SciELO - Scientific Electronic Library Online

 
 issue37Prevalence of Crib-Biting and Weaving in Stabled Horses Tie StallsComplications of surgical sterilization by ovariohysterectomy in female dogs: A systematic review author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Revista de Medicina Veterinaria

Print version ISSN 0122-9354On-line version ISSN 2389-8526

Rev. Med. Vet.  no.37 Bogotá July/Dec. 2018

https://doi.org/10.19052/mv.vol1.iss37.9 

Artículos

Infección con Fasciola hepatica en el ganado y hospederos intermediarios en 10 vaquerías de un municipio occidental de Cuba

Natural Infection with Fasciola hepatica in Host-Snails and Cattle in Ten Dairy Farms from a Western Municipality in Cuba

Infecção com Fascíola hepática no gado e hospedeiros intermediários em 10 leiterias de um município ocidental de Cuba

Adonis Pino Santos1 

Antonio A. Vázquez2 

Ingrid Doménech3 

Raydel Martínez4 

Jorge Sánchez5 

Elieser Martínez6 

1 Veterinarian and Zootechnician, Master in Parasitology, Laboratory of Parasitic Zoonosis, Institute of Tropical Medicine “Pedro Kourí”, Havana, Cuba. adonispino1985@yahoo.com

2 Biologist, Doctor of Science, Laboratory of Malacology, Institute of Tropical Medicine “Pedro Kourí”, Havana, Cuba. applesnail@hotmail.fr

3 Medical Doctor, Infectologist, Master of Science, Laboratory of Parasitic Zoonosis, Institute of Tropical Medicine “Pedro Kourí”, Havana, Cuba. orue@infomed.sld.cu

4 Department of Epidemiology, Institute of Tropical Medicine “Pedro Kourí”, Havana, Cuba.

5 Technician. Laboratory of Malacology, Institute of Tropical Medicine “Pedro Kourí”, Havana, Cuba. jsanchez@ipk.sld.cu

6 Veterinarian, Genetic Cattle Farm “Camilo Cienfuegos”, Consolación del Sur, Pinar del Río province, Cuba. kleinvet@gmail.com


Resumen

La fasciolosis es una trematodosis que afecta fuertemente al ganado de Cuba. Se estudiaron 10 vaquerías del municipio más occidental de Cuba para determinar la prevalencia de esta parasitosis en el ganado y en los hospederos intermediarios. Se recolectaron y estudiaron muestras fecales de 455 vacas lecheras seleccionadas al azar. Las muestras fueron conservadas a -20 oC hasta su estudio. La detección de la infección por Fasciola hepatica fue realizada a partir de un método de Elisa denominado FasciDIG®. El análisis e interpretación de los resultados demostró que 146 muestras fueran positivas a F. hepatica (32,09 %). Todas las vaquerías presentaron animales infectados con rangos de prevalencia entre las vaquerías que oscilaron de 9,5 % al 84 %. También fue posible encontrar las dos especies de hospederos intermediarios de este parásito en Cuba, Galba cubensis y Pseudosuccinea columella. Debe prestarse atención a la prevalencia en bovinos encontrada en este estudio para prevenir la aparición de brotes humanos de esta enfermedad.

Palabras clave: ganado; limneidos; Fasciola hepatica; trematodosis; Cuba

Abstract

Fasciolosis is a foodborne trematodosis affecting many cattle farms in Cuba. Ten dairy farms in western Cuba were studied to assess the prevalence in both intermediate and definitive hosts. A single stool sample from 455 dairy cows was taken and studied. The animals were randomly selected and the samples were kept at -20oC until infection was determined. Detection of the Fasciola hepatica infection was carried out using a non-commercial sandwich-ELISA called FasciDIG®. Results showed that 146 samples were positive for F. hepatica (32.09%) with every farm testing positive for F. hepatica infection, while prevalence ranged from 9.5% to 84% among farms. It was also possible to detect the presence of the two species of intermediate hosts of this trematode in Cuba, Galba cubensis and Pseudosuccinea columella. Main attention must be given to bovine prevalence found in this study in order to prevent eventual human outbreaks of this disease.

Keywords: cattle; lymnaeid snails; Fasciola hepatica; trematodosis; Cuba

Resumo

A fasciolose é uma trematoda que afeta fortemente ao gado de Cuba. Foram estudadas 10 leiterias do município mais ocidental de Cuba para determinar a prevalência desta parasitose no gado e nos hospedeiros intermediários. Se coletaram e estudiaram amostras fecais de 455 vacas leiteiras selecionadas aleatoriamente. As amostras foram conservadas a −20 oC até seu estudo. A detecção da infecção por Fascíola hepática foi realizada a partir de um método de Elisa denominado FasciDIG®. A análise e interpretação dos resultados demonstrou que 146 amostras foram positivas à F. hepática (32,09 %). Todas as leiterias apresentaram animais infectados com rangos de prevalência entre as leiterias que oscilaram de 9,5 % a 84 %. Também foi possível encontrar a duas espécies de hospedeiros intermediários deste parasita em Cuba, Galba cubensis e Pseudosuccinea columella. Deve prestar-se atenção à prevalência em bovinos encontrada neste estudo para prevenir a aparição de surtos humanos desta enfermidade.

Palavras-chave: gado; limneidos; Fasciola hepática; trematódea; Cuba

Introduction

Fasciola hepatica (also known as “the Liver Fluke”), is the main trematode responsible of fasciolosis, which affects bovines and goat livestock populations worldwide (1). The infection is not just a problem for cattle, but also a public health issue, considered as an increasingly relevant zoonosis in many countries (2). One of the most important aspects of fasciolosis infection is that the pathology and disease take place as early as three or four weeks after infection. During this time, the diagnosis can only be confirmed by coprology at two months post infection in cattle (3). This parasite can infect animals and last for years inside the definitive host without causing death. The fact that this parasite can persist for long periods of time suggests that the feces of infected animals can contaminate pastures and intermediate hosts, allowing it to extend in time the cycle of the parasite (4).

The epidemiology of fasciolosis is strongly related to the ecology of the snails that serve as intermediate hosts of the parasite. Lymnaeid snails are responsible for F. hepatica transmission worldwide (5). In Cuba, there are only two types of lymnaeid snails, Galba cubensis and Pseudosuccinea columella, whose susceptibility to F. hepatica infection has been proved (6, 7, 8), and their settlement in subtropical areas is favored by the high moisture associated with frequent rainfall and moderate temperatures. Other malacological studies (7,9,10,11) have been carried out in Cuba, which made it possible to understand the biology and population dynamics of lymnaeid snails.

On the other hand, between 1944 and 2007, at least seven major human outbreaks have been reported in Cuba, three of which occurred in the Pinar del Río province, involving more than 1000 people (12). This province is one of the most used for cattle breeding, but it is not frequent to find reports regarding the prevalence of fasciolosis in bovines. Nevertheless, it is well known that local endemic animal fasciolosis is commonly associated with human infection (13) and the reservoir role of domestic animals is related with transmission of human fasciolosis (14).

Taking into account the severe impact on Cuban bovine livestock farming due to fasciolosis (15,16) and the effect of this disease on the human population (12), the aim of this work was to determine the prevalence of Fasciola hepatica in cattle and its association with the intermediate hosts inhabiting in a rural area of the Pinar del Río province.

Material and Methods

The study was carried out in a livestock farming area (including 14 farms with 1528 bovines) located in the Consolación del Sur municipality, Pinar del Río province, Cuba, from February 2011 to March 2012. The entire area surrounding the rural community of “El Canal” is inhabited by more than one thousand people, whose main source of employment is stockbreeding.

Ten farms were randomly selected. The infection of F. hepatica in cattle was determined in each farm as well as in the collection of snails (Figure 1).

Figure 1 Map of the “El Canal” community, Consolación del Sur municipality, Pinar del Rio province, Cuba. Source (17). 

Study animals: A single stool sample from 455 dairy cows was studied. The animals were randomly selected, and the samples were kept at -20oC until the infection was determined. The totality of cattle was from dairy farms that grazed in open field pastures of mixed grasses (Panicum maximum, Brachiaria brizantha, Cynodon nlemfuensis) and legumes (Leucaena leucocephala and Pueraria phaseoloides). The cattle were also given harvested forages (Saccharum officinarum, Pennisetum purpureum).

Detection of Fasciola hepatica infection: It was carried out using a non-commercial sandwich-ELISA called FasciDIG®, which was developed for diagnosis in humans and later validated in animals (18,19).

Collection of snails: A total of 50 snails were collected from each bovine livestock farm using forceps and sieves (11). The mollusks were kept in moist conditions and taken to the Malacology Laboratory at the Institute of Tropical Medicine where they were subsequently dissected to identify larval stages of F. hepatica.

Results

F. hepatica infection in cattle

Considering the ten farms studied, 146 of a total of 455 collected faecal samples tested positive for F. hepatica (32.09%). Every farm was found to be infected with F. hepatica, which varied in prevalence with ranges from 9.5% to 84% among farms (Table 1).

It was also possible to detect the presence of the two species of intermediate hosts of F. hepatica in Cuba, Galba cubensis and Pseudosuccinea columella, with the former as the only one infected with F. hepatica (table 1).

Table 1 Fasciola hepatica infection in cattle and presence of the parasite in intermediate snails collected in the livestock 

Livestock Cattle Intermediate snails of F. hepatica
Total Infected by F. hepatica
No. (%) G. cubensis P. columella
108 80 26 (32.5) - -
115 63 6 (9.5) - 0
121 39 12 (30.8) - 0
122 35 16 (45.7) + 0
124 25 21 (84.0) - 0
125 87 15 (17.2) - -
126 20 5 (25.0) - 0
127 56 17 (30.4) + 0
130 25 17 (68.0) - 0
131 25 11 (44.0) + 0
Total 455 146 (32.09)

(0) snail species absence, (-) negative for F. Hepatica, (+) positive for F. hepatica

Freshwater snail associated to the livestock farms

Eight species of freshwater snails (six pulmonates and two caenogastropods) were found in the entire area. Detailed information about snail species and the type of ecosystem found in each farm is summarized in Table 2.

G. cubensis was found in every farm, while P. columella occurred only in two of them. The savanna habitat and the low species richness predominated, with the exception of the pond located nearby farm 125, where the highest number of snail species was found.

Table 2 Presence/absence of freshwater snails in the studied farms 

Livestock Habitat Families of fresh-water snails
Lymnaeidae Physidae Planorbidae Thiaridae Ampullariidae
G.cub P. col P. acu D.ana D.luc B.hel T. gra P. poe
108 Savanna 1 1 0 0 0 0 0 0
115 1 0 0 0 0 0 0 0
121 1 0 0 0 0 0 0 0
122 1 0 0 0 0 0 1 0
124 1 0 0 0 0 0 0 0
125 Pond 1 1 1 1 1 1 0 1
126 Savanna 1 0 1 0 0 0 0 0
127 1 0 0 0 0 0 0 1
130 1 0 1 0 0 0 0 0
131 1 0 1 0 0 0 0 0
(0) Absence (1) Presence G.cub= Galba cubensis; P. col= Pseudosuccinea columella; P.acu= Physa acuta; D.ana= Drepanotrema anatinum; D.luc= Drepanotrema lucidum; B.hel= Biomphalaria helophila; T.gra= Tarebia granifera; P. poe= Pomacea poeyana

Discussion

Fasciolosis causes significant economic losses worldwide in animal husbandry, mainly ruminants, estimated at US$ 3 billion per annum, due to reduction in meat and milk production (20). The Cuban bovine cattle is a product of a prolonged process of natural selection, of the descendants of the cattle Bos taurus introduced by the Spanish conquerors and of animal coming from Africa, mainly Bos indicus. This crossbreeding has allowed great adaptability to tropical climates and more resistance to the infectious diseases (21). However, and in spite of this, cattle losses due to F. hepatica infection are still reported every year (16,22).

In the present study the number of cattle infected found in the whole area can be due to a number of factors such as: (I) every farm is located in a suitable ecosystem for lymnaeid snails settlement; (II) bad management of livestock allows the encounter of both intermediate and definitive hosts; and (III) grazing animals usually drink contaminated water with metacercariae in the field. During the dry season, ponds and streams experience a significant shrinkage and snail populations are forced to concentrate in the remaining waters, which are at the same time the only one available for cattle. Thus, infection may increase severely under these conditions.

The levels of cattle infection (32.09% in the whole area) are a reflection of this problem. Since every infected animal is an excellent disseminator of the parasite (rates of excretion of F. hepatica eggs can reach thousands/day; see (4) for review), these numbers may actually be considered as very high. The prevalence found in this study also agrees with the values found in other countries (23,24,25,26), and similar results of infection rates have been found in Chile (30.1% of infected cattle) (24) and Zimbabwe with the Fasciola gigantica species (31.7% of infected cattle) (27). A higher prevalence of 46.58% has been reported in Ethiopia (28), and the level of infection in a study carried out in five districts of Vietnam varied from 60 to 76% (13).

Fasciolosis is considered the vector-borne disease that has the widest geographical distribution (1,29), placing it as the most prevalent helminthic infection in cattle in the tropics with a variable frequency from 30 to 90% (30). In Cuba, this disease is one of the most important parasitic diseases in livestock animals (12,31) and differences in prevalence of fasciolosis in different areas may be attributed to variations in ecological, climatic and animal husbandry practices (32).

The diagnosis by FasciDIG® allowed the quick detection of F. hepatica, especially because this technique only needs a single sample to detect coproantigens. It also provides positive results four weeks before egg excretion starts, preventing economic losses (15,19,33). Also, the use of feces rather than serum to perform the test has better practical and ethical advantages. This method has been validated in human and animals using stool samples (18,19,34) and has been successfully used in fasciolosis-endemic areas of South America like Colombia, Argentina, Peru, Uruguay, and Venezuela, leading to more accurate diagnosis of this disease (23,35,36).

Intermediate snail host found

Most of the snail species found (P. poeyana, P. cubensis, T. granifera, D. lucidum, G. cubensis and P. columella) were also identified by Cañete, Yong, Sánchez, et al. (37) and Gutiérrez, Hernández, and Sánchez (11) in studies conducted in similar ecosystems in the province of Pinar del Río. Diversity in freshwater snail communities may affect the distribution and abundance of several species, especially those acting as intermediate host of parasites (38). Galba cubensis have been found as a dominant species in low diversity habitats, whereas in highly diverse ecosystems it may occur with low abundance (39). Interestingly, G. cubensis populations were found in all dairies studied, while P. columella was found in two livestock, which enhances the idea of the former being the main agent responsible for fasciolosis in Cuba (6,7,11,40).

The higher ecological diversity observed in the pond belonging to farm 125 may be due to its ecological features (abundant aquatic vegetation, depth, area). The results obtained in the distribution of G. cubensis in the whole area agrees with the general pattern observed in Cuba in this species (mainly in areas of low diversity and high human activity) while on the contrary, P. columella has more affinity to sites with less human activity (7). Although P. columella has been found only in two sites, it does not diminish its importance as a transmitter of F. hepatica. Its role in the transmission of fasciolosis has been referred in laboratory conditions (6,11,41) and recently in nature for the first time in Cuba and the Caribbean (8). Natural infection of this species has also been reported in other countries like Brazil, Australia, and Argentina (42,43), and it was introduced in France with the possibility of transmission capacity (44).

The rates of infection found in every farm indicate that the F. hepatica life cycle is running perfectly in the whole study area. This fact may jump to the idea that, although the sampling of non-infected snail may occur in a particular area where cattle are infected, it does not necessarily mean that they do not exist. The transmission of any parasite is a probabilistic event that ultimately depends on the distribution of its hosts (45). Hence, sampling size is a key factor to detect infected snails in the field but it is not a determinant fact to prove transmission.

The epidemiology of any snail-borne disease is closely related to the ecology of the snails. To date there are approximately 100 known species of lymnaeids, some of which have been identified in the Americas (G. cubensis, P. columella, Galba truncatula, Lymnaea humilis, G. viatrix, among others) (5). As a result of a presumed endemism of fasciolosis in Cuba and that there are favorable conditions (high humidity and rainfall) for the settlement of lymnaeids, several studies have been developed to investigate the ecology and population dynamics of these snails (7,11,41,46).

These investigations have helped to understand more about the epidemiology of this disease, but there are still some problems, such as lack of medicines to treat animals and poor husbandry practices that undermine the control of fasciolosis (12). Main attention must be given to the bovine prevalence found in this study to prevent future outbreaks of this trematodosis, as has occurred over the last few years in this geographical area.

Acknowledgements

The authors are very grateful to the health authorities of Consolación del Sur, and to the leaders from the Empresa Genética Pecuaria “Camilo Cienfuegos” for granting us permission to collect the samples.

References

1. Mas-Coma S, Valero MA, Bargues MD. Effects of climate change on animal and zoonotic helminthiases. Rev Sci Tech. 2008;27:443-457. [ Links ]

2. World Health Organization. Action against worm. Washington: WHO; 2007. [ Links ]

3. Hillyer GV, Sanchez Z, de Leon D. Immunodiagnosis of bovine fascioliasis by enzyme-linked immunosorbent assay and immunoprecipitation methods. J Parasitol. 1985;71:449-54. [ Links ]

4. Fairweather I, Threadgold L, Hanna RB. Development of Fasciola hepatica in the Mammalian Host. In: Dalton JP, editor. Fascioliasis. London: CABI Publishing; 1999. p. 47-111. [ Links ]

5. Correa AC, Escobar JS, Durand P, et al. Bridging gaps in the molecular phylogeny of the Lymnaeidae (Gastropoda: Pulmonata), vectors of Fascioliasis. BMC Evol Biol. 2010;10:381. [ Links ]

6. Gutiérrez A, Yong M, Perera G et al. Fasciola hepatica (Trematoda: Digenea): its effect on the life history traits of Pseudosuccinea columella (Gasteropoda: Lymnaeidae), an uncommon interaction. Parasitol Res. 2002;88:535-9. [ Links ]

7. Vázquez A, Sánchez J, Hevia Y. Distribución y preferencia de hábitats de moluscos hospederos intermediarios de Fasciola hepatica en Cuba. Rev Cubana Med Trop. 2009;61:248-53. [ Links ]

8. Gutiérrez A, Vázquez AA, Hevia Y, et al. First report of larval stages of Fasciola hepatica in a wild population of Pseudosuccinea columella from Cuba and the Caribbean. J Helminthol. 2011;85:109-11. [ Links ]

9. Perera de Puga G, Ferrer JR, Arrinda C et al. Effectiveness of three biological control agents against Intermediate hosts of snail-mediated parasites in Cuba. Malacological Rev. 1990;23:47-52. [ Links ]

10. Perera G, Yong M, Ferrer J. Biological control of snail intermediate hosts by competitor Thiarid snails in cuba. J Med & AppL Malacol. 1993;5:97-101. [ Links ]

11. Gutiérrez A, Hernández DF, Sánchez J. Variation of snail's abundance in two water bodies harboring strains of Pseudosuccinea columella resistant and susceptible to Fasciola hepatica miracidial infection, in Pinar del Río Province, Cuba. Mem Inst Oswaldo Cruz. 2005;100:725-7. [ Links ]

12. Rojas L, Vázquez A, Domenech I et al. Fascioliasis: can Cuba conquer this emerging parasitosis? Trends Parasitol. 2010;26:26-34. [ Links ]

13. Nguyen TG, Le TH, Dao TH et al. Bovine fasciolosis in the human fasciolosis hyperendemic Binh Dinh province in Central Vietnam. Acta Trop. 2011;117:19-22. [ Links ]

14. Mas-Coma S. Epidemiology of fascioliasis in human endemic areas. J Helminthol . 2005;79:207-16. [ Links ]

15. Duménigo BE, Finlay CM. Detection and quantification of Fasciola hepatica antigens in sheep. Rev Cubana Med Trop . 1998;50:82-4. [ Links ]

16. Brito E, Hernández M, de la Fe P et al. Prevalence, liver confiscation and economic losses by Fasciola hepatica in bovine slaughterhouses of three provinces of the central region of Cuba. REDVET. 2010;11. [ Links ]

17. Pino A, Nuñez F, Martinez R et al. Prevalence and risk factors for intestinal parasitic infections in a rural community in “Consolación del Sur” municipality, Cuba. West Indian Med J. 2014;63:337-43. [ Links ]

18. Espino AM, Marcet R, Finlay CM. Detection of circulating excretory secretory antigens in human fascioliasis by sandwich enzyme-linked immunosorbent assay. J Clin Microbiol. 1990;28:2637-40. [ Links ]

19. Duménigo BE, Espino AM, Finlay CM. Detection of Fasciola hepatica antigen in cattle faeces by a monoclonal antibody-based sandwich immunoassay. Res Vet Sci. 1996;60:278-9. [ Links ]

20. FAO. Diseases of domestic animals caused by flukes: epidemiology, diagnosis and control of Fasciola, Paramphistome, Dicrocoelium, Eurytrema and Schistosome infections of ruminants in developing countries. Food and Agriculture Organisation. Rome: Animal Production and Health Div.; 1994. [ Links ]

21. Uffo O, Acosta A, Martínez S et al. Genetic characterization of Cuban Creole cattle using molecular tools. Biotecnol Apl. 2012;27:127-8. [ Links ]

22. Gonzalez R, Perez MY, Brito S. Fasciolosis bovina: Evaluación de las principales pérdidas provocadas en una empresa ganadera. Rev Salud Anim. 2007;29:167-75. [ Links ]

23. Torrel T. Detección de coproantígenos de Fasciola hepatica en ovinos y bovinos mediante un método de ELISA. Rev Investig Pecu. 1997;8:74-8. [ Links ]

24. Morales MA, Luengo J, Vásquez J. Distribución y tendencia de la fasciolosis en ganado de abasto de Chile, 1989-1995. Parasitol Dia. 2000;24:115-8. [ Links ]

25. Raymundo LA, Flores VM, Terashima A et al. Hyperendemicity of human fasciolosis in the Mantaro Valley, Peru: factors for infection with Fasciola hepatica. Rev Gastroenterol Peru. 2004;24:158-64. [ Links ]

26. Munguia-Xochihua JA, Ibarra-Velarde F, Ducoing-Watty A et al. Prevalence of Fasciola hepatica (ELISA and fecal analysis) in ruminants from a semi-desert area in the northwest of Mexico. Parasitol Res . 2007;101:127-30. [ Links ]

27. Pfukenyi DM, Mukaratirwa S. A retrospective study of the prevalence and seasonal variation of Fasciola gigantica in cattle slaughtered in the major abattoirs of Zimbabwe between. 1990 and. 1999. Onderstepoort J Vet Res. 2004;71:181-7. [ Links ]

28. Tadele T, Worku T. The prevalence and economic significance of bovine fasciolosis at Jimma Abattoir, Ethiopia. Internet J Vet Med. 2007;3:1-10. [ Links ]

29. Sturchler D. Fasciola hepatica: Convoluted life forms and names. Travel Med Infect Dis. 2018;21:85. [ Links ]

30. Rim HJ, Farag HF, Sornmani S et al. Food-borne trematodes: ignored or emerging? Parasitol Today. 1994;10:207-9. [ Links ]

31. Vazquez AA, Lounnas M, Sanchez J, et al. Genetic and infective diversity of the liver fluke Fasciola hepatica (Trematoda: Digenea) from Cuba. J Helminthol . 2016;90:719-25. [ Links ]

32. Berhe G, Berhane K, Tadesse G. Prevalence and economic significance of fasciolosis in cattle in Mekelle Area of Ethiopia. Trop Anim Health Prod. 2009;41:1503-4. [ Links ]

33. Espino AM. Inmunodiagnóstico de la fasciolosis humana y su aplicación en brotes epidémicos [Tesis para Doctor en Ciencias Médicas]. La Habana: Instituto de Medicina Tropical "Pedro Kourí"; 1997. [ Links ]

34. Espino AM, Finlay CM. Sandwich enzyme-linked immunosorbent assay for detection of excretory secretory antigens in humans with fascioliasis. J Clin Microbiol . 1994;32:190-93. [ Links ]

35. Li O, Leguía G, Espino AM et al. Detección de anticuerpos y antígenos para el diagnóstico de Fasciola hepatica en alpacas naturalmente infectadas. Rev Ivestig Vet Peru. 2005;16:143-53. [ Links ]

36. Moriena R, Álvarez J, Álvarez A, et al. Diagnóstico de Fasciola hepatica por detección de coproantígenos y coprología clásica: su comparación [Internet]. Available from: http://www1.unne.edu.ar/cyt/veterinarias/v-043.pdf. [ Links ]

37. Cañete R, Yong M, Sánchez J et al. Population dynamics of intermediate snail hosts of Fasciola hepatica and some environmental factors in San Juan y Martínez municipality, Cuba. Mem Inst Oswaldo Cruz . 2004;99:257-62. [ Links ]

38. Vázquez AA, Gutiérrez A, Sánchez J. Estudios de diversidad en comunidades de moluscos fluviales de importancia médica. Rev Cubana Med Trop . 2008;60:159-61. [ Links ]

39. Vázquez AA, Gutiérrez G. Ecología de moluscos fluviales de importancia médica y veterinaria en 3 localidades de La Habana. Rev Cubana Med Trop . 2007;59:149-53. [ Links ]

40. Yong Cong M, Perera de Puga G. The external and internal morphology of the intermediate hosts of Fasciola hepatica. Rev Cubana Med Trop . 1991;43:13-6. [ Links ]

41. Gutiérrez A, Pointier JP, Yong M et al. Evidence of phenotypic differences between resistant and susceptible isolates of Pseudosuccinea columella (Gastropoda: Lymnaeidae) to Fasciola hepatica (Trematoda: Digenea) in Cuba. Parasitol Res . 2003;90:129-34. [ Links ]

42. Prepelitchi L, Kleiman F, Pietrokovsky SM et al. First report of Lymnaea columella Say, 1817 (Pulmonata: Lymnaeidae) naturally infected with Fasciola hepatica (Linnaeus,1758) (Trematoda: Digenea) in Argentina. Mem Inst Oswaldo Cruz . 2003;98:889-91. [ Links ]

43. Pointier JP, Noya O, Alarcon de Noya B et al. Distribution of Lymnaeidae (Mollusca: Pulmonata), intermediate snail hosts of Fasciola hepatica in Venezuela. Mem Inst Oswaldo Cruz . 2009;104:790-6. [ Links ]

44. Pointier JP, Coustau C, Rondelaud D et al. Pseudosuccinea columella (Say. 1817) (Gastropoda, Lymnaeidae), snail host of Fasciola hepatica: first record for France in the wild. Parasitol Res . 2007;101:1389-92. [ Links ]

45. Lockyer AE, Jones CS, Noble L et al. Trematodes and snails: an intimate association. Can J Zool. 2004;82:251-69. [ Links ]

46. Calienes AF, Fraga J, Pointier JP et al. Detection and genetic distance of resistant populations of Pseudosuccinea columella (Mollusca: Lymnaeidae) to Fasciola hepatica (Trematoda: Digenea) using RAPD markers. Acta Trop . 2004;92:83-7. [ Links ]

Ethical Standards

2All animals were handled in strict accordance with good animal practice as defined by the Ethics and Management Committee for Laboratory Animals of the Institute of Tropical Medicine Pedro Kourí and all the animal work was approved by this committee.

How to cite this article: Pino Santos A, Vázquez AA, Doménech I, Martínez R, Sánchez J, Martínez E. Natural infection with Fasciola hepatica in host-snails and cattle in ten dairy farms from a western municipality in Cuba. Rev Med Vet. 2019;(37): 73-81. https://doi.org/10.19052/mv.vol1.iss37.9.

Recibido: 08 de Enero de 2017; Aprobado: 23 de Octubre de 2018

We declare that we have no conflicts of interest.

Creative Commons License Este es un artículo publicado en acceso abierto bajo una licencia Creative Commons