Skip to main content
Log in

Assessing the potential of fungi isolated from dieback-affected trees as biological control agents for prickly acacia (Vachellia nilotica subsp. indica)

  • Published:
BioControl Aims and scope Submit manuscript

Abstract

Prickly acacia (Vachellia nilotica subsp. indica, Family: Fabaceae) is an invasive woody weed in coastal and semi-arid rangelands of Australia. A prominent dieback event was observed on this species in 2010 in north-western Queensland. A Botryosphaeriaceae fungus, Cophinforma sp., was consistently isolated from symptomatic stem tissues. In preliminary studies, Cophinforma sp. and an isolate of Lasiodiplodia pseudotheobromae sourced from dieback-affected Parkinsonia aculeata (Family: Fabaceae) were found to be pathogenic to prickly acacia seedlings and juveniles. In this study, we investigated whether typical dieback symptoms could be replicated under glasshouse conditions and in the field following stem inoculations of these two fungi (either singly or in combination). In the glasshouse trial, stem lesions and leaf mortality were observed following stem inoculation by both of the test fungi although it was greatest in the presence of L. pseudotheobromae. However, no effects on plant growth or mortality were observed. In the field trials (located in central and north-western Queensland) both test fungi caused infection, but significant lesions were only induced by L. pseudotheobromae in central Queensland, and no treatment effects on plant growth or survival were observed at either site over the next two years. Prominent decline in plant vigour was observed in north-western Queensland two years after inoculation, but was presumed to be naturally occurring as it affected controls and neighbouring untreated plants equally. The test fungi were reisolated from lesions in both field and glasshouse trials, but were never found in adjacent tissue, suggesting that infection was successfully contained by the plant’s wound response. We found no potential for the tested fungal isolates to be effective biocontrol agents, although future studies should aim to initiate systemic infections.

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

  • Aghighi S, Fontanini L, Yeoh PB, Hardy GESJ, Burgess TI, Scott JK (2014) A conceptual model to describe the decline of European blackberry (Rubus anglocandicans), a weed of national significance in Australia. Plant Dis 98:580–589

    Article  CAS  PubMed  Google Scholar 

  • Almaraz-Sanchez A, Alvarado-Rosales D, Tlapal-Bolanos B, Espinoza-Victoria D (2012) Identification of fungi potentially antagonist to Phytophthora cinnamomi Rands in oak forest at the El Arrayanal, Colima and Tecoanapa, Guerrero. Revista Chapingo Serie Ciencias Forestales Y Del Ambiente 18:341–355

    Google Scholar 

  • Amponsah NT, Jones EE, Ridgway HJ, Jaspers MV (2014) Factors affecting Neofusicoccum luteum infection and disease progression in grapevines. Australas Plant Pathol 43:547–556

    Article  Google Scholar 

  • Chen SF, Morgan DP, Hasey JK, Anderson K, Michailides TJ (2014) Phylogeny, morphology, distribution, and pathogenicity of Botryosphaeriaceae and Diaporthaceae from English walnut in California. Plant Dis 98:636–652

    Article  Google Scholar 

  • Davidson JM, Werres S, Garbelotto M, Hansen EM, Rizzo DM (2003) Sudden oak death and associated diseases caused by Phytophthora ramorum. Plant Health Prog 4(1):21

    Article  Google Scholar 

  • Demirci E, Dane E, Eken C (2011) In vitro antagonistic activity of fungi isolated from sclerotia on potato tubers against Rhizoctonia solani. Turk J Biol 35:457–462

    Google Scholar 

  • Desprez-Loustau ML, Marcais B, Nageleisen LM, Piou D, Vannini A (2006) Interactive effects of drought and pathogens in forest trees. Ann For Sci 63:597–612

    Article  Google Scholar 

  • Dhileepan K, Shi B, Callander J, Teshome M, Neser S, Senaratne KADW (2018) Gall thrips Acaciothrips ebneri (Thysanoptera: Phlaeothripidae) from Ethiopia, a promising biological control agent for prickly acacia in Australia. Afr Entomol 26:237–241

    Article  Google Scholar 

  • Diplock N (2015) Parkinsonia dieback: Investigations into its cause, ecology and potential for biological control. PhD thesis, The University of Queensland

  • Diplock N, Galea VJ, van Klinken RD, Wearing A (2006) A preliminary investigation of dieback on Parkinsonia aculeata. In: Preston C, Watts JH, Crossman ND (eds) Proceedings of the 15th Australian weeds conference Adelaide, Australia, 24–28 September 2006. Weed Management Society of South Australia, pp 585–587

  • Fensham RJ, Fairfax RJ (2007) Drought-related tree death of savanna eucalypts: species susceptibility, soil conditions and root architecture. J Veg Sci 18:71–80

    Article  Google Scholar 

  • Fensham RJ, Fairfax RJ, Ward DP (2009) Drought-induced tree death in savanna. Glob Change Biol 15:380–387

    Article  Google Scholar 

  • Galea V, Goulter K (2013) Field evaluation of a bioherbicide for control of parkinsonia (Parkinsonia aculeata) in Australia. In: Abstract and programme book: The 19th Australasian plant pathology conference, Auckland, New Zealand, 25–28 November, 2013. Australasian Plant Pathology Society, p 43

  • Hallett SG, Paul ND, Ayres PG (1990) Botrytis cinerea kills groundsel (Senecio vulgaris) infected by rust (Puccinia lagenophorae). New Phytol 114:105–109

    Article  Google Scholar 

  • Haque A (2015) Investigation of the fungi associated with dieback of prickly acacia (Vachellia nilotica subsp. indica) in Northern Australia. PhD thesis, The University of Queensland

  • Haque A, Galea V, Bisset A, van Klinken RD (2012) A preliminary investigation of prickly acacia dieback (Acacia nilotica ssp.indica). In: Eldershaw V (ed) Eighteenth Australasian weeds conference, Melbourne, 8–11 October 2012. pp 131–134

  • Hasan S, Ayres PG (1990) The control of weeds through fungi - principles and prospects. New Phytol 115:201–222

    Article  Google Scholar 

  • Jaremo J, Palmqvist E (2001) Plant compensatory growth: a conquering strategy in plant-herbivore interactions? Evolut Ecol 15:91–102

    Article  Google Scholar 

  • Johnson GI, Mead AJ, Cooke AW, Dean JR (1992) Mango stem end rot pathogens—Fruit infection by endophytic colonization of the inflorescence and pedicel. Ann Appl Biol 120:225–234

    Article  Google Scholar 

  • Kaczynski KM, Cooper DJ (2013) Susceptibility of Salix monticola to Cytospora canker under increased temperatures and decreased water levels. For Ecol Manag 305:223–228

    Article  Google Scholar 

  • Kriticos Sutherst RW, Brown JR, Adkins SW, Maywald GF (2003) Climate change and the potential distribution of an invasive alien plant: Acacia nilotica ssp. indica in Australia. J Appl Ecol 40:111–124

    Article  Google Scholar 

  • Linaldeddu BT, Scanu B, Maddau L, Franceschini A (2014) Diplodia corticola and Phytophthora cinnamomi: the main pathogens involved in holm oak decline on Caprera Island (Italy). For Pathol 44:191–200

    Article  Google Scholar 

  • Lynch SC, Eskalen A, Zambino PJ, Mayorquin JS, Wang DH (2013) Identification and pathogenicity of Botryosphaeriaceae species associated with coast live oak (Quercus agrifolia) decline in southern California. Mycologia 105:125–140

    Article  CAS  PubMed  Google Scholar 

  • Mehl JWM, Slippers B, Roux J, Wingfield MJ (2011) Botryosphaeriaceae associated with Pterocarpus angolensis (kiaat) in South Africa. Mycologia 103:534–553

    Article  Google Scholar 

  • Mohali SR, Slippers B, Wingfield MJ (2009) Pathogenicity of seven species of the Botryosphaeriaceae on eucalyptus clones in Venezuela. Australas Plant Pathol 38:135–140

    Article  Google Scholar 

  • Palmer B, Lockett C, Dhileepan K (2012) Acacia nilotica subsp. indica (Benth.) Brenan—prickly acacia. In: Julien M, McFadyen R, Cullen J (eds) Biological control of weeds in Australia. CSIRO Publishing, Melbourne, pp 18–28

    Google Scholar 

  • Paul ND, Ayres PG (1986) Interference between healthy and rusted groundsel (Senecio-vulgaris L.) within mixed populations of different densities and proportions. New Phytol 104:257–269

    Article  Google Scholar 

  • Petrini O, Fisher PJ (1988) A comparative study of fungal endophytes in xylem and whole stem of Pinus sylvestris and Fagus sylvatica. Trans Br Mycol Soc 91:233–238

    Article  Google Scholar 

  • Raghavendra AKH, Bissett AB, Thrall PH, Morin L, Steinrucken TV, Galea VJ, Goulter KC, van Klinken RD (2017) Characterisation of above-ground endophytic and soil fungal communities associated with dieback-affected and healthy plants in five exotic invasive species. Fungal Ecol 26:114–124

    Article  Google Scholar 

  • Rodrigues AL, Pinho DB, Lisboa DO, Nascimento RJ, Pereira OL, Alfenas AC, Furtado GQ (2014) Colletotrichum theobromicola causes defoliation, stem girdling and death of mini-cuttings of eucalyptus in Brazil. Trop Plant Pathol 39:326–330

    Article  Google Scholar 

  • Sacdalan A, Galea V, Goulter K, Elliot L, Klinken RDv (2012) Preliminary investigations of the Mimosa pigra dieback phenomenon. In: Proceedings of 18th Australasian weeds conference, Melbourne, Victoria, Australia, 8–11 October 2012, Melbourne, Australia. pp 356–360

  • Salomon Ballina-Gomez H, Iriarte-Vivar S, Orellana R, Santiago LS (2010) Compensatory growth responses to defoliation and light availability in two native Mexican woody plant species. J Trop Ecol 26:163–171

    Article  Google Scholar 

  • Slippers B, Wingfield MJ (2007) Botryosphaeriaceae as endophytes and latent pathogens of woody plants: diversity, ecology and impact. Fungal Biol Rev 21:90–106

    Article  Google Scholar 

  • Smith H, Wingfield MJ, Petrini O (1996) Botryosphaeria dothidea endophytic in Eucalyptus grandis and Eucalyptus nitens in South Africa. For Ecol Manag 89:189–195

    Article  Google Scholar 

  • Steinrucken TV, Aghighi S, Hardy GESJ, Bissett A, Powell JR, van Klinken RD (2017a) First report of oomycetes associated with the invasive tree Parkinsonia aculeata Australas (Family: Fabaceae). Plant Pathol 46:313–321

    Google Scholar 

  • Steinrucken TV, Raghavendra AKH, Powell JR, Bissett A, Van Klinken RD (2017b) Triggering dieback in an invasive plant: endophyte diversity and pathogenicity. Australas Plant Pathol 46:157–170

    Article  CAS  Google Scholar 

  • Tennakoon KMS, Ridgway HJ, Jaspers MV, Jones EE (2018) Factors affecting Neofuscicoccum ribis infection and disease progression in blueberry. Eur J Plant Pathol 151:87–99

    CAS  Google Scholar 

  • Toh R, Galea VJ, Diplock N, van Klinken RD (2008) Evaluation of fungal isolates for potential use as mycoherbicides for seed bank reduction of Parkinsonia aculeata. In: van Klinken RD, Osten VA, Panetta FD, Scanlan JC (eds) Proceedings of the 16th Australian weeds conference, Cairns Convention Centre, North Queensland, Australia, 18–22 May, 2008. pp 284–286

  • Trakunyingcharoen T, Cheewangkoon R, To-anun C (2013) Phylogeny and pathogenicity of fungal species in the family Botryosphaeriaceae associated with mango (Mangifera indica) in Thailand. Int J Agric Technol 9:1535–1543

    Google Scholar 

  • Trakunyingcharoen T, Cheewangkoon R, To-anun C, Crous PW, van Niekerk JM, Lombard L (2014) Botryosphaeriaceae associated with diseases of mango (Mangifera indica). Australas Plant Pathol 43:425–438

    Google Scholar 

  • van Klinken RD, Campbell SD, Heard TA, McKenzie J, March N (2009) The biology of Australian weeds 54. Parkinsonia aculeata L. Plant Protect Q 24:100–117

    Google Scholar 

  • Wapshere AJ, Delfosse ES, Cullen JM (1989) Recent developments in biological control of weeds. Crop Protect 8:227–250

    Article  Google Scholar 

  • White TJ, Bruns T, Lee S, Taylor J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: PCR—protocols and applications—a laboratory manual, pp 315–322

  • Wilson CG, Pitkethley RN (1992) Botryodiplodia dieback of Mimosa pigra, a noxious weed in northern Australia. Plant Pathol 41:777–779

    Article  Google Scholar 

  • Wood AR, Ginns J (2006) A new dieback disease of Acacia cyclops in South Africa caused by Pseudolagarobasidium acaciicola sp.nov. Can J Bot 84:750–758

    Article  Google Scholar 

  • Yuan ZQ, Mohammed C (2001) Lesion development in stems of rough- and smooth-barked Eucalyptus nitens following artificial inoculations with canker fungi. For Pathol 31:149–161

    Article  Google Scholar 

  • Zhu H-Y, Tian C-M, Fan X-L (2018) Studies of Botryosphaerialean fungi associated with canker and dieback of tree hosts in Dongling Mountain of China. Phytotaxa 348:63–76

    Article  Google Scholar 

Download references

Acknowledgements

Mr. Victor Robertson, Mr. Lachlan Fowler, Dr. Mel Schneemilch and Ms. Heidi Robertson are thanked for their technical assistance. Special thanks to Mr. Allan Lisle and Dr. Syed Rizvi for their guidance during statistical analysis. Thanks to the Rockhampton Regional Council for access to a field site and to Mr Leonard Milner (Pink Lilly Station, Rockhampton) and Mr. Corbett Tritton (Silver Hills Station, Richmond) for the generous provision of access to their properties for research purposes and for kind assistance during the fieldwork. This study was funded by Australian Endeavour Postgraduate Award, Meat and Livestock Australia, BioHerbicides Australia Pty Ltd. and UniQuest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ahsanul Haque.

Additional information

Handling Editor: S. Raghu.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOC 71 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Haque, A., van Klinken, R.D., Goulter, K. et al. Assessing the potential of fungi isolated from dieback-affected trees as biological control agents for prickly acacia (Vachellia nilotica subsp. indica). BioControl 64, 197–208 (2019). https://doi.org/10.1007/s10526-018-09919-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10526-018-09919-9

Keywords

Navigation