Evaluation of fungal and bacterial antagonists for managing phytopathogen Fusarium moniliforme var. subglutinans Sheldon, causing Pokkah Boeng disease of sugarcane

Jump To References Section

Authors

  • Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand ,IN
  • Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand ,IN
  • Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand ,IN
  • Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand ,IN
  • Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand ,IN
  • Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand ,IN

DOI:

https://doi.org/10.18311/jbc/2017/15456

Keywords:

Bacillus sp., Fusarium sp., Pokkah boeng, Pseudomonas spp., Trichoderma spp
Biological control

Abstract

In the present investigation potential fungal and bacterial antagonists were tested under laboratory and field conditions against the phytopathogen Fusarium moniliforme var. subglutinans Sheldon, causing Pokkah Boeng disease of sugarcane. Different strains of fungal anatagonists viz; Trichoderma spp. (strains TCMS36, TCMS43, Th3, TCMS9, Th14) and bacterial antagonists viz; Pseudomonas fluorescens (strains Psf173 and Psf02) and Bacillus sp. were tested against the pathogen under in vitro conditions by employing dual culture technique and volatile assay. The results from dual culture revealed that TCMS36 showed the maximum radial growth inhibition i.e., 73.33 per cent followed by Th14 (69.01%), Psf02 (68.33%), Th3(66.04%),TCMS43 (64.7%), Bacillus sp. (63.95%) and TCMS9(63.74%). Volatile assay depicted that the maximum radial growth inhibition was found in TCMS36(70.01%) followed by TCMS9 (60.10%), Th3 (57.25%), Th14 (55.36%), Psf02 (50.83%) and Bacillus sp. (51.79%), while minimum growth inhibition was observed in Psf173 (40.49%). Further studies were conducted in field, where, Th 14, Psf02 and the consortium of both (Th 14+Psf 02) were tested through sett treatment. The minimum disease incidence was observed in the treatment where setts were treated with P. fluorescens (Psf02) followed by consortium (Th 14+Psf 02) and Th 14 i.e. 0.92%, 1.51% and 5.53%, respectively. The findings from research conclude that the fungal and bacterial antagonist strains can exert an inhibitory effect on the radial growth of Fusarium sp. as well as reduce the disease incidence in field. Application of these antagonists in field could be a better management tool without having to depend on hazardous chemicals.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Author Biography

Anshul Arya, Department of Plant Pathology, College of Agriculture, G. B. Pant University of Agriculture and Technology, Pantnagar – 263145, Uttarakhand

Plant Pathology

Downloads

Published

2018-04-06

How to Cite

Arya, A., Sharma, R., Sharma, G., Chandra Kabdwal, B., Negi, A., & Mishra, B. (2018). Evaluation of fungal and bacterial antagonists for managing phytopathogen <i>Fusarium moniliforme</i> var. <i>subglutinans</i> Sheldon, causing Pokkah Boeng disease of sugarcane. Journal of Biological Control, 31(4), 217–222. https://doi.org/10.18311/jbc/2017/15456

Issue

Section

Research Articles
Received 2017-02-09
Accepted 2018-03-01
Published 2018-04-06

 

References

Akrami M, Khiavi HK, Shikhlinski H and Khoshvaghtei H. 2012. Bio controlling two pathogens of chickpea Fusarium solani and Fusarium oxysporum by different combinations of Trichoderma harzianum, Trichoderma asperellum and Trichoderma virens under field conditions. Int J Agri Sci Res. 1(3): 41–45.

Brunner K, Peterbauer CK, Mach RL, Lorito M, Zeilinger S and Kubicek CP. 2003. The Nacetylglucosaminidase of Trichoderma atroviride is essential for chitinase induction by chitin of and major relevance to bio-control. Curr Gen. 43: 289–295. Crossref. PMid:12748812

Dal Bello GM, Mónaco CI and Cháves AR. 1997. Study of the effect of volatile metabolites of Trichoderma hamatum on the growth of phytopathogenic soil borne fungi. Rev Iberoam Micol. 14(3):131–4. PMid:17655390

Duttamajumdar SK. 2004. Bacterial diseases of sugarcane in india: a bird's eye view. In: Rao GP, Saumtally AS, Rott P, (Eds). Sugarcane pathology: bacterial and nematodes diseases, Science Publishers. pp. 15–50.

Khan MR, Khan SM and Mohiddin FA. 2004. Biological control of Fusarium wilt of chickpea through seed treatment with the commercial formulation of Trichoderma harzianum and/or Pseudomonas fluorescens. Phytopathol Mediterr. 43: 20–25.

Korsten L, De Jager ES, Paul I, Obagwu J and El-Ghaouth A. 2000. Alternative control of citrus postharvest diseases. Proc Int Soc Citriculture (in press)

Kullnig C, Mach RL, Lorito M and Kubicek CP. 2000. Enzyme diffusion from Trichoderma atroviride to Rhizoctonia solani is a prerequisite for triggering of Trichodermaech 42 gene expression before mycoparasitic contact. Appl Environ. Microbiol. 66: 2232–2234. Crossref. PMid:10788407 PMCid:PMC101480

Martin JP, Hong HL and Wismer CA. 1961. The corresponding heritability estimate for Pokkah boeng. In Sugar-cane diseases of the world. Vol. 1, Elsevier Publ. Co. New York. 542 p.

Mohamedy RSR and Alla MAA. 2013. Bio-priming seed treatment for biological control of soil borne fungi causing root rot of green bean (Phaseolus vulgaris L.). J Agri Tech. 9(3): 589–599.

Negi DS, Sharma PK and Gupta RK. 2014. Management of root-rot complex disease and assessment of plant growth promoting characters in vegetable pea with native and commercial antagonists through seed biopriming. Int J Rec Sci. 5(8): 1416–1421.

Papavizas GC. 1985. Trichoderma and Gliocladium: Biology, ecology, and potential for biocontrol. Ann Rev Phytopathol. 23: 23-54. Crossref.

Raza W, Faheem M, Yousaf S, Rajer FU and Yameen M. 2013. Volatile and non-volatile antifungal compounds produced by Trichoderma harzianum SQR-T037 suppressed the growth of Fusarium oxysporum f. sp. niveum. Sci Lett. 1(1): 21–24.

Sharfuddin C and Mohanka R. 2012. In vitro antagonism of indigenous Trichoderma isolates against phytopathogen causing wilt of lentil. Int J Life Sci Pharma Res. 2(3): 195–202.

Sivasithamparam K and Ghisalberti EL. 1998. Secondar metabolism in Trichoderma and Gliocladium, In: Kubicek CP, Harman GE, and Ondik KL (Eds). Trichoderma and Gliocladium: basic biology, taxonomy and genetics. Taylor and Francis, pp. 139–191.

Sundaramoorthy S and Balabaskar P. 2013. Trichoderma spp. against wilt of tomato caused by Fusarium oxysporum f. sp. lycopersici. J Appl Biol Biotech. 1(03): 36–40.

Vincent JM. 1947. Distortions of fungal hyphae in the presence of certain inhibitors. Phytopathology 48: 268–270. Crossref.

Vishwakarma SK, Kumar PL, Nigam A, Singh A and Kumar A. 2013. Pokkah Boeng: An emerging disease of sugarcane. J Pl Pathol Microbiol. 4(3): 1–5.

Wakker JH and Went FAF C. 1896. Overzicht van de Ziekten van het suikerriet op Java.

Zeininger S, Galhaup C, Payer K, Woo SL, Mach RL, Fekete C, Lorito M and Kubicek CP. 1999. Chitinase gene expression during mycoparasitic interaction of Trichoderma harzianum with its host. Fungal Genet Biol. 26:131–140. Crossref. PMid:10328983