Microbial assembly and association network in watermelon rhizosphere after soil fumigation for Fusarium wilt control

2021 ◽  
Vol 312 ◽  
pp. 107336
Author(s):  
An-Hui Ge ◽  
Zhi-Huai Liang ◽  
Ji-Ling Xiao ◽  
Yi Zhang ◽  
Qing Zeng ◽  
...  
2004 ◽  
Vol 103 (1) ◽  
pp. 9-17 ◽  
Author(s):  
A. Miguel ◽  
J.V. Maroto ◽  
A. San Bautista ◽  
C. Baixauli ◽  
V. Cebolla ◽  
...  

2014 ◽  
Vol 104 (12) ◽  
pp. 1314-1321 ◽  
Author(s):  
Tian Tian ◽  
Shi-Dong Li ◽  
Man-Hong Sun

Soil fumigation and biological control are two control measures frequently used against soilborne diseases. In this study, the chemical fumigant dazomet was applied in combination with the biocontrol agent (BCA) Clonostachys rosea 67-1 to combat cucumber wilt caused by Fusarium oxysporum f. sp. cucumerinum KW2-1. When the mycoparasite C. rosea 67-1 was applied after dazomet fumigation, disease control reached 100%, compared with 88.1 and 69.8% for dazomet and 67-1 agent, respectively, applied alone, indicating a synergistic effect of dazomet and C. rosea in combating cucumber Fusarium wilt based on analysis of Bliss Independence. To understand the synergistic mechanism, the effects of chemical fumigation on the colonization potential and activity of F. oxysporum f. sp. cucumerinum, and the interaction between the BCA and the pathogen were investigated. The results showed that growth of the pathogen decreased with increasing dazomet concentration subsequent to fumigation. When exposed to dazomet at 100 ppm, the fungal sporulation rate decreased by 94.4%. Severe damage was observed in fumigated isolates using scanning electron microscopy. In the greenhouse, disease incidence of cucumber caused by fumigated F. oxysporum f. sp. cucumerinum significantly decreased. Whereas germination of C. rosea 67-1 spores increased by >sixfold in fumigated soil, and its ability to parasitize fumigated F. oxysporum f. sp. cucumerinum significantly increased (P = 0.014).


HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 821C-821
Author(s):  
Timothy J Ng ◽  
James G. Kantzes

Twenty-five melon (Cucumis melo L.) cultigens were screened for resistance to fusarium wilt in a field infested with race 1 and race 2 of Fusarium oxysporum f.sp. melonis in 1993 and 1994. Plants were grown on clear plastic mulch using commercial production recommendations. The soil was fumigated with methyl isothiocyanate at a broadcast rate of 340 liters·ha–1 in 1993, and with dichloropropene at a broadcast rate of 136 liters·ha–1 in 1994. Resistance was determined by the percentage of plants surviving 8 weeks after transplanting. In general, highly resistant cultigens (>90% survival) and highly susceptible cultigens (<20% survival) performed consistently in the two experiments. However, differences in performance between the two years were noted for cultigens with intermediate resistance, and their performance may have contributed to the significant cultigen × year interaction in this study.


Plant Disease ◽  
1999 ◽  
Vol 83 (11) ◽  
pp. 1073-1073 ◽  
Author(s):  
G. Magnano di San Lio ◽  
S. O. Cacciola ◽  
A. Pane

Muskmelon (Cucumis melo L.) is very important economically to agriculture in Italy. The Sicily area accounts for ≈40% of the total muskmelon production. Fusarium wilt caused by Fusarium oxysporum f. sp. melonis (Leach & Currence) W.C. Snyder & H.N. Hans. is the most prevalent and damaging disease of muskmelon in Sicily. Use of cultivars with major resistance genes, Fom 1 and Fom 2, is the most effective control measure for combating the disease. During March 1999, severe infections of Fusarium wilt were noted in a commercial muskmelon crop, cv. Firmo F1, grown in plastic tunnels in Syracuse Province (eastern Sicily). The muskmelon seedlings had been transplanted into the tunnels during January 20 days after soil fumigation with methyl bromide. Firmo F1 possesses both Fom 1 and Fom 2 genes. Of 18,000 Firmo F1 plants, ≈6,500 showed symptoms consisting of stunting, vein clearing; leaf yellowing, wilting, and dying; brown necrotic streak; and gummy exudates on the basal portion of vines. A pinkish white mold developed on dead tissues when infected plants were kept at high relative humidity. The pathogenicity of both a single-conidium isolate of F. oxysporum f. sp. melonis from a symptomatic Firmo F1 plant and two isolates of races 0 and 1, recovered previously from other cultivars in Sicily and used as references, was tested with three differential muskmelon cultivars, Charentais T, Doublon, and CM 17187 (1), as well as three commercial cultivars, Ramon, Cassella, and Geamar (possessing Fom 1, Fom 2, and both Fom 1 and Fom 2 resistance genes, respectively). Muskmelon seedlings were inoculated by the root-dip method (3), using a suspension of 5 × 105 conidia per ml. Inoculated seedlings were transplanted to plastic pots filled with sterilized soil and placed in a greenhouse (25 to 30°C). Symptoms were scored 7 to 10 days after inoculation. The isolate from Firmo F1 was pathogenic to all cultivars tested, the race 0 isolate was pathogenic only to cv. Charentais T, and the race 1 isolate was pathogenic only to cvs. Charentais T, Doublon, and Ramon. F. oxysporum was reisolated from symptomatic plants. Based on its pathogenicity and symptomology, the isolate from Firmo F1 was classified as race 1,2y (yellows), according to the nomenclature proposed by Risser et al. (1). Race 1,2 poses a serious threat to muskmelon production in Sicily, because all currently used cultivars are susceptible to the race, and other control measures, such as preplant soil fumigation with methyl bromide and solarization, are not as effective as use of resistant cultivars. Further study is needed to establish which is the prevalent race of F. oxysporum f. sp. melonis in Sicily. This report confirms that race 1,2 occurs in all major muskmelon-production areas in Italy (2). References: (1) G. Risser et al. Phytopathology 66:1105, 1976. (2) G. Tamietti et al. Petria 4:103, 1994. (3) F. L. Wellman. Phytopathology 29:945, 1939.


1993 ◽  
Vol 42 (6) ◽  
pp. 858-864 ◽  
Author(s):  
R. GONZALEZ-TORRES ◽  
J. M. MELÉRO-VARA ◽  
J. GÓMEZ-VÁZQUEZ ◽  
R. M. JIMÉNEZ DÍAZ

Sign in / Sign up

Export Citation Format

Share Document