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Number of results: 10
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Abstract

In Cameroon, oil palm ( Elaeis guineensis Jacq.) is of economic importance. However, it is affected by vascular wilt presumed to be caused by Fusarium oxysporum f. sp. elaeidis (FOE). Accurate species identification requires molecular-based comparisons. The aim of this work was to molecularly identify Fusarium species associated with diseased oil palms and to determine the pathogenicity of selected isolates. Fungal samples of diseased palms were collected from the canopies and the soil of five oil palm estates of the Cameroon Development Corporation and characterized by sequencing and comparing the translation elongation factor 1a gene. The results revealed the presence of FOE from approximately 80% of the isolates. Cameroonian isolate within FOE clade 1 exhibited the greatest variability grouping with isolates from Suriname, Brazil and Democratic Republic of Congo. Other isolates found in FOE clade 2 formed a unique group which was comprised solely of isolates originating from Cameroon. Twenty-two isolates were chosen for pathogenicity tests. After a short time, 14 isolates were found to be pathogenic to oil palm seedlings. This study revealed the pathogenicity of FOE isolates from Cameroon and demonstrated that FOE in Africa is more diverse than previously reported, including a lineage not previously observed outside of Cameroon. Comparisons between all isolates will ultimately aid to devise appropriate control mechanisms and better pathogen detection methods.
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Authors and Affiliations

Rosemary Tonjock Kinge
1
ORCID: ORCID
Lilian Moforcha Zemenjuh
2
Evelyn Manju Bi
3
Godswill Ntsomboh-Ntsefong
4
Grace Mbong Annih
5
Eneke Esoeyang Tambe Bechem
2

  1. Department of Plant Sciences, Faculty of Science, University of Bamenda, Bamenda, Northwest Region, Cameroon
  2. Department of Plant Science, Faculty of Science, University of Buea, Buea, Southwest Region, Cameroon
  3. Department of Crop Production Technology, College of Technology, University of Bamenda, Bamenda, Northwest Region, Cameroon
  4. Department of Plant Biology, Faculty of Science, University of Yaounde 1, Yaounde, Center Region, Cameroon
  5. Department of Plant Biology, Faculty of Science, University of Dschang, Dschang, West Region, Cameroon
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Abstract

The effect of crude extracts of neem (Azadirachta indica) leaf, neem seed and garlic (Allium sativum) at concentrations ranging from 5% to 30% of the material in 100 ml of Potato Dextrose Agar on mycelial growth of Fusarium oxysporum f. sp. lycopersici was assessed. All the extracts inhibited mycellial growth at various levels. Dry neem seed extract gavel 100% inhibition of mycelial growth. Fresh neem leaf extract reduced mycelial growth with increasing concentration while in garlic there were no differences in growth inhibition among the various concentrations used. However garlic extracts decreased sporulation with increasing concentration and cultures grown on extract amended agar plates remained viable.

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Authors and Affiliations

Ogechi N. Agbenin
P.S. Marley
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Abstract

The objective of this study was to evaluate the antagonistic activity of Trichoderma spp. against wild pathogen Fusarium oxysporum F.28.1A, which causes wilt disease on sesame. Twenty-six isolates of Trichoderma spp. isolated from soil samples were tested to control F. oxysporum F.28.1A. Prescreening showed that five isolates were T-02B1, T-18B2, T-20B1, T-28B1, and T-29A1, based on the lowest values of colony radius of F. oxysporum F.28.1A. The selected isolates were identified by their ITS region as T. yunnanense T-02B1, T. lentiforme T-18B2, T. asperellum T-20B1, T. hamatum T-28B1, and T. hamatum T-29A1, with similarities around 96–100%. The isolates selected were able to produce enzymes including chitinase, exo-β-1,3-glucanase, and endo-β-1,3-glucanase at levels of 0.34–0.44, 0.017–0.034, and 0.032–0.121 UI · ml –1, respectively, which were considered to be a mechanism to prevent the growth of F. oxysporum F.28.1A. The isolates tested were applied in soil pots to prevent damage from F. oxysporum F.28.1A as a following experiment. The greenhouse experiment was arranged in a completely randomized design with 10 treatments, including a negative control, application of only F. oxysporum F.28.1A, application of both F. oxysporum F.28.1A and fungicide chemicals, application of both F. oxysporum F.28.1A and Trichoderma spp. DHCT, application of T. yunnanense T-02B1, application of T. lentiforme T-18B2, application of T. asperellum T-20B1, application of T. hamatum T-28B1, application of T. hamatum T-29A1 and a mixture of the five selected isolates of Trichoderma spp. with their total population equal to that in individual strain application. The results showed that the five mixed isolates of Trichoderma had a synergistic effect on the reduction of the disease’s prevalence by 35% compared to the negative control treatment.
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Authors and Affiliations

Nguyen Quoc Khuong
1
Cao Thi Thuy Trang
1
Do Thi Xuan
2
Le Thanh Quang
2
Tran Ngoc Huu
1
Ly Ngoc Thanh Xuan
3
Jun-Ichi Sakagami
4
Le Vinh Thuc
1

  1. Faculty of Crop Science, College of Agriculture, Can Tho University, Viet Nam
  2. Biotechnology Research and Development Institute, Can Tho University, Viet Nam
  3. Experimental and Practical Area, An Giang University – Vietnam National University, Ho Chi Minh City, Viet Nam
  4. Tropical Crop Science Laboratory, Faculty of Agriculture, Kagoshima University, Japan
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Abstract

Fusarium wilt is one of the most severe diseases of chickpea in the major growing areas of chickpea production in western Iran. To identify Fusarium spp. associated with chickpea plants showing symptoms of yellowing and wilting, 58 chickpea fields were sampled and 106 Fusarium spp. isolates were obtained from six different regions of Kermanshah Province in western Iran during 2018 and 2019 crop seasons. Thirty-six isolates obtained from stem or lower stem tissues were selected for pathogenicity, morphological and molecular identification using polymease chain reaction species-specific primers. Eleven isolates of Fusarium spp. were selected for sequence analyzing the translation elongation factor 1-α (EF-1α), and β-tubulin gene regions. Phylogenetic analysis of concatenated DNA sequences of both gene regions of these isolates plus other taxa revealed that 11 Fusarium spp. isolates were clustered into five distinct groups. Based on the results of morphological and molecular identification five Fusarium species were identified. Pathogenicity tests showed that F. oxysporum f. sp. ciceris and F. redolens isolates had the highest disease incidence on JG–62 and Bivenij cvs. and F. hostae, F. equiseti and F. acuminatum isolates had the lowest disease incidence. No sign of vascular discoloration was observed in longitudinal or transverse sections of chickpea plants affected by F. redolens isolates. Instead, brown to black necrosis was observed on the surface of tap-roots and crowns. No correlation was found between geographical distribution and pathogenicity of isolates. This is the first report of morphological, molecular and pathogenicity characteristics of F. redolens and F. hostae isolated from chickpea stems or lower stems in Iran.
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Authors and Affiliations

Hassan Younesi
1
ORCID: ORCID
Mostafa Darvishnia
1
ORCID: ORCID
Eidi Bazgir
1
ORCID: ORCID
Khosrow Chehri
2
ORCID: ORCID

  1. Department of Plant Protection, College of Agriculture and Natural Resources, Lorestan University, Khorramabad, Iran
  2. Department of Biology, Faculty of Sciences, Razi University, Kermanshah, Iran
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Abstract

Electrolyzed fertilizer solution (EFS) was produced by passing an irrigation solution through an electrolization chamber in order to suppress fungal disease caused by Fusarium oxysporum f. sp. cubense race 4 (Foc4) infecting banana plantlets. In the laboratory, EFS was prepared by electrolyzing solutions containing different amounts of potassium chloride and potassium nitrate. The results indicated a significant reduction in the conidial densities of Foc4 which was from 10 6 spores · ml –1 to a maximum of 10 1.3 spores · ml –1 and depended on the concentration of components in the input flow. Eventually the EFS produced from the lowest one was chosen to treat banana plantlets. Greenhouse experiments gave contradictory results of inoculated plantlets irrigated with or without EFS. The untreated banana plantlets virtually showed symptoms of infection such as discoloration of cross-cut corms, rapid wilting and dying within 60 days, while the treated ones kept their shapes and grew normally. The drastic fall in the microbial population in the rhizosphere of treated plants confirmed the activity of oxidation agents which is the major mechanism of disease suppression. The results suggest that further studies of EFS in the field as a potential technique in fighting Panama wilt in the banana industry are necessary.
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Authors and Affiliations

Vu Anh Nguyen
1
ORCID: ORCID
Ha Van Nguyen
2
Phai Duy Do
3
Hung Ngoc Tran
4

  1. Department of Environmental Physico-Chemistry, Institute of Environmental Technology, Vietnam Academy of Science and Technology, Hanoi, Viet Nam
  2. Department of Technology Application and Transfer, Institute of Environmental Technology, Vietnam Academy of Science and Technology, Hanoi, Viet Nam
  3. Central Analytical Laboratory, Soils and Fertilizers Research Institute, Hanoi, Viet Nam
  4. Department of Biotechnology, Fruit and Vegetable Research Institute, Hanoi, Viet Nam
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Abstract

A survey was conducted in February of 2004 on the outbreak of stem rot and wilt disease of pepper at the Kitabawa/Danzakara and Ajiwa irrigation sites in Northern Nigeria. Laboratory investigations revealed that it was elicited by Phytophthora capsici Leon. The disease caused severe loss in yield and USD 1 700.00 to USD 3 200.00 loss in revenue/ha. The disease was probably further aggravated by the presence of Fusarium sp. as well as ecto- and endoparasitic nematodes. Reasons for outbreak were elucidated and solutions proffered.

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Authors and Affiliations

Matthew Alegbejo
Abdulahi Lawal
Paul Chindo
Olalekan Banwo
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Abstract

Three plant extracts viz. bulbs of Allium sativum L. (Liliaceae), seeds of Annona squamosa L. (Annonaceae) and leaves of Vitex negundo L. (Verbenaceae) were evaluated against cowpea wilt pathogen, Fusarium oxysporum f. sp. ciceris by mycelial dry weight method under laboratory condtions. The mean mycelium dry weights of F. oxysporum of methanol and benzene extracts of A. sativum obtained from 125 g of crused dry plant material (bulbs) were 0.0113 and 0.0174 mg, respectively. This was followed by methanol and petroleum ether extracts of A. squamosa (0.2396 and 0.2381 mg). They effectively controlled mycelial growth of cowpea wilt pathogen, however V. negundo extracts did not cause any significant mycelium growth inhibition when compared to other plant extracts tested. Among the three plant extracts, methanol extracts of A. sativum bulbs could possibly be used for controlling F. oxysporum.

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Authors and Affiliations

Kitherian Sahayaraj
Sathasivam Karthick Raja Namasivayam
Jesu Alexander Francis Borgio
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Abstract

Spectroscopy has become one of the most used non-invasive methods to detect plant diseases before symptoms are visible. In this study it was possible to characterize the spectral variation in leaves of Solanum lycopersicum L. infected with Fusarium oxysporum during the incubation period. It was also possible to identify the relevant specific wavelengths in the range of 380–1000 nm that can be used as spectral signatures for the detection and discrimination of vascular wilt in S. lycopersicum. It was observed that inoculated tomato plants increased their reflectance in the visible range (Vis) and decreased slowly in the near infrared range (NIR) measured during incubation, showing marked differences with plants subjected to water stress in the Vis/NIR. Additionally, three ranges were found in the spectrum related to infection by F. oxysporum (510–520 nm, 650–670 nm, 700–750 nm). Linear discriminant models on spectral reflectance data were able to differentiate between tomato varieties inoculated with F. oxysporum from healthy ones with accuracies higher than 70% 9 days after inoculation. The results showed the potential of reflectance spectroscopy to discriminate plants inoculated with F. oxysporum from healthy ones as well as those subjected to water stress in the incubation period of the disease.

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Authors and Affiliations

Juan Carlos Marín Ortiz
Lilliana María Hoyos Carvajal
Veronica Botero Fernandez
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Abstract

Essential oils from four plants , i.e. geranium, rosa, lemon and mint were tested for their activity in vitro and in vivo against Rhizoctonia solani and Fusarium oxysporum f. sp. phaseoli, the cause of root rot and wilt of beans. In vitro, they were found to have an inhibitory effect against the mycelial growth of R. solani and F. oxysporum f. sp. phaseoli. Complete inhibition in fungal growth was observed at a concentration of 4% of each essential oil and Topsin M at 400 ppm as well. In greenhouse the four essential oils were tested as seed coating and/or foliar spray. Results of seed coating at a concentration of 1% clearly demonstrate a good protection of emerged bean seeds against invasion of R. solani and F. oxysporum f. sp. phaseoli compared with the fungicide treatment. A similar trend was observed in a lower extent when the essential oils were applied as bean seeds coating followed by seedlings foliar spray under field conditions. Obvious yield increase as bean green pods, in all treatments, was significantly higher than in the control.

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Authors and Affiliations

Nehal S. El-Mougy
Nadia G. El-Gamal
Mokhtar M. Abdel-Kader
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Abstract

This paper presents a preliminary report of Fusarium wilt of Roselle in the Nigerian savanna. Soil and plant samples were collected from eight experimental plots where plants showed Roselle wilt symptoms. Samples were analyzed for the presence of nematodes and wilt pathogens. The wilt causative organism Fusarium oxysporum was isolated together with nematodes of different genera. However, nematodes of the genus Helicotylenchus, Scutellonema and Hoplolaimus appeared to occur in higher densities than the others.

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Authors and Affiliations

Ogechi N. Agbenin
M.O. Ogunlana

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