Abiotic Conditions on Growth of Pseudomonas fluorescens (DS17R) and Its Ability to Produce Secondary Metabolites (Including Phenazines) Against Phytophthora colocasiae, the Causal Agent of Taro Leaf Blight

Author(s):  
Sameza Modeste Lambert
2014 ◽  
Vol 140 (2) ◽  
pp. 243-250 ◽  
Author(s):  
Modeste Lambert Sameza ◽  
Marie Ampere Bedine Boat ◽  
Séverin Tchameni Nguemezi ◽  
Lile Christere Nguemnang Mabou ◽  
Pierre Michel Jazet Dongmo ◽  
...  

Author(s):  
Zhang Hong ◽  
Kalhoro Muhammad Talib ◽  
Kalhoro Ghulam Mujtaba ◽  
Hou Dabin ◽  
Faqir Yahya ◽  
...  

Abstract Background Taro leaf blight, caused by a severely destructive oomycete fungus Phytophthora colocasiae, is responsible for threatening yield loss worldwide. The pathogen has the ability to germinate and spread rapidly to other plants during favorable conditions resulting in acute decline and even death, causing 100% crop loss. Farmers usually rely on highly toxic systemic fungicides to control the disease, which is effective, but residual effects and resistance of these agrochemicals is still a concern. Recently as returning to nature people tend to use chemical-free products, especially edible stuff produced in organic agriculture. Therefore, the use of bio-pesticides and phytochemicals is gaining special attention by scientists as they are ecofriendly non-hazardous, sustainable, and potent alternatives to control many virulent plant pathogens The present research was conducted to assess the antifungal potential of cinnamon essential oils against P. colocasiae. Materials and methods The essential oils from cinnamon bark were extracted using microwave-assisted hydrodistillation equipment, and then their chemical constituents were evaluated using ATR FTIR spectroscopy. The antifungal potential of essential oil was assessed against mycelium, sporangia, zoospore, leaf necrosis, and corms lesions under laboratory conditions at, 0.156, 0.312, 0.625, 1.25, 2.5, 5.0 mg/mL concentrations. Hymexazol was used as positive control and no essential oil as negative control, while each treatment have three replications and experiment repeated twice. Results The main component of oil was identified as cinnamaldehyde. The pathogen isolated from infected taro leaves was identified as P.colocasiae and then was used as a test fungus in the current study. Repeated experiments show maximum inhibition percentage of mycelial growth, zoospore germination, and sporulation of the fungus were observed at 0.625 mg/mL, whereas leaf necrosis was 100% inhibited at 1.25 mg/mL concentration. Conclusion This research can be a reference for easy, cost-effective and environment-friendly management and control of taro leaf blight with phytochemicals and plant essential oil derivatives. Graphic abstract


2014 ◽  
Vol 43 (1) ◽  
pp. 21-35 ◽  
Author(s):  
Vishnu Sukumari Nath ◽  
Vinayaka Mahabaleswar Hegde ◽  
Muthulekshmi Lajapathy Jeeva ◽  
Raj Shekar Misra ◽  
Syamala Swayamvaran Veena ◽  
...  

2017 ◽  
Vol 25 (30) ◽  
pp. 29929-29935 ◽  
Author(s):  
Séverin Nguemezi Tchameni ◽  
Staelle Njamou Mbiakeu ◽  
Modeste Lambert Sameza ◽  
Pierre Michel Dongmo Jazet ◽  
François Tchoumbougnang

Author(s):  
Manju Evelyn Bi ◽  
Ache Neh Teke ◽  
Suh Christopher ◽  
Mbong Grace Annih ◽  
Fokunang Charles

Globally the taro leaf blight (Phytophthora colocasiae) disease causes between 50 to 70% yield loss. Four taro landraces were planted in three agroecological zones of Cameroon; the Western Highlands (Bambui), Mono-Modal Humid Forest (Ekona), and the Bimodal Humid Forest (Nkolbisson) and evaluated for taro blight severity in four successive growing seasons in March and July, 2018 and 2019. Different concentrations of copper oxide (600 g)–Metalaxyl (120 g) fungicide were applied to control taro blight before and during plant growth. Results showed that, in all the field sites, the disease severity of Phytophthora colocasiae greatly decreased below 1.5 with varying concentrations of copper oxide (600 g)–Metalaxyl (120 g) fungicide applied at two-week intervals. The control field at Ekona recorded the highest taro blight severity of 7.8. There was no significant difference in taro blight severity (P≤0.05) between landraces treated with the different concentrations of copper oxide (600 g)–Metalaxyl (120 g) fungicide. Therefore, lower concentrations (0.33% and 0.27%) of copper oxide (600 g)–Metalaxyl (120 g) can be effectively used in the pre and post control of taro blight in the field. All the landraces in the screen house experiments were susceptible to P. colocasiae.   In all the zones, Landrace L2 (red petiole small leaves) was highly resistant to P. colocasiae and should be recommended to farmers for optimum taro production in the three agro-ecological zones and zones with similar characteristics.


Plant Disease ◽  
2008 ◽  
Vol 92 (1) ◽  
pp. 126-131 ◽  
Author(s):  
F. E. Brooks

Taro leaf blight disease, caused by Phytophthora colocasiae, is a major limiting factor in taro production worldwide. P. colocasiae is an aerial pathogen similar to P. infestans, causal agent of potato late blight disease, but occurs in warmer climates. In the year-round subsistence cropping systems of the Pacific Islands, resistant cultivars are essential. Breeding lines from Southeast Asia and Oceania were tested in American Samoa for resistance to taro leaf blight using a detached-leaf bioassay and field trials. Mean lesion diameters from bioassays were highly correlated with field estimates of the number of healthy leaves per plant and yield (corm weight). However, the bioassay did not adequately assess infection efficiency. Additional experiments revealed that attached leaves had smaller lesion diameters than detached leaves incubated in closed containers, but both were very highly correlated. Taro resistance increased with plant age and the second-oldest leaf was more resistant than the third-oldest leaf. The bioassay was a fast, space-saving, effective method of screening taro lines for post-penetration resistance to P. colocasiae. It also provided an easily standardized method of evaluating host–pathogen interactions under controlled conditions.


2013 ◽  
pp. 104-112 ◽  
Author(s):  
S. C. Miyasaka ◽  
K. Lamour ◽  
M. Shintaku ◽  
S. Shrestha ◽  
J. Uchida

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