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Deciphering the role of bacterial antimicrobial compounds in the Biocontrol of plant pathogenic fungi

Deciphering the role of bacterial antimicrobial compounds in the Biocontrol of plant pathogenic fungi

Introduction

Pathogen infection is one of the major causes of yield loss in agricultural and horticultural crops. The rapid increase of antimicrobial resistance in plant pathogens urged researchers to develop new fungicide molecules. Antagonistic bacteria are considered as ideal biocontrol agents due to their aggressive colonization and rapid growth in the rhizosphere. These bacteria mediate biocontrol by several mechanisms. A primary mechanism of pathogen inhibition is by the production of antimicrobial peptide compounds and other factors such as siderophore production and microbial cyanide, and lytic enzymes (O’Sullivan and O’Gara, 1992).

Antimicrobial peptides (AMP) are a diverse class of naturally occurring molecule produced as a first line of defense by the bacteria with broad spectrum of activity against plant pathogens. These are the biologically active secondary metabolite compounds that possess antimicrobial and antifungal activities. Secondary metabolites (SM) produced by certain microorganisms induce plant defense reactions leading to a systemic resistance to pathogen infection.

In recent days, AMPs are acting as an attractive alternative to traditional antibiotics due to their physicochemical properties and their wide array of activities. AMP kill the pathogenic fungi by interacting with their intracellular components. Characterization of the mode of action of AMP is essential to improve their activity and to accelerate their use as an effective antimicrobial agent.

Antimicrobial compounds are specific in killing microorganisms. They cause no harm to the environment.

Role of antimicrobial compounds produced by bacteria

Phenazines are group of aromatic heterocyclic compounds produced by Bacteria as a strategy to compete for nutrients or to improve other survival conditions (Laursen and Nielsen,2004) (Table 1). They interfere with electron flow and functional enzymes related to cellular respiration. Phenazine-1-carboxylic acid (PCA), a bright lemon-yellow pigment, was first isolated and identified from Pseudomonas aureofaciens in the 1930’s by Dr. Kluyver.

Pyrrole are the antimicrobial compounds produced during secondary metabolism in some bacteria, by the genera Pseudomonas and Burkholderia. Pyrrolnitrin was first isolated in the 1960s by Arima et al., (1964) from Pseudomonas pyrrocinia. Pyrrolnitrin inhibits fungal growth by inhibiting the respiratory electron transport system.

Siderophores are compounds of low molecular weight (around 400–2000 Da). The genus Pseudomonas produces a diverse variety of siderophores. Burkholderia genus also produces pyochelin (Meyer et al.,1995). Pyochelin (Pch) and pyoverdin (Pvd) have been most intensively studied. Siderophores regulate other virulence factors of pathogens and promote plant growth (Fedrizzi, 2006). They capture iron and make unavailable to the pathogens (Neilands, 1995). They control biofilm formation of the pathogens.

Hydrogen cyanide (HCN) is an extremely volatile compound. Its mechanism of action involves inhibition of the activity of cytochrome c oxidase, preventing production of adenosine triphosphate (ATP) (Spence et al., 2014). In addition to antimicrobial activity, this compound shows nematicidal activity. The presence of HCN together with pyrrolnitrin another antimicrobial compound, contributed to the death of the model nematode, Caenorhabditis elegans (Nandi et al. (2015).

Diacetyl phloro glucinol (2,4-DAPG) is a phenolic compound of natural origin produced mainly by the genus Pseudomonas (Meyer et al., 2009). Besides stimulating ISR (Weller et al., 2012) it stimulates exudate production by plant roots (Combes Meynet et al., 2011), becoming an important protector in disease-suppressive soils. Xylocandins or cepacidins are a complex of antifungal peptides isolated originally from Burkholderia cepacia (Bisacchi et al. 1987; Meyers et al. 1987) (Table 2).

Burkholdines are octapeptide compounds which possess antifungal activity by interfering with electron flow responsible for cellular respiration. The cyclic peptide compounds, iturins are subdivided into iturin, bacillomycin, and mycosubtilin, which cause cell leakage by forming pores in the cytoplasmic membrane.

Fengycins, which are also called plastathins, are composed of a hydroxylated fatty acid and ten amino acids, comprising fengicins A and B. The antifungal activity of fengycins is due to their ability to interact with lipid components of the fungal cytoplasmic membrane, such as ergosterol, which alter its structure and permeability in a dose-dependent manner, with an interesting application in biological control of fruit diseases (Toure et al. 2004., Ongena et al. 2005).

Surfactins are composed of a hydroxylated fatty acid and seven amino acids. These are not fungitoxic by themselves, but they express some antifungal activity in synergism with iturin A, which is essential for formation of a biofilm matrix and has surfactant properties, with the capacity to increase penetration of some substances (Deravel et al. 2014; Yanez-Mendizabal et al. 2012; Gong et al. 2014). Low concentrations of surfactin have been shown to induce several plant defense events in tobacco cells (Jourdan et al. 2009; Chowdhury et al. 2015).

A natural antimicrobial product named after Hollywood actor, Keanu Reeves is effective against fungi that cause diseases in both plants and humans, according to a study. The research, published in the Journal of the American Chemical Society, describes how the natural product group of “Keanumycins”, produced by the bacteria of the genus Pseudomonas, works against plant pests. Scientists have shown that the Keanumycins work “effectively” against the plant pest Botrytis cinerea which triggers gray mold rot and causes immense harvest losses every year. Studies have also found that the active ingredient in the Keanumycin molecules can inhibit the growth of fungi dangerous to humans like Candida albicans. This group of molecules, can act as an “environmentally friendly alternative” to chemical pesticides, and may also offer an alternative in the fight against drug-resistant fungi. The latest findings, shed more light on the mode-of-action of this potential natural product and may potentially aid the development of new pharmaceutical and agrochemical antifungals.

Table 1. Different types of antimicrobial compounds produced by bacteria

S.no

Antimicrobial compounds

Produced by Bacteria

1

Phenazines

Burkholderia, Streptomyces, Mycobacterium, and Xanthomonas (Pierson and Pierson, 2010)

2

Pyrroles

Pseudomonas and Burkholderia (Kilani and Fillinger, 2014)

3

Siderophores

Pseudomonas and Burkholderia (Scavino and Pedraza, 2013)

4

Hydrogen cyanide

Pseudomonas and Burkholderia (Fernando et al., 2005)

5

Diacetyl phloroglucinol

Pseudomonas (Meyer et al., 2009)

6

Pyrrolnitrin

Burkholderia pyrrocinia 2327 (Kwak and Shin, 2015)

7

Xylocandins

Burkholderia cepacia ATCC 39277 (Bisacchi et al., 1987; Meyers et al.,1987)

8

Burkholdines

Burkholderia ambifaria 2.2 N (Tawfik et al., 2010)

9

Occidiofungins

Burkholderia contaminans MS14 (Lu et al., 2016)

10

Cepalycin I and cepalycin II

Burkholderia cepacia JN106 (Abe and Nakazawa, 1994)

11

2-hydroxymethyl-chroman-4-one

Burkholderia cepacia (Kang et al., 2004)

12

Quinoline

Burkholderia cepacia (Moon et al., 1996)

13

Altericidins

Burkholderia contaminans (Kirinuki and Ichiba, 1986)

14

Cepaciamides

Burkholderia Cepacia D-202 (Toshima et al., 1999)

15

Syrbactin

Pseudomonas syringae pv. syringae (Amrein et al., 2004)

16

Phenylacetic Acid

Burkholderia sp. strain MP-1 (Kim et al., 2004)

17

Dichloromethane and methanol extracts

Burkholderia pyrrocinia strain RV1R2 (Silva et al., 2015)

18

Iturins

Bacillus subtilis (Shafi et al., 2017)

19

Bacillomycin

Bacillus amyloliquefaciens (Gu et al., 2017)

20

Mycosubtilin

Bacillus subtilis (Deravel et al., 2014)

21

Surfactin

Bacillus subtilis (Chowdhury et al., 2015)

Table 2. Bacterial antimicrobial compounds acting against fungi

S.no

Bacterial Antimicrobial compounds

Against fungi

Reference

1

Phenazine-1-carboxylic acid (PCA) or Shenqinmycin from Pseudomonas aureofaciens

Fusarium sp. wilt in watermelon, Phytophthora sp. blight in pepper, and sheath blight in rice

Yuan et al., 2008; Xu et al., 2015

2

Phenazine-1-carboxyamide (PCN) from Pseudomonas chlororaphis

Xanthomonas oryzae pv. oryzae, which cause Bacterial leaf blight in rice

 

Shanmugaiah et al.,2010

3

5-methyl-1-hydroxyphenazine (PYO) from Pseudomonas aeruginosa

Macrophomina phaseolina, which causes gray root rot in peanuts and soybean

Khare and Arora, 2011

4

Pyrrolnitrin from Burkholderia cepacia strain JBK9

R. solani, P. capsici, and
F. oxysporum.

Jung et al., 2018

5

Ornibactin from Burkholderia contaminans, MS14

X. citri pv. malvacearum, P. carotovorum, R. solanacearum,

P. syringae B301, Erwinia amylovora,

Escherichia coli, and Clavibacter michiganensis

Herrera, 2017

6

Cepacidin B from B. cepacia AF2001

Pythium ultimum in cucumbers and cotton plants

Lee et al., 2000

7

Bk-1229 and Bk-1097 from a culture of Burkholderia ambifaria 2.2 N

B. cinerea, A. solani, Phytophthora infestans, and Mycosphaerella fijiensis (an agent of black sigatoka disease in banana plants)

Tawfik et al., 2010

8

 

Occidiofungins from Burkholderia

A. alternata, Aspergillus fumigatus, R. solani

Lu et al., 2000

9

Cochliobolus heterostrophus, Geotrichum candidum

Wang et al., 2016

10

Quinoline derivatives from. B. cepacia PCII

P. capsici, R. solani, and F. oxysporum.

Yoshihisa et al., 1989

11

Iturin A from B. subtilis B47

R. solani, Penicillium chrysogenum, A. niger, F. oxysporum, V. dahliae

Yu et al. 2002, Gong et al.,

2006; Kim et al.,2010

12

Bacillomycin D from Bacillus subtilis AU195 and B. subtilis B-FS06

Aspergillus flavus in wheat and groundnut

Gu et al., 2017

13

Bacillomycin D produced by B. amyloliquefaciens SQR9 and B. amyloliquefaciens NJN-6

F. Oxysporum in cotton and castor

Moyne et al.,2001; Yuan et al.,2012

14

Fengycins produced by B. subtilis CPA-8

Peach rot caused by Monilinia laxa and Monilinia

fructicola

Yanez Mendizabal et al.,2012

15

Mycosubtilin from Bacillus

lettuce mildew caused by Bremia lactucae.

Deravel et al., 2014

Conclusion 

Microbial metabolism has inspired a large number of studies of bioactive compounds that can be used in biological control of plant diseases. The vast majority of natural antimicrobials come from microbial secondary metabolism, which provides benefits for the plants. These metabolites have the potential to be used in agro industry, especially in relation to pathogen control and environmental sustainability. There is a significant demand for production of new bioactive compounds that will replace the agrochemicals currently used in control of plant diseases due to increasing microbial resistance to currently used chemicals, confirming the need for development of new biological agents, from natural sources, that can be used in control of plant diseases.

Future researchable areas 

Studies on investigating new compounds from beneficial microbes against pathogenic organisms are required to develop the novel biomolecules formulation against the plant pathogens. It can be done in association with biotechnological studies by altering genome of beneficial organisms to develop more new antimicrobial compounds.

References

  • Arima, K., Imanaka, I., Kousaka, M., Fukuta, A and Tamura, G. 1964. Pyrrolnitrin, a new antibiotic substance, produced by Pseudomonas. Agricultural biology and chemistry. 28: 575–576.
  • Gong, Q., Zhang, C., Lu, F., Zhao, H., Bie, X and Lu, Z. 2014.Identification of bacillomycin D from Bacillus subtilis fmbJ and its inhibition effects against Aspergillus flavus. Food Control. 36: 8–14.
  • Kluyver, AJ. 1956. Pseudomonas aureofaciens and its pigments. Journal of Bacteriology.72: 406–411.
  • Laursen, JB and Nielsen, J. 2004. Phenazine natural products: biosynthesis, synthetic analogues, and biological activity. Chemical Reviews. 104: 1663–1685.
  • Meyer, SLF., Halbrendt, JM., Cart, LK., Skantar, AM., Liu, T., Abdelnabby, HME and Vinyard, BT. 2009.Toxicity of 2,4-diacetylphloroglucinol (DAPG) to plant parasitic and bacterial feeding nematodes. Journal of Nematology. 41:274–280.
  • Moon, SS., Kang, PM., Park, KS and Kim, CH. 1996. Plant growth promoting and fungicidal4-quinolinones from Pseudomonas cepacia. Phytochemistry. 42: 365–368.
  • Nandi, M., Selin, C., Brassinga, AKC., Belmonte, MF., Fernando, WD., Loewen, PC and De Kievit, TR.2015. Pyrrolnitrin and hydrogen cyanide production by Pseudomonas chlororaphis strain PA23 exhibits nematicidal and repellent activity against Caenorhabditis elegans. Public library of science. 31: 298-310.
  • Neilands, JB. 1995. Siderophores-structure and function of microbial iron transport compounds. Journal of biology and chemistry. 270: 26723–26726.
  • Shanmugaiah, V., Mathivanan, N and Varghese, B. 2010. Purification, crystal structure and antimicrobial activity of phenazine-1-carboxamide produced by a growth-promoting biocontrol bacterium, Pseudomonas aeruginosa MML2212. Journal of Applied of Microbiology. 108:703–711.
  • Sullivan, O and Gara, O. 1992. Traits of fluorescent Pseudomonas sp. Involved in suppression of plant root pathogens. Journal of Microbiology. 52: 78-82.
  • Weller, DM., Mavrodi, DV., Van Pelt, JA., Pieterse, CMJ., Van Loon, LC and Bakker, PAHM. 2012. Induced systemic resistance in Arabidopsis thaliana against Pseudomonas syringae pv. Tomato by 2,4-diacetylphloroglucinol-producing Pseudomonas fluorescens. Phytopathology. 102: 403–412.

Content contributors

  1. Sk. Menaaz Fathima, Department of Plant Pathology, College of Agriculture, Rajendranagar, Professor Jayashankar Telangana State Agricultural University, Hyderabad, Telangana, India.
  2. K. Sankari Meena, Indian Institute of Oilseeds Research, Hyderabad,
  3. B. Vidya Sagar, Department of Plant Pathology, College of Agriculture, Rajendranagar, Professor Jayashankar Telangana State Agricultural University, Hyderabad, Telangana, India

Last Modified : 9/7/2024



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