Moulting of parasitic nematodes

Nematodes are usually divided into two major groups, the Adenophora which are common in water and the Secernentea largely from soil. Most research on moulting has been done with the Secernentea, which include the majority of the parasitic forms. Cuticle composition and morphology is discussed in relation to the physiology and possible reasons for moulting in the Nematoda.     

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.     

Acetylcholinesterase secretion by parasitic nematodes. II. Trichostrongylus spp

Unusually high levels of acetylcholinesterase (AChE) were found in the nematode parasites Trichostrongylus axei, T. colubriformis and T, retortaeformis. In T. colubriformis the enzyme was located in the oesophageal and excretory glands of the parasitic stages. The highest level/unit wt was found in the fourth-stage larvae, which per worm had a comparable level to that in adult worms because the excretory gland was fully developed in the fourth-stage larvae. In acrylamide gel electrophoresis, T. axei and T. colubriformis AChE and esterases were similar but differed from those present in T. retortaeformis. Globulins prepared from the sera of sheep and guinea-pigs infected with T. colubriformis complexed with T. colubriformis and T. axei AChE, but not with esterases nor with AChE from T. retortaeformis, Nippostrongylus brasiliensis, Oesophagostomum radiatum or O. venulosum. Complexing of AChE to globulins did not inhibit the enzymic function of this enzyme.     

Genes and genomes of parasitic nematodes

Our knowledge of gene and genome organization in nematodes is growing rapidly, partly as a result of the Caenorhabditis elegans genome project. Here Martin Hammond and Ted Bianco review what is known about the organization of genes and genomes in parasitic nematode species, using information gained from molecular and cytological approaches. They suggest that there are implications not only for a wide range of problems in parasitology but also for our understanding of genome evolution in eukaryotes.     

Acetylcholinesterase secretion by parasitic nematodes. 3. Oesophagostomum spp

Acetylcholinesterase (AChE) activity in Oesophagostomum radiatum increased markedly during the fourth and early fifth stages of parasitic development and thereafter remained relatively constant in the mature parasites. Fourth stage Oe. radiatum maintained in vitro in a saline medium released AChE steadily for 4 h. Whereas the excretory glands of Oe. radiatum appeared to be the major site of AChE secretion, the highest concentration of the enzyme in Oe. venulosum was found in the cephalic tissues.Antibodies to Oe. radiatum AChE appeared in the serum of calves three weeks after primary infection with the parasite and were also found in the serum of neonatal calves and in the colostrum of their dams.Several soluble non-specific esterases were present in homogenates of adult Oe. radiatum and Oe. venulosum. In Oe. radiatum these esterases occurred both in gut tissue and excretory glands, and were present in secretions released in vitro by fourth-stage larvae. However, no antibodies against the esterases were detected in host serum.     

Intersex or sex reversal amongst plant parasitic nematodes.

The intersexuality amongst plant parasitic nematodes has been discussed to be an intermediate stage of sex reversal of male into female. We, hereby, suggest four possible reasons for the sex reversal, this being an intermediate stage - a so-called intersex phase: (1) gene mutation, (2) unusual numerical relationship between autosomes and sex chromosomes during fertilization, (3) effect of female sex hormone secreted by adult females alongwith the mating attractant, and (4) presence or absence of andrgenic hormone in males. The possible effect of female sex hormone on the synthesis of macromolecules which might play a role in sex reversal, is discussed in particular.     

Nematode-trapping fungi against parasitic cattle nematodes

Interactions between larvae of bovine gastrointestinal nematode parasites and nematode-trapping fungi, such as Arthrobotrys and Duddingtonia species and strains have been studied in Denmark. In this article J?rn Gr?nvold, Jens Wolstrup, Peter Nansen and Svend Aage Henriksen discuss how these fungi are able to grow, trap and kill parasitic nematode larvae, both on agar in the laboratory and in cattle faeces in the field.     

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.     

Mucosal immunity against parasitic gastrointestinal nematodes

The last two decades witnessed significant advances in the efforts of immunoparasitologists to elucidate the nature and role of the host mucosal defence mechanisms against intestinal nematode parasites. Aided by recent advances in basic immunology and biotechnology with the concomitant development of well defined laboratory models of infection, immunoparasitologists have more precisely analyzed and defined the different immune effector mechanisms during the infection; resulting in great improvement in our current knowledge and understanding of protective immunity against gastrointestinal (GI) nematode parasites. Much of this current understanding comes from experimental studies in laboratory rodents, which have been used as models of livestock and human GI nematode infections. These rodent studies, which have concentrated on Heligmosomoides polygyrus, Nippostrongylus brasiliensis, Strongyloides ratti/S. venezuelensis, Trichinella spiralis and Trichuris muris infections in mice and rats, have helped in defining the types of T cell responses that regulate effector mechanisms and the effector mechanisms responsible for worm expulsion. In addition, these studies bear indications that traditionally accepted mechanisms of resistance such as eosinophilia and IgE responses may not play as important roles in protection as were previously conceived. In this review, we shall, from these rodent studies, attempt an overview of the mucosal and other effector responses against intestinal nematode parasites beginning with the indices of immune protection as a model of the protective immune responses that may occur in animals and man.     

Production-based control of parasitic nematodes of cattle

Nematode parasite control in cattle is the goal of the parasitologist and the cattle producer. However, the language used to express the impact of that control has been a source of confusion between the two groups. Veterinary parasitologists speak in terms of reduction in worms or worm eggs, and cattle producers in terms of weight gain, milk production or calving rate. During the development of doramectin for cattle in temperate climates worldwide, the point came when we began to look for a different set of parameters to guide trial design and to communicate the results. In this paper, a series of published papers resulting from the yearling portion of this development programme are reviewed from the viewpoint of weight gain in relation to forage/feed availability. A pattern emerged that indicated that yearling cattle, when parasite control was effective (as indicated by egg counts) and forage was sufficient (as indicated by weather patterns), gained from 0.75 to 0.95 kg day(-1) in trials from the USA, Europe and Argentina. When parasite control or forage supply or both were insufficient, these rates of weight gain were significantly reduced. If more attention is spent on forage availability and weight-gain parameters when parasite-control programmes are designed, then researchers might communicate more meaningful information to producers on the value of parasite control.     

The FAR protein family of parasitic nematodes

Fatty acid–and retinol-binding proteins (FARs) belong to a unique family of excreted/secreted proteins (ESPs) found exclusively in nematodes. Much of our understanding of these proteins, however, is limited to their in vitro binding characteristics toward various fatty acids and retinol and has provided little insight into their in vivo functions or mechanisms. Recent research, however, has shown that FARs elicit an immunomodulatory role in plant and animal model systems, likely by sequestering lipids involved in immune signaling. This alludes to the intricate relationship between parasitic nematode effectors and their hosts.     

Recovery of parasitic nematodes from fish by digestion or elution.

Two methods, digestion and elution, were used to recover parasitic nematodes from 470 flatfish belonging to species in the family Pleuronectidae. Samples of similar fish were collected from market lots; half of each sample was subjected to digestion, and half was subjected to elution (sedimentation). The edible (flesh) and the inedible (viscera) portions of each fish were analyzed separately. The total number of nematodes recovered by digestion was 1,110, which was not significantly greater than the 922 nematodes recovered by elution. However, digestion recovered 1,062 nematodes of the anisakine genera Anisakis and Phocanema, which are potentially pathogenic for human consumers of raw of semiraw fish. This number is significantly greater than the 608 pathogenic nematodes recovered by elution. Digestion also recovered 242 more nematodes from the edible flesh than did elution. Conversely, more nonpathogenic nematodes were recovered by elution. Approximately half the fish (240) had been collected in Boston markets, and the other half (230) had been collected in San Francisco markets. Fish from San Francisco each contained an average of eight nematodes, and those from Boston contained an average of less than one nematode per fish.     

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