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Parasitic profile of traction equids in the semi-arid climate of Paraíba State, Northeastern, Brazil

Perfil parasitário de equídeos de tração em clima semiárido do Estado da Paraíba, Nordeste do Brasil

Abstract

The objective of this study was to determine the parasitological profiles of traction equids from the semi-arid climate of Paraíba (PB) State. We analyzed 96 equids that performed traction work, with no defined breed, males and females, and all older than 24 months. Among the analyzed animals, 51% were donkeys, 41.7% mules, and 7.3% horses. Fecal material and blood were collected for parasitological examination and to determine the packed cell volume (PCV), respectively. The samples were sent to the Veterinary Parasitology Laboratory, Veterinary Hospital - IFPB, Sousa-PB campus, and epidemiological questionnaires were provided to the owners. It was observed that 83.3% of equids tested positive for gastrointestinal parasites. Strongylidae was the most prevalent parasite (83.3%), followed by Giardia sp. (5.3%), and Eimeria sp. (2.1%). The mean eggs per gram (EPG) value of the fecal samples was 1143. Fecal analysis revealed that 78.9% of the larvae were from “small strongyles”. The presence of ectoparasites was not observed in the studied animals. The answers to our questionnaire revealed that 69.8% of the animals had never been dewormed and that the remaining 31.2% had only been dewormed once. We concluded that the prevalence of gastrointestinal parasites among traction equids in the municipality of Sousa-PB is high.

Keywords:
Traction animals; donkeys; horses; mules; parasitism; cyatosthome

Resumo

Objetivou-se determinar o perfil parasitológico de equídeos carroceiros no município de Sousa, Sertão da Paraíba. Foram analisados 96 equídeos que realizavam trabalho de tração, sem raça definida, machos e fêmeas, idade superior a 24 meses. Dentre os animais analisados 51% foram asininos, 41,7% muares e 7,3% equinos. Foi coletado material fecal para exames coproparasitológicos e sanguíneo para determinação do volume globular (VG), encaminhados ao Laboratório de Parasitologia Veterinária, Hospital Veterinário - IFPB, campus Sousa-PB. Foi aplicado questionários epidemiológicos aos proprietários. Observou-se que 83,3% dos equídeos carroceiros foram positivos nos exames parasitológicos fecais. Os Estrongilídeos foram os parasitos mais prevalentes (83,3%), seguidos por Giardia sp. (5,3%). e Eimeria sp. (2,1%). A média de OPG dos equídeos carroceiros foi 1143. Nas coproculturas, constatou-se que 78,9% das larvas eram de “pequenos estrôngilos”. Não foi observada a presença de ectoparasitas. Em 69,8% dos animais nunca haviam sido vermifugados e os demais 31,2% apenas uma vez. Concluiu-se que é alta a prevalência de parasitos gastrintestinais em equídeos carroceiros do município de Sousa-PB.

Palavras-chave:
Animais de tração; asininos; equinos; muares; parasitismo; ciatostomíneos

The use of traction equids is still very common in the interior of Brazil. They are important in the generation of income for families, especially through the collection of garbage and recyclables and the transport of materials ( PAZ et al., 2013 Paz CFR, Paganela JC, Oliveira DP, Feijó LS, Nogueira CEW. Biometric standard of traction horses in Pelotas, state of Rio Grande do Sul. Ciênc Anim 2013; 14(2): 159-163. ). Traction equids are used mainly in developing countries and are directly linked to jobs in agriculture, trade, and transport ( UPJOHN et al., 2014 Upjohn MM, Pfeiffer DU, Verheyen KL. Helping working Equidae and their owners in developing countries: monitoring and evaluation of evidence-based interventions. Vet J 2014; 199(2): 210-216. http://dx.doi.org/10.1016/j.tvjl.2013.09.065. PMid:24269105.
http://dx.doi.org/10.1016/j.tvjl.2013.0...
).

Among the diseases that affect the health of equids, those caused by parasites stand out because of the high associated morbidity ( BOTELHO et al., 2012 Botelho GG, Cassiano ALV, Botelho CFM, Botelho CFM. Análise hematológica, bioquímico-sérica e coproparasitológica de equinos criados em Seropédica, RJ. Rev Bras Med Vet 2012; 34(1): 69-72. ). Infection with gastrointestinal parasites is usually subclinical, resulting in significant losses in animals used for reproduction, sport, and work ( RIET-CORREA et al., 2001 Riet-Correa F, Schild AL, Méndez MC, Lemos RAA. Doenças de ruminantes e equinos. 2nd ed. São Paulo: Varela; 2001. ).

Infection with “small strongylus” or cyathostomines causes anemia, diarrhea, and reduced nutrient absorption, causing weight loss and decreased productivity ( MOLENTO, 2005 Molento MB. Parasite resistance on helminths of equids and management proposal’s. Cienc Rural 2005; 35(6): 1469-1477. http://dx.doi.org/10.1590/S0103-84782005000600041.
http://dx.doi.org/10.1590/S0103-8478200...
). The large strongyles are hematophagous parasites that are found in the mucosa of the cecum and colon of equids in the adult phase ( VAN DER KOLK & KROEZE, 2013 Van Der Kolk JH, Kroeze EJBV. Infectious diseases of the horse: diagnosis, pathology, management, and public health. London: Manson Publishing; 2013. ).

Gastrointestinal protozoa such as Eimeira sp., Giardia sp., and Cryptosporidium spp. cause intermittent diarrhea, anorexia, weight loss, and brittle hair ( GEURDEN et al., 2010 Geurden T, Vercruysse J, Claerebout E. Is Giardia a significant pathogen in production animals? Exp Parasitol 2010; 124(1): 98-106. http://dx.doi.org/10.1016/j.exppara.2009.03.001. PMid:19285075.
http://dx.doi.org/10.1016/j.exppara.200...
).

The most prevalent ectoparasites in equids include the ticks Amblyomma cajennense, Anocentor nitens, and Rhipicephalus (Boophilus) microplus . Tick infestation causes economic loss due to decreasing animal productivity and the expense associated with the use of tick preventives ( PRATA et al., 1996 Prata MCA, Alonso LS, Sanavria A. Parâmetros biológicos do estádio ninfal de Amblyomm cajennense (Fabricius, 1787) (Acari: Ixodidae) em coelhos. Rev Bras Cienc Vet 1996; 3(2): 55-57. http://dx.doi.org/10.4322/rbcv.2015.045.
http://dx.doi.org/10.4322/rbcv.2015.045...
).

There are no reports that describe the main parasites of traction horses, donkeys, and mules in the municipality of Sousa-PB. Therefore, the objective of this study was to identify the main parasites in working equids in the municipality of Sousa, arid midland of Paraíba.

This study was performed in the municipality of Sousa, Paraíba. The laboratory analyses were performed at the Veterinary Parasitology Laboratory (LPV), Veterinary Hospital, Federal Institute of Education Science and Technology of Paraíba (IFPB), Sousa-PB campus.

The number of animals required for analysis was calculated using an expected prevalence of 50% for gastrointestinal helminths, gastrointestinal protozoa, and ectoparasites since there are no previous reports detailing the prevalence of these parasites in equids in the semi-arid region of Paraíba. A minimum confidence level of 95% was also considered assuming a statistical error of 10% ( THRUSFIELD, 1995 Thrusfield M. Veterinary epidemiology. 2nd ed. Cambridge: Blackwell Science; 1995. ).

For the identification of helminths and protozoa in the equids, fecal samples were collected as advised by Gordon & Whitlock (1939) Gordon HM, Whitlock HV. A new technique for counting nematode eggs in sheep faeces. J Counc Sci Ind Res 1939; 12(1): 50-52. . Fecal analysis was performed in accordance with the study by Roberts & O’Sullivan (1950) Roberts FHS, O’Sullivan JP. Methods of egg cougars and laval cultures for strongyles infesting the gastrointestinal tract of cattle. Aust Agric Res 1950; 1(1): 99-102. http://dx.doi.org/10.1071/AR9500099.
http://dx.doi.org/10.1071/AR9500099 ...
, and the eggs per gram of feces (EPG) were calculated for each parasitic helminth. Centrifugation in Sucrose Solution (CFSS), the method developed by Tobie et al. (1938) Tobie J, Thomen LF, Sawitz W, D’Antoni JS, Peres C, Faust EC, et al. A critical study of clinical laboratory technics for the diagnosis of protozoan cysts and helminth eggs in feces 1. Am J Trop Med Hyg 1938; s1-18(2): 169-183. http://dx.doi.org/10.4269/ajtmh.1938.s1-18.169.
http://dx.doi.org/10.4269/ajtmh.1938.s1...
, was used to isolate protozoal cysts and oocysts as well as low-density eggs. For the quantification and identification of the larvae isolated in the fecal examinations, the method of Bevilaqua et al. (1993) Bevilaqua CML, Rodrigues ML, Cocordet D. Identification of infective larvae of some common nematode strongylids of horses. Rev Méd Vét 1993; 144(12): 989-995. was followed. To identify ectoparasites, inspection of the entire body of the animal was performed. For the determination of the PCV using the microhematocrit method ( FERREIRA et al., 1978 Ferreira JM No, Viana ES, Magalhães LM. Patologia clínica veterinária. Belo Horizonte: Rabelo and Brazil; 1978. ), blood samples were collected by jugular venipuncture into a tube containing EDTA anticoagulant (10%) and then sent to LPV.

An epidemiological questionnaire was provided to the owners of the traction equids, in which the cleanliness and nutrition of the animals were addressed. The following information was requested: owner's and animal’s signalment, management of the animal (nutrition and sanitation), and health history of the animal.

The data were analyzed using the chi-square test, followed by the Fisher's exact test at a 5% level of significance ( SERRA-FREIRE, 2002 Serra-Freire NM. Planejamento e análise de pesquisas parasitológicas. Niterói: Publisher of Fluminense Federal University; 2002. ).

We analyzed 96 equids that performed traction work in the municipality of Sousa-PB, with no defined breed, of both sexes, and of at least twenty-four months of age. Among the equids analyzed, 51% (49/96) were donkeys, 41.7% (40/96) mules, and 7.3% (7/96) horses.

It was observed that 83.3% (80/96) of the traction equids had positive fecal parasitological examinations. Piccoli et al. (2015) Piccoli C, Marques SMT, Appel G, Silveira E, Siqueira GB, Loos DE, et al. Helmintos intestinais em cavalos de trabalho e de lazer de Porto Alegre/RS. Sci Anim Health 2015; 3(1): 56-64. also detected a high prevalence of parasitic infection (82%) among traction horses in Porto Alegre, Rio Grande do Sul. Ferraro et al. (2008) Ferraro CC, Kloss AB, Souza DF, Deconto I, Biondo AW, Molento MB. Parasitological prevalence of cart-horses in Curitiba, Paraná. Rev Bras Parasitol Vet 2008;17(1 Suppl 1): 175-177. PMid:20059842. likewise identified a parasitological prevalence of 88% among traction horses in Curitiba, Paraná.

There was no statistically significant difference (p ≥ 0.05) in the prevalence of gastrointestinal parasites among the species evaluated ( Table 1 ).

Table 1
Number of infected animals and prevalence (%) of helminths and protozoa among traction equids in Sousa, Paraíba, Brazil.

Strongylidae were the most prevalent parasites (83.3%), followed by Giardia sp. (5.3%), and Eimeria sp. (2.1%). Infection with Strongylidae was also found to be common (96.03%) in traction and leisure horses in Porto Alegre, RS ( PICCOLI et al., 2015 Piccoli C, Marques SMT, Appel G, Silveira E, Siqueira GB, Loos DE, et al. Helmintos intestinais em cavalos de trabalho e de lazer de Porto Alegre/RS. Sci Anim Health 2015; 3(1): 56-64. ).

In the present work 5.3%(5/96) of the animals were positive for Giardia sp. and 2.1% (2/96) were positive for Eimeria sp. A similar prevalence for the genus Giardia (4%, 6/150) was found by Nasciutti et al. (2013) Nasciutti NR, Cabral DD, Cabral AD, Souza RR, Oliveira PM. Frequency of occurrence of Giardia sp. and Cryptosporidium spp. in equidae naturally infected and slaughtered in a slaughter house. Cienc Anim Bras 2013; 14(2): 253-257. in a slaughterhouse in the city of Araguari, Minas Gerais.

An association was observed between Strongylidae and the protozoa Giardia sp. in 8.2% (4/49) of the donkeys. Among the mules, 5% (2/40) were positive for the protozoa Eimeria sp. in combination with Strongylidae. Among the horses, 14.3% (1/7) had an association between Strongylidae and Giardia sp. In a study performed by Souza et al. (2009) Souza PN, Bomfim TC, Huber F, Abboud LC, Gomes RS. Natural infection by Cryptosporidium sp., Giardia sp. And Eimeria leuckarti in three groups of equines with different handlings in Rio de Janeiro, Brazil. Vet Parasitol 2009; 160(3-4): 327-333. http://dx.doi.org/10.1016/j.vetpar.2008.10.103. PMid:19117684.
http://dx.doi.org/10.1016/j.vetpar.2008...
on horses in Rio de Janeiro-RJ, an association was detected between Giardia sp. and Eimeria sp. This differed from the present study, in which no animal showed infection with more than one genus of protozoa.

It was observed that 85.7% of the male equids and 80% of the females were infected with gastrointestinal parasites. However, only among the horses was the difference between the sexes statistically significant (p ≤ 0.05) ( Table 2 ). However, low sampling of male horses may have interfered with the results and promoted this difference.

Table 2
Prevalence of helminths and protozoa among traction equids, according to sex, in Sousa, Paraíba, Brazil.

The mean (±SD) EPG of the traction equids was 1143(±1853). The donkeys possessed a statistically lower mean EPG (p ≤ 0.05) as compared to the other species at 807 (± 770), whereas the mule EPG average was 1571 (± 2682) and the horses was 1050 (± 800). On classifying by category, 35% (34/96) of the animals were classified as having low-level infection (<500), 28% (27/96) as medium (500-1000), and 37% (35/96) as high (>1000). The donkeys possessed the highest percentage of positive fecal examinations but the lowest level of parasitic disease, confirming the resistance of the species. Chitra et al. (2011) Chitra R, Rajendran S, Prasanna D, Kirubakaran A. Influences of age on the prevalence of parasitic infections among donkeys in Erode district, Tamilnadu, India. Vet World 2011; 4(6): 258-259. http://dx.doi.org/10.5455/vetworld.4.258.
http://dx.doi.org/10.5455/vetworld.4.25...
stated that, although donkeys are also known in India for their robustness, they are the species most vulnerable to parasitic infection.

Only among the horses did the prevalence of infection differ significantly (p ≤ 0.05) between the females and the males. In general for the traction equids, there was no statistically significant difference (p ≥ 0.05) in EPG between the sexes ( Table 3 ). Similar results were found by Ferraro et al. (2008) Ferraro CC, Kloss AB, Souza DF, Deconto I, Biondo AW, Molento MB. Parasitological prevalence of cart-horses in Curitiba, Paraná. Rev Bras Parasitol Vet 2008;17(1 Suppl 1): 175-177. PMid:20059842. when evaluating traction animals from Curitiba-Paraná, where the mean EPG for males was 1,492 and that for females was 1,322.

Table 3
Mean and standard deviation of eggs per gram (EPG) in male and female traction equids in Sousa, Paraíba, Brazil.

Mules aged ≥ 12 years had significantly higher EPG (p ≤ 0.05) as compared to mules in other age groups and to other species of the same age group ( Table 4 ). It was also observed that animals ≥ 12 years of age were more vulnerable (p ≤ 0.05) to high levels of parasitism. This finding was also made by Ferraro et al. (2008) Ferraro CC, Kloss AB, Souza DF, Deconto I, Biondo AW, Molento MB. Parasitological prevalence of cart-horses in Curitiba, Paraná. Rev Bras Parasitol Vet 2008;17(1 Suppl 1): 175-177. PMid:20059842. who observed an average EPG of 1438 (high level) in adult and geriatric animals. It has been shown that as they increase in age, equids develop a resistance where they may develop severe infections while remaining asymptomatic ( BOWMAN, 2014 Bowman DD. Georgis’ parasitology for veterinarians. 10th ed. Philadelphia: Saunders; 2014. ). Thus, equids of advanced age become sources of infection for younger animals.

Table 4
Relationship between mean EPG (± SD) and the equid age range.

No statistically significant difference was observed (p ≥ 0.05) when the EPG levels were evaluated in association with the PCV ( Figure 1 ). When evaluating gastrointestinal parasitism and hematology in horses and donkeys in São Luís, Maranhão, Ferreira et al. (2014) Ferreira GMS, Dutra FAF, Amorim EF Fo, Santos ACG. Gastrointestinal parasitism and hematology in horses and donkeys from the urban area of São Luís/MA, Northeast Brazil. Arch Vet Sci 2014; 19(2): 22-30. observed that the degree of parasitism was not responsible for the hematological alterations.

Figure 1
Packed cell volume (PCV) in relationship to the eggs per gram (EPG) levels among traction equids in Sousa, Paraíba, Brazil.

In the fecal examinations, it was found that 78.9% of the larvae were small strongyles or cyathostomes, followed by 7.1% Strongylus equinus, 3% Strongylus edentatus , 6% Strongylus vulgaris, and 5% Trichostrongylus axei ( Figure 2 ). It was observed that among the horses, S. vulgaris was present with the highest prevalence (12.8%). Similar results were obtained by Ferraro et al. (2008) Ferraro CC, Kloss AB, Souza DF, Deconto I, Biondo AW, Molento MB. Parasitological prevalence of cart-horses in Curitiba, Paraná. Rev Bras Parasitol Vet 2008;17(1 Suppl 1): 175-177. PMid:20059842. , with an average prevalence of 88% for the cyathostomes and 12% for S. vulgaris .

Figure 2
Percentage of gastrointestinal helminths infecting traction equids in Sousa, Paraíba, Brazil.

Although a thorough visual inspection was performed on all animals, the presence of ectoparasites was not observed. Perhaps the rusticity of these animals, coupled with the absence of a defined breed and the high temperatures present throughout the year, does not favor ectoparasite infestation. Rego et al. (2009) Rego DX, Schmeil BRP, Schiller JW, Silva MM, Ramos CG, Michelotto PV Jr. Incidence of endoparasites and ectoparasites in equines from the city of Curitiba - Paraná. Rev Acad Cien Agrar Amb 2009; 7(3): 281-287. also did not identify ectoparasites in 166 equines used for work and sport in Curitiba, Paraná. According to Chagas et al. (2001) Chagas ACS, Furlong J, Nascimento CB. Behavior and ecology of engorged females of the tick, Boophilus microplus in pastures of the grass, Brachiaria decumbens in Brazil. Braz J Vet Res Anim Sci 2001; 38(4): 188-191. , high temperatures do not provide an ideal environment for the breeding and survival of engorged female ticks, and at 20 °C the females are not very mobile. In Sousa-PB, the average annual temperature is 27 °C, and the average daytime temperature exceeds 35 °C. By contrast, in Curitiba-PR, the average annual temperature does not exceed 17.5 °C ( IBGE, 2010 Brazilian Institute of Geography and Statistics – IBGE [online]. 2010 [cited 2017 Feb 13]. Available from: https://www.ibge.gov.br/
https://www.ibge.gov.br/ ...
).

In the epidemiological questionnaire, 63.5% (61/96) of the owners replied that they possessed other equids in addition to the evaluated animal, and 60.4% (58/96) of the equids were maintained in direct contact with other species of animals. These included canines, felines, poultry, cattle, sheep, goats, and pigs.

Regarding the use of dewormers, 69.8% (67/96) of the equids had never been dewormed and the remaining 31.2% (29/96) had only been dewormed once. Of the dewormers used, the only compound cited was ivermectin. The most commonly used formulation was paste (51.7%, 15/29), followed by injectable (48.3%, 14/29). The limited use of dewormers may explain the high parasite burden found in this study, where it was observed that 65% (62/96) of the animals possessed EPG > 500 (medium to high).

None of the equids evaluated had been vaccinated. Furthermore, the term “vaccinated” was frequently confused with ”dewormed”, which denotes a low level of knowledge regarding animal health management possessed by the owners.

With regard to nutrition, 59.5% (57/96) of the equids in this study were fed a combination of grass and corn, 37.5% (36/96) were pasture-fed only, and 3% (3/96) were provided a mixture of pasture and a commercial ration. It is well known that little attention is paid to the quality of the food provided to traction equids. This may be one of the factors contributing to the high prevalence of parasitism observed in the present study. It has been proven that a well-balanced diet can improve the immune response of the host, and therefore limit the development of parasitic infections.

Inadequate nutrition and sanitation was observed in a study by Herd (1990) Herd RP. Equine parasite control-solutions to anthelmintic associated problems. Equine Vet Educ 1990; 2(2): 86-91. http://dx.doi.org/10.1111/j.2042-3292.1990.tb01396.x.
http://dx.doi.org/10.1111/j.2042-3292.1...
. According to the investigators in that study, forced labor, malnutrition, and stress were associated with parasitism, and severely impaired the health of the equids, even leading to death. However, despite being used all day for work under adverse environmental conditions, the traction equids in this study were resistant to parasitic disease. No affliction was reported that required removal of any of the equids from work.

We concluded that the prevalence of gastrointestinal parasites in traction equids in the municipality of Sousa-PB is high. However, no animal presented parasitic disease. Ectoparasites were not founded on the animals in this study. Increased awareness is required for owners to improve the cleanliness of these animals.

References

  • Bevilaqua CML, Rodrigues ML, Cocordet D. Identification of infective larvae of some common nematode strongylids of horses. Rev Méd Vét 1993; 144(12): 989-995.
  • Botelho GG, Cassiano ALV, Botelho CFM, Botelho CFM. Análise hematológica, bioquímico-sérica e coproparasitológica de equinos criados em Seropédica, RJ. Rev Bras Med Vet 2012; 34(1): 69-72.
  • Bowman DD. Georgis’ parasitology for veterinarians. 10th ed. Philadelphia: Saunders; 2014.
  • Brazilian Institute of Geography and Statistics – IBGE [online]. 2010 [cited 2017 Feb 13]. Available from: https://www.ibge.gov.br/
    » https://www.ibge.gov.br/
  • Chagas ACS, Furlong J, Nascimento CB. Behavior and ecology of engorged females of the tick, Boophilus microplus in pastures of the grass, Brachiaria decumbens in Brazil. Braz J Vet Res Anim Sci 2001; 38(4): 188-191.
  • Chitra R, Rajendran S, Prasanna D, Kirubakaran A. Influences of age on the prevalence of parasitic infections among donkeys in Erode district, Tamilnadu, India. Vet World 2011; 4(6): 258-259. http://dx.doi.org/10.5455/vetworld.4.258.
    » http://dx.doi.org/10.5455/vetworld.4.258
  • Ferraro CC, Kloss AB, Souza DF, Deconto I, Biondo AW, Molento MB. Parasitological prevalence of cart-horses in Curitiba, Paraná. Rev Bras Parasitol Vet 2008;17(1 Suppl 1): 175-177. PMid:20059842.
  • Ferreira GMS, Dutra FAF, Amorim EF Fo, Santos ACG. Gastrointestinal parasitism and hematology in horses and donkeys from the urban area of São Luís/MA, Northeast Brazil. Arch Vet Sci 2014; 19(2): 22-30.
  • Ferreira JM No, Viana ES, Magalhães LM. Patologia clínica veterinária. Belo Horizonte: Rabelo and Brazil; 1978.
  • Geurden T, Vercruysse J, Claerebout E. Is Giardia a significant pathogen in production animals? Exp Parasitol 2010; 124(1): 98-106. http://dx.doi.org/10.1016/j.exppara.2009.03.001. PMid:19285075.
    » http://dx.doi.org/10.1016/j.exppara.2009.03.001
  • Gordon HM, Whitlock HV. A new technique for counting nematode eggs in sheep faeces. J Counc Sci Ind Res 1939; 12(1): 50-52.
  • Herd RP. Equine parasite control-solutions to anthelmintic associated problems. Equine Vet Educ 1990; 2(2): 86-91. http://dx.doi.org/10.1111/j.2042-3292.1990.tb01396.x.
    » http://dx.doi.org/10.1111/j.2042-3292.1990.tb01396.x
  • Molento MB. Parasite resistance on helminths of equids and management proposal’s. Cienc Rural 2005; 35(6): 1469-1477. http://dx.doi.org/10.1590/S0103-84782005000600041.
    » http://dx.doi.org/10.1590/S0103-84782005000600041
  • Nasciutti NR, Cabral DD, Cabral AD, Souza RR, Oliveira PM. Frequency of occurrence of Giardia sp. and Cryptosporidium spp. in equidae naturally infected and slaughtered in a slaughter house. Cienc Anim Bras 2013; 14(2): 253-257.
  • Paz CFR, Paganela JC, Oliveira DP, Feijó LS, Nogueira CEW. Biometric standard of traction horses in Pelotas, state of Rio Grande do Sul. Ciênc Anim 2013; 14(2): 159-163.
  • Piccoli C, Marques SMT, Appel G, Silveira E, Siqueira GB, Loos DE, et al. Helmintos intestinais em cavalos de trabalho e de lazer de Porto Alegre/RS. Sci Anim Health 2015; 3(1): 56-64.
  • Prata MCA, Alonso LS, Sanavria A. Parâmetros biológicos do estádio ninfal de Amblyomm cajennense (Fabricius, 1787) (Acari: Ixodidae) em coelhos. Rev Bras Cienc Vet 1996; 3(2): 55-57. http://dx.doi.org/10.4322/rbcv.2015.045.
    » http://dx.doi.org/10.4322/rbcv.2015.045
  • Rego DX, Schmeil BRP, Schiller JW, Silva MM, Ramos CG, Michelotto PV Jr. Incidence of endoparasites and ectoparasites in equines from the city of Curitiba - Paraná. Rev Acad Cien Agrar Amb 2009; 7(3): 281-287.
  • Riet-Correa F, Schild AL, Méndez MC, Lemos RAA. Doenças de ruminantes e equinos 2nd ed. São Paulo: Varela; 2001.
  • Roberts FHS, O’Sullivan JP. Methods of egg cougars and laval cultures for strongyles infesting the gastrointestinal tract of cattle. Aust Agric Res 1950; 1(1): 99-102. http://dx.doi.org/10.1071/AR9500099.
    » http://dx.doi.org/10.1071/AR9500099
  • Serra-Freire NM. Planejamento e análise de pesquisas parasitológicas. Niterói: Publisher of Fluminense Federal University; 2002.
  • Souza PN, Bomfim TC, Huber F, Abboud LC, Gomes RS. Natural infection by Cryptosporidium sp., Giardia sp. And Eimeria leuckarti in three groups of equines with different handlings in Rio de Janeiro, Brazil. Vet Parasitol 2009; 160(3-4): 327-333. http://dx.doi.org/10.1016/j.vetpar.2008.10.103. PMid:19117684.
    » http://dx.doi.org/10.1016/j.vetpar.2008.10.103
  • Thrusfield M. Veterinary epidemiology 2nd ed. Cambridge: Blackwell Science; 1995.
  • Tobie J, Thomen LF, Sawitz W, D’Antoni JS, Peres C, Faust EC, et al. A critical study of clinical laboratory technics for the diagnosis of protozoan cysts and helminth eggs in feces 1. Am J Trop Med Hyg 1938; s1-18(2): 169-183. http://dx.doi.org/10.4269/ajtmh.1938.s1-18.169.
    » http://dx.doi.org/10.4269/ajtmh.1938.s1-18.169
  • Upjohn MM, Pfeiffer DU, Verheyen KL. Helping working Equidae and their owners in developing countries: monitoring and evaluation of evidence-based interventions. Vet J 2014; 199(2): 210-216. http://dx.doi.org/10.1016/j.tvjl.2013.09.065. PMid:24269105.
    » http://dx.doi.org/10.1016/j.tvjl.2013.09.065
  • Van Der Kolk JH, Kroeze EJBV. Infectious diseases of the horse: diagnosis, pathology, management, and public health. London: Manson Publishing; 2013.

Publication Dates

  • Publication in this collection
    24 May 2018
  • Date of issue
    Apr-Jun 2018

History

  • Received
    15 July 2017
  • Accepted
    03 Apr 2018
Colégio Brasileiro de Parasitologia Veterinária FCAV/UNESP - Departamento de Patologia Veterinária, Via de acesso Prof. Paulo Donato Castellane s/n, Zona Rural, , 14884-900 Jaboticabal - SP, Brasil, Fone: (16) 3209-7100 RAMAL 7934 - Jaboticabal - SP - Brazil
E-mail: cbpv_rbpv.fcav@unesp.br