SciELO - Scientific Electronic Library Online

 
vol.40 número3Níveis de glicerina bruta na ensilagem de capim Tifton 85 (Cynodon dactylon): perfil fermentativo e valor nutricionalEvolução dos preços das terras agrícolas no Paraná entre 1998 e 2015 índice de autoresíndice de assuntosPesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Revista de Ciências Agrárias

versão impressa ISSN 0871-018X

Rev. de Ciências Agrárias vol.40 no.3 Lisboa set. 2017

https://doi.org/10.19084/RCA16028 

ARTIGO

 

Aspects of epidemiology and control of gastrointestinal nematodes in sheep and cattle – Approaches for its sustainability

Aspectos de epidemiologia e controle de nematódeos gastrintestinais em ovinos e bovinos – Abordagens à sua sustentabilidade

Katia Denise Saraiva Bresciani1,2* , Willian Marinho Dourado Coelho3, Jancarlo Ferreira Gomes4,5, Lucas Shigaki de Matos2, Thais Rabelo dos Santos6, Celso Tetsuo Nagase Suzuki4, Luiz Gustavo Ferraz Lima1 and Carlos Noriyuki Kaneto1

1 Universidade Estadual Paulista (Unesp), Faculdade de Medicina Veterinária de Araçatuba, Araçatuba, São Paulo, Brasil. Rua Clóvis Pestana, 793, Jardim Dona Amélia, Araçatuba, São Paulo, CEP 16050-680, Brasil

2 Universidade Estadual Paulista (Unesp), Faculdade de Ciências Agrárias e Veterinárias, Jaboticabal, São Paulo, Brasil;

3 Universidade Estadual Paulista (Unesp), Faculdade de Engenharia de Ilha Solteira, Ilha Solteira, São Paulo, Brasil;

4 Universidade Estadual de Campinas (UNICAMP), Departamento de Sistemas de Informação do Instituto de Computação, Laboratory of Image Data Science - LIDS, Campinas, Brasil.

5 Universidade Estadual de Campinas  (UNICAMP), Faculdade de Ciências Médicas, Campinas, Brazil.

6Universidade Federal dos Vales do Jequitinhonha e Mucuri, Rondônia, Brasil.

(*E-mail: bresciani@fmva.unesp.br)


ABSTRACT

Gastrointestinal helminthosis in ruminants cause considerable economic losses, with marked impairment of productivity of these animals, especially in poor management systems and poor parasite control programs. Infections caused by these helminths represent an obstacle to the expansion of the sheep industry. Furthermore, high parasite burdens were associated with increased mortality in calves. The recommended methods for the control of gastrointestinal helminths not always have practical applicability. We discuss important epidemiological and control aspects concerning gastrointestinal nematodes in sheep and cattle. Thus, sustainable worm control practices are recommended. Each farm has a specific situation and a management system directed to a specific parasitic infection must be adopted.

Keywords: cattle, sheep, gastrointestinal helminths, epidemiology, control, sustainability.


RESUMO

Helmintíases gastrintestinais em ruminantes acarretam perdas econômicas relevantes, com marcante prejuízo da produção animal, especialmente em sistemas de maneio precários e em programas de controle parasitário deficientes. Infeções causadas por esses helmintos representam um obstáculo para a expansão do mercado ovino. Ademais, altas cargas parasitárias foram associadas à elevada mortalidade em bezerros. Os métodos recomendados para o controle de helmintos gastrintestinais nem sempre apresentam aplicação prática. Nós discutimos os aspectos importantes sobre nematodes gastrintestinais em ovinos e caprinos. Sendo assim, práticas de controle sustentáveis são recomendadas. Cada propriedade possui uma situação em particular e um sistema de maneio direcionado deve ser adotado para as infecções parasitárias específicas.

Palavras-chave: bovinos, ovinos, helmintos gastrintestinais, epidemiologia, controlo, sustentabilidade.


INTRODUCTION

Gastrointestinal helminthosis in ruminants are caused by trichostrongylid wormswhich are small, often have a capillary form, with copulatory bursa, and, excepting the lungworm Dictyocaulus, infect the digestive tract of animals and birds. The most important genera in ruminants are Haemonchus, Trichostrongylus, Cooperia, Nematodirus and Ostertagia.

These helminths represent a major obstacle to the expansion of the sheep industry (Amarante et al., 2004) and cause considerable economic losses, with marked impairment of these animals productivity, especially in poor management systems and poor parasite control programs (Santos et al., 2010). Gastrointestinal nematodes (GINs) are a major disease in beef cattle around the world, and its main consequence is a decrease in production (Charlier et al., 2014). In this review we discuss important epidemiological and control aspects about gastrointestinal nematodes in sheep and cattle, towards the sustainability of animal and parasites management.

EPIDEMIOLOGY AND BIOLOGY

Very common species in sheep, as Haemonchus contortus, Cooperia curticei and Trichostrongylus colubriformis can also infect cattle, and species that affect cattle, as H. placei, T. axei and C. punctata, can parasitize sheep. Heterologous infections are mild and over time the animals naturally eliminate them (Amarante et al., 1997).

Many publications discuss on parasitism in cattle under 24 months of age (Tongson and Balediata, 1972; Wymann et al., 2007; Jiménez et al., 2010). With the beginning of the development of the immune response to these helminths, from 18 to 24 months, the tendency would be to reduce the parasitic burden, with a decrease in the number of eggs excreted in faeces and diminished incidence of clinical cases of hookworm. However, it was observed the frequent occurrence of nematodes in adult animals (Waruiru et al., 1998; Chollet et al., 2000).

The resistance of sheep to infection by these wormsis correlated to seasonal variations, the type of nutrition (Vagenas et al., 2007), proximity of parturition (Fthenakis et al., 2012), genetic factors (Mpetile et al., 2015) and certain racial patterns (Bowdridge et al., 2015). Some studies have reported a higher predominance of H. contortus in sheep, confirming the observations of this nematode, being more prevalent in extensive regimes of tropical and subtropical regions (Liu et al., 2003; Tariq et al., 2008; Yoshihara et al., 2015).

In general, the life cycle of gastrointestinal nematodes comprises the following steps: adult helminths in the digestive tract of the host eliminate eggs in the faeces; the larvae hatch, and after a period of development up to the third stage (L3), they become infective in the environment. The sheep or cattle ingest the contaminated vegetation, and once in the digestive tract, the larvae molt twice and give rise to adult specimens of both sexes, which will continue the life cycle of the parasite. Thus, there is a parasitic life phase (within the host) with a prepatent period of 14-44 days after infection, depending on the species, and a free-living phase (in the environment), which occurs under appropriate conditions of temperature and humidity in about a week (Yoshihara et al., 2013).

Trichostrongylids are responsible for symptoms such as diarrhoea, anaemia, weight loss, emaciation, and may cause death, especially in young animals. The subclinical symptoms related to parasitism may affect weight gain, reproductive rates and even the immune condition of ruminants (Santos et al., 2010; Tariq, 2015).

PARASITOLOGICAL DIAGNOSIS

The counting of eggs shed in faecal samples is used for the diagnosis of infection by gastrointestinal helminths, especially nematodes and does not allow immediate identification of the corresponding genera. For this, faecal cultures are used, allowing the production of third stage larvae (L3), which can be morphologically identified. This method is laborious and requires at least a week to allow the isolation and identification of different genera of L3, and can be affected by a failure in the development from egg to infective larvae (Berrie et al., 1988).

Another technique being advocated is micromorphometry, being possible to classify the genus of 53% to 72% of eggs. This measurement method is very laborious and time-consuming (Georgi and McCulloch, 1989). Anyway, these techniques do not allow the identification of species, but only genera. In epidemiological studies in which species identification is essential, it is necessary the necropsy of deceased animals and euthanasia of infected animals in poor clinical condition for the collection of adult nematodes, which are then classified into species.

Due to the resistance of gastrointestinal helminths of ruminants to many used active ingredients, the awareness of veterinarians (the technicians responsible for the herd parasitological control) is of great importance in order to evaluate the anthelmintic efficacy of products to be used, with periodic monitoring by faecal examinations. Each farm features a special situation and a management system directed to the infections issues must be implemented.

KNOWN ANTHELMINTIC RESISTANCE IN RUMINANTS AND ITS DIAGNOSIS

The development of resistance to these products are likely to start as soon as they reach the market, due to the lack of effective options and the increasing pressure for the use of drug combinations against highly resistant isolates.

The administration of anthelmintics to animals is the primary control measure adopted to prevent damages caused by worms (Miller and Horohov, 2006). For many years, anthelmintics were effective in controlling intestinal parasites in ruminants. However, one consequence of the widespread use of these drugs has been the emergence of resistant nematodes, a problem that is widespread in the sheep farming systems worldwide (Lopes et al., 2009; Palcy et al., 2010; Soutielo et al., 2010; Almeida et al., 2013).

With the increasing problem of anthelmintic resistance, more emphasis has been placed on identifying herds or animals with helminth-induced production losses, and targeting anthelmintic treatment to these subgroups to preserve anthelmintic efficacy while preventing production losses (Charlier et al., 2014).

The broad-spectrum anthelmintics (the benzimidazoles group, the imidazothiazoles and the macrocyclic lactones) remove parasites in different stages of development. The narrow-spectrum compounds, like salicylanilides, substituted phenols and triclabendazole, have activity against fewer species of parasites (Tariq, 2015). Although the development of monepantel added another molecule to the antiparasitic compounds market, success in discovering new drugs has been limited (Kumarasingha et al., 2016).

SUSTAINABLE CONTROL

The recommended methods for the control of gastrointestinal helminths in organic production are balanced nutrition, pasture rotation, use of resistant breeds and alternate grazing of sheep and cattle (NCAT, 2004), but not always have practical applicability. The effectiveness of the latter in the decontamination of pastures is intrinsically dependent on the specificity of the parasites to the hosts (Rocha et al., 2008). The positive or negative effect of rotational grazing on the control of nematodes is directly dependent on the climatic conditions of each region. It was proved that nematodes with free-living stages can survive on pasture throughout the year (Amarante and Barbosa, 1995). Therefore, in most situations, more sustainable worm control practices are recommended (Amarante et al., 2014).

Thus, for an effective reduction of pasture contamination, it should be taken a rest for the pastures during an extended period of time, being economically unviable. To perform an integrated parasite management, knowledge of the ecology of the free living stages of sheep and cattle parasites is highly required. For example, in tropical areas, the average life of the larvae on the pasture is one to three months. In temperate climates the larvae can be viable for 180 to 540 days (O’Connor et al., 2006).

The use of different species of ruminants grazing in the same area can be a way to reduce the populations of nematode larvae, besides allowing the improvement of pasture management. This treatment allows the larvae of parasites in sheep species to be ingested by the cattle or vice versa, which are destroyed in the host (Amarante et al., 2004). Based on the principle of host specificity of the parasites, the consortium of animals of different species consists of a management measure to be recommended in order to minimize pasture contamination (Amarante et al., 2014).

In general, animals have great susceptibility to parasitism until puberty. The resistance increases in adulthood, but there are certain times and physiological conditions in which the adult animal becomes more susceptible (Miller and Horohov, 2006). The intrinsic relationship between the intensity of parasitism and the age of affected cattle was mentioned as an essential element in a control program of gastrointestinal worms based in their epidemiology. With the adoption of strategic anthelmintic measures, it is possible to increase its efficacy, but also the cost-effectiveness of the activity.

The distribution of gastrointestinal helminths populations in dairy cows and calves in this organic production system does not constitute a health risk for the animals. Measures such as rotational grazing, pasture rest periods and use of genetically resistant animals are approaches that match with the principles of organic livestock production and play an important role in controlling gastrointestinal nematodes (Barbosa da Silva et al., 2012).

Several strategies have been suggested for the control of parasites, including adequate food to supply the nutritional requirements of the animal, which favours its body condition to confront disease threats, especially worm infections (Bricarello et al., 2005). Finally, supplementary feeding and breeding strategies to improve resistance to nematodes can reduce the use of anthelmintic drugs to control worm infections (Amarante et al., 2014).

Forages with high condensed tannin content when provided to sheep and cattle, improve protein digestion and absorption of amino acids. Animals that have higher protein absorption produce more wool, meat and milk, as well as, it improves the ovulation rate in females (Yoshihara et al., 2013).

Therefore, plant-based products can be considered as a viable alternative (Tariq, 2015). Carica papaya, Terminalia arjuna (Tannin and ellagic acid), Fumaria parviflora (alkaloids and tannins) and Zingiber officinale (ginger) showed efficacy against gastrointestinal nematodes of ruminants. The possibility of resistance to plant-based drugs is lower than chemical anthelmintics (Bauri et al., 2015).

These plant extracts could be introduced into the drinking water of livestock, especially cattle. This method of parasite control is indeed cheap and easy to practice and could be adopted to complement the already in-use method of application of commercially available chemical anthelmintics (Ngozi et al., 2015).

The sustainable use of certain fungi and earthworms may reduce parasitism in pastures, but needs to be further investigated against different gastrointestinal nematode parasite species all over the world (Tariq, 2015). The coadministration of Duddingtonia flagrans and Monacrosporium thaumasium has been effective in controlling gastrointestinal helminths of adults and young sheep (Vilela et al., 2016).

Many epidemiological aspects related to gastrointestinal helminths of ruminants need to be better elucidated by research, which will allow a current updated overview of these helminth infections.

CONCLUSION

In this review were discussed important epidemiological and control aspects about gastrointestinal nematodes in sheep and cattle. The pasture rotation system has been used to control parasite populations in the pasture, although alternate grazing systems using different host species seem to be also a good option on this sense. Plant-based products can be considered a viable alternative and showed efficacy against gastrointestinal nematodes of ruminants. Sustainable use of certain fungi and earthworms may reduce parasitism, but each farm has a special situation and a management system directed to the specific parasitic infection must be adopted accordingly.

 

References        [ Links ]

Amarante, A.F.T. and Barbosa, M.A. (1995) - Seasonal variations in populations of infective larvae on pasture and nematode faecal egg output in sheep. Arquivo Brasileiro de Medicina Veterinária e Zootecnia, vol. 7, p. 127–133.         [ Links ]

Amarante, A.F.T.; Bagnola Jr., J.; Amarante, M.R.V. and Barbosa, M.A. (1997) - Host specificity of sheep and cattle nematodes in São Paulo State. Brazil. Veterinary Parasitology,vol. 73, n. 1-2, p. 89–104.         [ Links ]

Amarante, A.F.T.; Bricarello, P.A.; Rocha, R.A. and Gennari, S.M. (2004) - Resistance of Santa Ines Suffolk and Ile de France lambs to naturally acquired gastrointestinal nematode infections. Veterinary Parasitology, vol. 120, n. 1-2, p. 91–106. http://dx.doi.org/10.1016/j.vetpar.2003.12.004        [ Links ]

Amarante, M.R.; Bassetto, C.C.; Neves, J.H. and Amarante, A. F. (2014) - Species-specific PCR for the identification of Cooperia curticei (Nematoda: Trichostrongylidae) in sheep. Journal of Helminthology, vol. 88, n. 4, p. 447-452. http://dx.doi.org/10.1017/S0022149X13000412        [ Links ]

Barbosa da Silva, J.; Rangel, C.P.; Fonseca, A.H. and Soares, J.P.G. (2012) - Gastrointestinal helminths in calves and cows in an organic milk production system. Revista Brasileira de Parasitologia Veterinária, vol. 21, n. 2, p. 87-91. http://dx.doi.org/10.1590/S1984-29612012000200003        [ Links ]

Bauri, R.K.; Tigga, M.N. and Kullu, S.S. (2015) - A review on use of medicinal plants to control parasites. Indian Journal of Natural Products and Resources, vol. 6, n. 4, p. 268–277.         [ Links ]

Berrie, D.A.; East, I.J.; Bourne, A.S. and Bremner, K.C. (1988) - Differential recoveries from fecal cultures of larvae of some gastro-intestinal nematodes of cattle. Journal of Helminthology, vol. 62, n. 2, p. 110-114. https://doi.org/10.1017/S0022149X00011330        [ Links ]

Bowdridge, S.A.; Zajac, A.M. and David, R. (2015) - St. Croix sheep produce a rapid and greater cellular immune response contributing to reduced establishment of Haemonchus contortus. Veterinary Parasitology, vol. 208, p. 204–210. http://dx.doi.org/10.1016/j.vetpar.2015.01.019        [ Links ]

Bricarello, P.A.; Amarante, A.F.T.; Houdijk, J.G.M.; Rocha, R.A.; Cabral Filho, S.L. and Gennari, S.M. (2005) - Influence of dietary protein supply on resistance to experimental infections with Haemonchus contortus in Ile de France and Santa Ines lambs. Veterinary Parasitology, vol. 134, n. 1-2, p. 99-100. http://dx.doi.org/10.1016/j.vetpar.2005.05.068        [ Links ]

Charlier, J.; Voort, M.V.; Kenyon, F.; Skuce, P. and Vercruysse, J. (2014) - Chasing helminths and their economic impact on farmed ruminants.  Trends in Parasitology, vol. 30, n. 7, p. 361-367. http://dx.doi.org/10.1016/j.pt.2014.04.009        [ Links ]

Chollet, J.Y.; Jacquiet, P.; Cardinale, E.; N-Damkou-Ndamkou, C.; Diop, C.; Thiam, A. and Dorchies, P. (2000) - Cooperia pectinata and C. puncata, parasites of the abomasum of cattle in northern Cameroon (Central Africa). Veterinary Parasitology, vol. 88, n. 1-2, p. 135-138. http://dx.doi.org/10.1016/S0304-4017(99)00202-2        [ Links ]

Fthenakis, G.C.; Arsenos, G.; Brozos, C.;  Fragkou, I.A.; Giadinis, N.D.; Giannenas, I.; Mavrogianni, V.S.; Papadopoulos, E. and Valasi, I. (2012).  Health management of ewes during pregnancy. Animal Reproduction Science, vol. 130, n. 3-4, p. 198-212. http://dx.doi.org/10.1016/j.anireprosci.2012.01.016        [ Links ]

Georgi, J.R. and Mcculloch, C.E. (1989) - Diagnostic morphometry: identification of helminth eggs by discriminant analysis of morphometric data. Proceedings of the Helminthological Society of Washington, vol. 56, p. 44-57.         [ Links ]

Jiménez, A.E.; Fernández, A.; Alfaro, R.; Dolz, G.; Vargar, B.; Epe, C. and Schnieder, T. (2010) - A cross-sectional survey of gastrointestinal parasites with dispersal stages in feces from Costa Rican dairy calves. Veterinary Parasitology, vol. 173, n. 3-4, p. 236-246. http://dx.doi.org/10.1016/j.vetpar.2010.07.013        [ Links ]

Kumarasingha, R.; Preston, S.; Yeo, T.C.; Lim, D.S.L.; Tu, C.L.; Palombo, E.A.; Shaw, J.M.; Gasser, R.B. and Boag, P.R. (2016)  Anthelmintic activity of selected ethno-medicinal plant extracts on parasitic stages of Haemonchus contortusParasites & Vectors, vol. 9, art. 187. http://dx.doi.org/10.1186/s13071-016-1458-9        [ Links ]

Liu, Y.; Cao, X.M.; Tan, M.Y. and Ying, P.Y. (2003) - Parasite spectrum and seasonal epidemiology of gastrointestinal nematodes of sheep in highland pasture in Hunan, south part of China (in Chinese). Journal of Veterinary Science and Technology, vol. 39, p. 9-10.         [ Links ]

Lopes, W.D.; Santos, T.R.; Borges, F.A.; Sakamoto, C.A.M.; Soares, V.E.; Costa, G.H.N.; Camargo, G.; Pulga, M.E., Bhushan, C. and Costa, A.J.C. (2009) - Anthelmintic efficacy of oral trichlorfon solution against ivermectin resistant nematode strains in cattle. Veterinary Parasitology, vol. 166, n. 1-2, p. 98-102. http://dx.doi.org/10.1016/j.vetpar.2009.07.045        [ Links ]

Mpetile, Z.; Cloete, S.W.P.; Kruger; A.C.M.; Dzama, K. (2015) - Environmental and genetic factors affecting faecal worm egg counts in Merinos divergently selected for reproduction. South African Journal of Animal Science, vol. 45, n. 5, p. 510-520. http://dx.doi.org/10.4314/sajas.v45i5.8        [ Links ]

Miller, J.E. and Horohov, D.W. (2006) - Immunological aspects of nematode parasite control in sheep. Journal of Animal Science, vol. 84, p. 124-132.         [ Links ]

Ngozi, D.U.; Ohalete, C.N.; Ibiam, U.K. and Okechukwu, R.I. (2015) - Medicinal plants effectiveness against helminths of cattle. Journal of Applied Biosciences, vol. 86, p. 7909-7917. http://dx.doi.org/10.4314/jab.v86i1.6        [ Links ]

NCAT (2004) - NCAT´s Organic livestock workbook: guide for sustainable and allowed practices. National Center for Appropriate Technology. [cit. 2011-03-12].: <http://attra.nact.org/attra-pub/PDF/livestockworkbook.         [ Links ]pdf>.

O’Connor, L.J.; Walkden-Brown, S.W. and Kahn, L.P. (2006) - Ecology of the free-living stages of major trichostrongylid parasites of sheep. Veterinary Parasitology, vol. 142, n. 1-2, p. 1-5. http://dx.doi.org/10.1016/j.vetpar.2006.08.035        [ Links ]

Palcy, C.; Silvestre, A.; Sauve, C.; Cortet, J. and Cabaret, J. (2010) - Benzimidazole resistance in Trichostrongylus axei in sheep: Long-term monitoring of affected sheep and genotypic evaluation of the parasite. The Veterinary Journal, vol. 183, n. 1, p. 68-74. http://dx.doi.org/10.1016/j.tvjl.2008.09.012        [ Links ]

Rocha, R.A.; Bresciani, K.D.S.; Barros, T.F.M.; Fernandes, L.H.; Silva, M.B. and Amarante, A.F.T. (2008) - Sheep and cattle grazing alternately: Nematode parasitism and pasture decontamination. Small Ruminant Research, vol. 75, n. 2-3, p. 135-143. http://dx.doi.org/10.1016/j.smallrumres.2007.09.001        [ Links ]

Santos, T.R.; Lopes, W.D.Z.; Buzulini, C.; Borges, F.A.; Sakamoto, C.A.M.; Lima, R.C.A.; Oliveira, G.P.O. and Costa, A.J. (2010) - Helminth fauna of bovines from the Central Western Region, Minas Gerais State, Brazil. Ciência Rural, vol. 40, n. 4, p. 934-938. http://dx.doi.org/10.1590/S0103-84782010005000040        [ Links ]

Soutielo, R.V.G.; Coelho, W.M.D.; Oliveira, F.P.; Fonzar, J.F.; Luquetti, B.C.; Souza, R.F.P.; Seno, M.C.Z. and Amarante, A.F.T. (2010) - Evaluation of reduction in egg shedding of gastrointestinal nematodes in cattle following administration of anthelmintics. Revista Brasileira de Parasitologia Veterinária, vol. 19, n. 3, p. 183-185. http://dx.doi.org/10.1590/S1984-29612010000300011        [ Links ]

Tariq, K.A.; Chishti, M.Z.; Ahmad, F. and Shawl, A.S. (2008) - Epidemiology of gastrointestinal nematodes of sheep managed under traditional husbandry system in Kashmir Valley. Veterinary Parasitology, vol. 158, n. 1-2, p. 138-143. http://dx.doi.org/10.1016/j.vetpar.2008.06.013        [ Links ]

Tariq, K.A. (2015) - A Review of the Epidemiology and Control of Gastrointestinal Nematode infections of Small Ruminants. Proceedings of the National Academy of Sciences, India Section B: Biological Sciences, vol. 85, n. 2, p. 693-703. http://dx.doi.org/10.1007/s40011-014-0385-9        [ Links ]

Tongson, M.S. and Balediata, E. (1972) - Epidemiology of bovine parasitic gastroenteritis. Journal of Veterinary Medicine, vol. 11, p. 63-72.         [ Links ]

Vagenas, D.; Bishop, S.C. and Kyriazakis, I. (2007) - A model to account for the consequences of host nutrition on the outcome of gastrointestinal parasitism in sheep: model evaluation. Parasitology, vol. 134, p. 1279-1289. http://dx.doi.org/10.1017/S0031182007002624        [ Links ]

Vilela, V.L.R.; Feitosa, T.F.; Braga, F.R; de Araújo, J. V.; Santos, A.;, Morais, D.F.; Souto, D.V.O. and Athayde, A.C.R. (2016) - Coadministration of nematophagous fungi for biological control over gastrointestinal helminths in sheep in the semiarid region of northeastern Brazil. Veterinary Parasitology, vol. 221, p. 139–143. http://dx.doi.org/10.1016/j.vetpar.2016.03.027        [ Links ]

Waruiru, R.M.; Nansen, P.; Kyusgaard, N.C.; Thamsborg, S.M.; Munyua, W.K.; Gathuma, J.M.and Borg, H.O. (1998) - An abattoir survey of gastrointestinal nematode infections in cattle in the central highlands of Kenya. Veterinary Research Communications, vol. 22, n. 5, p. 325-334. http://dx.doi.org/10.1023/A:1006164805185        [ Links ]

Wymann, M.N.; Bonfoh, B.; Traore, K.; Tembely, S. and Zinsstag, J. (2007) - Species diversity and acquisition of gastrointestinal parasites in calves aged 0–13 months in periurban livestock production in Mali. Veterinary Parasitology, vol. 143, n. 1, p. 67–73. http://dx.doi.org/10.1016/j.vetpar.2006.07.025        [ Links ]

Yoshihara, E.; Minho, A.L. and Yamamura, M.H. (2013). Efeito anti-helmíntico de taninos condensados em nematódeos gastrintestinais de ovinos (Ovis aries). Semina: Ciências Agrárias, vol. 34, n. 6, p. 3935-3950. http://dx.doi.org/10.5433/1679-0359.2013v34n6p3935        [ Links ]

 

Received/recebido: 2016.03.03

Received in revised form/recebido em versão revista: 2016.07.09

Accepted/aceite: 2017.02.23

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons