Skip to main content
Log in

Potential for dissemination of Phytophthora cinnamomi by feral pigs via ingestion of infected plant material

  • Original Paper
  • Published:
Biological Invasions Aims and scope Submit manuscript

Abstract

Feral pigs have long been implicated as potential vectors in the spread of the devastating plant pathogen Phytophthora cinnamomi due to their rooting and wallowing activities which may predispose them as vectors of infested soil. In this study, we aim to determine whether feral pigs have the potential to act as vectors of plant pathogens such as P. cinnamomi through their feeding activity. The typically omnivorous diet of feral pigs may also lead to the passage of P. cinnamomi infected plant material through their digestive system. This study investigates the potential for feral pigs to pass viable P. cinnamomi in their faeces following the ingestion of millet seeds, pine plugs and Banksia leptophilia roots inoculated with P. cinnamomi. Recovery rates of P. cinnamomi from the millet seeds, pine plugs and B. leptophilia roots following a single ingested bolus were 33.2, 94.9 and 10.4 %, respectively supported by quantitative PCR analysis. These results demonstrate that P. cinnamomi remain viable within infected plant material following passage through the pig digestive tract, although the digestive processes reduce the pathogen’s viability. An inverse relationship was observed between the viability of infected material and passage time, suggesting that partially digested plant material provides protection for P. cinnamomi against the adverse environmental conditions of the pig digestive tract. Phytophthora cinnamomi remained viable for up to 7 days in larger pieces of colonised woody plant material such as the pine plugs. A plant infection trial using passaged P. cinnamomi colonised pine plugs showed that even material that remained in the digestive tract for 7 days was capable of infecting and killing healthy plants, susceptible to P. cinnamomi. This study provides compelling evidence that feral pigs have the ability to transport viable P. cinnamomi in their digestive tract.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Andjic V, Hardy GES, Cortinas MN, Wingfield MJ, Burgess TI (2007) Multiple gene genealogies reveal important relationships between species of Phaeophleospora infecting Eucalyptus leaves. Fed Eur Microbiol Soc Microbiol Lett 268:22–33

    Article  CAS  Google Scholar 

  • Argenzio RA, Southworth M (1974) Sites of organic acid production and absorption in gastrointestinal tract of the pig. Am J Physiol 228:454–460

    Google Scholar 

  • Asplund JM, Harris LE (1970) A technique and apparatus for the study of rate of passage of feed residues through the digestive tract of sheep. J Anim Sci 31:1199–1204

    Google Scholar 

  • Brasier CM (2008) The biosecurity threat to the UK and global environment from international trade in plants. Plant Pathol 57:792–808

    Article  Google Scholar 

  • Burgess TI, Stukely MJC, Jung T, White D, Hüberli D, Hardy GE. St. J (2010) Molecular characterisation of a Phytophthora hybrid swarm in native ecosystems and waterways in Western Australia. In: 5th IUFRO phytophthora diseases in forests and natural ecosystems, 7–12 March, Auckland and Rotorua

  • Carter R (2004) Arresting Phytophthora Dieback: the biological bulldozer. A report by the World Wildlife Fund and the WA Dieback Consultative Council

  • Choquenot D, McIlroy J, Korn T (1996) Managing vertebrate pests: feral pigs. Bureau of Resource Sciences, Australian Government Publishing Service, Canberra

  • Cooke DEL, Drenth A, Duncan JM, Wagels G, Brasier CM (2000) A molecular phylogeny of Phytophthora and related oomycetes. Fungal Genet Biol 30:17–32

    Article  CAS  PubMed  Google Scholar 

  • Erwin DC, Ribeiro OK (1996) Phytophthora diseases worldwide. American Phytopathological Society, St. Paul

    Google Scholar 

  • Feio CL, Bauwens L, Swinne D, De Meurichy W (1999) Isolation of Basidiobolus ranarum from ectotherms in Antwerp zoo with special reference to characterization of the isolated strains. Mycoses 42:291–296

    Article  CAS  PubMed  Google Scholar 

  • Gallo L, Siverio F, Rodríguez-Pérez AM (2007) Thermal sensitivity of Phytophthora cinnamomi and long-term effectiveness of soil solarisation to control avocado root rot. Ann Appl Biol 150:65–73

    Article  Google Scholar 

  • Giménez-Anaya A, Herrero J, Rosell C, Couto S, García-Serrano A (2008) Food habits of wild boars (Sus scrofa) in a Mediterranean coastal wetland. Wetlands 28:197–203

    Article  Google Scholar 

  • Graham GC, Mayers P, Henry RJ (1994) A simplified method for the preparation of fungal genomic DNA for PCR and RAPD analysis. Biotechniques 16:48–50

    CAS  PubMed  Google Scholar 

  • Gurevitch J, Padilla DK (2004) Are invasive species a major cause of extinctions? Trends Ecol Evol 19:470–474

    Article  PubMed  Google Scholar 

  • Hardham AR (2005) Phytophthora cinnamomi. Mol Plant Pathol 6:589–604

    Article  CAS  PubMed  Google Scholar 

  • Hardy GESJ, Huberli D, Dunstan W, Dell B (2007) The dynamics and management of Phytophthora in the jarrah (Eucalyptus marginata) forest of Western Australia. Brazil Phytopathol 32(Supplement):S87–S88

    Google Scholar 

  • Hüberli D, Tommerup I, Hardy G (2000) False-negative isolations or absence of lesions may cause mis-diagnosis of diseased plants infected with Phytophthora cinnamomi. Aust Plant Pathol 29:164–169

    Article  Google Scholar 

  • Keast D, Walsh LG (1979) Passage and survival of chlamydospores of Phytophthora cinnamomi Rands, the causal agent of forest dieback disease, through the gastrointestinal tracts of termites and wild birds. Appl Environ Microbiol 37:661–664

    CAS  PubMed Central  PubMed  Google Scholar 

  • Kliejunas JT, Ko WH (1976) Dispersal of Phytophthora cinnamomi on the Island of Hawaii. Phytopathology 66:457–460

    Article  Google Scholar 

  • Knudsen KEB, Jensen BB, Hansen I (1993) Digestion of polysaccharides and other major components in the small and large intestine of pigs fed on diets consisting of oat fractions rich in β-d-glucan. Br J Nutr 70:537–556

    Article  CAS  PubMed  Google Scholar 

  • Manners MJ (1976) The development of digestive function in the pig. Proceed Nutr Soc 35:49–55

    Article  CAS  Google Scholar 

  • Martin HL, Dale ML (2001) Potential of Cactoblastis cactorum as a vector for fungi pathogenic to pricklypear, Opuntia inermis. Biol Control 21:258–263

    Article  Google Scholar 

  • Masters KB (1979) Feral pigs in the south-west of Western Australia—final report to Feral Pig Committee. Department of Agriculture, Perth

    Google Scholar 

  • McCauley I, Matthews B, Nugent L, Mather A, Simons JA (2005) Evaluation of wireless sensors to measure the effect of microclimate on pig body temperature. In: Paterson JE (ed) Manipulating pig production X. Proceedings of the tenth biennial conference of the Australasian Pig Science Association (APSA). Christchurch

  • McLeod R (2004) Counting the cost: impact of invasive animals in Australia 2004. Cooperative Research Centre for Pest Animal Control, Canberra

    Google Scholar 

  • Schley L, Roper TJ (2003) Diet of wild boar Sus scrofa in Western Europe, with particular reference to consumption of agricultural crops. Mamm Rev 33:43–56

    Article  Google Scholar 

  • Shearer BL, Crane CE, Cochrane A (2004) Quantification of the susceptibility of the native flora of the South-West Botanical Province, Western Australia, to Phytophthora cinnamomi. Aust J Bot 52:435–443

    Article  Google Scholar 

  • Teague HS, Hanson LE (1954) The effect of feeding different levels of a cellulosic material to swine. J Anim Sci 13:206–214

    CAS  Google Scholar 

  • Tierney T, Cushman J (2006) Temporal changes in native and exotic vegetation and soil characteristics following disturbances by feral pigs in a California Grassland. Biol Invasions 8:1073–1089

    Article  Google Scholar 

  • van der Putten WH, Klironomos JN, Wardle DA (2007) Microbial ecology of biological invasions. Int Soc Microb Ecol 1:28–37

    Google Scholar 

  • White TJ, Bruns T, Lee S, Taylor J, Innis M, Gelfand D, Shinsky J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR protocols. A guide to methods and applications. Academic Press, Waltham

    Google Scholar 

  • Zevenhuizen LPTM, Bartnicki-Garcia S (1969) Structure of the insoluble hyphal wall glucan of Phytophthora cinnamomi. Biochemistry 8:1496–1502

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This research was supported under Australian Research Council’s Linkage Projects funding scheme (project number LP0561974) with animal ethics approval (AEC: R2082/07). The authors would like to thank Dr. T. Paap, Dr. W. Dunstan, P. Stasikowski, K. Thomas, Dr. T. Burgess and D. White.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Andrew Yufa Li.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, A.Y., Williams, N., Fenwick, S.G. et al. Potential for dissemination of Phytophthora cinnamomi by feral pigs via ingestion of infected plant material. Biol Invasions 16, 765–774 (2014). https://doi.org/10.1007/s10530-013-0535-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10530-013-0535-7

Keywords

Navigation