Halo Blight of Mungbean in Australia - Opinion - MDPI
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Opinion Halo Blight of Mungbean in Australia Araz Sedqi Abdullah *,† and Col Douglas Department of Agriculture and Fisheries, Hermitage Research Facility, Warwick 4370, Australia; col.douglas@daf.qld.gov.au * Correspondence: araz.solman@daf.qld.gov.au † Author also known as Araz Solman. Abstract: Halo blight, one of the major diseases of mungbean, is caused by the bacterium Pseudomonas savastanoi pv. phaseolicola. The pathogen infects the foliar parts of the plant, causing water-soaked spots that eventually develop surrounding yellow margins. The disease is particularly destructive under moderate temperature and high humidity, especially when it occurs during late vegetative through to early reproductive stage. In such conditions, severely infected crops could experience a yield loss up to 70%. Halo blight can be widespread on mungbeans grown in Southern Queensland and Northern New South Wales. However, due to its seedborne and cryptic nature of transmis- sion, the disease is likely to be under-reported. This report addresses major aspects of halo blight symptomology, pathology and epidemiology. Keywords: Vigna radiata; P. phaseolicola; bacterial disease; disease management 1. The Pathogen and Disease Symptoms Halo blight is a major mungbean disease caused by the foliar bacterium Pseudomonas savastanoi pv. phaseolicola. The disease was first reported in Queensland in the early 1980s and has since become a widespread constraint affecting the reliability and yield Citation: Abdullah, A.S.; Douglas, C. of mungbeans. The bacterium’s seedborne nature and broad host range contribute to Halo Blight of Mungbean in Australia. the widespread distribution of the halo blight disease. However, due to unfamiliarity Crops 2021, 1, 3–7. https://doi.org/ with disease symptoms and the possibility of mixed infections, halo blight is likely to be 10.3390/crops1010002 under-reported. Recent genomic analysis suggests the existence of several pathotypes of the causal agent of halo blight [1]. This highlights the significance of conducting annual Academic Editor: Il-Ryong Choi surveillance at a level sufficient to monitor and characterise pathogen virulences as they Received: 9 April 2021 respond to changes in host genotype and growing conditions. Virulences identified can Accepted: 13 May 2021 then be evaluated against current breeding lines and commercial varieties to inform and Published: 17 May 2021 direct future breeding activities. While halo blight can occur on seedlings early in the season, the main damage often Publisher’s Note: MDPI stays neutral occurs when the infection reaches the epidemic stage during and after flowering. Typical with regard to jurisdictional claims in symptoms of the disease initially appear as small, dark, circular spots. These eventually published maps and institutional affil- develop necrotic lesions surrounded by yellow margins (Figures 1 and 2). Advanced iations. lesions can join, giving rise to large necrotic areas scattered on both sides of the infected leaf (Figure 2B,C). Stress plants, including those exposed to waterlogging, high wind rainfall events or water stress, are more likely to show disease symptoms and suffer significant yield loss. Even stress associated with flowering may be sufficient to induce susceptibility Copyright: © 2021 by the authors. for significant halo blight disease. The disease is wind- and rain-dispersed, spreading the Licensee MDPI, Basel, Switzerland. infection to uninfected leaves and neighbouring plants throughout the crop. This article is an open access article Studies have shown that halo blight bacterium can rapidly reach high densities with- distributed under the terms and out causing visible disease symptoms [2]. This suggests that apparent lack of symptoms conditions of the Creative Commons is not indicative of a pathogen-free crop. In fact, dispersal of bacteria is likely to precede Attribution (CC BY) license (https:// symptom development, making physical movement of the pathogen within and between creativecommons.org/licenses/by/ crops less detectable. Symptoms can subsequently express following physical injury from 4.0/). Crops 2021, 1, 3–7. https://doi.org/10.3390/crops1010002 https://www.mdpi.com/journal/crops
Crops 2021, 1 4 Crops 2021, 1, FOR PEER REVIEW 2 rain and hail; these are thought to trigger a widespread pathogenic shift [2]. Therefore, rain and hail; movement of these are thought equipment throughto trigger a widespread and between pathogenic paddocks shouldshift be [2]. Therefore, carefully considered, movement of equipment through and between paddocks should be carefully as symptomless mungbeans can harbour the pathogen. Mechanical damage and physical considered, as symptomless movement maymungbeans spread thecan harbour disease the pathogen. across Mechanical the paddocks [3]. damage Growers and physical and agronomists movement may spread the disease across the paddocks [3]. Growers and agronomists should implement a ‘come clean-go clean’ approach, which has proven successful in many should implement a ‘come clean-go clean’ approach, which has proven successful in many other crops such as cotton [4]. Vehicles and machineries should be properly cleaned before other crops such as cotton [4]. Vehicles and machineries should be properly cleaned before leaving one paddock so that they arrive clean at the next paddock. leaving one paddock so that they arrive clean at the next paddock. Figure 1. Examples of mungbean leaves, cultivar Berken, showing halo blight symptoms. On the Figure 1. Examples of mungbean leaves, cultivar Berken, showing halo blight symptoms. On the cotyledons, symptoms initially appear as irregular shaped spots scattered throughout the tissue cotyledons, symptoms ((A) picture collected initially 6 days appear as irregular after inoculation). These can shaped spots join, causing scattered large, throughout the tissue irregular-shaped ((A) picture chlorotic collected lesions 6 days ((B) picture after 12 collected inoculation). These can days after inoculation). Onjoin, causingleaves, the trifoliate large,initial irregular-shaped symptomslesions chlorotic appear ((B) as regular-shaped, water-soaked picture collected 12 days circular spots surrounded after inoculation). On bythelarge chlorotic trifoliate leaves, initial margins ((C) picture collected 6 days after inoculation). These develop large necrotic lesions by symptoms appear as regular-shaped, water-soaked circular spots surrounded by large chlorotic margins ((C) picture collected 6 days after inoculation). These develop large necrotic lesions by about 12 days after inoculation (D). White arrows in A and B indicate the presence of chlorotic tissues. Black and red arrows in C and D indicate the presence of necrotic and water-soaked lesions, respectively.
Crops 2021, 1, FOR PEER REVIEW 3 about 12 days after inoculation (D). White arrows in A and B indicate the presence of chlorotic Crops 2021, 1 5 tissues. Black and red arrows in C and D indicate the presence of necrotic and water-soaked le- sions, respectively. Figure Figure 2. 2. The The ‘5Rs’ ‘5Rs’ diagnostic diagnostic scheme scheme showing showing symptom symptomprogression progressionon on aa halo halo blight blight infected infected leaf leaf (A). (A). (1) (1) Ringed Ringed with with yellow yellow margin, margin, (2) (2) rectangular rectangular shape shape lesions, lesions, (3) (3) restricted restricted by by the the leaf leaf veins, veins, (4) (4) reddish-brown reddish-brown colouration, colouration, (5) (5) rampant rampant throughout throughout the the leaf. leaf. Halo Halo blight blight symptoms symptoms on on the the upper upper (B) (B) and and lower lower (C) (C) sides sides of of the the leaf. leaf. 2.2.Pathogen PathogenSurvival Survivaland andDisease DiseaseSpread Spread The The causal agent of halo blight survives causal agent of halo blight survives thethe intercropping intercropping periods periods onon alternative alternative hosts, hosts, in infected seeds and plant debris from previous seasons. Infected seed represents in infected seeds and plant debris from previous seasons. Infected seed represents the themajor major mode mode of of survival survival andand transport transport ofof the the pathogen pathogen [3].[3]. The The pathogen pathogen can can invade invade the theplant plantthrough throughstomatal stomatal openings openings but, more but, morenotably, through notably, throughwounds and and wounds injuries cre- injuries ated by heavy rainfall and wind. The disease can be spread by created by heavy rainfall and wind. The disease can be spread by rain-splash, contactrain-splash, contact be- tween between wetwetleaves leaves andand irrigation irrigation water, water,asaswell wellasasbybypeople people andand animal animal movements movements through infested crops. Rain splash permits disease transmission, through infested crops. Rain splash permits disease transmission, especially when especially whentherethereis isa aprevailing prevailing wind that facilitates movement of the pathogen over long distances wind that facilitates movement of the pathogen over long distances (Figure 3). (Figure 3). Halo Halo blight blight flourishes flourishes ininmoderately moderatelylow lowtemperatures temperatures(18–26(18–26◦°C) with periods C) with periods ofof high high relative relative humidity (i.e., during and following heavily rainfall). The disease causes yieldyield humidity (i.e., during and following heavily rainfall). The disease causes loss loss by reducing by reducing leaf leaf areaarea available available for photosynthesis for photosynthesis [5]. Yield [5]. Yield losseslosses up toup to have 70% 70% have been been documented documented in heavily in heavily infected infected cropscrops [6]. [6].
Crops 2021, 1 6 Crops 2021, 1, FOR PEER REVIEW 4 Figure Figure 3. Schematic 3. Schematic representation representation of theof lifethe lifeof cycle cycle of Pseudomonas Pseudomonas savastanoi savastanoi pv. Phaseolicola, pv. Phaseolicola, causing causing halo halo blight blight of mung- of mungbeans. beans. 3. Management of Halo Blight 3. Management of Halo Blight Management of halo blight is difficult as there are no registered chemicals for effective Management in-crop control of halo Tolerance of the disease. blight is difficult level in as thethere seed are no such is low registered chemicals that, when for effec- conditions are tive in-crop only conducive, control oneofinfected the disease. seed Tolerance in 10,000 is level in the seed sufficient to startis low such that,[7]. an outbreak whenThiscon- ditions are conducive, only one infected seed in 10,000 is sufficient prompted many countries to undertake highly sensitive and specific testing protocols to to start an outbreak [7].the detect Thispresence prompted of many countries halo blight to undertake bacterium in seedhighly crops sensitive [8]. Crops and arespecific rejectedtesting whenpro- the bacterium is detected or observed in or near seed production sites. Currently,rejected tocols to detect the presence of halo blight bacterium in seed crops [8]. Crops are the when the Australian bacteriumAssociation Mungbean is detected requires or observed in orcrops all seed near seed to beproduction tested, based sites. onCurrently, DNA the Australian detection method, for Mungbean the presenceAssociation of the halorequires blightall seed crops bacterium to be in the tested, seed. Thisbased on DNA represents detectionstep a significant method, towardsfor the presence producing of the halo certified, haloblight blightbacterium free seed. in the seed. This testing Comprehensive represents a significant of seed crops forstep towards all the majorproducing certified, bacterial diseases halo will blight potential identify free seed.disease Comprehensive problems,test- ing of seed crops for all the major bacterial diseases will identify reducing the risk of pathogen spread. Diagnostic methods, such as those that employ potential disease DNA prob- markers, appear to be more robust in detecting bacterial pathogens such as halo blight,em- lems, reducing the risk of pathogen spread. Diagnostic methods, such as those that evenploy whenDNA markers, there appearsymptoms are no visible to be more onrobust in detecting the infected bacterial pathogens such as seeds [8,9]. halo blight, resistance Improved even whentothere halo are no has blight visible symptoms become availableon in thetheinfected last five seeds years[8,9]. through Improved variety releases resistance from National to halo blight has Mungbean become available Improvement. Opal-AU in the(released last five years 2020)through is a variety large greenreleases from National shiny-seeded mungbean Mungbean in the same Improvement. market classOpal-AUas Crystal (released 2020) is a and Jade-AU. large green Opal-AU shiny-seeded is adapted to Southern mungbean Queensland in theandsameNew market SouthclassWales as and Crystal and Jade-AU. represents the Opal-AU biggest singleisstep adapted forward to Southern in diseaseQueensland resistance for and New South mungbean. In Wales the niche andsmall represents green the biggest single shiny-seeded stepclass, market forward in disease Celera resistance2015) II-AU (released for mungbean. In the niche has good protection small from green halo blight. More details shiny-seeded on yield market andCelera class, agronomic II-AUperformance, (released 2015) disease profiles has good and marketing protection from halo of these areMore blight. provided detailsin on theyield Variety andManagement Packages at http://www.mungbean.org. agronomic performance, disease profiles and marketing au/agronomy.html of these are provided(accessedinonthe 17 May 2021). Variety Management Packages at http://www.mung- bean.org.au/agronomy.html (accessed on 17 May 2021). Author Contributions: A.S.A. conceived the idea of the paper, revised the literature and drafted the manuscript. C.D. drafted theA.S.A. Author Contributions: halo blight management conceived the idea section and provided of the paper, revised comments on and the literature the article. drafted All authors have read and agreed to the published version of the manuscript. the manuscript. C.D. drafted the halo blight management section and provided comments on the article.This Funding: Allresearch authorsreceived read andnoapproved the final external funding version other of theisarticle. than what specified in the acknowledgments.
Crops 2021, 1 7 Institutional Review Board Statement: Not applicable. Informed Consent Statement: Not applicable. Data Availability Statement: Not applicable. Acknowledgments: This paper has been developed as part of the National Mungbean Improvement Program (NMIP). The NMIP is a joint investment between the Department of Agriculture and Fisheries and Grains Research and Development Corporation aiming to improve productivity and reliability of the Australian mungbean industry. Conflicts of Interest: The authors declare no conflict of interest. References 1. Noble, T.J.; Young, A.J.; Kelly, L.A.; Barrerro, R.A.; Douglas, C.A.; Long, H.; Williams, B.; Mundree, S. Characterisation of the Pseudomonas savastanoi pv. phaseolicola population found in Eastern Australia associated with halo blight disease in Vigna radiata. Australas. Plant Pathol. 2020, 49, 515–524. [CrossRef] 2. Marques, A.S.d.A.; Samson, R. Population dynamics of Pseudomonas savastanoi pv. phaseolicola in bean, throughout the epiphytic and pathogenic phases. Pesqui. Agropecuária Bras. 2016, 51, 623–630. [CrossRef] 3. Noble, T.J.; Young, A.J.; Douglas, C.A.; Williams, B.; Mundree, S. Diagnosis and management of halo blight in Australian mungbeans: A review. Crop. Pasture Sci. 2019, 70, 195–203. [CrossRef] 4. Allen, S.; Kochman, J. Eliminating seed-borne inoculum of Fusarium oxysporum f. sp. vasinfectum in cotton. In Proceedings of the Beltwide Cotton Conference, Australian Cotton Cooperative Research Centre, Narrabri, Australia, 9–13 January 2001; pp. 139–140. 5. Bashan, Y. Mechanisms of symptom production by foliar bacterial pathogens. Phytoparasitica 1987, 15, 197–223. [CrossRef] 6. Ryley, M.; Douglas, C.; Ryan, M.; Tatnell, J.; Martin, W.; King, K.; Keller, L. Integrated management of foliar pathogens of mungbean in Australia. In Proceedings of the Australian Summer Grains Conference, Gold Coast, Queensland, Australia, 21 June 2010; pp. 1–9. 7. Taylor, J. The quantitative estimation of the infection of bean seed with Pseudomonas phaseolicola (Burkh.) Dowson. Ann. Appl. Biol. 1970, 66, 29–36. [CrossRef] 8. Rico, A.; Lopez, R.; Asensio, C.; Aizpun, M.T.; Asensio-S-Manzanera, M.C.; Murillo, J. Nontoxigenic strains of Pseudomonas syringae pv. phaseolicola are a main cause of halo blight of beans in Spain and escape current detection methods. Phytopathology 2003, 93, 1553–1559. [CrossRef] [PubMed] 9. Borowicz, B.; Maćkowiak, A.; Pospieszny, H. Improved identification of Pseudomonas savastanoi pv. phaseolicola at the molecular level. EPPO Bull. 2002, 32, 467–469. [CrossRef]
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