate the soil. The activity of root ectoparasitic nematodes could be modelled by multiplying the duration of activity by temperature, using the Q₁₀ curve if necessary (i.e. by the rate of activity). The soil environment imposes constraints on the animals that live in it. Populations are relatively static and inbred. The pore space also limits the properties of substances that link parasite with parasite (pheromones) and parasite with host (phytomones). The many additional complications that arise when plants are grown are depicted diagrammatically.     

Relationship between the successful infection by entomopathogenic nematodes and the host immune response

Reproduction of entomopathogenic nematodes requires that they escape recognition by a host's immune system or that they have mechanisms to escape encapsulation and melanization. We investigated the immune responses of larvae for the greater wax moth (Galleria mellonella), tobacco hornworm (Manduca sexta), Japanese beetle (Popillia japonica), northern masked chafer (Cyclocephala borealis), oriental beetle (Exomala orientalis) and adult house crickets (Acheta domesticus), challenged with infective juveniles from different species and strains of entomopathogenic nematodes. The in vivo immune responses of hosts were correlated with nematode specificity and survival found by infection assays. In P. japonica, 45% of injected infective juveniles from Steinernema glaseri NC strain survived; whereas the hemocytes from the beetle strongly encapsulated and melanized the Heterorhabditis bacteriophora HP88 strain, S. glaseri FL strain, Steinernema scarabaei and Steinernema feltiae. Overall, H. bacteriophora was intensively melanized in resistant insect species (E. orientalis, P. japonica and C. borealis) and had the least ability to escape the host immune response. Steinernema glaseri NC strain suppressed the immune responses in susceptible hosts (M. sexta, E. orientalis and P. japonica), whereas S. glaseri FL strain was less successful. Using an in vitro assay, we found that hemocytes from G. mellonella, P. japonica, M. sexta and A. domestica recognized both nematode species quickly. However, many S. glaseri in M. sexta and H. bacteriophora in G. mellonella escaped from hemocyte encapsulation by 24h. These data indicate that, while host recognition underlies some of the differences between resistant and susceptible host species, escape from encapsulation following recognition can also allow successful infection. Co-injected surface-coat proteins from S. glaseri did not protect H. bacteriophora in M. sexta but did protect H. bacteriophora in E. orientalis larva; therefore, surface coat proteins do not universally convey host susceptibility. Comparisons of surface coat proteins by native and SDS-PAGE demonstrated different protein compositions between H. bacteriophora and S. glaseri and between the two strains of S. glaseri.     

Cell cycle activation by plant parasitic nematodes

Sedentary nematodes are important pests of crop plants. They are biotrophic parasites that can induce the (re)differentiation of either differentiated or undifferentiated plant cells into specialized feeding cells. This (re)differentiation includes the reactivation of the cell cycle in specific plant cells finally resulting in a transfer cell-like feeding site. For growth and development the nematodes fully depend on these cells. The mechanisms underlying the ability of these nematodes to manipulate a plant for its own benefit are unknown. Nematode secretions are thought to play a key role both in plant penetration and feeding cell induction. Research on plant-nematode interactions is hampered by the minute size of cyst and root knot nematodes, their obligatory biotrophic nature and their relatively long life cycle. Recently, insights into cell cycle control in Arabidopsis thaliana in combination with reporter gene technologies showed the differential activation of cell cycle gene promoters upon infection with cyst or root knot nematodes. In this review, we integrate the current views of plant cell fate manipulation by these sedentary nematodes and made an inventory of possible links between cell cycle activation and local, nematode-induced changes in auxin levels.     

New approaches to control plant parasitic nematodes

Plant parasitic nematodes are a serious threat for crop production worldwide. This review summarizes our understanding of plant nematode interactions and presents new alternatives for nematode control in the field. Breeding for resistance has been a major goal for many important crop species like soybean, potato, tomato and sugar-beet. As a result numerous nematode-resistance genes have been identified, two of which have been cloned recently, Hs1 ^pro-1 from sugar-beet, giving resistance to the beet cyst nematode Heterodera schachtii, and Mi from tomato, giving resistance to the root-knot nematode Meloidogyne incognita. Also artificial resistance genes, coding for nematotoxic proteins or causing rapid death of feeding cells, have been elucidated. In the future, genetic engineering of nematode resistance will become more and more important for plant breeding. Transformation techniques will allow genes to be quickly introduced into susceptible breeding lines and then combined with each other to produce plant varieties with durable resistance. Received: 26 August 1998 / Received revision: 16 December 1998 / Accepted: 21 December 1998     

A sensory code for host seeking in parasitic nematodes

Parasitic nematode species often display highly specialized host-seeking behaviors that reflect their specific host preferences. Many such behaviors are triggered by host odors, but little is known about either the specific olfactory cues that trigger these behaviors or the underlying neural circuits. Heterorhabditis bacteriophora and Steinernema carpocapsae are phylogenetically distant insect-parasitic nematodes whose host-seeking and host-invasion behavior resembles that of some devastating human- and plant-parasitic nematodes. We compare the olfactory responses of Heterorhabditis and Steinernema infective juveniles (IJs) to those of Caenorhabditis elegans dauers, which are analogous life stages. The broad host range of these parasites results from their ability to respond to the universally produced signal carbon dioxide (CO(2)), as well as a wide array of odors, including host-specific odors that we identified using thermal desorption-gas chromatography-mass spectroscopy. We find that CO(2) is attractive for the parasitic IJs and C. elegans dauers despite being repulsive for C. elegans adults, and we identify a sensory neuron that mediates CO(2) response in both parasitic and free-living species, regardless of whether CO(2) is attractive or repulsive. The parasites' odor response profiles are more similar to each other than to that of C. elegans despite their greater phylogenetic distance, likely reflecting evolutionary convergence to insect parasitism.     

不同离体寄主及其成熟度对亚洲柑桔木虱存活的影响

【目的】亚洲柑桔木虱Diaphorina citri Kuwayama的虫口密度及活动与柑桔黄龙病的田间传播、流行有十分密切的关系,寻找合适的室内饲养条件能够便于观察和研究其生物学特性和传病机制。【方法】本文以九里香Murraya exotica(L.)Mant.、酸桔Citrus sunki Hort.ex Tanaka和马水桔Citrus reticulata Blanco.cv.Mashuiju 3种寄主植物不同成熟度离体梢为研究材料,(1)比较亚洲柑桔木虱卵分别在3种寄主植株和离体嫩梢上的孵化率;(2)比较3种寄主不同成熟度离体梢对各龄若虫存活率和蜕皮的影响;(3)比较3种寄主不同成熟度离体梢对成虫存活率的影响。【结果】(1)亚洲柑桔木虱在植株嫩梢上卵的孵化率高于离体嫩梢,九里香表现最明显;(2)低龄若虫在叶片未完全展开的离体嫩梢上存活率最高,而高龄若虫在完全展开的嫩梢上最高;(3)用离体成熟梢饲养柑桔木虱成虫存活率高于离体嫩梢,酸桔和马水桔离体梢饲养的存活率较九里香高。【结论】用寄主植物离体梢饲养的亚洲柑桔木虱卵孵化率和若虫、成虫存活率都较高而且较稳定,该方法可用于这种木虱的室内繁殖中。     

Preferential infectivity of entomopathogenic nematodes in an envenomed host

Entomopathogenic nematodes and parasitoid wasps are used as biological control agents for management of insect pests such as the Indian meal moth, Plodia interpunctella. The parasitoid wasp Habrobracon hebetor injects a paralytic venom into P. interpunctella larvae before laying eggs. A previous study reported that the entomopathogenic nematode Heterorhabditis indica preferentially infects P. interpunctella that have been envenomed by H. hebetor while results in this study showed a similar preference by the entomopathogenic nematode, Steinernema glaseri. We therefore tested four hypotheses for why nematode infection rates are higher in envenomed hosts: (1) elevated CO₂ emission from envenomed hosts attracts nematodes, (2) paralysis prevents hosts from escaping nematodes, (3) volatile chemicals emitted from envenomed hosts attract nematodes and increase infection, and (4) reduced immune defenses in envenomed hosts increase nematode survival. Results showed that envenomed P. interpunctella larvae emitted lower amounts of CO₂ than non-envenomed larvae. Physical immobilization of P. interpunctella larvae did not increase infection rates by S. glaseri but did increase infection rates by H. indica. Emissions from envenomed hosts were collected and analyzed by thermal desorption gas chromatography/mass spectrometry. The most abundant compound, 3-methyl-3-buten-1-ol, was found to be an effective cue for S. glaseri attraction and infection but was not an effective stimulus for H. indica. Envenomed P. interpunctella exhibited a stronger immune response toward nematodes than non-envenomed hosts. Altogether, we conclude that different mechanisms underlie preferential infection in the two nematode species: host immobilization for H. indica and chemical cues for S. glaseri.     

Relationship between intermediate host taxon and infection by nematodes of the genus Rhabdochona

We describe the intermediate and definitive hosts of the fish nematodes Rhabdochona coronacauda and R. denudata honshuensis and discuss the relationships between parasitism and the feeding habitats of their intermediate hosts. We found that the principal intermediate hosts of the two nematodes were filter-feeding mayflies of the genera Ephemera, Photamanthus and Isonychia. Ephemera strigata seemed to be the most important intermediate host of these nematodes. Adult R. coronacauda were found mainly in Hemibarbus longirostris and Rhinogobius flumineus, which are benthic fishes that feed on benthic aquatic insects, including E. strigata. For R. coronacauda, therefore, the feeding habits of the definitive hosts facilitate host alternation by this species. However, adult R. denudata honshuensis were found in cyprinids. In particular, Zacco temmincki was the principal natural definitive host in our study area. Since Z. temmincki is a swimming predator, E. strigata nymphs that burrow in the substrate are not the main prey of this species. This indicates that the transmission of R. denudata honshuensis hardly occurs from E. strigata nymph to Z. temmincki, suggesting another, unknown transmission route.     

Soil mediates the interaction of coexisting entomopathogenic nematodes with an insect host

We tested for soil substrate effects on the movement and infectivity of naturally co-occurring entomopathogenic nematodes Steinernema feltiae and Heterorhabditis marelatus, alone and in combination. We manipulated the presence and bulk density of soil and added Galleria mellonella baits within capped and perforated 15mL centrifuge tubes. Sampling tubes were then deployed in situ into field and laboratory settings as experimental traps for infective juveniles. In comparisons with standard soil collections from Lupinus arboreus rhizospheres, sampling tubes were equally sensitive to the presence of H. marelatus and more sensitive to S. feltiae. In laboratory microcosms, both EPN species infected Galleria at high frequencies in tubes lacking soil and in the absence of heterospecifics. Infection frequency of S. feltiae was unaffected by the presence of H. marelatus, but it declined with higher soil bulk density inside tubes. In contrast, detectable infection frequency by H. marelatus was reduced only marginally by the presence of soil but severely by the presence of S. feltiae. Thus, the presence of soil in tubes reversed the identity of dominant species infecting Galleria in tubes, an effect magnified when soils were compacted. Moreover, S. feltiae rarely moved into tubes lacking Galleria baits, whereas H. marelatus colonized unbaited tubes 4- to 5-fold more frequently than S. feltiae. In situ, sampling tubes acted as filters to reduce interference and contamination by fungal pathogens common in field soils. The method allows precision sampling with minimal soil disturbance while protecting bait insects from scavengers. Manipulation of tube design may allow selective sampling of EPN species, depending on the abiotic characteristics of soils, and the biology, behavior, and interspecific interactions of coexisting species.     

Mass production of entomopathogenic nematodes for plant protection

Entomopathogenic nematodes of the genera Heterorhabditis and Steinernema are commercially used to control pest insects. They are symbiotically associated with bacteria of the genera Photorhabdus and Xenorhabdus, respectively, which are the major food source for the nematodes. The biology of the nematode-bacterium complex is described, a historical review of the development of in vitro cultivation techniques is given and the current use in agriculture is summarised. Cultures of the complex are pre-incubated with the symbiotic bacteria before the nematodes are inoculated. Whereas the inoculum preparation and preservation of bacterial stocks follow standard rules, nematodes need special treatment. Media development is mainly directed towards cost reduction, as the bacteria are able to metabolise a variety of protein sources to provide optimal conditions for nematode reproduction. The process technology is described, discussing the influence of bioreactor design and process parameters required to obtain high nematode yields. As two organisms are grown in one vessel and one of them is a multicellular organism, the population dynamics and symbiotic interactions need to be understood in order to improve process management. Major problems can originate from the delayed or slow development of the nematode inoculum and from phase variants of the symbiotic bacteria that have negative effects on nematode development and reproduction. Recent scientific progress has helped to understand the biological and technical parameters that influence the process, thus enabling transfer to an industrial scale. As a consequence, costs for nematode-based products could be significantly reduced.     

The distribution of Epichloe typhina in natural plant populations of the host plant Calamagrostis purpurea

The distribution of the systemic fungus Epichloe typhina was studied in natural populations of the host grass Calamagrostis purpurea. By searching for stroma in field and dissecting and staining plant parts in the lab I found that E. typhina was only present in nutrient rich and more wet habitats and totally absent from nutrient poor areas. A greenhouse experiment showed that under high nutrient conditions infected plants produced significantly more shoots than did healthy plants, while no difference was found when plants were grown in low nutrient conditions. Thus, the results suggest that the occurrence as well as the effect of E. typhina is strongly affected by environmental factors similar to the case of other systemic diseases, such as rusts and smuts.     

Plant actin cytoskeleton re-modeling by plant parasitic nematodes

The cytoskeleton is an important component of the plant’s defense mechanism against the attack of pathogenic organisms. Plants however, are defenseless against parasitic rootknot and cyst nematodes and respond to the invasion by the development of a special feeding site that supplies the parasite with nutrients required for the completion of its life cycle. Recent studies of nematode invasion under treatment with cytoskeletal drugs and in mutant plants where normal functions of the cytoskeleton have been affected, demonstrate the importance of the cytoskeleton in the establishment of a feeding site and successful nematode reproduction. It appears that in the case of microfilaments, nematodes hijack the intracellular machinery that regulates actin dynamics and modulate the organization and properties of the actin filament network. Intervening with this process reduces the nematode infection efficiency and inhibits its life cycle. This discovery uncovers a new pathway that can be exploited for the protection of plants against nematodes.Key words: cytoskeleton, actin, actin depolymerizing factor, nematode, giant cells, syncytium, cytochalasin, taxol     

Arabidopsis thaliana as a new model host for plant-parasitic nematodes

We have established culture conditions for successful infection and development of several economically important cyst-forming and root-knot nematodes on Arabidopsis thaliana under monoxenic conditions. Complete life cycles were obtained with the sedentary cyst nematodes Heterodera schachtii, H. trifolii, H. cajani and the root-knot nematodes Meloidogyne incognita and M. arenariaas well as with the migratory nematode Pratylenchus penetrans. In contrast, H. goettingiana and Globodera rostochiensis were unable to develop on Arabidopsis roots. Tissue-culture quality agar and medium conditions optimized for hydroponic root culture were essential for successful infections. Detailed in-vivo observations were made inside Arabidopsis roots during the early infection stages of M. incognita and during complete development of H. schachtii. Seventy-four different ecotypes of Arabidopsis were screened for their susceptibility towards H. schachtii resulting in a range of infection rates. None of the ecotypes tested showed complete resistance in vitro. The use of Arabidopsis as a host for plant-parasitic nematodes will provide a new model system for the molecular genetic analysis of this interaction.     

Migratory plant parasitic nematodes as pests of cereals

Two field trials showed that initial populations of Tylenchus Bastian, Paratylenchus Micoletzky, Pratylenchus minyus Sher and Allen, P. crenatus Loof, P. penetrans Chitwood and Oteifa, Helicotylenchus pseudorobustus Golden and H. digonicus Perry did not decrease yield of cereals whereas a significant inverse relationship existed between populations of Tylenchorhynchus dubius Filipjev and yield of wheat. T. dubius and Longidorus spp. Filipjev were associated with early leaf-yellowing of barley, though difficulty in controlling nematodes failed to firmly link yield reduction with nematode populations. The possible variability in tolerance of cereals to nematodes is discussed.