Nematodes - available

Control ToolsDisease details
Sources of informationRisks
Main critical gapsConclusion
Score criteriaPrioritisation Model
Gap Analysis

Control Tools

Diagnostics availability

Commercial diagnostic kits available worldwide

Coprological (microscopical) tests and pepsinogen assays are available in the established veterinary laboratories across Europe. These tests are based on in-house protocols and are not standardized.

Commercially available kits and materials include:

  • McMaster, Flotac® and Fecpak® for microscopical examination of faecal samples (faecal egg counts)
  • Svanovir®-O. ostertagi-Ab for detection of antibodies against gastrointestinal nematodes in bovine milk (and serum) samples.

GAPS: 

  • There is a need for standardisation of available diagnostic methods to qualify and quantify parasite burdens.
  • Novel tests for the early detection of anthelmintic resistance and the interpretation of results.
  • Diagnostic systems based on the principle of identifying those animals that can cope with parasite infections without anthelmintic intervention, and to select individuals that require treatment. 

Commercial diagnostic kits available in Europe

Coprological (microscopical) tests and pepsinogen assays are available in the established veterinary laboratories across Europe. These tests are based on in-house protocols and are not standardized.

Commercially available kits and materials include:

  • McMaster, Flotac® and Fecpak® for microscopical examination of faecal samples (faecal egg counts)
  • Svanovir®-O. ostertagi-Ab for detection of antibodies against gastrointestinal nematodes in bovine milk (and serum) samples.

GAPS: 

  • There is a need for standardisation of available diagnostic methods to qualify and quantify parasite burdens.
  • Novel tests for the early detection of anthelmintic resistance and the interpretation of results.
  • Diagnostic systems based on the principle of identifying those animals that can cope with parasite infections without anthelmintic intervention, and to select individuals that require treatment.

Diagnostic kits validated by International, European or National Standards

None.

Diagnostic method(s) described by International, European or National standards

None.

Commercial potential for diagnostic kits in Europe

Moderate. Large for anthelmintic resistance management strategies.

DIVA tests required and/or available

Not applicable.

Opportunities for new developments

  • Further development of existing tests to make them suitable for high-throughput platforms.
  • Development of pen-side tests for user friendly (low input) on-farm monitoring and rapid detection of parasitic infections.

GAP: Multipathogen diagnosis, clinical disease indicators for health surveillance.

Vaccines availability

Commercial vaccines availability (globally)

None.

GAP: Vaccines for all the important gastrointestinal nematodes – in some cases (Haemonchus, Ostertagia) might have a market place as mono valent vaccines but the ambition should be polyvalent vaccines.

Commercial vaccines authorised in Europe

None.

GAPS: Development of effective vaccines and registration guidelines for helminth vaccines.

Marker vaccines available worldwide

None.

Marker vaccines authorised in Europe

None.

Effectiveness of vaccines / Main shortcomings of current vaccines

Prototype vaccines against Haemonchus contortus reduce worm numbers and worm egg output by > 90%.

Prototype vaccines against Ostertagia ostertagi reduce worm egg output by 60% during a two month challenge period. Main shortcomings include lack of cross-protection against other important nematodes and possible need for repeated administrations.

GAPS:

  • Required efficacy has been defined for some species by experimental infection and/or by modelling. There is a requirement to define efficacy in the field, probably at the level required to reduce or eliminate the economic impact of the disease.
  • Multivalent vaccines 

Commercial potential for vaccines in Europe

Native protein “prototype” vaccines are under development for Haemonchus and Ostertagia with support from the commercial sector.

GAPS: 

  • Effective recombinant vaccines to allow mass production are required.
  • Effective means of delivery 

Regulatory and/or policy challenges to approval

This whole area is undefined. How will the regulators treat a monovalent vaccine with 60% protection? Vaccines seem to be entirely in line with policy at a national, European and global level.

GAP: Helminth vaccine registration guidelines. We need to interact with the regulators to ensure the targets are acceptable.

Commercial feasibility (e.g manufacturing)

Recombinant vaccines can be produced on an industrial scale. The current native protein vaccines are not commercially feasible, except for specific niche markets (e.g. a native Haemonchus contortus vaccine in Southern Hemisphere countries).

GAPS:

  • Development of affordable large-scale expression systems that can produce recombinant helminth proteins with the same conformational and protective properties as the native antigens.
  • Concerted interaction between researchers, the commercial sector and end-users is required. 

Opportunity for barrier protection

Not applicable.

Opportunity for new developments

No vaccine yet.

Pharmaceutical availability

Current therapy (curative and preventive)

Anthelmintics.

The three current major families of anthelmintics are the benzimidazoles (BZ), macrocyclic lactones (ML) and imidazothiazoles & tetrahydropyrimidines (which include levamisole - LEV & pyrantel - PYR). A fourth new class for sheep (amino- acetonitrile derivative or AAD) will be available shortly

All anthelmintics used in livestock are very effective, reducing susceptible worm burdens (all parasitic stages) by at least 90% (BZ, PYR & LEV) up to 99% (ML, AAD).

Possible drawbacks of the use of anthelmintics may include: (a) the increasing incidence of anthelmintic resistance (AR); (b) reduced development of natural immunity against nematodes; and (c) consumer concerns (often not justified) regarding drug residues in food products and in the environment.

Nematodes in pigs are mainly controlled by application of anthelmintics (as above), cleaning of pens/change of bedding and pasture shifts between farrowings. MLs are widely used due to combined effect on sarcoptic mange.

GAPS: Means of optimising anthelmintic usage to both control nematodes and maintain efficacy.

Future therapy

The difficulties and cost of discovering new actives, can be compensated for in part through the introduction of novel mixtures, formulations and delivery systems. Instead of blanket treatments future treatment strategies could benefit from selective treatment of only those animal requiring treatment.

GAPS:

  • Short term – Introduction of anthelmintic combinations and/or novel formulations.
  • Long term – Development of in vivo parasite gene silencing technology (e.g.  RNAi) 

Commercial potential for pharmaceuticals in Europe

Large – based on current anthelmintic market. Also, meat consumption predicted to continue increasing globally until 2050. Therefore more pressure on grazing, increased intensification where feasible.

GAP: Statistics difficult to obtain because of different routes of distribution (e.g. vet/non-vet) and some generic companies do not submit figures.

Regulatory and/or policy challenges to approval

Safety studies and their interpretation, particularly in terms of tissue residues/withholding periods and environmental impact assessments.

GAPS: Knowledge transfer and exchange with policy makers and commerce to ensure global standardisation of regulatory requirements.

Commercial feasibility (e.g manufacturing)

Existing technology is adequate.

Opportunities for new developments

Current priority research targets for antiparasitics are orientated towards the companion animal market. Spin offs may lead to novel production animal (and human) anthelmintics.

Opportunities for novel therapeutics may arise from developing genome technologies e.g. dietary interventions which may influence parasite gene promotors directly and switch off key proteins.

GAP: Research into the control of parasite gene expression.

New developments for diagnostic tests

Requirements for diagnostics development

Identification of:

  • specific proteins or sequences for species differentiation
  • novel  biomarkers  and molecular markers for anthelmintic resistance
  • novel genetic markers associated with host resistance/resilience

Improvement and refinement of:

  • non-invasive and automated sampling (e.g. milk, meat-juice, body condition scoring)
  • pen-side diagnostics

GAPS:

  • Need for high throughput novel and affordable diagnostics for the farming and research communities.
  • Novel target proteins and morbidity markers 

Time to develop new or improved diagnostics

From short (1-2 years) to evaluate and improve reproducibility to long (³ 4 years) to develop more specific methods suitable for high-throughput platforms.

Cost of developing new or improved diagnostics and their validation

Requires research and costs will be relatively high. Return on investment moderate to low.

Research requirements for new or improved diagnostics

Need for high throughput novel and affordable diagnostics for the farming and research communities.

Novel target proteins and morbidity markers

Technology to determine virus freedom in animals

Not applicable.

New developments for vaccines

Requirements for vaccines development / main characteristics for improved vaccines

  • knowledge of protective immune responses
  • protective worm antigens
  • large-scale expression systems
  • effective antigen delivery systems
  • definition of the efficacy required for vaccines

GAPS: 

For most GI nematodes:

  • improved knowledge of protective immune responses
  • identification of protective worm antigens
  • development of affordable large-scale expression systems that can produce recombinant helminth proteins with the same conformational and protective properties as the native antigens
  • development of improved antigen delivery systems
  • knowledge on required vaccine efficacies 

Time to develop new or improved vaccines

5 to 20 years.

Cost of developing new or improved vaccines and their validation

Lower than the cost for development of conventional anthelmintics (e.g. no residue studies).

GAP: Funding is needed to bridge the gap between lab research and commercialisation.

Research requirements for new or improved vaccines

  • knowledge of protective immune responses
  • protective worm antigens
  • large-scale expression systems
  • effective antigen delivery systems
  • definition of the efficacy required for vaccines

New developments for pharmaceuticals

Requirements for pharmaceuticals development

Anthelmintics with new mode of actions. Current anthelmintics have a high broad-spectrum efficacy against most nematodes. Low or nil effect of a number of anthelmintics against Trichuris –for pigs/humans.

Time to develop new or improved pharmaceuticals

Around 10 years for new chemistry.

Cost of developing new or improved pharmaceuticals and their validation

Estimated to be approx 250 mil €.

Research requirements for new or improved pharmaceuticals

Additional screens to identify novel targets (e.g. parasite genes).

Disease details

Description and characteristics.

Pathogen

Only Nematoda of the gastrointestinal tract of ruminants and pigs are considered (Trichinella excluded). Large number of genera and species (annex1). Most important GI nematodes are:

  • Cattle -  Ostertagia ostertagi, Cooperia oncophora, Nematodirus helvetianus
  • Small ruminants – Teladorsagia circumcincta, Haemonchus contortus, Trichostrongylus colubriformis, T. vitrinus, Nematodirus spp.
  • Swine – Ascaris suum, Trichuris suis, Oesophagostomum spp.

GAPS:

  • Variations in biology of nematodes
  • Interspecies interactions 

Variability of the disease

Agent types: Some GI nematode species are more pathogenic than others (e.g. Ostertagia ostertagi more pathogenic in cattle than Cooperia spp and in sheep/goats Haemonchus contortus is more pathogenic than Trichostrongylus spp .). Within nematode species, no documented differences in pathogenicity between strains or regional isolates.

Host range: Differences in host susceptibility to GI nematodes occur between animal species and breeds (latter has mainly been described in small ruminants, to a lesser extent in cattle/swine) and within breeds between age classes (younger animals more susceptible), physiological status (pregnancy, lactation) to the level of the individual.

Temporal variability: In ruminants, parasitic gastroenteritis mainly occurs during the grazing period and will vary according to latitude. Management conditions (e.g. access to pastures, turn-out and housing periods) will determine infection levels. Selective control agents may suppress certain nematode species and allow others to flourish. As an example long acting macrocyclic lactones will suppress e.g. Teladorsagia or Ostertagia, and may allow e.g. Cooperia and Trichostrongylus to flourish.

Spatial variability: Important differences in the prevalence and importance of parasite species according to regions (sub-arctic, temperate & Mediterranean regions). For example, in Northern Europe Teladorsagia circumcincta is the most important GI nematode in sheep, while in temperate & Mediterranean regions Haemonchus contortus is more important).

GAPS: 

  • Parasite genetic variation and virulence.
  • Host genetic and nutritional factors influence the animals’ susceptibility to infection (resistance) and their ability to cope with the pathogenic affects (resilience). Both in turn can affect parasite epidemiology.
  • Currently, very few genetic markers are available to identify resistant vs. susceptible host individuals.
  • Little/no knowledge on population specific pathogenicity

Stability of the agent/pathogen in the environment

Environmentally very stable. Infectious L3 larvae can commonly survive up to one year on pasture and at low levels into subsequent years; infectious eggs (Ascaris, Trichuris, Nematodirus) can survive for several years on pasture or in stables.

GAPS:

  • Agents killing infectious eggs.
  • Larvicidal compounds/management on pasture 

Species involved

Animal infected/carrier/disease

Nematodes species are typically host-specific, but there are species overlaps in sheep and goats for example and some parasite species of sheep and goats can infect cattle and vice versa (see annex 1). Only one species (Trichostrongylus axei) may infect ruminants, pigs and horses.

Most animals are asymptomatic carriers.

Human infected/disease

Ascaris suum (and Trichuris spp. and occasionally other nematodes) can infect humans.

Vector cyclical/non-cyclical

No vectors.

Reservoir (animal, environmental)

Wild ruminants and wild boars (see comments on species specificity above).

GAP: The identification of wild-life as reservoir.

Description of infection & disease in natural hosts

Transmissibility

Eggs excreted by host need first to develop to an infectious stage (free living L3 or L1/2/3 in ovo). Host is infected by oral ingestion of the infectious stages.

Speed of development to the infectious stage is mainly determined by temperature and varies between one to many weeks. Moisture (rainfall) is important in facilitating the release of infective stages from the faeces onto pasture.

 

Pathogenic life cycle stages

Developing stages and adults.

Signs/Morbidity

Anorexia, diarrhoea, anaemia, cachexia, production losses (weight, milk, wool). Very high morbidity (i.e. production losses) in ruminants but lower in pigs.

Incubation period

Varies from weeks to months; most infections are chronic.

Infection is generally continuous when animals graze on pasture, but may be subject to seasonal variations.

Mortality

In the absence of control measures, mortality can be high, particularly with the more pathogenic species such as Haemonchus contortus, Nematodirus battus, Teladorsagia circumcincta & Ostertagia ostertagi.

Shedding kinetic patterns

Infected animals can excrete eggs more-or-less continuously.

Mechanism of pathogenicity

All GI nematodes induce anorexia and impair nutrient utilisation. Infections with nematodes are likely to have a higher impact in animals suffering from intercurrent diseases and/or under-nutrition than otherwise healthy animals.

Pathogenicity varies according to the nematode genus (species) and includes the following:

  • Ostertagia/Teladorsagia  influence protein digestion and utilisation and can cause diarrhoea.
  • Haemonchus – blood sucking worm inducing anaemia
  • Nematodirus – principle affect on water balance resulting in diarrhoea.
  • Ascaris – nutrient malabsorption, intestinal occlusion, pulmonary dysfunction, secondary bacterial infections in the lungs, possibly negative interactions with certain pathogens and vaccines.
  • Trichuris -  hemorrhagic diarrhoea (dysentery).

GAPS: Different elements of importance for pathogenesis are still unknown and their identification may be important to better understand rationale of production losses and for vaccine or drug development.

Pathogenic interaction during multi-pathogen infections are incompletely understood. 

Zoonotic potential

Reported incidence in humans

Ascaris suum – Only in Denmark (DK) the incidence has been studied: 3.0 per 10,000 children living in the urban area and 27.8 per 10,000 children in the rural population.  Estimated 200-500 cases/5 mill./year in DK but severe under reporting.

GAP: Studies required to assess prevalence of zoonotic nematodes in humans.

Estimated level of under-reporting in humans

Ascaris suum – limited reporting at all so unknown if under-reporting. But presumable serious under-reporting.

GAP: Severe under reporting. Need to inform medical doctors.

Risk of occurence in humans, populations at risk, specific risk factors

Ascaris suum - mainly children, farm environments and often related to use of pig slurry as fertiliser. A. suum in humans has been observed mainly in developed countries where A. lumbricoides is no longer common. In developing countries mainly A. lumbricoides is present in humans.

Symptoms described in humans

Ascaris suum - no recorded pathogenicity, but A. lumbricoides cause retarded growth and cognitive impairment, pneumonitis, abdominal pain (e.g. bile duct infections).

GAP: Need to assess symptoms in humans.

Likelihood of spread in humans

Ascaris  suum - low.

Impact on animal welfare and biodiversity

Both disease and prevention/control measures related

Clinical parasitic gastroenteritis (PGE) is a severe welfare problem. However, the use of effective anthelmintics therapeutically in the face of clinical disease generally is rapidly effective. Grazing and nutritional management, supported by the tactical use of anthelmintics can control diseases and thus maintain high levels of welfare. In some regions, mainly on small farms and in marginal areas, prevention/control measures are not regularly practised.

GAP: Consequences of low input and organic farming practices on infection outcomes and welfare are ill defined.

Endangered wild species affected or not (estimation for Europe / worldwide)

No.

Slaughter necessity according to EU rules or other regions

No.

Geographical distribution and spread

Current occurence/distribution

Worldwide distribution. All grazing/outdoor reared animals are exposed to infection.

In pigs reared indoors, individual prevalence varies between 0-50% in Ascaris suum, 0-5% in Trichuris suis, and 0-100% for Oesophagostomum spp. depending on age groups and management.

Epizootic/endemic- if epidemic frequency of outbreaks

Infections with GI nematodes are endemic.

Seasonal cycle (seasonality)

Pasture infectivity varies seasonally according to latitude and management.

In pigs infections occur all year round (in-door production); outdoors, development does not take place in winter.

GAP: Influence of climatic change.

Speed of spatial spread during an outbreak

NA

Transboundary potential of the disease

No, ubiquitous.

Seasonal cycle linked to climate

Yes.

Distribution of disease or vector linked to climate

No, ubiquitous (although regional differences in species spectrum). No vectors.

Outbreaks linked to extreme weather

Possible as climate will influence the development of pre-parasitic stages.

Sensitivity of disease or vectors to the effects of climate change (environmental changes/land use)

Very important. Nematode diseases found previously in sub-tropical regions are now causing problems in temperate regions (e.g. haemonchosis in northern Europe).

Potential for increasing drug resistance problems e.g. in a dry summer, the population in refugia may be affected.

GAPS: 

  • Relative significance of certain GI nematodes and levels of exposure may change.
  • Effect of refugia on drug resistance selection under temperate climate conditions 

Route of Transmission

Usual mode of transmission (introduction, means of spread)

All livestock reared outdoors are, to some extent, infected and most animals excrete eggs; infection is direct by the faeco-oral route. Introduction or spread of infection between farms or regions generally occurs via the movement of animals.

Occasional mode of transmission

Nematode eggs and larvae may be transported by e.g.  contaminated machinery, slurry, forage, on insects. This mode of transmission may be important for the introduction of species to a previously non-infected herd.

GAP: Importance of atypical mode of transmission.

Conditions that favour spread

Favourable climate (warm and humid weather), host density, pasture quality.

Detection and Immune response to infection

Mechanism of host response

In general, a T helper-2 type immune response is generated against GI nematode infections.

Ruminants - While this response seems to be effective against some nematode species (rapid development of some level of protective immunity against Cooperia oncophora and Nematodirus), other nematode species are affected to a lesser extent and can persist in older animals (e.g. Ostertagia).

Pigs - Immunity to reinfection with Ascaris suum but adults stay for prolonged time (concomitant immunity). Trichuris suis: all expelled and solid immunity after 7 to 8 weeks - but 5% may be low responders – continue to excrete eggs. Oesophagostomum spp.: cause life-long infections.

GAPS: 

Many aspects of the innate and acquired immune responses are not clearly defined e.g. molecular pattern recognition, Th1/Th2 balance, cells and pathways involved in the early stages of the immune response, defining essential components of the protective host immune response, and influence of host genotype and nutrition.

The development and maintenance of an immune response against nematodes may be an important component of the induced production losses. 

Immunological basis of diagnosis

Antibodies and antigens (in blood, milk, faeces and meat juice) can be used to detect nematode infections.

GAP: Standardised and widely available diagnostic techniques required.

Main means of prevention, detection and control

Sanitary measures

Grazing management (e.g. by rotational grazing, reduced grazing density, mixed grazing of different host species) can reduce pasture infection levels. Implementation of these practices is limited by the availability of labour, and/or suitable pastures and livestock.

Dung removal and removal of deep litter bedding in animal houses (or using slatted floors without bedding material) will reduce the contamination of the environment.

Mechanical and biological control

Currently not practised on a large scale. Bioactive forages can deliver parasitological and nutritional benefits. Biological control with nematophagous fungi is effective under experimental conditions.

GAPS:

  • Practical agronomics of bioactive forages needs further applied research.
  • Technical solutions for delivery of nematophagous fungi.
  • Development of other biological control methods 

Diagnostic tools

Ruminants

1) Coprological methods

These methods can be used for all gastrointestinal nematodes and all hosts. Coprology can be used to identify and quantify eggs and coproculture to identify L3.

2) Serological methods

Serum pepsinogen levels are used to assess the degree of damage/extent of exposure to abomasal nematode infections.

Antibody levels against crude extract of Ostertagia ostertagi in bulk-tank milk or serum are used to assess nematode exposure in adult cows. 

3) Morbidity markers

Morbidity markers have been described in sheep.

An estimation of the level of anaemia (FAMACHA), diarrhoea index (DISCO), body condition scoring (BODCON) and use of automated weighing  (LIVGAIN) are means of identifying individual animals that may benefit from treatment.

Pigs

Pig nematodes are mainly diagnosed by faecal examination for eggs and occasional reports from abattoir of milk spots in the liver, only indicative of recent Ascaris suum exposure. Elimination of worms observed by farmer reassures him/her of necessity to treat.

GAPS:

  • Conventional diagnosis of nematode infections is laborious and expensive, and often not informative in providing a decision on whether to treat or not.
  • A key problem is to identify those animals requiring treatment in order to avoid unnecessary use of anthelmintics.
  • Standardised, cost-efficient, control-relevant diagnostic tools are needed, both at group and individual level.
  • Value of morbidity markers needs to be further assessed in multicentre field trials.

 

Vaccines

None.

GAPS:

For most GI nematodes:

  • identification of protective worm antigens
  • development of affordable large-scale expression systems that can produce recombinant helminth proteins with the same conformational and protective properties as the native antigens
  • development of improved antigen delivery systems
  • improved knowledge of protective immune responses
  • knowledge on required vaccine efficacies 

Therapeutics

Control of GI nematodes in Europe relies largely on anthelmintics. The three current major families of anthelmintics are the benzimidazoles (BZ), macrocyclic lactones (ML) and imidazothiazoles & tetrahydropyrimidines (which include levamisole - LEV & pyrantel - PYR). A fourth new class for sheep (amino- acetonitrile derivative or AAD) will be available shortly

All anthelmintics used in livestock are very effective, reducing susceptible worm burdens (all parasitic stages) by at least 90% (BZ, PYR & LEV) up to 99% (ML, AAD).

Possible drawbacks of the use of anthelmintics may include: (a) the increasing incidence of anthelmintic resistance (AR); (b) reduced development of natural immunity against nematodes; and (c) consumer concerns (often not justified) regarding drug residues in food products and in the environment.

Nematodes in pigs are mainly controlled by application of anthelmintics (as above), cleaning of pens/change of bedding and pasture shifts between farrowings. MLs are widely used due to combined effect on sarcoptic mange.

GAP: New action class anthelmintics or combinations of products within the current classes would greatly assist in managing anthelmintic resistance.

Biosecurity measures effective as a preventive measure

Quarantine strategies can be useful in minimising the transmission of drug resistant parasite populations in animals.

Border/trade/movement control sufficient for control

None.

Prevention tools

Chemoprophylaxis – strategic use of anthelmintics based on nematode epidemiology.

The impact of parasitism can be mitigated using grazing management, optimised nutrition and selection of appropriate host genetics.

GAPS:

  • Vaccines.
  • Improved anthelmintic treatment strategies. Targeted treatment strategies should be developed and evaluated, to treat only those groups or individuals that require treatment in terms of control, health and/or production. This would limit selection pressure for anthelmintic resistance and reduce treatment costs.
  • Updated epidemiological information to reflect recent changes in management and the impact of climate and land use changes.

Surveillance

Little or no routine surveillance exists for endemic GI nematode infections.

GAPS:

  • Need for national capacity to undertake surveillance of nematode infections e.g. national reference laboratory.
  • Routine procedures to direct control strategies and to monitor their efficacy.
  • Routine procedures to monitor anthelmintic efficacy.

Past experiences on success (and failures) of prevention, control, eradication in regions outside Europe

Failure of anthelmintic-based control strategies for GI nematode infections in the southern hemisphere to remain sustainable.

Eradication is not a feasible option under most circumstances.

Costs of above measures

Costs of GI nematode infections and their control exceed all other production limiting diseases.

Disease information from the OIE

Disease notifiable to the OIE

No.

OIE disease card available

No.

OIE Terrestrial Animal Health Code (reference)

None.

OIE Terrestrial Manual (reference)

None.

Socio-economic impact

Zoonosis: Impact on affected individuals and/or aggregated DALY figures

Not available.

Ascaris suum infections do impact humans. Knowledge gained in controlling GI nematode infections in animals may provide  invaluable models for Soil Transmitted Helminth infections in humans.

The issue of drug resistance for human helminthiases may be of public health concern, particularly in view of growing drug pressure in the era of ‘preventive chemotherapy’, which is the large-scale application of anthelminthic drugs to at risk populations (e.g., school-aged children) in developing countries.  

GAPS: 

  • Assessing impact of Ascaris suum infections in humans
  • Better interactions between veterinary and human parasitologists which for example could lead to improved guidelines for evaluating the efficacy of anthelmintics in humans.

Zoonosis: cost of treatment and control of the disease in humans

Not available.

Direct impact (a) on production

It varies considerably between animal species, geographic area, farm, etc. Most losses within the EU are caused by effects on productivity

Ruminant nematodes: In growing animals subclinical infections can lead to reduced weight gains by 10 to 30%. In adult animals infections can result in milk yield losses (5 to 10% in cattle and up to 40%  in small ruminants). Other losses include lower conception rates, poor carcass quality, reduced wool yields

Pig nematodes: Largely unknown, some older reports on marked reduced reproductive performance and weight gain but several other studies have failed to show an impact. Liver condemnations up to 20 % in certain countries.

GAPS:

More information is required on:

  • Effects on susceptibility to other diseases (bacterial, viral infections and metabolic diseases) and vaccination responses.
  • Effects on fertility parameters
  • Effects on culling
  • Effects on carcass weight/quality.

Pig nematode – a need for  a suitable model to assess the impact on-farm 

Direct impact (b) cost of private and public control measures

Costs for control measures are borne by the farmer with no public financial support. Control of nematodes is largely dependent on the use of anthelmintics, with an estimated €2.8 billion spent on anthelmintics globally (the bulk of which in the major livestock producing regions of Europe, USA and Australasia).

GAP: The cost of disease on the farm level has been poorly described. Studies are needed in order to define the room for investment for the farmer to prevent production losses.

Indirect impact

According to FAO, the demand for food is expected to continue to grow as a result both of population growth and rising incomes. Annual meat production will have to grow by over 200 million tonnes to reach a total of 470 million tonnes in 2050; annual milk production is projected to increase from 580 to 1047 million tones. Reaching these targets will require an increase in the efficiency of production. Both milk and meat production from cattle and pigs are the most important sectors in animal farming in the EU. Nematode infections cause the highest productivity and economical losses in livestock. Combatting these infections is indispensable to increase efficiency of production.

GAPS:

Need for cost benefit and socio-economic analyses of the impact of:

  • GI nematodes on the quantity and quality of livestock products (impact on food security)
  • Ineffective helminth control on livestock production and the sustainability of rural communities

Trade implications

Impact on international trade/exports from the EU due to existing regulations

None.

Impact on EU intra-community trade due to existing EU regulations

None.

Impact on national trade due to existing regulations

None.

Main perceived obstacles for effective prevention and control

The persistence of infectious stages (see 1.3) limits the application of environmental control on pasture and in housing

Ruminants

Control currently is largely centred on the use of anthelmintics and dependence is not without risk. An emerging problem threatening worm control today is the spread of anthelmintic resistance (AR). The prevalence of resistance varies geographically, depending on the livestock species involved and the drugs used.

Benzimidazole-resistant and Macrocyclic lactones-resistant nematodes are widely reported in sheep/goats of several temperate European countries. Resistance to levamisole is present in sheep and goat parasites, though at a lower level.

In cattle AR has been reported, however, until now it is mainly limited to Macrocyclic lactones resistance to Cooperia spp.

Pigs

AR has been demonstrated for Oesophagostomum spp. in Denmark and Germany (pyrantel, levamisole, benzimidazoles), and may be an overlooked problem.

GAPS:

Overall

There is a lack of standardized techniques for the diagnosis of infection, the early detection of AR and the absence of systematic large-scale surveys to assess the importance of AR for ruminants in Europe.

Ruminants

Much of the research on non-pharmaceutical approaches has not yet been successfully transferred from the research environment to the field.

In the long run, vaccines may provide complementary measures for control, but their efficacy and value under commercial farming conditions is only just beginning (in Australia)

Farmers and veterinarians like simple, empirical solutions to diseases and their control: the control of parasitism with anthelmintics is still viewed like this and a major initiative is required to change these habits to those that are more attuned to local topography, weather, management etc

Pigs

Lack of means to remove the constant high infection pressure on permanently used premises. Also a high level of protection and associated low levels of immunity in early life, often results in major problems with liver condemnation dues to late infections and a lot of milk spots. 

Main perceived facilitators for effective prevention and control

Demonstrating and understanding the benefits of control measures in terms of profitability of the production system is the most important facilitator to implement effective control measures.

GAPS:

  • Knowledge transfer through peer experience and endorsement
  • Finding effective methods for enhancing uptake of best practices by farmers and veterinarians. 

Risk

Livestock welfare and production (both meat and dairy) are negatively affected by gastrointestinal nematode infections, which are one of the main constraints to efficient livestock production worldwide. Changing climate is likely to exacerbate parasitoses by increasing the level and duration of pasture infectivity.

Failure to optimise anthelmintic usage could lead to loss of effective worm control.

GAPS: 

  • Improved communication and implementation of holistic control strategies using improved diagnostics, host genetics, nutrition and pasture management to reduce the reliance upon anthelmintics.
  • Introduction of additional control measures, e.g. vaccines, bio-active forages, nutraceuticals, ovicidals. 

Main critical gaps

Conclusion

Failure to implement effective control threatens animal welfare and productivity and, in the long term, food security.

Sources of information

Name of expert group leader

Jozef Vercruysse - Laboratory of Parasitology, Gent University

Name of reviewers

Project Management Board

Date of preliminary approval

17th September 2010

Date of final approval

1st October 2010