Termite–gut-associated actinomycetes as biological control agents against phytopathogen Pyrrhoderma noxium
Cherrihan Adra A , Harrchun Panchalingam A and D. İpek Kurtböke A *A School of Science, Technology and Engineering, University of the Sunshine Coast (UniSC), Maroochydore BC, Qld 4558, Australia.
Cherrihan Adra is one of the UniSC graduates with first class Honours. She also holds a BSc in the Science Program where she majored in Chemistry and minored in Microbiology. She is now continuing with this research by conducting her PhD with Dr İpek Kurtböke relating to the application of actinomycetes as biological control agents through investigating their bioactive secondary metabolites. |
Harrchun Panchalingam has recently completed his PhD under Dr Kurtböke’s supervision. He is an international student from Sri Lanka and holds BSc from Monash University Malaysia and MSc from University of Peradeniya, Sri Lanka. His PhD project involved assessment of Trichoderma and actinomycetes spp. to control Pyrrhoderma noxium infections of heritage fig trees in Brisbane. Currently he is working as research assistant at (UniSC). His research interests are biological control of plant diseases, development of biofertilizers and bioremediation of hydrocarbons. |
Dr D. İpek Kurtböke is currently a senior lecturer at the University of the Sunshine Coast (UniSC) in Australia conducting research in applied, industrial and environmental microbiology. She is an internationally reputed actinomycetologist and she has been in the field of biodiscovery since 1982 conducting research into discovery of novel and potent therapeutic compounds produced by actinomycetes in Turkey, Italy, the UK, and Australia with leading pharmaceutical companies. She has been an Executive Board member of the World Federation of Culture Collections (WFCC) since 2000, currently serving her second term as the President of the Federation. She is also one of the members of the International Committee on Taxonomy of Viruses (ICTV)’s, Bacterial Viruses Subcommittee. She has editorial duties in different journals including Marine Drugs, Diversity and Frontiers Marine Science/Marine Biotechnology. |
Microbiology Australia 43(4) 190-193 https://doi.org/10.1071/MA22052
Submitted: 6 October 2022 Accepted: 19 October 2022 Published: 7 December 2022
© 2022 The Author(s) (or their employer(s)). Published by CSIRO Publishing on behalf of the ASM. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)
Abstract
Brown root-rot disease is caused by phytopathogenic white-rot basidiomycete fungus, Pyyrhoderma noxium. Currently, it is causing significant issues for the Brisbane hinterland in Queensland, Australia and killing many tree species throughout the greater Metropolitan area, including park and street trees located in Shorncliffe, Taringa, New Farm, Eagle Farm, West End, Hamilton, Indooroopilly, Brisbane River, and the City Centre. Brisbane trees being attacked are figs, poinciana, jacarandas, Chinese elms, Moreton Bay eucalypts, kauris, and hoop pines and these include both public and privately owned trees. A joint study between the University of the Sunshine Coast (UniSC) and the Brisbane City Council (BCC) aimed to assess the efficacy of different biological control agents to control infections in the region. In a substudy presented here, termite gut-associated actinomycetes were evaluated to determine their antifungal abilities against the pathogen.
Keywords: actinomycetes, antifungal agents, biological control, fermentation, microbial metabolism, Pyrrhoderma noxium, Streptomyces spp., termite guts.
References
[1] Zhou, LW et al.. (2018) Taxonomy and phylogeny of Pyrrhoderma: a redefinition, the segregation of Fulvoderma, gen. nov., and identifying four new species. Mycologia 110, 872–889.| Taxonomy and phylogeny of Pyrrhoderma: a redefinition, the segregation of Fulvoderma, gen. nov., and identifying four new species.Crossref | GoogleScholarGoogle Scholar |
[2] Tsang, KSW et al.. (2020) A preliminary examination of the bacterial, archaeal, and fungal rhizosphere microbiome in healthy and Phellinus noxius-infected trees. MicrobiologyOpen 9, e1115.
| A preliminary examination of the bacterial, archaeal, and fungal rhizosphere microbiome in healthy and Phellinus noxius-infected trees.Crossref | GoogleScholarGoogle Scholar |
[3] Wu, ZC et al.. (2020) Soil is not a reservoir for Phellinus noxius. Phytopathology 110, 362–369.
| Soil is not a reservoir for Phellinus noxius.Crossref | GoogleScholarGoogle Scholar |
[4] Hsiao, WW et al.. (2019) The pathogenicity of basidiospores of Phellinus noxius which causes brown root rot disease in Taiwan. Taiwania 64, 189–194.
| The pathogenicity of basidiospores of Phellinus noxius which causes brown root rot disease in Taiwan.Crossref | GoogleScholarGoogle Scholar |
[5] Sahashi, N et al.. (2012) Brown root rot of trees caused by Phellinus noxius in the Ryukyu Islands, subtropical areas of Japan. For Pathol 42, 353–361.
| Brown root rot of trees caused by Phellinus noxius in the Ryukyu Islands, subtropical areas of Japan.Crossref | GoogleScholarGoogle Scholar |
[6] Hodges, CS and Tenorio, JA (1984) Root disease of Delonix regia and associated tree species in the Mariana Islands caused by Phellinus noxius. Plant Dis 68, 334–336.
| Root disease of Delonix regia and associated tree species in the Mariana Islands caused by Phellinus noxius.Crossref | GoogleScholarGoogle Scholar |
[7] Farid, AM et al.. (2009) Pathogenicity of Rigidoporus microporus and Phellinus noxius against four major plantation tree species in peninsular Malaysia. J Trop For Sci 21, 289–298.
[8] Schwarze, FW et al.. (2012) Evaluation of an antagonistic Trichoderma strain for reducing the rate of wood decomposition by the white rot fungus Phellinus noxius. Biol Control 61, 160–168.
| Evaluation of an antagonistic Trichoderma strain for reducing the rate of wood decomposition by the white rot fungus Phellinus noxius.Crossref | GoogleScholarGoogle Scholar |
[9] Ashiglar SM et al. (2015) Aggressive root pathogen Phellinus noxius and implications for western Pacific Islands. In Proceedings of the 62nd Annual Western International Forest Disease Work Conference (Murray M, Palacios P, comps), 8–12 September 2014, Cedar City, UT, USA. pp. 79–81.
[10] Gray P (2017) Brown root rot Phellinus noxius. pp. 1–7. https://www.northerntreecare.com.au/wp-content/uploads/2021/09/Brown-Root-Rot.pdf
[11] Dann K et al. (2011) Phellinus noxius: a basidiomycete fungus impacting productivity of Australian avocados. In 7th World Avocado Congress.
[12] Bolland, L (1984) Phellinus noxius: cause of a significant root-rot in Queensland hoop pine plantations. Aust For 47, 2–10.
| Phellinus noxius: cause of a significant root-rot in Queensland hoop pine plantations.Crossref | GoogleScholarGoogle Scholar |
[13] Ribera, J et al.. (2016) In-vitro evaluation of antagonistic Trichoderma strains for eradicating Phellinus noxius in colonised wood. J Trop For Sci 28, 457–468.
[14] Bose R et al. (2022) Biological control of forest pathogens: success stories and challenges. In Trends of Applied Microbiology for Sustainable Economy. pp. 155–184. Elsevier.
[15] Yang, Y et al.. (2019) Antagonistic activity and mechanism of an isolated Streptomyces corchorusii stain AUH-1 against phytopathogenic fungi. World J Microbiol Biotechnol 35, 145.
| Antagonistic activity and mechanism of an isolated Streptomyces corchorusii stain AUH-1 against phytopathogenic fungi.Crossref | GoogleScholarGoogle Scholar |
[16] Wu, W et al.. (2022) Isolation and identification of symbiotic actinomycetes from termites in hainan and their activity against tropical plants pathogenic fungi. Chin J Trop Crops 43, 1240–1247.
| Isolation and identification of symbiotic actinomycetes from termites in hainan and their activity against tropical plants pathogenic fungi.Crossref | GoogleScholarGoogle Scholar |
[17] Selim, MSM et al.. (2021) Secondary metabolites and biodiversity of actinomycetes. J Genet Eng Biotechnol 19, 72.
| Secondary metabolites and biodiversity of actinomycetes.Crossref | GoogleScholarGoogle Scholar |
[18] Matsui, T et al.. (2012) Antibiotics production by an actinomycete isolated from the termite gut. J Basic Microbiol 52, 731–735.
| Antibiotics production by an actinomycete isolated from the termite gut.Crossref | GoogleScholarGoogle Scholar |
[19] Krishanti, N et al.. (2018) Antimicrobial production by an actinomycetes isolated from the termite nest. J Trop Life Sci 8, 279–288.
| Antimicrobial production by an actinomycetes isolated from the termite nest.Crossref | GoogleScholarGoogle Scholar |
[20] Sujada, N et al.. (2014) Termite nests as an abundant source of cultivable actinobacteria for biotechnological purposes. Microbes Environ 29, 211–219.
| Termite nests as an abundant source of cultivable actinobacteria for biotechnological purposes.Crossref | GoogleScholarGoogle Scholar |
[21] Khucharoenphaisan, K et al.. (2012) Isolation and identification of actinomycetes from termite’s gut against human pathogen. Asian J Anim Vet Adv 7, 68–73.
| Isolation and identification of actinomycetes from termite’s gut against human pathogen.Crossref | GoogleScholarGoogle Scholar |
[22] Gomes, EdB et al.. (2018) Actinomycetes bioactive compounds: biological control of fungi and phytopathogenic insect. Afr J Biotechnol 17, 552–559.
| Actinomycetes bioactive compounds: biological control of fungi and phytopathogenic insect.Crossref | GoogleScholarGoogle Scholar |
[23] Kurtböke, DI and French, JRJ (2007) Use of phage battery to investigate the actinofloral layers of termite gut microflora. J Appl Microbiol 103, 722–734.
| Use of phage battery to investigate the actinofloral layers of termite gut microflora.Crossref | GoogleScholarGoogle Scholar |
[24] Kurtböke, DI and French, JRJ (2008) Actinobacterial resources from termite guts for regional bioindustries. Microbiol Aust 29, 42–44.
| Actinobacterial resources from termite guts for regional bioindustries.Crossref | GoogleScholarGoogle Scholar |
[25] English, AL et al.. (2017) Evaluation of fermentation conditions triggering increased antibacterial activity from a near-shore marine intertidal environment-associated Streptomyces species. Synth Syst Biotechnol 2, 28–38.
| Evaluation of fermentation conditions triggering increased antibacterial activity from a near-shore marine intertidal environment-associated Streptomyces species.Crossref | GoogleScholarGoogle Scholar |
[26] Panchalingam, H et al.. (2022) Assessing the various antagonistic mechanisms of Trichoderma strains against the brown root rot pathogen Pyrrhoderma noxium infecting heritage fig trees. J Fungi 8, 1105.
| Assessing the various antagonistic mechanisms of Trichoderma strains against the brown root rot pathogen Pyrrhoderma noxium infecting heritage fig trees.Crossref | GoogleScholarGoogle Scholar |