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Parasitology research2011; 110(2); 657-662; doi: 10.1007/s00436-011-2537-7

Predatory activity of the fungus Duddingtonia flagrans in equine strongyle infective larvae on natural pasture in the Southern Region of Brazil.

Abstract: Biological control is an alternative method to reduce the population of parasites through natural predators. A promising option of biological control in the reduction of infective larvae on pasture is the use of nematophagous fungi. In this study, the efficacy of the nematophagous fungus Duddingtonia flagrans in controlling gastrointestinal nematode parasites in field-raised horses was tested. Ten foals with an average age of 12 months were divided in two groups: five males constituted the treated group and five females constituted the control group. Each group was introduced in a field of mixed pasture with approximately 5 ha. The treated group received the fungus D. flagrans at a concentration of 10(6) chlamydospores per kilogramme of animal body weight daily, mixed with horse food for 5 months. The control group did not receive the fungus. Samples were collected to perform eggs per gramme (EPG) counts weekly. Coproculture and collection of pasture were done monthly for larvae counting. No significant difference was observed in the EPG counting and in the number of larvae recovered from coprocultures, where cyathostomines, Strongylus and Trichostrongylus spp. were found after monthly larvae counting. No significant difference was observed in the EPG counts, and Trichostrongylus sp. was identified. The number of recovered larvae on pasture was significantly lower in the treated group in the last month of treatment, showing a reduction of 73.5% (p < 0.05). As such, the fungus was able to reduce the number of infective larvae in the pasture. Nevertheless, this did not reflect in a decrease of parasitic infection during the 5-month study period.
Publication Date: 2011-07-12 PubMed ID: 21748346DOI: 10.1007/s00436-011-2537-7Google Scholar: Lookup
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  • Journal Article

Summary

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The study investigates the effectiveness of the Duddingtonia flagrans fungus as a biological control agent against parasitic worm infections in horses. The results indicate that, even though the use of the fungus significantly reduced the number of infective larvae in the horses’ grazing pasture, it did not lead to a decrease in the parasitic infection levels of the horses themselves over five months.

Research Details

  • The study’s primary focus is to test the efficacy of using the fungus Duddingtonia flagrans for controlling gastrointestinal nematode parasites in field-raised horses. Nematodes, sometimes referred to as worms, are common parasites in horses and cause various health issues.
  • For this study, ten foals averaging 12 months of age were divided into two groups: one group of five males (treated group) and another of five females (control group). These foals were kept in a field of mixed pasture of approximately 5 hectares.
  • The treated group was given D. flagrans daily for five months mixed in with their food. The fungus was delivered at a dose of one million chlamydospores per kilogram of the horse’s body weight. Conversely, the control group did not receive the fungus.

Observations and Findings

  • Researchers took weekly and monthly samples from each group to monitor the change in parasitic infection levels. They looked at the number of eggs per gram (EPG) in the foals’ feces and the total number of larvae in the pasture area.
  • There was no significant difference observed in the EPG counts between the treated and control group and in the number of larvae recovered from the horses’ fecal cultures in which cyathostomines, Strongylus, and Trichostrongylus spp. were found.
  • In the final month of treatment, there was a marked reduction (73.5%) in the number of larvae found on the pasture area used by the treated group, indicating that the fungus was indeed effective at reducing the overall population of infective larvae in the environment.
  • The failure for these environmental reductions to translate into lower infection rates within the horses suggests that larvae populations within the body may not be significantly impacted by the use of D. flagrans.
  • The study concludes that despite D. flagrans reducing the number of infective larvae in the pasture, it did not alleviate the parasitic infection within the horses over the course of the five-month research period.

Implications

  • The partial success of the treatment implies that biocontrol methods like D. flagrans may have potential in controlling environmental reservoirs of equine parasites, but further research is needed to develop more efficient treatments for direct parasitic infections within horses.
  • These results highlight the complex nature of parasitic infections and the challenges faced in developing effective control strategies. Nevertheless, the success at reducing larvae in the environment underscores the potential value of integrating such biocontrol agents into broader pest management strategies.

Cite This Article

APA
de Almeida GL, Santurio JM, Filho JO, Zanette RA, Camillo G, Flores AG, da Silva JH, de la Rue ML. (2011). Predatory activity of the fungus Duddingtonia flagrans in equine strongyle infective larvae on natural pasture in the Southern Region of Brazil. Parasitol Res, 110(2), 657-662. https://doi.org/10.1007/s00436-011-2537-7

Publication

ISSN: 1432-1955
NlmUniqueID: 8703571
Country: Germany
Language: English
Volume: 110
Issue: 2
Pages: 657-662

Researcher Affiliations

de Almeida, Gisane Lanes
  • Postgraduate Program in Veterinary Medicine, Federal University of Santa Maria, S. Maria, Brazil.
Santurio, Janio Morais
    Filho, José Osvaldo Jardim
      Zanette, Régis Adriel
        Camillo, Giovana
          Flores, Alexandra Geyer
            da Silva, José Henrique Souza
              de la Rue, Mário Luiz

                MeSH Terms

                • Animals
                • Brazil
                • Duddingtonia / pathogenicity
                • Feces / parasitology
                • Female
                • Horse Diseases / parasitology
                • Horse Diseases / prevention & control
                • Horses
                • Larva / microbiology
                • Male
                • Parasite Egg Count
                • Pest Control, Biological / methods
                • Strongylida Infections / parasitology
                • Strongylida Infections / prevention & control
                • Strongylida Infections / veterinary
                • Strongylus / isolation & purification
                • Strongylus / microbiology
                • Trichostrongylus / isolation & purification
                • Trichostrongylus / microbiology

                References

                This article includes 20 references
                1. Eysker M, Mirck MH. The distribution of inhibited early third stage Cyathostominae larvae in the large intestine of the horse.. Z Parasitenkd 1986;72(6):815-20.
                  pubmed: 3799011doi: 10.1007/BF00925101google scholar: lookup
                2. Baudena MA, Chapman MR, Larsen M, Klei TR. Efficacy of the nematophagous fungus Duddingtonia flagrans in reducing equine cyathostome larvae on pasture in south Louisiana.. Vet Parasitol 2000 Apr 28;89(3):219-30.
                  pubmed: 10760412doi: 10.1016/s0304-4017(00)00201-6google scholar: lookup
                3. Silva AR, Araújo JV, Braga FR, Frassy LN, Tavela AO, Carvalho RO, Castejon FV. Biological control of sheep gastrointestinal nematodiasis in a tropical region of the southeast of Brazil with the nematode predatory fungi Duddingtonia flagrans and Monacrosporium thaumasium.. Parasitol Res 2009 Nov;105(6):1707-13.
                  pubmed: 19756749doi: 10.1007/s00436-009-1613-8google scholar: lookup
                4. Bonneau S, Maynard L, Tomczuk K, Kok D, Eun HM. Anthelmintic efficacies of a tablet formula of ivermectin-praziquantel on horses experimentally infected with three Strongylus species.. Parasitol Res 2009 Sep;105(3):817-23.
                  pubmed: 19488785doi: 10.1007/s00436-009-1460-7google scholar: lookup
                5. Mfitilodze MW, Hutchinson GW. Prevalence and abundance of equine strongyles (Nematoda: Strongyloidea) in tropical Australia.. J Parasitol 1990 Aug;76(4):487-94.
                  pubmed: 2380857
                6. Stromberg BE. Environmental factors influencing transmission.. Vet Parasitol 1997 Nov;72(3-4):247-56; discussion 257-64.
                  pubmed: 9460201doi: 10.1016/s0304-4017(97)00100-3google scholar: lookup
                7. Araujo JM, Araújo JV, Braga FR, Carvalho RO. In vitro predatory activity of nematophagous fungi and after passing through gastrointestinal tract of equine on infective larvae of Strongyloides westeri.. Parasitol Res 2010 Jun;107(1):103-8.
                  pubmed: 20369256doi: 10.1007/s00436-010-1841-ygoogle scholar: lookup
                8. Courtney CH. Seasonal transmission of equine cyathostomes in warm climates.. Vet Parasitol 1999 Aug 31;85(2-3):173-7; discussion 177-80, 215-25.
                  pubmed: 10485363doi: 10.1016/s0304-4017(99)00097-7google scholar: lookup
                9. Fernández AS, Larsen M, Nansen P, Grønvold J, Henriksen SA, Wolstrup J. Effect of the nematode-trapping fungus Duddingtonia flagrans on the free-living stages of horse parasitic nematodes: a pilot study.. Vet Parasitol 1997 Dec 31;73(3-4):257-66.
                  pubmed: 9477512doi: 10.1016/s0304-4017(97)00121-0google scholar: lookup
                10. Kahn LP, Norman TM, Walkden-Brown SW, Crampton A, O'Connor LJ. Trapping efficacy of Duddingtonia flagrans against Haemonchus contortus at temperatures existing at lambing in Australia.. Vet Parasitol 2007 May 15;146(1-2):83-9.
                  pubmed: 17349746doi: 10.1016/j.vetpar.2007.02.004google scholar: lookup
                11. Stear MJ, Doligalska M, Donskow-Schmelter K. Alternatives to anthelmintics for the control of nematodes in livestock.. Parasitology 2007 Feb;134(Pt 2):139-51.
                  pubmed: 17076922doi: 10.1017/S0031182006001557google scholar: lookup
                12. Waller PJ, Faedo M, Ellis K. The potential of nematophagous fungi to control the free-living stages of nematode parasites of sheep: towards the development of a fungal controlled release device.. Vet Parasitol 2001 Dec 28;102(4):299-308.
                  pubmed: 11731073doi: 10.1016/s0304-4017(01)00545-3google scholar: lookup
                13. Paraud C, Pors I, Chartier C. Efficiency of feeding Duddingtonia flagrans chlamydospores to control nematode parasites of first-season grazing goats in France.. Vet Res Commun 2007 Apr;31(3):305-15.
                  pubmed: 17216307doi: 10.1007/s11259-006-3467-1google scholar: lookup
                14. Larsen M, Nansen P, Grøndahl C, Thamsborg SM, Grønvold J, Wolstrup J, Henriksen SA, Monrad J. The capacity of the fungus Duddingtonia flagrans to prevent strongyle infections in foals on pasture.. Parasitology 1996 Jul;113 ( Pt 1):1-6.
                  pubmed: 8710410doi: 10.1017/s003118200006621xgoogle scholar: lookup
                15. Terrill TH, Larsen M, Samples O, Husted S, Miller JE, Kaplan RM, Gelaye S. Capability of the nematode-trapping fungus Duddingtonia flagrans to reduce infective larvae of gastrointestinal nematodes in goat feces in the southeastern United States: dose titration and dose time interval studies.. Vet Parasitol 2004 Apr 15;120(4):285-96.
                  pubmed: 15063939doi: 10.1016/j.vetpar.2003.09.024google scholar: lookup
                16. Braga FR, Araújo JV, Silva AR, Araujo JM, Carvalho RO, Tavela AO, Campos AK, Carvalho GR. Biological control of horse cyathostomin (Nematoda: Cyathostominae) using the nematophagous fungus Duddingtonia flagrans in tropical southeastern Brazil.. Vet Parasitol 2009 Aug 26;163(4):335-40.
                  pubmed: 19497672doi: 10.1016/j.vetpar.2009.05.003google scholar: lookup
                17. Larsen M. Biological control of helminths.. Int J Parasitol 1999 Jan;29(1):139-46; discussion 153-4.
                  pubmed: 10048826doi: 10.1016/s0020-7519(98)00185-4google scholar: lookup
                18. Xiao L, Herd RP, Majewski GA. Comparative efficacy of moxidectin and ivermectin against hypobiotic and encysted cyathostomes and other equine parasites.. Vet Parasitol 1994 May;53(1-2):83-90.
                  pubmed: 8091622doi: 10.1016/0304-4017(94)90020-5google scholar: lookup
                19. Silvina Fernández A, Henningsen E, Larsen M, Nansen P, Grønvold J, Søndergaard J. A new isolate of the nematophagous fungus Duddingtonia flagrans a biological control agent against free-living larvae of horse strongyles.. Equine Vet J 1999 Nov;31(6):488-91.
                20. Bird J, Herd RP. In vitro assessment of two species of nematophagous fungi (Arthrobotrys oligospora and Arthrobotrys flagrans) to control the development of infective cyathostome larvae from naturally infected horses.. Vet Parasitol 1995 Jan;56(1-3):181-7.
                  pubmed: 7732642doi: 10.1016/0304-4017(94)00663-wgoogle scholar: lookup

                Citations

                This article has been cited 2 times.
                1. da Silva ME, Braga FR, de Gives PM, Uriostegui MA, Reyes M, Soares FE, de Carvalho LM, Rodrigues FB, de Araújo JV. Efficacy of Clonostachys rosea and Duddingtonia flagrans in Reducing the Haemonchus contortus Infective Larvae. Biomed Res Int 2015;2015:474879.
                  doi: 10.1155/2015/474879pubmed: 26504809google scholar: lookup
                2. Buske R, Santurio JM, de Oliveira CV, Bianchini LA, da Silva JH, de la Rue ML. In vitro influence of temperature on the biological control activity of the fungus Duddingtonia flagrans against Haemonchus contortus in sheep. Parasitol Res 2013 Feb;112(2):473-8.
                  doi: 10.1007/s00436-012-3156-7pubmed: 23052786google scholar: lookup