A Rapid Technique for Identifying the Clones of Fusarium oxysporum f. sp. lycopersici Causing Crown- and Root-rot of Tomato

1975 ◽  
Vol 65 (6) ◽  
pp. 726 ◽  
Author(s):  
L. E. Sanchez
2006 ◽  
Vol 5 (2) ◽  
pp. 161-165 ◽  
Author(s):  
Khaled Hibar ◽  
Mejda Daami-Remadi . ◽  
Hayfa Jabnoun-Khiare . ◽  
Mohamed El Mahjoub .

Plant Disease ◽  
2001 ◽  
Vol 85 (7) ◽  
pp. 735-739 ◽  
Author(s):  
Y. Rekah ◽  
D. Shtienberg ◽  
J. Katan

The saltcedar shrub Tamarix nilotica grows as a weed in the Arava region of Israel. This weed is commonly found in cultivated fields naturally infested with Fusarium oxysporum f. sp. radicis-lycopersici, the causal agent of tomato crown and root rot. Young bushes, 20 to 40 cm tall, were randomly uprooted from different fields. The roots were cut into segments which were placed on Fusarium-selective medium. Although the plants did not show any symptoms of disease, the roots of the shrub were colonized by the pathogen. The incidence of infected saltcedar plants and level of root colonization by F. oxysporum f. sp. radicis-lycopersici decreased with increasing distance of the sampling location from a tomato field infected with crown and root rot. F. oxysporum f. sp. radicis-lycopersici was also isolated from chaff of inflorescence samples taken from mature T. nilotica shrubs. Identity of the pathogen isolates obtained from T. nilotica roots and chaff samples was verified by pathogenicity and vegetative compatibility tests. Roots of T. nilotica plants sown under greenhouse conditions in soil naturally infested with F. oxysporum f. sp. radicis-lycopersici became colonized by the pathogen. Uprooting and removing saltcedar plants throughout the season from fields not cultivated with tomatoes lowered the inoculum density of F. oxysporum f. sp. radicis-lycopersici in the soil from 611 to 6 and from 176 to 10 CFU/g of soil in the 1998-99 and 1999-2000 growing seasons, respectively. These results demonstrate that T. nilotica may contribute to the buildup of the pathogen populations in the absence of a susceptible host. Colonization of saltcedar by F. oxysporum f. sp. radicis-lycopersici is an additional mechanism for survival of this pathogen in the fields and for dissemination through the spread of infested seed or chaff of T. nilotica.


2013 ◽  
Vol 53 (2) ◽  
pp. 172-176 ◽  
Author(s):  
Wojciech Szczechura ◽  
Mirosława Staniaszek ◽  
Hanna Habdas

Abstract Fusarium oxysporum f. sp. radicis-lycopersici (FORL) leading to fusarium crown and root rot is one of the most destructive soilborne diseases of tomatoes occurring in greenhouse and field crops. Physiological races of FORL were not defined but nine vegetative compatibility groups (VGCs) were identified. Infection followed by wounds and natural holes and infection is not systemic. The optimum soil temperature for pathogen development is 18°C. Infection may cause plants to wilt and die completely or infection may lower fruit quality. Fusarium oxysporum f. sp. radicis-lycopersici has the ability to produce a specific enzyme, tomatinase, which breaks down α-tomatine and protects the pathogen. In contrast tomato also has a defence system which consists of the enzymes chitinase and β-1, 3-glucanase. Tomato resistance to Fusarium oxysporum f. sp. radicis-lycopersici is determined by a single dominant gene Frl, localized on the long arm of chromosome 9. It was introduced to cultivars from Licopersicum peruvianum (L.) Mill.


2015 ◽  
Vol 13 (4) ◽  
pp. e1009
Author(s):  
Ana I. Borrego-Benjumea ◽  
José M. Melero-Vara ◽  
María J. Basallote-Ureba

<p><em></em><em>Fusarium oxysporum</em> (<em>Fo</em>), <em>F. proliferatum</em> (<em>Fp</em>) and <em>F. solani</em> (<em>Fs</em>) are causal agents associated with roots of asparagus affected by crown and root rot, a disease inflicting serious losses worldwide. The propagule viability of <em>Fusarium</em> spp. was determined on substrate artificially infested with <em>Fo</em>5<em>, Fp</em>3<em> </em>or <em>Fs</em>2 isolates,<em> </em>amended with either poultry manure (PM), its pellet (PPM), or olive residue compost (ORC) and, thereafter, incubated at 30 or 35°C for different periods. Inoculum viability was significantly affected by these organic amendments (OAs) in combination with temperature and incubation period. The greatest reduction in viability of <em>Fo</em>5 and <em>Fs</em>2 occurred with PPM and loss of viability achieved was higher at 35°C than at 30ºC, and longer incubation period (45 days). However, the viability of <em>Fp</em>3 did not decrease greatly in most of the treatments, as compared to the infested and un-amended control, when incubated at 30ºC. After incubation, seedlings of asparagus `Grande´ were transplanted into pots containing substrates infested with the different species of <em>Fusarium</em>. After three months in greenhouse, symptoms severity in roots showed highly significant decreases, but <em>Fp</em>3 caused lower severity than <em>Fo</em>5 and <em>Fs</em>2. Severity reduction was particularly high at 30ºC (by 15 days incubation for <em>Fs</em>2 and by 30-45 days for <em>Fo</em>5), after PPM treatment, as well as PM-2% for <em>Fo</em>5<em> </em>and <em>Fs</em>2 incubated during 30 and 45 days at both temperatures, and with ORC (15-30 days incubation). Moreover, assessment of plants fresh weight showed significantly high increases in <em>Fo</em>5 and <em>Fs2</em>, with some rates of the three OAs tested, depending on incubation period and temperature.<br /><strong></strong></p>


HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 449D-449
Author(s):  
J.W. Scott ◽  
J.P. Jones

Lycopersicon pennellii accession LA 1277 was crossed to tomato (L. esculentum) and the F1 was backcrossed to tomato. Self-pollinated seed was saved from backcross plants and seedlings derived were inoculated with Fusarium oxysporum Schlecht f.sp. radicus-lycopersici Jarvis and Shoemaker, the causal agent of Fusarium crown and root rot (FCRR). Seed was saved from resistant plants that were self-pollinated and screened until homozygous resistance was verified five generations after the backcross. Three homozygous lines were crossed to Fla. 7547, a tomato breeding line susceptible to FCRR but resistant to Fusarium wilt races 1, 2, and 3. Subsequently, backcrosses were made to each parent and F2 seed were obtained. The three homozygous FCRR-resistant lines were also crossed to Ohio 89-1, which has a dominant gene for FCRR resistance presently being used in breeding programs. F2 seed were obtained from these crosses. These generations were inoculated with the FCRR pathogen. The resistant parents, F1, and backcross to the resistant parents were all healthy. The backcross to the susceptible parent and the F2 segregated healthy to susceptible plants in 1:1 and 3:1 ratios, respectively. Thus, the resistance from LA 1277 was inherited as a single dominant gene. This gene was different than the gene from Ohio 89-1 because susceptible segregants were detected in the F2 generation derived from the two resistant sources.


2019 ◽  
Vol 13 (1) ◽  
pp. 27-33
Author(s):  
A. Muslim ◽  
Mitsuro Hyakumachi ◽  
Koji Kageyama ◽  
Suwandi Suwandi ◽  
Rahmat Pratama

Background: Fusarium Oxysporum f.sp. Radicis-Lycopersici (FORL) caused Fusarium Crown and Root Rot of tomato (FCRR), it’s a serious constraint on tomato production and contributing to yield losses. Aims/Method: Using a rapid bioassay, Hypovirulent Binucleate Rhizoctonia (HBNR) was tested for their ability to reduce Fusarium Crown and Root Rot (FCRR) of tomato, caused by Fusarium oxysporum f.sp. radicis lycopersici (FORL). Roots of tomato seedlings growing on 2% water agar in plastic boxes were inoculated with living or dead mycelial disks of HBNR. After 24 h, the pathogen was applied at 0, 3, 6, and 9 cm away from the position of the HBNR. Results: When living HBNR was used, the treatments provided significant protection to tomato seedlings from FCRR infection at all distances tested. Tomato plants pre-inoculated with living HBNR at different times (12 h and 24 h before inoculation with the pathogen) and challenged with FORL showed significant reduction of FCRR lesion development. A significant reduction was still observed even when HBNR was inoculated simultaneously with or 12 h after inoculation of a pathogen. Seedlings treated with dead HBNR and culture filtrates also showed significantly reduced FCRR lesion development. When living HBNR were enveloped by a polycarbonate membrane filter, a significant reduction of FCRR lesion development was still observed. Conclusion: In all experiments, reduction of FCRR lesion development in seedlings treated with HBNR tended to decrease with longer distance from the inoculation point of FORL and HBNR. We developed a simple, rapid, and miniaturized bioassay for evaluating the efficacy of HBNR against FORL. The bioassays require only 12 - 18 days, which is at least 12 days less than the soil system employed by previous researchers.


Plant Disease ◽  
2001 ◽  
Vol 85 (7) ◽  
pp. 802-802 ◽  
Author(s):  
S. C. Bost

In the summer of 2000, tomato (Lycopersicon esculentum Mill.) plants in several commercial fields in southeastern and eastern Tennessee exhibited symptoms of Fusarium wilt. All cultivars on which symptoms were observed are classified as resistant to races 1 and 2 of the causal fungus, Fusarium oxysporum Schlechtend.:Fr. f. sp. lycopersici (Sacc.) W.C. Snyder and H.N. Hansen. Race 3 has been reported from several areas (1), but not from Tennessee, a major producer of fresh market tomatoes. F. oxysporum was consistently isolated from discolored vascular tissue on potato dextrose agar (PDA). Pathogenicity and race determination tests for six isolates representing three counties were conducted by inoculating cultivars susceptible to races 1, 2, and 3 (Rutgers); resistant to race 1 (Bradley, Roma VF); resistant to races 1 and 2 (Conquest, Florida 47); or resistant to races 1, 2, and 3 (Floralina). Inoculum suspensions were obtained from 1-week-old cultures grown on PDA. Seedlings were grown in commercial potting mix for 3 weeks. The roots were rinsed and submerged for 30 s in inoculum suspensions (1 × 107 conidia per ml). Seedlings were then transplanted into potting mix in metal flats and placed in a greenhouse. Natural light conditions provided a 12-h photoperiod, and day and night temperatures averaged 29 and 17°C, respectively. Within 4 weeks after inoculation, all isolates caused symptoms of Fusarium wilt in all cultivars except Floralina, indicating that the isolates were race 3. The pathogen was reisolated from the discolored vascular tissue of diseased plants. Among the cultivars most severely affected by all six isolates was Conquest, which is resistant to F. oxysporum f. sp. radicis-lycopersici, the cause of Fusarium crown and root rot. Reference: (1) M. L. Marlatt et al. Plant Dis. 80:1336, 1996.


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