The Farmers Cry: Impact of Heat Stress on Fusarium oxysporum f. sp. dianthi, Interaction with Fungicides
Archetypal fungal resistance is marked by deform macroscopic growth on artificial medium supplemented with fungicides and the overexpression of resistance proteins weaponries at the molecular level. The interaction of Fusarium oxysporum f.sp. dianthi. with fungicides viz., copper oxychloride, metalaxyl-mancozeb and, mancozeb under heat-stress condition was studied. We evidence the pathogen interrelatedness to elude combine heat and fungicides stress is chiefly governed by the differential over expression of a 22.9 kDa Resistant Heat Shock Protein (RHSP) and a 26.3 kDa housekeeping protein (HKP). Of the assayed fungicides, resistant protein suppression was a function of temperature rise acting as a positive variance for copper oxychloride; and as a negative variance for mancozeb and metalaxyl-mancozeb. This first report suggests predicting field temperature prior to application of fungicide of choice is keyed to avert resistance resurgence. We infer within the context of global warming, the interaction of F. oxysporum f.sp. dianthi with fungicides inherently fluctuates and lends credence for the expression of adaptive RHSP responsible for its resiliency, a predicament for the farmers cry.
Received: November 20, 2011;
Accepted: December 10, 2011;
Published: March 20, 2012
Fusarium wilts, caused by soilborne Fusarium oxysporum f.sp.
dianthi. (Prill. and Delacr.) W.C. Snyder and H.N. Hans, is the most
calamitous phytopathogen for tuberous crops (Agrios, 1988).
In India alone, 80-100% yield loss is associated with the F. oxysporum species
(Anjani et al., 2004). Tubers incessantly deteriorate
in store-house once the pathogen gain access to host even after pretreatment
with agrochemicals. Performing fungicides in the field harbours carbamate and
phenylamide derivatives as active ingredient notably for mancozeb and metalaxyl,
respectively. Despite the harmful effects of fungicides such as resistance and
cross-resistance within fungi, insects and weeds population (FRAC,
2009), fungicides form the scaffold strategy for extensive seed treatment
(Khanzada et al., 2002), while the used of some
bacterial isolates to control F. oxysporum f.sp. radicis-lycopersici
(Kerkeni et al., 2008) and F. oxysporum
f.sp. psidii (Srivastava et al., 2011)
proved to be effective.
Pioneer post genomics sequencing and comparative genomics studies revealed
pathogenicity mobility on Fusarium chromosomes (Ma
et al., 2010), providing substantial clue that Fusarium spp.
can adapt to weird conditions. Unquestionably, profiling resistance protein
weaponries under chronic stress conditions provide invaluable insight on F.
oxysporum f.sp. dianthi. inherent adaptability to key fungicides
and global warming trend. Reports on fungicides efficiency on F. oxysporum
strains (Amini and Sidovich, 2010; Taskeen-Un-Nisa
et al., 2011) focuses on variability in antifungal potential and
sensitivity. The lack of information how the pathogen proteome changes and pilot
adaptation to global heat-stress trends has hoodwinked farmers on the choice
of fungicides considering the global heating scenario. Given the commercialization
of registered metalaxyl-mancozeb blend (MAGNET® 8/64%w/w, RPC
AgroIndustries, India), we hypothesize its molecular effectiveness to halt resistant
proteins expression to be superior over mancozeb (INDOFIL Chemicals®,
India, 75%WP) and inorganic copper oxychloride (INDOFIL Chemicals®
India, 75%WP) in the context of global warming. This study was conducted to
analyse the expression of adaptive proteins in the virulent isolate F. oxysporum
f.sp. dianthi. obtained from sampling S. tuberosum L. farms in
India (West Bengal, Burdwan region) under combined heat- and fungicide- stress.
MATERIALS AND METHODS
Between June 2010 to December-2010, Fusarium isolates were recovered from infected potato (Solanum tuberosum L.) tubers on Yeast Extract Agar Peptone (YEAP) medium amended with 0.75 mg L-1 chloramphenicol and 0.25 mg L-1 ampicillin, within the state of West Bengal-India, Burdwan District. Subsequent to pathogenicity test on healthy tubers, the most virulent strain was identified by the Division of Plant Pathology-IARI, New Dehli (Ref. No. 3095/2010) and commercialized registered copper oxychloride, mancozeb and metalaxyl-mancozeb were assayed. Fifty millilitre sterile Liquid Potato Sucrose Medium (LPSM) were inoculated with 5 mm diameter mycelium plug in 100 mL Erlenmyer flask. Each fungicide concentration per flask were maintained at 10 and 50 mg kg-1 and incubated at 39 and 24°C, respectively for a photoperiod of 16/8 h day and night for 5 days with occasional shaking.
A second lot of controls: (1) Positive control void of fungicide but heat stress at 39°C and 2) negative control void of fungicide and heat stress in LPSM were cultured as mentioned above. Homogeneous fresh mycelium growth were harvested with a triple-fold cheesecloth and air-dried for 10 min on Whatmann paper N°1. One gram of each sample was crushed in a pre-chilled mortar and pestle, containing 0.1 g silica gel-G (Merck), 10 mg SDS (sodium dedocylsulphate) and 100 mM, Tris-HCl pH 7.2 buffer system [containing 0.1% β-mercaptoethanol, 0.1% ascorbic acid and 0.1% cysteine-HCl and 2 mM PMSF (phenylmethylsulphonylfluoride)]. Crushed samples were vortexed at 10,000 rpm/10 min/4°C and supernatants precipitated with 30% tricarboxylic acid. Pelleted samples were triple washed using 98.8% acetone and aliquots stored in 100 mM, Tris-HCl pH 7.2 buffer containing 2 mM PMSF at -20°C.
Proteome change analysis by SDS-PAGE was done as follows: Protein concentrations
were determined by the standard Bradford (1976) method
using Biorad® bovine serum albumin for calibration. All protein
samples were profiled on a 15% polyacrylamide gel (Merck) (Lemmli,
1970) at constant voltage for approximately 6 h. The gels were stained using
50% methanol and 7% glacial acetic acid, 0.2% Coomassie Blue R250 overnight.
The gels were destained in two steps: first with 50% methanol, 7% acetic acid
for 1 to 2 h and completed with 7% methanol and 7% acetic acid. The gels were
analyzed using Bangalore-genie precision molecular weight markers and photographed
using the ST4 Quantum Biogel documentation system. The experiment was carried
out in quadruplet and choice profile is represented.
Fungicides antifungal potential were evaluated using the food poison technique
(Grover and Moore, 1962) on YEAP at 24°C and percentage
radial growth inhibition were calculated for triplicates using Pandey
et al. (1982) method. Data were analyzed using Statistical Package
for Social Science (SPSS) 17.0 for the determination of mean and significant
differences. One way ANOVA and Tukeys test for estimation of smallest
significant difference (p = 0.05) were applied.
Mancozeb (M) exhibited a 100% radial growth inhibition at 500 mg kg-1,
while the maximum of metalaxyl-mancozeb (MM) and copper oxychloride (Ce) stood
at 58.77 and 76.01%, respectively at 500 mg kg-1. Hence, metalaxyl-mancozeb
blend emerged less active at 24°C compared to mancozeb as depicted in Fig.
1a and b.
Figure 2a and b depicts the impact of heat
stress on F. oxysporum f.sp. dianthi. interaction with fungicides.
It shows a differential expression pattern manifested by the overexpression
of a 26.3 kDa housekeeping protein (HKP) at all stress conditions. Amongst assayed
fungicides, metalaxyl-mancozeb blend at 24°C/50 mg kg-1 considerably
deactivated the expression of the 26.3 kDa HKP but induced a 56.7 kDa resistant
protein Fig. 2a (lane 2). Moreover, none of the fungicides
at 24°C/50 mg kg-1 suppressed the constitutively expressed 128.6
kDa protein (Fig. 2a; lane 2, 3, 4). No major inducible protein
was observed with mancozeb (lane 3) at 24°C/50 mg kg-1 but also
failed to suppress the 26.3 kDa HKP. The pathogen reacted violently with copper
oxychloride at 24°C/50 mg kg-1 (Fig. 2a, lane
4) leading to the induction of a 77.4 kDa resistant protein. On the other hand,
Fig. 2b (lane 2 and 4) revealed heat-stress single-handedly
suppressed resistance proteins encoders except the 22.9 kDa RHSP encoder.
||(a) Antifungal potentials of fungicides against F. oxysporum
f.sp. dianthi. Ce: copper oxychloride, M: Mancozeb, MM: Metalaxyl-mancozeb.
Significant inhibition at 500 mg kg-1; where no significant difference
exist at p = 0.05 (5%) according to Tukeys test. (b): Radial growth
inhibition after 5 days, 24°C at 500 mg kg-1. A: Mancozeb
(M), B: Metalaxyl-mancozeb (MM), C: Copper oxychloride (Ce), D: Control,
no fungicide and heat-stress
||(a) Lane 1 and 6-Control at 24°C, fungicide free. Lane
2-MM at 50 mg kg-1. Lane 3-M at 50 mg kg-1. Lane 4-Ce
at 50 mg kg-1. Lane 5 and 10-Molecular weight marker. All 50
mg kg-1 were cultured at 24°C in LPSM. Lane 7-MM at 10 mg
kg-1. Lane 8-M at 10 mg kg-1. Lane 9-Ce at 10 mg kg-1.
All 10 mg kg-1 were cultured at 39°C in LPSM. (b): Lane 1-Molecular
weight marker. Lane 2 and 4-heat stress (39°C), fungicide free. Lane
3-Heat stress free and fungicide free
However, the pathogen at 24°C-fungicide-free proliferated abundantly by
producing an array of proteins with major ones being 77.2, 69.9, 64.8, 56, 49.8,
45.9, 30.1, 26.3, 22.9, 18.2 and 17.7 kDa as depicted in Fig.
2b (lane 3).
Despite the huge application of fungicides, S. tuberosum L. is enticed
to low yield in some regions even when the crop escape foliar damages mediated
by the early and late blight diseases due to the presence of soil-borne Fusarium
spp. Its been proposed coupling abiotic inducers to pathogen elicitors is
a better as alternative to fungicides (Alkahtani et al.,
2011). In this study we described the first report evidencing that F.
oxysporum f.sp. dianthi. can effectively eludes carbamates, phenylamides
and, the blend of the two derive fungicide while responding to heat-stress using
principally a 22.9 kDa RHSP.
The present analysis shows more proteins are suppressed by copper oxychloride
at 39°C/10 mg kg-1 than at 24°C/50 mg kg-1 vis-à-vis
mancozeb and metalaxyl-mancozeb blend at same concentration. Implying, the pathogen
sensitivity under heat-stress decreases for mancozeb and metalaxyl-mancozeb
blend than copper oxychloride. Following, FRAC (2009)
reports, phenylamides (or metalaxyl) targets RNA polymerase I and show resistance
and cross resistance to the Oomycetes. This may imply inability of phenylamides
to halt de novo synthesis of rRNA in F. oxysporum f.sp. dianthi.
and also its structural determinant role in protein synthesis is blended with
mancozeb; inferring either resistance or antagonism occurs with a rise in temperature.
Furthermore, FRAC (2009) reported carbamates such as
mancozeb targets β-tubulin engaged in mitosis; but also exhibit resistance
in many fungal species. Gel profile illustrates expression of resistance proteins
expression manifested by overexpression of the 22.9 kDa RHSP and 26.3 kDa HKP
with respect to metalaxyl-mancozeb and mancozeb (Fig. 2a).
Mandal and Sinha (1992) reported copper chloride, ferric
chlorides, manganese sulfate, were efficient in controlling Fusarium oxysporum
f.sp. lycopersici. in accordance with our studies with copper oxychloride.
The inability for phenylamides and carbamates derivatives to suppress the
26.3 kDa HKP and the 22.9 kDa RHSP indicates with the current scenario of global
warming, farmers may experience further poor yield if the sequel reliance on
these fungicides are maintained vis-à-vis the ubiquitous nature of F.
oxysporum f.sp. dianthi. in the soil if field temperature is not
The low antifungal potential of metalaxyl-mancozeb blend at 24°C/500 mg kg-1 indicate some degree of antagonism exist blending metalaxyl and mancozeb with regard to F. oxysporum f.sp. dianthi. Contrary to this inhibitory result; lane 2 (Fig. 2a) indicates many proteins were suppressed by the blended fungicide at 24°C/500 mg kg-1; explicitly, inhibitory potential should be higher. This divergence may probably be due to suppression of genes not directly linked to the pathogen vital metabolic processes. Moreover, the induction of the 56.8 kDa resistant protein by this blend, could explain the ambiguity observed. Mancozeb possess manganese and zinc in its structure and copper oxychloride contain copper, indicative transitional metal fungicides under heat-stress may enhance the pathogen vulnerability.
Indubitably, F. oxysporum f.sp. dianthi. thermotolerance poses severe threat to tuberous crop production as global temperature increases. Overcoming field resistance and understanding adaptive strategies depends chiefly on how we probe into pathogens interaction with fungicides under heat stress conditions. Temporarily, while relying on fungicides for the time being, a keen prediction of the field temperature will serve as an indicator for the choice of fungicides with respect to the targeted predominant pathogen for a purposeful antifungal activity optimization. The simplicity of copper oxychloride, cost effectiveness, efficiency makes it suitable for controlling F. oxysporum f.sp. dianthi. under heat stress conditions; irrevocably, lends credence for curbing the farmers cry.
This research was funded by the Third World Academy of Sciences (TWAS), Trieste-Italy and the Department of Biotechnology (DBT), New Dehli, India in program FR number: 3240223450. We thank the Division of Plant Pathology-IARI, New Dehli for identifying the pathogen.
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